Winter Habitat Ecology, Use, and Availability for the Aransas-Wood Buffalo Population of Whooping Cranes

Author(s):  
Elizabeth H. Smith ◽  
Felipe Chavez-Ramirez ◽  
Luz Lumb
1996 ◽  
Vol 6 (1) ◽  
pp. 318-325 ◽  
Author(s):  
Steven W. Buskirk ◽  
Ma Yiqing ◽  
Xu Li ◽  
Jiang Zhaowen

2000 ◽  
Vol 37 (4) ◽  
pp. 589-602 ◽  
Author(s):  
Eliot L. Terry ◽  
Bruce N. Mclellan ◽  
Glen S. Watts

2020 ◽  
Vol 57 ◽  
pp. 125892
Author(s):  
Kristine L. Metzger ◽  
Sarah E. Lehnen ◽  
Steven E. Sesnie ◽  
Matthew J. Butler ◽  
Aaron T. Pearse ◽  
...  

Author(s):  
Aaron T. Pearse ◽  
Mary J. Harner ◽  
David M. Baasch ◽  
Greg D. Wright ◽  
Andrew J. Caven ◽  
...  

Animals ◽  
2020 ◽  
Vol 10 (12) ◽  
pp. 2454
Author(s):  
Yue Sun ◽  
Yanze Yu ◽  
Jinhao Guo ◽  
Minghai Zhang

Single-scale frameworks are often used to analyze the habitat selections of species. Research on habitat selection can be significantly improved using multi-scale models that enable greater in-depth analyses of the scale dependence between species and specific environmental factors. In this study, the winter habitat selection of red deer in the Gogostaihanwula Nature Reserve, Inner Mongolia, was studied using a multi-scale model. Each selected covariate was included in multi-scale models at their “characteristic scale”, and we used an all subsets approach and model selection framework to assess habitat selection. The results showed that: (1) Univariate logistic regression analysis showed that the response scale of red deer to environmental factors was different among different covariate. The optimal scale of the single covariate was 800–3200 m, slope (SLP), altitude (ELE), and ratio of deciduous broad-leaved forests were 800 m in large scale, except that the farmland ratio was 200 m in fine scale. The optimal scale of road density and grassland ratio is both 1600 m, and the optimal scale of net forest production capacity is 3200 m; (2) distance to forest edges, distance to cement roads, distance to villages, altitude, distance to all road, and slope of the region were the most important factors affecting winter habitat selection. The outcomes of this study indicate that future studies on the effectiveness of habitat selections will benefit from multi-scale models. In addition to increasing interpretive and predictive capabilities, multi-scale habitat selection models enhance our understanding of how species respond to their environments and contribute to the formulation of effective conservation and management strategies for ungulata.


2014 ◽  
Vol 128 (3) ◽  
pp. 272 ◽  
Author(s):  
Gilbert Proulx

Late-winter habitat use by the Fisher, Pekania pennanti (Erxleben, 1777) in northwestern Saskatchewan was assessed in February 2009, 2011, and 2012. A total of 78 Fisher tracks were recorded over 60 300 m of snowshoe surveys. Fisher tracks were significantly less frequent than expected in Tamarack (Larix laricina [Du Roi] K. Koch) stands with > 40% crown closure and mainly 0–10 m trees (P < 0.05) and in open areas. Fishers used other habitat types equal to availability, including muskeg and coniferous, mixed, and deciduous forest stands. Maintaining mosaics of forest stands of different seral stages interspersed with muskeg would meet the late-winter habitat needs of Fishers in the Boreal Plains Ecozone of northwestern Saskatchewan.


Polar Biology ◽  
2021 ◽  
Author(s):  
Carmen L. David ◽  
Fokje L. Schaafsma ◽  
Jan A. van Franeker ◽  
Evgeny A. Pakhomov ◽  
Brian P. V. Hunt ◽  
...  

AbstractSurvival of larval Antarctic krill (Euphausia superba) during winter is largely dependent upon the presence of sea ice as it provides an important source of food and shelter. We hypothesized that sea ice provides additional benefits because it hosts fewer competitors and provides reduced predation risk for krill larvae than the water column. To test our hypothesis, zooplankton were sampled in the Weddell-Scotia Confluence Zone at the ice-water interface (0–2 m) and in the water column (0–500 m) during August–October 2013. Grazing by mesozooplankton, expressed as a percentage of the phytoplankton standing stock, was higher in the water column (1.97 ± 1.84%) than at the ice-water interface (0.08 ± 0.09%), due to a high abundance of pelagic copepods. Predation risk by carnivorous macrozooplankton, expressed as a percentage of the mesozooplankton standing stock, was significantly lower at the ice-water interface (0.83 ± 0.57%; main predators amphipods, siphonophores and ctenophores) than in the water column (4.72 ± 5.85%; main predators chaetognaths and medusae). These results emphasize the important role of sea ice as a suitable winter habitat for larval krill with fewer competitors and lower predation risk. These benefits should be taken into account when considering the response of Antarctic krill to projected declines in sea ice. Whether reduced sea-ice algal production may be compensated for by increased water column production remains unclear, but the shelter provided by sea ice would be significantly reduced or disappear, thus increasing the predation risk on krill larvae.


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