Academic literature on the topic 'Sexually monomorphic birds'

Background and Aim: Many avian species are considered sexually monomorphic. In monomorphic bird species, especially in young birds, sex is difficult to identify based on an analysis of their external morphology. Accurate sex identification is essential for avian captive breeding and evolutionary studies. Methods with varying degrees of invasiveness such as vent sexing, laparoscopic surgery, steroid sexing, and chromosome inspection (karyotyping) are used for sex identification in monomorphic birds. This study aimed to assess the utility of a non-invasive molecular marker for gender identification in a variety of captive monomorphic birds, as a strategy for conservation. Materials and Methods: DNA was isolated from feather samples from 52 individuals representing 16 species of 11 families indigenous to both Indonesia and elsewhere. We amplified the chromodomain helicase DNA-binding (CHD) gene using polymerase chain reaction with MP, NP, and PF primers to amplify introns with lengths that differ between the CHD-W and the CHD-Z genes, allowing sex discrimination because the W chromosome is exclusively present in females. Results: Molecular bird sexing confirmed 33 females and 19 males with 100% accuracy. We used sequencing followed by alignment on one protected bird species (Probosciger aterrimus). Conclusion: Sex identification may be accomplished noninvasively in birds, because males only have Z sex chromosomes, whereas females have both Z and W chromosomes. Consequently, the presence of a W-unique DNA sequence identifies an individual as female. Sexing of birds is vital for scientific research, and to increase the success rate of conservation breeding programs.

The Hooded Plover Thinornis rubricollis is a threatened, sexually monomorphic wading bird that occurs in two allopatric populations in eastern and western Australia. We used a PCR-based molecular sexing technique to sex captured birds from both populations. We found 69% of adults captured at a salt-lake in Western Australia were male. We tested for a sex-bias in our trapping technique by examining the sex-ratio of eastern birds captured under circumstances analogous to the western capture operation. No sex-bias in the trapping technique was apparent although the sample size was low. This suggests that the male-bias at the lake was real. Any spatial or habitat-related segregation of the sexes must be investigated before we can conclude that the bias is a trait of the western population. If the bias occurs in the population as a whole, then the effective size of the breeding population will be less than that indicated by counts. If the sexes segregate to different sites or habitats, then spatially constrained threatening processes may lead to a skewed sex-ratio.

Telomeres are noncoding genetic repeats protecting the ends of linear chromosomes. Long telomeres are often associated with high individual survival, and interindividual variation in telomere length has recently been proposed as a proxy for individual quality. Therefore, one might expect individuals of either sex with long telomeres to be of higher intrinsic quality and to be preferred in the context of mate choice. Thus, in sexually monomorphic species where individuals discriminate mates on the basis of signals of intrinsic quality, mate choice should lead to assortative pairing by telomere length, and it should be associated with breeding performance. We tested these two predictions in the King Penguin (Aptenodytes patagonicus J.F. Miller, 1778), a sexually monomorphic seabird. Over 3 years of study and 73 penguin pairs under contrasting environmental conditions, we found strong assortative pairing by telomere length. Interestingly, only female telomere length was positively associated to chick survival up to fledging, and this relationship was only apparent when foraging conditions at sea were average. The positive link between telomere length and breeding success confirmed that telomere length is somehow related to individual biological state at a given time. The proximate mechanisms by which birds assess individual state related to telomere length remain to be discovered.

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.

Abstract We studied the intraspecific territorial defense behavior of wintering Willow Flycatchers (Empidonax traillii) in Costa Rica using a randomized playback experiment that exposed male and female birds to recordings of Willow Flycatcher songs and calls, Lesser Ground Cuckoo (Morococcyx erythropygius) vocalizations, and random noise. Flycatchers of both sexes responded most strongly to simulated conspecific territory intrusion, and the agonistic behaviors that we observed were similar to those seen during natural intraspecific encounters in winter. Both males and females engaged in song and aggressive behaviors in defense of territories, and there was no significant difference between the sexes in scored agonistic responses. The similarity between the sexes in intraspecific territorial defense behaviors and aggressiveness may account for both sexes of flycatchers using the same habitats at our study sites in Costa Rica, and wintering females defending territories against males. The Willow Flycatcher, a sexually monomorphic species, differs in this way from a number of sexually dimorphic passerines, in which behaviorally dominant males occur in more optimal winter habitats.

Avian plumage traits are the targets of both natural and sexual selection. Consequently, genetic changes resulting in plumage variation among closely related taxa might represent important evolutionary events. The molecular basis of such differences, however, is unknown in most cases. Sequence variation in the melanocortin-1 receptor gene ( MC1R ) is associated with melanistic phenotypes in many vertebrate taxa, including several avian species. The blue-crowned manakin ( Lepidothrix coronata ), a widespread, sexually dichromatic passerine, exhibits striking geographic variation in male plumage colour across its range in southern Central America and western Amazonia. Northern males are black with brilliant blue crowns whereas southern males are green with lighter blue crowns. We sequenced 810 bp of the MC1R coding region in 23 individuals spanning the range of male plumage variation. The only variable sites we detected among L. coronata sequences were four synonymous substitutions, none of which were strictly associated with either plumage type. Similarly, comparative analyses showed that L. coronata sequences were monomorphic at the three amino acid sites hypothesized to be functionally important in other birds. These results demonstrate that genes other than MC1R underlie melanic plumage polymorphism in blue-crowned manakins.

