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The Implication of Past and Present Landscape Patterns for Biodiversity Research Introduction and Overview

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Page 1: The Implication of Past and Present Landscape Patterns for Biodiversity Research Introduction and Overview

Landscape Ecology 18: 223–225, 2003.© 2003 Kluwer Academic Publishers. Printed in the Netherlands.

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The implication of past and present landscape patterns for biodiversityresearch: introduction and overview

Isabelle Poudevigne1 & Jacques Baudry2

1Landscape Systems Research Group, Faculte des Sciences, Universite de Rouen, 76821 Mont Saint Aignan, (E-mail: [email protected])2INRA – SAD Armorique, CS 84215, 65 Rue de Saint Brieuc, 35042 Rennes Cedex, France

Since its development in the early 1980s, the aim oflandscape ecology is to understand both the effectsof spatial patterns on ecological processes and thedevelopment of those spatial patterns. In Europe, hu-man activities have had a pronounced long term rolein shaping this heterogeneity so that Europe is nowthe most modified of any continent (Godron and For-man 1983). Therefore, research on how humans haveshaped landscapes is of utmost importance (Burel andBaudry 1999). If changes following the World War IIare a frequent topic, long term changes are also impor-tant (Berlung 1991) as they have, in interaction withthe physical environment, selected the regional speciespool. Indeed, present co-existence of species in thelandscape is thought to be the end product of a seriesof long term responses between species requirementsand environmental gradients of both natural and hu-man origin (Huston 1994). Despite potential adverseeffects, many long-term human disturbance regimeshave promoted biodiversity. In western Europe, tra-ditional ‘low intensity’ agriculture has often promotedhigh levels of diversity, or provided relict habitat forrare or threatened taxa (Green 1990). By analysingecological patterns and functioning at large spatial andtemporal scale, landscape ecology offers some of themost successful examples of the uptake of ecology inpolicy or management (Ormerod et al. 2002). If re-gional approaches are increasing (Suárez-Seoane et al.2002), landscape studies of a lesser extent (few km2)are still dominant.One of the most important current areas in which thestudy of landscape patterns, past and present, offers amajor path of research is in understanding the sustain-able management of biodiversity. This was the themeof a meeting of landscape ecologists held in Rouen,France in October 2001. Our aim with this array of

selected papers from the meeting is to share our out-look on current European trends and approaches tolandscape ecology.

Patterns of human activities in landscapes, whatheritage?

Cubizolle et al. (2003) give evidence that human ac-tivities, as early as the Iron age in France, had animportant influence on plant biodiversity whose reflec-tion we see today. Their analysis of mires in France,based on radiocarbon dates and pollen analysis, revealthat some activities such as the building of small dams,forest clearing, and cattle grazing have favoured peatinception. Ernoult et al. (2003) provide an analysisof changes in agricultural landscapes during the lastdecades. They do so by proposing two measures oflandscape organisation, i.e., how patterns deviate fromrandomness. The first measure deals with the spatialrelationships among the different categories of landuse intensity that form the landscape mosaic. The sec-ond measure assess the relationships between land usepatches and the physical environment. They demon-strate that changes in agriculture have led to morestochastic patterns.

Assessing the risks to biodiversity

This historical background explains why today manyrepresentative or threatened species are dispersedthrough environments, such as farmland, that are ineconomic use (Robinson and Sutherland 2002). Un-fortunately, recent changes in agricultural manage-ment and intensification have altered subtle equilibriabetween biota and patterns of use in both farmedand natural landscapes even on areas with strongconstraints to development (Poudevigne et al. 2002).

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Habitat alteration (including habitat loss, degradationand fragmentation) is now among the major risksof ecosystem degradation by these human activities(Whitfield et al. 2002). Many of these empirical stud-ies seek the variable that at different scales, frompatch to landscapes drive species distribution. Land-scape ecologists have proposed many measures toassess the relationship between spatial heterogeneityand biodiversity in landscapes (Cullinan and Thomas1992; McGarigal and Marks 1995), but few effec-tively relate pattern to process (Levin 1992). Classicalmetrics remain dissatisfying as correlation betweenspecies diversity indices and heterogeneity indices arenot always meaningful. A step further is to identifythe thresholds to which ecosystems can be modifiedwithout being irreversibly altered (Suter 1993).

