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t<br />

Cent re for<br />

Ecology & Hydrology<br />

N AT U RAL ENV I RO N M ENT RES EA RC H C O U N C I L


PLANTATT<br />

<strong>Attributes</strong> <strong>of</strong> <strong>British</strong> <strong>and</strong> <strong>Irish</strong> <strong>Plants</strong>:<br />

Status, Size, Life History,<br />

Geography <strong>and</strong> Habitats<br />

for use in connection with the<br />

New atlas <strong>of</strong> the <strong>British</strong> <strong>and</strong> <strong>Irish</strong> fl ora<br />

M. 0 . Hill, C. D. Preston & D. B. Roy<br />

Biological Records Centre<br />

NERC Centre for Ecology <strong>and</strong> Hydrology<br />

Centre tor Et ctotry entl Hydrology<br />

Bush Es te:e<br />

Penicuik<br />

Midlottna t<br />

6 326 OAS<br />

2004<br />

10 0 0 (T 4 - 2 0 0 1


@ NERC Copyright 2004<br />

Print ed in 2004 by Raven Marketing Group, Cambridgeshire<br />

ISBN I 870393 74 0<br />

The Cent re for Ecology <strong>and</strong> Hydrology (CEH) is one <strong>of</strong> t he Cent res <strong>and</strong> Surveys <strong>of</strong> the<br />

Nat ural <strong>Environment</strong> <strong>Research</strong> Council (NERC). Established in 1994, CEH is a mult idisciplinary,<br />

environmental research organisat ion wit h some 600 staf <strong>and</strong> well-equipped<br />

laboratories <strong>and</strong> fi eld facilities at nine sites t hroughout t he Unit ed Kingdom. CEH's<br />

mission is to "advance t he science <strong>of</strong> ecology, environmental microbiology <strong>and</strong> hydrology<br />

t hrough high quality <strong>and</strong> internationally recognised research leading to bett er<br />

underst<strong>and</strong>ing <strong>and</strong> quant ifi cat ion <strong>of</strong> the physical, chemical <strong>and</strong> biological processes relating<br />

to l<strong>and</strong> <strong>and</strong> freshwat er <strong>and</strong> living organisms wit hin t hese environments".<br />

The Biological Records Cent re is operated by CEH, based at CEH Monks Wood. BRC is<br />

joint ly funded by CEH <strong>and</strong> t he Joint Nature Conservation Committ ee (www.jncc.gov.uk),<br />

t he latter act ing on behalf <strong>of</strong> the statutory nat ure conservation agencies in Engl<strong>and</strong>,<br />

Scotl<strong>and</strong>,Wales <strong>and</strong> Nort hern Irel<strong>and</strong>. CEH <strong>and</strong> JNCC support BRC as an important<br />

component <strong>of</strong> t he developing National Biodiversity Network. BRC seeks to help<br />

nat uralists <strong>and</strong> research biologists to co-ordinate t heir eff ort s in studying the occurrence<br />

<strong>of</strong> plant s <strong>and</strong> animals in Britain <strong>and</strong> Irel<strong>and</strong>, <strong>and</strong> to make t he results <strong>of</strong> these st udies<br />

available to others.<br />

For furt her informat ion, visit www.ceh.ac.uk.<br />

Cover photograph shows the endemic plant Coincya wright ii on the cliffs <strong>of</strong> Lundy (courtesy <strong>of</strong><br />

Roger Key, English Nature).<br />

Published by<br />

Cent re for Ecology & Hydrology<br />

Monks Wood<br />

Abbot s Ripton<br />

Hunt ingdon<br />

Cambridgeshire<br />

PE28 2LS<br />

Copies can be ordered by writing to the above address or by telephoning<br />

0 1487 772400, or faxing 0 1487 772558.


CON TEN TS<br />

Int roduction<br />

Species, fam ilies, stat us <strong>and</strong> change 3<br />

Species <strong>and</strong> families . 3<br />

Native/afi en status . 3<br />

Conservation status . . . 3<br />

Rarity status . 3<br />

Change Index . 4<br />

Size <strong>and</strong> life history at tributes . . .<br />

Height <strong>and</strong> length .<br />

Perennation . 5<br />

Life form . . . . . 5<br />

Woodiness<br />

Clonality<br />

Geographic attributes<br />

European <strong>and</strong> wider distributions, <strong>and</strong> continentality . . 9<br />

Native distribution <strong>of</strong> species alien in Britain <strong>and</strong> Irel<strong>and</strong> . . . 10<br />

Counts <strong>of</strong> 10-km squares in the New Atlas . 10<br />

Climatic means 11<br />

H abitat att ributes . . . . . 12<br />

Coastal species . 12<br />

Broad Habitats . 12<br />

Ellenberg's indicator values . 14<br />

Light values (L) . 14<br />

Moisture values (F) . 15<br />

Reaction (R) . 16<br />

Nitrogen (N) . . . 16<br />

Sak tolerance (S) . . 17<br />

Listing <strong>of</strong> species with their attributes 18<br />

A ppendix 6 1<br />

Sources for plant height . . 6 1<br />

Defi nition <strong>of</strong> life forms . 6 1<br />

Examples <strong>of</strong> how fi fe-form criteria are applied . . 62<br />

Links between life forms <strong>and</strong> plant height . 63<br />

Clonality . 64<br />

Broad Habitats . 64<br />

Initial calculation <strong>of</strong> species' preferences for Broad Habitats . 68<br />

Extension <strong>and</strong> validation <strong>of</strong> species' preferences . 69<br />

Acknowledgem ent s 70<br />

Bibliography 7 1


IN TR OD UCTI ON<br />

In the course <strong>of</strong> our research on geographical distributions <strong>and</strong> climate change, we have<br />

frequent ly wanted to characterize the plants t hat const itute the wild fl ora <strong>of</strong> Britain <strong>and</strong> Irel<strong>and</strong>.<br />

Several sources <strong>of</strong> information were available, including t he Electronic Comparative Plant Ecology<br />

(Hodgson et al., 1994), t he Czech clonal plant database Clop la I (http.//www.butbn.cas.ce kfi mes/<br />

clopla I .htm), t he BSBI database (http://www.bsbi.org.uk/html/database.html), t he Ec<strong>of</strong>lora database<br />

(Fitter & Peat, 1994), <strong>and</strong> the indicator values <strong>of</strong> Ellenberg (Ellenberg et S., 1991). Inevitably, these<br />

sources were not sufi cient for our purposes, <strong>and</strong> we have gradually assembled our own set <strong>of</strong><br />

att ribute data, linked to t he database <strong>of</strong> the Biological Records Centre (BRC).<br />

The establishment <strong>of</strong> the National Biodiversity Network (NBN) provided an additional st imulus<br />

to the assembling <strong>of</strong> att ribute data, <strong>of</strong> ering a suitable platform for online searches for species<br />

att ributes. Some <strong>of</strong> the information published here is also available from the NBN gateway<br />

(www.searchnbn.net). In 2002, the publicat ion <strong>of</strong> the New Atlas <strong>of</strong> the <strong>British</strong> <strong>and</strong> <strong>Irish</strong> Flora (Preston,<br />

Pearman & Dines, 2002), toget her with results <strong>of</strong> a companion project to analyse change<br />

(Preston,Telfer et aL, 2002), allowed us to complete the dataset that is presented here.<br />

The dataset is partly old <strong>and</strong> partly new (Table 1). Biogeographic elements <strong>and</strong> Ellenberg values<br />

are taken with few modifi cat ions from earlier publications (Preston & Hill, 1997, 1999; Hill et<br />

1999). Information that depends directly on the New Atlas is either new or (Change Index) is<br />

taken from the text <strong>of</strong> the New Atlas. Data on t he Broad Habitats <strong>of</strong> plants are mostly drawn<br />

from an unpublished report (Preston et al., 2003). Information on plant height, perennat ion, life<br />

form <strong>and</strong> clonal growt h was assembled from a variety <strong>of</strong> fl oras <strong>and</strong> monographs, with some<br />

personal observation; it is a new compilat ion. Furt her details <strong>of</strong> t hese att ributes are provided in<br />

t he following pages. The attribute categories are tabulated (Tables 2- 13), with the numbe <strong>of</strong> taxa<br />

in each category listed in the column 'N='.


Table I . <strong>Attributes</strong>, codes <strong>and</strong> names listed as columns in PLA NTATT<br />

Colum n nam e<br />

(a) Status <strong>and</strong> taxonomic<br />

Taxon name<br />

Family<br />

Nat ive status<br />

Conservation status<br />

Rarity status<br />

Change Index<br />

(b) Size <strong>and</strong> life form<br />

Height (terrest rial)<br />

Length (aquatic)<br />

Perennation<br />

Life form<br />

Woodiness<br />

Clonal spread<br />

(c) Geography & climate<br />

Major Biome (European<br />

dist ribut ion)<br />

Eastern limit code<br />

Continentality in Europe<br />

O rigin <strong>of</strong> alien taxa<br />

Number <strong>of</strong> 10-km squares in<br />

Britain (including Isle <strong>of</strong> Man)<br />

Number. <strong>of</strong> 10-km squares in<br />

Irel<strong>and</strong><br />

Number <strong>of</strong> 10-km squares in<br />

Channel Isl<strong>and</strong>s<br />

January mean terhperature<br />

July mean temperature<br />

Annual precipitat ion<br />

(d) Habitat<br />

Coastal<br />

Broad Habitats<br />

Ellenberg indicator value<br />

A bbreviat<br />

ion<br />

Fam<br />

NS<br />

CS<br />

RS<br />

Chg<br />

Hght<br />

Len<br />

P I , P2<br />

LF1, LF2<br />

Clonel ,<br />

Clone2<br />

E I<br />

E2<br />

O rigin<br />

GB<br />

IR<br />

CI<br />

Tjan<br />

Tjul<br />

Prec<br />

Co<br />

Br Habitats<br />

Source or ot her comment<br />

Name in current flora (Stace, 1997)<br />

Stace (1997)<br />

New Atlas (Preston et al., 2002)<br />

Chefi ngs (2004)<br />

Calculated from New Atlas data<br />

New Atias (Preston et al., 2002)<br />

Several sources, listed below<br />

Several sources, listed below<br />

Mainly Clapham,Tutin & Warburg (1962)<br />

Clapham et al. ( 1962), heavily revised<br />

Mainly Clapham et al. ( 1962)<br />

Sources are listed below; clone2 is mainly blank<br />

Part <strong>of</strong> biogeographic element<br />

accor ding to Preston & Hill ( 1997)<br />

Part <strong>of</strong> biogeographic element<br />

according to Preston & Hill ( 1997)<br />

Preston & Hill ( 1997) plus additions<br />

New Atlas (Preston et al., 2002)<br />

New Atlas (Preston et al., 2002)<br />

New Atlas (Preston et al., 2002)<br />

New Atlas (Preston et al., 2002)<br />

Calculated from New Atlas plus climat ic data<br />

Calculat ed from New Atlas plus climat ic data<br />

Calculat ed from New Atlas plus climat ic data<br />

Calculated from New Atlas plus Ellenberg salt value<br />

Preston et al. (2003), plus previously unreported data<br />

for aliens<br />

L, F, R, N, S Hill et aL ( 1999)


SPE CIES, FAMILIES, S TA TUS A ND CHAN GE<br />

Species <strong>and</strong> families<br />

The list <strong>of</strong> 1885 taxa includes all nat ive <strong>British</strong> <strong>and</strong> <strong>Irish</strong> species, as well as natives <strong>of</strong> the Channel<br />

Isl<strong>and</strong>s not known from Britain or Irel<strong>and</strong>. There are no species restricted to the Isle <strong>of</strong> Man. All<br />

archaeophyt e species are included, plus a number <strong>of</strong> well-established neophytes.A small number<br />

<strong>of</strong> subspecies, hybrids <strong>and</strong> aggregate species are also included. The number <strong>of</strong> taxa has been<br />

slightly increased from the 1791 t hat were listed for Ellenberg indicator values (Hill et al., 1999).<br />

Most <strong>of</strong> t he addit ions are <strong>of</strong> neophytes, which, following the New Atlas (Preston et al., 2002), we<br />

now t hink t o be suffi cient ly common or potent ially interest ing to be included.<br />

The names <strong>of</strong> families have been abbreviated to four letters <strong>and</strong> follow Stace ( 1997).<br />

Native/alien status<br />

Species <strong>of</strong> uncertain stat us are classified as 'nat ive or alien'. Int roduced species have been<br />

classifi ed as archaeophytes, neophytes <strong>and</strong> casuals (Preston et al., 2002). Bot h archaeophytes <strong>and</strong><br />

neophytes are introduced species which are present in t he wild as naturalized populations, that is<br />

t hey are spreading vegetat ively or reproducing ef ectively by seed. An archaeophyte is a plant<br />

t hat became naturalized before AD 1500. A neophyte is one that was first int roduced after 1500,<br />

or was only present as a casual before 1500 <strong>and</strong> is naturalized now only because it was<br />

reint roduced subsequent ly. In contrast to archaeophytes <strong>and</strong> neophytes, a casual is a plant that is<br />

present only as populat ions which fail to persist in the wild for periods <strong>of</strong> more t han<br />

approximately fi ve years. Such a species is dependent on constant reint roduction (Macpherson et<br />

at , 1996).<br />

Hybrids between two alien parents which were introduced to the wild as hybrids (e.g. Crocosmia<br />

x crocosmiifl ora, Euphorbia x pseudovirgata) are classified as neophytes. Only hybrids between<br />

which have been formed spontaneously in the wild between two alien parents are classified as<br />

'AX'.<br />

Conservation status<br />

The conservat ion status <strong>of</strong> plant s is coded according to the system proposed by Hodgetts,<br />

Palmer & W igginton ( 1996); see also Palmer et al. ( 1997). This status is an assessment <strong>of</strong> threat<br />

rather t han rarity, alt hough closely related to rarity in that only species known at the time <strong>of</strong> the<br />

assessment in less t han 10 1 10-km squares have been allocated t o one <strong>of</strong> the categories listed.<br />

The stat us list ed is t hat given by Chefi ngs (2004). This replaces t he stat uses provided in the Red<br />

Data Book (W igginton, 1999) <strong>and</strong> Scarce plants in Britain (Stewart , Pearman & Preston, 1994).<br />

Cheffi ngs assigns a conservat ion status to nat ive species <strong>and</strong> archaeophytes, with only a few<br />

exceptions. PLA NTATT cannot be used to provide a complete list <strong>of</strong> threatened taxa as many<br />

subspecies listed by Cheffi ngs are not t reated separately by us.<br />

Rarity status<br />

Rarity status is based on counts <strong>of</strong> the number <strong>of</strong> 10-km squares in Britain <strong>and</strong> t he Isle <strong>of</strong> Man in<br />

which the plant was recorded as a nat ive in t he period 1987- 1999. Rare plants are those<br />

recorded in 1- 15 10-km squares during t his period; scarce plants are recorded in 16- 100.The<br />

t hresholds were those that were used in defining rare <strong>and</strong> scarce species for the Red Data Book<br />

<strong>and</strong> Scarce plants. Rarity status, however, is solely a measure <strong>of</strong> rarity rat her than threat, <strong>and</strong> is<br />

based on data from the New Atlas. Cheffi ngs assigns a conservat ion status to nat ive species <strong>and</strong><br />

archaeophyt es, with only a few except ions. PLANTATT cannot be used to provide a complete<br />

list <strong>of</strong> t hreat ened taxa as many subspecies listed by Cheffi ngs are not t reated separately by us.<br />

Alien species have by defi nition no nat ive records, <strong>and</strong> therefore are not given a rarity status.


Table 2. Nat ive stat us, Conservation stat us <strong>and</strong> Rarity stat us<br />

At tribute <strong>and</strong> codes N= Explanation<br />

(a) Native status<br />

(b) Conservation status<br />

(c) Rarity status<br />

(d) Change Index<br />

AC 12 Alien casual; many are crop plants<br />

A N 259 Neophyte, alien introduced after 1500<br />

A R 15 1 A rchaeophyte, alien introduced before 1500<br />

AX 1 Spontaneous hybrid between two alien parents<br />

1362 Native, not endemic<br />

NA 46 Native or alien (nat ive status doubtful)<br />

N E 47 Native endemic<br />

N H 7 Spontaneous hybrid between two native parents<br />

CR 20 Critically endangered<br />

D D I Data defi cient<br />

EN 34 Endangered<br />

EW 4 Ext inct in the wild<br />

EX 10 Ext inct<br />

VU 119 Vulnerable<br />

(values)<br />

933 Present, not rare or scarce<br />

234 Rare ( 1- 15 10-km squares in Britain, 1987- 1999)<br />

254 Scarce (16- 100 10-km squares in Britain, 1987- 1999)<br />

27<br />

(blank) 423 Alien taxa<br />

Absent from Britain <strong>and</strong> Isle <strong>of</strong> Man as a native, but native in<br />

Irel<strong>and</strong> or t he Channel Isl<strong>and</strong>s<br />

12 Apparently ext inct (not recorded since 1986)<br />

2 Insufi cient data available to assess rarity<br />

Change between 1930- 1960 <strong>and</strong> 1987- 1999<br />

Change Index<br />

The Change Index (Telfer et al., 2002) measures the relat ive magnitude <strong>of</strong> change, comparing the<br />

period 1930- 1960 with 1987- 1999. It is explained in more detail in t he Appendix. It ranges from<br />

-4.78 for the critically endangered Gahum tricornutum to 4.70 for t he much more frequent ly<br />

recorded Prunus laurocerasus. The Change Index has not been calculated for species not included<br />

in the fi rst Atlas <strong>of</strong> the <strong>British</strong> Flora (Perring & Walters, 1962). Consequent ly, several aliens such as<br />

Amsinckia micrantha <strong>and</strong> Crassula helmsii, which have increased spectacularly in the intervening<br />

period, lack a value for the Change Index.


SIZE A ND LI FE HIS TOR Y A TTRIB UTES<br />

H eight <strong>and</strong> length<br />

Heights, measured in cent imet res, are given for terrestrial (or emergent) plants <strong>and</strong> lengths (cm)<br />

for submerged aquatic plants. A few amphibious or emergent plants such as Persicaria amphibia<br />

are scored for both height <strong>and</strong> length.<br />

These values are int ended as a general indication <strong>of</strong> the size <strong>of</strong> the plant. For procumbent plants,<br />

heights are an indicat ion <strong>of</strong> the height <strong>of</strong> the less procumbent shoots. For scapose plants <strong>and</strong><br />

ferns, heights are not stem lengths but leaf lengths. Likewise, lengths for isoetids (i.e. linear-leaved<br />

rosette-forming root ed aquat ics) are in fact leaf lengths. For example Lobelia dortmanna has<br />

length 4 cm, which is certainly not the length <strong>of</strong> t he scape.<br />

Height <strong>and</strong> length values were drawn from a variety <strong>of</strong> sources, which are detailed in the<br />

Appendix.<br />

Perennat ion<br />

The categories are annual, biennial <strong>and</strong> perennial. Biennial is used as a short h<strong>and</strong> to denote also<br />

monocarpic perennials. For example Car /Ma vulgaris <strong>and</strong> Heracleum mantegazzianum normally<br />

take several years to reach maturity but are categorized as biennials. The sources <strong>of</strong> data for<br />

perennation are most ly t he same as t hose used for height <strong>and</strong> length. In a few cases (e.g. Linum<br />

catharticum), we have relied on personal communication <strong>and</strong> scientifi c papers rat her than fl oras.<br />

A relat ively small number <strong>of</strong> species fall into more t han one <strong>of</strong> these categories. The secondary<br />

category is intended to be either less frequent or equally frequent. Thus Poe annua has primary<br />

perennation category P I =annual <strong>and</strong> secondary category P2 = perennial. Several fl oras suggest<br />

t hat Cardamine flexuosa <strong>and</strong> Montia fontana can be annual, biennial or perennial. These have been<br />

coded as PI = p, P2 = a <strong>and</strong> PI = a, P2 = p respectively.<br />

Life form<br />

The Raunkiaer system <strong>of</strong> life forms was set out by Clapham,Tutin & Warburg (1962), who listed<br />

life forms for most species. Their assignments provide an excellent starting point but contain<br />

numerous inconsistencies. Life forms have been fully revised for PLANTATT. Following German<br />

<strong>and</strong> Swiss aut hors (e.g. Lindacher, 1995), the category <strong>of</strong> helophytes or marsh plants has been<br />

omitt ed. The majority <strong>of</strong> t hese can grow in places that are not permanently fl ooded in winter.<br />

The position <strong>of</strong> the overwintering buds in such situations is taken as a guide to t heir life form.<br />

An additional life form <strong>of</strong> annual water plants has been added, so t hat t he category t herophytes<br />

are all terrest rial.<br />

As with perennat ion, a secondary life form is given for some species. Details <strong>of</strong> how life forms<br />

were assigned <strong>and</strong> the relation <strong>of</strong> life form to plant height are given in t he Appendix.<br />

Woodiness<br />

Woodiness is an attribut e that applies to some chamaephytes, nanophanerophytes <strong>and</strong><br />

phanerophytes. All ot her life forms are t reated as herbaceous. Three categories are recognized,<br />

woody, semi-woody <strong>and</strong> herbaceous. Although we have been guided in part by Clapham,Tutin &<br />

W arburg ( 1962), we have not hesitated to express our own opinions where these diff er.


Table 3. Size <strong>and</strong> life history attributes other t han clonality; counts <strong>of</strong> primary<br />

att ributes are in the column N 1=, count s <strong>of</strong> secondary attributes are in N 2=<br />

Attribute or code N 1= N2= Explanat io n<br />

(a) Height (cm) Hght Height (leaf length for scapose plants <strong>and</strong> ferns)<br />

(b) Length (cm) Len Length (aquatic plants; leaf length for isoetids)<br />

(c) Perennation PI P2 Primary <strong>and</strong> secondary type <strong>of</strong> perennation<br />

a 455 14 Annual<br />

b 96 14 Biennial, including monocarpic perennials<br />

p 1334 42 Perennial<br />

(d) Life form L Fl LF2 Primary <strong>and</strong> secondary fi fe form (see Table Al )<br />

(e) Woodiness<br />

Ch 148 24 Chamaephyte<br />

Gb 32 Bulbous geophyte<br />

Gn 134 11 Non-bulbous geophyte (rhizome, corm or tuber)<br />

hc 8 11 50 Hemicryptophyte<br />

Hy 124 34 Perennial hydrophyt e (perennial water plant)<br />

H z 25 1 Annual hydrophyte (aquatic therophyte)<br />

Ph 108 15 Mega-, meso- <strong>and</strong> microphanerophyte<br />

Pn 73 2 1 Nanophanerophyte<br />

T h 430 14 Therophyte (annual l<strong>and</strong> plant)<br />

1651 Herbaceous<br />

sw 27 Semi-woody<br />

Vt 207 Woody<br />

Clonality<br />

Clonal growt h is defi ned here as vegetative reproduct ion combined with lateral spread. Like<br />

perennat ion, clonality may have more t han one value for a given species, refl ecting the various<br />

ways in which clonal growth may occur. In some species t here are varieties with clonal growt h<br />

(Arrhenatherum elatius van bulbosum, Caltha palustris var. radicans) while the normal form is not<br />

markedly clonal. In these two species, the variety with clonal growth is less frequent than the<br />

type variety, so that both plants are given Clone] = 0 (not spreading clonally) as the primary<br />

state, whereas Clone2 = D Rg <strong>and</strong> Sto12 respectively. Two species with proliferous<br />

infl orescences really ought to have been assigned to three categories, namely Juncus bulbosus<br />

(N ode2, Irreg <strong>and</strong> omitted DRi) <strong>and</strong> Butomus umbellatus (Rhiz2, DRg <strong>and</strong> omitted D Ri). It did<br />

not seem wort h having a third column just for these two, so the inflorescence character has<br />

been omitt ed.


Table 4. Cat egor ies <strong>of</strong> clonality; counts <strong>of</strong> primary attributes are in the column<br />

N 1=, count s <strong>of</strong> secondary attributes are in N 2=<br />

Attribute or code N 1 = N 2= Explanat io n<br />

(I) Clonafi ty Gone Clone2<br />

0 1228 Little or no vegetative spread<br />

Ogr 25 Tussock-forming graminoid, may slowly spread<br />

Ot b 26 Tuberous or bulbous, slowing cloning by <strong>of</strong> sets<br />

D Ra 20 10 Detaching ramets above ground (<strong>of</strong>t en axillary)<br />

D Rg 4 16 Detaching ramets at or below ground<br />

D Ri 11 Detaching ramets on infl orescence<br />

D R1 1 Detaching rarnets on leaves (Hammarbya)<br />

D Rp 1 Detaching ramets on prot hallus (Trichomanes)<br />

Frag 7 Fragmenting as part <strong>of</strong> normal growth<br />

Ir reg 38 17 Irregularly fragmenting (mainly water plants)<br />

Leaf 1 Plantlets formed on leaves (Cardamine pratensis)<br />

N ode l 19 20 Short ly creeping <strong>and</strong> rooting at nodes<br />

N ode2 76 9 Ext ensively creeping <strong>and</strong> rooting at nodes<br />

Rhiz l 152 8 Rhizome shortly creeping<br />

Rhiz2 209 15 Rhizome far-creeping<br />

Root 37 3 Clones formed by suckering from roots<br />

St ol l 14 Short ly creeping, stolons in illuminated medium<br />

St o12 26 5 Far-creeping by stolons in illuminated medium<br />

T ip 5 Tip rooting (the stems <strong>of</strong>ten turn downwards)<br />

The following comments may be helpful in distinguishing the clonal categories.<br />

I. The category Ogr is rather poorly defi ned. If a perennial graminoid (grass, sedge or rush) is<br />

repeatedly mown or heavily grazed, it may gradually form clones, even though this is not the<br />

normal condition.<br />

2. The category Ot b assumes that the ground is litt le disturbed. If there is regular disturbance,<br />

t he <strong>of</strong> sets will be dispersed to new sites <strong>and</strong> t he plant would then be indicated as DRg<br />

(detaching ramets at or below ground).<br />

3. The small category Frag applies to duckweeds <strong>and</strong> Azola<br />

4. The categories N ode (creeping <strong>and</strong> root ing at nodes), Rhiz (rhizomatous or with<br />

subterranean stolons) <strong>and</strong> Stol (stoloniferous in the illuminated medium, eit her air or<br />

water) are divided into two, according to whether they spread a short distance in a season<br />

or are far-creeping. For rhizomatous plants, a rule <strong>of</strong> t humb is that a species whose new<br />

shoots arise at a distance less t han a quarter <strong>of</strong> the height <strong>of</strong> the plant is short ly creeping,


while those that spread further are deemed to be far-creeping. Analogous distinct ions are<br />

made for N ode <strong>and</strong> Stol.<br />

5. The distinction between Node <strong>and</strong> Stol is that in N ode the horizontal or decumbent<br />

stem extends with indeterminate growth, rooting at the leafy nodes <strong>and</strong> not forming a new<br />

stem axis at each rooted position. In St ol, a new stem axis normally arises at the point <strong>of</strong><br />

root ing, or the stolon is determinate, bending upwards <strong>and</strong> not progressing with<br />

indeterminat e growt h.<br />

6. In the tip-rooting category, T ip, leafy stems that are not obviously stolons turn down at the<br />

apex <strong>and</strong> root there.


GE OGRAPHI C A TTRIB UTES<br />

Euro ean <strong>and</strong> wider distribut ions <strong>and</strong> cont inent alit<br />

The categorizat ion <strong>of</strong> taxa to biogeographic elements <strong>and</strong> their designat ion as 'continental' or<br />

ot herwise (Table 5) follow Preston & Hill ( 1997), with minor revisions <strong>and</strong> t he addit ion <strong>of</strong> the<br />

hyperoceanic category from a subsequent paper (Preston & Hill, 1999). Element s are provided<br />

for nat ive species <strong>and</strong> some archaeophytes; for archaeophyt es the classifi cation describes the<br />

archaeophyt ic range. In addition, some but not all alien species originat ing in Europe have also<br />

been assigned to biogeographic elements for PLANTATT <strong>and</strong> designated as continental.<br />

Geographic att ribut es are not provided for some hybrids.<br />

Table 5. European <strong>and</strong> wider dist ribution, <strong>and</strong> continentality<br />

Att ribut e<br />

<strong>and</strong> codes<br />

N = Ex planat io n


Native distribution o s ecies alien in Britain <strong>and</strong> Irel<strong>and</strong><br />

The native dist ribution <strong>of</strong> aliens (Table 6) is taken from the New Atlas. This information is<br />

provided for neophytes <strong>and</strong> some archaeophytes. In Table 6, taxa present in two areas are<br />

included in bot h totals but taxa are excluded from the totals if they are only doubtfully native in<br />

the relevant area.<br />

Table 6. Nat ive dist ribution <strong>of</strong> species alien in Britain <strong>and</strong> Irel<strong>and</strong><br />

Code N = Explanat ion<br />

Am 24 North America<br />

Am4 22 West ern North America<br />

Am6 5 Eastern North America<br />

As 10 Asia east <strong>of</strong> 60°E<br />

As I 24 Asia between 60°E <strong>and</strong> I 20°E<br />

As2 9 Asia E <strong>of</strong> I 20°E<br />

Aus 3 Aust ralia<br />

Crop 15 Crop plant, does not have a native range<br />

Eur 149 Europe<br />

Gard 13 Garden or igin, does not have a native range<br />

NHem 6 N Hemisphere (Europe,Asia <strong>and</strong> Nort h America)<br />

NZ 4 New Zeal<strong>and</strong><br />

SAf 5 Southern Africa<br />

SAm 20 South America <strong>and</strong>/or Cent ral America<br />

Unk 10 Unknown<br />

Counts o I O-km s uares in the New Atlas<br />

For each taxon, the number <strong>of</strong> 10-km squares in Britain, Irel<strong>and</strong> <strong>and</strong> the Channel Isl<strong>and</strong>s is.<br />

enumerated (Table 7). For most natives, only t he native distribution has been counted (blue dots<br />

in the New Atlas). For the small number <strong>of</strong> nat ive species in which it proved impossible even to<br />

attempt to delimit the nat ive range in the New Atlas, the count is for all squares. For alien taxa,<br />

all squares with records have been counted. Squares have been counted without regard to date,<br />

so that Otanthus maritimus, ext inct in Britain, is recorded from 23 squares t here.<br />

10


Table 7. Counts <strong>of</strong> squares <strong>and</strong> climat ic means<br />

Attribute<br />

(a) Counts<br />

GB<br />

Min Max Explanation<br />

IR 0 985 Irel<strong>and</strong><br />

Counts <strong>of</strong> 10-km squares<br />

0 2805 Great Britain <strong>and</strong> Isle <strong>of</strong> Man<br />

CI 0 14 Channel Isl<strong>and</strong>s<br />

(b) Climatic means Mean values for 10-km squares<br />

Tian - 1.3 7.0 January mean temperat ure (°C)<br />

Tjul 10.4 17.0 July mean temperature (°C)<br />

Prec 553 32 18 Annual precipitation (mm)<br />

Climatic means<br />

Climat ic values for plants were calculated as t he mean climate <strong>of</strong> the 10-km squares where they<br />

occur in Britain, Irel<strong>and</strong> <strong>and</strong> the Channel Isl<strong>and</strong>s, averaging over the squares enumerated for the<br />

counts. Climate data for 10-km squares were taken from baseline climate summaries <strong>of</strong> t he UK<br />

Climate Impacts Programme (Hu Ime & Jenkins, 1998). These baseline summaries were<br />

const ructed by interpolat ion <strong>of</strong> daily weat her measurements from individual met stat ions,<br />

averaged over the 30-year period 1961- 1990 (Barrow et al., 1993).


HA BI TA T A TTRIB UTES<br />

Coastal species<br />

Species are deemed to be coastal if 80% <strong>of</strong> occupied squares are on the coast <strong>and</strong> if they depend<br />

on coastal habitat. Most coastal species have Ellenberg salt values (S values, defi ned below)<br />

greater than 0. Those with Ellenberg S = 0 were scrutinized carefully to ascertain whether their<br />

habitat was indeed coastal.<br />

Broad Habitats<br />

The preferences <strong>of</strong> species for Broad Habitats <strong>of</strong> the UK BAP are listed in the column labelled Br<br />

Habitats. Species' main habitat (s) are_list ed. No species is deemed to have a preference for<br />

more t han four habitats. Minor habitats are ignored. For more informat ion about Broad<br />

Habitats <strong>and</strong> species' preferences, refer to the Appendix.


Table 8. Coastal species <strong>and</strong> preferences for Broad H abitats<br />

A ttribut e<br />

<strong>and</strong> codes<br />

N = Explanat io n<br />

(a) Co Coastal species<br />

Co 145 At least 80% <strong>of</strong> occupied squares contain sea at high tide<br />

(b) Br Nabs Broad Habitats<br />

3 10 Broad leaved, mixed <strong>and</strong> yew woodl<strong>and</strong><br />

2 32 Coniferous woodl<strong>and</strong><br />

3 543 Boundary <strong>and</strong> linear features (eg hedges, roadsides, walls)<br />

4 198 A rable <strong>and</strong> horticultural (includes orchards, excludes domest ic gardens)<br />

5 22 Improved grassl<strong>and</strong><br />

6 163 Neut ral grassl<strong>and</strong> (includes coarse Arrhenatherum grassl<strong>and</strong>)<br />

7 2 18 Calcareous grassl<strong>and</strong> (includes lowl<strong>and</strong> <strong>and</strong> montane types)<br />

8 89 Acid grassl<strong>and</strong> (includes non-calcareous s<strong>and</strong>y grassl<strong>and</strong>)<br />

9 10 Bracken<br />

10 83 Dwarf shrub heat h (cover <strong>of</strong> dwarf shrubs at least 25%)<br />

I I 254<br />

12 4 1<br />

Fen, marsh <strong>and</strong> swamp (not wooded; includes flushes, rush-pastures, springs <strong>and</strong><br />

mud communit ies)<br />

Bog (on deep peat; includes bog pools as well as acid lowl<strong>and</strong> valley mires on<br />

slight ly shallower peat)<br />

13 174 St<strong>and</strong>ing wat er <strong>and</strong> canals<br />

14 149 Rivers <strong>and</strong> st reams<br />

I S 103 Montane habitats (acid grassl<strong>and</strong> <strong>and</strong> heat h with montane species)<br />

16 292<br />

Inl<strong>and</strong> rock (heterogeneous - includes quarries, limestone pavement, clif s, screes<br />

<strong>and</strong> skeletal soils over rock)<br />

17 231 Built-up areas <strong>and</strong> gardens<br />

18 74 Supra littoral rock (does not include maritime grassl<strong>and</strong>)<br />

19 135 Supra littoral sediment (st r<strong>and</strong>lines, shingle, coastal dunes)<br />

2 1 65 Littoral sediment (includes saltmarsh <strong>and</strong> saltmarsh pools)<br />

23 1 Inshore sublittoral sediment (only Zostera marina)


Ellenbe s indicator values<br />

Ellenberg defi ned seven major scales, <strong>of</strong> which fi ve are presented here. The two that are<br />

omitted, T (temperat ure) <strong>and</strong> K (cont inentality), correspond quite closely to the major biome<br />

<strong>and</strong> east ern limit categories defi ned for European dist ribut ions by Preston & Hill (1997). Neither<br />

T nor K values are satisfactory in an oceanic climate such as that <strong>of</strong> Britain; t hose for K are<br />

particularly unreliable, especially as Ellenberg's defi nition was geographical rather than climat ic.<br />

The fi ve remaining scales have values defi ned in the tables that follow. The values are based on<br />

those <strong>of</strong> Ellenberg et at (1991). They are mostly reproduced from a previous publication (Hill et<br />

al., 1999), with some additions because <strong>of</strong> the ext ra species included here. A few example<br />

species are given for each value, by way <strong>of</strong> explanation.<br />

Light values (L)<br />

The full range <strong>of</strong> Ellenberg values for light (Table 9) is not represent ed in the <strong>British</strong> fl ora. For<br />

canopy t rees, light values refer to the tolerance <strong>of</strong> t he sapling stage <strong>of</strong> the life cycle.<br />

Table 9. Ellenberg values for light (L)<br />

Code N = Explanat io n<br />

0 Plant in deep shade (no examples for Britain or Irel<strong>and</strong>)<br />

2 4 Between 1 <strong>and</strong> 3 (Epipogium aphyllum, Neottia nidus-avis,Trichomenes speciosum)<br />

Shade plant, most ly less than 5% relative illuminat ion, seldom more than 30%<br />

3 20 illumination when t rees are in full leaf (Ga hurn odoraturn, Listera cordate, Mercurialis<br />

perennis)<br />

4 70 Between 3 <strong>and</strong> 5 (Circaea lutetiono, Lamiastrum galeobdolum, Poa nérnoralis)<br />

Semi-shade plant, rarely in full light, but generally with more than 10% relat ive<br />

5 120 illumination when t rees are in leaf (Carex pendula, Hyacinthoides non-scripta, Primula<br />

vulgaris)<br />

6 2 13 Between 5 <strong>and</strong> 7 (Anthriscus sylvestris, Digitalis purpurea, Teucriurn scorodonia)<br />

7 680<br />

8 576<br />

9 202<br />

Plant generally in well lit places, but also occurring in part ial shade (Arrhenatherurn<br />

elatius, Carex flacco, Poo trivialis,Vicia cracca)<br />

Light-loving plant rarely found where relat ive illumination in summer is less than 40%<br />

(Cardarnine hirsute, Orchis morio,Thymus polytrichus,Vacciniurn oxycoccus)<br />

Plant in full light, found mostly in full sun (Aster tripolium, Mel/ lotus albus, Poa compressa,<br />

Primula farinosa)<br />

14


M oisture values (F)<br />

Unlike the ot her Ellenberg values, moisture is on a scale <strong>of</strong> I to 12 (Table 10). We use the<br />

abbreviation F from the German Feuchtigkeit.<br />

Table 10. Ellenberg values for moisture (F)<br />

Code N = Explanat ion<br />

1 3<br />

Indicator <strong>of</strong> ext reme dryness, restricted to soils that <strong>of</strong>t en dry out for some time<br />

(Corynephorus canescens, Helianthemum apenninum, Koeleria vallesiana)<br />

2 28 Between 1 <strong>and</strong> 3 (Clinopodium acinos, Saxifraga tridactyfi tes, Sedum acre)<br />

3 168<br />

4 378<br />

5 492<br />

Dry-site indicator, more <strong>of</strong>t en found on dry ground than in moist places (Asplenium<br />

trichomanes, Centaurea scabiosa, Spergularia rubra)<br />

Between 3 <strong>and</strong> 5 (Arctium minus, Hefi ctotrichon pratense, Iris foetidissima,Thymus<br />

polytrichus)<br />

Moist-site indicator, mainly on fresh soils <strong>of</strong> average dampness (Anthriscus sylvestris,<br />

Euphorbia amygdaloides, Hyacinthoides non-scripta, Solarium nigrum)<br />

6 226 Between 5 <strong>and</strong> 6 (Agrostis stolonifera, Empetrum nigrum, Rumex crispus)<br />

7 14 1<br />

8 170<br />

9 126<br />

10 64<br />

I I 34<br />

12<br />

55<br />

Dampness indicator, mainly on constant ly moist or damp, but not on wet soils (Carex<br />

Dactylorhiza maculata, Pulicaria dysenterica, Ranunculus repens)<br />

Between 7 <strong>and</strong> 9 (Cardamine pratensis, Equisetum telmateia, Phalaris arundinacea, Schoenus<br />

nigricans)<br />

Wet-site indicator, <strong>of</strong>t en on water-saturated, badly aerated soils (Drosera rotundif<strong>of</strong>i a,<br />

Myosotis scorpioides,Vaccinium oxK occus, Viola palustris)<br />

Indicator <strong>of</strong> shallow-water sites that may lack st<strong>and</strong>ing water for ext ensive periods<br />

(Afi sma plantago-aquatica, Carex limosa, Ranunculus fi ngua,Typha latif<strong>of</strong>i a)<br />

Plant root ing under water, but at least for a time exposed above, or plant fl oat ing on<br />

t he surface (Lemna minor, Nuphar lutea, Sagit aria sagittifolia, Schoenoplectus lacustris)<br />

Submerged plant, permanently or almost constantly under water (Isoetes lacustris,<br />

Potamogeton crispus, Ranunculus circinatus, Zostera marina)<br />

15


Reaction (R)<br />

Reaction (Table I I) refers to environmental acidity, which would ordinarily be measured by pH.<br />

Except for water plants, R values refl ect preferences for soil acidity.<br />

Table I I . Ellenberg values for reaction (R)<br />

Code N = Ex planat io n<br />

Indicator <strong>of</strong> ext reme acidity, never found on weakly acid or basic soils (Andromeda<br />

polifolia, Lycopodium clavatum, Rubus chamaemorus, Ulex minor)<br />

Between I <strong>and</strong> 3 (Agrostis curtisii, Calluna vulgaris, Drosera rotundif<strong>of</strong>i a, Po lygala serpyllifolia)<br />

Acidity indicator, mainly on acid soils, but exceptionally also on nearly neutral ones<br />

(Agrostis vinealis, Dactylorhiza M a de ra, Ga lium saxatile, Pteridium aquilinum)<br />

Between 3 <strong>and</strong> 5 (Agrostis capillaris, Carex panicea,Juncus eff usus,Teucrium scorodonia)<br />

Indicator <strong>of</strong> moderately acid soils, only occasionally found on very acid or on neutral to<br />

basic soils (Cardamine pratensis, Cirsium palustre, Rubus idaeus, Ulex eumpaeus)<br />

Between 5 <strong>and</strong> 7 (Ammophila arenaria, Carex sylvatica, L<strong>of</strong>i um perenne, Ranunculus ficaria)<br />

Indicator <strong>of</strong> weakly acid to weakly basic conditions; never found on very acid soils<br />

(Agrimonia eupatoria,Atriplex prostrata, Nuphar lutea, Phleum pretense)<br />

Between 7 <strong>and</strong> 9 (Artemisia vulgaris, Carduus nutans, Iris foetidissima, Viola hirsuta)<br />

Indicator <strong>of</strong> basic reaction, always found on calcareous or other high-pH soils (Bunium<br />

bulbocastanum, Clinopodium calamintha, Dryopteris submontana, Primula farMosa)<br />

Nitrogen (N)<br />

Nitrogen values (Table 12) are in fact a general indication <strong>of</strong> preference for soil fert ility. They are<br />

closely correlated with t he st ress values <strong>of</strong> Grime ( 1979, 200 1), low N values corresponding to<br />

plants with high st ress tolerance (Grime et al., 1997) <strong>and</strong> vice-versa.<br />

Table 12. Ellenberg values for nitrogen (N)<br />

Code N= Explanat io n<br />

1<br />

84<br />

Indicator <strong>of</strong> ext remely infertile sites (Agrostis curtisii, Cli nopodium acinos, Drosera<br />

rotundifolia, Rubus chamaemorus)<br />

2 323 Between 1 <strong>and</strong> 3 (Aira praecox, Carex panicea, Linum catharticum, Scabiosa columbaria)<br />

3 286<br />

Indicator <strong>of</strong> more or less infert ile sites (Centaured scabiosa, Go lium saxatile, Pimpinella<br />

saxifraga,Teucrium scorodonia)<br />

4 245 Between 3 <strong>and</strong> 5 (Agrostis capillaris, Cirsium palustre, Plantago lanceolata, Primula vulgaris)<br />

5<br />

342<br />

Indicator <strong>of</strong> sites <strong>of</strong> intermediate fert ility (Angelica sylvestris, Digitalis purpurea, Iris<br />

foetidissima,Trifolium pratense)<br />

6 3 19 Between 5 <strong>and</strong> 7 (Cirsium arvense, Glyceria fluitans, Poa trivialis, Rumex crisp s)<br />

7 223<br />

Plant <strong>of</strong>ten found in richly fertile places (Atriplex prostrate, Epilobium hirsutum, Stellaria<br />

media,Typha latifolia)<br />

8 55 Between 7 <strong>and</strong> 9 (Beta vulgaris, Galium aparine, Lamium album, Urtica dioica)<br />

9 8<br />

Indicator <strong>of</strong> ext remely rich situat ions, such as cattle resting places or near pollut ed<br />

rivers (Arctium laPpa,Artemisia absinthium, Hyoscyamus niger, Rumex obtusifolius)


Salt tolerance (5)<br />

Values for salt tolerance (Table 13) start at zero, corresponding to no tolerance <strong>of</strong> salt.<br />

