The functional significance of grooming behaviour in higher primates : the case of free-living chimpanzees

As a contribution to the existing knowledge of grooming in primates five and a half years of grooming data were examined from a group of free-living chimpanzees (Pan troglodytes) in the Budongo Forest, Uganda, to investigate various functional significances of grooming behaviour within the context of social reinforcement. The fission–fusion social structure of chimpanzees results in group members not moving around as a single unit, but forming temporary units as the need arises. This reduces opportunities for individuals to groom others and therefore, based on time and association constraints alone, grooming was as expected found to be unevenly distributed among group members. Grooming patterns found among this group of chimpanzees were comparable to those observed in other free-living populations with variations possibly being attributed to resource base, population numbers and differences in age-sex class composition. One of the suggested social benefits of grooming is that it is used to enhance reproductive success, either by allowing males to enhance their proximity to oestrous females, or by influencing female choice through the development of affiliative relationships with males. Grooming was found to increase between males and females, whilst females displayed sexual receptivity through the presence of anogenital swellings and grooming may be a strategy used by males to increase their access to copulation opportunities, whereas females may use grooming to increase protection from harassment by less preferred males during swollen periods and also increase the likelihood of copulation with preferred partners. Based on the availability of oestrous females, copulations between males and adult females occurred significantly less frequently than expected, whereas copulations between males and subadult females occurred significantly more frequently than expected. Overall a positive correlation was found between grooming of females by males and frequency of copulations. Due to concerns regarding the validity of different sampling methods, scan-focal and ad libitum sampling methods were compared to establish if results from different sampling methods were similar. Results from the scan-focal and ad libitum sampling methods had very few discrepancies, and it is suggested that ad libitum sampling methods which record behaviour types whenever they occur, may be more beneficial for species which don’t move around as a single unit and live in environments where visibility is reduced, therefore increasing the possibility of recording individuals or behaviours that are observed infrequently. Scan-focal sampling may be more beneficial in studying species which move around together in habitats which are conducive to greater visibility, therefore allowing all or most group members to be observed simultaneously.Thesis (DPhil)--University of Pretoria, 2009.Zoology and Entomologyunrestricte

Origin of the Helminth Community of an Exotic Invasive Lizard, the Brown Anole, Anolis sagrei (Squamata: Polychrotidae), in Southwestern Taiwan

v. ill. 23 cm.Also available through BioOne: http://www.bioone.org/doi/abs/10.2984/65.3.383QuarterlyComposition of the helminth community of the brown anole, Anolis sagrei, an exotic invasive species in Taiwan, was studied to identify the emigration point of this lizard. A total of 5,757 helminths was found, of which 5,734 (99.6%) were the nematode Cyrtosomum penneri. Also found were the digenean Mesocoelium monas (21, 0.4%) and one each of the nematodes Parapharyngodon sp. (female) and Acuariidae gen. sp. (larva). Cyrtosomum penneri has previously been reported in A. sagrei in Florida, supporting the contention that the Taiwan population of A. sagrei originated from Florida. This report provides a basis upon which future A. sagrei parasite studies in Taiwan can be based, and a helminth list for A. sagrei is included for future reference

