Academic literature on the topic 'Sink population'

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Journal articles on the topic "Sink population"

1

EBERHART-PHILLIPS, LUKE J., and MARK A. COLWELL. "Conservation challenges of a sink: the viability of an isolated population of the Snowy Plover." Bird Conservation International 24, no. 3 (2014): 327–41. http://dx.doi.org/10.1017/s0959270913000506.

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SummarySource-sink dynamics are easily overlooked when formulating recovery objectives for threatened species. This could lead to unrealistic criteria imposed on sink populations, which in turn might restrict an entire metapopulation from being delisted. Therefore, an understanding of the viability of subpopulations within the context of a metapopulation is needed to develop appropriate recovery objectives. Consequently, we used 11 years of mark-recapture, productivity, and movement data to analyse the viability of a small, geographically isolated population of the Snowy PloverCharadrius nivosus, a shorebird listed as threatened under the U.S. Endangered Species Act. Simulations confirmed that the focal population in northern California is a sink that relies upon immigrants from neighbouring populations. Furthermore, these source populations will increase within the next 50 years and are likely to achieve the delisting requirements. However, the northern California population is unlikely to reach the delisting criteria given the current vital rate estimations. Management scenarios demonstrated that lethal predator removal and reducing human disturbance facilitate population recovery and may partially alleviate the reliance upon immigration. However, the use of nest exclosures reduced population growth because they are known to compromise adult survival. These results highlight the importance of maintaining viable source populations and re-evaluating the recovery objectives of metapopulations with active sinks.
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2

Heinrichs, Julie A., Joshua J. Lawler, Nathan H. Schumaker, Chad B. Wilsey, and Darren J. Bender. "Divergence in sink contributions to population persistence." Conservation Biology 29, no. 6 (2015): 1674–83. http://dx.doi.org/10.1111/cobi.12540.

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3

Gaggiotti, Oscar E. "Population Genetic Models of Source–Sink Metapopulations." Theoretical Population Biology 50, no. 2 (1996): 178–208. http://dx.doi.org/10.1006/tpbi.1996.0028.

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4

Zwolak, Rafał, and Kerry R. Foresman. "Deer mouse demography in burned and unburned forest: no evidence for source–sink dynamics." Canadian Journal of Zoology 86, no. 2 (2008): 83–91. http://dx.doi.org/10.1139/z07-126.

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Deer mouse ( Peromyscus maniculatus (Wagner, 1845)) populations increase dramatically after wildfires. These increases are puzzling because there are no obvious food sources or vegetation cover in severely burned areas. We conducted a capture–mark–recapture study of deer mice in a mosaic of burned and unburned montane forests in western Montana to determine if their postfire increase could be explained by source–sink dynamics, with burned areas acting as a sink. When overall mouse densities were very low, the vast majority of the population was found in burned areas. Mice appeared regularly in unburned forest only when the densities were high. This pattern is precisely opposite to the expected results if the sink hypothesis were correct. Moreover, mice in burned areas did not show decreased body mass, reproductive performance, or survival when compared with mice in unburned areas. Age structure and sex ratio did not differ between burned and unburned sites. We conclude that burned areas do not function as population sinks; rather, they represent high-quality habitat for deer mice.
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5

Munguia, Pablo. "Role of sources and temporal sinks in a marine amphipod." Biology Letters 11, no. 2 (2015): 20140864. http://dx.doi.org/10.1098/rsbl.2014.0864.

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Spatially structured habitats challenge populations to have positive growth rates and species often rely on dispersing propagules to occupy habitats outside their fundamental niche. Most marine species show two main life stages, a dispersing stage and a sedentary stage affecting distribution and abundance patterns. An experimental study on Corophium acherusicum, a colonial tube-building amphipod, showed the strong influence that a source population can have on new habitats. More importantly, this study shows the effect of temporal sinks where newly established populations can show reduced growth rates if the propagule supply from a source is removed. Sink populations had a reduction in abundance and became male-biased as females left colonies. The consequences arising from short-term dispersal and temporal sinks could be due to different selection pressures at the source and sink populations. These consequences can become reflected in long-term dynamics of marine populations if we shift focus to non-random dispersal models incorporating behaviour and stage-dependent dispersal.
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6

Draheim, Hope M., Jennifer A. Moore, Dwayne Etter, Scott R. Winterstein, and Kim T. Scribner. "Detecting black bear source–sink dynamics using individual-based genetic graphs." Proceedings of the Royal Society B: Biological Sciences 283, no. 1835 (2016): 20161002. http://dx.doi.org/10.1098/rspb.2016.1002.