Table 13. Ellenberg values for salt tolerance (S)<br />

Explanat ion<br />

Absent from saline sites; if in coastal situations, only accidental <strong>and</strong> non-persistent if<br />

subjected to saline spray or water (85% <strong>of</strong> the fl ora)<br />

Slightly salt-tolerant species, rare to occasional on saline soils but capable <strong>of</strong> persisting<br />

in the present <strong>of</strong> salt (includes dune <strong>and</strong> dune-slack species where the ground water is<br />

fresh but where some inputs <strong>of</strong> salt spray are likely) (Calystegia sepium, Chenopodium<br />

album, Oenanthe crocata, Sedum angfi cum)<br />

Species occurring in both saline <strong>and</strong> non-saline situat ions, for which saline habitats are<br />

not stro ngly predominant (Atriplex prostrata, Elytrigia repens, Phragmites australis, Rumex<br />

crispus)<br />

Species most common in coastal sites but regularly present in freshwater or on nonsaline<br />

soils inl<strong>and</strong> (includes strictly coastal species occurring in sites such as cliff crevices<br />

<strong>and</strong> s<strong>and</strong> dunes that are not obviously salt-af ected) (Cakile maritima, Cochlearia <strong>of</strong>ficinalis,<br />

Juncus gerardii, Spergularia rupicola)<br />

Species <strong>of</strong> salt meadows <strong>and</strong> upper saltmarsh, subject to at most only very occasional<br />

tidal inundation (includes species <strong>of</strong> brackish conditions, i.e. <strong>of</strong> consistent but low<br />

salinity) (Atriplex littoralis, Elytrigia atherica, Glaux maritima,Triglochin maritimum)<br />

Species <strong>of</strong> the upper edge <strong>of</strong> saltmarsh, where not inundated by all tides (includes<br />

obligate halophytes <strong>of</strong> clif s receiving regular salt spray) (Aster trip<strong>of</strong>i um, Crithmum<br />

maritimum, Puccinellia maritima, Suaeda vera)<br />

Species <strong>of</strong> mid-level saltmarsh (Atriplex portulacoides, Cochlearia anglica, Limonium vulgare)<br />

Species <strong>of</strong> lower saltmarsh (Spartina anglica, Suaeda maritima)<br />

Species more or less permanently inundated in sea water (Zostera spp.)<br />

Species <strong>of</strong> extremely saline conditions, in sites where sea water evaporates,<br />

precipitating salt (Safi cornia europaea agg.; these could equally well be t reated as<br />

species <strong>of</strong> t he lower marsh)


LIS TIN G OF SPE CIES WI TH THEIR A TTRIB UTES<br />

The listing <strong>of</strong> species with their attributes has 32 columns. Codes used in these columns are set<br />

out in the foregoing tables. The short <strong>and</strong> full names <strong>of</strong> the columns are given here (Table 14), as<br />

are the pages on which the tables <strong>of</strong> codes appear<br />

Table 14. Plant attributes cross-referenced to tables <strong>and</strong> page numbers where t hese<br />

are described more fully<br />

Short name Attribute Table N o Page<br />

Taxon name Name in New At las 1 2<br />

Fam Family (4-letter abbreviation) 1 2<br />

NS Native status 2 4<br />

CS Conservation status 2 4<br />

RS Rarity status 2 4<br />

Chg Change Index 2<br />

Hght Height in cm (terrest rial) 3 6<br />

Len Length in cm (aquatic) 3 6<br />

PI Perennat ion - primary 3 6<br />

P2 Perennation - secondary 3 6<br />

LF 1 Life form - primary 3 6<br />

LF2 Life form - secondary 3 6<br />

Woodiness 3 6<br />

Clone 1 Clonal spread .- primary 4 7<br />

Clone 2 Clonal spread - secondary 4 7<br />

E I Major Biome (European di stribution) 5 9<br />

E2 Eastern limit code 5 9<br />

C' Continentality in Europe 5 9<br />

O rigin Origin <strong>of</strong> alien taxa 6 10<br />

GB Number <strong>of</strong> 10-km squares in Britain (including Isle <strong>of</strong> Man) 7 1 I<br />

IR Number <strong>of</strong> I 0-km squares in Irel<strong>and</strong> 7 I I<br />

CI Number <strong>of</strong> 10-km squares in Channel Isl<strong>and</strong>s<br />

7 I I<br />

Tjan January mean temperature 7 I I<br />

Tjul July mean temperature 7 I I<br />

Prec Annual precipitation 7<br />

Co Coastal 8 13<br />

Br Habitats Broad Habitats 8 13<br />

Ellenberg indicator value - light 9 14<br />

Ellenberg indicator value - moisture 10 15<br />

ft Ellenli erg indicator value - reaction I I 16<br />

Ellenberg indicator value - nit rogen 12 16<br />

Ellenberg indicator value - salt tolerance 13 17<br />

18


Taxo n name Fa m NS CS RS C hg Hght Len 1 P2 LF 1 LF2 W lo ne l C lo ne 2 E l E2 C Ori in G B IR C I r an r ul Prec Co Br Habitats L F R N S<br />

Acae na no vae-se l<strong>and</strong>iae Rosa A N 11 C h ode2 A us , NZ 82 9 3 .8 15 .2 83 1 3 , 10 , 18 , 19 8 3 6 3<br />

Acer campestre Acer N n 0 .35 15 00 Ph 7 3 1389 0 3 .6 15 .7 839 1, 3 5 5 7 6<br />

A cer plata noides Acer A N 3000 Ph 7 3 c Eur 14 19 43 3 .4 15 .2 903 1, 3, 17 4 5 7 7 '<br />

Ace r pseu dop latanus A cer A N -0 .40 3000 Ph 7 3 c Eur 2 59 9 942 1 3 .6 14 .6 1083 1, 3, 17 4 5 6 6<br />

Ace ras anthm pop hor um O rch N s -0 .76 40 G n 9 1 109 0 3 .6 16 .3 690 7 7 1 4 8 3<br />

Achillea millefolium A ste N n 0.29 45 C h h hiz2 5 5 277 4 968 1 3 .5 14 .5 110 3 6 7 5 6 4<br />

Ach illea ptarmica A ste N n -0.6 5 60 hc h hiz l 5 5 2 38 2 492 3 .3 14 .3 1146 11 7 7 5 3<br />

Acon itu m nap ell us Ranu NA 5 100 G n h hiz t 7 3 104 0 4 .0 15 .8 964 1, 3 . 14 , 17 5 7 7 6<br />

Acon iturn nap ellus se ns . lat. Ranu NA s 1.4 2 100 G n h hiz l 7 3 104 0 4 .0 15 .8 964 1, 3 , 14 , 17 5 7 7 6<br />

Acor us calam us A ra c A N 0.69 112 Hy h hiz2 Unk 5 15 17 3 .6 15 .8 770 13 , 14 8 10 7 71<br />

Actaea spica ta Ranu N s -0.44 60 G n h hiz l 4 6 33 0 2 .5 14 .3 10 54 16 3 5 8 6<br />

Adiantum cap illus- ven eris A dia N 5 0.54 30 hc 9 1 38 29 5 .2 15 .2 110 1 16 4 7 8 3<br />

Adonis annua Ranu A R V U -2.19 40 Th 9 1 234 3 3 .8 16 .0 745 4 7 4 7 4<br />

Adox a m osehatellin a Adox N n -0 .05 12 Gn h hiz l 5 6 1720 2 3 .3 14 .9 1005 1 4 5 6 5<br />

Aegopodium dagraria A pia A R -0 .45 100 hc h hiz2 7 4 Eur, A s 1 2533 8 19 1 3 .6 14 .6 1064 3, 17 6 5 6 71<br />

Aes culus hippoca stanum Hip p A N 1.0 8 32 00 Ph Eur 2 186 557 I 3.6 14 .8 10 14 3 , 17 5 5 7 7<br />

Aethusa cynap ium A pia NA n -0 .4 1 100 T h 7 3 164 0 0 3.6 15 .5 863 3, 4 , 17 6 4 7 6<br />

Agrimo nia eup atoria Ro sa N n -0 .89 60 hc 8 4 1859 532 3.8 15 .1 953 6 7 4 7 4<br />

Agrimo nia proc ere Ro sa N n -0 .38 100 hc 7 3 8 19 16 1 3.9 15 .1 10 26 1, 3 , 6 5 6 7 5<br />

Agros tem ma githago Cary A R EW -0 .75 10 0 T h Unk 8 15 96 3 .9 15 .6 852 4 7 5 6 5<br />

Agros tis can ine Po ac N n 60 hc to12 5 6 1609 36 1 3 .5 14 .5 1128 11, 13 7 7 3 3<br />

Agros tis can ine sen s.lat. Poac N n 1.3 2 60 hc iz2 St o12 5 6 19 37 44 3 3 .4 14 .3 114 5 8 , 11 7 6 3 3<br />

Agros tis cap illaris Poet N n 1.2 8 62 hc iz2 5 4 2758 922 1 3 .5 14 .5 1104 8 6 5 4 4<br />

Agro stis curtisii Poac N n -0 .26 60 he 8 1 207 0 4 .9 15 .8 1082 8 , 10 7 6 2 1<br />

Agros tis gigantea Poac A R 1.39 80 hc iz2 8 5 16 13 109 3 .6 15 .3 889 3, 4 7 6 6 71<br />

Agros tis stolonifera Poac N n 3 .66 4 5 hc to12 6 6 2 77 6 977 1 3 .6 14 .5 110 1 4, 6 7 6 7 6<br />

Agrostis vinea lis Poac N n 60 he iz2 7 3 1126 150 3 .3 14 .0 1200 8, 10 7 6 3 2<br />

Aire ca ryop hy llea Poa c N n -0 .52 25 Th 8 3 2046 6 56 1 3 .7 14 .6 1087 10 , 16 8 2 5 2<br />

Aire praeco x Po ac N n -0.19 10 Th 8 2 2450 6 59 1 3 .5 14 .3 1149 8 , 16 8 2 4 2<br />

Aj uga cha maep itys La mi NA V U r -0 .62 20 hc 8 3 43 0 3 .8 16 .5 7 13 4 , 7 71 4 8 2<br />

Aj uga py ramid alis La rni N 5 -0 .34 30 hc 4 3 106 8 3 .3 12 .6 1425 10 , 16 7 ' 5 5 2<br />

Aj uga reptans La m i N n -0 .56 30 hc to 12 7 3 2439 7 17 3 .4 14 .6 1095 1 5 7 5 5<br />

Alchem illa ac utiloba Ro sa N r 60 hc 5 3 c 15 0 1.6 13 .2 969 6 7 4 6 5<br />

Alch emilla alpina Ro sa N n -0 .6 1 15 hc 1 3 384 4 1.6 12 .1 1843 7 , 15 , 16 7 5 4 3<br />

Alch emilla filica ulis Ro sa N n 30 hc 4 3 1407 308 2 .9 14 .1 1185 7, 15 . 16 8 6 6 3<br />

Alch emilla glabra Ro sa N n 40 hc 5 3 127 1 223 2.6 13 .4 1338 6 , 15 . 16 7 6 6 4<br />

Alch emilla gla uce scens Ro sa N s 15 hc 5 3 c 20 3 2.0 13 .3 14 08 7 T 5 7 5<br />

Alch emilla glomerulans Ro sa N s 30 hc 2 3 57 0 0 .4 11.5 19 78 8 , 15 7 5 5 4<br />

Alchem illa micans . Ro sa N V U r 40 hc 5 3 c 4 0 2 .0 13 .5 10 56 7 7 5 7 5<br />

Alchem illa min ima Ro sa N E V U r 5 hc 4 1 3 0 1.7 13 .5 166 7 7 71 6 8 3<br />

Alchem illa mollis Rosa A N 60 hc Eur 805 17 3.5 15 .0 10 09 3 , 17 6 5 7 6<br />

Alchem illa monticola Rosa N r 35 hc 5 3 c 9 0 1.3 13 .0 10 84 6 7 4 6 4<br />

Alchem illa sub crena ta Rosa N EN r 35 hc 5 3 c 2 0 0 .9 12 .6 1125 6 7 4 6 5<br />

Alchem illa vulgaris agg . Rosa N n -0 .0 1 35 hc 5 3 19 35 496 3.1 14 .1 1179 6 , 7 , 15 , 16 T 5 6 4<br />

Alchemilla wichu rae Rosa N s 20 hc 4 3 6 5 0 0 .9 12 .0 1992 7 71 5 5 3<br />

Alchemilla xa nthoc hlora Rosa N n 40 . hc 7 3 1060 24 0 2 .8 13 .9 1174 6 , 7 6 5 6 4


Tax on name Fam NS CS RS Chg. Hght Len P1 P2 LF 1 LF2 W Clona l Clo ne2 El E2


S<br />

Taxon name Fam NS CS RS Chg Hght Len 1 P2 LF1 LF2 W Clonel Clone2 El E2 C Origin GB IR CI Tja n Tjul Prec Co Br Habitats L F R N<br />

Anthoxanthum aristatum Poac AN -2.65 40 Th 0 Eur 93 0 I 3.9 16.0 775 4, 17 7 4 4 5<br />

Anthoxanthum odoratum Poac N n 0.90 50 hc 0 6 4 2782 965 14 3.5 14.4 1106 6 7 6 4 3<br />

Anthriscus caucalis Apia N n -0.16 70 Th 0 7 3 659 471 12 3.9 15.71 747 3, 4, 8 71 5 6 5<br />

Anthriscus sylvestris Apia N n -0.19 100 hc 0 5 5 2480 805 5 3.6 14.6 1039 3 6 5 7 T<br />

Anthylris vulneraria Faba N n 0.45 60 he 0 5 3 1798 465 9 3.7 14.6 1030 7 8 4 7 2<br />

Anfi rrhinum maj us Scro AN 2.84 30 Ch 0 Eur 1043 84 8 3.9 15.7' 837 3, 17 8 3 7' 5<br />

Apera interrupta Poac AN 0.80 40 Th 0 8 4 Eur, As l 104 0 0 3.4 15.9 671 3, 4, 16 9 5 8 6<br />

Apera spica-venti Poac AR -0.21 100 Th 0 5 4 326 1 3 3.7 16.0 726 3, 4 7i 4 5 5<br />

Aphanes arvensis Rosa N n 10 Th 0 7 3 1608 432 4 3.7 15.0 956 4, 16 8 4 6 4<br />

Aphanes arvensis agg. Rosa N n -0.32 10 Th 0 7 3 2302 659 14 3.6 14.7 1038 4, 8, 16 7 4 6 4<br />

Aphanes australis Rosa N n 10 Th 0 7 3 1549 230 14 3.5 14.6 1070 8, 16 7 4 5 4<br />

Apium grayeolens Apia N n -0.63 80 hc 0 8 4 519 82 8 4.3 15.8 849 13 8 8 7 7<br />

Apium inundatum Apia N n -0.54 30 so Hy Irreg 7 2 9271 351 6 3.8 14.8 1023 11, 13 71 10 6 4<br />

Apium nodiflorum Apia N n -0.31 60 100 Hy Irreg 8 4 1661 855 12 4.0 15.2 961 14 7 10 7 7'<br />

Apium repens Apia N CR r 15 hc Node2 7 3 3 0 0 3.6 16.4 651 13 9 9 7 7<br />

Aquilegia vulgaris Ranu N n 1.70 100 hc 0 7 3 1504 197 5 3.6 15.0 986 1, 3, 16 6 4 6 5<br />

Arabidopsis thaliana Bras N n 1.21 30 Th 0 7 4 2218 509 13 3.5 14.8 1034 16, 17 8 3 6 2<br />

Arabis alpina Bras N EN r 15 Ch 0 1 4 1 0 0 2.5 11.8 3218 16 7 5 71 3<br />

Arabis glabra Bras N VU s -1.16 100 hc 0 7 4 151 0 1 3.5 16.0 686 8 7 3 8 5<br />

Arabis hirsuta Bras N n -1.02 40 p he 0 5 6 1042 143 4 3.3 14.6 1104 7, 16 7 5 8 3<br />

Arabis petraea Bras N s -0.64 25 Ch 0 1 5 78 2 0 1.7 11.9 1966 15, 16 9 3 8 1<br />

Arabis scabra Bras N VU r 20 Ch 0 9 3 1 0 0 4.4 16.5 844 16 7 3 8 2<br />

Arbutus unedo Eric N o 1.18 500 Ph w O 9 1 0 8 0 4.7 14.4 1335 1, 16 6 5 71 2<br />

Arctium lappa Aste AR 0.51 150 hc h 0 7 4 971 4 1 3.8 16.0 769 3 9 5 7 9<br />

Arctium minus Aste N n -0.41 150 hc h 0 7 5 2424 846 14 3.7 14.7 1051 3 6 4 7 5<br />

Arctostaphybos alpinus Eric N s -0.22 20 Ch w Node2 1 6 134 0 0 1.6 11.6 1750 15 7 6 2 2<br />

Arctostaphylos uva-ursi Eric N n -0.75 20 Ch w Node2 4 6 473 37 0 2.1 12.3 1615 10, 15 7 5 2 2<br />

Arenaria ciliata Cary N o 6 Ch 0 1 3 0 1 0 2.6 12.9 1454 15 9 5 8 2<br />

Arenaria norvegica Cary N r 0.21 6 a Ch Th 0 1 3 16 1 0 2.5 12.3 1904 16 9 3 8 2<br />

Arenaria serpyllifolia Cary N n -0.76 30 Th 0 8 4 2147 522 13 3.6 14.9 986 16 8 3 T 5<br />

Armeria arenaria Plum N o 20 Ch 0 8 2 0 0 5 6.1 16.9 843 Co 18, 19 8 3 6 2<br />

Armada maritima Plum N n -0. 14 15 Ch 0 3 6 1137 319 14 3.9 14.1 1265 Co 18, 21 8 7 5 5<br />

Armoracia rusticana Bras AR 0.05 150 hc Rhiz2 Crop 1532 111 10 3.8 15.6 850 3 8 5 7 Tj<br />

Arnoseris minima Aste AR EX -3.72 30 Th 0 7 3 83 0 0 3.6 16.1 685 4 7 4 3 3<br />

Arrhenatherurn elatius Poac N n 0.37 150 hc 0 DRg 7 3 2678 958 13 3.6 14.5 1089 3, 6 7 5 7 7<br />

Artemisia absinthium Aste AR -0.46 90 Ch sw 0 7 4 1005 41 6 3.8 15.6 861 3, 16, 17 7 4 7 9<br />

Art emisia campestris Aste N EN r -0,42 60 Ch sw Rhizl 7 4 c 9 0 0 3.3 16. 1 620 3, 8 8 3 6 5<br />

Artemisia norvegica Aste N VU r 8 hc h 0 1 3 3 0 0 0.9 10.9 1982 15 9 4 4 1<br />

Artemisia vulgaris Aste AR -0.20 150 hc h 0 7 4 2109 489 12 3.7 14.9 984 3, 17 7 4 8 7<br />

Arum italicum Arac N s 2.09 60 Gn h Rhizl 9 1 39 0 8 5.5 16.2 962 1, 3 4 5 6 6<br />

Arum maculatum Arae N n -0.28 50 Gn h Rhizl 7 3 1604 650 11 3.9 15.3 931 1 4 5 7 7'<br />

Asparagus <strong>of</strong> icinalis Lili N n 1.78 150 Gn h 0 7 1 17 7 7 5.4 15.9 953 3, 18, 19 7 5 6 5<br />

Asparagus <strong>of</strong> icinalis<br />

subsp.<strong>of</strong>ficinalis<br />

Lili AR 150 Gn h 0 7 4 5871 7 4 3.8 16.2 713 3 7j 5 6 5,<br />

Asparagus <strong>of</strong>i cinalis<br />

I<br />

subsp.prostratus Uh N VU r 30 Gn 0 7 1 171 7 7 5.9 15.9 950 18, 19 8 4 6 3


S<br />

Taxon name Fam NS CS RS Chg li ght Len 1 P2 LF1 LF2 W Clonel Clone2 El E2 C Origin GB IR CI Tjan Tjul Prec Co Br Habitats L F R N<br />

Asperula cynanchica Rubi N n -0.47 50 hc Rhiz2 7 3 329 47 3 4.0 15.9 842 7 7 8 2<br />

Asp leniurn adianturn-nigrum Asp N n 45 hc 0 7 3 2146 708 14 3.7 14.6 1110 3, 16 6 5 5<br />

Asp lenium adianturn-nigrum<br />

sens.lat Asp N n 0.35 45 hc 0 8 3 2146 708 14 3.7 14.6 1110 3 6 5 5<br />

Asp lenium marinum Asp N n 0.02 35 hc 0 8 2 530 172 12 4.4 14.0 1261 Co 18 9 5 5<br />

Asp leniurn obovatum Asp N s -0.18 30 hc 0 9 1 135 19 11 5.3 15.4 1197 16 5 4 3<br />

Asp lenium onopteris Asp N o 45 hc 0 9 1 0 34 0 4.6 14.5 1200 1, 3, 16 5 7 3<br />

Asp leniurn ruta-muraria Asp N n 0.15 12 hc 0 7 6 2184 898 11 3.7 14.7 1074 3, 16, 17 7 7 2<br />

Asp leniurn septentrionale Asp N s -0.08 15 hc 0 7 3 55 2 0 2.5 13.2 1825 16 8 2 2<br />

Aspleniurn trichomanes Asp N n 0.07 35 hc 0 8 6 2294 911 12 3.6 14.5 1121 3, 16, 17 5 8 2<br />

Asplenium viride Asp N n -0.21 20 hc 0 4 6 435 43 0 2.0 12.8 1701 15, 16 4 8 3<br />

Aster (alien N American taxa) Aste AN 150 hc Rhizl Am 1211 53 5 3.7 15.3 934 3, 17, 21 7 7 6<br />

Aster lanceolatus Aste AN 120 hc Rhizl Am6 211 5 0 3.9 15.8 844 3, 17 7 7 6<br />

Aster lanceolatus x novi-belgii<br />

(A. x salignus) Aste AN 150 hc Rhizl Gard 373 9 0 3.8 15.6 890 3, 17 7 7 6<br />

Aster linosyris Aste N r -0.10 50 hc 0 7 3 c 9 0 0 4.9 15.8 1006 Co 18 8 8 1<br />

Aster novae-angliae Aste AN 200 hc Rhizl Am6 83 0 1 3.9 16.1 806 3 7 7' 6<br />

Aster novi-belgii Aste AN 150 hc Rhir l Am6 557 12 3 3.7 15.2 936 3, 17 7 7 6<br />

Aster tripolium Aste N n -0.44 100 hc 0 7 5 703 267' 3 4.3 14,8 1109 Co 21 9 7 6<br />

Astragalus alpinus Faba N VU r 30 hc 0 1 6 4 0 0 -0.9 11.0 1275 7, 15 9 6 2<br />

Astragalus danicus Faba N n -0.88 30 hc 0 7 6 c 242 3 0 3.3 14.8 745 7 8 8 2<br />

Astragalus glycyphyllos Faba N n -0.36 100 hc 0 7 3 357 0 0 3.4 15.7 711 1, 3, / 6 6 7 3<br />

NJ<br />

1‘ ) Athyrium distentifolium Wood N s 0.38 30 hc 0 1 6 98 0 0 0.3 11.2 2098 15 6 3 4<br />

Athyrium filix-femina Wood N n 0.25 90 hc 0 5 6 2574 849 12 3.5 14.4 1132 1, 16 5 5 6<br />

Athyriurn flexile Wood NE VU r 20 hc 0 1 1 16 0 0 -0.9 10.7 1753 15, 16 7 3 4<br />

Atriplex glabriuscula Chen N n -0.93 33 Th 0 5 2 780 159 10 4.2 14.4 1163 Co 19 9 7 8<br />

Atriplex laciniata Chen N n 0.38 30 Th 0 7 1 418 92 13 4.5 14.8 979 Co 19 9 7 7<br />

Atriplex littoralis Chen N n 1.59 100 Th 0 7 6 362 36 3 4.2 15.4 822 Co 19 9 7 6<br />

Atriplex longipes Chen N s 90 Th 0 4 3 39 0 0 4.2 15.6 982 Co 21 9 7 8<br />

Atrip/ex patula Chen N n -0.34 87 Th 0 6 4 2318 787 12 3.7 14.8 1013 3, 4 7 7 7<br />

Atriplex pedunculata Chen N CR r 30 Th 0 7 4 20 0 0 3.9 16.4 603 Co 21 91 7 8<br />

Atriplex portulacoides Chen N n 0.06 80 Pn 0 9 1 322 68 10 4.6 15.7 869 Co 21 9 8 6<br />

Atriplex praecox Chen N s 10 Th 0 4 3 62 0 0 3.6 12.8 1503 Co 19 9 7 6<br />

Atriplex prostrata Chen N n 1.10 100 Th 0 6 4 1847 349 5 3.9 15.1 955 3, 4, 19, 21 8 7 7<br />

Atropa belladonna Sola N n -0.33 150 hc 0 7 3 414 0 0 3.6 16.1 717 1, 3 5 6 6<br />

Avena fatua Poac AR 1.17 150 Th 0 Eur 1556 170 5 3.71 15A 849 3, 4 71 7 7<br />

Avena sativa Poac AC 150 Th 0 Eur 728 131 4 3.9 15A 903 4 7 7 7<br />

Avena strigosa Poac AC -3.01 120 Th 0 Crop 270 72 6 4.0 14.6 1042 4 7 5 5<br />

Azol a filicuboides . Azol AN 2.76 1 Hy Frag Am4, SAm 660 21 9 4.0 16.0 774 13, 14 7 11 8 8<br />

Baldellia ranunculoides Alis N n -1.08 20 20 Hy 0 Sto12 8 2 536 344 6 4. 1 15.1 974 13, 14 8 10 6 2<br />

Bal ota nigra Lami AR -0.37 100 hc Rhiz2 8 3 1365 70 12 3.8 15.7 797 3 71 4 8 6<br />

Barbarea intermedia Bras AN 1.92 60 hc 0 Eur 735 207 7 3.7 15.0 975 4 8 5 6 7<br />

Barbarea stricta Bras AN 0.50 100 p hc 0 5 4 c Eur, Asl 104 1 0 3.7 15.9 705 11, 13, 14 8 7 7 8<br />

Barbarea verna Bras AN 1.34 90 b Th hc 0 Eur 514 28 7 4, 1 15.6 943 3 8 5 6 6<br />

Barbarea vulgaris Bras N n -0.02 90 p hc 0 7 4 1869 615 3 3.7 15.0 943 3, 14 7 6 7 8<br />

Bartsia alpina Scro N r -0.10 22 hc Rhizl 1 3 18 .".0 0 0.4 11.9 2069 7, 11, 15 5 8 71 2


S<br />

Taxon name Fam NS CS RS Chg Hght Len 1 P2 LF1 LF2 W Clonel Clone2 El E2 C Origin GB IR CI Tja n Tjul Prec Co Br Habitats L F R N<br />

Bell is pe rennis Aste N n 0.89 8 hc h Rhizl 7 3 2797 984 14 3,5 14.5 1105 6 8 5 6 4<br />

Berberis vulgaris Serb NA n -0 61 250 Pn w Rhizl 7 3 974 26 1 3.4 15.2 892 1, 3 7 4 8 3<br />

Baru la erecta Apia N n -0.02 100 Hy h Irreg 7 3 1111 265 1 3.8 15.5 843 11 7 10 7 7<br />

Beta vulgaris Chen N n 1.23 150 b he h 0 9 1 607 205 14 4.6 15.4 952 Co 18, 19 9 5 7 8<br />

Betula nana Betu N s -0.09 100 Pn w Rhizl 2 6 125 0 0 0.71 11.5 1585 10, 12, 15 7 8 1 1<br />

Betula pendula Betu N n -0.23 2500 Ph w o 5 4 2293 390' 0 3.3 14.6 1073 1 7 5 4 4<br />

Betula pubescens Betu N n 0.40 2000 Ph w 0 5 4 2399 779 0 3.4 14.4 1123 1 7 7 4 4<br />

Bidens cernua Aste N n -0.54 67 Th 0 7 6 874 281 2 3.9 15.5 883 13, 14 8 9 7 7<br />

Bide ns tripartita Aste N n -0.43 67 Th o 7 5 1055 222 5 3.9 15.5 884 11, 13 8 8 7 7<br />

Blacks tonia perfoliata Gent N n 0.12 45 Th 0 9 2 7871 198 2 4.0 15.8 812 7 8 5 8 2<br />

Blechnum spicant Blec N n -0.39 50 hc o 7 3 2159 831 9 3.5 14. 1 1198 1, 2, 10, 16 5 6 3 3<br />

Blysmus compressus Cype N n -1.28 37 hc Rhiz2 7 3 c 384 0 3.2 15.2 840 11 8 8 8 3<br />

Blysmus rufus Cype N n -0.53 37' hc Rhiz2 4 3 367 7 0 3.8 13.6 1371 Co 21 8 8 7 4<br />

Bo lboschoe nus maritimus Cype N n 0.00 100 Hy Rhizl DRg 8 4 766 21 7 4.3 15.1 1020 Co 21 8 10 8 7'<br />

Bo trychium lunaria Ophi N n -0.43 15 Gn 0 5 6 1109 13 1 3.0 13.8 1259 7, 16 8 4 6 2<br />

Brachy podium pinnatum Poac N n 0.15 90 he Rhizl 7 4 612 2 0 3.6 15.9 745 7 7 3 8 3<br />

Brachy podium sylvaticum Poac N n -0.17 95 he 0 7 3 2310 78 12 3.7 14.7 1062 1 6 5 6 5<br />

Brassica napus Bras AN 2.88 130 b Th hc 0 Gard 1758 14 7 3.6 15.1 914 3, 4, 17 7 4 7 7<br />

Brassica nigra Bras NA n -0.02 150 Th 0 7 3 1080 5 11 4.0 15.8 822 3, 4 8 5 7 6<br />

Brassica oleracea Bras NA s 0.90 130 Pn sw 0 8 2 98 1 4.9 15.6 922 17, 18 8 4 71 8<br />

Brassica rapa Bras AR 0.74 100 b Th hc 0 7 4 1407 63 7 3.9 15.0 993 4 7 5 7 6<br />

Briza maxima Poac AN 62 Th 0 0 3 Eur 239 11 4.6 15.8 932 3, 17, 19 7 3 4 2<br />

Briza media Poac N n 0.75 62 he Rhizl 7 3 1853 58 2 3.5 14.9 971 7 8 5 7 3<br />

Briza minor Poac AR 0.28 55 Th 0 9 1 92 8 5.2 16. 1 919 4 7 4 5 5<br />

Bromopsis benekenii Poac N s 0.25 105 hc 0 7 3 c 64 0 3.0 15.3 896 1 5 5 7 5<br />

Bromopsis erecta Poac N n -0.01 110 hc 0 7 3 798 4 3 3.7 15.9 764 7 7 4 5 3<br />

Bromopsis inermis Poac AN 1.71 150 hc Rhiz2 7 4 Eur, Asl 263 0 3.6 15.9 757 3 8 4 8 5<br />

Bromopsis ramosa Poac N n -0.18 170 hc 0 7 3 1887 45 0 3.5 14.9 995 1 4 6 7 7<br />

Bromus commutatus Poac N n 1.07 95 Th 0 7 3 675 3 0 3.9 16. 1 772 3 7 4 8 6<br />

Bromus hordeaceus Poac N n -0.37 80 Th o 8 3 2406 83 14 3.71 14.7 1051 4, 6 8 4 71 4<br />

Bromus racemosus Poac N n 0.74 95 Th 0 7 3 516 7 0 4.0 15.8 852 3, 6 6 6 7 8<br />

Bromus secalinus Poac AR -1.15 90 Th 0 Unk 403 1 4 3.9 15.8 816 4 6 4 5 4<br />

Bryonia dioica Cucu N n -0.50 400 Gn 0 9 2 1004 4 3.6 16.0 726 3 7 5 7 7<br />

Bu ddleja davidii Budd AN 3.73 500 Ph w 0 As 1434 26 14 3.9 15.4 930 3, 17 7 5 7 5<br />

Bu nium bulbo cas tanum Apia N r 0. 14 50 Gn 0 8 2 13 0 3.3 16.3 633 4 71 4 9 4<br />

Bupleururn baldense Apia N EN r 10 Th 0 9 1 3 8 6.1 16.5 808 Co 18, 19 9 3 8 2<br />

Bupleurum falcatum Apia AN 100 hc 0 8 5 Eur, As 8 0 3.4 16.0 776 3 6 3 9 3<br />

Bupleurum rotun difolium Apia AR EW -4.58 30 Th 0 Eur? 287 1 3.8 16.0 753 4 8 3 9 4<br />

Bupleurum tenuissimum Apia N s -0.97 50 Th 0 8 3 161 0 4.2 16.4 684 3, 6 9 7 8 4<br />

Butomus umbellatus Buto N n -0.04 150 150 Hy Rhiz2 DRg 7 4 685 0 3.71 16.0 715 13, 14 7i 11 71 71<br />

Buxus sempervirens Buxa N r 2.54 500 Ph w O 9 2 2 0 3.7 16.6 716 1, 3 4 4 8 5<br />

Cakile maritima Bras N n -0.38 30 Th h 0 6 3 576 131 13 4.4 14.6 1011 Co 19 9 6 7 7<br />

Calamagrostis canescens Poac N n -0.33 120 hc h Rhiz2 5 4 c 293 0 0 3.4 157 723 11 7 9 7 5<br />

Calamagrostis epigej os Poac N n 0.47 200 hc h Rhiz2 5 5 936 9 4 3.7 15.7 812 3, 11 7 7 7 6<br />

Calamagrostis purpurea Poac N r 150 hc h Rhiz2 4 4 10 0 0 1.6 13.1 1346 1, 11 71 8 6 3<br />

Calamagrostis scotica Poac NE VU r 100 hc h Rhizl 4 1 1 0 0 3.6 12.8 888 11 8 8 6 4


Taxon name Fam NS CS RS Chg_ Hght Len P1 P2 LF1 LF2 W Clonel Clone2 E1 E2 C Origin GB IR CI Tjan Tjul Prec Co Br Habitats L F R N S<br />

Calamagrostis stricta Poac N r -0.74 100 hc Rhiz1 2 6 22 6 0 2.9 14.2 928 11 9 9 4 2<br />

Calendula <strong>of</strong>ficinalis Aste AN 50 a Th 0 Unk 764 24 10 4.0 15.7 822 3, 17 8 5 7 7<br />

Callitriche brutia Cal N 25 a Hz Node2 9 1 213 63 3 4.1 14.9 1087 13 8 10 5 5<br />

Ca Ilitriche hamulata Cal N 80 a p Hz Hy Node2 Irreg 5 2 1758 282 6 3.3 14.2 1162 13, 14 7 11 6 5<br />

Callitriche hamulata sens.lat Cal N 1.12 25 80 a p Hz Hy Node2 lrreg 6 3 1758 282 6 3.3 14.2 1162 11, 13, 14 7 10 5<br />

Callitriche hermap hm ditica Cal N 0.21 50 p Hy Irreg 4 6 392 115 0 3.1 13.7 1120 13 7 12 7 5<br />

Callitriche obtusangula Cal N 1.35 60 Hy Irreg 8 2 757 157 4 4.1 15.7 840 13, 14 7 11 7 6 1<br />

Ca llitriche platycarpa Cal N 15 100 p Hz Hy Node2 lrreg 7 3 1006 173 5 3.7 15.1 947 11, 13 6 10 7 7 0<br />

Callitriche stagnalis Cal N 15 60 p Hz Hy Node2 Irreg 7 3 1488 346 5 3.71 14.6 1083 13 7 10 6 6 1<br />

Ca & riche stagnalis sens.lat Cal N n 1.51 15 80 p Hz Hy Node2 Irreg 7 3 2647 769 11 3.5 14.4 1105 11, 13, 14 6 10 6 6<br />

Callitriche truncata Cal N s 0.47 20 Hz 0 Irreg 9 1 52 1 2 4. 1 16.1 719 13, 14 7 12 7 7<br />

Eric N n -0.64 60 Ch Pn 0 Nodel 5 3 2434 905 11 3.5 14.3 1157 10, 12 7 6 2 2


Taxon name Fan/ NS CS RS Chg Hght Len 1 P2 LF1 LF2 W Clonel Clone2 El E2 C Origin GB IR CI Tjan Tjul Prec Co Br Habitats L F R N S<br />

Carex binervis Cype N n -0.17 90 hc 0 7 / 1927 647 3 3.3 14.0 1243 8, 10, 16 7 6 3 2<br />

Carex buxbaumii Cype N VU r 70 hc Rhizl 4 4 c 3 1 0 3.3 13.5 1410 11 8 8 7 2<br />

Carex capillaris Cype N s -0.35 40 hc Ogr 2 6 120 0 0 1.2 11.9 1636 7 9 6 8 2<br />

Carex caryophyllea Cype N n -0.20 15 hc Rhizl 7 4 1866 437 11 3.4 14.7 1079 7 7 4 7 2<br />

Carex chordorrhiza Cype N VU r 40 hc Rhiz2 2 6 c 4 0 0 1.4 11.9 1176 11 9 9 4 3<br />

Carex curia Cype N n 0.17 50 hc Rhizl 4 6 1190 219 0 2.7 13.6 1303 11 8 9 3 2<br />

Carex davalliana Cype N EX x 25 hc 0 7 3 c 1 0 0 4.0 16.3 833 11 9 9 8 2<br />

Carex depauperata Cype N CR r 60 hc Rhizl 9 2 9 1 0 4. 1 15.8 823 3 5 4 71 4<br />

Carex di<strong>and</strong>ra Cype N n 0.22 60' hc Rhizl 5 6 378 294 0 3.6 14.4 1042 11 8 9 5 3<br />

Carex digitate Cype N s 0.04 15 hc 0 5 3 c 39 0 0 3.3 15.5 859 1, 16 5 5 8 4<br />

Carex dioica Cype N n -0.35 30 hc Rhizl 2 6 1100 204 0 2.7 13.2 1404 11 8 9 6 2<br />

Carex distans Cype N n -0.47 72 hc 0 8 3 814 213 9 4.3 15.0 1039 Co 21 8 6 7 5<br />

Carex disticha Cype N n -0.03 90 hc Rhiz2 7 4 12271 48 1 3 3.6 15.0 910 11 7 8 6 4<br />

Carex divisa Cype N s -0.35 70 hc Rhizl 9 2 162 1 4.4 16.4 727 6 8 7 7 6<br />

Carex divulsa Cype N n 82 hc 0 8 4 780 24 4.2 15.8 844 3, 6, 7 7' 4 7 6<br />

Carex echinata Cype N n -0.75 40 hc 0 5 3 2100 78 3.4 14.1 1207 11, 12, 14 8 8 3 2<br />

Carex elate Cype N n -0.32 95 Hy hc 0 7 5 294 22 3.8 15.2 903 11 7 10 7 5<br />

Carex elongate Cype N s 0.06 80 hc 0 5 4 c 72 1 3.6 15.5 899 1 5 8 6 6<br />

Carex erk etorum Cype N s -0.46 17 hc Rhizl 5 4 c 33 2.9 15.3 801 7 6 4 7 1<br />

Carex extensa Cype N n -0.23 40 hc Ogr 8 3 440 19 4.5 14.5 1228 Co 21 8 7 7 5<br />

Carex filiformis Cype N r 0.23 50 hc Rhiz2 7 4 c 13 3.5 16.3 708 6, 7 7 7 8 5<br />

NJ Carex /lam a Cype N n 0.53 50 hc Rhiz2 8 3 2706 95 3.5 14.5 1104 7, 11 7 5 6 2<br />

in Carex fi ava Cype N VU r 70 hc 0 5 3 1 3.2 14.7i 1585 1, 11 7i 9 8 2<br />

Carex hirta Cype N n 0.17 70 hc Rhiz2 7 3 1958 57 3.7 15.0 963 6 T 7 7 6<br />

Carex hostiana Cype N n -0.05 57 hc 0 7 3 1578 42 3.2 13.8 1290 11 8 9 6 2<br />

Carex humifi s Cype N s -0.01 10 hc Ogr 7 5 c 30 3.9 16. 1 845 7 8 3 8 2<br />

Carex lachenalii Cype N r -0.22 20 hc Rhizl 1 6 9 -1.1 10.4 1948 11, 15 8 7 4 1<br />

Carex laevigata Cype N n -0.01 120 hc 0 7 1 1012 29 3.6 14.4 1240 1, 16 5 8 5 4<br />

Carex lasiocarpa Cype N n 0.73 120 Hy hc Rhiz2 4 6 461 16 3.1 13.6 1383 11 8 10 6 3<br />

Carex fi mosa Cype N n 0.14 40 Hy hc Rhiz2 4 6 423 19 3.3 13.4 1431 11, 12 8 10 4 1<br />

Carex magellanica Cype N s -0.02 40 hc Rhizl 4 6 131 1.7 12.8 1808 12 9 9 2 1<br />

Carex marifi ma Cype N s -1.34 18 hc Rhiz2 1 6 83 3.6 12.9 964 Co 19 9 8 7 2<br />

Carex microglochin Cype N VU r 12 hc Rhiz2 1 3 1 -0.7 11.0 1855 11 9 9 8 2<br />

Carex montane Cype N s 0.68 35 hc Rhizl 7 3 c 48 4.0 15.5 1193 6, 8 7 6 4 1<br />

Carex muricata Cype N n 85 he 0 8 4 912 6 1 3.8 15.4 939 3, 7, 8 T 4 6 4<br />

Carex nigra Cype N n -0.01 70 hc Rhiz2 5 4 2582 87 3.5 14.3 1131 11 7 8 4 2<br />

Carex norvegica Cype N VU r 30 hc 0 1 6 6 -0.8 10.8 1901 15 8 7 7 2<br />

Carex ornithopoda Cype N r 0.28 15 hc 0 4 3 15 0 2.1 13.8 1272 7, 16 8 3 9 3<br />

Carex otrubae Cype N n -0. 14 100 hc 0 8 4 1636 40 9 4.0 15.3 939 11 6 8 7 7<br />

Carex Ova rls Cype N n -0.21 90 hc 0 5 4 2422 74 7 3.4 14.3 1138 3, 10 7 7 5 4<br />

Carex pallescens Cype N n -0.51 60 hc 0 5 4 1596 18 1 3.0 14.2 1236 1 6 6 5 4<br />

Carex panicea Cype N n -0.31 50 hc Rhiz2 5 3 2526 89 6 3.5 14.3 1139 11 8 8 4 2<br />

Carex paniculata<br />

Cype N n -0.11 150<br />

hc Hy 0 7 3<br />

1516 50 5 3.7 14.9 1036 1, 11 6 9 6 6,<br />

Carex pauciflora<br />

Cype N n -0.59 25'<br />

hc<br />

Rhizl 4 6<br />

377 0 1.7 12.1 1789 12<br />

8 9 1 1<br />

Carex pendula Cype N n 1.30 150 hc 0 8 3 1409 30 10 3.9 15.3 928 1, 14 5 8 7 6<br />

