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230 results for “population decline”

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dryad32/100

Data from: Harvest and density-dependent predation drive long-term population decline in a northern ungulate

<p><span>The relative effect of top-down versus bottom-up forces in regulating and limiting wildlife populations is an important theme in ecology. Untangling these effects is critical for a basic understanding of trophic dynamics and effective management. We examined the drivers of moose (<em>Alces alces</em>) population growth by integrating two independent sources of observations within a hierarchical Bayesian population model. This analysis used one of the largest existing spatiotemporal datasets on ungulate population dynamics globally. We documented a 20% population decline over the period examined. Moose population growth was negatively density-dependent. Although the mechanisms producing density-dependent suppression of population growth could not be determined, the relatively low densities at which moose populations were documented suggests it could be due primarily to density-dependent predation. Predation </span>primarily limited population growth, except at low density, where it was regulating. <span>Harvest appeared to be largely </span>additive<span> and contributed to population declines.</span> Our results, highlight how <span>population dynamics are context dependent and vary strongly across gradients in climate, forest type, and predator abundance. These results help clarify long-standing questions in population ecology and highlight the complex relationships between natural and human-caused mortality in driving ungulate population dynamics. </span></p>

opencc-zeroFeb 2022View details →
dryad32/100

Genotype data for: Population genetics reveals divergent lineages and ongoing hybridization in a declining migratory fish species complex

<p>Deciphering the effects of historical and recent demographic processes responsible for the spatial patterns of genetic diversity and structure is a key objective in evolutionary and conservation biology. Using population genetic analyses, we investigated the demographic history, the contemporary genetic diversity and structure, and the occurrence of hybridization and introgression of two species of anadromous fish with contrasting life history strategies and which have undergone recent demographic declines, the allis shad (<em>Alosa alosa</em>) and the twaite shad (<em>Alosa fallax</em>). We genotyped 706 individuals from 20 rivers and 5 sites at sea in Southern Europe at thirteen microsatellite markers. Genetic structure between populations was lower for the nearly semelparous species <em>A. alosa</em>, which disperses greater distances compared to the iteroparous species, <em>A. fallax</em>. Individuals caught at sea were assigned at the river level for <em>A. fallax</em> and at the region level for A. alosa. Using an approximate Bayesian computation framework, we inferred that the most likely long term historical divergence scenario between both species and lineages involved historical separation followed by secondary contact accompanied by strong population size decline. Accordingly, we found evidence for contemporary hybridization and bidirectional introgression due to gene flow between both species and lineages. Moreover, our results support the existence of at least one distinct species in the Mediterrannean sea: <em>A. agone</em> in Golfe du Lion area, and another divergent lineage in Corsica. Overall, our results shed light on the interplay between historical and recent demographic processes and life history strategies in shaping population genetic diversity and structure of closely related species. The recent demographic decline of these species' populations and their hybridization should be carefully considered while implementing conservation programs.</p>

opencc-zeroMay 2022View details →
zenodo32/100

Distribution. Now restricted to the Channel Country of SW Queensland and the Lake Eyre Basin in NE South Australia. Descriptive notes. Head-body 95-120 mm, tail 105-160 mm, ear 23-29 mm, hindfoot 32-37 mm; weight 30-50 g. The Fawn Hopping Mouse has body form typical of hopping mice, with very long hindfeet, long tail with distal brush of longer hairs, very long ears, and large protruberant eyes. Dorsal fur is of variable color, from pale pinkish fawn to gray; ventral fur white. Unlike most other hopping mice, it has no throat pouch, but males have a glandular area of naked skin on the chest. Habitat. Occurs in low shrublands and tussock grasslands on stony ("gibber") plains and claypans. Shows marked habitat segregation from the Dusky Hopping Mouse (N. fuscus), which is closely associated with sandy substrates. Food and Feeding. The Fawn Hopping Mouse is mostly granivorous, but also eats other plant material (stems, leaves) and occasionally invertebrates. It uses succulent, salt-adapted plants around edges of claypans as a source of water. Breeding. Reproduction is probably largely opportunistic and aseasonal, with high reproductive output from near-continuous breeding after periods of high rainfall; reported littersize is 1-5, most commonly three; gestation period 38-43 days for nonlactating females. Females may mature later than other hopping mice, with reproductive maturity reached at about six months. Activity patterns. Terrestrial and nocturnal. Fawn Hopping Mice shelter during day in burrow systems that are typically simpler and shallower than those of other hopping mice. Movements, Home range and Social organization. Fawn Hopping Mice generally live singly or in small groups; typically uncommon within range, but population density may increase by an order of magnitude following periods of high rainfall. Status and Conservation. Classified as Near Threatened on The IUCN Red List. The Fawn Hopping Mouse has shown marked decline in range (estimated at greater than 50%), and presumably population size, since European settlement of Australia. This is mostlikely due to predation by the introduced house cat and Red Fox (Vulpes vulpes), and to habitat degradation associated with pastoralism. Bibliography. Brazenor (1934), Burbidge et al. (2008), Finlayson (1939), Gould (1853), Jackson & Groves (2015), Murray et al. (1999), Ogilby (1892), Thomas (1921h), Van Dyck & Strahan (2008), Waite (1898), Watts & Aslin (1981), Woinarski et al. (2014), Wood Jones (1925). in Muridae

