Mortality patterns in a protected population of isards (Rupicapra pyrenaica)

2001 ◽  
Vol 79 (11) ◽  
pp. 2072-2079 ◽  
Author(s):  
Georges Gonzalez ◽  
Jean-Paul Crampe

We considered variation in mortality over 8 years in a protected population of isards (Pyrenean chamois; Rupicapra pyrenaica) within the Pyrenean National Park using monthly systematic skull collection. After testing the stationary-type pattern of estimates of mortality of the living population, we (i) analysed the composition of a sample of dead animals in terms of age and sex; (ii) investigated temporal patterns of mortality and their relationship with winter severity; (iii) tested for sexual differences in mortality rates in this weakly sexually dimorphic species. Of 588 animals found dead from natural causes, 114 were kids (19.4%). No statistical differences existed in the composition of the sample according to sex (the ratio of males to females was 1/1.13). Age at death did not differ significantly between the sexes or among years. A positive relationship was found between winter severity (expressed as cumulative snowfall) and mortality rates for both kids and adults. During mild winters, the mortality rate was low (a mean of 38.4 carcasses per year versus 124 per year in severe winters) and was concentrated on the oldest animals, mainly males. Based on 303 skulls more than 1 year old, annual survivorship curves revealed a period of low mortality (prime age) extending to 9 and 10 years of age for males and females, respectively, followed by a period of increasing mortality (senescence). Our results are commented on in light of recent publications on the demography of populations of large herbivores.

PLoS ONE ◽  
2021 ◽  
Vol 16 (3) ◽  
pp. e0237687
Author(s):  
Mariya P. Dobreva ◽  
Joshua G. Lynton-Jenkins ◽  
Jaime A. Chaves ◽  
Masayoshi Tokita ◽  
Camille Bonneaud ◽  
...  

Darwin’s finches are an iconic example of adaptive radiation and evolution under natural selection. Comparative genetic studies using embryos of Darwin’s finches have shed light on the possible evolutionary processes underlying the speciation of this clade. Molecular identification of the sex of embryonic samples is important for such studies, where this information often cannot be inferred otherwise. We tested a fast and simple chicken embryo protocol to extract DNA from Darwin’s finch embryos. In addition, we applied minor modifications to two of the previously reported PCR primer sets for CHD1, a gene used for sexing adult passerine birds. The sex of all 29 tested embryos of six species of Darwin’s finches was determined successfully by PCR, using both primer sets. Next to embryos, hatchlings and fledglings are also impossible to distinguish visually. This extends to juveniles of sexually dimorphic species which are yet to moult in adult-like plumage and beak colouration. Furthermore, four species of Darwin’s finches are monomorphic, males and females looking alike. Therefore, sex assessment in the field can be a source of error, especially with respect to juveniles and mature monomorphic birds outside of the mating season. We caught 567 juveniles and adults belonging to six species of Darwin’s finches and only 44% had unambiguous sex-specific morphology. We sexed 363 birds by PCR: individuals sexed based on marginal sex specific morphological traits; and birds which were impossible to classify in the field. PCR revealed that for birds with marginal sex specific traits, sexing in the field produced a 13% error rate. This demonstrates that PCR based sexing can improve field studies on Darwin’s finches, especially when individuals with unclear sex-related morphology are involved. The protocols used here provide an easy and reliable way to sex Darwin’s finches throughout ontogeny, from embryos to adults.