Carex pilulifera Cype N n -0.04 35 hc 0 7 3 2111 44 8 3.3 14.1 1197 8 7 5 3 2


R N<br />

6 6<br />

5 2<br />

7 3<br />

3 2<br />

7 5<br />

6 6<br />

7 7<br />

4 2<br />

7 2<br />

7 3<br />

6 4<br />

7 6<br />

6 5<br />

6 3<br />

5 4<br />

6 2<br />

onel Clone2 El E2 C Origin GB IR CI Tjan Tjul Pree Co Br Habitats L F<br />

7<br />

8,<br />

9<br />

8<br />

8<br />

4<br />

71<br />

8 1<br />

8<br />

8<br />

7<br />

3<br />

4<br />

7'<br />

8 1<br />

8<br />

754 11<br />

1239 11, 16<br />

1125 Co 18<br />

1541 15<br />

936 11<br />

1063 1, 14<br />

814 11, 14<br />

1193 11<br />

1699 15, 16<br />

2262 15<br />

823 3, 6, 7<br />

841 1, 14<br />

1050 1<br />

1904 15<br />

1072 11<br />

1169 11, 14, 19<br />

16.0<br />

13.9<br />

15.4<br />

10.6<br />

13.1<br />

14.8<br />

15.7<br />

14.0<br />

11.5<br />

11.3<br />

15.7<br />

15.7<br />

14.8<br />

11.3<br />

14.6<br />

14.2<br />

3.8<br />

3.3<br />

5.3<br />

-1.2<br />

3.1<br />

3.7<br />

3.9<br />

3.3<br />

0.7<br />

0.3<br />

3.6<br />

3.8<br />

3.6<br />

-0.1<br />

3.3<br />

3.5<br />

3<br />

4<br />

7<br />

0<br />

0<br />

5<br />

41<br />

0<br />

0<br />

0<br />

1<br />

0<br />

2<br />

0<br />

1<br />

9<br />

72<br />

656<br />

42<br />

0<br />

0<br />

675<br />

160<br />

731<br />

0<br />

0<br />

48<br />

102<br />

608<br />

0<br />

230<br />

855<br />

672<br />

1874<br />

56<br />

17<br />

4<br />

1879<br />

1186<br />

1924<br />

31<br />

71<br />

1043<br />

417<br />

1899<br />

83<br />

913<br />

2337<br />

7 4<br />

7 2<br />

8 2<br />

1 6<br />

4 1<br />

7 3<br />

7 4<br />

5 6<br />

1 6<br />

1 6<br />

7 3<br />

7 2<br />

7 5<br />

2 6<br />

5 6<br />

5 6<br />

hizl<br />

hizz21 h<br />

hiz2<br />

hiz2<br />

hIz21 h<br />

hiz2<br />

hizl<br />

a,<br />

84 2 1<br />

1200 11,14<br />

13.9<br />

3.1<br />

2<br />

434<br />

1168<br />

7 3<br />

2 0<br />

7 3 1<br />

8 6 0<br />

7 2 0<br />

s 6 0<br />

4 5 3<br />

7 6 1<br />

4 2 0<br />

s 5 0<br />

7 71 1<br />

7 3<br />

7 2<br />

7 3<br />

6 5<br />

6 5<br />

8 3<br />

6 3<br />

a 3<br />

8 3<br />

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8<br />

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7<br />

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8<br />

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6<br />

9<br />

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7<br />

7<br />

71<br />

8<br />

8<br />

9<br />

8<br />

9<br />

8<br />

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4<br />

s<br />

4<br />

9<br />

7<br />

1194 14<br />

1278 11, 19<br />

731 13<br />

947 7<br />

895 1<br />

962 Co 18, 19<br />

868 3, 6, 17<br />

1578 11, 14<br />

950 1<br />

936 13, 14<br />

1027 Co 18<br />

878 7, 17<br />

744 3<br />

836 3, 4, 17<br />

1093 6, 7<br />

632 6, 7<br />

980 7, 19<br />

1063 Co 19, 21<br />

841 Co 21<br />

1170 10<br />

825 Co 18<br />

896 3, 16, 17,<br />

763 1<br />

1166 1<br />

797 1<br />

2003 15, 16<br />

2178 . 15, 16<br />

14.2<br />

13.9<br />

16.4<br />

15.3<br />

15.4<br />

15.9<br />

15.0<br />

13.9<br />

15.2<br />

15.0<br />

15.1<br />

15.5<br />

16.1<br />

15.4<br />

14.5<br />

15.6<br />

15.1<br />

14.3<br />

16.1<br />

15.4<br />

16.5<br />

15.5<br />

16.2<br />

14.7<br />

16.2<br />

11.4<br />

11.3<br />

3.4<br />

3.8<br />

3.9<br />

3.9<br />

3.6<br />

5.7<br />

3.6<br />

3.4<br />

3.6<br />

3.8<br />

4.8<br />

4.1<br />

4.0<br />

3.8<br />

3.6<br />

3.8<br />

4.0<br />

3.8<br />

4.4<br />

5.8<br />

5.5<br />

4.0<br />

3.7<br />

3.7<br />

3.8<br />

0.4<br />

0.8<br />

6<br />

5<br />

0<br />

10<br />

9<br />

10<br />

2<br />

1<br />

12<br />

3<br />

14<br />

10<br />

3<br />

5<br />

11<br />

2<br />

14<br />

0<br />

8<br />

0<br />

2<br />

14<br />

0<br />

0<br />

0<br />

0<br />

0<br />

761<br />

179<br />

0<br />

243<br />

52<br />

8<br />

30<br />

42<br />

140<br />

304<br />

172<br />

494<br />

1<br />

56<br />

975<br />

125<br />

710<br />

3<br />

17<br />

0<br />

0<br />

357<br />

0<br />

31<br />

0<br />

0<br />

0<br />

2203<br />

477<br />

24<br />

1131<br />

1488<br />

79<br />

303<br />

296<br />

1693<br />

955<br />

463<br />

1216<br />

153<br />

884<br />

2658<br />

1239<br />

1811<br />

111<br />

457<br />

3<br />

3<br />

1361<br />

233<br />

131<br />

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7 4<br />

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7 2<br />

7 4<br />

8 3<br />

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18<br />

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7 3<br />

7 3<br />

7 3<br />

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hizl


Taxon name Fam NS CS RS Chg Hght Len P1 P2 LF1 LF2 W Clonal Clone2 El E2 C Origin GB IR CI Tja n Tjul Prec Co Br Habitats L F R N S<br />

Cerastium arvense Cary N n -1.05 30 p Ch Rhiz2 5 6 814 39 0 3.3 15.3 773 8 8 4 5. 3 0<br />

Co a st/UM brachypetalum Cary AN 30 a Th 0 8 3 Eur 2 0 0 3,4 16.3 657 3, 7 9 3 8 2 0<br />

Cerastiurn cerastoides Cary N s -0.05 12 p Ch Nodal 1 3 29 0 0 -0.4 10.8 1994 15 8 8 5 4 0<br />

Cerastiurn diffusum Cary N n 0.38 23 a Th 0 7 3 1174 247 12 4.0 14.6 1062 Co 18, 19 9 4 61 3 1<br />

Cerastium fontanum Cary N n 1.40 30 p Ch Rhizl Nodal 5 4 2805 985 14 3.5 14.4 1106 6 7 5 5 4 0<br />

Cerastium glomeratum Cary N n 1.44 30 a Th 0 8 3 2631 823 14 3.6 14.5 1079 3, 5 7 5 6 5 0<br />

Cerastium nigrescens Cary NE VU r 5 p Ch 0 4 1 2 0 0 3.0 11.5 1256 16 9 3 5 1 0<br />

Cerastiurn pumilum Cary N s -0.171 11 a Th 0 7 3 87 0 0 4,1 16.2 806 7 8 2 8 1 0<br />

Cerastium sernidec<strong>and</strong>rum Cary N n 0.50 14 a Th 0 7 3 1117 61 12 3.7 15.3 846 8, 18, 19 8 3 6 3 0<br />

Cerastium tomentosurn Cary AN 2.97 30 p Ch Rhiz2 Node2 Eur 1303 140 8 3.7 15.2 898 3, 17, 19 8 3 7 5 1<br />

Ceratocapnos claviculata Furna N n 0.57 75 a Th ' 0 7 1 1122 20 2 3.3 14.6 1111 1, 9 5 5 4 5 0<br />

Ceratochloa carinata Poac AN 2.09 80 p hc 0 Am4 183 1 2 3,8 16. 1 744 3, 4 8 5 6 6 0<br />

Ceratoch/oa cathartica Poac AN 0.63 100 p hc 0 Am, SAm 184 0 9 4.2 16.1 796 3 , 4 7i 4 5, 5 0<br />

Ceratophyllum demersum Gera N n 0.87 100 p Hy Irreg 6 6 927 62 1 3,7 15.8 770 13 7 12 7 7<br />

Ceratophyllum submersum Cera N n 0.39 100 p Hy Irreg 7 4 208 3 5 3,9 16.3 705 13 7 12 8 8<br />

Ceterach <strong>of</strong> icinarum AspI N n -0.30 20 p he 0 9 2 1093 787 9 4.0 15.0 1061 3, 16 7 3 8 1<br />

Chaenorhinum minus Scro AR -0.63 25 a Th 0 7 3 1468 170 0 3.6 15.3 899 3, 4, 17 8 4 7 4<br />

Chaerophyllum temulum Apia N n -0.64 100 b hc 0 7 3 1786 0 5 3.6 15.4 890 3 6 5 71 7i<br />

Chamaecyparis lawsoniana Cupr AN 4100 p Ph w 0 Arn4 827 46 4 3.6 15.3 965 17 5 5 6 4<br />

Chamaemelum nobile Aste N n -0.92 30 p hc h Node2 8 2 308 115 13 4.6 15.7 990 8 8 7 5 5<br />

Charnerion angustifolium Onag N n -0.01 150 p Gn hc h Root 5 6 2603 650 10 3.4 14.5 1075 3, 17 6 5 6 5<br />

Chelidonium rnaj us Papa AR -0.72 90 p he h 0 7 5 1662 220 9 3.7 15.3 905 3 6 5 8 7<br />

Chenopodium album Chen N n 100 a Th h 0 6 5 2340 782 14 3.7 14.8 1018 4 7 5 71 71 1<br />

Chenopodium album agg. Chen N n -0.73 100 a Th h 0 6 5 2340 782 14 3.7 14.8/ 1018 4 7 5 7 7 1<br />

Chenopodiurn bonus-henricus Chen AR -1.79 50 p hc h 0 Eur 1363 81 1 3,4 15.2 883 3 8 5 7 8 0<br />

Chenopodium<br />

chenopodioides Chen N s -0.17 30 a Th h 0 7 4 39 0 2 4.2 16.7 612 Co 6, 21 8 7 7 8 4<br />

Chenopodiurn ficifoliurn Chen AR 1.90 90 a Th h 0 7 4 745 11 7 3.9 16. 1 745 4 7 6 6 7 0<br />

Chenopodiurn glaucurn Chen AR -1.32 50 a Th h 0 7 6 157 2 2 4.0 16. 1 724 17 8 6, 7i 9 3<br />

Chenopodiurn hybridum Chen AR -0.32 100 a Th h 0 7 6 285 0 1 3.7 16.2 695 4 7 4 7 7 0<br />

Chenopodiurn murale Chen AR -1.63 100 a Th h 0 8 4 412 8 13 4.2 16.0 797 4 8 6 6 7 0<br />

Chenopodiurn polyspermum Chen AR 0.62 50 a Th h 0 7 4 998 8 12 3.9 16.0 794 4 7 6 7 8 0<br />

Chenopodiurn rubrum Chen N n' 1.00 70 a Th h 0 7 4 1267 142 8 3.8 15.7 800 4, 11 7 7 7 8 1<br />

Chenopodiurn urbicurn Chen AR 1 -4.57 100 a Th h 0 7 4 239 1 0 4.0 16.1 762 4 71 5 71 7t<br />

Chenopodiurn Chen AR VU -2.60 35 a Th h 0 8 4 180 0 6 4. 1 16.1 752 Co 15, 19 7 4 7 9<br />

Chrysanthemum segetum Aste AR -1.80 60 a Th h 0 8 3 1682 471 10 3.8 14.8 1022 4 7 5 6 5<br />

Chrysospleniurn alternifolium Saxi N n 0.62 20 p he h Sto12 3 6 790 0 0 2.8 14.4 1042 11, 14 5 8 6 6<br />

Chrysosplenium<br />

oppositifolium Saxi N n -0.36 15 p Ch hc h Node2 7 2 2067 688 6 3.4 14.3 1168 1, 14 5 9 5 5<br />

Cicendia filiformis Gent N s -0.70 10 a Th h 0 9 2 66 371 5 5.4 15.6 1063 10 9, 8 3 2<br />

Cicerbita alpina Aste N VU r 130 p hc h Rhiz2 4 3 4 0 0 -1.3 10.5 1375 15, 16 7 6 6 6<br />

Cicerbita rnacrophylla Aste AN 175 p hc h Rhiz2 Eur 724 42 0 3.3 14.9 920 3, 17 7 5 6 6<br />

Cichorium intybus Aste AR . -1.27' 110 p hc h 0 8 4 1312 60 10 3.8 15.5 840 3 5 4 7 5<br />

Cicuta virosa Apia N s 0.55 150 p Hy h 0 5 5 c 139 139 0 3.5 14.8 926 1/ , 13, 14 7 10 7 5<br />

Circaea alpina Onag N 5 . 30 p Gn h Rhiz2 4 6 40 0 0 2.2 13.0 1836 1 4 71 5; 5<br />

tJ


Taxon name Fam NS CS RS Ch Hght Len P P2 LF1 LF2 W Clonal Clone2 El E2 C Origin GB IR CI T an T'ul Prec Co Br Habitats L F R N S<br />

Circaea alpina x lutetiana (C<br />

x intermedia) Onag NH n 0.48 45 Gn Rhiz2 7 3 570 49 0 2.7 13.4 1477 1 6 6<br />

Circaea lutetiana Onag N n -0.38 60 Gn Rhiz2 7 3 2053 748 8 3.7 14,9 1041 1 6 6<br />

Cirsium acaule Aste N n -0.52 15 hc Rhial 7 3 734 0 3 3.7 16.1 742 7 4 3<br />

Cirsium arvense Aste N n 0.47 120 Gn Root 7 5 2736 968 14 3.6 14.5 1092 3, 4, 6 6 6<br />

Cirsium dissectum Aste N n -0. 14 60 hc Rhizl 7 1 539 553 2 4.0 15.0 1043 11 8 2<br />

Cirsium eriophorum Aste N n -0.08 150 hc 0 7 3 447 0 0 3.6 16.0 745 7 4 5<br />

Cirsium heterophyllum Aste N n -0.44 120 he Rhizl 4 4 761 1 0 2.0 12.9 1476 6, 16 6 5<br />

Cirsium palustre Aste N n 0.15 175 hc 0 5 4 2697 95 12 3.5 14.5 1105 11, 14 8 4<br />

Cirsium tuberosurn Aste N VU r 0.41 80 hc o 8 2 17 0 3.9 16.1 882 7 6 3<br />

Cirsium vulgare Aste N n 0.80 150 hc 0 7 4 2789 98 14 3.5 14.5 1103 3, 5, 6, 7 5 6<br />

Cladium mariscus Cype N n 0.11 200 Hy Gn Rhir l 8 4 232 25 1 4.1 14.7 1085 11 10 4<br />

Claytonia perfoliata Port AN 0.50 30 a Th 0 Am4 704 10 3.6 15.6 768 4, 17, / 9 6 5<br />

Claytonia sibirica Port AN 1.28 40 a p Th hc 0 As2, Am4 1166 2 6 3.2 14.4 1092 1, 3 7' 6<br />

Clematis vitalba Ranu N n 0.00 3000 p Ph 0 7 3 954 0 4.0 16.0 815 3 4 5<br />

Clinopodium acinos Lami N n -1.59 22 a Th 0 7 3 551 0 3.6 15.8 778 16 2 1<br />

Clinopodium ascendens Lami N n 0.04 60 P hc Rhizl 7 3 657 6 2 4.2 15.9 854 3, 16 5 6<br />

Clinopodium calamintha Lami N s -0.31 60 P hc Rhiz2 9 2 129 4 3.7 16.4 641 3 3 3<br />

Clinopodium menthifolium Lami N EN r 60 p hc Rhizl 7 3 1 0 4.8 16.3 844 1 5 5<br />

Clinopodium vulgare Lami N n -0.67 77 P hc Rhizl 7 6 1317 2 3.5 15.4 880 7 4 4<br />

Cochlearra anglica Bras N n 0.02 40 b hc 0 7 1 297 9 0 4.5 15.6 917 Co 21 8 6<br />

Cochlearia atlantica Bras NE DD r 20<br />

t.. )<br />

P he 0 4 1 2 0 4.4 12.8 1830 Co 18 6 5<br />

CO Cochlearia danica Bras N n 3.31 25 a Th 0 7 1 588 13 14 4.5 14.9 1056 Co 3, 18 6 5<br />

Cochlearia micacea Bras NE s 10 b p hc 0 1 1 32 0 0.2 11.4 2221 15 2<br />

Cochlearia <strong>of</strong>ficinalis Bras N n 30 P hc 0 3 6 1051 27 2 3.9 14.0 1246 Co 18, 21 6 5<br />

Cochlear la <strong>of</strong>ficinalis sens.lat Bras N n -0.18 30 b p hc 0 3 6 1245 30 3 3.7 13.9 1287 18 7 i 4<br />

Cochleada pyrenaica Bras N s 30 b p hc 0 1 3 124 0 1.5 12.9 1567 11, 16 7 3<br />

Coeloglossum viride Orch N n -1.34 22 P Gn 0 4 6 964 21 0 3.2 14.1 1148 7 4 2<br />

Coincya monensis Bras N s 0.43 50 b hc 0 8 2 61 3 4.2 14.8 1037 3, 17, 19 4 3<br />

Coincya wrightii Bras NE VU r 90 P Ch hc 0 7 1 1 0 5.8 15.7 986 Co 18 4 3<br />

Colchicum autumnale Li li N n -0. 14 35 p Gn Dtb 7 3 301 1 0 3.6 15.8 809 6 6 4<br />

Colutea arborescens Faba AN 400 p Ph 0 Eur 166 0 3.7 16.3 671 3, 17 4 3<br />

Conium maculatum Apia AR -0.02 250 b hc 0 8 4 1847 47 13 3.9 15.2 915 3 8<br />

Conopodium maj us Apia N n -0.19 40 a Gn 0 7 1 2520 75 7 3.5 14.5 1102 1, 6 5 5<br />

Consolida aj acis Ranu AN 60 a Th 0 Eur 360 7 3.8 16.2 703 3, 4, 17 4 4<br />

Convallaria maj alis Li li N n 0,25 25 P Gn Rhiz2 5 3 439 0 3.3 15.5 831 1, 7 5 5<br />

Convolvulus arvensis Cony N n -0.70 100 P Gn Rhiz2 8 4 1841 43 14 3.8 15.2 929 3, 4 4 6<br />

Conyza canadensis Aste AN 1.12 100 a Th 0 Am 1048 11 10 3.8 16.0 766 3, 4, 17, 19 4 6<br />

Corallorhiza trifida Orch N s 0.61 22 p Gn 0 4 6 c 102 0 0 2.5 13.5 956 1, 2 5 4<br />

Cori<strong>and</strong>rum sativum Apia AN 50 a Th 0 Eur? 201 2 3 3.9 16.0 763 3, 17 4 5<br />

Cornus sanguinea Corn N n -0.06 400 P Ph Root 7 3 1179 52 1 3.7 15.8 810 1, 3 5 6<br />

Cornus sericea Corn AN 300 p Pn Ph 0 Nodal Am 421 111 0 3.5 15.0 936 1, 3, 17 7 6<br />

Cornus suecica Corn N n -0.42 20 p hc Rhiz2 2 3 218 0 0 0.9 11.6 1853 10, 15 6 1 2<br />

Coronopus didymus Bras AN 1.77 18 a Th 0 Unk 1284 315 14 4.1 15.5 921 4, 17 5 6 7<br />

Coronopus squamatus Bras AR 0.33 25 a Th 0 8 3 1290 149 9 4.0 15.7 821 3, 4 5 7 7<br />

Corrigiola litoralis Cary N CR r -0.96 25 a Th 0 8 2 2 0 0 6.2 16.0 1052 Co 19 7 5 5


S<br />

,<br />

Taxon name Fam NS CS RS Chg Hght Len P1 P2 LF1 LF2 W Clonel Clone2 El E2 C Origin GB IR CI Tjan Tjul Prec Co Br Habitats L F R N<br />

Corylus avellana Beth N n -0.54 600 p Ph w 0 7 3 2470 870 5 3.5 14.6 1094 1, 3 4 5 6 6<br />

Cory nephorus canes cens Poac N r 0.01 32 P hc h 0 8 3 22 0 3 4. 1 16.2 649 Co 19 9 1 3 1<br />

Cotoneaster bullatus Rosa AN 400 p Ph w 0 As l 237 10 0 3.7 15.3 965 1, 3, 16, 17 7 4 7 4<br />

Cotoneaster cambricus Rosa AN EN 150 p Pn vv 0 7 1 Eur 1 0 0 5,4 15.5 796 7, 16 8 3 7 2<br />

Cotoneaster horiz ontalis Rosa AN 100 p Pn w 0 As 1 855 63 2 3.8 15.5 933 3, 16, 17 8 3 8 4<br />

Cotoneaster integrifolius Rosa AN 100 p Pn w 0 As l 537 103 2 3.9 14.7 1194 3, 17 7 3 7 4<br />

Cotoneaster microphyllus<br />

agg. Rosa AN 1.54 100 Pn w 0 Asl 576 135 3 3.9 14.7 1174 3, 16, 17 7 3 7 4<br />

Cotoneaster simonsii Rosa AN 3.55 300 Pn Ph w 0 Asl 973 122 5 3.7 14.9 1086 3, 10, 16, 17 6 5 6 4<br />

Crambe maritima Bras N n 0.29 62 hc h 0 7 3 25 1 46 11 4.8 15.5 938 Co 19 9 5 8 7<br />

Crassula aquatica Cras NA VU 8 a Hz h 0 Nodel 7 6 c 2 0 0 3.2 14.0 1459 14 8 9 5 5<br />

Crassula helmsii Cras AN 10 30 p Hy Ch h Irreg Node2 Aus, NZ 604 8 8 3.8 15.8 826 13, 14 7 10 6 7<br />

Crassula tillaea Cras N $ 0.86 5 a Th h 0 9 2 104 0 11 4.1 16.2 734 3 8 7 4 2<br />

Crataegus laevigata Rosa N n 0.32 1000 Ph w 0 7 3 597 0 1 3.5 16.2 674 1 5 5 7 5<br />

Crataegus m onogyna Rosa N n -0.76 1000 Ph w 0 7 3 2496 946 13 3.6 14.7 1073 1, 3 6 5 7 6<br />

Crepis biennis Aste N n -0.02 120 hc 0 7 3 288 th 0 3.7 16.3 711 3, 6 8 5 7 6<br />

Crepis capillaris Aste N n -0.17 75 a b Th hc 0 7 3 2525 907 14 3.6 14.6 1074 7 7 4 7 4<br />

Crepis foetida Aste AR EN 60 a hc Th 0 8 4 33 0 2 4.0 16.4 707 Co 19 9 4 6 3<br />

Crepis morns Aste N r -1.20 60 hc 0 7 3 c 75 0 0 1.7 13.2 1079 7 8 5 7 5<br />

Crepis paludosa Aste N n -0.27 80 hc 0 5 3 1162 357 0 2.7' 13.4 1334 11, 16 6 7 6 4<br />

Crepis praemorsa Aste N EN 60 hc 0 7 4 c 1 0 0 1.71 13.3 1333 7 8 3 9 3<br />

Crepis vesicaria Aste AN 0.60 80 hc 0 Eur 1227 302 14 4.1 15.7 858 3, 5, 6, 17 8 5 7 7<br />

Crithmurn maritimum Apia N n 0.23 45 hc 0 9 1 301 138 14 5.1 15.4 1042 Co 18 9 6 7 5<br />

Crocosmia aurea x poli sh (C.<br />

x crocosmiiflora) Irid AN 3.11 60 Gn Rhizl ORg Gard 1446 731 12 4.0 14.6 1129 1, 3, 17 7 6 4 4<br />

Cruciata laevipes Rubi N n -0.77 60 hc Rhiz2 7 4 1475 0 1 3.2 15.2 892 6 6 5 7 5<br />

Cryptogramma crispa Adia N n -0.63 15 hc 0 4 3 466 23 1.8 12.9 1678 10, 15, 16 7 5 2 3<br />

Cuscuta epithyrnum Cuse N n -1.28 1 a Th Sto12 8 4 494 27 1 4.3 15.9 846 10 7 6 2 2<br />

Cuscuta europaea Cusc N s 0.04 2 a Th Sto12 7 4 126 0 3.7 16.4 679 14 6 7 6 7<br />

Cymbalaria muralis Scro AN<br />

-0.10 8,<br />

Ch<br />

Node2<br />

Eur 2059 619 1 3.7 15.0 990 3, 16, 17, 19 7 5 7 6<br />

Cynodon dactylon<br />

Poac NA VU r -0.10 30<br />

hc<br />

Rh1z2 Node2 8 5<br />

2 0 6.4 15.6 1156 3, 5, 17 8 4 7 5<br />

Cynoglossum ge rmanicurn Bora N VU r -0.52 75 hc 0 7 3 c 50 0 3.71 16.5 676 1 6 5 8 71<br />

Cynoglossum <strong>of</strong>i cinale Bora N n -1.09 75 hc 0 7 4 718 42 3.9 15.8 780 7, 19 8 4 8 6<br />

Cynosurus cristatus Poac N n 0.02 75 hc 0 7 3 2745 962 1 3.5 14.5 1103 6 7 5 6 4<br />

Cyperus fuscus Cype N VU r -0.32 20 a Th 0 8 4 11 0 4.4 16.6 758 13 9 8 5 4<br />

Cyperus longus Cype N s 2.22 100 he Rhizl 8 3 33 0 1 5.7 16.1 943 11, 13 8 9 7 5<br />

Cypripedium calceolus Orch N CR r 30 Gn Rhizl 5 6 c 22 0 2.2 13.9 1270 7 5 4 8 4<br />

Cystopteris dickie ana Wood N VU r 20 hc 0 ? ? 5 0 0.9 12.3 1379 16 5 7 8 2<br />

Cystopteris fragilis Wood N n -0.69 20 hc 0 3 6 1118 191 2.6 13.5 1361 16 6 7 8 4<br />

Cystopteris montana Wood N r -0.25 15 hc Rhiz2 4 6 22 0 -0.2 11.3 2151 15, 16 5 7 9 2<br />

Cytisus seopar/us Faba N n 0.00 200 Pn w 0 7 3 2288 553 1 3.4 14.6 1085 3 8 5 4 4<br />

Daboe cia cantabrica Eric N o 0.12 50 Ch Pn w 0 8 1 0 33 4.5 14.4 1265 10 8 5 3 2<br />

Dactylis glomerata Poac N n -0.06 120 he h 0 8 4 2707 981 1 3.6 14.5 1091 6 7 5 7 6<br />

Dacty/orhiza fuchsii Orch N n 0.33 50 Gn h 0 7 4 2214 774 3.5 14.7 1063 11 7 8 7 3<br />

Dactylorhiza incarnata Orch N n -0.33 45 Gn h 0 5 4 1189 331 3.6 14.4 1127 11 8 9 6 2<br />