Population genetics of a lethally managed medium-sized predator

Globally, levels of human–wildlife conflict are increasing as a direct consequence of the expansion of people into natural areas resulting in competition with wildlife for food and other resources. By being forced into increasingly smaller pockets of suitable habitat, many animal species are at risk of becoming susceptible to loss of genetic diversity, inbreeding depression and the associated inability to adapt to environmental changes. Predators are often lethally controlled due to their threat to livestock. Predators such as jackals (black backed, golden and side striped; Canis mesomelas, C. aureus and C. adustus, respectively), red foxes (Vulpes vulpes) and coyotes (C. latrans) are highly adaptable and may respond to ongoing persecution through compensatory reproduction such as reproducing at a younger age, producing larger litters and/or compensatory immigration including dispersal into vacant territories. Despite decades of lethal management, jackals are problematic predators of livestock in South Africa and, although considered a temporary measure, culling of jackals is still common. Culling may affect social groups, kinship structure, reproductive strategies and sex-biased dispersal in this species. Here, we investigated genetic structure, variation and relatedness of 178 culled jackals on private small-livestock farms in the central Karoo of South Africa using 13 microsatellites. Genetic variation was moderate to high and was similar per year and per farm. An absence of genetic differentiation was observed based on STRUCTURE, principal component analysis and AMOVA. Relatedness was significantly higher within farms (r = 0.189) than between farms (r = 0.077), a result corroborated by spatial autocorrelation analysis. We documented 18 occurrences of dispersal events where full siblings were detected on different farms (range: 0.78–42.93 km). Distance between identified parent–offspring varied from 0 to 36.49 km. No evidence for sex-biased dispersal was found. Our results suggest that in response to ongoing lethal management, this population is most likely able to maintain genetic diversity through physiological and behavioural compensation mechanisms.APPENDIX S1. Supplementary methods.SUPPLEMENTARY TABLES. TABLE S1. Primer details for microsatellite loci used to genotype black-backed jackals (Canis Mesomelas). TABLE S2. Per-locus summary statistics as calculated in Cervus v3.0.7. The non-exclusion probabilities and combined non-exclusion probabilities (final row, italics) are relevant indicators of the power of the loci for parentage and sibship analyses. TABLE S3. Summary statistics for 20 sampling localities (farms) with >1 sample and for all farms pooled. Produced using the basicStats command of the diveRsity package v1.9.90 in R v3.6.2 and RStudio v1.2.5033. Standard deviation was calculated across loci in Microsoft Excel (stdev.s). Sampling localities with only one sample are not shown. TABLE S4. Summary statistics per year and for all years pooled. Produced using the basicStats command of the diveRsity package v1.9.90 in R v3.6.2 and RStudio v1.2.5033. Standard deviation was calculated across loci in Microsoft Excel (STDEV.S). TABLE S5. Pairwise FST values between farms with the full dataset (below diagonal) and associated significance at a level of 0.05 (above diagonal), where significant values are indicated by a “+” and non-significant values by a “−”. Calculated in Arlequin 3.5.2.2. TABLE S6. Pairwise FST values between farms with relatives removed (below diagonal) and associated significance at a level of 0.05 (above diagonal), where significant values are indicated by a “+” and non-significant values by a “−”. Calculated in Arlequin 3.5.2.2. TABLE S7. Comparison of mean pairwise relatedness (r) between years and mean individual inbreeding coefficients (F) between years. P-values for the Wilcoxon tests for difference in means are shown on the inside of the table (bordered by grey), with P-values for inbreeding comparisons shown below the diagonal (bottom left) and P-values for relatedness comparisons shown above the diagonal (top right). The mean F for each year is shown in the left-most column “outside” the main table, with the mean r for each year shown in the top row “outside” the main table. The numbers in parentheses after each year are the number of observations/data points for that year (number of samples for F and number of pairwise relatedness comparisons for r).SUPPLEMENTARY FIGURES. FIGURE S1. STRUCTURE HARVESTER results for (a) Delta K values and (b) probability (-LnPr) of K = 1–27 averaged over 20 runs and (c) genetic differentiation between the jackal sample locations (farms) based on STRUCTURE analysis (performed with K = 2–6) of 1 = GV, 2 = BB, 3 = BR, 4 = BD, 5 = DS, 6 = GG, 7 = HK, 8 = KD, 9 = KW, 10 = KK, 11 = KT, 12 = NG, 13 = ND, 14 = OG, 15 = RV, 16 = RE, 17 = RT, 18 = RD, 19 = SG, 20 = SK, 21 = VR, 22 = WK, 23 = CL, 24 = KR, 25 = WB and 26 = TD. FIGURE S2. STRUCTURE HARVESTER results for (a) Delta K values and (b) probability (-LnPr) of K = 1–27 averaged over 20 runs and (c) genetic differentiation between the jackal sample locations (farms) based on STRUCTURE analysis (performed with K = 2–6 and K = 14) of 1 = GV, 2 = BB, 3 = BD, 4 = DS, 5 = GG, 6 = HK, 7 = KW, 8 = KT, 9 = NG, 10 = ND, 11 = OG, 12 = RV, 13 = RE, 14 = RD, 15 = SG, 16 = SK, 17 = VR, 18 = WK and 19 = CL. After removing relatives, some localities had no samples, hence fewer sampling localities as compared to the full dataset. Note: The Evanno method (DeltaK) does not evaluate K = 1. FIGURE S3. Principal component analysis (PCA) of the different jackal sampling locations (farms) with related individuals removed. FIGURE S4. Plot comparing the relatedness estimates using six estimators and simulated individuals of known relatedness. Di, Dyadic likelihood estimator “DyadML”; LL, Lynch-Li estimator; LR, Lynch and Ritland estimator; QG, Queller and Goodnight estimator; Tri, Triadic likelihood estimator “TrioML”; W, Wang estimator. Plot produced with ggplot2 3.3.0 (Wickham, 2016). FIGURE S5. Results of the spatial autocorrelation analysis for A females and B males. The blue line indicates the autocorrelation coefficient of the data, with the 95% confidence interval at each distance class indicated by the black error bars, as determined by 1000 bootstrap resampling replicates. The red dashed lines indicate the 95% confidence interval around the null hypothesis (no spatial structure, i.e. rauto = 0), as determined by permutation (999 steps). Thus, if the error bars around the blue line do not overlap with the red dashed lines in a distance class, then genotypes were more (positive rauto) or less (negative rauto) similar than expected under the null hypothesis in that distance class. Such cases are indicated with an asterisk (*).The National Zoological Gardens, Pretoria and the University of South Africa.https://zslpublications.onlinelibrary.wiley.com/journal/14697998hj2023BiochemistryGeneticsMicrobiology and Plant Patholog

