de Vere 2007 Biol Flora C. dissectum.pdf - The Whitley Wildlife ...

de Vere 2007 Biol Flora C. dissectum.pdf - The Whitley Wildlife ... de Vere 2007 Biol Flora C. dissectum.pdf - The Whitley Wildlife ...

20.08.2015 Views

883Cirsium dissectum© 2007 The AuthorJournal compilation© 2007 BritishEcological Society,Journal of Ecology,95, 876–894Table 2 ContinuedSite CodeNVC CommunityEBCM24cEKSM24cEMSM24cEMMM24cWDBM24EACM16bEMOM16bERWM16bEBBSD14bWKFSD14dEWFS24cOphioglossum vulgatum – – – – – – – – I (1) – –Parentucellia viscosa – – – – – – – – II (1–2) – –Pedicularis palustris I (1) – – – – – – – – – –Pedicularis sylvatica – – – – – – IV (1–3) – – – –Phragmites australis – – – – – – – – – – V (1–7)Plantago lanceolata – – III (1–3) – I (1) – – – I (1) III (1–7) –Plantago major I (1) – – – – – – – – – –Polygala serpyllifolia – I (1) – – – – III (1) – – – –Polygala vulgaris – – – – – – – – – I (1) –Polytrichum sp. – – I (1) – – – – – – – –Potentilla anserina – – – – – – – – V (6–9) II (3–5) –Potentilla erecta IV (1–5) V (2–4) V (1–4) V (2–4) IV (1–4) V (1–4) V (1–4) V (1–4) – – –Potentilla reptans – – – – – – – – V (1–8) – –Prunella vulgaris II (1–4) I (1) I (1) – II (1) – – I (4) – I (1) –Pteridium aquilinum – – – – – I (7) – I (1) – – –Pulicaria dysenterica – – – – – – – – III (1) V (1–8) –Pyrola rotundifolia – – – – – – – – – I (1) –Quercus robur seedling – – II (1) – I (1) – – – – – –Ranunculus acris – I (1–2) – – V (1) – – – V (1–3) V (1–4) –Ranunculus flammula IV (2–8) – I (1) – IV (1–4) – I (1) – V (1–3) V (1–5) –Ranunculus repens III (1–6) – III (1) – – – – – – – –Rhinanthus minor – – – – – – – – – III (1–3) –Rubus caesius – – – – – – – – – I (1) –Rubus fruticosus agg. I (1) – – – – – I (2) I (1) – – –Rumex acetosa – I (1) III (1–2) – III (1) – – – – – II (2)Sagina sp. – – – – – – I (1) – – – –Salix repens III (1) – – I (1) – IV (1–4) II (1–3) V (1–5) II (5–8) V (1–7) –Scutellaria galericulata – – – – – – – – – I (1) –Scutellaria minor II (1–2) III (1–3) I (1) IV (1–3) I (1) – – – – – –Senecio jacobaea I (1) – – – – – – – – – –Serratula tinctoria – I (1–4) III (1–2) V (1–3) – – II (1) I (1) – – –Sphagnum sp. – V (8–8) IV (3–5) V (3–6) I (6–8) II (1–5) – – – – –Stachys palustris – – – – – – – – – – II (1)Succisa pratensis II (1–7) V (2–5) V (1–6) IV (2–6) IV (1–5) – II (1) IV (1–4) – – I (1)Symphytum officinale – – – – – – – – – – IV (1–5)Taraxacum officinale agg. I (1) – – – I (1) – – – – – –Thalictrum flavum – – – – – – – – – – IV (1–5)