Dactylorhiza lapponica Orch N s 21 Gn h 0 4 3 15 0 3.2 12.5 1910 11 5 8 6 2


F R N S<br />

77 53 23 0 0<br />

6 7 3<br />

8 7 2 0<br />

6 7 2 1<br />

10 5 3 0<br />

Br Habitats<br />

12<br />

11<br />

11<br />

11<br />

11<br />

13<br />

7, 8<br />

1<br />

1<br />

17<br />

6, 7<br />

17<br />

1, 6<br />

8, 10<br />

12, 13<br />

4<br />

3, 16<br />

7<br />

16<br />

15<br />

8, 9<br />

3, 4, 17<br />

3, 4, 17<br />

15<br />

10<br />

3, 4, 16, 17<br />

3, 16, 17<br />

3, 6, 17<br />

3, 6, 17<br />

1, 3, 16<br />

3, 18, 19<br />

1, 3<br />

16<br />

7, 16<br />

3, 16<br />

15, 16<br />

11, 12<br />

12, 14<br />

12<br />

7, 16<br />

1, 16<br />

1, 16<br />

1<br />

11 .<br />

1, 2<br />

1, 15, 16<br />

El E2 C Origin GB IR CI Tjan Tjul Prec Co<br />

1221<br />

1237<br />

849<br />

1244<br />

978<br />

707<br />

1160<br />

760<br />

890<br />

796<br />

989<br />

913<br />

1099<br />

1177<br />

1211<br />

738<br />

805<br />

797<br />

979<br />

2845<br />

1120<br />

777<br />

783<br />

1686<br />

1465<br />

810<br />

790<br />

863<br />

863<br />

729<br />

898 Co<br />

921<br />

1191<br />

1584<br />

1151<br />

2311<br />

1422<br />

1337<br />

1269<br />

1734<br />

1373<br />

1160<br />

1075<br />

659<br />

1114<br />

1772<br />

W Clonel Clone2<br />

h 0<br />

h 0<br />

h 0<br />

h 0<br />

h 0<br />

h 0<br />

h 0<br />

w 0<br />

w 0<br />

h 0<br />

h 0<br />

h 0<br />

h 0 DRi<br />

h Ogr<br />

h 0<br />

h 0<br />

LF2<br />

65 74 2 5 0<br />

5 7 6 0<br />

4 7 8 0<br />

4 71 3 1<br />

65 75 8 4<br />

5 2 3<br />

9 2 1<br />

4 7i 6<br />

5 3 5 3 2<br />

2 7 1<br />

3 4 1<br />

6 4 5<br />

4 5 5<br />

4 5 5<br />

5 2 2<br />

4 1 2<br />

4 71 6<br />

h 0<br />

0<br />

0<br />

sw<br />

sw<br />

w 0<br />

h 0<br />

h 0<br />

h 0<br />

Taxon name Fam NS CS RS Chg Hght Len P1 P2 LF1<br />

40 p Gn<br />

30 p Gn<br />

50 p Gn<br />

25 p Gn<br />

30 p Gn<br />

30 a Hz<br />

40 p hc<br />

100 p Pn<br />

100 p Pn<br />

100 a Th<br />

100 b hc<br />

120 b hc<br />

150 p hc<br />

60 p hc<br />

70 p hc<br />

100 a Th<br />

60 a Th<br />

37 p Ch<br />

20 p Ch<br />

6 p Ch<br />

150 b hc<br />

35 a Th<br />

50 a Th<br />

10 p Ch<br />

8 p Ch<br />

60 a Th<br />

80 p Ch<br />

200 b hc<br />

200 b hc<br />

150 b hc<br />

9 p Ch<br />

80 p hc<br />

10 p Ch<br />

35 b hc<br />

50 a Th<br />

5<br />

Ch<br />

13<br />

hc<br />

5<br />

hc<br />

5<br />

hc<br />

10<br />

Ch<br />

60<br />

hc<br />

80<br />

he<br />

80<br />

hc<br />

60<br />

hc<br />

150<br />

hc<br />

80<br />

hc<br />

f.a<br />

c)<br />

57 77 76<br />

sw Rhiz2<br />

sw Rhiz2<br />

h 0<br />

h 0<br />

h 0<br />

h 0<br />

hc<br />

76 78 7 7<br />

3 4 5<br />

5 6 5<br />

4 9 3<br />

5 7 2<br />

6 7 6<br />

5 71 3<br />

99 22 1 1<br />

9 2 1<br />

4 7 2<br />

6 2 3<br />

6 5 5<br />

8 5 4<br />

9 4 4<br />

6 4 5<br />

6 3 2<br />

h 0<br />

sw Node2<br />

Rhizl<br />

0<br />

0<br />

0<br />

0<br />

0<br />

0<br />

0<br />

w Node2<br />

0<br />

0<br />

0 Rhizl<br />

0<br />

0<br />

0


N<br />

IR<br />

Origin<br />

LF2<br />

1 P2<br />

Chg<br />

RS<br />

n<br />

n<br />

n<br />

x<br />

s<br />

CS<br />

5<br />

5<br />

2<br />

4<br />

3<br />

8<br />

5<br />

4<br />

4<br />

5<br />

5<br />

5<br />

1<br />

4<br />

5<br />

2<br />

4<br />

2<br />

R<br />

6 5<br />

6 5<br />

5 2<br />

6 4<br />

5 9,<br />

5 7<br />

3 5<br />

4 7<br />

5<br />

5<br />

7<br />

9 5<br />

NS<br />

N<br />

N<br />

N<br />

N<br />

N<br />

AN<br />

AR<br />

N<br />

N<br />

N<br />

N<br />

N<br />

N<br />

N<br />

N<br />

N<br />

N<br />

N<br />

AN<br />

AN<br />

N<br />

N<br />

N<br />

N<br />

N<br />

N<br />

N<br />

AN<br />

AN<br />

N<br />

N<br />

N<br />

N<br />

N<br />

N<br />

N<br />

N<br />

N<br />

N<br />

N<br />

N<br />

N<br />

N<br />

NE<br />

N<br />

N<br />

Fam<br />

Dry o<br />

Taxon name<br />

Dryopteris filix-mas<br />

0.03<br />

0.24<br />

NHem<br />

LF1<br />

hc<br />

hc<br />

he<br />

hc<br />

he<br />

Th<br />

hc<br />

hc<br />

Hz<br />

Hz<br />

Hy<br />

hc<br />

hc<br />

Hy<br />

hc<br />

hc<br />

hc<br />

Hy<br />

Hy<br />

Hy<br />

he<br />

he<br />

he<br />

hc<br />

Ch<br />

hc<br />

he<br />

he<br />

hc<br />

hc<br />

hc<br />

hc<br />

hc<br />

hc<br />

he<br />

hc<br />

hc<br />

Gn<br />

Gn<br />

Gn<br />

Gn<br />

Gn<br />

Gn<br />

Gn<br />

Gn<br />

Gn<br />

Hght Len<br />

120<br />

120<br />

50<br />

80<br />

60<br />

120<br />

67<br />

90<br />

5 10<br />

5 10<br />

10<br />

60<br />

35<br />

60<br />

8<br />

30<br />

60<br />

45<br />

300<br />

300<br />

110<br />

105<br />

55<br />

125<br />

30<br />

20<br />

10<br />

4<br />

75<br />

150<br />

60<br />

75<br />

75<br />

60<br />

75<br />

75<br />

75<br />

30<br />

80<br />

60<br />

45<br />

42<br />

65<br />

60<br />

22<br />

90<br />

0.10<br />

0.75<br />

0.36<br />

-0.24<br />

1.07<br />

0.66<br />

-0.11<br />

,<br />

n<br />

n<br />

s<br />

n<br />

r<br />

n<br />

n<br />

r<br />

n<br />

n<br />

n<br />

F<br />

EN<br />

Hy<br />

p<br />

he<br />

9 4<br />

6<br />

9 71<br />

9 7<br />

9 7<br />

4<br />

L F<br />

5<br />

5<br />

7<br />

6<br />

8<br />

6<br />

9<br />

8<br />

7 10<br />

71 10<br />

7 10<br />

8<br />

8<br />

8 10<br />

6<br />

9<br />

8<br />

8 11<br />

W Clonel Clone2 El E2 C<br />

0 7 6<br />

0 5 6<br />

0 4 2<br />

0 4 3<br />

0 9 3<br />

0<br />

0 9 1<br />

0 7 4<br />

0 Nodel 7 3<br />

0 Nodel 5 4 c<br />

Rhiz2 5 6<br />

Rhiz2 4 3<br />

0 7 2<br />

Rhiz2 6 5<br />

Rhiz2 7 3<br />

Rhizl 5 3<br />

Rhiz2 7 6<br />

Irreg 8 1<br />

Irreg<br />

Irreg<br />

0 5 4<br />

Rhiz2 8 3<br />

Rhiz2 8 3<br />

Rhiz2 6 4<br />

w Node2 2 6<br />

Rhizl 1 3<br />

Stoll 1 6<br />

Node2<br />

0<br />

Rhiz2 8 5<br />

0 9 2<br />

0 7 3<br />

0 7 3<br />

Rhizl 5 6<br />

0 7 3<br />

0 7 4<br />

0 7 4<br />

0 5 4<br />

0 7 5<br />

hc<br />

0.47<br />

0.91<br />

0.00<br />

0.02<br />

0.60<br />

0.37<br />

0.37<br />

VU<br />

67<br />

8<br />

6<br />

6<br />

7<br />

1<br />

4<br />

3<br />

3<br />

6<br />

71<br />

5<br />

6<br />

5<br />

3<br />

5<br />

7<br />

5<br />

1<br />

4<br />

4<br />

3<br />

4<br />

4<br />

3<br />

4<br />

6<br />

771<br />

7<br />

7<br />

7<br />

7<br />

2<br />

6<br />

6<br />

4<br />

6<br />

71<br />

6<br />

6<br />

5<br />

5<br />

71<br />

7<br />

5<br />

8<br />

7<br />

9<br />

7<br />

7<br />

8<br />

5<br />

7i<br />

6<br />

7 6 11<br />

7<br />

9<br />

9<br />

7<br />

7<br />

8<br />

8<br />

7<br />

7<br />

71<br />

7<br />

6<br />

6<br />

7<br />

71<br />

6<br />

6<br />

7<br />

4<br />

3<br />

8<br />

3<br />

2<br />

3<br />

2<br />

7<br />

Co Br Habitats<br />

1, 2<br />

1, 2<br />

15, 16<br />

1, 2<br />

16<br />

17<br />

4<br />

7<br />

13<br />

13<br />

13, 14<br />

13, 14<br />

11, 12, 13<br />

11<br />

Co 21<br />

11<br />

11<br />

11<br />

13, 14<br />

13, 14<br />

1, 3<br />

Co 19, 21<br />

Co 19<br />

3, 4, 19<br />

10, 12, 15<br />

11, 16<br />

11, 15<br />

14, 15, 16<br />

3, 4, 17<br />

11, 14<br />

3, 16, 17<br />

3, 16, 17<br />

11, 14<br />

11, 14<br />

11<br />

1, 3, 14, 17<br />

3, 17<br />

16<br />

1, 7<br />

1<br />

11<br />

1<br />

1<br />

1<br />

1<br />

3, 4<br />

Prec<br />

1096<br />

1096<br />

1810<br />

1998<br />

1527<br />

785<br />

848<br />

822<br />

1365<br />

1072<br />

924<br />

1348<br />

1348<br />

1098<br />

1130<br />

1323<br />

1182<br />

1259<br />

936<br />

836<br />

981<br />

863<br />

1050<br />

1046<br />

1381<br />

1832<br />

1880<br />

1357<br />

972<br />

971<br />

937<br />

1091<br />

1104<br />

1146<br />

996<br />

893<br />

834<br />

1328<br />

946<br />

808<br />

915<br />

774<br />

728<br />

820<br />

721<br />

1087<br />

Tjul<br />

14.5<br />

14.5<br />

12.6<br />

13.4<br />

13.7<br />

16.0<br />

15.9<br />

15.6<br />

14.2<br />

14.71<br />

15.2<br />

13.2<br />

14.0<br />

14.5<br />

15.3<br />

13.5<br />

14.4<br />

14.2<br />

15.1<br />

15.8<br />

14.9<br />

15.9<br />

14.5<br />

14.6<br />

13.2<br />

11.9<br />

11.6<br />

13.6<br />

15.0<br />

15.0<br />

16.0<br />

14.5<br />

14.5<br />

14.3<br />

14.9<br />

15.5<br />

15.9<br />

13.8<br />

15.3<br />

15.7<br />

15.3<br />

16.0<br />

16.3<br />

14.3<br />

16.1<br />

14.5<br />

CI Tjan<br />

13 3.5<br />

13 3.5<br />

0 1.9<br />

0 2.7<br />

0 2.1<br />

10 4.0<br />

7 4.7<br />

9 3.8<br />

3 3.7<br />

0 3.6<br />

1 3.6<br />

0 1.4<br />

7 3.7<br />

10 3.5<br />

0 4.6<br />

4 3.1<br />

2 4.0<br />

3 3.7<br />

3 3.6<br />

3 3.7<br />

0 3.3<br />

8 4.6<br />

9 4.4<br />

13 3.6<br />

0 2.7<br />

0 1.0<br />

0 0.9<br />

2 3.0<br />

9 3.7<br />

12 3.8<br />

12 4.4<br />

10 3.5<br />

8 3.5<br />

3 3.4<br />

11 3.8<br />

0 3.6<br />

7 3.9<br />

0 3.0<br />

0 3.6<br />

0 3.6<br />

3 3.9<br />

0 3.8<br />

0 3.6<br />

0 2.8<br />

0 3.6<br />

12 3.5<br />

928<br />

928<br />

5<br />

1<br />

0<br />

4<br />

0<br />

41<br />

79<br />

19<br />

89<br />

0<br />

330<br />

756<br />

5<br />

267<br />

95<br />

286<br />

424<br />

15<br />

122<br />

41<br />

180<br />

837<br />

236<br />

1<br />

0<br />

423<br />

400<br />

795<br />

0<br />

894<br />

758<br />

812<br />

824<br />

24<br />

0<br />

13<br />

161<br />

0<br />

160<br />

9<br />

0<br />

0<br />

0<br />

921<br />

GB<br />

2650<br />

2650<br />

308<br />

1<br />

33<br />

370<br />

79<br />

1066<br />

212<br />

33<br />

366<br />

14<br />

962<br />

2577<br />

15<br />

1236<br />

574<br />

889<br />

1696<br />

808<br />

1669<br />

370<br />

572<br />

2530<br />

1359<br />

218<br />

236<br />

1226<br />

2005<br />

2036<br />

371<br />

2630<br />

2347<br />

2417<br />

2070<br />

937<br />

1171<br />

60<br />

1218<br />

86<br />

447<br />

134<br />

235<br />

10<br />

8<br />

2666<br />

Am<br />

Am<br />

0.27<br />

0.32<br />

-0.28<br />

-0.01<br />

-0.29<br />

-0.41<br />

-0.76<br />

1.42<br />

3.88<br />

0.12<br />

0.07<br />

-0.39<br />

0.38<br />

-0.18<br />

-0.41<br />

-0.25<br />

1.66<br />

0.16<br />

0.08<br />

0.26<br />

-0.39<br />

0.19<br />

-0.08<br />

n<br />

n<br />

n<br />

n<br />

n<br />

n<br />

n<br />

NZ<br />

Am<br />

Ch<br />

0Rhiz2 7 7 43<br />

0 7 3<br />

0 7 3<br />

0 7 1<br />

Rhiz2 4 5<br />

Rhiz2 3 6<br />

n<br />

n<br />

n<br />

n<br />

n<br />

n<br />

n<br />

n<br />

s<br />

n<br />

s<br />

n<br />

s<br />

n<br />

r<br />

x<br />

n<br />

EN<br />

CR<br />

0.39


F R N S<br />

10 6 4<br />

78 76 6 3<br />

7 5 4<br />

4 8 5<br />

8 5 5<br />

8 7 6<br />

8 8 3<br />

5, 7 6<br />

1 P2 LF1 LF2 W<br />

Gn Hy<br />

Gn<br />

Gn<br />

Gn<br />

Gn<br />

Gn<br />

Gn<br />

Gn<br />

Chg<br />

0.42<br />

0.30<br />

0.18<br />

0.11<br />

RS<br />

n<br />

n<br />

n<br />

s<br />

-0.35<br />

0.41<br />

-0. 12<br />

1.59<br />

-0.11<br />

-0.94<br />

n<br />

n<br />

s<br />

Gn<br />

7 1 1<br />

56 22 2 2<br />

8 2 1<br />

8 2 1<br />

6 4 1<br />

5 7 3<br />

5 7 2<br />

3 7 2<br />

3 8 2<br />

11 4 1<br />

CI<br />

8<br />

0<br />

8<br />

0<br />

0<br />

0<br />

3<br />

0<br />

0<br />

0<br />

13<br />

0<br />

0<br />

2<br />

0<br />

5<br />

0<br />

11<br />

1<br />

E2 C Origin<br />

6<br />

6<br />

6<br />

6<br />

5 Eur, As<br />

6<br />

3<br />

6<br />

Eur<br />

1<br />

1<br />

1<br />

0<br />

2<br />

1<br />

6<br />

4<br />

SAm<br />

Eur<br />

0<br />

6<br />

6 c<br />

3<br />

6<br />

4<br />

4<br />

2<br />

2<br />

1<br />

Ch Pn<br />

Ch Pn<br />

Pn<br />

Ch Pn<br />

Ch Pn<br />

Pn<br />

b Th hc<br />

Ch<br />

Ch<br />

Ch<br />

Hy<br />

hc<br />

hc<br />

hc<br />

hc<br />

Th<br />

Th<br />

Th<br />

Th<br />

Th<br />

Th<br />

Th<br />

Th<br />

Th<br />

Th<br />

hc<br />

hc<br />

Th<br />

Ch Pn sw<br />

Ph<br />

hc<br />

Ch<br />

hc<br />

Fight Len<br />

100<br />

100<br />

60<br />

60<br />

120<br />

90<br />

180<br />

60<br />

15<br />

60<br />

60<br />

120<br />

60<br />

60<br />

80<br />

50<br />

20<br />

25<br />

20<br />

20<br />

60<br />

60<br />

60<br />

50<br />

40<br />

40<br />

15<br />

20<br />

40<br />

9<br />

9<br />

10<br />

10<br />

60<br />

75<br />

60<br />

90<br />

60<br />

600<br />

150<br />

70<br />

40<br />

r<br />

n<br />

o<br />

o<br />

n<br />

r<br />

n<br />

r<br />

-0.91<br />

-0.07<br />

0.33<br />

-0. 11<br />

2.37<br />

1.52<br />

0.18<br />

-0.79<br />

-0.20<br />

0.36<br />

-0.36<br />

99 44 21<br />

9 7 2<br />

8 2 1<br />

4 6 4<br />

4 6 4<br />

4 7 2<br />

4 6 6<br />

4 6 5<br />

3 7 3<br />

3 7 3<br />

3 6 3<br />

3 7 3<br />

4 7 7<br />

3 6 3<br />

4 6 5<br />

5 7 7<br />

4 8 5<br />

5 8 5<br />

8 6 7<br />

5 6 6<br />

3 7 3<br />

4 8 5<br />

Br Habitats L<br />

11<br />

1, 11, 14<br />

11<br />

11<br />

6<br />

1, 16<br />

11<br />

11<br />

1, 3, 17<br />

10, 12<br />

10<br />

10, 13, 14<br />

10, 12<br />

10, 12<br />

10<br />

3, 16<br />

15, 16<br />

3, 16, / 7<br />

3, 16<br />

13<br />

12<br />

11<br />

11<br />

12<br />

19<br />

19<br />

19<br />

18, 19<br />

3, 4<br />

3, 16, 17<br />

3, 16, 17<br />

3, 16, 17<br />

3, 16, 17<br />

3, 16<br />

3, 5<br />

19<br />

3, 4<br />

3, 16, 17<br />

1, 3<br />

11<br />

1<br />

3, 4, 7, 19<br />

Prec Co<br />

1116<br />

1108<br />

1091<br />

1406<br />

740<br />

1269<br />

950<br />

1224<br />

716<br />

1011<br />

1226<br />

1395<br />

1593<br />

1230<br />

1047<br />

774<br />

1653<br />

904<br />

1121<br />

1435<br />

1194<br />

1006<br />

1394<br />

1307<br />

902<br />

902<br />

959 Co<br />

996 Co<br />

880<br />

997<br />

844<br />

918<br />

1011<br />

809<br />

856<br />

1010 Co<br />

804<br />

848<br />

904<br />

974<br />

827<br />

838<br />

Tjul<br />

14.4<br />

14.0<br />

14.5<br />

12.7<br />

16.3<br />

13.7<br />

15.2<br />

14.0<br />

15.6<br />

15.9<br />

14.0<br />

14.0<br />

13.7<br />

14.0<br />

15,5<br />

15.9<br />

10.6<br />

15.9<br />

14.5<br />

14.1<br />

14.1<br />

15.4<br />

13.6<br />

13.6<br />

15.2<br />

15.2<br />

15.5<br />

15.6<br />

15.8<br />

14.9<br />

15.5<br />

15.2<br />

14.7<br />

15.9<br />

16.1<br />

152<br />

15.7<br />

15.6<br />

15.4<br />

15.2<br />

16. 1<br />

15.6<br />

Tjan<br />

3.5<br />

3.0<br />

3.4<br />

1.8<br />

4.1<br />

2.9<br />

3.8<br />

3.4<br />

3.4<br />

5.7<br />

3.5<br />

4.3<br />

4.0<br />

3.4<br />

6.0<br />

3.8<br />

-1.2<br />

4.6<br />

3.3<br />

4.4<br />

3.4<br />

4.5<br />

2.7<br />

3.1<br />

3.8<br />

3.8<br />

5.0<br />

5.3<br />

4.6<br />

3.5<br />

3.7<br />

3.6<br />

3,4<br />

IR<br />

847<br />

112<br />

704<br />

35<br />

0<br />

334<br />

426<br />

129<br />

0<br />

0<br />

712<br />

24<br />

10<br />

781<br />

1<br />

80<br />

0<br />

34<br />

55<br />

70<br />

831<br />

14<br />

100<br />

560<br />

167<br />

167<br />

13<br />

33<br />

80<br />

40<br />

11<br />

177<br />

423<br />

25<br />

1<br />

106<br />

80<br />

97<br />

483<br />

410<br />

0<br />

2<br />

GB<br />

2494<br />

238<br />

2534<br />

170<br />

2<br />

1561<br />

1248<br />

170<br />

614<br />

19<br />

1999<br />

0<br />

0<br />

1962<br />

6<br />

974<br />

10<br />

292<br />

341<br />

8<br />

2134<br />

17<br />

575<br />

1516<br />

1666<br />

1666<br />

74<br />

195<br />

338<br />

359<br />

123<br />

1074<br />

2180<br />

141<br />

46<br />

291<br />

929<br />

907<br />

1254<br />

1715<br />

704<br />

369<br />

Clonel Clone2 El<br />

Rhiz2 5<br />

Rhiz2 5<br />

Rhiz2 5<br />

Rhiz2 4<br />

Rhiz2 8<br />

Rhiz2 5<br />

Rhiz2 8<br />

Rhiz2 2<br />

0<br />

w 0 8<br />

w 7<br />

w 8<br />

w 0 7<br />

w Nodel 7<br />

w O 8<br />

0 5<br />

0 1<br />

0<br />

0<br />

Rhizl DRa<br />

Rhiz2<br />

Rhiz2<br />

Rhiz2<br />

Ogr<br />

0<br />

0<br />

0<br />

0<br />

0<br />

0<br />

0<br />

0<br />

0<br />

0<br />

0<br />

0<br />

0<br />

r<br />

n<br />

r<br />

n<br />

n<br />

n<br />

n<br />

s<br />

n<br />

n<br />

s<br />

n<br />

n<br />

NS CS<br />

N<br />

N<br />

N<br />

N<br />

AN<br />

N<br />

N<br />

N<br />

AN<br />

N<br />

N<br />

N<br />

N<br />

N<br />

N<br />

N<br />

N VU<br />

AN<br />

AN<br />

N<br />

N<br />

N VU<br />

N<br />

N<br />

N<br />

N<br />

N<br />

N<br />

AR<br />

N<br />

N<br />

N<br />

N<br />

AN<br />

AR VU<br />

N<br />

AR<br />

AR<br />

N<br />

N<br />

N<br />

AN<br />

Taxon name Fam<br />

Equi<br />

Equi<br />

Equi<br />

Equi<br />

Equi<br />

Equi<br />

Equi<br />

Equi<br />

Ranu<br />

Eric<br />

Eric<br />

Eric<br />

Eric<br />

Eric<br />

Eric<br />

Aste<br />

Aste<br />

Aste<br />

Orob<br />

Eno<br />

Cype<br />

Cype<br />

Cype<br />

Cype<br />

Gera<br />

Gem<br />

Gem<br />

Gera<br />

Gem<br />

Bras<br />

Bras<br />

Bras<br />

Bras<br />

Bras<br />

Apia<br />

Apia<br />

Bras<br />

Bras<br />

Cela<br />

Aste<br />

Euph<br />

Euph<br />

1<br />

1<br />

-0.11<br />

1<br />

1<br />

0.38<br />

0.47<br />

11<br />

8 4<br />

0 3,9<br />

2 4.6<br />

4.7<br />

2 3.7<br />

8 4.0<br />

0 3.9<br />

3.9<br />

9 4.1<br />

2 3.6<br />

Eur<br />

11<br />

8 3<br />

8 3<br />

0.52<br />

-0.02<br />

-0.41<br />

-0.80<br />

-0.65<br />

1.05<br />

0.15<br />

-0.15<br />

-0.22<br />

0.98<br />

n<br />

Unk<br />

Gard<br />

7 3<br />

7 3<br />

7 3<br />

7 3 c Eur<br />

11<br />

w Root<br />

h Rhizl<br />

h 0<br />

h Root<br />

n<br />

n<br />

n<br />

4 71 5<br />

3<br />

4<br />

4, 17<br />

715<br />

783<br />

973<br />

16.1<br />

15.8<br />

14.9<br />

1 3.7<br />

3 3.9<br />

12 3.8<br />

0<br />

125<br />

642<br />

169<br />

1039<br />

2114<br />

Eur<br />

5 6 6<br />

8 3<br />

8 5<br />

h Root<br />

h 0<br />

h 0<br />

hc<br />

Th<br />

Th<br />

80<br />

20<br />

40<br />

-1.18<br />

-0.77<br />

AN<br />

AR<br />

AR<br />

Euph<br />

Euph<br />

Euph


F R N S<br />

5 57 45 0<br />

7 5 3<br />

7 5 3<br />

0<br />

0<br />

3<br />

0<br />

0<br />

0<br />

0<br />

0<br />

0<br />

1<br />

0<br />

3<br />

,<br />

Taxon name Fam NS CS RS Chg_ Hght Len P1 P2 LF1 LF2 W Clonel Clone2 El E2 C Origin GB IR CI Tjan Tjul Prec Co Br Habitats L<br />

Euphorbra hyberna Euph N VU r 52 p hc 0 8 2<br />

2 137 0 5.2 14.9 1203 1, 3 5<br />

Euphorbia lathyris Euph AR 2.16 120 b Ch 0 8 3<br />

956 21 13 3.8 15.8 804 3, 16, 17 6<br />

Euphorbia paralias Euph N n -0.35 52 Ch 0 9 1<br />

182 65 8 5./ 15.6 987 Co 19 9<br />

Euphorbia peplis Euph N EW x -1.49 5 Th 0 9 1<br />

26 1 8 5.8 16. 1 969 Co 19 9<br />

Euphorbia peplus Euph AR -0.17 30 Th 0 8 3<br />

1911 52 14 3.8 15.1 950 4, 17 7<br />

Euphorbia platyphyllos Euph AR -0.24 70 Th 0 8 3<br />

248 0 3.9 16.3 733 4 7<br />

Euphorbia portl<strong>and</strong>ica Euph N n -0.09 35 Ch 0 8 /<br />

148 8 14 5.3 15.4 1060 Co 18, 19 8<br />

Euphorbia serrulata Euph NA VU r 1.20 65 Th 0 8 3<br />

13 0 4. 1 16.3 812 1, 3 5<br />

Euphrasia anglica Scro NE n 20 Th 0 7 1<br />

375 5 0 4. 1 15.3 1081 10, 16 71<br />

Euphrasia arctica Scro N n 30 Th 0 5 1<br />

1095 47 0 3.2 13.6 1315 6, 11 7<br />

Euphrasia cambrica Scro NE VU r 8 Th 0 1 1<br />

5 0 2.8 13.2 2458 15 8<br />

Euphrasia campbelliae Scro NE r 10 Th 0 4 1<br />

11 0 4.0 12.5 1638 10, 11 8<br />

Euphrasia confusa Scro N n 20 Th 0 5 1<br />

970 3 3 3.2 13.8 1267 7, 8, 16 8<br />

Euphrasia foulaensis Scro N s 6 Th 0 4 1<br />

143 0 3.6 12.4 1263 Co 18, 21 8<br />

Euphrasia frigida Scro N s 20 Th 0 1 4<br />

118 0 1.5 11.8 1981 15, 16 81<br />

Euphrasia heslop-hanisonii Scro NE r 15 Th 0 4 1<br />

20 0 3.7 12.6 1695 Co 21 8<br />

Euphrasia marshallii Scro NE r 12 Th 0 4 1<br />

39 0 3.8 12.3 1334 Co 18 8<br />

Euphrasia micrantha Scro N n 25 Th 0 7 3<br />

941 19 0 3.0 13.2 1400 8, 10 7<br />

Euphrasia nemorosa Scro N n 35 Th 0 7 3<br />

1498 20 71 3.6 14.8 1037 7, 10<br />

Euphrasia <strong>of</strong>i cinalis agg. Scro N n -1.61 30 Th 0 6 3<br />

2600 87 12 3.5 14.4 1131 6, 7, 8, 10 8<br />

Euphrasia ostenfeldii Scro N r 12 Th 0 2 1<br />

85 1 2.8 12.2 1694 16 9<br />

Euphrasia pseudokerneri Scro NE s 20 Th 0 7 1<br />

167 0 3.7 16.1 753 7 7'<br />

Euphrasia rivularis Scro NE r 15 Th 0 4 1<br />

14 0 2.3 13.2 2450 15, 16 7<br />

Euphrasia rostko viana Scro N n 35 Th 0 5 3<br />

29 1 12 1 3.7 14.3 1336 6 71<br />

Euphrasia rotundifolia Scro NE EN r 10 Th 0 4 1<br />

4<br />

3.5 12.4 1004 Co 18 8<br />

Euphrasia salisburgensis Scro N o 12 Th 0 2 3<br />

0 3 4.6 14.7 1134 16 7<br />

Euphrasia scottica Scro N n 25 Th 0 4 3<br />

601 7 2.5 12.8 1575 10, 15 8<br />

Euphrasia tetraquetra Scro N n 15 Th 0 7 1<br />

313 10 1 4.7 14.9 1105 6, 10 8<br />

Euphrasia vigursii Scro NE VU r 20 Th 0 7 1<br />

33<br />

5.4 15.3 1263 10<br />

Exact, /um pusillum Gent N o 8 Th 0 8 2<br />

0<br />

6.8 16.7 712 19 9<br />

Fagopyrum esculentum Poly AN -0.53 60<br />

Th 0<br />

Asl ? 501<br />

3.8 15.8 788 4 8<br />

Fagus sylvatica Faga N n -0.62 3000<br />

Ph sAf<br />

7 3 2397 79 3.5 14.7 1061 1 3<br />

Fallopia convolvulus Poly AR -1.31 100<br />

Th 0<br />

6 4 2139 51 3.7 14.9 971 3, 4 7<br />

Fallopia dumetorum Poly N s -0.33 200<br />

Th 0<br />

7 5 69<br />

3.9 16.4 784 1, 3 6<br />

Fallopia j aponica Poly AN 1.83 200<br />

Gn Rhiz2<br />

As2 2060 68 1 3.7 14.8 1043 3, 14, 17 6<br />

Fallopia sachalinensis Poly AN 1.05 300<br />

Gn Rhiz2<br />

As2 507 6 3.7 15.3 976 3 6<br />

Festuca altissima Poac N n 0.83 120<br />

hc 0<br />

7 3 241 8 2.6 13.6 1410 1, 16 3<br />

Festuca arenaria Poac N S 75<br />

hc Rhiz2<br />

7 1 108<br />

4.2 15.4 828 19 8<br />

Festuca armoricana Poac N o 40<br />

hc 0<br />

7 1 0<br />

6.2 16.9 796 19 8<br />

Festuca arundinacea Poac N n 1.71 120<br />

hc 0<br />

8 4 2082 55 7 3.6 14.9 980 6, 7 8<br />

Festuca filiformis Poac N n 35<br />

hc Ogr<br />

7 2 821 6 4 3.0 14.3 1100 8 8<br />

Festuca gigantea Poac N n 0.46 125<br />

hc 0<br />

7 3 1885 35 0 3.6 15.1 981 1 5<br />

Festuca huonii Poac N a 25<br />

hc 0<br />

7 0 0 7 6.4 16.5 780 16, 18 8<br />

Festuca lemanii Poac NA r 66<br />

hc 0<br />

7 1 71 1 3.4 15.3 1079 7, 8, / 6 8<br />

Festuca longifolia Poac N VU r 40<br />

hc 0<br />

7 1 15 6 4.8 16.2 751 8 8<br />

Festuca ovina Poac N n 43<br />

hc Ogr<br />

5 5 1788 5 4 3.5 14.5 1109 7, 8 7<br />

3<br />

0


NS CS RS Chg_ Hght Len P1 P2 LFI LF2 W Clonal Clone2 El E2 C Origin GB IR CI Tjan Tjul Prec Co Br Habitats L F R N S<br />

n -0.15 45 p hc h Ogr 3 6 2718 726 13 3.5 14.4 1118 7, 8 7 5 4 2 0<br />

n -0. 16 80 p hc h O 5 4 1976 569 4 3.6 14.9 985 6 7 6 6 6 0<br />

Taxon name Fam<br />

Festuca ovina agg. Poac<br />

Festuca pratensis Poac<br />

Festuca pratensis x Lolium<br />

perenne (x Festulolium<br />

6 71 6<br />

5 6 5<br />

62 35 2 2<br />

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4 7 3<br />

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4 6 71<br />

790 80 3.5 15.5 851 6<br />

iz2 3 6 2799 974 1 3.5 14.5 1104 3, 5, 6, 2/<br />

iz2 3 6 2799 974 1 3.5 14.5 1104 6<br />

gr DRi 2 6 801 182 2.7 12.7 1592 15, 16<br />

Eur 21 0 3.8 16.4 647 3, 4<br />

7 3 85 0 3.71 16.4 660 3, 4<br />

7 3 788 105 1 3.6 15.1 904 16<br />

9 2 132 0 3.8 16.3 687 4<br />

8 3 980 78 3.8 15.5 832 3<br />

iz2 5 5 2692 967 3.5 14.5 1105 11<br />

izl DRg 7 4 578 8 3.6 15.8 776 7<br />

0 3 Eur 961 60 1 4.1 15.9 823 3, 16, 17<br />

oI2 7 4 2380 819 3.5 14.6 1091 1, 7<br />

ol2 Gard 740 20 3.7 15.5 863 3, 17<br />

7 4 712 56 3.8 15.8 881 1<br />

8 2 58 0 4.4 16.5 680 Co 19, 21<br />

7 3 2459 930 1 3.6 14.7 1069 1<br />

7 3 98 0 3.6 16.3 688 6<br />

SAm 367 542 4.3 14.3 1223 3, 17<br />

9 1 423 330 1 4.5 14.8 1086 4<br />

9 2 482 180 11 4.2 14.9 997 3, 16<br />

8 3 307 16 0 3.6 15.5 763 4<br />

8 1 1200 368 13 4.0 14.9 1004 4<br />

7 1 31 0 0 6.5 15.8 1073 3, 4<br />

8 3 1978 304 12 3.6 15.0 912 3, 4<br />

8 3 128 0 0 3.6 16.1 703 4<br />

7 1 191 37 2 4.1 14.8 978 3, 4<br />

8 1 Eur 13 0 1 5.4 16. 1 958 ' 3, 4, 17<br />

7 4 116 0 0 3.5 16.2 702 4<br />

b DRa 8 3 c 1 0 0 2.9 14.7 1008 16<br />

Otb DRg 7 3 c 212 0 0 3.0 15.1 861 1, 3, 14, 16<br />

Otb DRg 8 3 Eur 1763 36 5 3.5 15.2 919 1, 3, 17<br />

0 7 3 c Eur 352 0 1 3.7 16.2 725 3, 17<br />

0 7 3 616 43 0 3.8 15.8 791 4, 16<br />

0 5 5 1135 138 1 3.6 14.9 1011 4<br />

0 7 2 32 01 0 3.7 15.6 789 4<br />

0 5 4 999 84 0 3.1 14.5 1043 4<br />

0 5 3 1725 409 1 3.6 14.8 1025 3<br />

0 5 5 2508 623 4 3.5 14.5 1073 3<br />

0 SAm 429 2 9 3.8 16. 1 721 4, 17<br />

0 SAm 524 5 6 3.8 16.0 778 3, 4, 17<br />

0 7 3 2672 960 14 3.6 14.6 1080 3, 4, 17<br />

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loliaceum) Poac NH n 65<br />

Festuca rubra Poac N n 72<br />

Festuca rubra agg. Poac N n 2.96 72<br />

Festuca vivipara Poac N n 0.13 44<br />

Filago gallica Aste AR CR 0.01 20<br />

Filago lutescens Aste NA VU s -0.34 25<br />

Filago minima . Aste N n -0.91 20<br />

Filago pyramidata Aste AR EN -1.14 30<br />

Filago vulgaris Aste N n -1.20 35<br />

Filipendula ulmaria Rosa N n -0.10 120<br />

Filipendula vulgaris Rosa N n -0.07 50<br />

Foeniculum vulgate Apia AR 1.17 250<br />

Fragaria vesca Rosa N n -1.09 30<br />

Fragaria x ananassa Rosa AN 0.42 40<br />

Frangula alnus Rham N n -0.16 500<br />

Frankenia laevis Fran N s 0.03 8<br />

Fraxinus excelsior Olea N n -0.73 2500<br />

Fritillaria meleagris Lili NA s 0.86 30<br />

Fuchsia magellanica Onag AN 1.85 150<br />

Fumaria bastardii Fuma N n 0.39 75<br />

Fumaria capreolata Fuma N n 0.31 100<br />

Fumaria densillora Fuma AR -0.37 52<br />

Fumaria muralis Fuma N n 1.75 100<br />

Fumaria occidentalis Fuma NE s 0.04 100<br />

Fumaria <strong>of</strong>i cinalis Fuma AR -0.34 52<br />

Fumaria parvillora Fuma AR -0.55 471<br />

Fumaria purpurea Fuma N s 0.25 60<br />

Fumaria reuteri Fuma AN -0.62 100<br />

Fumaria vaillantii Fuma AR -0.51 42<br />

Gagea bohemica Lili N VU r 9<br />

Gagea lutea Lili N n 0.16 25<br />

Galanthus nivalis Lili AN 3.01 22<br />

Galega dfi cinalis Faba AN 150<br />

Galeopsis angustifi lia Lami AR -3.31 50<br />

Galeopsis bifida Lami N n 100<br />

Galeopsis segetum Lami AR EX 50<br />

Galeopsis speciosa Lami AR -1.82 100<br />

Galeopsis tetrahit Lami N n 100<br />

Galeopsis tetrahit agg. Lami N n -0.61 100<br />

Galinsoga parVillora Aste AN 0.63 80<br />

Galinsoga quadriradiata Aste AN 1.071 80<br />

Garium aparine Rubi N n -0.09 150<br />

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35 86 65<br />

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Taxon name Fan/ NS CS RS Chg li ght Len 1 P2 LF1 LF2 W Clonel Clone2 El E2 C Origin GB IR CI Tjan Tjul Prec Co Br Habitats L F R N<br />

Galiurn boreale Rubi N n -0.52 45 hc h Rhiz2 5 6 561 101 0 2.2 12.8 1580 7, 16 7 5 7 3<br />

Galium conshictum Rubi N r 40 hc h Rhizl 9 1 12 0 5 5.0 16.5 799 13 8 9 3 2<br />

Galium mollugo Rubi N n 0.04 112 hc h Rhiz2 5 3 1665 0 14 3.5 15.3 905 7 7 4 7 4<br />

Galiurn odoratum Rubi N n -0.62 45 hc h Rhiz2 7 3 1836 350 1 3.4 14.7 1086 1 3 5 71 6<br />

Gahm palustre Rubi N n 0.07 75 hc h Rhizl 5 4 2652 932 9 3.5 14.5 1105 11 7 9 5 4<br />

Galium parisiense Rubi NA $ -0.57 30 Th h O 9 2 63 0 0 3.7 16.3 693 3 8 3 7 2<br />

Galium pumilum Rubi N r -1.32 35 hc h Nodel 7 3 65 0 0 3.7 16.2 754 7 7 4 8 3<br />

Galium saxatile Rubi N n -0. 15 30 hc h Node2 7 2 2489 793 9 3.5 14.3 1148 8, 9 6 6 3 3<br />

Galturn spurium Rubi AN -1.871 100 Th h O 7 6 c NHem 55 0 0 3.9 16.1 755 4 71 5 8 5<br />

Galiurn sterneri Rubi N n 0.69 30 hc h Nodel 4 2 273 35 0 2.0 13.0 1457 7, 16 9 4 7 1<br />

Galium tricomutum Rubi AR CR -4.78 50 Th h 0 8 4 386 1 0 3.8 16.1 736 4 7 4 7 4<br />

Galium uliginosum Rubi N n -0.14 60 hc h Rhizl 5 5 1435 102 0 3.2 14.9 96 1 11 7 9 6 4<br />

Galium verurn . Rubi N n -0.85 75 hc h Rhiz2 5 5 2516 730 14 3.5 14.6 1045 7 7 4 6 2<br />

Gastridium ventricosum Poac NA $ -0.48 50 Th h o 9 1 159 0 2 4.6 16.3 839 4, 7 9 3 8 2<br />

Gaudinia fragilis Poac NA s 45 Th h 9 2 47 0 2 4.5 16.2 865 3, 6 8 5 6 6<br />

Gaultheria shallon Eric AN 150 Pn w Rhiz2 Am4 179 14 1 3.6 14.9 1077 1, 10 3 4 4 3<br />

Genista anglica Faba N n -1.09 50 Ch Pn wi 0 7 1 858 0 0 3.0 14.6 1019 10 8 5 3 2<br />

Genista pilosa Faba N r -0.26 40 Ch Pn wo 0 7 3 23 0 0 5.0 15.6 1011 10 8 5 4<br />

Genista tind oria Faba N n -0.77 60 Ch Pn w 0 7 3 932 0 1 3.6 15.6 880 6 8 6 71 2<br />

Gentiana nivalis Gent N VU r 15 Th 0 1 3 4 0 -0.5 11.2 1853 15, 16 9 5 7 3<br />

Gentiana pneurnonanthe Gent N s -0.31 40 hc 0 7 4 130 0 3.7 15.7 806 8, 10 8 7 4 1


Taxo n name Fam NS CS RS Chg._ Hght Len P1 P2 LF 1 LR2 W Clona l Clo ne2 El E2 C Origin GB IR CI Tjan Tjul Prec Co Br Habitats L F R N S<br />

Hordelymus europaeus Poac N s 0. 12 120 p hc 0 7 3 185 1 0 3.2 15.5 788 1 6 4 7 7 0<br />

Hordeum distichon Poac AC 75 a Th 0 Cro p 714 76 3 3.8 15.4 898 3, 4 8 4 7 7 0<br />

Hordeum distichon sensi at Poac AC 87 a Th 0 Crop 714 76 3 3.8 15.4 898 3, 4 8 4 71 7 0<br />

Hordeum j ubatum Poac AN 60 p hc 0 As2, Am 349 6 1 3.5 15.4 800 3, 5 9' 6 7 6 2<br />

Hordeum marinum Poac N s -0.85 37 a Th 0 9 1 146 0 1 4.3 16.4 720 6 9 6 8 6 4<br />

Hordeum murinum Poac AR I -0.04 60 a Th 0 8 4 1497 48 14 3.8 15.6 817 3, 17 8 4 7 6 0<br />

Hordeum secalinum Poac N n -0. 19 70 p he 0 7 3 926 30 0 3.8 16.0 742 5 8 6 7 6<br />

Hordeum vulgare Poac AC 100 a Th 0 Cro p 196 8 1 3.8 15.6 833 3, 4 9 4 71 7<br />

Hornungia petraea Bras N s 0.31 10 a Th 0 7 3 56 0 3 3.5 14.8 116 1 16 9 2 8 1<br />

Hottonia palustris Prim N n -0 .63 120 p Hy brag 7 3 463 2 0 3.6 16.0 697 13 7 11 7 5<br />

Humulus lupu/us Cann N n -0 .09 450 p hc Rhiz2 7 4 1273 0 8 3.8 15.8 833 3 6 7 7 8<br />

Huperzia selago Lyco N n -0 .41 10 p Ch sw 0 2 6 989 234 0 2.7 13.2 1472 15, 16 7 6 2 2<br />

Hyacinthoides hispanica Lili AN L 60 p Gb OM Eur 847 76 12 3.9 15.5 866 1, 3 , 17 5 4 6 6<br />

Hyacinthoides non-scripta Lili N n -0.4 1 50 p Gb Ot b 7 1 243 9 760 13 3.6 14.6 1092 1, 9 5 5 5 6<br />

Hydrilla vert icillata Hydr N r 100 p Hy DRa DRg 8 5 c 2 1 0 3.5 14.2 1555 13 6 12 9 3<br />

Hydrocharis morsus-ranae Hyd r N n -0 .89 50 p Hy Stoll 7 4 323 84 2 3.9 15.8 772 13 7 11 7 7<br />

Hydrocotyle ranunculoides Apia AN 20 40 p Hy lrreg Am 43 0 0 4.0 16.6 680 13, 14 7 10 7 7<br />

Hydrocotyle vulgaris Apia N n -0 .53 20 p hc Node2 8 2 2091 842 10 3.7 14.4 1126 11 8 8 6 3<br />

Hymenophyllum tunbrigense Hym e N n -0 .54 8 p hc Rhiz l 7 0 197 112 0 3.8 14.0 1567 16 4 6 2 3<br />

Hymenophyllum wilsonii Hyme N n -0 .87 10 p hc Rhiz l 5 0 577 176 0 3.1 13.1 1685 1, 16 5 5 3 3<br />

Hyoscyamus niger Sob AR , - 1.38 80 b hc<br />

0<br />

8 4<br />

796 87 5 4.0 15.7 799 4<br />

8 4 7 9<br />

Hypericum <strong>and</strong>rosaemum Clus N n 0.78 80 p Pn w 0<br />

9 2<br />

1139 744 8 4.0 14.8 1184 1, 3<br />

S 6 6 , 5<br />

Hypericum calycinum Clus A N<br />

0.74 60 p Ch Pn w Rhiz2<br />

Eur<br />

702 63 2 4.0 15.6 884 3<br />

5 71 5, 5<br />

Hypericum canadense Clus AN<br />

20 a Th<br />

0<br />

Am<br />

0 3 0 4.6 14.4 1252 11, 14 8 9 2 2<br />

Hypericum elodes Clus N n -0 .46 20 40 hc Hy Node2 7 1 583 260 7 4.2 14.8 1194 11 8 10 3 2<br />

Hypericum hirsutum Clus N n -0 .18 100 hc 0 7 4 1276 10 0 3.3 15.3 832 6, 7 6 5 7 5<br />

Hypericum humilusum Clus N n -0 .40 10 Ch 0 7 3 1732 428 12 3.6 14.8 1085 3 7 6 4 3<br />

Hypericum Iinadilolium Clus N r 0.09 40 hc Ch 0 8 1 14 0 9 5.5 15.8 1069 16 71 3 3 2<br />

Hypericum maculatum Clus N n 2.11 60 hc Rhiz2 5 3 1180 300 0 3.6 15.0 1016 1, 3 , 16 6 6 5 5<br />

Hypericum montanum Clus N n -0 .49 80 hc 0 7 3 269 0 0 3.8 15.6 867 1, 3 7 4 8 2<br />

Hypericum co l oratura Clus N n 80 hc Rhiz2 Root 8 4 1906 385 6 3.6 15. 1 95 1 7 7 4 7 5<br />

Hypericum pulchrum Clus N n -0.32 60 hc 0 7 2 2427 887 9 3.5 14.3 1148 10, 16 6 5 4 3<br />

Hypericum tetrapterum Clus N n -0 .41 60 hc Stoll 7 3 2 101 842 11 3.71 14.9 1025 11 71 8 6 4<br />

Hypericum undulatum Clus N s -0 .12 60 hc Stol l 8 1 81 0 0 5.6 15.5 1152 11 8 8 4 2<br />

Hypochaeris glabra Ast e N n - 1.01 20 a Th 0 8 3 270 5 14 4.0 15.9 754 8 8 4 4 2<br />

Hypochaeris maculata Aste N VU r -0 .10 60 p hc 0 7 4 c 17 0 1 3.9 16.1 710 7 8 4 8 3<br />

Hypochaeds radicata Aste N n 0.6 1 60 p hc 0 8 3 272 5 977 14 3.5 14.5 1104 6 8 4 5 3<br />

/beds amara Bras N s - 1.21 35 a Th 0 8 2 471 0 0 3.5 16.3 710 7 71 4 8 3<br />

Ilex aquifolium Aqui N n -0. 16 1500 p Ph w 0 8 2 235 3 86 1 14 3.6 14.7 1079 1 5 5 5 5<br />

Illecebrum vedicillatum Cary N r -0 .60 20 a Th h 0 Nodal 8 2 37 ' 0 0 5.6 15.7 1062 3, 13 8 7 3 2<br />

Impatiens capensis Bals AN 0.71 60 a Th h 0 Am6 323 1 0 3.7 16.2 723 13, 14 7 9 7 6<br />

Impatiens gl<strong>and</strong>ulifera Bals AN 1.85 200 a Th h 0 As l 1599 286 6 3.7 15.1 957 14 6 8 7 7<br />

Impatiens noli-tangere Bals N s -0 .77 60 a Th h 0 7 5 2 1 0 0 2.6 13.9 1833 1 4 71 71 6<br />

Impatiens p<strong>and</strong>fi ora Bals AN<br />

0.10 100 a Th h 0<br />

AO 470 1 0 3.5 15.7 82 1 1<br />

4 5, 7 8<br />

/nu/a conyzae<br />

Ast e N n -0 .15 125 p hc h 0 7 3<br />

860 0 7 3.9 15.9 82 1 7, 16<br />

7 3 8 3<br />

Mula crithmoides Ast e N e 0.09 95 p hc Ch h 0 9 1 121 19 8 5. 1 16.1 869 Co 18 9 6 7 5<br />

l a<br />

V


Taxon name Fam NS CS RS Chg_ Hght Len P1 P2 LF1 LF2 W Clonal Clone2 El E2 C Origin GB IR CI Tjan Tjul Prec Co Br Habitats F R N<br />

Mu la helenium Aste AR -0.80 150 p hc 0 Eur, As l 631 100 3 4.0 15.1 973 3, 17 6 5<br />

Mu la salicina Aste N o 60 p hc Rhiz2 7 5 c 0 3 0 4.7 14.9 1017 16 9 3<br />

Iris foetidissima Ind N n 1.47 80 p hc Rhizl 8 2 728 0 14 4.2 16.1 821 1 8 5<br />

Iris germanica Ind AN 95 p hc Rhizl Gard 211 1 3 3.9 16.0 734 3, 17 6 4<br />

Iris pseudacorus Irid N n 0.16 150 p Gn Hy Rhiz2 8 3 2563 959 10 3.7 14.6 1081 11 6 6<br />

(sail s tinctoria Bras AR 1.08 150 b p hc 0 Eur, As 102 2 1 3.8 16.0 733 3, 16 8 3<br />

Isoetes echinospora Isoe N n 0.65 15 p Hy 0 4 6 178 32 0 3.2 13.0 1613 13 1 5 2<br />

Isoetes histrix lsoe N r 4 p hc 0 9 1 3 0 5 6.6 16.2 829 16 5 1<br />

Isoetes lacustris Isoe N n 0.95 25 p Hy 0 4 4 522 147 0 2.8 12.9 1660 13 1 4 1<br />

Iso lapis cernua Cype N n 0.23 15 a p Th hc 0 9 1 242 215 10 4.8 14.8 1181 11 5 3<br />

(so lapis setacea Cype N n 0.53 15 a p Th he 0 7 4 2038 638 10 3.5 14.4 1149 11, 14 5 3<br />

Jasione montana Camp N n -1.08 50 hc 0 7 3 1076 420 14 4.0 14.8 1152 8, 10 4 2<br />

Jug bans regia Jugl AN 2400 Ph w 0 Eur?, Asl ? 803 11 3 3.7 15.9 779 1, 3 8 7<br />

Juncus acutiflorus Junc N n 1.16 100 he Rhiz2 7 3 2498 845 11 3.5 14.5 1115 11 4 2<br />

Juncus acutus Junc N s 0.01 150 hc Ogr 9 1 41 28 12 5.4 15.7 1031 Co 19 7 3<br />

Juncus alpinoarticulatus June N $ -0. 12 30 hc Rhizl 4 6 53 0 0 0.7 12.1 1477 11 7 2<br />

Juncus ambiguus Junc N n 17 Th 0 8 3 175 50 1 4.4 14.9 999 Co 19, 21 71 5<br />

Juncus articulatus Junc N n 1.26 60 hc IRhiz2 8 4 2740 956 11 3.5 144 1108 11 6 3<br />

Juncus balticus Junc N s -0.34 45 Gn Rhiz2 2 6 92 0 0 3.3 13.1 1012 Co 19 5 2<br />

Juncus bigIumis June N s -0.17 12 hc Ogr 1 6 37 0 0 0.5 11.4 2194 11, 15 8 2<br />

Juncus bufonius June N n 25 Th 0 6 6 1986 724 3 3.6 14.6 1102 3, 11, 13, 14 6 5<br />

Juncus bufonius sensi at. Junc N n 1.13 25 Th 0 6 6 2736 937 14 3.5 14.5 1105 3, / , 13, 14 6 5<br />

La<br />

co Juncus bulbosus June N n 0.34 30 90 hc Hy Node2 Irreg 5 3 2250 827 8 3.5 14.2 1180 14 1 4 2<br />

Juncus capitatus Junc N 5 Th 0 8 3 12 0 10 6.3 16.1 889 10 5 1<br />

Juncus castaneus Junc N s -0.40 30 he Rhiz2 1 6 44 0 0 0.1 11.2 2291 15 7 3<br />

Juncus compressus Junc N n -1.09 30 Gn Rhizl 7 4 430 4 1 3.6 15.9 746 6, 11 7 5<br />

Juncus conglomeratus Junc N n 0.84 100 hc Ogr 7 3 2622 798 4 3.5 14.4 1117 11 4 3<br />

Juncus effusus Junc N n 1.06 120 hc Ogr 8 3 2753 974 13 3.5 14.4 1108 8, 11 4 4<br />

Juncus filiformis Junc N s 0.79 30 hc Ogr 4 6 32 0 0 2.3 13.6 1530 13 6 4<br />

Juncus foliosus Junc N n 25 Th 0 8 2 218 88 2 4.3 14.7 1241 11, 13 6 6<br />

Juncus gerardii June N n -0. 13 30 hc Rhiz2 6 6 919 271 11 4.2 14.4 1174 Co 21 7 6<br />

Juncus infi exus Junc N n 0.04 90 hc Ogr 8 4 1758 631 9 3.8 15.2 925 6, 11 71 5<br />

Juncus maritimus June N n -0.26 100 Gn Ogr 8 3 390 196 11 4.7 15.1 1081 Co 21 8 5<br />

Juncus pygmaeus Junc N EN r 8 Th 0 9 1 4 0 0 6.7 15.9 965 3 4 2<br />

Juncus squarrosus Junc N n 30 p hc Ogr 7 2 1849 484 0 3.1 13.8 1254 8, 12 2 2<br />

Juncus subnodulosus Junc N n 0.15 120 p hc Rhizl 8 3 680 224 2 3.9 15.5 838 11 8 4<br />

JUnCUS tenuis Junc AN 0.83 40 p hc Ogr Am, SAm 1053 145 3 3.6 14.6 1267 1, 3, 13 5,1 4<br />

Juncus trifidus Ju nc N n -0.38 30 p hc Ogr 1 4 177 0 0 1.0 11.5 2162 15 2 2<br />

Juncus triglumis Junc N n -0.38 20 p hc Ogr 1 6 200 0 0 0.9 11.8 2085 11, 16 6 2<br />

Jun/penis communis Cupr N n -0.42 500 p Ph Ch w O 5 6 1020 145 0 2.8 13.4 1380 7, 10, 15, 16 5 3<br />

Kickxia elatine Scro AR -0.18 25 a Th 0 8 3 911 41 11 4.1 16.0 813 4 6 5<br />

Kickxia spuria Scro AR -0.071 25 a Th 0 8 3 622 0 2 3.9 16.2 737 4 7 5<br />

Knautia arvensis Dips N n -0.88 100 p hc 0 7 4 1707 478 4 3.8 15.2 919 6, 7 8 4<br />

Kobresia sitnpliciuscula Cype N r 0.58 20 p he 0 1 6 18 0 0 -0.1 11.5 2044 11, 15 6 1<br />

Koeleria macrantha Poac N n -0.29 50 p hc 0 7 6 1250 266 7 3.7 14.7 989 7 7 2<br />

Koeleria vallesiana Poac N r 40 p hc 0 8 2 4 0 0 4.5 16.4 868 7 8 1


S<br />

L F R N<br />

8 9 6 1<br />

6 5 7 7<br />

8 4 7 6<br />

8 5 7 6<br />

8 4 7 7<br />

6 12 7 6<br />

4 5 7 6<br />

7 5 7 8<br />

7 4 7 6<br />

7 5 7 7<br />

71 5 7 6<br />

5 6 7 8<br />

6 5 7 7<br />

6 4 7 7<br />

7 4 6 3<br />

Br Habitats<br />

11, 16<br />

3, 17<br />

19<br />

3, 17<br />

3, 16<br />

13<br />

1<br />

3, 17<br />

3, 4<br />

4<br />

4<br />

3, 17<br />

3, 4, 17<br />

3, 17<br />

1, 2, 17<br />

LF2 W Clonal Clone2 El E2 C Origin GB IR CI Tjan Tjul Prec Co<br />

2175<br />

884<br />

601 Co<br />

741<br />

693<br />

839<br />

855<br />

911<br />

842<br />

1097<br />

877<br />

869<br />

1027<br />

1059<br />

1049<br />

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1 P2<br />

Taxon name Fam NS CS RS Chg Hght Len<br />

6<br />

700<br />

75<br />

200<br />

200<br />

300<br />

60<br />

60<br />

30<br />

25<br />

30<br />

35<br />

30<br />

95<br />

4600<br />

7j 6, 5 3<br />

7 6 5 3<br />

3 6 7 6<br />

7 3 8 4<br />

9 5 7 6<br />

71 4 8 3<br />

6 5 4 3<br />

8 6 7 6<br />

7 9 7 4<br />

7 6 6 5<br />

71 4 8 2<br />

6 5 7 6<br />

6 5 7 6<br />

9 6 7 8<br />

9 4 5 5<br />

8 9 8 71<br />

7 4 7 4<br />

7 11 7 8<br />

7 11 7 6<br />

7 11 7' 7<br />

71 12 71 5<br />

8 6 6 4<br />

8 4 7' 3<br />

8 5 6 3<br />

7 4 7 6<br />

8 4 8 6<br />

7 4 5 4<br />

8 5 7 8<br />

9 4 7 7'<br />

2, 17<br />

2, 17<br />

1, 3<br />

4, 7<br />

19<br />

3, 18<br />

8, 15<br />

3, 6, 7<br />

11<br />

6<br />

3<br />

3<br />

3, 17, 18, 19<br />

18<br />

3, 4, 16<br />

13<br />

4<br />

13<br />

11, 13<br />

13, 14<br />

11, 13<br />

6<br />

7<br />

7<br />

3, 4, 17<br />

3, 19, 21<br />

3<br />

6<br />

3, 17<br />

1134<br />

1133<br />

955<br />

718<br />

886 Co<br />

782<br />

1172<br />

742<br />

823<br />

1079<br />

835<br />

776<br />

942<br />

1023 Co<br />

875<br />

766<br />

717<br />

739<br />

986<br />

787<br />

832<br />

1103<br />

918<br />

960<br />

801<br />

786<br />

1074<br />

629<br />

757<br />

Ph<br />

Ph<br />

Gn<br />

Th<br />

Gn<br />

hc<br />

Gn<br />

Th<br />

hc<br />

hc<br />

hc<br />

Gn<br />

Ph<br />

Pn<br />

Th<br />

hc<br />

Th<br />

Hy<br />

Hy<br />

Hy<br />

Fly<br />

hc<br />

hc<br />

hc<br />

Th<br />

hc<br />

hc<br />

hc<br />

Th<br />

3000<br />

3700<br />

30<br />

60<br />

20<br />

300<br />

40<br />

75<br />

120<br />

80<br />

200<br />

120<br />

600<br />

300 b<br />

100 a<br />

90<br />

30<br />

0.5<br />

0.4<br />

0.3<br />

1<br />

60<br />

35<br />

20<br />

40<br />

60<br />

50<br />

120<br />

40<br />

LO<br />

0<br />

p<br />

3


Taxon name Fam NS CS RS Chg Hght Len P1 P2 LF1 LF2 W Clonal Clone2 E/ E2 C Origin GB IR CI Tjan Tjul Prec Co Br Habitats L F R N<br />

Lobelia dortm anna Camp N n -0.05 - 4 p Hy h 0<br />

4 3<br />

570, 178 0 3.0 12.9 1635 13<br />

8 12 5 1<br />

Lobelia urens Camp N VU r -0. 19 70 p hc h 0<br />

8 1<br />

12 0 0 4.7 16.1 988 8, 10<br />

8 8 4 2<br />

Lobularia maritima Bras AN ' 2.34 30 a p Th hc h 0 0 3 Eur 738 33 13 4.0 15.71 854 18, 19 9 3 71 4<br />

Loiseleuria procum bens Eric N n -0.58 25 p Ch w Node2 1 6 182 0 0 0.9 11.4 1994 15 9 5 2 2<br />

Lolium multifl orum Poac AN : -1.06 100 a b Th hc h 0 Eur 2069: 340 10 3.6 14.9 968 5 7 5 7 7<br />

Lolium perenne Poac N n -0.29 50 p hc h 0 8 3 2743 964 14 3.6 14.5 1096 3, 6 8 5 6 6<br />

Lolium te m ulentum Poac AR -4.05 90 a Th h 0 Eur 341 37' 7 4.0 15.6 855 4 7 4 8 7<br />

Lonice ra p ericlym e num Capr N n -0.11 600 p Ph w 0 Node2 8 2 2622 943 14 3.6 14.5 1102 1 5 6 5 5<br />