Distribution. Now restricted to the Channel Country of SW Queensland and the Lake Eyre Basin in NE South Australia. Descriptive notes. Head-body 95-120 mm, tail 105-160 mm, ear 23-29 mm, hindfoot 32-37 mm; weight 30-50 g. The Fawn Hopping Mouse has body form typical of hopping mice, with very long hindfeet, long tail with distal brush of longer hairs, very long ears, and large protruberant eyes. Dorsal fur is of variable color, from pale pinkish fawn to gray; ventral fur white. Unlike most other hopping mice, it has no throat pouch, but males have a glandular area of naked skin on the chest. Habitat. Occurs in low shrublands and tussock grasslands on stony ("gibber") plains and claypans. Shows marked habitat segregation from the Dusky Hopping Mouse (N. fuscus), which is closely associated with sandy substrates. Food and Feeding. The Fawn Hopping Mouse is mostly granivorous, but also eats other plant material (stems, leaves) and occasionally invertebrates. It uses succulent, salt-adapted plants around edges of claypans as a source of water. Breeding. Reproduction is probably largely opportunistic and aseasonal, with high reproductive output from near-continuous breeding after periods of high rainfall; reported littersize is 1-5, most commonly three; gestation period 38-43 days for nonlactating females. Females may mature later than other hopping mice, with reproductive maturity reached at about six months. Activity patterns. Terrestrial and nocturnal. Fawn Hopping Mice shelter during day in burrow systems that are typically simpler and shallower than those of other hopping mice. Movements, Home range and Social organization. Fawn Hopping Mice generally live singly or in small groups; typically uncommon within range, but population density may increase by an order of magnitude following periods of high rainfall. Status and Conservation. Classified as Near Threatened on The IUCN Red List. The Fawn Hopping Mouse has shown marked decline in range (estimated at greater than 50%), and presumably population size, since European settlement of Australia. This is mostlikely due to predation by the introduced house cat and Red Fox (Vulpes vulpes), and to habitat degradation associated with pastoralism. Bibliography. Brazenor (1934), Burbidge et al. (2008), Finlayson (1939), Gould (1853), Jackson &amp; Groves (2015), Murray et al. (1999), Ogilby (1892), Thomas (1921h), Van Dyck &amp; Strahan (2008), Waite (1898), Watts &amp; Aslin (1981), Woinarski et al. (2014), Wood Jones (1925).

opennotspecifiedNov 2017View details →
zenodo32/100

Humid tropical vertebrates are at lower risk of extinction and population decline in forests with higher structural integrity

<p>The four Excel workbooks contain processed data in the form of humid tropical forest area under each of multiple values of the Structural Condition Index (SCI), Forest Structural Integrity Index (FSII), and Human Footprint (HFP) for Mammal, Bird, Reptile and Amphibian species. The associated README text file contains metadata to describe the data in the xlsx workbooks. Python code to replicate geospatial analyses and R code to replicate statistical analyses are provided in the respective scripts. ArcGIS Pro is required to be installed prior to running the Python script.</p>

opencc-by-4.0Aug 2022View details →
dryad32/100

Molecular and quantitative genetic variation within and between populations of the declining grassland species Saxifraga granulata