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Source–sink dynamics affects population connectivity, spatial genetic structure and population viability for many species. We introduce a novel approach that uses individual-based genetic graphs to identify source–sink areas within a continuously distributed population of black bears ( Ursus americanus ) in the northern lower peninsula (NLP) of Michigan, USA. Black bear harvest samples ( n = 569, from 2002, 2006 and 2010) were genotyped at 12 microsatellite loci and locations were compared across years to identify areas of consistent occupancy over time. We compared graph metrics estimated for a genetic model with metrics from 10 ecological models to identify ecological factors that were associated with sources and sinks. We identified 62 source nodes, 16 of which represent important source areas (net flux > 0.7) and 79 sink nodes. Source strength was significantly correlated with bear local harvest density (a proxy for bear density) and habitat suitability. Additionally, resampling simulations showed our approach is robust to potential sampling bias from uneven sample dispersion. Findings demonstrate black bears in the NLP exhibit asymmetric gene flow, and individual-based genetic graphs can characterize source–sink dynamics in continuously distributed species in the absence of discrete habitat patches. Our findings warrant consideration of undetected source–sink dynamics and their implications on harvest management of game species.
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7

Murphy, Michael T. "Source-Sink Dynamics of a Declining Eastern Kingbird Population and the Value of Sink Habitats." Conservation Biology 15, no. 3 (2001): 737–48. http://dx.doi.org/10.1046/j.1523-1739.2001.015003737.x.

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8

Robinson, Hugh S., Robert B. Wielgus, Hilary S. Cooley, and Skye W. Cooley. "SINK POPULATIONS IN CARNIVORE MANAGEMENT: COUGAR DEMOGRAPHY AND IMMIGRATION IN A HUNTED POPULATION." Ecological Applications 18, no. 4 (2008): 1028–37. http://dx.doi.org/10.1890/07-0352.1.

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9

Donker, Scott A., and Charles J. Krebs. "Evidence for source - sink dynamics in a regional population of arctic ground squirrels (Urocitellus parryii plesius)." Wildlife Research 39, no. 2 (2012): 163. http://dx.doi.org/10.1071/wr11167.

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Context Variable demographic rates can manifest themselves between habitat types in the form of source–sink dynamics where populations in sink habitats would not exist without the addition of migrants from source habitats. Aims Arctic ground squirrels (Urocitellus parryii pleisus (Osgood, 1900)) occupy a large geographic area in northern Canada and live in a variety of habitat types, including boreal forest, low-elevation meadows and alpine meadows, providing an opportunity to investigate the possible existence of source–sink dynamics. Methods We hypothesised that arctic ground squirrels in the south-western Yukon exhibit demographic characteristics indicative of source–sink dynamics. Boreal forest habitat could be a sink in spite of previous high squirrel densities, whereas meadows could be a source. We investigated this by mark–recapture live-trapping and radio-telemetry. Key Results In the boreal forest in the Kluane region, we found reduced recruitment, reduced population growth rates (λ), and reduced survivorship for radio-collared individuals that moved from low-elevation meadows into the boreal forest. There was no evidence from radio-collared juveniles of dispersal from high-density ground squirrel populations in alpine meadows down into boreal forest. Conclusions Boreal forest is a sink habitat for arctic ground squirrels. Source–sink dynamics observed between low-elevation meadow and boreal forest habitats appear to result from increased predation pressure in the boreal forest. The result has been a near extirpation of boreal forest arctic ground squirrels in the Kluane region since 1998. Implications Because the source areas of low-elevation meadows occupy only 7–9% of the lowland habitat, recolonisation of boreal forest sites has been very slow. Whereas alpine populations remain high in 2011, boreal forest populations remain near zero. Alpine populations do not appear to be a source for the boreal forest.
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10

Xiao, Zeping, Manyu Bi, Yexi Zhong, Xinghua Feng, and Hongzhi Ma. "Study on the Evolution of the Source-Flow-Sink Pattern of China’s Chunyun Population Migration Network: Evidence from Tencent Big Data." Urban Science 5, no. 3 (2021): 66. http://dx.doi.org/10.3390/urbansci5030066.

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We construct a comprehensive analysis framework of population flow in China. To do so, we take prefecture-level administrative regions as the basic research unit of population flow and use source-sink theory and flow space theory. Additionally, we reveal the dynamic differentiation of population flow patterns and the evolution of population source-flow-sink systems. We try to provide a theoretical basis for the formulation of population development policies and regional spatial governance. The results show the following: (1) The Hu Huanyong Line has a strong spatial lock-in effect on population flow. Additionally, provincial capital cities, headed by Hangzhou, Nanjing, and Hefei, have played an increasingly prominent role in population flow. (2) The developed eastern coastal areas have undertaken China’s main population outflow. The net population flow is spatially high in the middle of the region and low on the two sides, exhibiting an “inverted U-shaped” pattern. Furthermore, the borders of the central provinces form a continuous population inflow area. (3) The hierarchical characteristics of the population flow network are obvious. Strong connections occur between developed cities, and the effect of distance attenuation is weakened. The medium connection network is consistent with the traffic skeleton, and population flow exhibits a strong “bypass effect”. (4) The source and sink areas are divided into four regions similar to China’s three major economic belts. The 10 regions can be refined to identify the main population source and sink regions, and the 18 regions can basically reflect China’s level of urbanization. The network of the population flow source-flow-sink system exhibits notable nesting characteristics. As a result, it creates a situation in which the source areas on both sides of the east and the west are convective to the middle. The hierarchical differentiation of the source-flow sink system is related to the differences between the east and the west and between the north and the south, as well as local differences in China.
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