scholarly journals Spatial Capture-Recapture for Categorically Marked Populations with An Application to Genetic Capture-Recapture

2018 ◽  
Author(s):  
Ben C. Augustine ◽  
J. Andrew Royle ◽  
Sean M. Murphy ◽  
Richard B. Chandler ◽  
John J. Cox ◽  
...  

AbstractRecently introduced unmarked spatial capture-recapture (SCR), spatial mark-resight (SMR), and 2-flank spatial partial identity models (SPIM) extend the domain of SCR to populations or observation systems that do not always allow for individual identity to be determined with certainty. For example, some species do not have natural marks that can reliably produce individual identities from photographs, and some methods of observation produce partial identity samples as is the case with remote cameras that sometimes produce single flank photographs. These models share the feature that they probabilistically resolve the uncertainty in individual identity using the spatial location where samples were collected. Spatial location is informative of individual identity in spatially structured populations with home range sizes smaller than the extent of the trapping array because a latent identity sample is more likely to have been produced by an individual living near the trap where it was recorded than an individual living further away from the trap. Further, the level of information about individual identity that a spatial location contains is determined by two key ecological concepts, population density and home range size. The number of individuals that could have produced a latent or partial identity sample increases as density and home range size increase because more individual home ranges will overlap any given trap. We show this uncertainty can be quantified using a metric describing the expected magnitude of uncertainty in individual identity for any given population density and home range size, the Identity Diversity Index (IDI). We then show that the performance of latent and partial identity SCR models varies as a function of this index and produces imprecise and biased estimates in many high IDI scenarios when data are sparse. We then extend the unmarked SCR model to incorporate partially identifying covariates which reduce the level of uncertainty in individual identity, increasing the reliability and precision of density estimates, and allowing reliable density estimation in scenarios with higher IDI values and with more sparse data. We illustrate the performance of this “categorical SPIM” via simulations and by applying it to a black bear data set using microsatellite loci as categorical covariates, where we reproduce the full data set estimates with only slightly less precision using fewer loci than necessary for confident individual identification. The categorical SPIM offers an alternative to using probability of identity criteria for classifying genotypes as unique, shifting the “shadow effect”, where more than one individual in the population has the same genotype, from a source of bias to a source of uncertainty. We discuss the difficulties that real world data sets pose for latent identity SCR methods, most importantly, individual heterogeneity in detection function parameters, and argue that the addition of partial identity information reduces these concerns. We then discuss how the categorical SPIM can be applied to other wildlife sampling scenarios such as remote camera surveys, where natural or researcher-applied partial marks can be observed in photographs. Finally, we discuss how the categorical SPIM can be added to SMR, 2-flank SPIM, or other future latent identity SCR models.

1995 ◽  
Vol 52 (7) ◽  
pp. 1499-1508 ◽  
Author(s):  
Charles K. Minns

A data set assembled from published literature supported the hypotheses that (i) home range size increases allometrically with body size in temperate freshwater fishes, and (ii) fish home ranges are larger in lakes than rivers. The allometric model fitted was home range = A∙(body size)B. Home ranges in lakes were 19–23 times larger than those in rivers. Additional analyses showed that membership in different taxonomic groupings of fish, the presence–absence of piscivory, the method of measuring home range, and the latitude position of the water bodies were not significant predictive factors. Home ranges of freshwater fish were smaller than those of terrestrial mammals, birds, and lizards. Home ranges were larger than area per fish values derived by inverting fish population and assemblage density–size relationships from lakes and rivers and territory–size relationships in stream salmonids. The weight exponent (B) of fish home range was lower than values reported for other vertebrates, 0.58 versus a range of 0.96–1.14. Lake–river home range differences were consistent with differences reported in allometric models of freshwater fish density and production.


2021 ◽  
pp. NULL
Author(s):  
Rowena P. Hamer ◽  
Georgina E. Andersen ◽  
Bronwyn A. Hradsky ◽  
Shannon N. Troy ◽  
Riana Z. Gardiner ◽  
...  

Mammalia ◽  
2018 ◽  
Vol 82 (2) ◽  
pp. 188-192 ◽  
Author(s):  
Matthis Petit ◽  
Thomas Denis ◽  
Ondine Rux ◽  
Cécile Richard-Hansen ◽  
Rachel Berzins

AbstractKnowledge of the jaguar population is needed in French Guiana that faces an increase of human-jaguar conflicts. We carried out a camera trap survey to assess jaguar local density and home range size in a preserved coastal area of French Guiana. We ran spatially explicit capture recapture (SECR) models. In our model, the scale parameterσ, that is linked to the home range size, was larger for males (σ=3.87±0.59 SE km) than for females (σ=2.33±0.30 SE km). The assessed jaguar density was 3.22±0.87 SE ind. 100 km−2, which should be considered as an optimal density in a French Guiana coastal area.