Jeanneret et al. (2003) compare the distribution ofcarabids, spiders and butterflies in two Swiss agri-cultural landscapes. They conclude that landscapemetrics are of little use, while information on habitatmosaic provide information. It also appears that thevariables explaining most of the variance in speciesdistribution are different in the two landscapes, asare the reactions of the different groups of species.This work calls for comparative studies along land-scape gradients. Millán de la Peña et al. (2003) foundlittle correlation between the landscape descriptorsthey investigated, such as the amount of cropland,and the richness and species composition of smallmammal communities on agricultural land in westernFrance. They nevertheless found effects on mammaldemography: intensification of agriculture had re-duced the density of rare and habitat specialist specieswhile favouring habitat-generalists. Mennechez et al.(2003), investigating on the effects of habitat loss andfragmentation on butterfly population functioning withclassical measures, argue that spatial heterogeneity intheir case study affects dispersal more than demog-raphy. With this organism-centred point of view, theauthors then propose the definition of a new parame-ter, the minimal patch area needed to establish a localpopulation in highly fragmented landscapes.

Looking beyond France, in Africa, Fritz et al.(2003) observe that the extension of agriculture alongrivers in the Mid Zambezi valley, Zimbabwe, impactson most wild species. But they also define a thresh-old value of field size above which there seems tobe an acceleration of the decrease in wildlife densityand diversity. Definition of such thresholds may bean important asset in determining priorities for themanagement of degraded ecosystems.

Modelling and field testing the risks

Rather than synthesising the landscape system withmetrics, some scientists have chosen to model thesesystems, in an attempt to capture manageable aspectsof their complexity that are often beyond field exper-imentation and assessment (Jaberg and Guisan 2002).Baudry et al. (2003) model dairy farm landscapes witha measure which both considers the landscape andthe species. Connectivity is described as a measure oflandscape structure and species characteristics basedon individual area requirements and dispersal distance.Results reveal that for one farming system, landscapeconnectivity remains the same over years (in a 7-yearmodel experiment), while it is significantly differ-ent between two intensive and traditionally extensivefarming systems). This work also suggests the im-portance of considering the temporal dimensions ofspatial heterogeneity metrics. Similarly, Cousins et al.(2003) present a model which explores the effects ofgrazing frequency and intensity on plant persistence,and the relative effects of grassland size and pattern.These models aim at exploring the effects of furtherfragmentation and habitat loss on the persistence ofspecies or plant functional groups. This generation ofmodels aim to be valuable tools for managers, both todefine threshold risk values, and do simulations of thepotential impacts of landscape planning decisions.

Most landscape ecology research is based on a cor-relative approach, mainly because of the scale andcomplexity of the landscape systems. Large scale andin vivo experimentation, because it is either unaf-fordable or technically unfeasible, is rarely, with fewexceptions (Bradley and Ormerod 2002; Donlan et al.2002), a possible way of testing hypotheses proposedby the correlative studies that often characterize land-scape ecology. Equally, landscape ecologists have sofar rarely moved beyond the realms of pattern amongspecies and communities. Yet, in that field, analy-sis of spatial genetic structuring can yield interestingpossibilities. Arnaud et al. (2003), working the landsnail Helix aspersa, test landscape-based geographicaldistance to an isolation by distance model. This analy-sis allowed them to test the hypothesis that migrationarises along functional pathways such as roadsideverges, hedges or irrigation canal embankments.

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Acknowledgements

The guest editors would like to thank David Mladenofffor his support, Steve Ormerod for his enthusiasticcomments, the new born IALE France associationfor their participation and the Agence de l’Eau SeineNormandie for financing this special issue.

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