2002 ◽  
Vol 80 (8) ◽  
pp. 1437-1441 ◽  
Author(s):  
P Neuhaus ◽  
K E Ruckstuhl

Animals that differ in reproductive status and body size have different needs in terms of foraging and resting. In most social ungulates this leads to sexual segregation, probably because of incompatibilities between the activity budgets of males and females. Since most studies on behavioural differences between the sexes have been done on sexually dimorphic species, we decided to look at a system in which males and females are similar in body size. We studied time budgets, synchrony of behaviour, and bite rates of plains zebras (Equus burchelli) to evaluate the factors that enable these extremely social ungulates to stay in stable mixed-sex family groups throughout the year. As we predicted, time budgets were similar among males, lactating females, pregnant females, and non-reproductive females. Furthermore, we observed close synchronization of behaviours between females that differed in reproductive status and males. Lactating females, however, did take more bites per minute when foraging than either pregnant or non-reproducing females or males. We assume that the higher bite rates of lactating females were due to the extra costs of producing milk for their foal. We concluded that the special harem mating system, and for females the year-round possibility of conceiving, force the animals to synchronize their time budgets, which might be a major reason for the lack of difference in body size between males and females.


2020 ◽  
Author(s):  
Mariya P. Dobreva ◽  
Joshua G. Lynton-Jenkins ◽  
Jaime A. Chaves ◽  
Masayoshi Tokita ◽  
Camille Bonneaud ◽  
...  

AbstractDarwin’s finches, endemic to the Galapagos and Cocos islands, are an iconic example of adaptive radiation and evolution under natural selection. Comparative genetic studies using embryos of Darwin’s finches have shed light on the possible evolutionary processes underlying the speciation of this clade. Molecular identification of the sex of embryonic samples is important for such studies, where this information often cannot be inferred otherwise. We tested a fast and simple chicken embryo protocol for extraction of genomic DNA on Darwin’s finch embryos. In addition, we suggest modifications to two of the previously reported PCR primer sets for CHD1, a gene used for sexing in adult passerine birds. The sex of all 29 tested embryos of six species of Darwin’s finches was determined successfully by PCR, using both primer sets. Hatchlings/nestlings and fledglings are also impossible to distinguish visually. This includes juveniles of sexually dimorphic species which are yet to moult in adult-like plumage and beak colouration. Furthermore, four species of Darwin’s finches are monomorphic, males and females looking alike. Therefore, sex assessment in the field can be a source of error, especially with respect to juveniles and mature monomorphic birds outside of the mating season. We caught 567 juveniles and adults belonging to six species of Darwin’s finches and only 44% had unambiguous sex-specific morphology. We sexed 363 birds by PCR, including individuals sexed based on marginal sex specific morphological traits (N=278) and birds which were impossible to classify in the field (N=39). For birds with marginal sex specific traits, PCR results revealed a 13% sexing error rate. This demonstrates that PCR based sexing can improve field studies on Darwin’s finches, especially when individuals with unclear sex-related morphology are involved. The protocols used here provide an easy and reliable way to sex Darwin’s finches throughout ontogeny, from embryos to adults.


Zootaxa ◽  
2017 ◽  
Vol 4237 (3) ◽  
pp. 583
Author(s):  
TAKUJI TACHI

Sexual dimorphism is a phenomenon in which the male and female of a species differ in features of the external morphology such as size, shape, colour, or the development of appendages. In the Diptera, stalked compound eyes, leg modifications and wing patterns are well-known examples of sexual dimorphism (McAlpine 1979; Zeil 1983; Adler & Adler 1991; Meyerrochow & Reid 1994; Wilkinson & Dodson 1996; Sivinski 1997; Baker & Wilkinson 2001; Eberhard 2002; Puniamoorthy et al. 2008). Males and females of sexually dimorphic species are often described as separate species due to the dissimilarity in external characters, thus leading to problems in identification and proper association of the sexes. In contrast to characters that are usually involved in sexual dimorphism, leg chaetotaxy is considered one of the invariable character systems, irrespective of sex, in the tribe Siphonini of the Tachinidae, and is thus widely used in keys to genera and species (O’Hara 1989; Andersen 1996). Species’ identification by DNA barcoding has been used in various groups of organisms (Hebert et al. 2003; Ratnasingham & Hebert 2013). In insects, males, usually more easily identified by morphological characters (e.g., postabdominal features) than females, are often used for barcoding. The identification of females will improve as sequence data accumulate, such as data from pairs collected in copula. In this paper, I describe sexual dimorphism in the Japanese endemic species of tachinid fly Ceromya glaucescens Tachi & Shima, 2000 of the tribe Siphonini, and use molecular and morphological data for the identification of this species. Sequence data of C. silacea (Meigen, 1824) are also included for comparison. 


