Native vegetation cover thresholds associated with species responses

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Native vegetation cover thresholds associated with species responses. / Lindenmayer, David B.; Fischer, Jörn; Cunningham, Ross B.
in: Biological Conservation, Jahrgang 124, Nr. 3, 01.08.2005, S. 311-316.

Publikation: Beiträge in ZeitschriftenZeitschriftenaufsätzeForschungbegutachtet

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Lindenmayer DB, Fischer J, Cunningham RB. Native vegetation cover thresholds associated with species responses. Biological Conservation. 2005 Aug 1;124(3):311-316. doi: 10.1016/j.biocon.2005.01.038

Bibtex

@article{03c627276b514ed0929bc62dbe5ddd81,
title = "Native vegetation cover thresholds associated with species responses",
abstract = "We examined data on bird and reptile assemblages in a plantation landscape in southern New South Wales, south-eastern Australia, for evidence of threshold responses to the amount of native eucalypt vegetation in circular areas of 2000 and/or 1000 m around field survey sites. These circular areas contained varying proportions of native Eucalyptus and exotic radiata pine Pinus radiata forest thereby providing a basis for examining potential threshold effects in relation to the area of native vegetation cover. For bird species richness or the probability of detection of individual bird species we found no empirical evidence of a threshold response to the area of native vegetation cover, or any other potential explanatory variables. All relationships were characterised by considerable variability in the response data. “Broken-stick” relationships which involved sudden change points did not fit the response data better than smooth relationships obtained from generalised additive or linear models. As with birds, there was no evidence that a threshold model between lizard richness and the amount of native vegetation within 1000 m described the relationship any better than a smooth, continuous or other type of relationship. Several related factors may explain our results. An important one is that species-specific responses to landscape conditions mean that marked thresholds will not be seen for an aggregate measure like species richness at a given value for a given landscape variable. Another is that factors other than the amount of native vegetation may significantly influence underlying patterns of species occurrence. This highlights a need to be aware of the potential effects of various ecological processes, even when a substantial amount of native vegetation cover remains.Our findings do not rule out the possibility of the existence of threshold relationships. However, irrespective of the choice of measure of predictor variable (e.g., the amount of native vegetation cover), it will often be difficult to detect and estimate threshold responses due to high inherent variability – a characteristic of the vast majority of ecological datasets. Furthermore, even if it is possible to estimate functional (threshold) forms and although they might be useful from an explanatory perspective, in most instances they are likely to be of limited value in a predictive sense. This calls into question the practical significance of the threshold concept.",
keywords = "Biology, Landscape, threshold, Conservation, Habitat fragmentation, experiment, Vertebrates, Birds, Reptiles",
author = "Lindenmayer, {David B.} and J{\"o}rn Fischer and Cunningham, {Ross B.}",
note = "Funding Information: Work at Tumut has been supported by major grants from Land and Water Forest Research and Development Corporation, Forest and Wood Products Research and Development Corporation, Rural Industries Research and Development Corporation, the Australian Research Council, and the NSW Department of Land and Water Conservation. Other supporting bodies for various projects in the Tumut regions NSW include National Parks and Wildlife Service, State Forests of NSW, Environment Australia, Brookfield Zoo (Chicago), The Pratt Foundation, Jim Atkinson and Di Stockbridge (private donation), the Ecological Society of Australia (J.F.), the Linnean Society of NSW (J.F.), and the Royal Zoological Society of NSW (J.F.). Mr. C. MacGregor, Mr. M. Crane, Mr. D. Michael and the Canberra Ornithologists Group assisted with the collection of data on birds at Tumut. Several people helped with the collection of pitfall data, and we particularly thank E. Flowers. Ms. N. Munro and Ms. M. Ruibal kindly assisted in the collection of scientific articles on the topics addressed in this paper. Comments from the other contributors to this series of papers on thresholds (particularly Jim Radford and Gary Luck) as well as very perceptive comments from Peter Cale and Denis Saunders greatly improved earlier versions of this manuscript. Work on the reptile fauna at Tumut was sanctioned by Animal Experimentation Ethics Committee of The Australian National University.",
year = "2005",
month = aug,
day = "1",
doi = "10.1016/j.biocon.2005.01.038",
language = "English",
volume = "124",
pages = "311--316",
journal = "Biological Conservation",
issn = "0006-3207",
publisher = "Elsevier B.V.",
number = "3",

}

RIS

TY - JOUR

T1 - Native vegetation cover thresholds associated with species responses

AU - Lindenmayer, David B.

AU - Fischer, Jörn

AU - Cunningham, Ross B.