Lonicera xylosteum Capr AN 0.58 200 p Pn w 0 7 4 Eur, As1 242 16 0 3.4 15.2 874 1, 3 5 5 7 6<br />

Lotus angustissimus Faba N $ -0.23 30 a Th h 0 8 3 55 0 12 5.7 16.2 952 8 8 3 4 3<br />

Lotus corniculatus Faba N n 1.09 40 p hc h 0 8 5 2801 975 14 3.5 14.5 1104 6, 7 7 4 6 2<br />

Lotus glab er Faba N n -0.55 90 p hc h 0 8 3 509 0 4 3.9 16. 1 732 3, 6, 7 7 7 7 5<br />

Lotus pe dunculatus Faba N n -0.06 60 p he h 0 Rhizl 7 3 2380 729; 13 3.6 14.7i 1072 11 7 8 6 4<br />

Lotus s ubbillorus Faba N s 0.22 30 a Th h 0 8 2 861 8 14 5.8 16.0 987 8 7 5 6 5<br />

Ludwigia palustris Onag N r 0. 19 15 p Th Hy h Node2 8 3 11 0 3 4.6 16.6 812 13 8 9 4 4<br />

Lupinus arboreus Faba AN 1 1.84 200 Pn w 0 Am4 341 21 11 4.2 15.7 825 3. 19 9 4 7 3<br />

Lupinus polyphyl/us Faba AN : 150 hc h 0 Am4 215 3 1 3.2 15.2 828 3, 14, 17 7 5 5 5<br />

Luron ium natans Alis N s 0.24 50 Hy h Sto12 7 2 91 3, 0 3.3 14.71 1229 13, 14 8 11 5 3<br />

Luzula arcuata Junc N r -0.43 10 he h Rhizl 1 3 22 0 0 0.0 10.8 2044 15, 16 9 5 2 2<br />

Luzula campestris Junc N n -0.18 15 hc h Rhiz2 7 3 2725 835 14 3.5 14.5 1100 6 7 4 5 2<br />

Luzula forsteri Junc N n 0.25 35 hc h 0 9 2 309 0 5 4.2 16.2 859 1 4 4 5 2<br />

Luzula multillora Junc N n 0.28 50 hc h 0 3 6 2451 834 7 3.5 14.3 1148 8 7 6 3 3<br />

Luzula pallidula Junc N VU r 30 hc h 0 5 5 c 2 0, 0 3.4 16.3 553 1, 11 7f 7 5 2<br />

Luzula pilosa June N n -0.35 32 hc h 0 5 4 2132 266 1 3.2 14.4 1127 1, 2 5 5 5 3<br />

Luzula spicata June N n -0.72 25 hc h Rhizl 1 3 189 0 0 1.0 11.5 2085 7, 15, 16 8 5 3 2<br />

Luzula sylvatica Jun c N n -0.02 80 hc h Rhizl 7 3 2058 621 4 3.3 14.1 1208 1, 16 5 5 4 4<br />

Ly chnis alpina Cary N VU r 20 Ch h 0 2 3 2 0 0 0.5 12.0 1640 15 8 3 4 2<br />

Lychnis flos-cuculi Cary N n -0.79 75 he h 0 7 4 2569 765 9 3.5 14.5 1095 11 71 9 6 4<br />

Lychnis viscaria Cary N VU r 0.01 45 Ch h 0 7 4 c 28 0 0 2.2 13.8 926 16 8 3 4 2<br />

Lycium Sola AN 0.13 250 Pn w Root As 1104 68 9 3.8 15.7 784 3, 19 8 5 7 4<br />

Lyciurn barbarum Sola AN 250 Pn w Root As 3, 19 8 5 7 4<br />

Lycium chinense Sola AN 250 Pn Ph w Root As 3, 19 8 5 7 4<br />

Lycop e rsicon e sculentum Sola AN 150 a Th h 0 SAm 523 41 4.0 15.6 876 17 71 5 71 8<br />

Lyc opodie lla inundata Lyco N s -0.65 5 Ch h Nodal 5 3 233' 18 3.5 14.9 1122 10, 12 9 9 2 1<br />

Lycopodium annotinum Lyco N s -0.38 10 Ch sw Node2 2 6 171 0 0.7 11.7 1760 10, 15 6 6 3 3<br />

Lycopodium clavatum Lyco N n -0.52 15 Ch sw Node2 5 6 948 81 2.4 13.3 1368 10 7 5 1 2<br />

Lycopus europaeus Lami N n -0.01 100 hc h Rhizl 7 4 1689 347 3.8 15.2 995 11 7 8 7 6<br />

Lysichiton am ericanus Arac AN 110 hc h Rhizl Am4 174 24 3.9 15.1 1073 13, 14 4 9 6 8<br />

Lysimachia nem orum Prim N n -0.46 20 Ch hc h Node2 7 2 2217 740 3.4 14.4 1150 1 5 7 4 5<br />

Lysimachia nummularia Prim N n -0.02 5 hc Ch h Node2 7 3 1266 227 3.7 15.5 895 6, 11, 14 5 7 5 5<br />

Lysimachia punctata Prim AN , 4.62 120 hc h Rhiz1 Eur 1127 48 3.5 15.1 999 1, 3, 17 6 6 7 5<br />

Lys ima chia thyrsillora Ri m N s 0.38 70 hc Hy h Rhiz2 4 6 51 0 2.7 14.2 1200 11, 13 8 10 4 3<br />

Lysimachia vulgaris<br />

Prim N n 0.22 105<br />

hc h Rhiz2<br />

7 5<br />

1227f 288 3.71 15.2 943 11<br />

7i 9 71 5,<br />

Lythrum hyssopifolium Lyth AR VU -1.12 15<br />

Th h 0<br />

8 4<br />

112 3 3.9 16.0 777 4<br />

8 6 6 4<br />

Lythrum portula Lyth N n 0.32 8 Th Hz h 0 Nodel 7 3 1262 321 3.8 14.8 1084 11, 13 8 9 5 3<br />

Lythrum salicaria Lyth N n -0.08 120 hc h 0 7 5 1692 827 4.0 15.0 1024 11 7 9 7 5


Taxon name Fam NS CS RS Chg_ Hght Len 1 P2 LF1 LF2 W Clonel Clone2 El E2 C Origin GB IR CI Tjan Tjul Prec Co Br Habitats L F R N S<br />

Mahonia aquifoliurn<br />

Berb AN 1.61 150 Pn w Rhiz2 Am4 991 4 2 3.4 15.6 786 1, 3 4 6 5<br />

Maianthemurn bifolium Li li NA VU r 0.32 20 Gn h Rhiz2 5 5 0 4 0 0 2.9 15.0 753 1, 2 5 3 3<br />

Malus domestica Rosa AR 1000 Ph w 0 Gard 1532 327 8 3.7 15.0 975 3 5 6 7'<br />

Malus sylvestris sens.lat. Rosa N n 0.57 1000 Ph w 0 7 3 2023 598 11 3.7 15.0 975 1, 3 5 6 6<br />

Malus sylvestris sens.str. Rosa N n 1000 Ph w 0 7 3 1335 218 0 3.7 15.1 964 3 5 6 6<br />

Ma Iva moschata Maly N n -0.04 80 hc h 0 7 3 1423 0 10 3.7 15.6 871 6 3 7 4<br />

Ma Iva neglecta<br />

Maly AR -0.22 60 Th h 0 7 3 1196 70 14 3.8 15.7 781 3 4 8 71<br />

Melva pusilla Maly AN 50 a Th h 0 7 5 c Eur, As 107 6 1 4.1 16.0 788 3, 17, 19 5 5 5<br />

Ma Iva sylvestris Maly AR -0.30 150 p he h 0 8 4 1788 354 14 3.8 15.3 899 3, 17 4 8 7<br />

Marrubium vulgere Lami N s -2.02 60 p hc h Rhizl 8 4 46 0 0 4.6 16.1 861 7 5 7 8<br />

Matricaria discoidea Aste AN -0.49 35 a Th h 0 As2?, Am? 2677 945 14 3.6 14.5 1086 3, 4 5 7 7<br />

Matricaria recutita Aste AR 0.92 60 a Th h O 8 3 1588 51 11 3.7 15.5 868 3, 4 5 7 7<br />

Matteuccia struthiopteris Wood AN 60 p hc h O 4 6 c NHem 74 4 3.2 14.7 1108 1 8 7 7<br />

Matthiola incana Bras AN 0.75 80 p Pn sw O 9 1 Eur 107 2 5.0 15.9 874 Co 18, 19 3 5 2<br />

Matthiola sinuata Bras NA VU r 60 b hc h O 9 1 19 8 5.4 15.6 1089 Co 18, 19 3 7 2<br />

Meconopsis cambrica Papa N s 2.36 60 p hc h O 5 1 54 77 3.5 14.0 1321 1 5 7 5<br />

Medicago arabica Faba N n 0.69 60 a Th h O 9 2 744 0 1 4.2 16.2 781 3, 17 5 6 5<br />

Medicago lupulina Faba N n -0.43 50 a p Th hc h o 7 4 2064 686 1 3.8 15.0 963 7, 17 4 8 4<br />

Medicago minima Faba N s -1.97 20 a Th h O 8 4 54 0 3.9 16.5 623 8 3 7 2<br />

Medicago polymorphe Faba N s -1.34 60 a Th h o 9 2 118 0 1 5.0 16.4 801 8 4 5 5<br />

Medicago sativa Faba N s -0.56 90 p hc h 0 Rhir l 8 4 c 54 0 3.5 16.2 604 3, 6 4 6 5<br />

Medicago sativa<br />

subsp falcata Faba N s 60 hc h Rhizl 8 4 c 541 01 3.51 16.2 604 3 3 7 3<br />

Medicago sativa subsp.sativa Faba AN 90 hc h 0 Crop 1065 17 3.8 15.8 768 3, 6 4 6 5<br />

Melampyrum arvense Scro AN -0.49 60 a Th h 0 7 3 c Eur 50 0 3.6 16.2 692 3, 4, 16 4 8 3<br />

Melampyrum cristatum Scro N r -0.88 50 a Th h 0 7 4 c 62 0 3.4 16.3 606 3 3 8 2<br />

Melampyrum pratense Scro N n -0.88 60 a Th h 0 5 4 1696 323 3.2 14.3 1220 1, 2 5 2 3<br />

Melampyrurn sylvaticum Scro N r -0.58 35 a Th h 0 4 3 75 20 1.5 12.5 1532 1, 16 5 2 2<br />

Merica nutans Poac N n -0.17 60 hc h Rhiz1 5 5 c 408 0 1.9 13.0 1483 1, 7, 16 5 7 3<br />

Merica uniflora Poac N n -0.04 60 hc h Rhir l 7 3 1511 246 3,5 15.0 1015 1 5 7 5<br />

Mehlotus elbus Faba AN -0.20 150 a hc Th h 0 Eur?, Asl ? 913 15 3.7 15.8 778 3 3 7 4<br />

Mefi lotus altissimus Faba AR 0.73 150 hc h 0 7 3 1122 16 3.8 15.8 785 3, 17 6 7 7<br />

Melilotus indicus Faba AN -1.59 40 Th h 0 Eur, As 1 427 12 1 3.8 15.7 790 3, 17 5 71 71<br />

Melilotus <strong>of</strong>i cinalis Faba AN 0.02 150 hc h 0 Eur?, Asl ? 1142 26 3.7 15.7 790 3, 17 5 7 5<br />

Melissa <strong>of</strong>ficinalis Lami AN 1.73 60 hc h Rhizl Eur 667 36 4.1 15.9 854 3, 17 5 7 6<br />

Melittis melissophyllum Lami N s -0.47 60 hc h Rhizl 7 3 119 0 5.1 15.7 1091 1, 3 4 7 5<br />

Menthe aquatica Lami N n -0.11 90 hc h Rhiz2 7 3 2475 922 3.7 14.7 1065 11 8 7 5<br />

Mentha arvensis Lami N n -1.30 60 hc h Rhiz2 5 6 1965 428 3.6 14.9 1017 4, 11 7i 71 6<br />

Mentha pulegium Lami N VU r -0.70 30 hc h Rhiz2 8 3 242 45 4.4 15.9 869 6, 13 7 5 7<br />

Mentha spicata Lami AR 1.69 90 hc h Rhiz2 Crop 1563 74 3.5 15.0 942 3, 17 5 7 7<br />

Menthe suaveolens Lami N $ -0.32 100 hc h Rhiz2 9 2 118 0 5.4 15.5 1151 3 8 6 6<br />

Menyanthes trifoliata Meny N n -0.04 30 150 Gn Hy h Rhiz2 5 6 1905 756 3.4 14.1 1201 11 10 4 3<br />

Mercurialis annua Euph AR 0.28 50 Th h 0 9 2 793 55 1 4.0 16.0 779 3, 4, 17 5 7 7<br />

Mercurialis perennis Euph N n -0.65 40 hc h Rhiz2 7 3 2214 4 3.2 14.8 1045 1 6 7 7<br />

Mertensia maritima Bora N s -0.53 60 hc h 0 2 3 222 29 3.8 13.4 1083 Co 19 5 T 7<br />

Mespilus germanica Rosa AR 900 Ph w o Eur 98 1 4.4 16.1 861 1, 3, 17 4 6 6


Taxon name Fam NS CS RS Chg. Hght Len P1 P2 LF1 LF2 W Clonal Clone2 El E2 C Origin GB IR CI Tja n Tjul Prec Co Br Habitats L F R N S<br />

Meum athamanticum Apia N s -0.40 60 p hc 0 4 3 164 0 0 1.6 12.9 1459 3, 6 8 5 4 3<br />

Mibora minirna<br />

Poac N r -0.01 8 a Th<br />

0<br />

8 2<br />

7, 0 10 5.8 16.1 861 Co 19<br />

9 3 71 1<br />

Milium effusum<br />

Poac N n 0.31 150 p hc<br />

0<br />

5 6<br />

1391 91 0 3.6 15.3 928 1<br />

4 5 6 5<br />

Milium vernale Poac N 0 5 a Th 0 9 1 0 0 2 6.8 16.6 718 19 9 3 6 2<br />

Mimulus Scro AN -0.47 50 p hc Node2 Am4, SAm 1767 237 5 3.2 14.3 1106 13, 14 7 9 6 5<br />

Mimulus guttatus Scro AN 50 p hc Node2 Am4 996 44 4 3.2 14.5 1020 13, 14 7 9 6 6<br />

Mimulus guttatus x luteus (M<br />

x robert sin<br />

Scro AN<br />

50 p hc<br />

Node2<br />

Gard<br />

473, 125 0 3.1 14.0 1162 13, 14 7 8 7i 5<br />

Mimulus luteus<br />

Scro AN<br />

50 p hc<br />

Node2<br />

SAm<br />

186 5 0 2.8 13.6 1144 13, 14 7 9 5 5<br />

Mimulus moschatus Scro AN 40 p hc Node2 Am4 361 13 2 3.3 14.6 1099 13, 14 7 8 5 5<br />

Minuartia hybrida Cary N s -1.70 20 a Th 0 9 2 294 0 1 3.5 16.0 716 7 9 3 8 3<br />

Minuartia recurva Cary N o 5 p Ch 0 1 3 0 1 0 4.8 14.2 1414 15 8 4 3 1<br />

Minuartia rubella Cary N r 0.01 6 p Ch 0 1 6 71 0 0 0.8 11.2 1679 15 8 4 7 1<br />

Minuartia sedoides Cary N s -0.75 8 p Ch 0 1 3 76' 0 0 1.2 11.4 2095 15 8 5 4 2<br />

Minuart ia stricta Cary N EN r 10 p Ch 0 1 6 1 0 0 0.4 12.1 1443 11 9 9 5 2<br />

Minuartia verna Cary N s -0.42 15 p Ch 0 4 5 139 30 0 2.7 13.9 1215 7, 16 8 4 7 1<br />

Misopates orontium Scro AR -0.89 50 a Th 0 8 4 488 24 11 4.3 15.9 864 4 7 5 6 6<br />

Moehringia trinervia<br />

Cary N n -0.40 40 a Th<br />

0<br />

7 3<br />

1990 259, 4 3.5 15.0 982 1<br />

4 5 7 6<br />

Moenchia erecta<br />

Cary N n -0.65 12 a Th<br />

0<br />

8 2<br />

418 0 14 4.2 16.0 823 8<br />

9 4 4 3<br />

Molinia caerulea Poac N n -0.34 130 p hc Ogr 5 4 2244 897 6 3.5 14.2 1179 12 7 8 3 2<br />

Moneses uniflora Pyro N VU r 0.14 4 p hc Rhizl 4 6 27 0 0 2.0 13.0 985 2 4 5 4 1<br />

Monotropa hypopitys Mono N<br />

-h.<br />

n -1.09 30 p Gn Rhizl 7 6 288 24 0 3.7 15.8 817 1 4 5 6 2<br />

to Montia fontana<br />

Port N n 0.14 20 a p Th Hy Nodal<br />

5 3<br />

21971 547, 14 3.4 14. 1 1198 11<br />

71 9 5 3<br />

Muscari neglectum<br />

Lili NA VU r 1.55 30 p Gb<br />

Gib DRg 8 4<br />

13 0 0 3.3 16.3 590 3, 8<br />

7 3 7 5<br />

Mycelis muralis Aste N n 0.01 100 p hc 0 7 3 1302 0 0 3.3 15.2 944 1, 16 4 5 7 5<br />

Myosotis alpestris Bora N r -0.22 25 p hc 0 1 6 7 0 0 -0.1 11.6 1623 7, 15, 16 8 4 8 2<br />

Myosotis arvensis Bora AR -0.34 40 a Th 0 5 4 2577 748 8 3.5 14.6 1056 3, 4 7 5 6 6<br />

Myosotis discolor Bora N n 0.14 25 a Th 0 7 3 23171 521 14 3.5 14.4 1088 6 7 5 5 3<br />

Myosotis taxa Bora N n 0.65 40 b hc 0 5 6 2409 757 8 3.5 14.5 1085 11 7 9 6 5<br />

Myosotis ramosissima Bora N n 0. 11 25 a Th 0 8 3 1174 52 14 3.8 15.5 823 8, 16 8 3 6 3<br />

Myosotis scorpioides Bora N n -0.77 57 p hc Hy Stoll 7 4 2291 662 3 3.5 14.7 1037 11, 14 7 9 6 6<br />

Myosotis secunda Bora N n 0.52 55 p hc Stoll 7 1 1736 498 6 3.3 14.0 1237 11 6 9 5 4<br />

Myosotis sicula Bora N o 15 a Th 0 9 1 0 0 2 6.2 17.0 794 19 6 7 6 3<br />

Myosotis stolonifera Bora N s 0.77 20 p hc Stoll 4 1 115 0 0 1.6 13.2 1362 11, 14 8 9 5 4<br />

Myosotis sylvatica Bora N n 2. 18 47 p hc 0 7 5 1690 24 4 3.4 15.1 931 1 6 5 7 5<br />

Myosoton aquaticum Cary N n 0.00 100 p hc Nodal 7 4 927 0 0 3.6 16.0 747 11, 13, 14 7 8 7 8<br />

Myosurus nnnimus Ranu NA n -0.66 8 a Th 0 7 3 339 0 2 3.8 16.3 691 4 8 7 6 5<br />

Myrica gale<br />

Myri N n -0.75 150 p Pn<br />

Rhiz2<br />

5 2<br />

976, 553 0 3.4 13.8 1353 12<br />

8 9 3 2<br />

Myriophyllum alternifl orum Halo N n 1.00 120 p Hy<br />

Irreg<br />

5 2<br />

1390 327 3 3.2 13.8 1299 13, 14 7 12 5 3<br />

Myriophyllum aquaticum Halo AN ,<br />

200 p Hy<br />

Irreg SAm 268 2 7 4.3 16.1 838 13<br />

7 12 5 3<br />

Myriophyllum spicatum Halo N n 0.63 250 p Hy<br />

Irreg 7 5<br />

1409 373 7 3.7 15.1 907 13, 14 7 12 7 7<br />

Myriophyllum verticillatum Halo N n -0.89 300 p Hy Irreg DRa 7 6 360 130 0 3.8 15.7 765 13, 14 7 12 7 7<br />

Mynt is odorata<br />

Apia AN<br />

-0.25 180 p hc<br />

0<br />

Eur 1152 147, 0 3.0 14. 1 1084 3, 17<br />

7 6 7 71<br />

Naj as flexilis<br />

Naja N s 0.48 30 a Hz<br />

0 4 6<br />

28 28 0 4.1 13.8 1338 13<br />

6 12 7 4 1<br />

Naj as marina Naja N VU r 97 a Hz 0 8 6 c 4 0 0 3.9 16.1 600 13 5 12 9 6 0<br />

Narcissus pseudonarcissus Lili N n 0.87 35 p Gb Otb 8 2 646 0 3 3.7 15.6 920 3 7' 5 6 5 0


Fam NS CS RS Chg_ Hght Len 1 P2 LF1 LF2 W Clonal Clone2 El E2 C Origin GB IR CI Tjan Tjul Prec Co Br Habitats L F R N S<br />

Lili Poac N n -0.32 -0.68 45 40 he hc 0 Rhizl 5 3 1 2051 1628 560 716 3 0 33.3 2 14.0 13.8 1226 1296 8 12 79 32 21 0<br />

Orch N EX n x -0.91 47 30 Gn 0 7 9 4 1 742 1 99 24 0 3.5 4.7 15.2 14.8 1107 938 7, 1 16 4 87 25 0<br />

Lami AR -1.23 100 he Rhizl 7 4 478 6 1 3.7 15.9 761 3, 7 4 7 6 0<br />

Nymp N n -0.13 150 Hy Rhizt 5 4 1140 452 0 3.6 15.1 975 13, 14 11 7 6<br />

Nymp N s 0.87 150 Hy Rhizl 4 6 68 0 0 1 7 12.5 1680 13 11 6 4<br />

Nymp N n 1.02 150 Hy Rhizl 7 3 1511 340 5 3.6 14.8 1090 13 11 6 4<br />

Meny N s 2.81 200 Hy Irreg Rhiz2 7 5 45 0 0 3.5 16.4 603 13, 14 11 7 6<br />

Apia Scro N n -0.35 -0.46 150 50 Th 0 7 5 2320 865 7 3.7 14.7 1047 6 5 6 5 0<br />

p Hz Hy 0 7 4 505 183 0 3.8 15.6 792 11 10 7 6<br />

Apia N n -0.04 150 he Hy 0 8 2 1599 633 12 4.0 14.8 1124 11, 14 ' 9 6 7<br />

Apia N n -1.18 0.19 100 80 Hy hc Hy 0 Node2 7 3 1 804 235 101 45 6 0 3.9 3.7 15.8 16.0 771 718 11 14 10 9 78 6 0<br />

Apia N n -0.36 0.48 100 hc 0 9 8 2 1 241 551 118 0 0 3 4.3 4.4 15,4 16.2 957 849 6 11 87 86 53 3 0<br />

Apia N s 0.37 100 hc 0 8 3 76 0 0 3.7 16.3 661 6 9 7 5 0<br />

Onag AN 1.02 100 hc 0 Am, SAm 1185 38 11 3.9 15.8 839 3, 16, 17, 19 4 6 4 0<br />

Onag AN 100 hc 0 Am? 614 9 2 3.9 15.9 777 3, 16, 17, 19 4 6 4 0<br />

Onag AX 100 hc 0 125 2 1 3.7 15.9 798 3, 16, 19 3 6 5 0<br />

Onag AN 80 he 0 Am? 217 0 4.2 15.9 921 3, 16, 17, 19 4 6 3 0<br />

Onag AN 100 he 0 Am 966 24 1 4.0 15.9 832 3, 16, 19 4 6 5 0<br />

Faba N NA VU n r -0.76 0.27 60 15 a Th he 0 9 7 4 1 265 10 0 5,6 3,6 15.8 16.2 999 710 Co 7 1 8 42 8 32 0 1<br />

Faba N n -0.45 60 Ch he sw Rhiz2 7 3 1664 178 1 3.8 15.3 878 7 4 6 3 0<br />

Aste Faba AR N n -0.82 0.66 200 70 Ch hc hc sw 0 87 4 724 778 0 5 3.6 3.7 16.0 15.9 718 733 6, 3, 7 17 4 86 37 0<br />

Ophi N s 10 Gn Root 5 2 72 12 4.3 13.3 1252 8 6 5 2 1<br />

Ophi N VU r 4 Gn Root 9 1 1 0 6,7 16.2 848 8 6 5 2<br />

Ophi N n 30 Gn Root 7 6 1474 209 3.6 15.1 964 6, 7 7 7 3<br />

Ophi N n 0.72 30 Gn Root 7 6 1474 209 3.6 15.1 964 6 7 7 3<br />

Orch N VU n r 0.83 45 35 Gn 0 9 2 936 6 182 0 3,9 4.0 15.7 16.4 807 766 7 4 89 23<br />

Orch N n -1.34 60 Gn 0 7 3 264 31 3.7 15.8 803 1. 7, 11 5 9 2<br />

Taxon name<br />

Nardus stdcta<br />

Narthecium ossifragum<br />

Neotinea maculata<br />

Neottia nidus-avis<br />

Nepeta cataria<br />

Nuphar lutea<br />

Nuphar pumila<br />

Nymphaea alba<br />

Nymphoides pe/tata<br />

Odontites vernus<br />

Oenanthe aquatica<br />

Oenanthe crocata<br />

Oenanthe fistulosa<br />

Oenanthe fluviatilis<br />

Oenanthe lachenalii<br />

Oenanthe pimpinelloides<br />

Oenanthe silaifolia<br />

Oenothera<br />

Oenothera biennis<br />

Oenothera biennis x<br />

glazoviana (0 . x fallax)<br />

Oenothera cambrica<br />

Oenothera glazioviana<br />

Onobrychis<br />

Orionis reclinata<br />

Orionis repens<br />

Ononis spinosa<br />

Onopordum acanthium<br />

Ophioglossum azoricum<br />

Ophioglossum lusitanicum<br />

Ophioglossum vulgatum<br />

Ophioglossum vulgatum<br />

sens.lat<br />

Ophrys apifera<br />

Ophrys fuciflora<br />

Ophrys insectifera<br />

Ophrys sphegodes<br />

Orchis laxiflora<br />

Orchis mascula<br />

Orchis militaris<br />

Omhis morio<br />

Orchis purpurea<br />

Orchis simia<br />

Orchis ustulata<br />

Oreopteris limbosperma<br />

Origanum vulgare<br />

Orch N s o -Oi l 20 50 Gn 0 98 2 4 c 62 0 0 8 1 4.0 6.4 16.3 16.7 729 800 6, 7 11 49 98 3 2<br />

Orch N n -0.72 40 Gn 0 7 3 1962 475 9 3.5 14.7 1073 1, 7, 16 5 7 4<br />

Orch N VU n r -0.98 45 20 Gn 0 7 4 3 c 931 19 124 0 0 8 3,4 3.9 16.3 15.8 694 801 6, 7 7 43 7 9 3 2<br />

Orch N s -0.56 50 Gn 0 7 3 36 0 1 4.0 16.5 748 1 4 8 3<br />

Orch N VU<br />

Orch N s r -1.77 30 15 Gn 0 87 3 265 10 0 0 3.8 3.5 16.4 15.7 697 777 7 34 8 2<br />

Thel N n -0.18 90 hc 0 7 3 1585 138 0 2.8 13.7 1323 1, 16 6 4 3<br />

Lami N n -0.10 65 Ch hc 0 Nodal 8 5 1148 179 0 3.7 15.3 898 7, 16 4 7 4


S<br />

P2 LF1 LF2 W Clonel Clone2 E1 E2 C Origin GB IR CI Tjan Tjul Prec Co Br Habitats L F R N<br />

Gb Mb DRg 8 3 Eur 1139 8 12 3.7 15.5 848 1, 3, 7, 8 8 3 6 4<br />

Th Gb Otb 0 9 7 2 1002 33 20 0 12 0 3,6 3.9 15.5 16.2 773 935 8 1, 3 5 71 5 4 7 5<br />

4 3<br />

p Th Gn 0 8 7 2 3 92 3 42 0 7 2 4.0 7.0 16.4 13.7 1493 832 8, 16 10 8 3 3 7 2<br />

3 6 0 0 4.5 16.5 753 Co 18 8 4 8 5<br />

34 0 2671 5 0 0 4.1 3.6 16.4 16.2 782 713 3, 18 7 8 3 98 2 3<br />

2 160 122 11 4.9 15.5 1004 1, 3, 16 4 5 6 5<br />

3 800 0 14 4.0 16.1 774 4, 5 7 4 8 6<br />

3 25 0 12 4.9 16.3 776 3, 6 7 4 7 2<br />

2 422 30 4 4.1 15.7 890 10 7 5 3 2<br />

3 c 71 0 0 3.1 15.3 666 3, 7 71 6 71 6<br />

6 228 7 0 1.4 12.2 1568 2, 10, 16 5 51 5 3<br />

2 735 576 4 4.2 14.5 1225 1, 11 6 9 5 4<br />

5 1 2393 23 791 6 2 3 3.4 5.1 14.4 16.0 1138 874 Co 1, 19 2, 16 4 9 26 4 5 2 4<br />