The Known Distribution of an Invasive Lizard, the Brown Anole (Anolis sagrei Duméril & Bibron, 1837), in Taiwan

The Brown Anole (Anolis sagrei) has become an invasive species in some parts of the Americas and in some localities in the Pacific region. In Taiwan A. sagrei was recorded for the first time in 2000 in Santzepu, southwestern Taiwan, and was subsequently recorded in Chisintang, eastern Taiwan, during 2006. For future monitoring and research, we describe the known distribution of A. sagrei in Taiwan by plotting GPS coordinates of localities where A. sagrei was observed during surveys (conducted on an ad hoc basis since this species was first discovered in Taiwan) or where specimens have been collected on GIS User Community aerial photographs that were divided into 100 x 100-m grids. We recorded this invasive lizard in southwestern Taiwan in an area spanning approximately 237 ha and in an approximately 8-ha area in eastern Taiwan. Since A. sagrei is easily spread by human activities, and because not all areas could be thoroughly surveyed, we conclude that the current actual distribution of A. sagrei in Taiwan is probably more extensive than shown. We believe that the eradication of A. sagrei in Taiwan through removal is unrealistic, and propose that ongoing efforts should focus on managing this species

Brown hyena habitat selection varies among sites in a semi-arid region of southern Africa

In the last 50 years, the human impact on ecosystems has been greater than during any other time period in human history (Millennium Ecosystem Assessment 2003). Large carnivores face anthropogenic threats worldwide, specifically persecution, habitat degradation, and habitat fragmentation (Everatt et al. 2014; Groom et al. 2014; Ripple et al. 2014; Wolfe et al. 2015). Because large carnivores often occupy high trophic levels, their presence influences species at lower levels through trophic cascades (Ripple et al. 2014). Natural experiments, taking advantage of large carnivore management, have shown that large predators provide fundamental ecosystem and economic services that help maintain healthy and diverse ecosystems (Ripple et al. 2014). Additionally, carnivores play an important role in other ecosystem processes, for example, scavenging carnivores may provide regulatory services, such as waste removal, nutrient cycling, and disease regulation. Such services add stability to ecosystems and ensure energy flow through multiple trophic levels (DeVault et al. 2003; Wilson and Wolkovich 2011)

Accelerating cryoprotectant diffusion kinetics improves cryopreservation of pancreatic islets

Funder: W. D. Armstrong Fund (School of Technology, University of Cambridge)Abstract: Cryopreservation offers the potential to increase the availability of pancreatic islets for treatment of diabetic patients. However, current protocols, which use dimethyl sulfoxide (DMSO), lead to poor cryosurvival of islets. We demonstrate that equilibration of mouse islets with small molecules in aqueous solutions can be accelerated from > 24 to 6 h by increasing incubation temperature to 37 °C. We utilize this finding to demonstrate that current viability staining protocols are inaccurate and to develop a novel cryopreservation method combining DMSO with trehalose pre-incubation to achieve improved cryosurvival. This protocol resulted in improved ATP/ADP ratios and peptide secretion from β-cells, preserved cAMP response, and a gene expression profile consistent with improved cryoprotection. Our findings have potential to increase the availability of islets for transplantation and to inform the design of cryopreservation protocols for other multicellular aggregates, including organoids and bioengineered tissues

Evaluation of a Theory-Informed Implementation Intervention for the Management of Acute Low Back Pain in General Medical Practice: The IMPLEMENT Cluster Randomised Trial