AbstractSexual imprinting is one of several known non - genetical, yet social factors which influence mate preferences and might play a role in the evolution of novel traits. We introduced a red bill as a novel trait in a monomorphic estrildid finch, the Javanese mannikin Lonchura leucogastroides. We established three different imprinting groups in which the father only, the mother only or none of the parents had a red bill. After reaching maturity we tested the offspring in double choice tests for a response to birds of the opposite sex with a naturally coloured black bill or with an artificially coloured red bill. Neither males nor females showed a preference for potential mates with a red bill. Males and females raised by a red bill father showed even a strong rejection to conspecifics of the opposite sex with a red bill. This is in contrast to a previous imprinting study in the Javanese mannikin under similar conditions (Witte et al., 2000) in which males and females became sexually imprinted on conspecifics adorned with a red feather on the forehead. It seems that not all kinds of novel traits birds can be sexually imprinted on. We could show in the present study that the red bill is a meaningful trait in female mate choice, i.e. females responded to males with and without a red bill in a similar way as do females imprinted on natural type parents to males with and without other artificial adornments (Witte & Curio, 1999). We could confirm an interaction between the red bill and the natural attractiveness of males as found in a previous study (Witte & Curio, 1999). Our study opens up questions about what traits are really learned and why some traits are not learned during imprinting.

Abstract Many seabirds are monomorphic and lack obvious ornamentation; thus the mechanisms and signaling systems that mediate mate choice can be elusive. We investigated the possibility that a unique characteristic of wing molt in most species of Sterna terns acts as a sexually selected indicator of fitness. Many terns replace a variable number of primaries and sometimes secondaries twice or occasionally three times each year. Some have suggested that this repeated wing molt may serve as an honest indicator of fitness in mutual mate choice. If this molt-signaling hypothesis is valid, one would expect there to be assortative mating with respect to the extent of repeated wing molt. We tested this prediction by examining 262 breeding pairs of Common Terns (Sterna hirundo) from colonies in Buzzards Bay, Massachusetts. Using banding records and plumage characters, we were often able to distinguish young birds making their first breeding attempt from older birds which may have maintained past pair bonds. We found evidence of assortative mating with respect to repeated wing molt in newly formed pairs, which supports the notion of wing molt as a sexually selected character. Muda del Ala y Apareamento Asociativo en Sterna hirundo: Una Prueba de la Hipótesis de la Muda-Señalización Resumen. Muchas aves marinas son monomórficas y no tienen ornamentaciones obvias; por tanto, los mecanismos y los sistemas de señales que media la selección de pareja son evasivos. Investigamos la posibilidad de que una característica única de la muda en la mayoría de las especies de charranes (Sterna spp.) funcione como un indicador de la aptitud sexualmente seleccionado. Muchos charranes substituyen un número variable de primarias y a veces de secundarias dos veces, u ocasionalmente tres veces, cada año. Algunos autores han sugerido que esta muda repetida podría servir como un indicador honesto de la aptitud durante la selección mutua de las parejas. Si esta hipótesis de la muda-señalización fuera válida, se esperaría que existiera apareamiento asociativo con respecto al grado de la muda repetida de las alas. Para poner a prueba esta predicción, examinamos 262 parejas reproductivas de Sterna hirundo, en colonias en la Bahía Buzzards, Massachusetts. Usando registros de anillamiento y caracteres del plumaje, pudimos distinguir con frecuencia los charranes jóvenes que hacían su primer intento de aparearse de los más viejos que pudieron haber mantenido enlaces con parejas anteriores. Encontramos evidencia de apareamento asociativo con respecto a la muda repetida de las alas en parejas nuevas, lo que apoya la noción de que la muda del ala sería un caracter seleccionado sexualmente.