8<br />

7<br />

7<br />

9<br />

8<br />

7<br />

8<br />

7<br />

4<br />

8<br />

9<br />

5<br />

SAm 541 65 14 4.4 15.8 861 3, 17, 19 7 3 4 2<br />

Unk 998 32 11 3.9 15.8 843 3, 17 7 4 6' 5<br />

SAm 137 10 12 4.3 16.1 784 3, 17 7 4 6 8<br />

Aus, NZ 323 11 8 3.8 15.7 782 3, 17 7 4 6 4<br />

SAT 146 5 11 4.6 15.8 927 3, 17 6 5 6 5<br />

SAm 67 1 11 5.1 16.1 892 3, 17 6 5, 6 5<br />

SAl 10 0 10 5.9 16.1 861 3, 4 7 4 6 5<br />

As2, Am 396 27 4 3.8 15.7 895 3, 17 6 5 6 5<br />

6 311 24 0 1.7 12.1 1940 15, 16 7 6 5 3<br />

5 c 3 0 0 0.4 11.5 1392 7 9 4 8 2<br />

3 16 0 0 2.5 12.9 1141 7, 18, 19 9 3 8 2<br />

Crop 359 6 6 4.0 16.0 787 1, 4, 17 9 3 7 6<br />

3 874 48 6 3.7 15.7 759 4 7 4 6 5<br />

4 1875 402 13 3.7 15.0 910 3, 4 7 5 6 5<br />

2 357' 33 6 4. 1 15.9 776 4 7 4 8 4<br />

3 1712 370 14 3.8 15.3 877 3, 4 71 5 71 6<br />

3 Eur? 1600 190 12 3.7 15.3 868 3, 4, 17 7 4 7 8<br />

1 109 / 5 4.4 16.4 709 Co 18, 19, 21 9 6 7 4<br />

2 1 347 165 101 63 11 5 5.1 4.5 15.4 15.7 1129 876 Co 3, 21 5 7 8 67 7 6 5<br />

2 1336 3171 14 4.1 15.6 865 16, 17 71 4, 8 5<br />

4 714 0 0 3.2 15.3 877 1 3 61 7 6<br />

6 1091 302 0 3.0 13.7 1236 11 8 8 7 3<br />

4 1011 0 7 3.8 16.0 774 3, 6, 7 7 4 7 5<br />

3 1744 583 1 3.3 14.0 1226 11 8 8 5 2<br />

3 2118 744 9 3.4 14.1 1202 10, 12, 14 8 8 3 2<br />

Eur 1753 88 11 3.6 15.2 915 1, 3, 17 6 5 6 7<br />

6 2013 644 11 3.7 14.9 986 11, 13 7 10 6 6<br />

0<br />

0<br />

0<br />

0<br />

0<br />

0<br />

0<br />

0<br />

Rhiz1<br />

0<br />

Rhiz2<br />

Rhiz1<br />

Rhiz1<br />

Node2<br />

DRg<br />

Node2<br />

DRa<br />

DRg<br />

DRg<br />

Rhiz1<br />

0<br />

0<br />

0<br />

0<br />

0<br />

0<br />

0<br />

0<br />

0<br />

0<br />

0<br />

0<br />

0<br />

Rhiz2<br />

0<br />

0<br />

0<br />

0<br />

0<br />

Rhiz2 klieg<br />

p Th Gn<br />

a Gn Th<br />

Gn<br />

a Gn Th<br />

p Th Gn<br />

a Gn Th<br />

Gn<br />

a Gn Th<br />

Ch<br />

hc<br />

hc<br />

hc<br />

hc<br />

a hc Th<br />

Gb<br />

a hc Th<br />

Gb<br />

Gb<br />

Gb<br />

Th<br />

hc<br />

hc<br />

hc<br />

Th<br />

Th<br />

Th<br />

Th<br />

Th<br />

Th<br />

Th<br />

Th<br />

Th<br />

hc<br />

Gn<br />

hc<br />

hc<br />

hc<br />

hc<br />

hc<br />

Hy hc<br />

Taxon name Fam NS CS RS Chg Hght Len<br />

Ornithogalum angustifolium Li li AN : 1.05 30<br />

Ornithogalum pyrenaicum Li li N s 0.14 75<br />

Ornithopus perpusillus Faba N n -0.18 10<br />

Ornithopus pinnatus Faba N r 8<br />

Orobanche alba Orob N s -0.38 25<br />

Orobanche artemisiaecampestris<br />

Orob N EN r 60<br />

Orobanche caryophyllacea Orob N VU r 0.01 40<br />

Orobanche elatior Orob N n -0.33 75<br />

Orobanche he derae Orob N n 0.20 60<br />

Orobanche minor Orob N n -0.20 60<br />

Orobanche purpurea Orob N VU r 0.50 45<br />

Orobanche rapum-genistae Orob N s -0.35 85<br />

Orobanche reticulata Orob N r 60<br />

Odin ha s ecunda Pyro N n -0.40 5<br />

Os m unda regalis Osmu N n 0.56 160<br />

Otanthus maritimus Aste N EX x -1.49 30<br />

Oxalis acetosella Oxa N n -0.74 10<br />

Oxalis art iculata Oxa AN 25<br />

Oxalis corniculata Oxa AN 1.62 15<br />

Oxalis de bilis Oxa AN 20<br />

Oxalis exilis Oxa AN 5<br />

Oxalis incarnata Oxa AN 20<br />

Oxalis latifolia Oxa AN 20<br />

Oxalis pes-caprae Oxa AN 30<br />

Oxalis stricta . Oxa AN -0.09 40<br />

Oxyria digy na Poly N n -0.71 30<br />

Oxytropis campestris Faba N VU r. 20<br />

Oxytropis hail ed Faba N r 0.16 13<br />

Panicum mil aceum Poac AC 100<br />

Papaver argemone Papa AR -1.79 45<br />

Papaver dubium Papa AR 0.23 60<br />

Papaver hybridum Papa AR -0.35 50<br />

Papaver rhoeas Papa AR -0.41 60<br />

Papaver s om nife rum Papa AR . 2.54 100<br />

Parapholis incurva Poac N s, 0.09 10<br />

Parapholis strigosa Poac N n 0.14 25<br />

Parentucellia viscosa Scro N n 0.64 50<br />

Parietaria j udaica Urti N n1 0.08 52<br />

Paris guadrifolia Lili N n1 -0.68 40<br />

Parnassia palustris Saxi N n; -0.84 20<br />

Pastinaca sali va Apia N ni -0.39 180 b<br />

Pedicularis palustris Scro N n -0.88 60 b<br />

Pedicularis sylvatica Scro N n -1.28 25 P<br />

Pentaglottis sempervirens Bora AN , 1.81 100 p<br />

Persicaria amphibia Poly N n 0.27 60 200 p


F R N S<br />

77 6 6<br />

6 71 7<br />

CI Tja n<br />

0 3.3<br />

9 3.7<br />

10 3.7<br />

12 3.6<br />

1 3.6<br />

1 3.8<br />

0 1.6<br />

0 3.8<br />

0 2.8<br />

12 4. 1<br />

2 3.6<br />

5 5.3<br />

0 3.8<br />

5 5.3<br />

10 4.2<br />

3 4.1<br />

IR<br />

43<br />

740<br />

434<br />

934<br />

93<br />

31<br />

5<br />

145<br />

10<br />

582<br />

569<br />

0<br />

0<br />

0<br />

42<br />

0<br />

GB<br />

1355<br />

2041<br />

1881<br />

2578<br />

296<br />

203<br />

446<br />

390<br />

335<br />

1328<br />

1825<br />

6<br />

5<br />

6<br />

401<br />

482<br />

10<br />

184<br />

47<br />

2449<br />

1102<br />

80<br />

10171<br />

33<br />

219<br />

1927<br />

26<br />

2294<br />

2429<br />

2182<br />

2115<br />

3<br />

14<br />

55<br />

8<br />

1460<br />

1144<br />

1191<br />

885<br />

1343<br />

3<br />

LF2 W Clonal Clone2 E1 E2 C Origin<br />

Rhiz1 5 5<br />

0 7 6<br />

0 8 6<br />

0 7 5<br />

0 7 5<br />

0 7 3<br />

Rhizl 2 6<br />

Rhiz2 As 1<br />

Rhiz2 Eur<br />

Rhiz2 Eur<br />

Rhiz2 7 3<br />

0 8 2<br />

0 7 3 Eur<br />

0 8 3<br />

0 Crop<br />

0 8 2<br />

0 8 3<br />

0 Eur<br />

0 5 4 c<br />

Gn Rhiz2 5 6<br />

0 Eur?<br />

0 9 1 Eur<br />

Rhiz2 5 6<br />

Rhir / 2 6<br />

0 8 3<br />

0 8 3<br />

0 7 4 c<br />

0 7 4<br />

0 8 4<br />

Gn Rhiz2 6 6<br />

0 7 3<br />

w 0 1 3<br />

h 0 7 3<br />

h 0 5 3<br />

h 0 7 3<br />

w 0 4 5 c Eur, As<br />

w 0 Am4<br />

he h 0 8 3<br />

h 0 7 5<br />

h Rhiz2 Sto12 4 3 Eur<br />

h Sto12 5 3 c<br />

LF1<br />

hc<br />

Th<br />

Th<br />

Th<br />

Th<br />

Th<br />

he<br />

Gn<br />

Gn<br />

Gn<br />

Gn<br />

Th<br />

Th<br />

Th<br />

hc<br />

hc<br />

hc<br />

he<br />

he<br />

Hy<br />

Th<br />

Th<br />

Gn<br />

hc<br />

Th<br />

hc<br />

hc<br />

hc<br />

hc<br />

Hy<br />

he<br />

Ch<br />

hc<br />

hc<br />

hc<br />

Ph<br />

Ph<br />

Th<br />

hc<br />

hc<br />

hc<br />

1 P2<br />

6 8 65 7 8<br />

8 6 9<br />

6 6 2<br />

4 5 6<br />

5 5 7<br />

5 6 6<br />

7 7 7<br />

2 6 1<br />

3 5 2<br />

3 6 2<br />

4 7 5<br />

5 8 6<br />

5 8 4<br />

5 71 7<br />

ChQ Hght Len<br />

-0.44 80<br />

-0.41 75<br />

-0.04 100<br />

-0.95 80<br />

-0.06 40<br />

-0.90 75<br />

-0.58 30<br />

0.59 150<br />

0.01 70<br />

0.80 30<br />

-0.15 120<br />

50<br />

50<br />

-0.68 50<br />

-0.34 75<br />

0.12 100<br />

0.29 200<br />

0.03 100<br />

-0.07 150<br />

0.23 200<br />

-0.32 120<br />

45<br />

-0.22 40<br />

-0.30 50<br />

-0.56 17<br />

50<br />

-0.10 60<br />

150<br />

-0.33 100<br />

0.43 270<br />

0.45 60<br />

20<br />

0.07 120<br />

-0. 16 50<br />

-0.73 80<br />

4600<br />

5500<br />

0.771 80<br />

-0.06 95<br />

20<br />

13<br />

RS<br />

n<br />

n<br />

n<br />

n<br />

n<br />

s<br />

n<br />

n<br />

r<br />

n<br />

0 0 4.1<br />

21 0 2.6<br />

0 3.6<br />

6 3.6<br />

10 3.7<br />

6 4.1<br />

8 0 2.4<br />

0 -0.7<br />

6 9 4.5<br />

8 4 3.5<br />

0 3.3<br />

3 3.5<br />

10 3.5<br />

11 3.7<br />

14 3.8<br />

0 -1.1<br />

0 5.4<br />

0 3.9<br />

0 4.1<br />

2 3.2<br />

1 3.2<br />

10 3.9<br />

8 3.8<br />

6 4 3.4<br />

0 3.5<br />

n<br />

r<br />

9 7 5 7<br />

4 7 6<br />

5 6 5<br />

6 4 4<br />

5 6 4<br />

3 5 3<br />

s<br />

n<br />

75<br />

6<br />

n<br />

s<br />

n<br />

n<br />

r<br />

n<br />

n<br />

n<br />

n<br />

r<br />

r<br />

s<br />

r<br />

Taxon name Fam NS CS<br />

N<br />

N<br />

N<br />

N<br />

N<br />

N<br />

N<br />

AN<br />

AN<br />

AN<br />

N<br />

N EN<br />

AN CR<br />

N<br />

AR<br />

N<br />

N<br />

AR<br />

N<br />

N<br />

AN<br />

AN<br />

N<br />

N<br />

N<br />

N<br />

N<br />

N<br />

N<br />

N<br />

N<br />

N VU<br />

N VU<br />

N<br />

NA VU<br />

AN<br />

AN<br />

AR<br />

N<br />

AN<br />

N<br />

-C.<br />

G.%<br />

43 78 4 2<br />

5 71 6<br />

Br Habitats<br />

6<br />

11, 13, 14<br />

4, 11<br />

3, 4<br />

13, 14<br />

13, 14<br />

7, 15<br />

3<br />

1, 3<br />

3<br />

14<br />

19<br />

8<br />

8, 19<br />

3, 17<br />

3, 4<br />

19<br />

5<br />

11<br />

11, 14<br />

3, 17<br />

4, 17<br />

1, 16<br />

11, 15<br />

19<br />

3, 6<br />

8<br />

3, 6<br />

3, 6<br />

11<br />

1, 16<br />

10, 15<br />

1, 10<br />

7<br />

1, 3<br />

2<br />

2<br />

3, 4<br />

7<br />

3, 17<br />

3, 16<br />

Prec Co<br />

1021<br />

1093<br />

958<br />

1077<br />

1003<br />

780<br />

1588<br />

1149<br />

1000<br />

941<br />

1002<br />

774 Co<br />

613<br />

774<br />

819<br />

751<br />

599 Co<br />

1127<br />

631<br />

1044<br />

856<br />

760<br />

1515<br />

1770<br />

918 Co<br />

942<br />

621<br />

1023<br />

1047<br />

1055<br />

1048<br />

1829<br />

1279<br />

806<br />

826<br />

1054<br />

1223<br />

795<br />

781<br />

985<br />

1153<br />

Tjul<br />

14.8<br />

14.8<br />

15.1<br />

14.6<br />

15.2<br />

15.9<br />

12.2<br />

14.8<br />

13.9<br />

15.3<br />

14.8<br />

16.7<br />

16.5<br />

16.7<br />

15.8<br />

16.2<br />

16.7<br />

13.5<br />

16. 1<br />

14.6<br />

15.5<br />

15.9<br />

13.1<br />

10.8<br />

15.3<br />

15.1<br />

16.2<br />

14.8<br />

14.7<br />

14.7<br />

14.8<br />

10.6<br />

15.5<br />

16.3<br />

16.4<br />

14.7<br />

14.1<br />

15.9<br />

16.0<br />

14.9<br />

11.5<br />

10 5 7 6<br />

67<br />

71<br />

78<br />

93<br />

54 73 5 2<br />

5 4 4<br />

4 8 3<br />

5 6 5<br />

6 3 4<br />

7 2 2<br />

5 71 6<br />

12<br />

21<br />

2<br />

b<br />

4 86 3 2<br />

4 7 4<br />

5 6 3<br />

n<br />

n<br />

4 7 4<br />

16<br />

1153<br />

11.5<br />

0 3.5<br />

3<br />

h Sto12 4 1<br />

hc<br />

13<br />

r<br />

NE VU<br />

4 7 2<br />

3<br />

7<br />

786<br />

1094<br />

14.9<br />

14.5<br />

0 3.0<br />

12 3.5<br />

89<br />

72<br />

2629<br />

h Sto12 Eur<br />

h Sto12 7 3<br />

hc<br />

hc<br />

13<br />

-0.59 12<br />

n<br />

AN<br />

N


CI Tja n<br />

12 5.2<br />

3 3.6<br />

0 3.6<br />

0 3.6<br />

0 3.0<br />

0 5.1<br />

0 3.9<br />

0 3.0<br />

2 3.3<br />

6 3.7<br />

0 0.8<br />

2 4.0<br />

14 4.1<br />

14 3.5<br />

14 3.5<br />

8 3.8<br />

0 3.5<br />

1 3.5<br />

0 3.4<br />

0 0.6<br />

6 3.7<br />

14 3.5<br />

6 4.6<br />

1 3.1<br />

2 3.6<br />

0 -0.6<br />

0 1.1<br />

5 3.4<br />

13 5.9<br />

5 3.2<br />

2 3.7<br />

10 3.5<br />

2 3.6<br />

11 3.6<br />

0 1.9<br />

14 6.3<br />

1 2.8<br />

0 3.7<br />

11 3.4<br />

3.5<br />

3.6<br />

3.1<br />

1.2<br />

1 3.7f<br />

3.7<br />

1 3.6<br />

IR<br />

0<br />

24<br />

109<br />

391<br />

0<br />

74<br />

309<br />

484<br />

116<br />

25<br />

0<br />

10<br />

303<br />

985<br />

975<br />

405<br />

0<br />

308<br />

251<br />

2<br />

0<br />

985<br />

0<br />

3<br />

0<br />

0<br />

0<br />

297<br />

0<br />

0<br />

12<br />

928<br />

423<br />

903<br />

0<br />

0<br />

0<br />

0<br />

717<br />

665<br />

0<br />

0<br />

0<br />

480<br />

819<br />

906<br />

GB<br />

11<br />

312<br />

584<br />

1938<br />

1<br />

0<br />

500<br />

1523<br />

444<br />

1009<br />

65<br />

137<br />

1445<br />

2804<br />

2766<br />

1295<br />

1243<br />

949<br />

1163<br />

72<br />

83 1<br />

2792<br />

72<br />

169<br />

1063<br />

8<br />

62<br />

1865<br />

54<br />

1960<br />

132<br />

2766<br />

1637<br />

2721<br />

16<br />

16<br />

18<br />

153<br />

2150<br />

2176<br />

268<br />

48<br />

10<br />

19371<br />

2030<br />

2605<br />

Origin<br />

Clone2 El E2 C<br />

5 2<br />

7 2<br />

7 3<br />

' 7 4<br />

1 4<br />

7 1<br />

7 1<br />

4 6<br />

W Clonel<br />

h Sto12<br />

h Rhiz2<br />

h 0<br />

h 0<br />

h O<br />

h O<br />

h o<br />

h 0<br />

w 0<br />

w 0<br />

w 0<br />

0<br />

0<br />

Rhiz1<br />

0<br />

0<br />

Rhiz1<br />

0<br />

0<br />

0<br />

Rhiz2<br />

0<br />

0<br />

0<br />

Rhiz2<br />

0<br />

0<br />

Rhiz2<br />

0<br />

0<br />

0<br />

Rhiz2<br />

Rhiz2<br />

0<br />

0<br />

0<br />

0<br />

0<br />

0<br />

0<br />

Rhiz2<br />

Rhiz2<br />

Rhiz2<br />

0<br />

0<br />

0<br />

LF2<br />

LF1<br />

hc<br />

Hy<br />

hc<br />

hc<br />

hc<br />

hc<br />

hc<br />

hc<br />

Ph<br />

Ph<br />

Ph<br />

Th<br />

hc<br />

hc<br />

he<br />

hc<br />

hc<br />

Gn<br />

Gn<br />

hc<br />

hc<br />

Th<br />

hc<br />

hc<br />

hc<br />

hc<br />

hc<br />

he<br />

Th<br />

he<br />

he<br />

hc<br />

hc<br />

hc<br />

hc<br />

Th<br />

Ch<br />

Ch<br />

Ch<br />

Ch<br />

Gn<br />

Gn<br />

Gn<br />

Th<br />

Th<br />

Th<br />

1 P2<br />

Hght Len<br />

9<br />

10 10<br />

100<br />

70<br />

5<br />

8<br />

3<br />

8<br />

2500<br />

4200<br />

3000<br />

200<br />

6<br />

15<br />

15<br />

15<br />

6<br />

40<br />

50<br />

40<br />

70<br />

20<br />

35<br />

100<br />

50<br />

22<br />

40<br />

30<br />

10<br />

75<br />

100<br />

58<br />

75<br />

70<br />

90<br />

25<br />

10<br />

10<br />

15<br />

25<br />

80<br />

40<br />

80<br />

20<br />

30<br />

30<br />

Chg<br />

0<br />

0<br />

-0.03<br />

-0.16<br />

-0.31<br />

0<br />

0<br />

0<br />

0<br />

0<br />

0<br />

0<br />

0<br />

0<br />

2<br />

0<br />

0<br />

3<br />

0<br />

0<br />

0<br />

0<br />

0<br />

1<br />

R N<br />

8 2<br />

4 2<br />

7 6<br />

7 3<br />

8 2<br />

4 2<br />

4 2<br />

6 2<br />

5 2<br />

5 2<br />

2 2<br />

7 7<br />

6 4<br />

6 4<br />

6 7<br />

6 4<br />

7 3<br />

6 2<br />

71 4<br />

7 3<br />

7 5<br />

6 7<br />

5 2<br />

6 5<br />

7 4<br />

3 2<br />

6 3<br />

6 4<br />

5 5<br />

6 5<br />

7 6<br />

6 5<br />

6 5<br />

6 6<br />

7 6<br />

6 4<br />

9 1<br />

8 2<br />

2 2<br />

6 3<br />

7 6<br />

7 3<br />

5 5<br />

71 6<br />

6 7<br />

7 6<br />

F<br />

3<br />

10<br />

5<br />

4<br />

8<br />

8<br />

8<br />

8<br />

5<br />

3<br />

6<br />

4<br />

6<br />

5,<br />

5<br />

7<br />

4<br />

6<br />

5<br />

5<br />

5<br />

5<br />

3<br />

5<br />

4<br />

5<br />

5<br />

6<br />

4<br />

5<br />

9<br />

5<br />

5<br />

6<br />

5<br />

4<br />

6<br />

3<br />

71<br />

5<br />

5<br />

3<br />

5<br />

5<br />

51<br />

5<br />

L<br />

8<br />

8<br />

7<br />

71<br />

9<br />

7<br />

8<br />

8<br />

7f<br />

7<br />

7<br />

7<br />

8<br />

71<br />

7<br />

8<br />

8<br />

6<br />

5<br />

7<br />

7<br />

7<br />

8<br />

5<br />

9<br />

6<br />

7<br />

8<br />

8<br />

4<br />

7<br />

7<br />

7<br />

7<br />

5<br />

9<br />

9<br />

7<br />

8<br />

8<br />

4<br />

5<br />

4<br />

71<br />

7<br />

7<br />

Br Habitats<br />

7, 16<br />

13<br />

6<br />

7<br />

11<br />

10, 12<br />

10, 11<br />

11, 12<br />

2<br />

1, 2, 17, 19<br />

2<br />

3, 4<br />

3, 6, 18<br />

6, 7<br />

3, 5<br />

15, 21<br />

7<br />

1, 10<br />

1, 6<br />

15<br />

7, 8<br />

3, 4, 5, 6<br />

19<br />

1<br />

3<br />

15, 16<br />

15, 16<br />

6, 19<br />

3<br />

1<br />

11, 13, 14<br />

3, 5, 6, 7<br />

3, 5, 6, 7<br />

1, 3, 6<br />

16<br />

3, 4, 17<br />

7<br />

7<br />

8, 10, 12<br />

7<br />

1<br />

1, 16<br />

1<br />

3, 4<br />

4, 17<br />

3, 4, 17<br />

Prec Co<br />

871<br />

1040<br />

819<br />

958<br />

752<br />

1270<br />

1475<br />

1305<br />

1302<br />

889<br />

1930<br />

896<br />

1065<br />

1105<br />

1102<br />

1248 Co<br />

804<br />

1235<br />

1147<br />

2142<br />

790<br />

1105<br />

741 Co<br />

959<br />

850<br />

1907<br />

2252<br />

1134<br />

935<br />

1015<br />

948<br />

1102<br />

1017<br />

1095<br />

1246<br />

923<br />

1037<br />

783<br />

1200<br />

1114<br />

829<br />

1091<br />

1061<br />

1008<br />

1039<br />

1073<br />

Tjul<br />

16,1<br />

14.8<br />

15.5<br />

15.0<br />

13.6<br />

14.7'<br />

13.7<br />

13.6<br />

14.0<br />

15.5<br />

11.7'<br />

15.6<br />

14.8<br />

14.5<br />

14.5<br />

14.0<br />

15.6<br />

14.3<br />

14.7<br />

11.5<br />

15.8<br />

14.5<br />

16.4<br />

14.5<br />

15.6<br />

10.5<br />

11.6<br />

14.3<br />

16.3<br />

14.8<br />

15.2<br />

14.5<br />

14.8<br />

14.5<br />

13.9<br />

16.3<br />

15.0<br />

16.2<br />

14. 1<br />

14.4<br />

16.0<br />

15.1<br />

13.1<br />

14.9<br />

14.8<br />

14.6<br />

-0.83<br />

-0.76<br />

RS<br />

e<br />

S.<br />

n<br />

n<br />

x<br />

o<br />

n<br />

n<br />

Am4<br />

Eur<br />

0.40<br />

'<br />

s.<br />

Eur<br />

4 5<br />

0 3<br />

8 4<br />

8 4<br />

6 5<br />

3 4<br />

7 5<br />

5 5<br />

7 3<br />

DRi 1 6<br />

8 6<br />

6 4<br />

DRi 8 4<br />

0.16<br />

1.35<br />

0.09<br />

-0.28<br />

-0.79<br />

-1.67<br />

-0.88<br />

-0.31<br />

hc<br />

p<br />

n<br />

n<br />

n<br />

n<br />

n<br />

n<br />

n1<br />

s<br />

ni<br />

e<br />

s:<br />

0.83<br />

0.63<br />

-0.05<br />

0.21<br />

7 3<br />

1 3<br />

2 6<br />

7 ?<br />

9 1<br />

5 6<br />

5 6<br />

6 6<br />

6 6<br />

Nodel 6 4<br />

5 4 c<br />

9 1<br />

5 3 c<br />

8 1<br />

7 2<br />

7 3<br />

7 3<br />

7 5<br />

4 3<br />

6 5<br />

6 6<br />

6 6<br />

n.<br />

r :<br />

s<br />

n.<br />

s'<br />

n<br />

n.<br />

n<br />

n<br />

r<br />

r '<br />

r ,<br />

n.<br />

n<br />

n<br />

n<br />

s<br />

r<br />

Taxon name Fam NS CS<br />

N VU<br />

N<br />

N<br />

N<br />

NA EX<br />

N<br />

N<br />

N<br />

AN<br />

AN<br />

N<br />

AC<br />

N<br />

N<br />

N<br />

N<br />

N<br />

N<br />

N<br />

N<br />

N<br />

N<br />

N<br />

AN<br />

N<br />

N VU<br />

N<br />

N<br />

N<br />

N<br />

AN<br />

N<br />

N<br />

N<br />

N<br />

NA<br />

N VU<br />

N<br />

N<br />

N<br />

N<br />

N<br />

N VU<br />

AR<br />

N<br />

N<br />

Eur<br />

-0.48<br />

NHem<br />

1.33<br />

0.27<br />

-1.55<br />

0.60<br />

1.10<br />

1.17<br />

-0.04<br />

-0.10<br />

-0.37<br />

-0.50<br />

-1.14<br />

0.27<br />

0.34<br />

-0.70<br />

n:<br />

n1<br />

I


Taxon name Fam NS CS RS Chg_ Hght Len P1 P2 LF1 LF2 W Clonal Clone2 El E2 C Origin GB IR CI Tjan Tjul Prec Co Br Habitats L F R N S<br />

Polygonum boreale Poly N $ 20 a Th 0 4 2 109 0 0 3.6 12.4 1084 4 7 5 6 0<br />

Polygonum maritimum Poly N EN r 0.21 20 p Ch 0 9 1 16 1 4 6.0 16.2 950 Co 19 9 3 4 3<br />

Polygonum oxyspermum Poly N n 0.01 20 a Th 0 6 3 305 75 9 4.6 14.8 1102 Co 19 9 6 8 3<br />

Polygonum runvagum Poly AR 20 a Th 0 7 3 274 0 4 3,9 16. 1 738 4 8 4 5 0<br />

Polypodiurn cambricum Poly N n 40 P hc Gn Rhizl 9 1 196 157 1 4.4 15.1 1102 3, 16 6 5 3 0<br />

Polypodiurn inte rje ctum Poly N n 40 p hc Gn Rhizl 7 2 1188 487 12 3.9 14.9 1074 1, 3, 16 5 5 3 0<br />

Polypodium vulgare Poly N n 40 P hc Gn Rhizl 5 3 1795 523 1 3.5 14.3 1158 1, 3, 16 5 5 3 0<br />

Polypodiurn vulgare sens.lat Poly N n -0.03 40 p hc Gn Rhir l 6 3 2496 916 12 3,5 14.4 1133 1 5 5 3 0<br />

Polypogon rnonspeliensis Poac N $ 0.60 80 a Th 0 9 1 45 0 0 4.3 16.6 661 6 8 8 6 3<br />

Polystichum aculeaturn Dryo N n 0.54 60 p hc 0 7 5 1618 314 3 3.2 14.4 1145 1, 16 5 5 5 0<br />

Polystichurn fonchitis Dryo N n -0.76 30 p hc 0 4 6 181 20 0 1.4 12.1 1857 7, 15, 16 6 5 3 0<br />

Polystichurn setiferurn Dryo N n 1.47 120 p hc 0 9 2 1249 748 10 4,1 15.0 1032 1 4 5 6 0<br />

Populus alba Sail AN 2000 p Ph w Root Eur, As 1 1531 116 10 3.6 15.3 867 3, 17, 19 6 6 6 0<br />

Populus alba x tremula (P. x I<br />

cane s ce ns) Sali AN 0.97 3000 p Ph w Root Eur 1145 110 7 3.8 15.6 819 1, 3 6 6 5 0<br />

Populus nigra sens.lat Sali N n 0.65 3000 p Ph w Root 7 4 692 66 2 3.6 15.7 800 3, 14 6 8 7 0<br />

Populus tremula Sall N n 0.88 2000 p Ph w Root 5 5 2248 414 7 3.3 14.5 1102 1, 16 6 5 6 0<br />

Potarnogeton acutifolius Pota N VU r 0.05 100 p Hy DRa 7 3 35 0 0 4.0 16.4 702 13 7 12 6 0<br />

Potamogeton alpinus Pota N n 0.30 280 p Hy lrreg DRa 4 6 5371 142 1 3.1 14.1 1188 13 71 12 5 1<br />

Potamogeton be rchto ldii Pota N n 1.66 60 p Hy DRa 5 6 1461 317 3.6 14.7 1027 13, 14 7 12 5 0<br />

Potarnogeton co/oratus Pota N s 0.03 70 p Hy Meg Rhiz2 8 3 142 140 4.1 15.1 893 13 7 11 5 0<br />

Potamogeton compressus Pota N s -1.68 90 p Hy DRa 5 5 134 0 3.4 15.9 697 13 7 12 4 -<br />

Potamogeton crispus Pota N n 150 p Hy Rhiz2 DRa 8 5 1541 358 3.7 15.2 893 13, 14 7 12 6 /<br />

Potamogeton epihydrus Pota N VU r 0.11 190 p Hy lrreg DRa 5 0 2 0 4.5 13.0 1288 13 8 12 / 0<br />

Potamogeton filiformis Pota N s 0.63 30 p Hy Rhiz2 DRg 4 6 161 63 3.6 13.3 1109 13 7 12 5 1<br />

Potamogeton friesii Pota N $ -1.06 150 p Hy DRa 5 6 270 43 3.6 15.4 782 13 7 12 5 0<br />

Potamogeton gramineus Pota N n 0.67 80 p Hy lrreg Rhiz2 5 6 473 163 3.3 13.8 1170 13, 14 7 12 3 0<br />

Potamogeton grarnineus x<br />

lucens (P. x zizii) Pota NH S 120 p Hy Meg Rhiz2 100 92 3.5 14.3 1138 13, 14 7 12 4 0<br />

Potamogeton grarnineus x<br />

perfoliatus (P. x nite ns) Pota NH n 250 p Hy Irreg Rhiz2 216 113 3.5 13.6 1257 14 7 12 5 1<br />

Potarnogeton lucens Pota N n 0.25 250 p Hy Irreg Rhiz2 7 4 456 171 I 3.7 15.5 832 13, 14 7 12 6 0<br />

Potarnogeton natans Pota N n 100 p Hy Irreg Rhiz2 5 6 2340 648 6 3.5 14.5 1091 11, 13, 14 7 11 4 0<br />

Potamogeton nodosus Pota N r -0.18 250 p Hy Me g Rhiz2 8 6 15 0 0 3.9 16.4 761 14 6 12 5 0<br />

Potamogeton obtusifolius Pota N n 0.96 190 p Hy DRa 5 6 601 155 0 3.4 14.7 994 13 7 12 5 0<br />

Potarnogeton pectinatus Pota N n 230 p Hy Rhiz2 DRg 6 6 1165 242 4 3.8 15.3 844 13, 14 6 12 7 2<br />

Potarnogeton perfoliatus Pota N n 300 p Hy Meg Rhiz2 5 6 1056 275 0 3.5 14.6 1026 13, 14 7 12 5 1<br />

Potam ogeton polygonifolius Pota N n 10 70 p Hy hc Irreg Rhiz2 7 2 1841 582 5 3.3 13.9 1254 11, 12, 13 8 10 2 0<br />

Potamogeton praelongus Pota N n -0.26 300 p Hy lrreg Rhiz2 4 6 252 90 0 3.2 14.1 1178 13 7 12 5 1<br />

Potamogeton pusillus Pota N n 0.77 70 p Hy DRa 8 6 806 146 1 3.6 15.1 877 13 7 12 6 1<br />

Potamogeton rutilus Pota N r 0. 18 45 p Hy DRa 4 3 13 0 0 3.8 12.9 1115 13, 14 7 12 5 0<br />

Potarnogeton trichoide s Pota N n 0.57 100 p Hy DRa 8 4 185 0 1 3.8 16.2 739 13, 14 6 12 6 0<br />

Potentil la anglica Rosa N n 0.11 25 p hc Sto12 7 3 1248 733 4 4.0 15.0 1045 6 7 5 5 0<br />

Potent) Ila ans erina Rosa N n -0.23 25 p hc Sto12 5 6 2662 973 12 3.6 14.6 1083 6 8 7 6 2<br />

Potentilla argentea Rosa N n -0.78 30 p hc 0 7 4 323 0 5 3.6 16.0 704 3, 8 8 3 2 0<br />

Potent" Ila crantzir Rosa N s -0.21 20 p hc 0 2 4 98 0 0 0.7 12.0 1855 7, 16 8 5 2 0<br />

Co


,<br />

Taxon name Fam NS CS RS Chg Fight Len 1 P2 LF1 LF2 W Clonel Clone2 El E2 C Origin GB IR CI Tjan Tjul Prec Co Br Habitats L F R N S<br />

Potent/ ha erecta Rosa N n -0.50 25 hc h 0 5 4 2700 947 12 3.5 14.4 1118 8 7 7 3 2<br />

Potentilla fruticosa Rosa N r 1.44 100 Pn w 4 6 8 7 0 2.8 13.7 1366 16 8 6 8 2<br />

Potentilla ne um anniana Rosa N s -0. 17 10 hc h 0 7 3 128 0 0 3.1 14.7 994 7, 16 7 3 8 1<br />

Potentilla palustris Rosa N n -0.21 50 Gn Hy h Rhiz2 5 6 1672 721 'I 3.4 14.0 1186 11 8 9 5 3<br />

Potentilla reptans Rosa N n -0.62 30 hc h Sto12 8 4 1882 769 11 3.8 15.1 959 6 71 5 7i 5<br />

Potent/ Ila rupestris Rosa N VU r 60 hc h 0 9 3 4 01 0 3.0 13.8 934 16 7 4 6 2<br />

Potentilla sterilis Rosa N n -0.30 15 hc h Stoll 7 2 2167 742 8 3.6 14.7 1071 1 5 5 5 5<br />

Primula elatior Prim N s 0.01 20 hc h 0 7 3 c 38 0 0 3.3 16.3 591 1 4 5 7 6<br />

Primula farinosa Prim N s -0.46 5 hc h 0 4 5 103 0 0 2.2 13.8 1194 7, 11 9 8 9 2<br />

Primula scotica Prim NE e -0.18 5 hc h 0 4 1 42 0 0 3.6 12.4 1026 Co 6, 19 9 4 71 2<br />

Primula veris Prim N n -0.32 15 hc h 0 7 4 1632 369 6 3 7 15.2 900 6, 7 7 4 7 3<br />

Primula vulgaris Prim N n 0.16 15 hc h 0 7 3 2651 934 11 3.5 14.5 1108 1, 16 5 5 6 4<br />

Prune lla vulgaris Lami N n 0.60 30 hc h Nodel 6 6 2783 970 14 3.5 14.4 1106 6, 7 7 5 8 4<br />

Prunus avium Rosa N n 1.29 2500 Ph w Root 7 3 2136 431 7 3.4 14.8 1024 1 4 5 6 6<br />

Prunus cerasifera Rosa AN 3.43 800 Ph w Eur, As 1 900 11 4 3.7; 15.8 803 1, 3, 17 6 5 7 6<br />

Prunus cerasus Rosa AR 0.90 800 Ph w Root Eur 706 339 7 3.9 15.2 961 1, 3 6 5 6 5<br />

Prunus domestica Rosa AR 2.19 800 Ph w Root Eur 1656 406 8 3.7 15.2 928 3, 17 7 5 7 6<br />

Prunus laurocerasus Rosa AN 4.70 600 Ph w Eur 1253 345 4 3.8 15.3 953 1, 17 4 6 5 6<br />

Prunus lusitanica Rosa AN , 800 Ph w Eur 468 31 1 3.8 15.5 876 1, 17 6 5 7 6<br />

Prunus padus Rosa N n 0.58 1500 Ph w 5 5 1089; 189 2.71 13.8 1240 1 5 6 6 71<br />

Prunus spinosa Rosa N n 0.40 400 Ph w Root 7 3 23081 917 3.7 14.8 1032 3 6 5 7 6<br />

Pseud<strong>of</strong>umaria lutea Furna AN 0.59 30 hc h 0 Eur 1425 39 3.6 15.4 876 3, 17 6 6 8 5<br />

-le<br />

C . Ps e udorchis albida Orch N n -0.88 20 Gn h 0 4 3 385 110 2.6 13.0 1534 7, 8 8 5 6 2<br />

Pseudotsuga menziesii Pina AN ! 5800 Ph w Am4 900 13 3.4 15.0 1035 1, 2, 17 6 6 4 4<br />

Pteridium aquilinum Denn N n -0.71 150 Gn Rhiz2 7 6 2685 964 / 3.5 14.5 1109 1, 9 6 5 3 3<br />

Puccinellia dis tans Poac N n 3.02 60 hc 0 5 4 405 39 4.1 14.9 859 3, 21 8 8 7 7<br />

Puccinellia fasciculata Poac N s -0.51 50 hc 0 8 2 97 11 4.5 16.4 722 6 8 7 7 7<br />

Puccinellia maritima Poac N n -0.27 80 hc Node2 5 1 788 201 4.1 14.4 1162 Co 21 9 8 7 6<br />

Puccinellia rupestris Poac N s -0.40 40 b Th hc 0 8 1 148 0 4.5 16.2 756 Co 6, 19 9 7 7 5<br />

Pulicaria dysenterica Aste N n -0.08 80 hc Rhiz2 8 4 14971 391 1 4.0 15.5 885 6, 11 71 71 7 4<br />

Pulicaria vulgaris Aste N VU r -0.551 45 Th 0 7 4 121 0 4.0 16.5 696 8 9 8 6 7<br />

Pulmonaria longifolia Bora N s -0.01 40 hc 0 7 1 21 0 4.7 16.5 810 1, 3 6 4 6 5<br />

Pulmonaria obscura Bora N VU r,<br />

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Pulmonaria <strong>of</strong>i cinalis Bora AN<br />

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Pulsatilla vulgaris Ranu N s -0.50 30 hc 0 7 3 c 691 0 3.3 16.0 664 7 71 3 8 3<br />

Pyrola media Pyro N 5 -1.09 10 hc Rhizl 4 4 258 47 2.2 13.0 1197 2, 10 5 4 5 2<br />

Pyrola rninor Pyro N n -0.55 7 hc Ch Rhizl 4 6 558 50 2.6 13.9 1089 1, 16 5 5 4 2<br />

Pyrola rotun difolia Pyro N s' -0.08 12 hc Rhizl 5 4 155 13 2.9 14.2 1072 2, 19 6 7 7 3<br />

Pyrus communis sens.lat Rosa AR 1.49 1500 Ph w Root Eur?, As l ? 781 6 3.8 15.9 801 1, 3, 17 7 5 6 7<br />

Pyrus cornm unis sens.str. Rosa AR 1500 Ph w Root Gard 3, 17 7l 5 6 71<br />

Pyrus cordata Rosa NA EN r 400 Ph w Root 7 1 9 0 5.4 15.9 1129 3 6 5 5 4<br />

Quercus cerris Faga AN 2.32 3500 Ph w Eur 1247 42 1 3.8 15.6 862 1, 3, 17 6 4 6 6<br />

Quercus ilex Faga AN ' 2.37 2500 Ph w 9 1 Eur 802 22 1 4.1 15.9 824 1, 17, 19 6 3 7 4<br />

Quercus petraea Faga N e 0.14 3000 Ph w 7 3 1832 549 3.5 14.6 1136 1 6 6 3 4 0<br />

Quercus robur Faga N n -0.60 3000 Ph w 7 3 2310 663 1 3.5 14.71 1049 1, 3 71 5 5 4 0<br />

Radio/a linoides Lina N n -0.87 6 a Th h 0 7 3 548 115 I I 4.2 14.7 1061 10 8 7 4 2 1<br />

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Taxon name Fam NS CS RS Chg Hght Len P1 P2 LF1 LF2 W Clonel Clone2 El E2 C Origin GB IR CI Tjan Tjul Prec Co Br Habitats L F R N<br />

Ranunculus acris Ranu N n 0.30 - 75 p hc 0 3 5 2780 968 13 3.5 14.4 1106 6 6 4<br />

Ranunculus aquatilis Ranu N n 90 a Hz 0 Irreg 7 3 1123 157 4 3.6 15.2 860 13, 14 1 7 5<br />

Ranunculus aquatilis sens.lat Ranu N n -1.37 90 a Hz 0 Irreg 6 3 1830 430 6 3.6 15.3 860 13, 14 1 7 5<br />

Ranunculus arvensis Ranu AR -3.771 60 a Th 0 8 4 824 2 3 3.7 15.9 742 4 7 6<br />

Ranunculus auncomus Ranu N n -0.33 40 p hc 0 5 3 1379 226 1 3.3 15.1 922 1 6 5<br />

Ranunculus baudotii Ranu N n -0.04 60 a Hz 0 Node2 8 3 361 61 5 4.4 15.3 905 13 1 7 6<br />

Ranunculus bulbosus Ranu N n -0.48 40 p hc 0 6 3 2259 616 14 3.6 14.8 1004 6, 7 7 4<br />

Ranunculus circinatus Ranu N n -0.34 75 p Hy Irreg 7 5 575 76 0 3.7 15.8 753 13, 14 1 7 7<br />

Ranunculus ficaria Ranu N n 0.16 25 p Gn Otb DRa 8 3 2648 820 14 3.6 14.5 1084 1, 3 6 6<br />

Ranunculus flammula Ranu N n -0.60 50 p hc Hy Nadel 7 3 2651 938 11 3.5 14.4 1122 11 5 3<br />

Ranunculus fluitans Ranu N n 1.96 300 p Hy 1rreg Node2 7 3 373 3 0 3.3 15.4 798 14 1 7 6<br />

Ranunculus he derace us Ranu N n 0.10 9 23 a p Hz Hy 0 Node2 8 2 1703 551 8 3.6 14.5 1093 11, 13 1 5 5<br />

Ranunculus lingua Ranu N n 1.70 120 p hc Hy Rhiz2 7 4 537 210 0 3.7 15.2 868 11 1 6 7<br />

Ranunculus muricatus Ranu AN 40 a Th 0 0 3 Eur 18 1 0 5.0 15.6 864 4 5 5<br />

Ranunculus omiophyllus Ranu N n 0.52 9 25 a p Hz Hy 0 Node2 8 2 813 151 1 3.7 14.7 1180 11 1 5 4<br />

Ranunculus ophioglossifolius Ranu N EN r 40 a Th 0 8 3 4 0 2 4.9 16.5 824 13 7 5<br />

Ranunculus paludosus Ranu N o 40 p he Rhizl 9 1 0 0 4 6.1 16.9 843 6 6 3<br />

Ranunculus parviflorus Ranu N n -0.08 40 a Th 0 6 2 497 0 11 4.3 16.0 834 6 6 5<br />

Ranunculus peltatus Ranu N n 90 a Hz 0 Irreg 6 3 990 151 5 3.5 15.2 908 11, 13, 14 I l 5 6<br />

Ranunculus penicillatus Ranu N n 180 p Hy Irreg 7 3 706 284 0 3.8 15.2 942 14 1 8 5<br />

Ranunculus repens Ranu N n 0.55 60 p hc Sto12 5 5 2784 983 14 3.5 14.5 1105 3, 6 6 7<br />

Ranunculus reptans Ranu N EN r 10 p hc Hy Sto12 4 6 9 0 0 2.6 13.7i 1467 13 6 2<br />

Ranunculus sardous Ranu NA n 0.24 45 a Th 0 7 3 544 0 12 4.1 15.9 800 3, 6, 13 6 7<br />

Ranunculus sceleratus Ranu N n -0.05 60 a Th 0 5 6 1492 353 6 3.8 15.4 861 11, 13, 14 8 8<br />

Ranunculus trichophy llus Ranu N n -0.07 60 a Hz 0 Wag 3 6 1121 259 6 3.7 15.2 861 11, 13 1 6 6<br />

Ranunculus tripartitus Ranu N VU s -1.09 9 25 a p Hz 0 8 1 79 1 0 5.2 15.8 1024 13 1 6 3<br />

Raphanus raphanistrum Bras N n -1.39 70 a p Th hc 0 8 3 1862 259 13 4.6 15.0 1079 4, 19 6 6<br />

Raphanus raphanistrum<br />

subsp.maritimus Bras N 80 b p hc 0 9 1 325 108 13 4.7 15.1 1093 19 7 5<br />

Raphanus raphanistrum<br />

s ubsp.raphanistrum Bras AR 60 p he 0 8 3 1797 237 8 3.6 15.0 941 4 6 6<br />

Reseda lutea Rese NA n 0.39 75 hc 0 8 3 1276 0 7 3.6 15.7 808 3 7 5<br />

Reseda luteola Rese AR 0.69 150 hc 0 8 4 1660 428 12 3.8 15.3 879 3, 17 8 6<br />

Rhamnus cathartica Rham N n -0.04 600 Ph 0 7 4 857 88 0 3.6 15.8 783 1, 3 7 6<br />

Rhinanthus angustifolius Scro AN -0.10 60 a Th 0 5 4 Eur, As 1 90 0 0 3.1 14.6 809 3, 4, 7 7 2<br />

Rhinanthus minor Scro N n -0.49 50 a Th 0 5 3 2629 850 6 3.5 14.4 1115 6 6 4<br />

Rhodode ndron ponticum Eric AN 1.83 500 Ph 0 Nadel Eur 1966 507 6 3.5 14.6 1111 1, 10, 16 3 3<br />

R hynchospora alba Cype N n -0.43 30 hc Rhizl 5 6 624 407 0 3.6 14.0 1400 12 2 1<br />

R hy nch osp ora fusca Cype N s 0.02 30 hc Rhiz2 5 2 46 94 0 4.4 14.7 1205 12 3 1<br />

Ribes alpinum Gros N s 0.45 200 Pn Ph 0 4 3 50 0 0 2.3 14.2 1084 1, 3, 16 8 6<br />

R ibe s nigrum Gros AN 1.76 200 Pn 0 5 4 Eur, As1 1749 213 2 3.4 14.9 995 1, 3, 14 6 6<br />

Ribes rubrum Gros NA n 1.79 200 Pn 0 7 2 1874 0 2 3.3 15.1 944 1 7 6<br />

Ribes spicatum Gros N 5 -0.12 200 Pn 0 5 3 c 118 0 0 2.0 13.2 1095 1, 16 7 6<br />

Ribes uva-crispa Gros AN 0.72 100 Pn 0 7 3 Eur 2130 312 4 3.4 14.8 1006 1, 3 7 6<br />

Robinia pseudoacacia Faba AN 2700 Ph Root Am6 566 1 4 3.7 16.0 748 3, 17 6 6<br />

Romulea columnae hi d N VU r 6 Gn Otb 9 1 2 0 14 6.2 16.5 842 Co 18, 19 5 2


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Taxon name Fam NS CS RS Chg Hght Len 1 P2 LFI LF2 W Clonel Clone2 El E2 C Origin GB IR CI Tjan T'ul Prec Co Br Habitats L F R N<br />

Samolus valer<strong>and</strong>i Prim N n -0.42 45 hc 0 8 6 845 411 12 4.3 15.1 1013 11 8 8 8 5<br />

Sanguisorba minor Rosa N n -0.16 50 hc 0 8 4 1216 84 6 3.7 15.6 844 7 7 4 8 3<br />

Sanguisorba <strong>of</strong>fi cinalis Rosa N n -0.23 120 hc 0 5 6 946 12 0 3 2 15.1 938 6 7 7 6 5<br />

Sanicula europaea Apia N n -0.98 40 hc o Rhizl 7 3 2025 634 0 3.5 14.7 1090 1 4 5, 7 5<br />

Saponaria <strong>of</strong>ficina(is Cary AR 0.29 90 hc Rhiz2 7 3 1246 256 9 3.9 15.5 890 3, 17 8 5 6 6<br />

Sarcocornia perennis Chen N s -0.22 30 Ch 0 9 1 80 4 1 4.4 16.4 702 Co 21 9 8 8 6<br />

Saussurea alpina Aste N n -0.51 45 hc Stoll 1 5 237 21 0 1.6 11.9 20 10 7, 15, 16 8 6 6 3<br />

Saxifraga aizoides Saxi N n -0.61 20 Ch Node2 1 3 422 17 0 1.7 12.3 1799 7, 11, 15, 16 8 9 6 2<br />

Saxifraga cernua Saxi N VU r 15 hc DRa DRi 1 6 5 0 0 0.5 11.7 2265 15, 16 6 6 7 1<br />

Saxifraga cespitosa Sax/ N VU r -0. 10 10 Ch 0 1 6 13 0 0 -0.4 10.7 2003 15, 16 71 5 71 1<br />

Saxifraga granulate Saxi N n -0.26 36 hc DRa 7 3 975 6 0 3 1 15.1 853 6, 7 8 5 6' 4<br />

Saxifraga hirculus Saxi N VU r -0.30 20 hc Rhiz/ 2 6 20 16 0 2.4 13.2 1253 11 8 9 6 2<br />

Saxifraga hirsuta Saxi N o 1.39 30 hc Stoll 7 1 0 36 0 5.0 14.6 1334 1, 15, 16 6 7 5 2<br />

Saxifraga hypnoides Saxi N n -0.54 20 Ch Node2 4 1 406 61 0 2.0 12.8 1697 7, 15, 16 7 5 6 3<br />

Saxifraga nivalis Saxi N s -0.50 15 hc 0 1 6 72 1 0 0 6 11.5 2099 15, 16 6 6, 71 3<br />

Saxifraga oppositifolia Saxi N n -0.45 3 Ch Node2 1 6 276 22 0 1.8 12.1 1980 7, 15, 16 8 6 8 2<br />

Saxifraga rivularis Saxi N r 0.19 10 hc Rhizl DRa 1 6 21 0 0 -0.3 10.8 1941 11, 15 6 9 5 2<br />

Saxifraga rosacea Saxi N EW x 20 Ch 0 4 2 2 31 0 4.4 14.3 1312 16 7 4 8 4<br />

Saxifraga spathularis Saxi N o 40 hc Ch Stoll 7 0 0 137 0 4.7 14.4 1328 16 6 8 3 2<br />

Saxifraga stellaris Saxi N n -0.58 20 hc Ch o 1 3 440 61 0 1.8 12.3 1811 11, 15, 16 8 8 5: 3<br />

Saxifraga tridactylites Saxi N n -0.12 10 Th 0 8 3 985 316 11 3.9 15.3 921 16 7 2 7 2<br />

Scabiosa columbaria Dips N n -0.71 70 hc 0 7 3 804 0 0 3,5 15.6 831 7 8 3 8 2<br />

Sc<strong>and</strong>ix pecten-veneris Apia AR -3.65 50 Th 0 8 4 780 94 6 3.8 15 7 792 4 7 4 7 4<br />

S che uchz e ria palustris Sche N VU r 22 hc Rhiz2 4 6 c 14 1 0 2.2 13.9 1380 12 9 9 3 1<br />

Schoenoplectus lacustris Cype N n 0 .47 2 10 Hy Rhizl 6 4 1202 535 0 3.7 14.9 1013 13. 14 8 11 71 6<br />

Schoenoplectus pungens Cype NA r 60 Hy Rhizl 7 3 0 0 1 6.1 16.7 869 Co / 9 8 10 7 7'<br />

Schoenoplectus<br />

tabemaemontani Cype N n 0.67 150 Hy Rhizl 8 5 702 192 4.2 15.3 917 11, 13 9 10 8 7<br />

Schoenoplectus ttigueter Cype N CR r 125 Hy Rhizl 7 5 8 3 4.7 16.5 799 14 8 10 7 7<br />

Schoenus ferw gineus Cype N VU r 40 hc o 4 3 3 0 0 4 12.4 1113 11 8 9 7 2<br />

Schoenus nigricans Cype N n -0.53 75 hc 0 8 4 763 484 3.9 13.9 1261 11 8 8 71 2<br />

Scilla autumnatis Lili N s -0.37 20 Gb Otb 9 1 49 0 1 5.9 16.2 939 Co 10, 18 9 3 6/ 1<br />

Scilla Verna Lili N n 0.12 10 Gb Otb DRg 7 1 310 29 4.6 13.9 1103 6, 10 8 5 5 3<br />

Scirpoides holos choenus Cype N VU r 0.21 100 hc 0 8 4 3 0 5.2 16.3 909 Co 19 8 8 7 6<br />

Scirpus sylvaticus Cype N n 0.02 120 hc Rhizl 7 4 871 102 3.4 15.2 921 1, 11 6 8 6 6<br />

S cleranthus annuus Cary N n -2.68 20 Th 0 7 3 983 69 3.6 15.2 883 4, 8, 10, 16 71 4 4 4<br />

S cleranthus perennis Cary N EN r -0.11 20 Ch o 7 3 11 0 3 3 16.0 656 8, 16 81 3 4 2<br />

Scorzonera humilis Aste NA VU r 50 hc 0 7 3 4 0 4 8 16. 1 1097 6 8 7 5 2<br />

Scrophularia auriculata Scro N n -0.21 120 hc 0 8 2 1490 504 3.9 15.4 918 11, 14 7 8 7 7<br />

Scrophularia nodos a Scro N 6 -0.37 100 hc 0 7 4 2327 850 3.6 14.7 1069 1, 3 5 6 7 6<br />

Scrophularia s corod onia Scro AN , 0.75 100<br />

hc<br />

0 8 1 Eur 68 0 1 5.8 16.0 1033 3, 16, 18 71 4 6 6<br />

Scrophularia umbrosa Scro N n 0.72 100<br />

hc<br />

0 7 4 c<br />

196 14 3.1 14.9 868 1, 14<br />

7 9 7 7<br />

Scrophularia vernalis Scro AN . 0.54 65 p hc 0 Eur 192 0 3.3 15.3 769 1, 3 5 5 7 7<br />

Scutellaria galericulate Lami N n -0.39 50 hc Rhizl 5 4 1751 212 3.6 14.9 1055 11 7 8 6 5<br />

Scutellaria minor Lami N 6 0.03 20 hc Rhizl 8 2 803 136 4.1 14.9 1191 11 7 9 4 2<br />

Secale cereale Poac AC , 150 Th 0 Eur 134 71 4.0 15.8 852 3, 4 8 5 71 7<br />

/


Taxon name Fam NS CS RS Chg Hght Len 1 P2 LF1 LF2 W Clone') Clone2 El E2 C Origin GB IR CI T an T ul Prec Co Br Habitats L F R N S<br />

Sedum acre Cras N n -0.24 10 Ch Node2 Irreg 7 3 2108 504 12 3.7 14.9 995 16 8 2 7 2 1<br />

Sedum album Cras AR 2.41 20 Ch Node2 Irreg 9 2 1603 517 13 3.8 15.1 948 3, 16, 17 8 3 6 2 0<br />

Sedum anglicum Cras N n -0.21 5 Ch Node2 Irreg 7 1 988 393 14 4. 1 14.3 1321 16, 18 8 3 4 2<br />

Sedum forsterianum Gras N s 1.54 20 Ch Node2 Irreg 8 1 122 0 0 3.6 14.8 1239 3, 16 7 3 5 1<br />

Sedum rosea Cras N n -0.41 35 hc 0 1 6 524 82 0 21 12.6 1728 15, 16 7 6 6 3<br />

Sedum rupestre Gras AN 2.20 30 Ch Node2 Irreg Eur 1212 70 4 3.7 15.5 905 3, 16 7 2 5 4<br />

Sedum telephium Cras N n -0.34 60 hc 0 7 5 1197 0 0 3.5 15.0 1032 1, 3, 16 7 5 7 5<br />

Sedum villosum Cras N s -0.76 10 Ch 0 2 3 211 0 0 1.6 12.9 1273 11 8 9 6 2<br />

Selaginella selaginoides Se la N n -0.47 9 Ch Nodal 4 6 988 288 0 2.8 13.0 1443 7, 11 8 7 6 2<br />

Selinum carvifolia Apia N VU r 100 hc 0 7 3 3 0 0 3.4 16.1 595 11 7 7 8 4<br />

Sempervivum tectorum Cras AN 40 Ch Stoll Eur 500 42 2 3.5 15.3 871 3, 17 8 2 4 1<br />

Senecio aquaticus Aste N n -0.92 80 p hc 0 7 3 2304 919 1 3.6 14.5 1109 11, 14 7 8 6 5<br />

Senecio cambrensis Aste NE r 30 hc 0 7 1 14 0 0 3.6 15.0 804 3, 17 8 5 7 7<br />

Senecio cineraria Aste AN<br />

2.73 60<br />

Ch Pn sw 0<br />

0 3 Eur 256 8 5 4.4 15.9 837 3, 17, 18, 19 9 3 7 3<br />

Senecio erucifolius Aste N n -0.03 120<br />

hc<br />

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7 4<br />

1276 30 0 3.8 15.8 783 3, 6<br />

7 5 7 5<br />

Senecio fluviatilis Aste AN<br />

0.03 150<br />

hc<br />

Rhiz2<br />

7 4 Eur, As l 184 25 0 3.3 14.6 1018 1, 11, 13, 14 7 8 6 7<br />

Senecio j acobaea Aste N n 0.11 125<br />

b hc<br />

0 Root 7 4<br />

2725 982 14 3.6 14.5 1102 3, 6, 7, 8 7 4 6 4<br />

Senecio paludosus Aste N CR r 175 hc 0 7 4 c 7 0 0 3.4 16.2 573 11, 13 7 9 7 6<br />

Senecio smithii Aste AN 100 hc 0 SAm 62 0 0 3.4 12.3 1072 3, 6 8 7 6 7<br />

Senecio squalidus Aste AN 0.771 50 a p Th Ch 0 Gard 1494 75 4 3.7 15,5 850 3, 17 8 4 7 7<br />

Senecio sylvaticus Aste N n 0,09 70 a Th 0 7 3 1853 238 12 3.6 14.9 987 2, 8, 9 7 5 5 6<br />

Senecio viscosus Aste AN 0.63 60 a Th 0 7 3 Eur 1747 69 1 3.4 15.1 920 3, 17, 19 8 5 7 6<br />