Introduction: This cluster randomised trial evaluated an intervention to decrease x-ray referrals and increase giving advice to stay active for people with acute low back pain (LBP) in general practice. Methods: General practices were randomised to either access to a guideline for acute LBP (control) or facilitated interactive workshops (intervention). We measured behavioural predictors (e.g. knowledge, attitudes and intentions) and fear avoidance beliefs. We were unable to recruit sufficient patients to measure our original primary outcomes so we introduced other outcomes measured at the general practitioner (GP) level: behavioural simulation (clinical decision about vignettes) and rates of x-ray and CT-scan (medical administrative data). All those not involved in the delivery of the intervention were blinded to allocation. Results: 47 practices (53 GPs) were randomised to the control and 45 practices (59 GPs) to the intervention. The number of GPs available for analysis at 12 months varied by outcome due to missing confounder information; a minimum of 38 GPs were available from the intervention group, and a minimum of 40 GPs from the control group. For the behavioural constructs, although effect estimates were small, the intervention group GPs had greater intention of practising consistent with the guideline for the clinical behaviour of x-ray referral. For behavioural simulation, intervention group GPs were more likely to adhere to guideline recommendations about x-ray (OR 1.76, 95%CI 1.01, 3.05) and more likely to give advice to stay active (OR 4.49, 95%CI 1.90 to 10.60). Imaging referral was not statistically significantly different between groups and the potential importance of effects was unclear; rate ratio 0.87 (95%CI 0.68, 1.10) for x-ray or CT-scan. Conclusions: The intervention led to small changes in GP intention to practice in a manner that is consistent with an evidence-based guideline, but it did not result in statistically significant changes in actual behaviour. Trial Registration: Australian New Zealand Clinical Trials Registry ACTRN01260600009853

Early ultrasound surveillance of newly-created haemodialysis arteriovenous fistula

IntroductionWe assess if ultrasound surveillance of newly-created arteriovenous fistulas (AVFs) can predict nonmaturation sufficiently reliably to justify randomized controlled trial (RCT) evaluation of ultrasound-directed salvage intervention.MethodsConsenting adults underwent blinded fortnightly ultrasound scanning of their AVF after creation, with scan characteristics that predicted AVF nonmaturation identified by logistic regression modeling.ResultsOf 333 AVFs created, 65.8% matured by 10 weeks. Serial scanning revealed that maturation occurred rapidly, whereas consistently lower fistula flow rates and venous diameters were observed in those that did not mature. Wrist and elbow AVF nonmaturation could be optimally modeled from week 4 ultrasound parameters alone, but with only moderate positive predictive values (PPVs) (wrist, 60.6% [95% confidence interval, CI: 43.9–77.3]; elbow, 66.7% [48.9–84.4]). Moreover, 40 (70.2%) of the 57 AVFs that thrombosed by week 10 had already failed by the week 4 scan, thus limiting the potential of salvage procedures initiated by that scan’s findings to alter overall maturation rates. Modeling of the early ultrasound characteristics could also predict primary patency failure at 6 months; however, that model performed poorly at predicting assisted primary failure (those AVFs that failed despite a salvage attempt), partly because patency of at-risk AVFs was maintained by successful salvage performed without recourse to the early scan data.ConclusionEarly ultrasound surveillance may predict fistula maturation, but is likely, at best, to result in only very modest improvements in fistula patency. Power calculations suggest that an impractically large number of participants (>1700) would be required for formal RCT evaluation

Multigene phylogeny of the Mustelidae: Resolving relationships, tempo and biogeographic history of a mammalian adaptive radiation

<p>Abstract</p> <p>Background</p> <p>Adaptive radiation, the evolution of ecological and phenotypic diversity from a common ancestor, is a central concept in evolutionary biology and characterizes the evolutionary histories of many groups of organisms. One such group is the Mustelidae, the most species-rich family within the mammalian order Carnivora, encompassing 59 species classified into 22 genera. Extant mustelids display extensive ecomorphological diversity, with different lineages having evolved into an array of adaptive zones, from fossorial badgers to semi-aquatic otters. Mustelids are also widely distributed, with multiple genera found on different continents. As with other groups that have undergone adaptive radiation, resolving the phylogenetic history of mustelids presents a number of challenges because ecomorphological convergence may potentially confound morphologically based phylogenetic inferences, and because adaptive radiations often include one or more periods of rapid cladogenesis that require a large amount of data to resolve.</p> <p>Results</p> <p>We constructed a nearly complete generic-level phylogeny of the Mustelidae using a data matrix comprising 22 gene segments (~12,000 base pairs) analyzed with maximum parsimony, maximum likelihood and Bayesian inference methods. We show that mustelids are consistently resolved with high nodal support into four major clades and three monotypic lineages. Using Bayesian dating techniques, we provide evidence that mustelids underwent two bursts of diversification that coincide with major paleoenvironmental and biotic changes that occurred during the Neogene and correspond with similar bursts of cladogenesis in other vertebrate groups. Biogeographical analyses indicate that most of the extant diversity of mustelids originated in Eurasia and mustelids have colonized Africa, North America and South America on multiple occasions.</p> <p>Conclusion</p> <p>Combined with information from the fossil record, our phylogenetic and dating analyses suggest that mustelid diversification may have been spurred by a combination of faunal turnover events and diversification at lower trophic levels, ultimately caused by climatically driven environmental changes. Our biogeographic analyses show Eurasia as the center of origin of mustelid diversity and that mustelids in Africa, North America and South America have been assembled over time largely via dispersal, which has important implications for understanding the ecology of mustelid communities.</p