Incorporating Estimates of Group Size in Sightability Models for Wildlife

ABSTRACT Sightability models have been used to estimate population size of many wildlife species; however, a limitation of these models is an assumption that groups of animals observed and counted during aerial surveys are enumerated completely. Replacing these unknown counts with maximum observed counts, as is typically done, produces population size estimates that are negatively biased. This bias can be substantial depending on the degree of undercounting occurring. We first investigated a method-of-moments estimator of group sizes. We then defined a population size estimator using the method-of-moments estimator of group sizes in place of maximum counts in the traditional sightability models, thereby correcting for bias associated with undercounting group size. We also provide associated equations for calculating the variance of our estimator. This estimator is an improvement over existing sightability model techniques because it significantly reduces bias, and variance estimates provide near nominal confidence interval coverage. The data needed for this estimator can be easily collected and implemented by wildlife managers with a field crew of only 3 individuals and little additional flight or personnel time beyond the normal requirements for developing sightability models.     

Quantifying sexual selection: a comparison of competing indices with mating system data from a terrestrially breeding salamander

Calculations for quantifying the potential for sexual selection remain controversial. Many indices have been promoted in the literature, but each has unique sets of advantages and disadvantages. Using marbled salamanders, I evaluated the performance of several measures by manipulating intensity of sexual selection in experimental breeding replicates of varying operational sex ratio. Theory predicts that sexual selection among males will be higher when sex ratio is male‐biased and lower when female‐biased. I used microsatellite data to assign hatchling parentage, estimate adult fitness, and calculate several indices of inequality for quantifying sexual selection. Opportunity for selection and Morisita index always conformed to theoretical expectations, which was not the case for index of resource monopolization, standardized Morisita index, or binomial skew index. Although I conclude that opportunity for selection is advantageous in sexual selection studies because of its link to formal theory, this should be tested against the null hypothesis of random variation in ambiguous cases. In the present study, although variation in both reproductive and mating success was high when quantified using opportunities for selection, it was only significantly greater than random expectations for reproductive success. This study provides further empirical support for the continued use of opportunity for selection in sexual selection studies. © 2010 The Linnean Society of London, Biological Journal of the Linnean Society, 2010, 99 , 73–83.     

The two groups of sensilla in the ventral coxal hairplate of Carausius morosus have different roles during walking

Abstract. The ventral coxal hairplate (cxHPv) of the stick insect Carausius morosus Br. (Phasmida: Bacteriidae) contains two morphologically distinct groups of sensilla designated as group 1 and 2 (Gl, G2). The function of these sensilla during walking was tested by selectively ablating one or both groups on one middle leg in thirty-four animals. It has previously been shown that ablation of the entire hairplate leads to two kinds of errors: the operated leg swings farther forward and the adjacent caudal leg ends its swing more to the rear relative to the operated leg. Following selective ablation of cxHPv Gl on the middle leg, the first kind of error is more pronounced, indicating that this group contributes more to limiting forward protraction during the swing. Following ablation of cxHPv G2, the second kind of error is more evident, indicating that during stance this group contributes more to the target information influencing the swing end-point of the adjacent caudal leg. These results are interpreted to reflect the phasic and phasic-tonic response characteristics of Gl and G2 hairs, respectively.