Senecio vulgaris Aste N n -1.08 37 a Th 0 8 3 2630 942 14 3.6 14.6 1075 3, 4, 17 7 5 7 7<br />

Serapias parviflora Orch NA r 30 p Gn 0 9 1 1 0 0 6.0 16.2 1048 6 8 4 7 3<br />

Seriphidium maritimum Aste N n -0.42 50 p Ch hc Rhiz2 7 2 222 20 1 4.3 15.8 783 Co 21 9 7 8 6<br />

Serratula tinctoria Aste N n -0.21 70 p hc 0 7 3 945 0 2 3.8 15.5 965 7 7 6 6 2<br />

Seseli libanotis Apia N VU r 60 b hc 0 7 5 c 4 0 0 3.7 16.4 645 7 7 4 8 3<br />

Sesleria caerulea Poac N s -0.09 45 p he 0 5 3 76 89 0 3.1 13.9 1262 7, 16 7 6 8 2<br />

Setaria viridis Poac AN 0.80 70 a Th 0 Unk 431 27 5 3.9 15.9 798 3, 4, 17 7 4 7 7<br />

Sherardia arvensis Rubi N n -0.94 40 a Th 0 8 3 1635 369, 12 3.9 15.2 916 7, 16 7 4 6 4<br />

Sibbaldia procumbens Rosa N s -0.75 5 p hc 0 1 6 133 0 0 0.4 11.3 2109 15 8 5 4 3<br />

Sibthorpia europaea Scro N s -0.14 5 p Ch Node2 7 1 107 9 8 5.3 15.5 1189 3, 14 5 7 5 5<br />

Silaum silaus Apia N n -0.42 100 p hc 0 7 4 963 0 0 3.6 15.8 743 6 8 5 7 4<br />

Silene acaulis Cary N n -0.47 10 p Ch 0 1 3 236 9 0 1.9 11.8 1937 7, 15, 16 8 5 6 1<br />

Silene conica Cary N $ -1.05 35 a Th 0 5 4 59j 0 10 4.0 16.0 702 8, 19 8 3 4 2<br />

Silene dioica Cary N n -0.44 90 hc Ch 0 5 3 2514 263 14 3 4 14.6 1065 1 5 6 6 7<br />

Silene gallica Cary AR -2.78 45 a Th 0 9 2 455 31 11 4,2 15.7 877 3, 4 7 4 5 5<br />

Silene latifolia Cary AR -0.88 100 p hc 0 8 4 1954 211 13 3.6 15,1 911 3 7 4 7 6<br />

Silene noctiflora Cary AR -2.04 50 a Th 0 7 3 686 22 1 3.7 15.8 736 4 7 4 7 6<br />

Silene nutans Cary N $ -0.39 80 p hc 0 7 4 52 0 10 4.3 15.7 883 16 5 3 8 4<br />

Sfi ene <strong>of</strong>i tes Cary N r -0.36 80 p hc 0 7 3 c 18 0 0 3.2 16.1 625 3, 8 8 3 7 2<br />

Silene uniflora Cary N n -0.39 28 p hc 0 5 2 943 236 13 4.0 14.1 1263 Co 18 8 6 6 4<br />

Silene vulgaris Cary N n -1.26 80 p hc 0 8 5 1710 280 8 3.7 15.3 897 3, 6 7 4 8 5<br />

Silybum marianum Aste AR -0.07 100 b a hc Th 0 0 3 Eur 552 64 6 4.0 15.8 781 3 8 4 8 6<br />

Simethis planifolia Lili N o 42 p Gn 0 5 2 0 4 0 5.7 15.1 1324 10 71 5 4 3<br />

Sinapis alba Bras AR -0.90 90 a Th 0 8 3 1082 162 10 3.8 15.5 832 3, 4 7 4 7 6


Taxon name Fam NS CS RS Chg Hght Len P1 P2 LF1 LF2 W Cb nel Clone2 El E2 C Origin GB IR CI Tian Tjul Prec Co Br Habitats L F R N S<br />

Sinapis aneensis Bras AR , -1 76 90 a Th h 0 7 4 2373 772 11 3.7 14.7 1012 3, 4, 17 8 5 7 7'<br />

Sison amomum Apia N n -0.19 100 b hc h 0 9 2 790 0 0 3.9 16.2 756 3 7 4 7 5<br />

Sisymbrium altissimum Bras AN -0,84 100 a Th h 0 Eur 614 29 3 3.7 15.6 771 3, 17 8 5 6 4<br />

Sisymbrium <strong>of</strong>i cinale Bras AR i -0.21 95 a b Th hc h 0 8 3 21171 775 13 3.8 15.0 973 3, 4, 17 71 4 7 7<br />

Sisymbrium orientale Bras AN -0.24 80 Th h 0 Eur 864 75 10 3.8 15.6 815 3, 17 7' 4 7 5<br />

Sisyrinchium be rm udiana Irid N o -1.80 23 hc h 0 6 0 0 43 0 4.5 14.4 1290 6, 13 8 8 6 3<br />

Sium latifolium Apia N s -1.83 200 Hy h 0 7 4 259 34 0 3.7 15.9 702 11, 14 7 10 7 7<br />

Smyrnium olusatrum Apia AR 0.66 150 he h 0 Eur 803 327 13 4.4 15.5 907 3 T 5 7 7<br />

Solanum dulcamara<br />

So la N n -0.11 225<br />

Pn Ch sw Node2<br />

8 5<br />

1918, 533 14 3.8 15.2 945 3, 11, 14 71 8 71 7<br />

Solanum nigrum<br />

So la NA n 0.44 60<br />

Th<br />

0<br />

8 5<br />

1258E 0 14 3.9 15.9 809 4<br />

7 5 7 8<br />

Solanum sarachoides So la AN 60 a Th 0 SAm 88 0 4 3.8 16.1 696 4, 17 7 4 7 7<br />

Solanum tubemsum So la AN 100 Gn Rhiz1 SAm 625 56 5 3.9 15.4 883 4 7 4 6 7<br />

So leiro lia soleirolii Urti AN 2.36 10 Ch Node2 0 2 Eur 773 130 11 4.3 15.7 906 3, 17 4 8 7 6<br />

Solidago canadensis Aste AN 200 hc Rhiz1 Am 981 24 3.6 15.6 833 3, 17 8 5 6 6<br />

Solidago gigantea Aste AN 200 hc Rhiz1 Am 645 1 3.5 15.5 854 3, 17 8 5 5 6<br />

Solidago virgaurea Aste N n -0.89 70 he 0 5 5 2043 492 3.4 14.2 1217 10, 16 5 5 4 3<br />

Sonchus arvensis Aste N n -0.12 150 hc Rhiz2 7 4 2320 806 3.8 14.8 1013 4 8 6 7' 6<br />

Sonchus asper Aste N n 0.78 150 a Th 0 8 3 2584 961 1 3.7 14.6 1070 3, 4 T 5 7 6<br />

Sonchus oleraceus Aste N n -0.42 150 Th 0 8 3 2358 924 1 3.71 14.8 1031 3, 4 71 5 71 71<br />

Sonchus palustris Aste N s, 0.18 250 he 0 7 4 51 0 3.8 16.4 615 11 7 8 7 7'<br />

Sorbus anglica Rosa NE VU r 200 Pn w 0 7 1 14 1 3.8 15.2 1082 1, 16 6 4 8 4<br />

Sorbus aria Rosa N n 1500 Ph w 0 7 3 225 2 3.8 16.3 774 1 6 4 7 4<br />

u-i<br />

u, Sorbus aria agg, Rosa N n' 0.82 1000<br />

Ph w 0<br />

7 3<br />

341 75 3.8 16.3 780 17<br />

6 5 7 4<br />

Sorbus arrane nsis Rosa NE VU r<br />

750<br />

Ph w 0<br />

4 1<br />

1 0 2.5 12.1 1530 16<br />

71 4 4 3<br />

Sorbus aucuparia Rosa N n 0.86 1500 Ph w 0 5 5 2472 749 3.4 14.4 1128 1, 2, 16 6 6 3 4<br />

Sorbus bristoliensis Rosa NE EN r , 1000<br />

Ph w 0<br />

7 1<br />

1 0 4.4 16.5 844 1, 16<br />

6 4 8 4<br />

Sorbus de von iensis Rosa NE s , 1500<br />

Ph w 0<br />

7 1<br />

32 11 5.0 15.4 1171 1, 3<br />

6 5 6 5<br />

Sorbus domestica Rosa N CR r 1 500<br />

Ph w Root<br />

3<br />

4 0 4.5 16.5 857 16<br />

6 4 8 3<br />

Sorbus e minens<br />

Rosa NE VU r 600<br />

Ph w 0<br />

7<br />

8, 0 4.4 16.2 878 1<br />

6 5 71 5<br />

Sorbus hibernica<br />

Rosa NE o 600<br />

Ph w 0<br />

7<br />

0' 63 4.5 14.6 1035 1, 3, 16 6 5 7 5<br />

Sorbus intermedia Rosa AN 1000 Ph w 0 Eur 686 17 3.5 15.2 901 1, 3, 17 6 6 8 7<br />

Sorbus lanc as triensis Rosa NE r 500 Ph w 0 7 9 0 3.3 14.8 1285 16 8 4 7 3<br />

Sorbus leptophylla Rosa NE CR r 300 Pn Ph w 0 7 3 0 2.9 14.5 1501 16 5 5 7 5<br />

Sorbus leyana<br />

Rosa NE CR r<br />

200<br />

Pn w 0<br />

7<br />

2 0, 2.5 14.0 1687 16<br />

7 5 8 4<br />

Sorbus minima<br />

Rosa NE VU r ' 300<br />

Pn Ph w 0<br />

7<br />

1 0' 2.2 14.0 1523 16<br />

6 4 8 3<br />

Sorbus porrigentiformis Rosa NE 5 , 500<br />

Ph w 0<br />

7<br />

30 0 3.8 15.2 1273 16<br />

7' 5 7' 5<br />

Sorbus ps e udotennica Rosa NE VU r<br />

700<br />

Ph w 0<br />

4<br />

1 0 2.5 12.1 1530 16<br />

7 4 4 3<br />

Sorbus rupicola Rosa N s 200 Pn w 0 4 2 98 13 2.9 13.6 1405 16 8 4 7 3<br />

Sorbus subcuneata<br />

Rosa NE VU r 1000<br />

Ph w 0<br />

7 1<br />

4, 0 4.0 14.9 1380 1<br />

6 5 4 4<br />

Sorbus torminalis<br />

Rosa N n 0.22 1900<br />

Ph w Root<br />

7 3<br />

573 0 3.9 16.0 804 1<br />

4 5 6 5<br />

Sorbus vexans Rosa NE VU r 600 Ph w 0 7 1 4 0 4.2 14.9 1409 1, 16 6 5 4 4<br />

Sorbus wilmottiana Rosa NE CR r 600 Ph w 0 7 1 1 0 4.4 16.5 844 1, 16 6 4 8 3<br />

Sparganium angus tifolium Spar N n 1.66 100 Hy h Rhiz2 4 3 652 207' 3.0 12.9 1571 13 8 11 4 2<br />

Sparganium emersum Spar N n 0.61 60 Hy h Rhiz2 5 6 1426 393 3.6 15.0 982 13, 14 7 11 7 6<br />

Sparganium erectum Spar N n 0.48 150 Hy h Rhiz2 7 6 2129 766 3.7' 14.9 1000 11, 13 7' 10 7 7<br />

Sparganium natans Spar N n : -0.13 50 Hy h Rhiz2 5 6 508 267 3.3 13.8 1303 13 7 11 6 3


S<br />

Taxon name Fam NS CS RS Chg_ Hght Len P1 P2 LF1 LF2 W Clonel Clone2 El E2 C Origin GB IR CI Tian Tjul Prec Co Br Habitats L F R N<br />

Spartina alternitiora Poac AN -0.22 110 p hc Rhiz2 Am 12 0 0 4.1 15.7 760 Co 21 9 9 8 7<br />

Spartina anglica Poac NE n 0.11 130 p hc Rhiz2 7 1 251 71 1 4.6 15.7 904 Co 21 9 9 8 6<br />

Spartina maritima Poac N s -0.55 50 p hc Rhiz2 8 2 571 0 0 4.1 16.6 625 Co 21 9 9 8 5<br />

Spergula arvensis Cary N o -2.30 30 a Th 0 6 4 0 0 9 6.3 16.7 811 4 7 4 5 5<br />

Spergularia bocco ne i Cary AN -0.22 10 a Th 0 9 1 Eur 18 0 9 5.9 16.3 901 16, 17, 19 9 4 6 7<br />

Spergularia marina Cary N n 1.83 10 a Th 0 8 6 680 185 8 4.3 14.6 1094 Co 3, 21 8 8 8 6<br />

Spergularia media Cary N n -0.24 15 p Ch 0 8 4 659 186 0 4.2 14.6 1125 Co 21 8 8 8 5<br />

Spergularia rubra Cary N n 0.05 15 a Th 0 8 3 1363 66 13 3.5 14.9 983 8, 17 8 3 4 2<br />

Spergulatia rupicola Cary N n 0.30 10 Ch 0 7 0 239 169 13 5.2 15.1 1105 Co 18 9 6 6 5<br />

Spiranthes aestivalis Orch N EX x 40 hc 0 7 3 1 0 2 5.6 16.5 822 11 9 8 8 2<br />

Spiranthes romanz <strong>of</strong>fi ana Orch N s 0.45 25 hc 0 4 0 21 44 0 4.4 14. 1 1248 11 8 8 6 4<br />

Spiranthes spiralis Orch N n -0.95 15 hc 0 8 3 655 117 13 4.4 15.9 884 7 8 4 6 3<br />

Spirodela polyrhiza Lemn N n -0.18 0.8 Hy Frag 8 6 535 991 2 3.9 15.9 768 13 71 11 7 7<br />

Stachys alpina Lami AN 100 hc 0 7 3 Eur 3 0 0 3.1 14.7 1007 1, 3 7 5 8 7<br />

Stachys arvensis Lami AR -1.17 25 Th 0 8 2 1418 206 13 4.0 15.3 964 3, 4 8 5 5 5<br />

Stachys germanica Lami N EN r -0.27 80 hc 0 7 3 10 0 0 3.4 16. 1 66 1 3 7 3 8 5<br />

Stachys <strong>of</strong>ficinalis Lami N n -0.62 60 he 0 7 3 1571 38 4 3.6 15.4 940 6, 7 7 5 5 3<br />

Stachys palustris Larni N n 0.01 100 Gn Rhiz2 5 6 2346 919 9 3.71 14.6 1079 11, 14 7 8 7 7<br />

Stachys palustris x sylvatica<br />

(S. x ambigua) Lami NH n 100 hc Rhiz2 1020 1171 4 3.5 14.7 1086 3, 14 7 6 6 6<br />

Stachys sylvatica Lami N n -0.49 100 hc Rhiz2 7 4 2462 806 12 3.6 14.7 1064 3 6 6 7 8<br />

Stellaria graminea Cary N n -0.02 80 hc Rhizl 5 4 2446 852 8 3.5 14.6 1065 6 7 6 5 4<br />

i n<br />

cn Stellaria holostea Cary N n -0.56 60 Ch Rhiz1 Nodel 7 4 2372 671 7 3.5 14.7 1058 1 5 5 6 6<br />

Stellaria media Cary N n 50 Th 0 Nodel 6 5 2749 962 14 3.6 14.5 1095 3, 4 7 5 6 7<br />

Stellaria nemorum Cary N n 0.21 60 hc Rhizl 5 3 432 0 0 2.7 14.2 1027 1, 14 4 6 6 7<br />

Stellaria media egg. Cary N n 0.03 50 Th 0 Nodal 6 5 2749 962 14 3.6 14.5 1095 3, 4 7 5 5 6<br />

Stellaria neglecta Cary N n 0.42 80 Th 0 Nodel 7 3 775 4 0 3.9 15.6 911 1, 3 6 7 6 7<br />

Stellaria pallida Cary N n 1.17 50 Th 0 Nodel 8 4 593 27 13 4.0 15.8 766 3, 19 7 4 4 4<br />

Stellaria palustris Cary N n -0.89 60 hc Rhizl Nodel 5 5 389 73 1 3.6 15.5 793 11 7 8 6 4<br />

Stellaria uliginosa Cary N n -0.10 40 he Rhizl 7 3 2570 798 9 3.5 14.4 1128 11, 14 7 8 5 5<br />

Stratiotes ab ides Hydr NA r 1.65 50 Hy Stoll DRa 5 4 c 65 0 0 3.5 16.1 596 13 7' 11 7 6<br />

Suaeda maritima Chen N n -0.47 30 Th 0 8 5 525 141 6 4.3 14.9 1094 Co 21 9 8 8 6<br />

Suaeda vera Chen N s -0.11 120 Pn w 0 9 1 47 0 1 4. 1 16.4 620 Co 19, 21 9 7 8 5<br />

Subularia aquatica Bras N n 0.73 6 Hz h 0 4 6 324 33 0 2.4 12.6 1789 13 7 11 5 2<br />

Succisa pratensis Dips N n -0.57 100 he h 0 Rhizl 7 4 2633 934 2 3.5 14.4 1124 6 7 7 5 2<br />

Symphoricarpos albus Capr AN 1.74 200 Pn w Rhiz2 Am 2067 744 4 3.6 14.9 992 1, 3, 17 5 5 6 7<br />

Symphytum asperum x<br />

<strong>of</strong> icinale (S. x upl<strong>and</strong> icum) Bora AN 135 hc h 0 Eur 1924 399 8 3.6 15.0 952 3 6 5 7 7<br />

Symphy tum <strong>of</strong>ficinale Bora N n 0.34 135 hc h 0 7 3 1263 189 10 3.7 15.4 871 11 7 7 7 8<br />

- -<br />

Symphytum orientale Bora AN 1.83 70 hc h 0 Eur 442 2 3 3.71 16.0 719 3 6 4 7 6<br />

Symphytum tuberosum Bora N n 0.11 55 hc h 0 7 3 407 0 0 2.5 13.5 1047 1, 3 6 6 6 6<br />

Sybnga vulgaris Olea AN 4.48 700 Ph w Rhir l Eur 1296 163 4 3.6 15.3 881 3, 17 6 5 6 5<br />

Tamus communis Dios N n -0.41 400 Gn h 0 9 2 1421 0 4 3.8 15.7 850 1, 3 6 5 7 6<br />

Tanacetum parthenium Aste AR 0.23 54 Ch hc h 0 Eur 2126 413 11 3.5 14.9 980 3, 17 7 4 7 6<br />

Tanacetum vulgare Aste N n -0.23 120 hc h Rhizl 5 5 2004 0 10 3.5 15.0 958 3 7 6 7 7<br />

Taraxacum Aste N n 0.43 30 hc h 0 6 6 2778 974 14 3.5 14.5 1104 3, 5, 17 7 5 7 6


W Clonel Clone2 El E2 C Origin GB IR CI Tja n Tjul Prec Co Br Habitats L F R N S<br />

w 0<br />

7 3 1881 260 7 3 5 15.1 976 1 4 4 7 5 0<br />

h 0<br />

7 3 509 11 12 3 4 15.0 949 8 8 3 2 2 0<br />

h 0<br />

Am4 308 20 2 3.6 15.2 974 1, 3, 17 3 8 6 4 0<br />

h 0<br />

3 6 c 99, 0, 0 3 71 16. 1 774 7 71 3 8 3 0<br />

h 0<br />

3 6 26 0 0 3.6 16. 1 617 13 7 9 7 6 0<br />

h 0<br />

7 3 c Eur 12 0 0 3.6 16.3 767 3, 4, 7, 16 9 2 8 2 0<br />

sw Rhizl<br />

8 3 c Eur 72 2 0 4.2 15.7 856 3, 7, 16 8 2 8 1 0<br />

h Rhiz2<br />

8 4 24 12 I 4.0 15.8 740 11, 13, 14 7 8 8 4 1<br />

h Rhiz2<br />

8 2 2322 588 1 3.5 14.5 1150 1, 9, 16 6 4 4 3<br />

h Rhiz2<br />

1 6 409' 23 2.0 12.1 1845 7, 11, 15, 16 8 7 6 3<br />

h 0<br />

5 4 669 91 3.7 15.8 762 11 7 8 7 5<br />

h Rhiz2<br />

5 5 504 89 3.4 14.0 1185 16, 19 7 4 6 3<br />

h Rhiz2<br />

7 6 171 54 3.9 15.5 869 1, 11 6 8 7' 5<br />

h 0<br />

7 1 145 0 3 6 16.2 762 7 8 3 8 3<br />

h 0<br />

7 5 1600 143 1 3 7 15.3 858 3, 4 7 4 7 6<br />

h 0<br />

4 3 70 0 2 0 13.5 1314 16 8 4 6 1<br />

h 0<br />

8 4 9 0 3,3 16.0 732 3, 16 8 4 8 2<br />

w 0<br />

Am4 574 7 1 3.6 15.4 977 2, 17 4 5 5 4<br />

sw Node2<br />

5 3 2246 486 1 3.4 14.2 1175 7, 16 8 4 6 2<br />

sw Node2<br />

7 3 455 3 3.7 16. 1 752 7 8 4 8 2<br />

sw Node2<br />

5 3 c 9 0 3,3 16.2 606 8 8 2 5 2<br />

w 0<br />

7 4 896 5 20 0 2.4 3 5 15.5 14.4 1064 873 1 5 5 6 5 6<br />

R<br />

B<br />

B<br />

B<br />

C<br />

L<br />

T<br />

7 3 84 0 3.3 15.6 816 1 4 5 7 6<br />

1 6 156 0 0 6 11.6 1964 7, 11 8 9 7 2<br />

Am4 267 11 3.2 14.3 1131 1 3 6 7 7<br />

Eur 11 1 4.0 16.3 739 6 7 3 6 5<br />

8 4 389 0 3.7 16.2 707 4 8 4 8 4<br />

7 5 2178, 824 3.71 14.9 1004 3 7 5 7 71<br />

9 1 708 77 4. 1 15.9 792 3, 6 8 5 7 6 1<br />

7 4 1749 124 1 3.6 15.3 87 1 6 8 4 7 5 0<br />

DRp 7 0 162 62 3.8 14.2 1390 16 2 7 7 3 0<br />

4 6 c 1 0 2.8 14.0 858 12 8 9 2 2 0<br />

4 6 1553, 629 0 3.2 13.71 1312 10, 12 8 8 2 1 0<br />

DRg 4 6 514 0 0 1,8 12.6 1277 1, 2, 10 5 6 3 3 0<br />

8 4 1205 56 14 3.8 15.5 84 1 8 9 3 5 2 1<br />

9 1 3 0 2 6 5 16.2 867 16 9 4 5 2 0<br />

8 4 1996 381 14 3.7 15.1 939 3, 16, 19 8 4 6 4 0<br />

7 3 2548 942 14 3 6 14.6 1072 6 71 4 6 5, 0<br />

8 4 7531 42 6 4.0 16.0 764 6 8 7 7 6 2<br />

9 1 148 5 13 4.6 16.3 767 8 9 3 5 2 0<br />

Eur 1940 214 11 3.5 15.0 943 3, 5 7 5 7 6 0<br />

9 1 3 0 4 6.4 16.4 883 3, 18 8 2 5 2 1<br />

w 0<br />

w 0<br />

h Rhizl<br />

h 0<br />

h 0<br />

h 0<br />

h 0<br />

h 0<br />

h 0<br />

h Rhizl<br />

h Rhizl<br />

h Ogr<br />

h Rhiz2<br />

h 0<br />

h 0<br />

h 0<br />

h 0<br />

h Node2<br />

h 0<br />

h 0<br />

h 0<br />

h<br />

T<br />

T<br />

Crop 196 1 5 4.0 16. 1 780 3 7 4 6 5 0<br />

h O


Taxon name Fam NS CS RS Chg Hght Len P1 P2 LF1 LF2 W Clonal Clone2 El E2 C Od in GB IR CI T an T uI Prec Co Br Habitats I. F R N S<br />

Trifolium incamatum<br />

subsp.molinerti Faba N VU r 20 Th 0 9 1 3 0 4 6 4 16.4 883 Co 18 6 2 51 2<br />

Trifolium medium Faba N n -0.53 45 hc 0 5 4 2050 208 2 3.4 14.8 1008 6 7 4 6 4<br />

Trifolium micranthum Faba N n 0.62 7 Th 0 9 2 909 52 13 4.1 15.9 848 8, 17 8 5 5 5<br />

Trifolium occidentale Faba N a 10 hc Ch Node2 7 0 21 9 12 6.3 15.9 940 Co 18 9 4 6 2<br />

Trifolium ochroleucon Faba N s -0.84 45 he 0 7 3 1271 0 0 3.4 16.3 595 3. 6 7 5 8 2<br />

Trifolium om ithop odioide s Faba N n 0.42 12 Th 0 8 2 281 18 14 4.8 16. 1 874 8 9 6 5 3<br />

Trifolium pratense Faba N n -0.18 45 hc 0 7 4 2745 976 14 3.6 14.5 1100 6. 7 7 5 7 5<br />

Trifolium repens Faba N n 1.31 20 hc Ch Node2 5 4 2798 981 14 3.5 14.5 1105 6 7 5 6 6<br />

Trifolium scabrum Faba N n -0.39 20 Th 0 9 2 390 12 11 4.5 15.9 831 8 9 3 7 2<br />

Trifoliurn sguamosum Faba N s -0.32 40 Th 0 9 1 116 0 6 4.5 16.5 757 Co 6, 19 9 6 7 6<br />

Trifolium striatum Faba N n -0.11 20 Th 0 8 3 848 31 12 4.0 15,7 805 8 8 3 5 2<br />

Trifolium strictum Faba N VU r 15 Th 0 9 2 4 0 2 5.8 15.9 874 16 9 2 5 2<br />

Trifolium subterraneum Faba N n -0. 10 10 Th 0 9 2 337 1 13 4.5 16.2 805 8, 18 8 3 4 2<br />

Trifolium suffocatum Faba N s 0.14 5 Th 0 9 1 96 0 13 4.8 16.4 774 8 8 4 4 2<br />

Triglochin maritimum Junc N n -0.44 55 hc Rhizl 5 6 8371 251 5 4.2 14.3 1181 Co 21 8 7 7 5<br />

Triglochin palustre Junc N n -0,22 55 hc Rhiz2 5 6 2196 71 5 3.4 14.2 1145 11 8 9 6 2<br />

Trinia glauca Apia N r 0.12 20 hc 0 8 3 6 0 4.9 16.4 889 7 9 2 8 1<br />

Tripleurospermum inodorum Aste AR 60 Th 0 7 4 2119 42 12 3.6 14.9 967 4. 17 8 5 6 6<br />

Tripleurospermum maritimum Aste N n 60 Ch hc 0 3 6 757 27 3 4.4 14.5 1132 Co 18, 19 8 5 6 6<br />

Tnpleurosp ennum maritimum<br />

sens.lat. Aste N n 0.3 1 60 p Th hc 0 3 6 757i 27 3 4.4 14,5 1132 4, 17 18, 19 8 5 6 6<br />

tri<br />

co Trisetum flavescens Poac N n -0.13 80 he 0 7 3 1734 36 6 3.6 15.2 900 6, 7 7 4 7 4<br />

Triticum aestivum Poac AC 150 Th 0 Crop 741 5 4 3.8 15.6 861 3, 4 8 5 7 7<br />

Trollius europaeus Ranu N n -0.73 60 hc 0 4 3 856 0 2.2 13.0 1517 11, 16 7 7 6 4<br />

Tsuga he terophylla Pina AN 4600 Ph w 0 Am4 598 1 0 3.4 14.9 1102 1, 2, 17 6 6 3 3<br />

Tuberaria guttata Cist N VU r 15 Th h 0 9 1 5 1 4 5.71 15.5 1069 10 9 2 5 1<br />

Tussilago farfara Aste N n -0.65 30 Gn h Rhiz2 5 4 2618 90 7 3.5 14.5 1085 16 7 6 6 6<br />

Typha angustifolia Typh N n 0.35 300 Hy h Rhiz2 7 4 776 6 6 3.7 15.8 775 11 8 10 7 7<br />

Typha latifolia Typh N n 1.01 275 Hy h Rhiz2 8 6 1860 68 9 3.8 15.1 958 11 8 10 7 7<br />

Ulex europaeus Faba N n -0.34 200 Pn w 0 7 1 2518 95 14 3.6 14.6 1090 10 7 5 5 3<br />

(fl ex gallii Faba N n 0.20 150 Pn w 0 7 1 918 38 11 4.1 15.0 1099 10 7 6 3 2<br />

Ulex minor Faba N n 0.20 100 Pn w 0 8 1 197 4 3.9 16.4 745 10 8 6 1 2<br />

Ulmus glabra Ulrna N n -0.28 3000 Ph w 0 7 3 2338 60 0 3.4 14.7 1056 1 4 5 7 6<br />

Ulmus minor Ulrna N n 0.75 3100 Ph w Root 7 3 641 9 3.9 16. 1 764 1, 3 5 5 7 7<br />

Ulmus plotii Ulma NE s 2000 Ph w Root 7 1 128 0 3.4 16.0 667 3 5 5 7 7<br />

Litmus procera Ulma NA n -0.48 3300 Ph w Root 7 3 13171 0 3.7 15.8 819 3 5 5 8 6<br />

Umbilicus rupestris Cras N n -0. 12 38 hc h 0 9 1 784 65 i 14 4.3 14.9 1125 3, 16 6 4 5 4<br />

Urtica dioica Urti N n 0.28 150 hc h Rhiz2 Sto12 5 4 2773 98 13 3.6 14.5 1102 3, 14, 17 6 6 7 8<br />

Urtica urens Urti AR -0.70 60 Th h 0 8 4 1924 28 14 3.7 15.0 914 4, 17 8 5 6 8<br />

Utricularia australis Lent N s 60 Hy h DRa 5 5 162 5 0 4.0 15.0 1120 13 7 12 5 3<br />

Utricularia intermedia<br />

sens.lat. Lent N n 0.40 20 Hy h DRa 4 6 412 15 0 3.1 13.2 1545 11, 12, 13 8 12 4 2<br />

Utricularia intermedia<br />

sens.str. Lent N n 20 Hy h DRa ? ? 13 8 12 4 2<br />

Utricularia minor Lent N n 0.20 40 Hy h DRa 5 6 628 377 1 3.6 13.9 1321 11, 12 8 12 4 2


S<br />

Taxon name Fam NS CS RS Chg_ Hght Len P2 LF1 LF2 W Clonel Clone2 E1 E2 C Origin GB IR CI Tjan Tjul Prec Co Br Habitats L F R N<br />

Utricularia ochroleuca Lent N i 20 Hy h DRa ? ? 11, 13 8 12 3 1<br />

Utricularia stygia Lent N i 20 Hy h DRa ? ? 11, 13 8 12 5 2<br />

Utricularia vulgaris seno lat. Lent N n 0.47 100 Hy h DRa 5 5 744 301 0 3.6 14.4 1148 13 7j 12 6 4<br />

Utricularia vulgaris sens.str. Lent N s 100 Hy h DRa 7 4 159 77 0 3.8 15.3 874 11 7 12 7 4<br />

Vaccinium microcarpum Eric N s 0.81 30 Ch h Node2 4 6 100 0 0 0.9 11.9 1339 12 7 8 1 1<br />

Vaccinium myrtillus Eric N g -0.61 50 Ch Pn w Rhiz2 4 4 1886 701 1 3.3 13.9 1243 10, 16 6 6 2 2<br />

Vaccinium oxycoccos Eric N n 0.28 30 Ch h Node2 4 6 725 246 0 3.0 14.0 1229 12 8 9 2 1<br />

Vaccinium uliginosum Eric N n -0.39 50 Ch Pn w Rhiz2 2 6 252 0 0 1.1 11.7i 1897 12, 15, 16 71 6 2 2<br />

Vaccinium vitis-idaea Eric N n -0. 18 30 Ch w Rhiz2 2 6 938 89 0 2.2 12.9 1474 2, 10, 15 6 5 2 2<br />

Valeriana dioica Vale N n -0.67 35 hc h Sto12 7 3 1171 0 0 3.2 15.3 896 11 8 8 6 3<br />

Valeriana <strong>of</strong>i cinalis Vale N n -0.64 175 hc h 0 Rhizl 5 5 2408 808 0 3.4 145 1115 11 6 8 6 5<br />

Valeriana pyrenaica Vale AN -0.35 110 hc h 0 Eur 195 8 0 2.7 13.8 1151 1, 3 5 7 5 5<br />

Va lerianella carinata Vale AR 2.15 15 Th h 0 8 3 547t 66 13 4.3 15.8 93 1 3, 17 8 4 8 4<br />

Valerianella dentata Vale AR -1.86 15 Th h 0 7 3 600 45 4 3.9 15.7 800 4 8 4 7 4<br />

Valerianella eriocarpa Vale AN -0.69 15 Th h 0 9 2 Eur 59 0 6 4.5 16.0 826 3, 16 8 3 8 3<br />

Valerianella locusta Vale N n -0.11 15 Th h 0 7 3 1358 238 9 3.9 15.3 925 3, 16, 19 8 4 6 4<br />

Valerianella rimosa Vale AR CR -2.55 15 Th h 0 7 3 181 27 0 4.3 15.9 860 4 8 4 8 3<br />

Verbascum lychnids Scro N s -0 .23 150 hc h 13 7 3 42 0 0 4.1 16.5 790 3, 7 71 3 71 3<br />

Verbascum nigrum Scro N n -0.12 120<br />

hc h 0<br />

7 4<br />

479, 0 8 3.9 16.2 742 3<br />

7 4 7 6<br />

Verbascum pulverulentum Scro NA s 0.94 135<br />

hc h 0<br />

9 2<br />

51 0 0 3.4 16.1 624 3, 16<br />

8 3 7 5<br />

Verbascum thapsus Scro N n 0.27 200 hc h 0 7 4 1874 375 12 3.7 15.2 918 3 7 4 7 5<br />

Verbascum virgatum Scro AN 0.35 100 hc h 0 8 2 Eur 339 13<br />

in<br />

3 4.2 15.8 870 3, 5, 17, 19 8 4 5 5<br />

so Verbena <strong>of</strong>i cinalis Verb AR -0.43 67 hc h 0 8 5 8571 90 10 4 1 15.8 859 3, 16 8 5 71 6<br />

Veronica agrestis Scro AR -0.38 10 a Th h 0 7 3 1715 177 9 3.5 15.0 963 3, 4, 17 7 6 6 7<br />

Veronica alpina Scro N s -0 .29 12 Ch h 0 1 4 35 0 0 -0.7 10.9 1783 15 8 6 5 2<br />

Veronica anagallts -aquabca Scro N n 0.05 50 a p Hz Hy h Nodel 8 5 1225 459 3 3.7 15.1 899 13, 14 7 10 7 7<br />

Veronica arvensis Scro N n 0.48 25 a Th h 0 8 3 2614 793 14 3.5 14.6 1077 3, 4, / 6 8 4 6 5<br />

Veronica be cca bunga Scro N n -0.31 45 Hy Ch h Nodel 7 4 2333 912 9 3.6 14.7 1034 11, 14 7f 10 6 6<br />

Veronica catenata Scro N n 0.37 50 a p Hz Hy h Nodel 7 6 956 249 4 3.8 15.6 816 13, 14 8 10 7 8<br />

Veronica chamaedrys Scro N n -0.50 30 Ch hc h Node2 5 4 2609 945 14 3.5 14.5 1095 1, 3, 6 6 5 6 5<br />

Veronica Milormis Scro AN 2.69 5 hc Ch h Node2 Eur 2013 397 9 3.6 14.9 990 3, 17 7 6 7 7<br />

Veronica froticans Scro N s 0.11 14 Ch sW 0 1 3 26 0 0 -0 .5 11.2 182 1 15, 16 8 5 7 2<br />

Veronica hecieriforia Scro AR 0.57 30 a Th h 0 8 3 1944 346 14 3.71 15.1 918 1, 3, 4, 17 6 5 7j 6<br />

Veronica m ontana Scro N n 0.48 15 Ch h Node2 7 3 1808 506 0 3.6 14.9 1029 1 4 6 6 6<br />

Veronica <strong>of</strong> icinalis Scro N n -0.84 23 Ch h Nodel 5 3 2507 754 8 3.4 14.4 1125 7, 8 6 5 4 4<br />

Veronica persica Scro AN -0.37 30 a Th h 0 Nodal Eur 2232 722 13 3.7 14.9 993 3, 4, 17 6 5 7 7<br />

Veronica polka Scro AN 0.07 10 a Th h 0 8 4 Eur, Asl 1237 107 8 3.8 15.5 867 4, 17 7 4 7 5<br />

Veronica praecox Scro AN 15 a Th h 0 8 3 c Eur 6 0 0 3.3 16.3 618 3, 4, 8 8 2 8 1<br />

Veronica scutellata Scro N n -0.06 25 hc h Nodel 5 4 1877 576 3 3.4 14.3 1129 11, 13 8 9 5 3<br />

Veronica serpyllifolia Scro N n 0.80 10 hc h Node2 5 6 2652 884 11 3.5 14.5 1104 3, 5, 11 7 5 6 5<br />

Veronica spicata Scro N s 0.13 45 hc Ch h Nodel 7 4 c 28 0 0 3.7 15.3 949 7, 16 8 3 7 2<br />

Veronica triphyllos Scro AR EN -0.82 15 a Th h 0 7 3 c 33 0 0 3.5 16.1 690 3, 4 7 4 7 3<br />

Veronica vema Scro N VU r -0.64 15 a Th h 0 7 4 c 71 0 0 3.3 16.2 618 8 8 2 5 1<br />

Viburn um lantana Capr N n 0.37 600 Ph w 0 7 3 537 0 0 3.8 16.2 763 1, 3 7 5 7 5<br />

Viburnu m opulus Capr N n -0.15 400 Ph w 0 7 6 1854 565 1 3.6 15.0 1019 1 6 7 6 6<br />

Vicia bithynica Faba N s -0.52 60 hc h 0 9 1 74 0 4 4.4 16. 1 827 3 7 4 6 4


Taxon name Fam NS CS RS Chg. Hght Len P1 P2 LF1 LF2 W Clonel Clone2 El E2 C Origin GB IR CI Tjan Tjul Prec Co Br Habitats L F R N $<br />

Vicia cracca Faba N n -0.37 120 p hc Rhir l 5 5 2647 938 10 3.6 14.5 1083 3, 11 7 6 5 0<br />

Vicia laba Faba AN 100 a Th 0 Cro 377, 5 2 3.71 16.1 734 4, 17 8 4 71 0<br />

Vicia hirsuta Faba N n 0.05 80 a Th 0 7 3 1925' 285 12 3.7 15.2 926 3, 6 7 5 6 0<br />

Vicia lathyroides Faba N n -0.36 10 a Th 0 7 3 501 27 11 3.8 15.2 808 8, 19 8 3 3 0<br />

Vicia lutea Faba N s -0.85 50 a Th 0 9 2 58 0 7 4.8 15.9 844 Co 18, 19 7 4 5 1<br />

Vicia orobus Faba N s -0.34 60 p hc 0 7 2 214 15 0 3.0 13.8 1410 16 7 5 4<br />

Vicia parvillora Faba N s -1.05 60 a Th 0 9 2 136 0 0 3.9 16.3 695 3, 4 7 5 5<br />

Vicia sativa Faba N n 0.19 90 a Th 0 8 3 1930 472 14 3.7 14.9 991 6 7 4 4<br />

Vicia sepium Faba N n -0.43 60 p hc Rhizl 5 4 2615 945 4 3.5 14.5 1095 3, 6 6 5 6<br />

Vicia sylvatica Faba N n -0.71 150 p hc Rhizl 5 4 623 57 0 3.1 14.3 1119 1, 3, 16 7 5 5<br />

Vicia tetrasperma Faba N n 0.45 60 a Th 0 7 3 1159 0 10 3.9 15.9 804 3, 4, 6 7 5 6<br />

Vicia villosa Faba AN 150 a Th 0 8 3 c Eur 147, 2 3 3.8 16.1 757 3, 4 7 4 5<br />

Vinca maj or Apoc AN 1.49 35 p Ch Tip Eur 1336 231 12 4.0 15.6 873 1, 3, 17 5 6 6<br />

Vinca minor Apoc AR 0.48 15 p Ch Node2 Eur 1359 12 8 3.7 15.3 893 1, 3, 17 4 6 7<br />

Viola arvensis \do AR -0.29 40 a Th 0 7 4 2065 33 11 3.6 15.0 940 4 8 4 6<br />

Viola canina Vio N n -0.87 18 p hc 0 5 4 1030. 18 3.5 14.7 1008 8, 10 8 4 2<br />

Viola hilt s<br />

Vio N n -0.46 15 P hc<br />

0 Rhir l 7 4<br />

964, 1 3.7 15.71 795 7<br />

7 4 2<br />

Viola kitaibeliana<br />

\do N VU r<br />

10 a Th<br />

0 8 3<br />

2<br />

6.7 16.6 814 19<br />

9 3 2<br />

Viola lactea Vio N s -1.08 15 hc 0 7 1 183 2 5.0 15.8 1025 10 7 6 2<br />

Viola lutea Vio N n -0.69 20 hc Rhiz2 4 3 536 1 2.0 13.3 1281 7, 8, 16 8 5 2<br />

Viola odorata Vio N n -0.19 15 hc Sto12 7 3 1340 9 3.8 15.7 833 7 5 5 7<br />

Viola palustris Vio N n -0.30 15 hc Rhiz2 5 3 1880 56 3.3 13.9 1262 11, 14 7 9 2<br />

a,<br />

0 Viola persicifolia Vio N EN r -0.62 25 hc 0 7 4 c 18 1 3.9 15.4 826 11 7 8 3<br />

Viola reichenbachiana Vio N n 0.20 13 hc 0 7 3 1128 28 3.8 15.5 869 1 4 6 5<br />

Viola riviniana Vio N n 1.07 18 hc 0 Root 7 3 2741 96 1 3.5 14.4 1112 1, 7, 16 6 5 4<br />

Viola rupestris Vio N r 5 hc 0 7 5 c 7 1,6 13.3 1393 7 8 3 2<br />

Vio/a tricolor Vio N n -1.52 20 p Th hc 0 7 3 1691 24 3.4 14.6 992 4, 8, 19 8 4 4<br />

Viscum album Vise N n 0.97 100 Ch Pn w 0 7 3 923 3.8 15.9 788 3, 17 7 5 5<br />

Vulpia bromoides Poac N n 0.18 37 Th 0 9 2 1777 51 1 3.8 15.0 1006 3 8 4 3<br />

Vulpia ciliata Poac N s 0.78 37 a Th 0 9 1 109 4.0 16.3 716 8 9 2 2<br />

Vulpia fasciculata Poac N s 0.37 55 a Th 0 9 1 109 1 5.0 15.8 911 Co 19 9 3 2<br />

Vulpia myuros Poac AR 1.55 62 a Th 0 8 4 1134 11 i 3.9 15.6 866 3, 17 8 3 3<br />

Vulpia unilateralis Poac AN -0.56 35 a Th 0 9 2 Eur 39 3.6 16.2 705 3, 7 9 3 2<br />

Wahlenbergia hederacea Camp N n -0.30 5 p hc Node2 8 1 314 4 4.1 14.9 1280 11, 14 6 8 3<br />

Wolfi a arrhiza Lemn N s -0.03 0.1 p Fly Frag 8 4 48 4.4 16.6 752 13 7 11 7<br />

Woodsia alpina Wood N r 0.11 8 p hc 0 2 6 22 0.4 11.6 2371 15, 16 7 4 2<br />

Woodsia ilvensis Wood N EN r -0.10 10 p hc 0 2 6 14 1.3 12.4 2108 16 7 3 2<br />

Zannichellia palustris Zann N n 0.17 50 p Hy Irreg Rhiz2 8 6 1196 20 3.8 15.5 820 13, 14 7 12 7<br />

Zea mays Poac AC 300 a Th 0 Crop 92 1 1 4.0 15.9 820 4, 17 8 3 7<br />

Zostera angustifolia Zost N s -0.68 30 p Hy Rhiz2 ? ? 131 27 6 4.3 15.0 926 Co 21 7 12 5<br />

Zostera marina Zost N n -0.86 50 p Hy Rhiz2 6 6 296 68 13 4.5 14.6 1156 Co 21, 23 6 12 6<br />

Zostera noltei Zost N s -0.51 12 p Hy Rhiz2 8 5 159, 36 4 4.2 14.9 1020 Co 21 8 11 5


