Kyle Finn

Kyle Finn
University of Pretoria | UP · Department of Zoology and Entomology

Doctor of Philosophy

About

17
Publications
3,860
Reads
How we measure 'reads'
A 'read' is counted each time someone views a publication summary (such as the title, abstract, and list of authors), clicks on a figure, or views or downloads the full-text. Learn more
90
Citations
Introduction
I am generally interested in animal movements, activity patterns, and gene flow across the landscape and how the environment has shaped their behaviour and choices in their daily lives. My current research on mole-rats will help me to understand the evolution of sociality and how ecological contraints in the environment has shaped their behaviour influencing dispersal decisions.
Education
January 2019 - December 2022
University of Pretoria
Field of study
  • Zoology
January 2016 - December 2016
Rhodes University
Field of study
  • Zoology
August 2006 - May 2009
University of Florida
Field of study
  • Wildlife Ecology

Publications

Publications (17)
Article
Full-text available
Groups of wild animals can vary considerably in their composition, including in the proportion of group members who are male or female, that is the within-group sex ratio. Variation in within-group sex ratios can arise from active adjustment of litter sex ratios by mothers, from sex differences in mortality, dispersal and immigration , or from stoc...
Article
Selection pressures underpinning the evolution of mammalian sociality and body mass variation have spurred great interest for several decades. Because they inhabit a wide range of geographic localities and habitats, African mole-rat subspecies of Cryptomys hottentotus present a unique opportunity to further our understanding of intra- and interspec...
Data
Supporting information for our study "Damaraland mole-rats do not rely on helpers for reproduction or survival", published in Evolution Letters 7(4): 203–215. doi: 10.1093/evlett/qrad023
Article
Full-text available
In eusocial invertebrates and obligate cooperative breeders, successful reproduction is dependent on assistance from non-breeding group members. Although naked (Heterocephalus glaber) and Damaraland mole-rats (Fukomys damarensis) are often described as eusocial and their groups are suggested to resemble those of eusocial insects more closely than g...
Thesis
Full-text available
The Natal mole-rat (Cryptomys hottentotus natalensis) is a social subspecies of African mole-rat related to the common mole-rat (Cryptomys hottentotus hottentotus). They inhabit mesic grassland in eastern South Africa from coastal regions to well over 2000m elevation. There have been a few studies on their physiology and reproductive suppression, b...
Article
Full-text available
The social mole-rats of the family Bathyergidae show elaborate social organisation that may include division of labour between breeders and non-breeders as well as across non-breeders within their groups. However, comparative behavioural data across the taxa are rare and contrasts and similarities between species are poorly understood. Field studie...
Article
Full-text available
Dispersal from the natal site to breeding sites is a crucial phase in the life history of animals and can have profound effects on the reproductive ecology and the structure of animal societies. However, few studies have assessed dispersal dynamics in subterranean mammals and it is unknown whether dispersal distances are constrained by living under...
Article
Sub-lethal effects, such as oxidative stress, can be linked to various breeding and thermophysiological strategies, which themselves can be linked to seasonal variability in abiotic factors. In this study, we investigated the subterranean, social living Natal mole-rat (Cryptomys hottentotus natalensis), which, unlike other social mole-rat species,...
Article
Full-text available
Differences in individual locomotor activity patterns may be linked to a number of ecological factors, such as changes in ambient temperature or photoperiod. Observations on subterranean mammals suggest that they exhibit diel rhythms despite the lack of visual cues in their underground burrows, but it is unknown how seasonality and individual chara...
Article
Full-text available
African Herp News 78:52-53
Preprint
Full-text available
Damaraland mole-rats ( Fukomys damarensis) are usually viewed as a eusocial or obligate cooperative breeder in which successful reproduction is dependent on help from closely related group members. However, because longitudinal studies of mole-rats in their natural environment are uncommon, the extent to which successful reproduction by breeders re...
Article
Geomagnetic sensitivity is present in a variety of vertebrates, but only recently has attention focused on subterranean mammals. We report the potential use of a magnetic compass in wild Damaraland mole-rats (Fukomys damarensis) during dispersal at two sites in the Kalahari region of South Africa. When the distance traveled was greater than 250 m,...
Article
Full-text available
We report instances of mole snakes (Pseudaspis cana) inhabiting mole-rat burrows in various locations of southern Africa. We also report instances that we believe to be predation of mole-rats by mole snakes.
Article
Full-text available
Eusocial societies are characterized by a clear division of labour between non-breeding workers and breeding queens, and queens often do not contribute to foraging, defence and other maintenance tasks. It has been suggested that the structure and organization of social mole-rat groups resembles that of eusocial insect societies. However, the divisi...
Article
We studied the correlates of population density and body size, growth rates, litter size, and group size in Damaraland mole-rats (Fukomys damarensis (Ogilby, 1838)) at two study sites with contrasting population densities. Group size, litter size, and the probability of recapture were independent of study site. However, body size differed between t...
Thesis
Full-text available
Population density may exert changes in a variety of behavioural and physiological characters in animals. However, the effects of density-dependence and dispersal are poorly studied in subterranean rodents due to the difficulties involved in observing such effects in wild populations. Using the cooperative breeding Damaraland mole-rat (Fukomys dama...
Article
Full-text available
The breeding population of the endangered Florida panther (Puma concolor coryi) is confined to the southern portion of the Florida peninsula. During the 20th century, a combination of isolation and small population size resulted in increased inbreeding. This ultimately led to a genetic restoration program in 1995 to alleviate correlates of inbreedi...