884N. de Vere© 2007 The AuthorJournal compilation© 2007 BritishEcological Society,Journal of Ecology,95, 876–894Table 2 ContinuedEWFS24cWKFSD14dEBBSD14bERWM16bEMOM16bEACM16bWDBM24EMMM24cEMSM24cEKSM24cEBCM24cSite CodeNVC CommunityTrifolium dubium – – – – – – – – – I (1) –Trifolium fragiferum – – – – – – – – IV (1–5) III (1–5) –Trifolium pratense – – – – I (1–4) – – – III (1–5) V (1–5) –Trifolium repens II (1–4) – – – II (1–5) – – – IV (1–5) II (1) –Ulex gallii – – – II (4–6) – V (6–8) – – – – –Ulex minor – – – – – – V (1–5) I (1) – – –Veronica scutellata I (1) – – – – – – – – – –Viola canina – – – – – – IV (1–2) – – – –Viola palustris – II (1–2) – – V (1–4) – – – – – –Ten 2 × 2 m quadrats were surveyed at each of 11 sites; in each quadrat all species were identified and abundance estimated using the Domin scale. Roman numerals indicate species frequency (the number of quadratsa species occurs within): I, 1–20%; II ,21–40%; III ,41–60%; IV, 61–80%; V, 81–100%. The numbers in brackets are the Domin range across the quadrats. Site codes: EKS (Knowstone Moor), EMM (MamburyMoor) and EMS (Meshaw Moor) are rhos pasture sites in Devon; WDB (Drostre Bank) is a rhos pasture in Wales; EAC (Aylesbeare Common) is a heath in Devon and EBC (Baddesley Common), EMO (MarlpittOak) and ERW (Rans Wood) are New Forest heaths. EBB (Braunton Burrows) is a dune slack in Devon and WKF (Kenfig) a dune slack in Wales. EWF is within Wicken Fen, Cambridgeshire. Sites were assignedto NVC communities using MAVIS Plot Analyser v. 1 (Rodwell 1991, 1995, 2000; Smart 2000).defoliated plants are seen frequently in cattle-grazedsites. In a growth-room experiment Ross (1999) discoveredthat C. dissectum is reasonably robust in its ability towithstand defoliation. Defoliated plants (with all of theleaves removed) showed a 35% decrease in root relativegrowth rate (RGR) and a 63% increase in shoot RGR;this allowed leaf biomass to be replaced in less than8 weeks. Replacement of the leaves depended onadequate nitrogen supply but was not particularly sensitiveto low concentrations of phosphorus.(B) OTHER PLANTSCirsium dissectum is susceptible to being out-competedby plants that are able to increase biomass more rapidly,especially when nutrient levels are increased throughthe effects of fertiliser addition or natural succession(see section V(B) below). In an open greenhouseexperiment where C. dissectum plants were grown withand without a grass competitor (Agrostis capillaris),the below-ground presence of the grass reduced theaverage biomass of C. dissectum by a factor of 5.8(Jongejans 2004).V. Responses to the environment(A) GREGARIOUSNESSCirsium dissectum can be locally abundant in sites withsuitable conditions. It reproduces vegetatively via longrhizomes and typically forms dense patches within allhabitat types. In the British Isles, density varied from 4rosettes m –2 in a Welsh rhos pasture to 24 rosettes m –2in a sand dune slack at Braunton Burrows, Devon.Jongejans (2004) recorded higher densities for plants inthe Netherlands: in five grasslands density varied from18 to 133 rosettes m –2 .Figure 4 illustrates the patches of rosettes foundwithin a small population at Wicken Fen, Cambs. Thesize of each patch was measured and the geneticidentity of 35 plants throughout the population wasdetermined using 8 microsatellite loci. Plants with thesame multilocus genotype belong to the same clone. Eachpatch generally contains more than one multilocusgenotype suggesting that patches often contain morethan one clone (de Vere 2007).(B) PERFORMANCE IN VARIOUS HABITATSTable 3 compares morphological variation in plantsgrowing in three different community types. The differencesbetween the populations are due to phenotypicplasticity and genetic differentiation (de Vere 2007).There is considerable variation in the proportion ofplants that flower at different sites; de Vere (2007)showed a significant positive relationship between theproportion of C. dissectum rosettes that flower and themean vegetation height within the community (r 2 = 0.544,β = 0.753, t = 4.99, P < 0.001).