A PPE NDIX<br />

Sources or Mot hei ht<br />

Plant heights have been calculated from a range <strong>of</strong> sources <strong>and</strong> have been subject to personal<br />

adjust ment . The main sources were Clapham,Tut in & Warburg ( 1962), Stace ( 1991, 1997) <strong>and</strong><br />

Sell & Murrell ( 1996). Values that were thought to be too big, especially the height <strong>of</strong><br />

procumbent species, were modifi ed using informat ion in Butcher (1961).<br />

A nearly complet e set <strong>of</strong> additional height values was taken from sources including Flora lberica<br />

(Cast roviejo et al., I 986-), a Czech fl ora (Dostal, 1958) <strong>and</strong> BSBI h<strong>and</strong>books such as Crucifers <strong>of</strong><br />

Great Britain <strong>and</strong> Irel<strong>and</strong> (Rich, 1991). Other such sources included Aeschimann & Burdet ( 1994),<br />

Hutchinson & Thomas ( 1966), Jermy, Chater & David (1982), Mei kle ( 1984), Page ( 1997) <strong>and</strong><br />

Preston ( 1995). The new values were checked against t hose derived from the main sources. For<br />

t hose species where t here was a dif erence <strong>of</strong> more than a factor <strong>of</strong> 1.5 between the two<br />

sources, the discrepancy was resolved by making a judgement as to which seemed most suitable<br />

for <strong>British</strong> conditions. In addition, all heights <strong>of</strong> pteridophytes <strong>and</strong> <strong>of</strong> trees <strong>and</strong> shrubs exceeding<br />

5 m have been critically examined.<br />

A difi culty with creeping or procumbent plants is that the fl oras give shoot lengt h but not plant<br />

height. For several such plants, the canopy height was estimated by Hill, using descriptions <strong>and</strong><br />

personal experience. Likewise Preston estimated t he heights <strong>of</strong> Aizoaceae (cf Preston & Sell,<br />

1989).<br />

Many diffi culties in assigning height to a plant remain. The height <strong>of</strong> a fern is taken to be the<br />

length <strong>of</strong> its fronds. Scapose plants such as Pinguicula lusitanica may be very small except for their<br />

scape. In several scapose genera (e.g. Bellis, Pilosella, Pinguicula, Plantago, Primula, Pyrola), t he length<br />

<strong>of</strong> the leaves is used as a measure <strong>of</strong> size. On the other h<strong>and</strong>, rosette plants with substantial<br />

infl orescences (e.g. Sempervivum tectorum) have been accorded t he height <strong>of</strong> their infl orescence<br />

rather t han t he lengt h <strong>of</strong> t he leaves. It was impossible to be completely consistent. Maximum<br />

height is a general indication <strong>of</strong> the size <strong>of</strong> the plant rather than a precise measure.<br />

The result ing table is inevitably a complex result <strong>of</strong> cited values <strong>and</strong> personal judgement. It was<br />

clear that aut hors repeat each ot her <strong>and</strong> that their informat ion is <strong>of</strong>t en wrong. Overestimates<br />

abound because botanists take pleasure in ext reme values. For example, <strong>British</strong> authors <strong>and</strong> Flora<br />

Europaea (Tutin et al., 1964- 1980) give t he height <strong>of</strong> Ulmus glabra as 40 m, higher than any ot her<br />

elm. This is clearly unrealistic, but authors' copying <strong>of</strong> height data has meant that the value 40 m<br />

is constantly repeated. Fortunately Bean ( 1950- 1951) indicates a more realist ic value <strong>of</strong> 30 m,<br />

which has been used here. We have in many ot her cases t ried to drive height s down from<br />

ext reme to typical values, by selecting the publication with the lowest values.<br />

De tuition o Ii e orms<br />

Life forms (Raunkiaer, 1934) are an example <strong>of</strong> what are now called 'plant funct ional types' (cf.<br />

Box, 1996). A modifi ed version <strong>of</strong> Raunkiaer's system was set out by Clapham,Tutin & Warburg<br />

( 1962), who specifi ed a life form for almost all species. Their assignments are a valuable starting<br />

point but contain many inconsistencies. For PLANTATT, they have been comprehensively<br />

revised. The categories were partially redefi ned (Table A l).<br />

6 1


Table A I . Life form categor ies from Clapham ,Tutin & W arburg ( 1962) <strong>and</strong> revised<br />

categories<br />

Category<br />

(CTW )<br />

Phanerophyte,<br />

mega-, meso-<br />

Phanerophyte,<br />

micro-<br />

Phanerophyte,<br />

nano-<br />

Defi nition (CTW ) PLA NTAT T Defi nit io n (database)<br />

>8 m Ph Mega-, meso- <strong>and</strong> microphanerophyte<br />

2-8 m Ph (combined with taller phanerophytes)<br />

25 cm-2 m Pn Nanophanerophyte<br />

Chamaephytes 0-25 cm Ch Chamaephyte<br />

Hemicryptophytes<br />

W intering buds at soil<br />

surface<br />

hc Hemicryptophyte<br />

Herbs with wintering<br />

Geophyt es buds below the soil Gb, Gn Geophytes<br />

surface<br />

Helophyt es Marsh plants (not recognized)<br />

Hydrophytes Water plants Hy<br />

Therophytes<br />

Passing unfavourable<br />

season as seeds<br />

Hz<br />

T h<br />

62<br />

Perennat ing buds submerged during<br />

winter<br />

Annual water plant<br />

Annual l<strong>and</strong> plant, including those living<br />

on summer mud<br />

The redefi ned categories are generally self-explanatory. As the database contains plant heights,<br />

the dist inctions between phanerophytes <strong>and</strong> chamaephytes, <strong>and</strong> distinct ions within<br />

phanerophytes, are not ent irely necessary. If required, new categories can be derived using<br />

combinations <strong>of</strong> character's. For example German authors such as Mueller-Dombois & Ellenberg<br />

( 1974) generally allow chamaephytes to be up to 50 cm tall <strong>and</strong> distinguish a category <strong>of</strong> dwarf<br />

shrubs (denot ed by Z - Zwergstraucher). These are woody or semi-woody chamaephytes. It<br />

would be possible to reconstruct t his category from our database, allowing for t he fact that<br />

ordinary maximum heights <strong>of</strong> many <strong>of</strong> these bushes might be up to 100 cm.<br />

Ot her categories included by Mueller-Dombois & Ellenberg ( 1974) are lianes, epiphytes <strong>and</strong><br />

errant hydrophytes (unattached water plants). They defi ne Hemicryptophytes as plants that die<br />

back to near the ground in the unfavourable season. Although worked out in some detail, their<br />

scheme remains somewhat tentative <strong>and</strong> we have not adopted it.<br />

Exam les o how li e- orm criteria are a lied<br />

The criteria given above result in many discrepancies between our defi nit ions <strong>of</strong> life for m <strong>and</strong><br />

those <strong>of</strong> Clapham,Tutin & Warburg ( 1962). For example, t he distinction between geophytes <strong>and</strong>


hemicryptophytes is <strong>of</strong>ten hard to apply with rhizomatous perennials. In principle, plants whose<br />

new shoots penet rate the surface before the advent <strong>of</strong> winter are hemicryptophytes, while those<br />

whose shoots remain well buried are geophytes. Thus Phragmites australis, with a relatively deep<br />

rhizome (Preston & Cr<strong>of</strong>t , 1997), has the life forms perennial Hy <strong>and</strong> Gn. In Carex acutiformis,<br />

however, many new shoots have already emerged by the autumn (Preston & Cr<strong>of</strong>t, 1997). It is<br />

also less strongly aquatic. It is t herefore given the life forms hc <strong>and</strong> Hy.<br />

In general, biennials have been classifi ed as hemicryptophytes, but a few such as Euphorbia lathyris,<br />

which are elongated from the beginning, are chamaephytes.<br />

It is inst ructive to consider some ot her cases (Table A2), which will not be discussed in detail.<br />

Table A 2. Som e cases where life-form ( LF) is difficult to apply or where our concept<br />

dif ers from t hat <strong>of</strong> C lapham,Tut in & W arburg ( 1962)<br />

Links between Ii e orms <strong>and</strong> lent hei ht<br />

Because chamaephytes <strong>and</strong> our two categories <strong>of</strong> phanerophytes are defi ned on the basis <strong>of</strong><br />

height, an eff ort was made to defi ne life forms consistently by reference to plant height (Table<br />

A3). Sometimes, as in Artemisia campestris, t he overwintering buds are at a substantially lower<br />

height t han the height <strong>of</strong> the mature plant. Therefore, this scheme has not been followed exact ly<br />

but has been used as a guide.<br />

63


These defi nitions are necessarily imprecise. However, knowing that Ca !tuna vulgans has a typical<br />

maximum height <strong>of</strong> 60 cm suggests that it will <strong>of</strong>ten grow as a chamaephyte <strong>and</strong> <strong>of</strong>t en as a<br />

nanophanerophyte. This is indeed the case; C. vulgaris is the classic dwarf shrub.<br />

Table A 3. Chamaephyte <strong>and</strong> phanerophyte categories in relation to plant height<br />

Typical maximum<br />

plant height (cm )<br />

3-39 Ch<br />

40-69 Ch<br />

70-299 Pn<br />

300-399 Pn<br />

400- Ph<br />

Primary life form Secondary life form<br />

Cionality<br />

Clonality can be defined in various ways. In an enumeration for Cent ral Europe, Klime§ et al.<br />

( 1997) defi ned clonal growt h as synonymous with vegetat ive multiplicat ion, which results in t he<br />

production <strong>of</strong> new, genetically identical descendants (ramets) with the potential to become<br />

independent <strong>of</strong> t he mot her organism. According to this definition, plants that produce a new<br />

ramet each year but do not spread laterally (for example many orchids) are clonal. Klime§ et aL<br />

recognize 21 diff erent clonal types. These are described in Klimet 's excellent website Clopla<br />

(http://wwri butInn.cas.cz/klimes/clopla .htm); all species <strong>of</strong> Central Europe, including the majority <strong>of</strong><br />

<strong>British</strong> <strong>and</strong> <strong>Irish</strong> plants, are assigned to one or more clonal types.<br />

Here we adopt a more familiar defi nit ion <strong>of</strong> clonal growth, namely vegetative reproduction<br />

combined with lateral spread — i.e. spreading through the formation <strong>of</strong> clonal patches or clumps,<br />

or through fragmentation <strong>and</strong> subsequent dispersal <strong>of</strong> plant parts.<br />

Broad Habit ats<br />

The Broad Habitat Classifi cation, developed as part <strong>of</strong> the UK Biodiversity Action Plan (Jackson,<br />

2000; UK Biodiversity Group, 1998; UK Biodiversity Steering Group, 1995), provides a<br />

comprehensive framework for surveillance <strong>of</strong> the UK countryside.We categorized the habitats <strong>of</strong><br />

plants by t heir preferences for Broad Habitats.<br />

In the UK Biodiversity Action Plan (UK Biodiversity Steering Group, 1995), 37 Broad Habitat<br />

categories were defi ned. These included some habitats, such as limestone pavements, that are<br />

quite narrow but were specified because t hey are priority habitats for conservat ion. In a later<br />

publication (UK Biodiversity Group, 1998), the number <strong>of</strong> terrest rial <strong>and</strong> freshwater Broad<br />

Habitats was reduced to 17. Limestone pavements were included in the Broad Habitat inl<strong>and</strong><br />

rock. Ten coastal <strong>and</strong> marine Broad Habitats were added shortly aft erwards (UK Biodiversity<br />

Group, 1999). Out <strong>of</strong> the 27 Broad Habitats, 2 1 support vascular plants (see Table 8, above).<br />

64<br />

Pn<br />

Ph


Broad Habitats are intended to be comprehensive <strong>and</strong> exclusive. In other words, every place in<br />

which a vascular plant is found ought to belong to one <strong>and</strong> only one Broad Habitat. Although<br />

the defi nit ions <strong>of</strong> Broad Habitats are in many cases obvious, t here was a need for more precise<br />

circumscript ion to defi ne t he boundaries between them. For terrest rial <strong>and</strong> freshwater habitats<br />

this guidance is now available (Jackson, 2000). The guidance not only gives writt en defi nit ions, but<br />

relates Broad Habitat s to the units <strong>of</strong> t he National Vegetation Classifi cation (NVC; Rodwell,<br />

1991-2000).<br />

Jackson's (2000) notes for guidance are the basis <strong>of</strong> the cross-reference <strong>and</strong> defi nitions used here<br />

(Table A4). In a small number <strong>of</strong> cases, we have diverged from her interpretations. The basis <strong>of</strong><br />

our disagreement was <strong>of</strong>t en the scale at which we wished to view the vegetation. Thus we have<br />

t reated bog pools as st rictly bog features (not as open water) <strong>and</strong> we treat rock-free maritime<br />

grassl<strong>and</strong> as neut ral grassl<strong>and</strong> (not as supralitt oral rock). Ot her interpretat ions are possible but<br />

result in fl orist ically less homogeneous Broad Habitats.<br />

Table A 4. Assignment <strong>of</strong> N VC com munities to Broad Habitats for t he purpose <strong>of</strong><br />

ascribing habitat preferences. Sequential runs <strong>of</strong> numbers are indicated by hyphens, e.g. 2 1-<br />

23, which signifi es t he sequence 2 1,22,23. Some NVC communit ies were assigned to two Broad<br />

Habitats; where this is t he case, the community is marked by an asterisk, to show that it is also<br />

listed under another Broad Habitat.<br />

N o Nam e N VC com munities<br />

Broad leaved, mixed <strong>and</strong> yew W I- 17,19<br />

woodl<strong>and</strong><br />

2 Coniferous woodl<strong>and</strong> W I8<br />

3 Boundary <strong>and</strong> linear feat ures W 2 I-23,24*; OV I 8*, I 9*,21*,22*,24*,25*,27<br />

4 A rable <strong>and</strong> horticult ural O V I- 11, 13, 14- 17, 18* , 19*,2 1* ,22*,36<br />

5 Improved grassl<strong>and</strong> MG6*,7; OV 12,23*,25*<br />

6 Neutral grassl<strong>and</strong> W 24; MC9- 1 2; MG I-5,6*; MG8- I 3; 0 V28*<br />

7 Calcareous grassl<strong>and</strong> CG I- 14<br />

8 Acid grassl<strong>and</strong> U I - 6,19<br />

9 Bracken U 20; W 25<br />

10 Dwarf shrub heath H I- 10,12,16,18,2 1; M I5*,16; 0 V 34<br />

11 Fen, marsh <strong>and</strong> swamp M4- 14,22-24,25*,26-38; S - I 9,20*,22-28; OV 26,28*,29-<br />

12 Bog M 1-3,15*, 17-21,25*<br />

13 St<strong>and</strong>ing water <strong>and</strong> canals A I-7,8*,9*,10,(11- 16)* , 19*,20*, 21-24<br />

14 Rivers <strong>and</strong> st reams A 8*,9*,( 1 I - I 6)*,17,18,19*,20*<br />

15 Montane habitats H I 3- 15,17,19,20,22; U7- I5,18; W 20<br />

16 Inl<strong>and</strong> rock U 16, 17,2 1; 0 V37-40,4 I*<br />

17 Built-up areas <strong>and</strong> gardens 0 V 20,23*,24*,41* ,42<br />

18 Supralittor al rock MC 1-8<br />

19 Supralittor al sediment H I I; SD I- 19<br />

2 1 Littor al sediment 520,21; SM I-28<br />

65


It is pertinent here to consider the defi nitions, drawing attention to less obvious features <strong>and</strong> to<br />

where we have dif ered from Jackson (2000).<br />

BH I Broad leaved, mixed <strong>and</strong> yew woodl<strong>and</strong><br />

Broad leaved woodl<strong>and</strong> is defi ned as woodl<strong>and</strong> with broadleaved trees having at least 20% canopy<br />

cover. In practice, most woodl<strong>and</strong> has closed canopy. Juniper scrub is included in this type if it is<br />

large enough to result in a woodl<strong>and</strong> understorey (W 19). Other scrub types are treated as edge<br />

features (BH3), because hedges are <strong>of</strong>ten where they occur. The underscrub community W 24 is<br />

shared between woodl<strong>and</strong> (BH1) <strong>and</strong> neutral grassl<strong>and</strong> (BH6).<br />

8 H 2 Coniferous woodl<strong>and</strong><br />

This category is clearly defi ned <strong>and</strong> corresponds to nat ive pine woodl<strong>and</strong> (W 18) in the NVC.<br />

St<strong>and</strong>s <strong>of</strong> planted conifers normally have a subset <strong>of</strong> the normal broadleaved woodl<strong>and</strong> fl ora<br />

growing under them. There is no corresponding NVC type. Planted conifers have therefore<br />

been under-represented, <strong>and</strong> the fern Dryopteris dilatata, which is t he commonest vascular plant<br />

in upl<strong>and</strong> conifer plantations, did not appear as a conifer specialist in our fl oristic database, but its<br />

preference was added by us later<br />

BH 3 Boundary <strong>and</strong> linear feat ures<br />

Apart from scrub that forms hedges, boundary <strong>and</strong> linear features are not directly crossreferenced<br />

to the NVC. They include hedges, t ree-lines, walls, earth banks, grass strips <strong>and</strong> dry<br />

ditches. Note that roads, t racks <strong>and</strong> railways in urban areas belong to the urban BH I7.<br />

BH 4 A rable <strong>and</strong> horticultural<br />

Commercial orchards are included here, as well as fi eld crops. Note that hort iculture here is<br />

defi ned as commercial hort iculture <strong>and</strong> does not include domestic gardens <strong>and</strong> allotments, which<br />

are included in BH 17. The NVC communit ies classifi ed as OV 1- 11,13-19,2 1,22,36 are included<br />

here.<br />

BH 5 Im proved grassl<strong>and</strong><br />

This has few characteristic species, <strong>and</strong> is typically dominated by sown ryegrass Lolium perenne or<br />

clover Trifolium repens. OV I2, the Poo annua-Myosotis arvensis community, is indicated in <strong>British</strong><br />

Plant Communities (Rodwell, 1991-2000) as being mainly a disturbed element in improved pasture<br />

<strong>and</strong> has been included here.<br />

8 H 6 N eutral grassl<strong>and</strong><br />

The mesot rophic grassl<strong>and</strong> types MG I-6,8- 13 are the core <strong>of</strong> t he neutral grassl<strong>and</strong> category.<br />

Coastal grazing marsh is included here. Four <strong>of</strong> the coastal clif grassl<strong>and</strong>s, MC9- I2, are not<br />

necessarily or normally rocky <strong>and</strong> have been included here in BH6. OV28, an inundation<br />

grassl<strong>and</strong>, is shared between BH6 <strong>and</strong> BH 1 I.<br />

BH 7 Calcareous grassl<strong>and</strong><br />

By convention, this includes all NVC types included in the CG class. As a result, montane<br />

calcareous vegetation is in BH7, along with chalk grassl<strong>and</strong>.<br />

BH 8 Acid grassl<strong>and</strong><br />

Only lowl<strong>and</strong> <strong>and</strong> subalpine grassl<strong>and</strong> are included here; vegetation types that would normally be<br />

found above the timberline are in BH I5. Communities U I-6 form the core <strong>of</strong> this type. The<br />

fern community U 19 is treated in BH8. It is usually a mosaic element in grassl<strong>and</strong>, though it also<br />

occurs on steep banks by rivers <strong>and</strong> could therefore be included also in the broad defi nit ion (not<br />

used here) <strong>of</strong> BH I4.<br />

66


BH 9 Bracken<br />

This is small type, defi ned as unwooded l<strong>and</strong> dominated by bracken Pteridium aquilinum. 8H9 has<br />

few characterist ic species, because it is usually a derivative <strong>of</strong> grassl<strong>and</strong> or forest. Just two NVC<br />

types, U20 <strong>and</strong> W 25, are included here.<br />

BH 10 Dwarf shrub heat h<br />

The heath type BH 10 includes vegetation with at least 25% cover <strong>of</strong> Ericaceae or dwarf gorse<br />

Ulex minor. Coastal heath is included in this category, except for dune heath, which is assigned to<br />

BHI9. Dwarf shrub communit ies on blanket bogs are st rictly included in BH I2, but this is a<br />

relat ively minor habitat for them <strong>and</strong> has not been recognized in t he cross-reference. The<br />

st<strong>and</strong>ard heathl<strong>and</strong> communities H 1- 10,12,16,18,21, toget her with the wet heath communities<br />

M 15,16 form the core <strong>of</strong> this community. The bizarre 0 V34, a chive M um schoenoprasum<br />

community forming a mosaic element on shallow soils in coastal heath, is included here.<br />

B14 1 I Fen, marsh <strong>and</strong> swamp<br />

This is a very wide category <strong>and</strong> includes reedbeds, swamps, tall-herb fens, fl ushes, springs,<br />

marshes, rush-past ures <strong>and</strong> wet grassl<strong>and</strong>. Mud communities <strong>of</strong> dried-up ponds <strong>and</strong> riverbeds<br />

(e.g. 0 V30) have been included here, although they belong more st rictly to BH I3 <strong>and</strong> BH I4<br />

unless they are very ext ensive (>0.25 ha). Types M4- 14,22-38, all swamp communities except<br />

Scirpus maritimus S2 1, <strong>and</strong> OV 26,28-33,35 are included. We have excluded the bog-like<br />

communities (Erico-Sphagnion) that are found in very acid lowl<strong>and</strong> valley-mires.<br />

BH I 2 Bog<br />

Bogs are defi ned strictly only as ombrot rophic bogs. However, we have lumped all Erico-<br />

Sphagnion vegetation, including M21, in BH 12 even if it the vegetation occurs in valley mires,<br />

toget her with bog pool vegetation M 1-3. This is to prevent the characteristic species <strong>of</strong> BH 11<br />

being too heterogeneous. The NVC types included are M1-3,15,17-21,25.<br />

BH I 3 St<strong>and</strong>ing water <strong>and</strong> canals<br />

Only aquatic vegetat ion has been cross-referenced to this type, i.e. communit ies A l - 16,19-24.<br />

Mud communities <strong>and</strong> marginal vegetation are referred to BH11.<br />

BH I 4 Rivers <strong>and</strong> st reams<br />

This Broad Habitat is t reated in much the same way as BH I3. According to t he strict defi nition,<br />

all vegetation between the banks <strong>of</strong> a river counts as belonging to BH I4. For the purposes <strong>of</strong><br />

defi ning characteristic species, river-bank vegetat ion has been t reated as belonging to other types<br />

such as inl<strong>and</strong> rock. Thus t he communities included in BHI4 are A8,9,11-20. Several <strong>of</strong> these<br />

communities are also characteristic <strong>of</strong> B1-113.<br />

BH 1 S Mont ane habit at s<br />

This type is defined by having distinctive arctic-alpine species, provided that they are not<br />

calcicolous. Calcareous montane vegetation is included in BH7. BH 15 includes montane heaths<br />

H I3- 15,17,19,20,22, grassier types U7- I5,18, <strong>and</strong> a willow scrub type W 20.<br />

BH I 6 Inl<strong>and</strong> rock<br />

This heterogeneous Broad Habitat includes limestone pavement, cliff s, caves, scree, quarries <strong>and</strong><br />

vegetation on skeletal soils over rock. Communities U 16,17,2 1 <strong>and</strong> 0 V37-4 1 are assigned to<br />

BH 16.<br />

BH I 7 Built-up areas <strong>and</strong> gardens<br />

Urban habitats were largely ignored by the NVC surveyors. Most <strong>of</strong> the characteristic species<br />

are neophytes, while t he commonest species are widespread nat ives <strong>and</strong> archaeophytes (Hill, Roy<br />

67


& Thompson, 2002). Very few NVC communities are really characteristic <strong>of</strong> the built<br />

environment. Pavement <strong>and</strong> wall communities 0 V20,42 are assigned wholly to BH I7;<br />

0 V23,24,4 I are assigned to BH 17 but shared with other Broad Habitats.<br />

BH 18 Supra littoral rock<br />

It is clear from the Habitat Statement for supralitt oral rock (UK Biodiversity Group, 1999) that<br />

maritime grassl<strong>and</strong> is not included. For that reason, MC9- 11,12 have been treated as neutral<br />

grassl<strong>and</strong>, BH6. Only MCI-8 are included in BH I8.<br />

BH 19 Supralittoral sedim ent<br />

This includes str<strong>and</strong>lines, shingle, machair <strong>and</strong> coastal dunes. It includes all the NVC types SD I-<br />

19, toget her with the dune heath type H I I .<br />

BH 20 Littoral Rock<br />

Intert idal rock normally lacks vascular plants <strong>and</strong> no vascular-plant species or vegetat ion type is<br />

characterist ic <strong>of</strong> it.<br />

BH 2 I Littoral sediment<br />

This includes saltmarshes <strong>and</strong> saltmarsh pools.<br />

BH 23 Inshore sublittoral sediment<br />

One vascular plant. Zostero marina, occurs in this habitat, which is not considered furt her<br />

Initial calculation o s ecies' re erences or Broad Habitats<br />

For the majority <strong>of</strong> species, habitat preferences were based on quadrat data. Two major datasets<br />

were available, the original data used to derive the association tables in <strong>British</strong> Plant Communities<br />

(NVC; Rodwell, 1991-2000) <strong>and</strong> quadrat samples collected for Count ryside Survey 2000,<br />

CS2000 (Haines-Young et aL, 2000).<br />

The quadrat data used to create the NVC categories were supplied by JNCC as an MS Access<br />

database. This had been created from fi les in the format <strong>of</strong> the VESPAN package (Malloch, 1985).<br />

There was no information on the NVC community to which each quadrat had been assigned.<br />

Therefore, the computer program TABLEFIT (Hill, 1996) was used to assign 312 16 quadrats to<br />

NVC communities using species' Domin scores. The median goodness-<strong>of</strong>-fi t was 67%. Only four<br />

samples had no fi t; t hese were assigned to a community by personal judgement . NVC plant<br />

communit ies were then attributed to Broad Habitats using the cross-reference outlined above<br />

(Table A4). All CS2000 samples had been allocated to BAP Broad Habitat types in the fi eld.<br />

Aft er quadrats had been assigned to Broad Habitats, species' frequencies in each Broad Habitat<br />

were calculated. Frequencies were used to calculate preferences for Broad Habitats. For each<br />

species s <strong>and</strong> BH h, we calculated an odds-ratio index:<br />

Qsh<br />

= observed odds for species s in habitat h / expected odds<br />

nsh<br />

/ (ns+ "sh + 0.5)<br />

esh/ Os+ esh)<br />

where<br />

nsh = observed number <strong>of</strong> occurrences <strong>of</strong> species s in BH h<br />

ns+ = 1h nsh = total number <strong>of</strong> occurrences <strong>of</strong> speCies s<br />

esh = expected number <strong>of</strong> occurrences <strong>of</strong> species s in BH h.<br />

68


The expected number <strong>of</strong> occurrences<br />

where<br />

esh<br />

= ns N h / N +<br />

Nh = number <strong>of</strong> quadrat samples in BH h<br />

N 4. = E h N h = total number <strong>of</strong> quadrat samples.<br />

Species s was deemed to have a preference for BH h if<br />

Qsh 4.<br />

Extension <strong>and</strong> validation o s ecies' re erences<br />

Many rare, scarce or uncommon native species are not represented either in the NVC quadrats<br />

or in CS2000 samples. Furt hermore, t here was the possibility that uneven sampling <strong>of</strong> Broad<br />

Habitats could have resulted in some wrong indications <strong>of</strong> preference.<br />

First, we ext ended the list <strong>of</strong> BH preferences to species not adequately sampled by the NVC or<br />

CS2000, using the text prepared for the New Atlas, together with other literature sources (e.g.<br />

Stewart, Pearman & Preston, 1994; W igginton, 1999). Much <strong>of</strong> the initial work was done by Bill<br />

Meek (CEH); t he resulting table <strong>of</strong> preferential species was checked by D.A. Pearman (BSB1), as<br />

well as by ourselves <strong>and</strong> ot her CEH staf . In addition, preferences were checked against ot her<br />

data in PLANTATT For example, species attributed to BH I3 (St<strong>and</strong>ing water <strong>and</strong> canals) <strong>and</strong><br />

BH 14 (Rivers <strong>and</strong> streams) were checked for their Ellenberg moisture (F) values. Those for<br />

which F


A CKN O WLED GEMEN TS<br />

Much <strong>of</strong> the work presented here was support ed by funding from the W ildlife <strong>and</strong> Countryside<br />

Division <strong>of</strong> Defra <strong>and</strong> its predecessor DETR. The immediate stimulus was a project to interpret<br />

the New Atlas <strong>of</strong> the <strong>British</strong> <strong>and</strong> <strong>Irish</strong> Flora (Preston et al., 2003). A requirement for non-spatial<br />

attributes <strong>of</strong> plants was written into the 2002 programme <strong>of</strong> work for the National Biodiversity<br />

Network (NBN). Informat ion on native status was prepared for the New Atlas <strong>and</strong> presented<br />

there (Preston, Pearman & Dines, 2002). The Ellenberg indicator values were developed under<br />

the DETR-funded ECO FACT programme <strong>and</strong> published separately (Hill et al., 1999).<br />

The other main ot her source <strong>of</strong> funding was from our parent body the <strong>Natural</strong> <strong>Environment</strong><br />

<strong>Research</strong> Council. Not only have they generously support ed the Biological Records Centre<br />

(BRC) <strong>and</strong> NBN over the years, but they have allowed us to fi nd additional t ime to work our<br />

data up into publishable form. The geographical classifi cat ion <strong>of</strong> European distributions (Preston<br />

& Hill, 1997) was developed with support from NERC's special programme on global<br />

environmental change,TIGER.<br />

Some elements <strong>of</strong> t his work have been funded by the Joint Nat ure Conservation Committee<br />

through t heir joint sponsorship <strong>of</strong> BRC. Other aspects were supported by t he Countryside<br />

Council for Wales, English Nat ure, Scottish <strong>Natural</strong> Heritage, <strong>Environment</strong> <strong>and</strong> Heritage Service<br />

(Northern Irel<strong>and</strong>) <strong>and</strong> Plantlife as part <strong>of</strong> the analysis <strong>of</strong> New Atlas data.<br />

Publication <strong>of</strong> this booklet has been jointly funded by CEH <strong>and</strong> Defra.<br />

We are grateful to the following for particular help:<br />

De fra<br />

Andrew Stott (overall guidance <strong>and</strong> long-term support)<br />

Debbie Boobyer (Broad Habitats <strong>and</strong> analysis <strong>of</strong> New Atlas data)<br />

BSBI<br />

David Pearman (Broad Habitats)<br />

Cambridge University<br />

Peter Sell (unpublished fl ora draft s)<br />

English Nature<br />

Roger Key (Cover photograph)<br />

JNCC<br />

Ian St rachan (NVC quadrat data)<br />

CEH<br />

Bob Bunce (Ellenberg values)<br />

Jon Cooper (liaison with NBN)<br />

Julie Gaunt (graphic design)<br />

Bill Meek (Broad Habitats)<br />

Owen Mountford (Ellenberg values, European fl oras, species attributes)<br />

Peter Rothery (Change index)<br />

Mark Telfer (Change index)<br />

70


B IB LI OGRA PH Y<br />

Aeschimann, D. & Burdet, H.M. ( 1994) Fiore de la Suisse. Editions du Grif on, Neuchatel.<br />

Barrow, E.M., Hu Ime, M. <strong>and</strong> Jiang,T. (1993) A 1961-90 baseline climatology <strong>and</strong> future climate<br />

change scenarios for Great Britain <strong>and</strong> Europe. Part 1: 1961-90 Great Britain baseline climatology.<br />

Climatic <strong>Research</strong> Unit, Norwich, 43pp. (plus maps).<br />

Bean,W.J. ( 1950- 1951) Trees <strong>and</strong> shrubs hardy in the <strong>British</strong> Isles. 7 edn. John Murray, London.<br />

Box, E.O. ( 1996) Plant functional types <strong>and</strong> climate at the global scalej ournal <strong>of</strong> Vegetation Science,<br />

7, 309-320.<br />

Butcher, R.W. ( 1961) A new illustrated <strong>British</strong> fl ora. Leonard Hill, London.<br />

Castrovielo, S. et al., eds. ( 1986-) Flora iberica: plantas vasculares de la Peninsula iberica e Islas<br />

Baleares. Vol. 1 -. Real Jardin Botanico, Madrid.<br />

Cheffi ngs, C. (2004) New plant status lists for Great Britain. 8581 News, 95, 36-43.<br />

Clapham, A.R.,Tut in,T.G. & Warburg, E.F. ( 1962) Flora <strong>of</strong> the <strong>British</strong> Isles. 2 edn. Cambridge<br />

University Press, Cambridge.<br />

Dostald . ( 1958) Klic k Opine kvetene CSR. 2 edn. Ceskoslovenske Akademie Ved, Prague.<br />

Ellenberg, H.,Weber, H. E., Dull, R.,W irt h,V,Werner,W. & Paulissen, D. ( 1991) Zeigerwerte von<br />

Pfl anzen in Mitt eleuropa. Scripta Geobotanica, 18, 1-248.<br />

Fitt er, A.H. & Peat, H.J. ( 1994) The Ecological Flora Database. Journal <strong>of</strong> Ecology, 82, 4 15-425.<br />

Grime, J. R ( 1979) Plant strategies <strong>and</strong> vegetation processes. John W iley, Chichest er.<br />

Grime, J. P. (2001) Plant strategies, vegetation processes, <strong>and</strong> ecosystem properties.W iley, Chichester.<br />

Gr imel .R,Thompson, K., Hunt, R., Hodgson, J.G., Cornelissen, J.H.C., Rorison, 1.H., Hendry, G.A.F,<br />

Ashenden,T.W.,A skew,A.R, B<strong>and</strong>, S.R., Booth, R.E., Bossard, C.C., Campbell, B.D., Cooper,<br />

J.E.L., Davison, A.W., Gupta, PL., Hall,W , H<strong>and</strong>, D.W., Hannah, M.A., Hillier, S.H., Hodkinson,<br />

D.J., Jahli,A ., Liu, Z., Mackey, J.M.L., Matthews, N., Mowforth, M.A., Neal,A.M., Reader, R.J.,<br />

Reiling, K., Ross-Fraser,W , Spencer, R.E., Sutton, F.,Tasker, D.E., Thorpe, P.C. & W hitehouse, J.<br />

( 1997) Integrated screening validates primary axes <strong>of</strong> specialisation in plants. Oikos, 79, 259-<br />

281.<br />

Haines-Young, R.H., Barr, C.J., Black, H.1.J., Briggs, D.J., Bunce, R.G.H., Clarke, R.T , Cooper, A.,<br />

Dawson, F.H., Firbank, L.G., Fuller, R.M., Furse, MI , Gillespie, M.K., Hill, R., Hornung, M.,<br />

Howard, D.C., McCann,T , Morecr<strong>of</strong>t, M.D., Petit, S., Sier,A.R.J., Smart , S.M., Smith, G.M., Stott,<br />

A.R, St uart , R.C. & Watkins, J.W. (2000) Accounting for nature: assessing habitats in the UK<br />

countryside. Depart ment <strong>of</strong> the <strong>Environment</strong>,Transport <strong>and</strong> the Regions, London.<br />

Hill, M.O. ( 1996) Tablefit version 1.0, for identification <strong>of</strong> vegetation types. Institute <strong>of</strong> Terrestrial<br />

Ecology, Huntingdon.<br />

Hill, M.O., Mountford, J.O., Roy, D.B. & Bunce, R.G.H. (1999) Ellenberg's indicator values for <strong>British</strong><br />

plants. ECO FACT Volume 2 technical annex. Institute <strong>of</strong> Terrestrial Ecology, Huntingdon.<br />

Hill, M.O., Roy, D.B. & Thompson, K. (2002) Hemeroby, urbanity <strong>and</strong> ruderality: bioindicators <strong>of</strong><br />

disturbance <strong>and</strong> human impact. Journal <strong>of</strong> Applied Ecology, 39, 708-720.<br />

Hodgson, J.G., Grime, J.R, Hunt, K. & Thompson, K. ( 1994) The electronic comparative plant ecology.<br />

Chapman & Hall, London.<br />

Hodgetts, N., Palmer, M. & W igginton, M. ( 1996) The Pink Book <strong>of</strong> <strong>Plants</strong>: lists <strong>of</strong> vascular <strong>and</strong> nonvascular<br />

plant species which are nationally threatened, localised or protected in Great Britain.<br />

JNCC, Peterborough.


Hu Ime, M. & Jenkins, G. ( 1998) Climate change scenarios for the United Kingdom: summary report<br />

Climate <strong>Research</strong> Unit, Norwich.<br />

Hutchinson, G. & Thomas, B.A. ( 1996) Welsh ferns: clubmosses, quillworts <strong>and</strong> horsetails. 7 edn.<br />

National Museums <strong>and</strong> Galleries <strong>of</strong> Wales, Cardif .<br />

Jackson, D.L. (2000) Guidance on the interpretation <strong>of</strong> the Biodiversity Broad Habitat Classifi cation<br />

(terrestrial <strong>and</strong> freshwater types): Defi nitions <strong>and</strong> the relationship with other habitat classifi cations.<br />

JNCC Repor t No. 307. JNCC, Peterborough.<br />

Jermy, A.C., Chater, A.O. & David, R.W. ( 1982) Sedges <strong>of</strong> the <strong>British</strong> Isles. Botanical Society <strong>of</strong> the<br />

<strong>British</strong> Isles, London.<br />

Klim8 , L., Klimegova J Hendriks, R. & van Groenendael, J. ( 1997) Clonal plant architecture: a<br />

comparative analysis <strong>of</strong> form <strong>and</strong> funct ion. In The ecology <strong>and</strong> evolution <strong>of</strong> clonal plants (eds H.<br />

de Kroon & J. van Groenendael), pp. 1-29. Backhuys, Leiden.<br />

Lindacher, R. ( 1995) PHANART: Datenbank der Gefasspfl anzen Mitteleuropas. Vertiffentlichungen<br />

des Geobotanischen Institutes der ETH, Stiftung RUbel, Zurich, I 25, 1-436.<br />

Macpherson, P., Dickson, J.H., Ellis, R.G., Kent, D.H. & Stace, C.A. ( 1996) Plant status<br />

nomenclature. M I News, 72, 13-16.<br />

Malloch,A.J.C. ( 1985) VESPAN: FORTRAN programs for h<strong>and</strong>ling <strong>and</strong> analysis <strong>of</strong> vegetation data <strong>and</strong><br />

species distributions. Depart ment <strong>of</strong> Biological Sciences, University <strong>of</strong> Lancaster.<br />

Meikle, R.D. ( 1984) Willows <strong>and</strong> poplars <strong>of</strong> Great Britain <strong>and</strong> Irel<strong>and</strong>. Botanical Society <strong>of</strong> t he <strong>British</strong><br />

Isles, London.<br />

Mueller-Dombois, D. & Ellenberg, H. ( 1974) Aims <strong>and</strong> methods <strong>of</strong> vegetation ecology. John W iley &<br />

Sons, New York.<br />

Page, C.N. ( 1997) The ferns <strong>of</strong> Britain <strong>and</strong> Irel<strong>and</strong>. Cambridge University Press, Cambridge.<br />

Palmer, M.A., Hodgetts, N.G.,W igginton, Mj ., Ing, B. & Stewart , N.F. ( 1997) The application to t he<br />

Brit ish fl ora <strong>of</strong> the World Conservation Union's revised red list criteria <strong>and</strong> the signifi cance<br />

<strong>of</strong> red lists for species conservation. Biological Conservation, 82, 2 19-226.<br />

Perring, EH. & Walters, S.M. ( 1962) Atlas <strong>of</strong> the <strong>British</strong> Flora.Thomas Nelson & Sons, London.<br />

Preston, C.D. ( 1995) Pondweeds <strong>of</strong> Great Britain <strong>and</strong> Irel<strong>and</strong>. Botanical Society <strong>of</strong> the <strong>British</strong> Isles,<br />

London.<br />

Preston, C.D. & Cr<strong>of</strong>t, J.M. ( 1997) Aquatic <strong>Plants</strong> in Britain <strong>and</strong> Irel<strong>and</strong>. Harley Books, Colchester.<br />

Preston, C.D. & Hill, M.O. ( 1997) The geographical relationships <strong>of</strong> Brit ish <strong>and</strong> <strong>Irish</strong> vascular<br />

plants. Botanical Journal <strong>of</strong> the Linnean Society, 124, I - 120.<br />

Preston, C.D. & Hill, M.O. ( 1999) The geographical relationships <strong>of</strong> the <strong>British</strong> <strong>and</strong> <strong>Irish</strong> fl ora: a<br />

comparison <strong>of</strong> pteridophytes, fl owering plants, liverworts <strong>and</strong> mosses. Journal <strong>of</strong> Biogeography,<br />

26, 629-642.<br />

Preston, C.D., Pearman, D.A. & Dines,T.D., eds. (2002) New atlas <strong>of</strong> the <strong>British</strong> <strong>and</strong> <strong>Irish</strong> Flora.<br />

Oxford University Press, Oxford.<br />

Preston, C.D. & Sell, RD. ( 1989) The Aizoaceae naturalized in the <strong>British</strong> Isles. Watsonia, 17, 217-<br />

245.<br />

Preston, C.D.,Telfer, M.G.,Arnold, H.R., Carey, RD., Cooper, J.M., Dines,T.D., Hill, M.O., Pearman,<br />

D.A., Roy, D.B. & Smart , S.M. (2002) The changing fl ora <strong>of</strong> the UK. DEFRA, London.<br />

Preston, C.D.,Telfer, M.G., Roy, D.B., Carey, RD., Hill, M.O., Meek,W.R., Rot hery, P. Smart,<br />

Smith, G.M.,Walker, K.J. & Pearman, D.A. (2003) The changing distribution <strong>of</strong> the fl ora <strong>of</strong> the<br />

United Kingdom: technical report Report to DEFRA on CEH project C0 1093. CEH Monks<br />

Wood, Huntingdon.<br />

72


Raunkiaer, C. ( 1934) The life forms <strong>of</strong> plants <strong>and</strong> statistical plant geography. Oxford University Press,<br />

Oxford.<br />

Rich,T.C.G. ( 1991) Crucifers <strong>of</strong> Great Britain <strong>and</strong> Irel<strong>and</strong>. Botanical Society <strong>of</strong> the Brit ish Isles,<br />

London.<br />

Rodwell, J.S. ( 1991-2000) <strong>British</strong> plant communities. Cambridge University Press, Cambridge.<br />

Sell, P. & Murrell, G. ( 1996) Flora <strong>of</strong> Great Britain <strong>and</strong> Irel<strong>and</strong>. Volume 5 Butomaceae-Orchidaceae.<br />

Cambridge University Press, Cambridge.<br />

Stace, C.A. ( 1991) New fl ora <strong>of</strong> the <strong>British</strong> Isles. Cambridge University Press, Cambridge.<br />

Stace, C.A. ( 1997) New flora <strong>of</strong> the <strong>British</strong> Isles. 2 edn. Cambridge University Press, Cambridge.<br />

Stewart, A., Pearman, D.A. & Preston, C.D., eds. ( 1994) Scarce plants in Britain. JNCC,<br />

Peterborough.<br />

Telfer, M.G., Preston, C.D. & Rothery, P. (2002) A general method for the calculation <strong>of</strong> relat ive<br />

change in range size from biological atlas data. Biological Conservation, 107, 99- 109.<br />

Tutin,T.G., Heywood,V.H., Burges, NA ., Moore, D.M.,Valent ine, D.H., Walters, S.M. & Webb, D.A.<br />

( 1968- 1980) Flora Europaea. Volumes 2-5. Cambridge University Press, Cambridge.<br />

Tutin,I G., Heywood,V.H., Burges, N.A.,Valent ine, D.H.,Walters, S.M. & Webb, D.A. ( 1964) Flora<br />

Europaea. Volume I. Cambridge University Press, Cambridge.<br />

UK Biodiversity Group ( 1998) Action Plan Volume 2:Terrestrial <strong>and</strong> freshwater habitats. English<br />

Nat ure, Peterborough.<br />

UK Biodiversity Group ( 1999) Tranche 2 Action Plans.Volume S. Maritime species <strong>and</strong> habitats.<br />

English Nat ure, Peterborough.<br />

UK Biodiversity Steering Group ( 1995) Biodiversity: the UK Steering Group Report. Volume 1,<br />

Meeting the Rio challenge; Volume 2: Action plans. HMSO, London.<br />

W igginton, M.J., ed. ( 1999) <strong>British</strong> Red Data Books. I Vascular plants, 3 edn. Joint Nature<br />

Conservat ion Committee, Peterborough.<br />

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