Questions

Questions (4)
Question
I'm assessing geneflow, relatedness and dispersal patterns in social mole-rats. They live in groups (4-15 animals) with high reproductive skew, 1 reproductive female and 1-2 reproductive males, with overlapping generations. The other group members are usually offspring of the breeders and don't contribute to breeding. Some unrelated immigrants do occur. I'm using SPAGeDI to estimate dispersal distances. Now some papers recommend removing offspring in genetic analyses so that you don't include pre-dispersal individuals. So I did that for Fst, relatedness coeff, and isolation by distance. For dispersal distances initially I thought to use just the reproductive individuals, but my sample size for females is 32 so I used all adults regardless of reproductive status getting me 84 males and 97 females. I used a population density equal to the expected number of breeding individuals per group in my study area, not the total number of individuals I captured. The values for males did not converge (no matter what density I used), and the predicted neighborhood size for females is 3 times than what I observed through captures. The predicted neighborhood size for both sexes combined is fairly accurate.
So a few questions: 1) when estimating dispersal distances through genetic methods do I limit my dataset to just reproductive individuals or use all the individuals even if there is overlapping generations? 2) specifically for SPAGeDi the population density you specify, is it the number of breeders per sq km or the total number of individuals (census density)? 3) assuming i used an accurate population density for the adult females, is the neighborhood size accurate? Thank you in advance
Question
I have widely inaccurate spatial distances in my "Pairwise Spatial and genetic distances written in column form" table output from SPAGeDI 1.5. For example SPAGeDi measures the distance between points -29.325094, 29.707921 and -29.322181, 29.707929 as 0.001178km (Spatial dist (km) column), but they are actually +/- 320m apart! I have entered the lat and long as decimal degrees (Lat = -29.322710, Long = 29.716432) in columns labeled X and Y. I have also specified Num Coords in the second line of my file as "-2". Are the spatial distances something else entirely and not the distance between GPS points?
Question
Hello all, I am analyzing body mass between small mammals and testing if it varies between sexes, reproductive status (breeding/non-breeding), and season (wet/dry). Would it be alright to have one variable called reproductive class as a factor with 4 variables: reproductive male, reproductive female, non-reproductive male, non-reproductive female. Is it possible to then use this in a linear model like body mass ~ reproductive class * season ?
Does sex and reproductive status have to be separate terms?
Additionally if I have significant differences between males and females, can I group the two sexes together to see if body mass overall changes with season?
Thank you
Question
Hi all,
Due to quarantine my uni is closed and I can't get any hands on help with analysis for a manuscript. My study is looking at dispersal distances of small mammals in two populations and how dispersal distances are affected by population density. It seems pretty straight forward except that my study sites are two different shapes and one of my co-authors thinks that I should find a way to statistically correct for this difference since my results could simply be due to animals migrating outside of the boundaries for study site B and therefore dispersal distances are shorter than what actually occurs.
Study site A: mostly square with area of 3km2, with a low population density and higher mean dispersal distance
Study site B: a long rectangle 4km by 0.5km, with a high population density and lower mean dispersal distance.
It was suggested that I build a model and let the program do random walks in and out of the study sites to mimic dispersing individuals. Then test whether the model correctly represents what is actually happening. However neither of my advisors has any experience in movement ecology. Ideally it would be nice to account for actual home ranges within the study sites since being able to see how theoretical movement would happen in a polygon (or how often individuals may move out of it) based on actual locations of home ranges would be exceedling helpful.
So my questions are
1: is this extra modeling step necessary or is it overkill?
2: what program(s) (open source please) could I use to do this?
3: how do I do this? can you provide tutorials and examples to help me figure this out, or terms to search for?
I have novice R and QGIS skills by the way. Thank you very much in advance!

Network

Cited By