<p class="MsoNormal"><span>Formerly common plant species are expected to be particularly susceptible to recent habitat fragmentation. We studied the population genetics of 19 recently fragmented <em>Saxifraga granulata</em> populations (max. distance 61 km) in Luxembourg and neighbouring Germany using RAPD markers and a common garden experiment. We assessed (1) the relationships between plant fitness, quantitative genetic variation, molecular genetic variation and population size, and (2) the relative importance of genetic drift and selection in shaping genetic variation. Molecular genetic diversity was high but did not correlate with population size, habitat conditions or with plant performance. Genetic differentiation was low (<em>F</em><sub>ST</sub> = 0.079 ± 0.135) and there was no isolation by distance. Longevity, clonality and the long-lived seed bank of <em>S. granulata</em> may have prevented strong genetic erosion and genetic differentiation among populations. H</span><span>owever, genetic distinctness increased with decreasing genetic diversity indicating that random genetic drift occurred in the studied populations. Quantitative and molecular gen</span><span>etic variation were correlated and their differentiation (<em>Q</em><sub>ST </sub>vs. <em>F</em><sub>ST</sub>) among <em>S. granulata</em> populations was similar, suggesting that mainly random processes have shaped the quantitative genetic differentiation among populations. However, pairwise quantitative genetic distances increased with geographic and climatic distances, even when adjusted for molecular genetic distances, indicating diversifying selection. Our results indicate that long-lived clonal species may be buffered at least temporarily against the negative effects of fragmentation. The relationship between quantitative genetic and geographic distance may be a more sensitive indicator of selection than <em>Q</em><sub>ST</sub> - <em>F</em><sub>ST</sub> differences.</span></p>

opencc-zeroOct 2022View details →
dryad32/100

Data from: Population structure and historical demography of South American sea lions provide insights into the catastrophic decline of a marine mammal population

Understanding the causes of population decline is crucial for conservation management. We therefore used genetic analysis both to provide baseline data on population structure and to evaluate hypotheses for the catastrophic decline of the South American sea lion (Otaria flavescens) at the Falkland Islands (Malvinas) in the South Atlantic. We genotyped 259 animals from 23 colonies across the Falklands at 281 bp of the mitochondrial hypervariable region and 22 microsatellites. A weak signature of population structure was detected, genetic diversity was moderately high in comparison with other pinniped species, and no evidence was found for the decline being associated with a strong demographic bottleneck. By combining our mitochondrial data with published sequences from Argentina, Brazil, Chile and Peru, we also uncovered strong maternally directed population structure across the geographical range of the species. In particular, very few shared haplotypes were found between the Falklands and South America, and this was reflected in correspondingly low migration rate estimates. These findings do not support the prominent hypothesis that the decline was caused by migration to Argentina, where large-scale commercial harvesting operations claimed over half a million animals. Thus, our study not only provides baseline data for conservation management but also reveals the potential for genetic studies to shed light upon long-standing questions pertaining to the history and fate of natural populations.

opencc-zeroDec 2015View details →
dryad32/100

Data from: Patterns of mammalian population decline inform conservation action

1. Evaluations of wildlife population dynamics have the potential to convey valuable information on the type of pressure affecting a population and could help predict future changes in the population's trajectory. Greater understanding of different patterns of population declines could provide a useful mechanism for assessing decline severity in the wild and identifying those populations that are more likely to exhibit severe declines. 2. We identified 93 incidences of decline within 75 populations of mammalian species using a time-series analysis method. These included: linear, quadratic convex (accelerating) declines, exponential concave (decelerating) declines, and quadratic concave declines (representing recovering populations). Excluding linear declines left a dataset of 85 declines to model the relationship between each decline-curve type and a range of biological, anthropogenic, and time-series descriptor explanatory variables. 3. None of the decline-curve types were spatially or phylogenetically clustered. The only characteristic that could be consistently associated with any curve-type was the time at which they were more likely to occur within a time-series. Quadratic convex declines were more likely to occur at the start of the time-series, while recovering curve shapes (quadratic concave declines) were more likely at the end of the time-series. 4. Synthesis and applications: The ability to link certain factors with specific decline dynamics across a number of mammalian populations is useful for management purposes as it provides decision-makers with potential triggers upon which to base their conservation actions. We propose that the identification of quadratic convex declines could be used as an early-warning signal of potentially severe decline dynamics. For such populations, increased population monitoring effort should be deployed to diagnose the cause of its decline and avert possible extinctions. Conversely, the presence of a quadratic concave decline suggests that the population has already undergone a period of serious decline but is now in the process of recovery. Such populations will require different types of conservation actions, focussed on enhancing their chances of recovery.

opencc-zeroDec 2015View details →
dryad32/100

Data from: Sixty years of anthropogenic pressure: a spatio-temporal genetic analysis of brown trout populations subject to stocking and population declines

