scholarly journals Sex identification in embryos and adults of Darwin’s finches

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.

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.


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.


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.


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. 


Genetics ◽  
2000 ◽  
Vol 155 (4) ◽  
pp. 1757-1772 ◽  
Author(s):  
Scott L Page ◽  
Kim S McKim ◽  
Benjamin Deneen ◽  
Tajia L Van Hook ◽  
R Scott Hawley

Abstract We present the cloning and characterization of mei-P26, a novel P-element-induced exchange-defective female meiotic mutant in Drosophila melanogaster. Meiotic exchange in females homozygous for mei-P261 is reduced in a polar fashion, such that distal chromosomal regions are the most severely affected. Additional alleles generated by duplication of the P element reveal that mei-P26 is also necessary for germline differentiation in both females and males. To further assess the role of mei-P26 in germline differentiation, we tested double mutant combinations of mei-P26 and bag-of-marbles (bam), a gene necessary for the control of germline differentiation and proliferation in both sexes. A null mutation at the bam locus was found to act as a dominant enhancer of mei-P26 in both males and females. Interestingly, meiotic exchange in mei-P261; bamΔ86/+ females is also severely decreased in comparison to mei-P261 homozygotes, indicating that bam affects the meiotic phenotype as well. These data suggest that the pathways controlling germline differentiation and meiotic exchange are related and that factors involved in the mitotic divisions of the germline may regulate meiotic recombination.


Diversity ◽  
2021 ◽  
Vol 13 (4) ◽  
pp. 147
Author(s):  
Mariana Villegas ◽  
Catherine Soos ◽  
Gustavo Jiménez-Uzcátegui ◽  
Shukri Matan ◽  
Keith A. Hobson

Darwin’s finches are a classic example of adaptive radiation involving differential use of dietary resources among sympatric species. Here, we apply stable isotope (δ13C, δ15N, and δ2H) analyses of feathers to examine ecological segregation among eight Darwin’s finch species in Santa Cruz Island, Galápagos collected from live birds and museum specimens (1962–2019). We found that δ13C values were higher for the granivorous and herbivorous foraging guilds, and lower for the insectivorous finches. Values of δ15N were similar among foraging guilds but values of δ2H were higher for insectivores, followed by granivores, and lowest for herbivores. The herbivorous guild generally occupied the largest isotopic standard ellipse areas for all isotopic combinations and the insectivorous guild the smallest. Values of δ2H provided better trophic discrimination than those of δ15N possibly due to confounding influences of agricultural inputs of nitrogen. Segregation among guilds was enhanced by portraying guilds in three-dimensional isotope (δ13C, δ15N, and δ2H) space. Values of δ13C and δ15N were higher for feathers of museum specimens than for live birds. We provide evidence that Darwin’s finches on Santa Cruz Island tend to be generalists with overlapping isotopic niches and suggest that dietary overlap may also be more considerable than previously thought.


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