N1 - Funding Information: Work at Tumut has been supported by major grants from Land and Water Forest Research and Development Corporation, Forest and Wood Products Research and Development Corporation, Rural Industries Research and Development Corporation, the Australian Research Council, and the NSW Department of Land and Water Conservation. Other supporting bodies for various projects in the Tumut regions NSW include National Parks and Wildlife Service, State Forests of NSW, Environment Australia, Brookfield Zoo (Chicago), The Pratt Foundation, Jim Atkinson and Di Stockbridge (private donation), the Ecological Society of Australia (J.F.), the Linnean Society of NSW (J.F.), and the Royal Zoological Society of NSW (J.F.). Mr. C. MacGregor, Mr. M. Crane, Mr. D. Michael and the Canberra Ornithologists Group assisted with the collection of data on birds at Tumut. Several people helped with the collection of pitfall data, and we particularly thank E. Flowers. Ms. N. Munro and Ms. M. Ruibal kindly assisted in the collection of scientific articles on the topics addressed in this paper. Comments from the other contributors to this series of papers on thresholds (particularly Jim Radford and Gary Luck) as well as very perceptive comments from Peter Cale and Denis Saunders greatly improved earlier versions of this manuscript. Work on the reptile fauna at Tumut was sanctioned by Animal Experimentation Ethics Committee of The Australian National University.

PY - 2005/8/1

Y1 - 2005/8/1

N2 - We examined data on bird and reptile assemblages in a plantation landscape in southern New South Wales, south-eastern Australia, for evidence of threshold responses to the amount of native eucalypt vegetation in circular areas of 2000 and/or 1000 m around field survey sites. These circular areas contained varying proportions of native Eucalyptus and exotic radiata pine Pinus radiata forest thereby providing a basis for examining potential threshold effects in relation to the area of native vegetation cover. For bird species richness or the probability of detection of individual bird species we found no empirical evidence of a threshold response to the area of native vegetation cover, or any other potential explanatory variables. All relationships were characterised by considerable variability in the response data. “Broken-stick” relationships which involved sudden change points did not fit the response data better than smooth relationships obtained from generalised additive or linear models. As with birds, there was no evidence that a threshold model between lizard richness and the amount of native vegetation within 1000 m described the relationship any better than a smooth, continuous or other type of relationship. Several related factors may explain our results. An important one is that species-specific responses to landscape conditions mean that marked thresholds will not be seen for an aggregate measure like species richness at a given value for a given landscape variable. Another is that factors other than the amount of native vegetation may significantly influence underlying patterns of species occurrence. This highlights a need to be aware of the potential effects of various ecological processes, even when a substantial amount of native vegetation cover remains.Our findings do not rule out the possibility of the existence of threshold relationships. However, irrespective of the choice of measure of predictor variable (e.g., the amount of native vegetation cover), it will often be difficult to detect and estimate threshold responses due to high inherent variability – a characteristic of the vast majority of ecological datasets. Furthermore, even if it is possible to estimate functional (threshold) forms and although they might be useful from an explanatory perspective, in most instances they are likely to be of limited value in a predictive sense. This calls into question the practical significance of the threshold concept.

AB - We examined data on bird and reptile assemblages in a plantation landscape in southern New South Wales, south-eastern Australia, for evidence of threshold responses to the amount of native eucalypt vegetation in circular areas of 2000 and/or 1000 m around field survey sites. These circular areas contained varying proportions of native Eucalyptus and exotic radiata pine Pinus radiata forest thereby providing a basis for examining potential threshold effects in relation to the area of native vegetation cover. For bird species richness or the probability of detection of individual bird species we found no empirical evidence of a threshold response to the area of native vegetation cover, or any other potential explanatory variables. All relationships were characterised by considerable variability in the response data. “Broken-stick” relationships which involved sudden change points did not fit the response data better than smooth relationships obtained from generalised additive or linear models. As with birds, there was no evidence that a threshold model between lizard richness and the amount of native vegetation within 1000 m described the relationship any better than a smooth, continuous or other type of relationship. Several related factors may explain our results. An important one is that species-specific responses to landscape conditions mean that marked thresholds will not be seen for an aggregate measure like species richness at a given value for a given landscape variable. Another is that factors other than the amount of native vegetation may significantly influence underlying patterns of species occurrence. This highlights a need to be aware of the potential effects of various ecological processes, even when a substantial amount of native vegetation cover remains.Our findings do not rule out the possibility of the existence of threshold relationships. However, irrespective of the choice of measure of predictor variable (e.g., the amount of native vegetation cover), it will often be difficult to detect and estimate threshold responses due to high inherent variability – a characteristic of the vast majority of ecological datasets. Furthermore, even if it is possible to estimate functional (threshold) forms and although they might be useful from an explanatory perspective, in most instances they are likely to be of limited value in a predictive sense. This calls into question the practical significance of the threshold concept.

KW - Biology

KW - Landscape

KW - threshold

KW - Conservation

KW - Habitat fragmentation

KW - experiment

KW - Vertebrates

KW - Birds

KW - Reptiles

UR - http://www.scopus.com/inward/record.url?scp=16844382696&partnerID=8YFLogxK

UR - https://www.mendeley.com/catalogue/72e3dba1-d5af-3b07-b18f-4807a8dff4ca/

U2 - 10.1016/j.biocon.2005.01.038

DO - 10.1016/j.biocon.2005.01.038

M3 - Journal articles

VL - 124

SP - 311

EP - 316

JO - Biological Conservation

JF - Biological Conservation

SN - 0006-3207

IS - 3

ER -

DOI