Anthropogenic habitat modification is accelerating, threatening the world's biodiversity.Understanding species' responses to anthropogenic modification is vital for halting species' declines. However, this information is lacking for globally threatened amphibians, informed primarily by small community-level studies. We integrated >126,000 verified citizen science observations of frogs, with a global continuous measure of anthropogenic habitat modification for a continental scale analysis of the effects of habitat modification on frogs.We derived a modification index -accounting for anthropogenic stressors such as human habitation, agriculture, transport, and energy production -for 87 species (36% of all Australian frog species). We used this index to quantify and rank each species' tolerance of anthropogenic habitat modification, then compiled traits of all the frog species and assessed how well these equipped species to tolerate modified habitats. Most of Australia's frog species examined were adversely affected by habitat modification. Habitat specialists and species with large geographic range sizes were the least tolerant of habitat modification. Call dominant frequency, body size, clutch type, and calling position (i.e., from vegetation) were also related to tolerance of habitat modification. There is an urgent need for improved consideration of anthropogenic impacts and improved conservation measures to ensure the long-term persistence of frog populations, particularly focused on specialists and species identified as intolerant of modified habitats.
Anthropogenic habitat modification is accelerating, threatening the world’s biodiversity. Understanding species’ responses to anthropogenic modification is vital for halting species’ declines. However, this information is lacking for globally threatened amphibians, informed primarily by small community-level studies. We integrated >126,000 verified citizen science observations of frogs, with a global continuous measure of anthropogenic habitat modification for a continental scale analysis of the effects of habitat modification on frogs. We derived a modification index – accounting for anthropogenic stressors such as human habitation, agriculture, transport, and energy production – for 87 species (36% of all Australian frog species). We used this index to quantify and rank each species’ tolerance of anthropogenic habitat modification, then compiled traits of all the frog species and assessed how well these equipped species to tolerate modified habitats. Most of Australia’s frog species examined were adversely affected by habitat modification. Habitat specialists and species with large geographic range sizes were the least tolerant of habitat modification. Call dominant frequency, body size, clutch type, and calling position (i.e., from vegetation) were also related to tolerance of habitat modification. There is an urgent need for improved consideration of anthropogenic impacts and improved conservation measures to ensure the long-term persistence of frog populations, particularly focused on specialists and species identified as intolerant of modified habitats.
Urban environments are novel ecosystems, with increased chemical, sound, and light pollution differentially impacting many animals. Understanding the impacts of urban environments on biodiversity is the first step to understanding how to best mitigate biodiversity losses in an increasingly urbanizing world. Analyses with broad geographic and taxonomic coverage can offer critical context for informing urban biodiversity conservation.But such studies are currently lacking, especially for under-studied but likely highly impacted taxa such as frogs. Our objective was to document frog diversity in relation to urban environments at continental, regional, and local scales. We used FrogID dataan opportunistic citizen science dataset generated by volunteers recording calling frogs using a smartphone and validated by expertsthroughout continental Australia, to calculate species richness, Shannon diversity, and phylogenetic diversity of frogs in urban and non-urban areas, as well as along a continuous urbanization gradient. The overall species richness of frogs was, on average, 57% less in urban than non-urban areas across six ecoregions. Further, we found significantly lower frog diversity in urban environments compared with non-urban environments across the country, with an average reduction of 59% species richness, 86% Shannon diversity, and 72% phylogenetic diversity. We also found evidence for a steady decrease in frog diversity along an urbanization gradient, with no obvious thresholds. Our results highlight the negative impacts of urbanizationat a continental scaleon frog diversity, and clearly highlight the necessity to consider frog diversity in future urban land development decisions.
Temperature is a crucial environmental component that imposes physiological constraints and ultimately produces variation in life-history traits. Temperatures experienced by mothers can influence offspring phenotypes, including growth and sex ratios, especially in ectothermic species. However, mechanisms by which thermal information can be passed onto offspring have been underexplored. Here, we investigated corticosterone as a potential mediator of thermal maternal effects. We held female jacky dragons (Amphibolurus muricatus) in two different thermal regimes (short [7 h] or long [11 h] basking treatments), then quantified plasma corticosterone levels and tested for correlations between the resulting corticosterone levels and reproductive outputs. Lizards in the long-bask treatment had significantly higher corticosterone levels than those in the short-bask treatment. Maternal corticosterone, in turn, had sex-dependent effects on offspring hatching size but was not associated with maternal reproductive effort or offspring sex or growth. In contrast, maternal body condition was strongly positively related to both reproductive output (including clutch size and total number of eggs) and offspring size at hatching but had no effect on offspring growth. Basking treatment also interacted with condition and corticosterone to affect egg mass and hatchling snout-vent length, respectively. When we tested for relationships between corticosterone levels and body condition, we found corticosterone to be negatively related to condition in long-bask lizards but only in the postbreeding season. These findings indicate that thermal opportunity alters physiology, with potential consequences for fitness. Moreover, the results suggest interactive influences of temperature, corticosterone, and condition as mediators of maternal effects.
Urban environments are novel ecosystems, with increased chemical, sound, and light pollution differentially impacting many animals. Understanding the impacts of urban environments on biodiversity is the first step to understanding how to best mitigate biodiversity losses in an increasingly urbanizing world. Analyses with broad geographic and taxonomic coverage can offer critical context for informing urban biodiversity conservation. But such studies are currently lacking, especially for under-studied but likely highly impacted taxa such as frogs. Our objective was to document frog diversity in relation to urban environments at continental, regional, and local scales. We used FrogID data — an opportunistic citizen science dataset generated by volunteers recording calling frogs using a smartphone and validated by experts — throughout continental Australia, to calculate species richness, Shannon diversity, and phylogenetic diversity of frogs in urban and non-urban areas, as well as along a continuous urbanization gradient. The overall species richness of frogs was, on average, 57% less in urban than non-urban areas across six ecoregions. Further, we found significantly lower frog diversity in urban environments compared with non-urban environments across the country, with an average reduction of 59% species richness, 86% Shannon diversity, and 72% phylogenetic diversity. We also found evidence for a steady decrease in frog diversity along an urbanization gradient, with no obvious thresholds. Our results highlight the negative impacts of urbanization — at a continental scale — on frog diversity, and clearly highlight the necessity to consider frog diversity in future urban land development decisions.
Biodiversity is under tremendous pressure in the Anthropocene (Johnson et al., 2017;Sullivan et al., 2017). Habitat loss (e.g. deforestation) and fragmentation have undoubtedly driven species declines and extinctions (Dirzo et al., 2014;Young et al., 2016), but even subtle changes in temperature, resource availability, noise or light pollution caused by human modification can contribute to de-
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