Abstract

Loss of habitat, specifically deforestation, is a major driver of biodiversity loss. Species-area relationship (SAR) models traditionally have been used for estimating species richness, species loss as a function of habitat loss, and extrapolation of richness for given areas. Sampling-species relationships (SSRs) are interrelated yet separate drivers for species richness estimates. Traditionally, however, SAR and SSR models have been used independently and not incorporated into a single approach. We developed and compared predictive models that incorporate sampling effort species-area relationships (SESARS) along the entire Atlantic Forest of South America, and then applied the best-fit model to estimate richness in forest remnants of Interior Atlantic Forest of eastern Paraguay. This framework was applied to non-volant small mammal assemblages that reflect different tolerances to forest loss and fragmentation. In order to account for differences in functionality we estimated small mammal richness of 1) the entire non-volant small mammal assemblage, including introduced species; 2) the native species forest assemblage; and 3) the forest-specialist assemblage, with the latter two assemblages being subsets of the entire assemblage. Finally, we geospatially modeled species richness for each of the three assemblages throughout eastern Paraguay to identify remnants with high species richness. We found that multiple regression power-law interaction-term models that only included area and the interactions of area and sampling as predictors, worked best for predicting species richness for the entire assemblage and the native species forest assemblage, while several traditional SAR models (logistic, power, exponential, and ratio) best described forest-specialist richness. Species richness was significantly different between assemblages. We identified obvious remnants with high species richness in eastern Paraguay, and these remnants often were geographically isolated. We also found relatively high predicted species richness (in relation to the entire range of predicted richness values) in several geographically-isolated, medium-size forest remnants that likely have not been considered as possible priority areas for conservation. These findings highlight the importance of using an empirical dataset, created using sources representing diverse sampling efforts, to develop robust predictive models. This approach is particularly important in geographic locations where field sampling is limited yet the geographic area is experiencing rapid and dramatic land cover changes. When combined, area and sampling are powerful modeling predictors for questions of biogeography, ecology, and conservation, especially when addressing habitat loss and fragmentation.

Highlights

  • IntroductionThe Earth’s surface is covered by more than 4 billion ha of forest habitats that account for approximately 31% of the total land area of the planet [2]

  • We are currently in the sixth mass extinction on our planet, the Anthropocene [1]

  • We identified all of the models where all of their included parameters included were significantly contributing to the SESAR

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Summary

Introduction

The Earth’s surface is covered by more than 4 billion ha of forest habitats that account for approximately 31% of the total land area of the planet [2]. 3.3 million ha of net forest loss occurred from 2010–2015 [2], resulting in the fragmentation of key habitats on the planet. The primary driver for mammal extinction is the loss and fragmentation of habitat [3], and this potentially includes large numbers of poorly known or species yet to be described [4,5]. The Atlantic Forest of South America has experienced extreme levels of deforestation [7]. 12% and 20% of the original Atlantic Forest remains in Brazil and Paraguay, respectively [10,11]. A logical subsequent question is what is the effect of this deforestation on regional biodiversity?

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