884N. <strong>de</strong> <strong>Vere</strong>© <strong>2007</strong> <strong>The</strong> AuthorJournal compilation© <strong>2007</strong> BritishEcological Society,Journal of Ecology,95, 876–894Table 2 ContinuedEWFS24cWKFSD14dEBBSD14bERWM16bEMOM16bEACM16bWDBM24EMMM24cEMSM24cEKSM24cEBCM24cSite Co<strong>de</strong>NVC CommunityTrifolium dubium – – – – – – – – – I (1) –Trifolium fragiferum – – – – – – – – IV (1–5) III (1–5) –Trifolium pratense – – – – I (1–4) – – – III (1–5) V (1–5) –Trifolium repens II (1–4) – – – II (1–5) – – – IV (1–5) II (1) –Ulex gallii – – – II (4–6) – V (6–8) – – – – –Ulex minor – – – – – – V (1–5) I (1) – – –Veronica scutellata I (1) – – – – – – – – – –Viola canina – – – – – – IV (1–2) – – – –Viola palustris – II (1–2) – – V (1–4) – – – – – –Ten 2 × 2 m quadrats were surveyed at each of 11 sites; in each quadrat all species were i<strong>de</strong>ntified and abundance estimated using the Domin scale. Roman numerals indicate species frequency (the number of quadratsa species occurs within): I, 1–20%; II ,21–40%; III ,41–60%; IV, 61–80%; V, 81–100%. <strong>The</strong> numbers in brackets are the Domin range across the quadrats. Site co<strong>de</strong>s: EKS (Knowstone Moor), EMM (MamburyMoor) and EMS (Meshaw Moor) are rhos pasture sites in Devon; WDB (Drostre Bank) is a rhos pasture in Wales; EAC (Aylesbeare Common) is a heath in Devon and EBC (Bad<strong>de</strong>sley Common), EMO (MarlpittOak) and ERW (Rans Wood) are New Forest heaths. EBB (Braunton Burrows) is a dune slack in Devon and WKF (Kenfig) a dune slack in Wales. EWF is within Wicken Fen, Cambridgeshire. Sites were assignedto NVC communities using MAVIS Plot Analyser v. 1 (Rodwell 1991, 1995, 2000; Smart 2000).<strong>de</strong>foliated plants are seen frequently in cattle-grazedsites. In a growth-room experiment Ross (1999) discoveredthat C. <strong>dissectum</strong> is reasonably robust in its ability towithstand <strong>de</strong>foliation. Defoliated plants (with all of theleaves removed) showed a 35% <strong>de</strong>crease in root relativegrowth rate (RGR) and a 63% increase in shoot RGR;this allowed leaf biomass to be replaced in less than8 weeks. Replacement of the leaves <strong>de</strong>pen<strong>de</strong>d ona<strong>de</strong>quate nitrogen supply but was not particularly sensitiveto low concentrations of phosphorus.(B) OTHER PLANTSCirsium <strong>dissectum</strong> is susceptible to being out-competedby plants that are able to increase biomass more rapidly,especially when nutrient levels are increased throughthe effects of fertiliser addition or natural succession(see section V(B) below). In an open greenhouseexperiment where C. <strong>dissectum</strong> plants were grown withand without a grass competitor (Agrostis capillaris),the below-ground presence of the grass reduced theaverage biomass of C. <strong>dissectum</strong> by a factor of 5.8(Jongejans 2004).V. Responses to the environment(A) GREGARIOUSNESSCirsium <strong>dissectum</strong> can be locally abundant in sites withsuitable conditions. It reproduces vegetatively via longrhizomes and typically forms <strong>de</strong>nse patches within allhabitat types. In the British Isles, <strong>de</strong>nsity varied from 4rosettes m –2 in a Welsh rhos pasture to 24 rosettes m –2in a sand dune slack at Braunton Burrows, Devon.Jongejans (2004) recor<strong>de</strong>d higher <strong>de</strong>nsities for plants inthe Netherlands: in five grasslands <strong>de</strong>nsity varied from18 to 133 rosettes m –2 .Figure 4 illustrates the patches of rosettes foundwithin a small population at Wicken Fen, Cambs. <strong>The</strong>size of each patch was measured and the genetici<strong>de</strong>ntity of 35 plants throughout the population was<strong>de</strong>termined using 8 microsatellite loci. Plants with thesame multilocus genotype belong to the same clone. Eachpatch generally contains more than one multilocusgenotype suggesting that patches often contain morethan one clone (<strong>de</strong> <strong>Vere</strong> <strong>2007</strong>).(B) PERFORMANCE IN VARIOUS HABITATSTable 3 compares morphological variation in plantsgrowing in three different community types. <strong>The</strong> differencesbetween the populations are due to phenotypicplasticity and genetic differentiation (<strong>de</strong> <strong>Vere</strong> <strong>2007</strong>).<strong>The</strong>re is consi<strong>de</strong>rable variation in the proportion ofplants that flower at different sites; <strong>de</strong> <strong>Vere</strong> (<strong>2007</strong>)showed a significant positive relationship between theproportion of C. <strong>dissectum</strong> rosettes that flower and themean vegetation height within the community (r 2 = 0.544,β = 0.753, t = 4.99, P < 0.001).

Hooray! Your file is uploaded and ready to be published.

Saved successfully!

Ooh no, something went wrong!