Background The sex of an individual organism plays such an important role in its life cycle that researchers must know a bird’s sex to interpret key aspects of its biology. The sexes of dimorphic species can be easily distinguished, but sexing monomorphic bird species often requires expensive and time-consuming molecular methods. The Little Stint (Calidris minuta) is a numerous species, monomorphic in plumage but showing a small degree of reversed sexual size dimorphism. Females are larger than males but the ranges of their measurements overlap, making Little Stints difficult to sex in the field. Our aim was to develop reliable sexing criteria for Little Stints in different stages of primary moult during their stay on the non-breeding grounds in South Africa using DNA-sexed individuals and discriminant function analysis. Methods We caught 348 adult Little Stints in 2008–2016 on their non-breeding grounds at Barberspan Bird Sanctuary. To molecularly identify the birds’ sex we used P2/P8 primers and DNA isolated from blood samples collected in the field. We used Storer’s dimorphism index to assess the degree of sexual size dimorphism. Then we divided our sample into two groups: before or during and after primary moult. For each group we developed two functions: one using wing length only and the other a combination of morphometric features including wing, tarsus and total head length. Then we used a stepwise procedure to check which combination of measurements best discriminated sexes. To validate our result we used a jack-knife cross-validation procedure and Cohen-kappa statistics. Results All the morphometric features we measured were bigger in DNA-sexed females than in males. Birds with fresh primaries had on average 2.3 mm longer wings than those with worn primaries. A discriminant function using wing length (D1) correctly sexed 78.8% of individuals before moult, and a stepwise analysis showed that a combination of wing length and tarsus (D2) correctly identified the sex of 82.7% of these birds. For birds with freshly moulted primaries a function using wing length (D3) correctly classified 83.4% of the individuals, and a stepwise analysis revealed that wing and total head length (D4) classified 84.7%. Discussion Sexual size differences in Little Stints might be linked to their phylogenetics and breeding biology. Females are bigger, which increases their fecundity; males are smaller, which increases their manoeuverability during display flights and hence their mating success. Little Stints show an extreme lack of breeding site fidelity so we did not expect a geographical cline in their biometrics. Sexing criteria available for Little Stints in the literature were developed using museum specimens, which often shrink, leading to misclassification of live birds. The sexing criteria we developed can be used for studies on Little Stints at their non-breeding grounds and on past data, but should be applied cautiously because of the overlapping ranges.

Abstract Many species have evolved alternate phenotypes, thus enabling individuals to conditionally produce phenotypes that are favorable for reproductive success. Examples of this phenomenon include sexual dimorphism, alternative reproductive strategies, and social insect castes. While the evolutionary functions and developmental mechanisms of dimorphic phenotypes have been studied extensively, little attention has focused on the evolutionary covariance between each phenotype. We extend the conceptual framework and methods of morphological integration to hypothesize that dimorphic traits tend to be less integrated between sexes or social castes. In the case of social insects, we describe results from our recent study of an ant genus in which workers have major and minor worker castes that perform different behavioral repertoires in and around the nest. In the case of birds, we describe a new analysis of a family of songbirds that exhibits plumage coloration that can differ greatly between males and females, with apparently independent changes in each sex. Ant head shape, which is highly specialized in each worker caste, was weakly integrated between worker castes, whereas thorax shape, which is more monomorphic, was tightly integrated. Similarly, in birds, we found a negative association between dimorphism and the degree of integration between sexes. We also found that integration decreased in fairy wrens (Malurus) for many feather patches that evolved greater dichromatism. Together, this suggests that the process of evolving increased dimorphism results in a decrease in integration between sexes and social castes. We speculate that once a mechanism for dimorphism evolves, that mechanism can create independent variation in one sex or caste upon which selection may act.

Unambiguous gender identification (ID) is needed to assess parameters in studies of population dynamics, behavior, and evolutionary biology of Caribbean Flamingo (Phoenicopterus ruber ruber) and other birds. Due to its importance for management and conservation, molecular (DNA-based) avian gender ID assays targeting intron-size differences of the Chromosome Helicase ATPase DNA Binding (CHD) gene of males (CHD-Z) and females (CHD-W) have been developed. Male (ZZ) and female (WZ) genotypes are usually scored as size polymorphisms through agarose or acrylamide gels. For certain species, W-specific restriction sites or multiplex polymerase chain-reaction (PCR) involving CHD-W specific primers are needed. These approaches involve a minimum of three steps following DNA isolation: PCR, gel electrophoresis, and photo-documentation, which limit high throughput scoring and automation potential. In here, a short amplicon (SA) High-resolution Melting Analysis (HRMA) assay for avian gender ID is developed. SA-HRMA of an 81-Base Pair (bp) segment differentiates heteroduplex female (WZ) from homoduplex male (ZZ) genotypes by targeting Single-nucleotide Polymorphisms (SNPs) instead of intron-size differences between CHD-Z and CHD-W genes. To demonstrate the utility of the approach, the gender of Caribbean Flamingo (P. ruber ruber) (17 captive from the Dallas Zoo and 359 wild from Ria Lagartos, Yucatan, Mexico) was determined. The assay was also tested on specimens of Lesser Flamingo (P. minor), Chilean Flamingo (P. chilensis), Saddle-billed Stork (Ephippiorhynchus senegalensis), Scarlet Ibis (Eudocimus ruber), White-bellied Stork (Ciconia abdimii), Roseate Spoonbill (Platalea ajaja), Marabou Stork (Leptoptilos crumeniferus), Greater Roadrunner (Geococcyx californianus), and Attwater's Prairie Chicken (Tympanuchus cupido attwateri). Although the orthologous 81 bp segments of Z and W are highly conserved, sequence alignments with 50 avian species across 15 families revealed mismatches affecting one or more nucleotides within the SA-HRMA forward or reverse primers. Most mismatches were located along the CHD-Z gene that may generate heteroduplex curves and thus gender ID errors. For such cases, taxon and species-specific primer sets were designed. The SA-HRMA gender ID assay can be used in studies of avian ecology and behavior, to assess sex-associated demographics and migratory patterns, and as a proxy to determine the health of the flock and the degree by which conservation and captive breeding programs are functioning.