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Full-Text Articles in Life Sciences

Modelling Non-Euclideanmovement And Landscape Connectivity In Highly Structured Ecological Networks, Chris Sutherland, Angela Fuller, J. Royle Dec 2014

Modelling Non-Euclideanmovement And Landscape Connectivity In Highly Structured Ecological Networks, Chris Sutherland, Angela Fuller, J. Royle

Environmental Conservation Faculty Publication Series

1. Movement is influenced by landscape structure, configuration and geometry, but measuring distance as perceived by animals poses technical and logistical challenges. Instead, movement is typically measured using Euclidean distance, irrespective of location or landscape structure, or is based on arbitrary cost surfaces. Arecently proposed extension of spatial capture-recapture (SCR)models resolves this issue using spatial encounterhistories of individuals to calculate least-cost paths (ecological distance: Ecology, 94, 2013, 287) thereby relaxingthe Euclidean assumption. We evaluate the consequences of not accounting for movement heterogeneity whenestimating abundance in highly structured landscapes, and demonstrate the value of this approach for estimatingbiologically realistic space-use patterns …


Modelling Non-Euclideanmovement And Landscape Connectivity In Highly Structured Ecological Networks, Chris Sutherland, Angela Fuller, J. Royle Dec 2014

Modelling Non-Euclideanmovement And Landscape Connectivity In Highly Structured Ecological Networks, Chris Sutherland, Angela Fuller, J. Royle

Chris Sutherland

1. Movement is influenced by landscape structure, configuration and geometry, but measuring distance as perceived by animals poses technical and logistical challenges. Instead, movement is typically measured using Euclidean distance, irrespective of location or landscape structure, or is based on arbitrary cost surfaces. A
recently proposed extension of spatial capture-recapture (SCR)models resolves this issue using spatial encounter
histories of individuals to calculate least-cost paths (ecological distance: Ecology, 94, 2013, 287) thereby relaxing
the Euclidean assumption. We evaluate the consequences of not accounting for movement heterogeneity when
estimating abundance in highly structured landscapes, and demonstrate the value of this approach for …


Density And Cover Preferences Of Black-And-Rufous Elephant-Shrews (Rhynchocyon Petersi) In Chome Forest Reserve, Tanzania, Stephanie Coster, David Ribble May 2014

Density And Cover Preferences Of Black-And-Rufous Elephant-Shrews (Rhynchocyon Petersi) In Chome Forest Reserve, Tanzania, Stephanie Coster, David Ribble

David O Ribble

The objective of this study was to determine the density and habitat preference of the Black-andrufous elephant-shrew (Rhynchocyon petersi) in Chome Forest Reserve, Tanzania. Chome Forest (143km2) is located in the South Pare Mountains and provides critical habitat for endangered R. petersi. Twelve 300m transects were cut through the centre of the forest in an east-west direction and the number of elephant-shrew nests within 2.5 meters on each side of the transects was recorded. The mean number of nests per 100m transect (0.39 ± 0.47 [1SE]) translated to a density estimate of 19 elephant-shrews per km2 (SE=23). Nest sites tended …


Plasticity In Female Mate Choosiness: A Result Of Variation In Perceived Predation Risk And The Interaction Of Female Age And Male Density, Ashley Atwell May 2014

Plasticity In Female Mate Choosiness: A Result Of Variation In Perceived Predation Risk And The Interaction Of Female Age And Male Density, Ashley Atwell

School of Biological Sciences: Dissertations, Theses, and Student Research

In many species, female mate choices can be a strong source of sexual selection. Females often prefer a certain male phenotype, and this can be due to benefits females gain from mating with preferred males. However, such benefits can sometimes be outweighed by the cost of searching for a preferred male. These costs and benefits often change concomitantly with changes in environmental (e.g., predator abundance and conspecific density) and internal factors (e.g., female age). Thus, female mate choosiness (the degree to which preferences for certain males are expressed) should often be plastic. Plasticity in female mate choosiness may be complicated …