2002 ◽  
Vol 80 (9) ◽  
pp. 1578-1583 ◽  
Author(s):  
Christopher P Yourth ◽  
Mark R Forbes ◽  
Robert L Baker

A few studies have shown that male and female invertebrates differ in immunity and that these differences appear related to differences in sexual dimorphism and gender differences in life histories. Melanotic encapsulation of foreign objects in insects is one form of immunity. The damselfly Lestes forcipatus Rambur is moderately sexually dimorphic, and much is known about patterns of mass gain in congeners relating to differences in life history between males and females. In this study, females were more immunoresponsive than males under controlled temperatures, following emergence, and at a time when parasitic mites were challenging these hosts. However, males and females that overlapped in mass at emergence did not differ in their immune responses. Males in better condition at emergence were more immunoresponsive than lighter males, but this relation was not found in females. Sex differences in immune expression may have implications for how females versus males are able to deal with challenges from parasites, under varying environmental conditions.


2021 ◽  
Author(s):  
Thomas E White ◽  
Amy Locke ◽  
Tanya Latty

Abstract Structurally coloured sexual signals are a conspicuous and widespread class of ornament used in mate choice, though the extent to which they encode information on the quality of their bearers is not fully resolved. Theory predicts that signalling traits under strong sexual selection as honest indicators should evolve to be more developmentally integrated and exaggerated than nonsexual traits, thereby leading to heightened condition dependence. Here we test this prediction through examination of the sexually dimorphic faces and wings of the cursorial fly Lispe cana. Males and females possess structural UV-white and golden faces, respectively, and males present their faces and wings to females during close-range, ground-based courtship displays, thereby creating the opportunity for mutual inspection. Across a field-collected sample of individuals, we found that the appearance of the faces of both sexes scaled positively with individual condition, though along separate axes. Males in better condition expressed brighter faces as modelled according to conspecific flies, whereas condition scaled with facial saturation in females. We found no such relationships for their wing interference pattern nor abdomens, with the latter included as a nonsexual control. Our results suggest that the structurally coloured faces, but not the iridescent wings, of male and female Lispe cana are reliable guides to individual quality and support the broader potential for structural colours as honest signals. They also highlight the potential for mutual mate choice in this system, while arguing for one of several alternate signalling roles for wing interferences patterns among the myriad taxa which bear them.


Author(s):  
Mary Jane West-Eberhard

Distinctive male and female traits are perhaps the most familiar of all divergent specializations within species. In cross-sexual transfer, discrete traits that are expressed exclusively in one sex in an ancestral species appear in the opposite sex of descendants. An example is the expression of brood care by males in a lineage where ancestral females are the exclusive caretakers of the young, as in some voles (Thomas and Birney, 1979). Despite the prominence of sexual dimorphism and sex reversals in nature, and an early explicit treatment by Darwin, discussed in the next section, cross-sexual transfer is not often recognized as a major factor in the evolution of novelty (but see, on animals, Mayr, 1963, pp. 435-439; Mayr, 1970, p. 254; on plants, Iltis, 1983). When more widely investigated, cross-sexual transfer may prove to rival heterochrony and duplication as an important source of novelties in sexually dimorphic lineages. For this reason, I devote more attention here to cross-sexual transfer than to these other, well-established general patterns of change. The male and female of a sexually dimorphic species may be so different that it is easy to forget that each individual carries most or all of the genes necessary to produce the phenotype of the opposite sex. Sex determination, like caste determination and other switches between alternative phenotypes, depends on only a few genetic loci or, in many species, environmental factors (Bull, 1983). There is considerable flexibility in sex determination and facultative reversal in some taxa. Among fish, for example, there is even a species wherein sex is determined by juvenile size at a critical age (Francis and Barlow, 1993). The sex determination mechanism, whatever its nature, leads to a series of sex-limited responses, often coordinated by hormones and not necessarily all occurring at once. A distinguishing aspect of sexually dimorphic traits in adults is that there is often a close homology between the secondary sexual traits that are differently modified in the two sexes.