Ecography ◽  
2015 ◽  
Vol 39 (7) ◽  
pp. 676-688 ◽  
Author(s):  
M. G. Efford ◽  
D. K. Dawson ◽  
Y. V. Jhala ◽  
Q. Qureshi

2015 ◽  
Vol 61 (3-4) ◽  
pp. 157-161
Author(s):  
Charles J. Randel ◽  
Nova J. Silvy

Kit fox (Vulpes macrotis) life history and ecology has been extensively studied in the Great Basin and California's Central Valley, with fewer studies in hot desert regions resulting in regional knowledge gaps. To augment our understanding of kit fox life history and ecology, we conducted a 2-year radio-telemetry study of the desert kit fox (V. m. arsipus) in southeastern California. Fifty-six desert kit foxes were fitted with morality-sensitive radio collars between October 2012 and August 2014 with individuals located five to seven nights per week to determine home range size and population density. Mean home range was 15.77 ± 1.03 km2 (95% fixed kernel) and 18.48 ± 1.77 km2 (minimum convex polygon), and larger than all, but one previous study. We found no difference in home range size based on sex or year. Home range overlaps were significantly larger for mated (79.3% ± 1.35%) than unmated pairs (20.9% ± 1.01%) and consistent with previous studies. Population size was estimated at 88 individuals using open population models, resulting in an estimated density of 0.34/km2 (range 0.26–0.47/km2) which is higher than previously reported. Our study represents the first home range and population density study for desert kit foxes in California and provided critical knowledge of this understudied kit fox population.


2017 ◽  
Vol 44 (4) ◽  
pp. 316 ◽  
Author(s):  
K. S. Richardson ◽  
C. Rouco ◽  
C. Jewell ◽  
N. P. French ◽  
B. M. Buddle ◽  
...  

Context The Australian brushtail possums (Trichosurus vulpecula) introduction to New Zealand has exacted a heavy toll on native biodiversity and presented the country with its greatest wildlife reservoir host for bovine tuberculosis (TB). Management efforts to control both possums and TB have been ongoing for decades, and the biology of possums has been studied extensively in Australia and New Zealand over the past 50 years; however, we still do not have a clear understanding of its home-range dynamics. Aims To investigate determinants of home range size by using a uniquely large dataset in the Orongorongo Valley, a highly monitored research area in New Zealand and compare our findings with those of other studies. Methods Possum density was estimated, for subpopulations on four 13-ha cage-trap grids, by the spatially explicit capture–mark–recapture analysis of trapping data from 10 consecutive months. Home ranges were estimated from trap locations using a 100% minimum convex polygon (MCP) method for 348 individuals and analysed with respect to grid, age and sex. Key results Mean (standard error) possum density, estimated as 4.87 (0.19), 6.92 (0.29), 4.08 (0.21) and 4.20 (0.19) ha–1 for the four grids, was significantly negatively correlated with mean MCP home-range size. Grid, age, and the interaction of age and sex were significantly related to home-range size. Older possums had larger home ranges than did younger possums. When ‘juvenile cohort’ and ‘adult cohort’ data were analysed separately, to investigate the significant interaction, males in the ‘adult cohort’ had significantly larger home ranges than did females, with the grid effect still being apparent, whereas neither sex nor grid effects were significant for the ‘juvenile cohort’. Conclusions Our findings indicate that, in addition to density, age and sex are likely to be consistent determinants of possum home-range size, but their influences may be masked in some studies by the complexity of wild-population dynamics. Implications Our findings have strong implications regarding both disease transmission among possums and possum management. The fact that adult males occupy larger home ranges and the understanding that possum home range increases as population density decreases are an indication that males may be the primary drivers of disease transmission in possum populations. The understanding that possum home range increases as population density decreases could be a direct reflection of the ability of TB to persist in the wild that counteracts current management procedures. If individuals, and particularly males, infected with TB can withstand control measures, their ensuing home-range expansion will result in possible bacteria spread in both the expanded area of habitation and new individuals becoming subjected to infection (both immigrant possums and other control survivors). Therefore, managers should consider potential approaches for luring possum males in control operations.


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