Testing for human impacts in the mismatch of living and dead ostracode assemblages at nested spatial scales in subtropical lakes from the Bahamian archipelago

Paleobiology ◽  
2018 ◽  
Vol 44 (4) ◽  
pp. 758-782
Author(s):  
Andrew V. Michelson ◽  
Susan M. Kidwell ◽  
Lisa E. Park Boush ◽  
Jeanine L. Ash

AbstractNaturally time-averaged accumulations of skeletal remains—death assemblages—provide reliable, albeit temporally coarse, information on the species composition and structure of communities in diverse settings, and their mismatch with local living communities usually signals recent human-driven ecological change. Here, we present the first test of live–dead mismatch as an indicator of human stress using ostracodes. On three islands along a gradient of human population density in the Bahamas, we compared the similarity of living and death assemblages in 10 lakes with relatively low levels of human stress to live–dead similarity in 11 physically comparable lakes subject to industrial, agricultural, or other human activities currently or in the past. We find that live–dead agreement in pristine lakes is consistently excellent, boding well for using death assemblages in modern-day and paleolimnological biodiversity assessments. In most comparison of physically similar paired lakes, sample-level live–dead mismatch in both taxonomic composition and species’ rank abundance is on average significantly greater in the stressed lakes; live–dead agreement is not lower in all samples from stressed lakes, but is more variable. When samples are pooled for lake-level and island-level comparisons, stressed lakes still yield lower live–dead agreement, but the significance of the difference with pristine lakes decreases—species that occur dead-only (or alive-only) in one sample are likely to occur alive (or dead) in other samples. Interisland differences in live–dead agreement are congruent with, but not significantly correlated with, differences in human population density. This situation arises from heterogeneity in the timing and magnitudes of stresses and in the extent of poststress recovery. Live–dead mismatch in ostracode assemblages thus may be a reliable indicator of human impact at the sample level with the potential to be a widely applicable tool for identifying impacted habitats and, perhaps, monitoring the progress of their recovery.

2019 ◽  
Author(s):  
Anderson A. Eduardo ◽  
Lucas A. B. O. Santos ◽  
Mônica C. Rebouças ◽  
Pablo A. Martinez

AbstractPrevious work on Chagas Disease disease at large spatial scales has not explored how interaction with humans can affect projections for geographical distribution of environmental suitability of vector species. Here, we compare niche-based species distribution models with climatic variables as predictors (SDMclim) and with climatic variables + human population density (SDMHuman). Our results show that accounting for human population density helps refine the models to finer geographical scales. Also, different spatial patterns of accumulated environmental suitability were obtained by SDMclim and SDMHuman. Moreover, projections were more accurate for SDMHuman than for SDMclim. Our results show that considering human populations in SDMs for epidemiologically relevant triatomiane species can improve our understanding of macroecology and biogeography of environmental suitability for vectors of Chagas disease.


Alpine Botany ◽  
2021 ◽  
Author(s):  
Christian Körner ◽  
Davnah Urbach ◽  
Jens Paulsen

AbstractMountains are rugged structures in the landscape that are difficult to delineate. Given that they host an overproportional fraction of biodiversity of high ecological and conservational value, conventions on what is mountainous and what not are in need. This short communication aims at explaining the differences among various popular mountain definitions. Defining mountainous terrain is key for global assessments of plant species richness in mountains and their likely responses to climatic change, as well as for assessing the human population density in and around mountainous terrain.


2013 ◽  
Vol 86 ◽  
pp. 166 ◽  
Author(s):  
O. Maurin ◽  
T.J. Davies ◽  
K. Yessoufou ◽  
B.H. Daru ◽  
B.S. Bezeng ◽  
...  

2018 ◽  
Vol 18 (3) ◽  
Author(s):  
Camila Fernanda Moser ◽  
Fernanda Rodrigues de Avila ◽  
Roberto Baptista de Oliveira ◽  
Juliano Morales de Oliveira ◽  
Márcio Borges-Martins ◽  
...  

Abstract This work aimed to catalog the species of reptiles of the Sinos River Basin based on records from scientific collections and data collected in the field. We recorded 65 species, including 46 snakes, nine lizards, five turtles, four amphisbaenians and one caiman. Snakes composed most of the recorded specimens (91.3%), and the three most representative are venomous and of medical importance. The most urban region of the basin (Lowland) has the highest number of records. This fact may be a reflection of the high human population density in this region, which would have favored the encounter of specimens and their sending to scientific collections and research centers. It is worth highlighting that most species with few specimens in the collections are also rarely observed in the wild, such as Clelia hussani and Urostrophus vautieri. This observation makes it feasible that these populations are small or that they are declining.


Land ◽  
2018 ◽  
Vol 7 (4) ◽  
pp. 136 ◽  
Author(s):  
Caitlin Cunningham ◽  
Karen Beazley

Biodiversity hotspots are rich in endemic species and threatened by anthropogenic influences and, thus, considered priorities for conservation. In this study, conservation achievements in 36 global biodiversity hotspots (25 identified in 1988, 10 added in 2011, and one in 2016) were evaluated in relation to changes in human population density and protected area coverage between 1995 and 2015. Population densities were compared against 1995 global averages, and percentages of protected area coverage were compared against area-based targets outlined in Aichi target 11 of the Convention on Biological Diversity (17% by 2020) and calls for half Earth (50%). The two factors (average population density and percent protected area coverage) for each hotspot were then plotted to evaluate relative levels of threat to biodiversity conservation. Average population densities in biodiversity hotspots increased by 36% over the 20-year period, and were double the global average. The protected area target of 17% is achieved in 19 of the 36 hotspots; the 17 hotspots where this target has not been met are economically disadvantaged areas as defined by Gross Domestic Product. In 2015, there are seven fewer hotspots (22 in 1995; 15 in 2015) in the highest threat category (i.e., population density exceeding global average, and protected area coverage less than 17%). In the lowest threat category (i.e., population density below the global average, and a protected area coverage of 17% or more), there are two additional hotspots in 2015 as compared to 1995, attributable to gains in protected area. Only two hotspots achieve a target of 50% protection. Although conservation progress has been made in most global biodiversity hotspots, additional efforts are needed to slow and/or reduce population density and achieve protected area targets. Such conservation efforts are likely to require more coordinated and collaborative initiatives, attention to biodiversity objectives beyond protected areas, and support from the global community.


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