Author(s):  
Daniel Enrique Rodriguez Bauza ◽  
Patricia Silveyra

Exercise-induced bronchoconstriction (EIB) is a common complication of athletes and individuals who exercise regularly. It is estimated that about 90% of patients with underlying asthma (a sexually dimorphic disease) experience EIB; however, sex differences in EIB have not been studied extensively. With the goal of better understanding the prevalence of EIB in males and females, and because atopy has been reported to occur at higher rates in athletes, in this study, we investigated sex differences in EIB and atopy in athletes. A systematic literature review identified 60 studies evaluating EIB and/or atopy in post-pubertal adult athletes (n = 7501). Collectively, these studies reported: (1) a 23% prevalence of EIB in athletes; (2) a higher prevalence of atopy in male vs. female athletes; (3) a higher prevalence of atopy in athletes with EIB; (4) a significantly higher rate of atopic EIB in male vs. female athletes. Our analysis indicates that the physiological changes that occur during exercise may differentially affect male and female athletes, and suggest an interaction between male sex, exercise, and atopic status in the course of EIB. Understanding these sex differences is important to provide personalized management plans to athletes with underlying asthma and/or atopy.


Author(s):  
Tatiana Sella Tunis ◽  
Israel Hershkovitz ◽  
Hila May ◽  
Alexander Dan Vardimon ◽  
Rachel Sarig ◽  
...  

The chin is a unique anatomical landmark of modern humans. Its size and shape play an important role from the esthetic perspective. However, disagreement exists in the dental and anthropological literature regarding the sex differences in chin and symphysis morphometrics. The “sexual selection” theory is presented as a possible reason for chin formation in our species; however, many other contradictory theories also exist. This study’s aims were therefore to determine how chin and symphysis size and shape vary with sex, and to discuss “sexual selection” theory as a reason for its formation. Head and neck computed tomography (CT) scans of 419 adults were utilized to measure chin and symphysis sizes and shapes. The chin and symphysis measures were compared between the sexes using an independent-samples t-test, a Mann–Whitney test, and the F-statistic. The chin width was significantly greater in males than in females (p < 0.001), whereas the chin height, area, and size index were significantly greater in females (p < 0.001). Symphysis measures did not differ significantly between the sexes. Size accounted for 2–14% of the chin variance and between 24–33% of the symphysis variance. Overall, the chin was found to be a more heterogeneous anatomical structure than the symphysis, as well as more sexually dimorphic.


The Auk ◽  
1984 ◽  
Vol 101 (3) ◽  
pp. 551-555 ◽  
Author(s):  
Patrick J. Weatherhead ◽  
Drew J. Hoysak

Abstract Observations of the behavior of roosting male Red-winged Blackbirds (Agelaius phoeniceus) indicated that after hatching year (AHY) males were dominant over hatching year (HY) males. This dominance resulted in AHY males occupying central roost positions in dense vegetation and HY males occupying edge positions in sparse vegetation. Overall, the birds preferred positions over deep water, although the edge positions of HY males were over deeper water than were the positions of AHY males. These results are consistent with the two-strategies roosting hypothesis (Weatherhead 1983), in that the dominance of older males allows them access to roost positions with relatively low vulnerability to predation. In this study, these positions also appeared to be microclimatically superior. These results also suggest that the bright plumage of adult males of sexually dimorphic species may be advantageous in some nonbreeding situations in addition to their more commonly recognized role in reproduction.


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