scholarly journals Estimating the proportion of a beluga population using specific areas from connectivity patterns and abundance indices

Ecosphere ◽  
2021 ◽  
Vol 12 (6) ◽  
Author(s):  
Jean‐François Ouellet ◽  
Robert Michaud ◽  
Michel Moisan ◽  
Véronique Lesage
2011 ◽  
Vol 76 (3) ◽  
pp. 403-428 ◽  
Author(s):  
Jack M. Broughton ◽  
Michael D. Cannon ◽  
Frank E. Bayham ◽  
David A. Byers

The use of body size as an index of prey rank in zooarchaeology has fostered a widely applied approach to understanding variability in foraging efficiency. This approach has, however, been critiqued—most recently by the suggestion that large prey have high probabilities of failed pursuits. Here, we clarify the logic and history of using body size as a measure of prey rank and summarize empirical data on the body size-return rate relationship. With few exceptions, these data document strong positive relationships between prey size and return rate. We then illustrate, with studies from the Great Basin, the utility of body size-based abundance indices (e.g., the Artiodactyl Index) when used as one component of multidimensional analyses of prehistoric diet breadth. We use foraging theory to derive predictions about Holocene variability in diet breadth and test those predictions using the Artiodactyl Index and over a dozen other archaeological indices. The results indicate close fits between the predictions and the data and thus support the use of body size-based abundance indices as measures of foraging efficiency. These conclusions have implications for reconstructions of Holocene trends in large game hunting in western North America and for zooarchaeological applications of foraging theory in general.


2020 ◽  
Vol 276 ◽  
pp. 804-814 ◽  
Author(s):  
Xiaoqin Wang ◽  
Yafei Tan ◽  
Omer Van den Bergh ◽  
Andreas von Leupoldt ◽  
Jiang Qiu

2006 ◽  
Vol 84 (8) ◽  
pp. 1210-1215 ◽  
Author(s):  
Pei-Jen L. Shaner

Food availability often drives consumer population dynamics. However, food availability may also influence capture probability, which if not accounted for may create bias in estimating consumer abundance and confound the effects of food availability on consumer population dynamics. This study compared two commonly used abundance indices (minimum number alive (MNA) and number of animals captured per night per grid) with an abundance estimator based on robust design model as applied to the white-footed mouse ( Peromyscus leucopus (Rafinesque, 1818)) in food supplementation experiments. MNA consistently generated abundance estimates similar to the robust design model, regardless of food supplementation. The number of animals captured per night per grid, however, consistently generated lower abundance estimates compared with MNA and the robust design model. Nevertheless, the correlations between abundance estimates from MNA, number of animals captured, and robust design model were not influenced by food supplementation. This study demonstrated that food supplementation is not likely to create bias among these different measures of abundance. Therefore, there is a great potential for conducting meta-analysis of food supplementation effect on consumer population dynamics (particularly in small mammals) across studies using different abundance indices and estimators.


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