Analyses of historical samples can provide invaluable information on changes to the genetic composition of natural populations resulting from human activities. Here, we analyze 21 microsatellite loci in historical (archived scales from 1927-1956) and contemporary samples of brown trout (Salmo trutta) from six neighbouring rivers in Denmark, to compare the genetic structure of wild populations before and after population declines and stocking with non-local strains of hatchery trout. We show that all populations have been strongly affected by stocking, with admixture proportions ranging from 14 to 64%. Historical population genetic structure was characterized by isolation-by-distance and by positive correlations between historical effective population sizes and habitat area within river systems. Contemporary population genetic structure still showed isolation-by-distance, but also reflected differences among populations in hatchery trout admixture proportions. Despite significant changes to the genetic composition within populations over time, dispersal rates among populations were roughly similar before and after stocking. We also assessed whether population declines or introgression by hatchery strain trout should be the most significant conservation concern in this system. Based on theoretical considerations, we argue that population declines have had limited negative effects for the persistence of adaptive variation, but admixture with hatchery trout may have resulted in reduced local adaptation. Collectively, our study demonstrates the usefulness of analyzing historical samples for identifying the most important consequences of human activities on the genetic structure of wild populations.

opencc-zeroDec 2009View details →
dryad32/100

Data for spatial and temporal refugia for an insect population declining due to climate change

<p>Insect declines have been reported worldwide, although the particular causes of the declines may be complex and are poorly understood. Meadow spittlebugs were one of the most abundant insects in the coastal prairie along the California coast 40 years ago but have largely disappeared. Evidence links this decline to changing climatic conditions, which have reduced survival of eggs and neonates. We identified several refugia where meadow spittlebug populations have persisted amidst unfavorable conditions. Protection from desiccating winds was the common attribute of these refugia. Following a wet year, adult meadow spittlebugs were able to disperse from one refuge that we studied to recolonize coastal prairie habitats, although populations declined over the next two drier years. Because of their previous high abundance, loss of meadow spittlebugs is likely to affect the functioning of this widespread habitat, including energy transfer, their host plants, and their predators. In addition, meadow spittlebugs are unusual in having been the subject of extensive physiological and long-term ecological data, so they can serve as a bellwether species, indicating the effects of climate change.</p>

opencc-zeroJul 2021View details →
ClinicalTrials.gov32/100

HOme-based Brain Monitoring With a GARment-EEG to Study Cognitive Decline in the Aging Population

ClinicalTrials.gov study NCT06993207. IPD Sharing: UNDECIDED. Countries: 1. Publications: 2.

restrictedIPD-UNDECIDEDFeb 2026View details →
ClinicalTrials.gov32/100

Effects of Real-time Feedback During Decline Walking on Kinematic and Kinetic Gait Parameters in a Healthy Population

ClinicalTrials.gov study NCT04763850. IPD Sharing: YES. Countries: 1. Publications: 2.

controlledIPD-YESFeb 2026View details →
dryad32/100

Data from: Sixty years of anthropogenic pressure: a spatio-temporal genetic analysis of brown trout populations subject to stocking and population declines

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publicMar 2010View details →
dryad32/100

Data from: At risk of population decline? An ecological and genetic approach to the threatened palm species Butia eriospatha (Arecaceae) of southern Brazil

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publicAug 2013View details →
dryad32/100

Data from: Harvest and density-dependent predation drive long-term population decline in a northern ungulate

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publicFeb 2022View details →
dryad32/100

Data from: Variation in thermal niche of a declining river-breeding frog: from counter-gradient responses to population distribution patterns

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publicApr 2018View details →
dryad32/100

Data from: Ancient, but not recent, population declines have had a genetic impact on alpine yellow-bellied toad populations, suggesting potential for complete recovery

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publicFeb 2017View details →
dryad32/100

Data from: Climatic effects on population declines of a rare wetland species and the role of spatial and temporal isolation as barriers to hybridization

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publicDec 2017View details →
dryad32/100

Data from: The large-scale drivers of population declines in a long-distance migratory shorebird

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publicSep 2017View details →
dryad32/100

Data from: The enemy of my enemy is my friend: native pine marten recovery reverses the decline of the red squirrel by suppressing grey squirrel populations

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publicFeb 2018View details →
dryad32/100

Data from: Genetic structure of populations of whale sharks among ocean basins and evidence for their historic rise and recent decline

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publicApr 2014View details →

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dandi-nwb
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Last verified 2026-04-30Open record

International Brain Laboratory public data

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ibl
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Last verified 2026-04-29Open record

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Last verified 2026-04-29Open record