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ABSTRACT: The bird beak is mainly functioned as feeding and attacking, and its shape has extremely important significance for survival and reproduction. In chickens, since beak shape could lead to some disadvantages including pecking and waste of feed, it is important to understand the inheritance of chicken beak shape. In the present study, we firstly established 4 indicators to describe the chicken beak shapes, including upper beak length (UL), lower beak length (LL), distance between upper and lower beak tips (DB) and upper beak curvature (BC). And then, we measured the 4 beak shape indicators as well as some production traits including body weight (BW), shank length (SL), egg weight (EW), eggshell strength (ES) of a layer breed, Rhode Island Red (RIR), in order to estimate genetic parameters of chicken beak shape. The heritabilities of UL and LL were 0.41 and 0.37, and the heritabilities of DB and BC were 0.22 and 0.21, indicating that beak shape was a highly or mediumly heritable. There were significant positive genetic and phenotypic correlations among UL, LL, and DB. And UL was positively correlated with body weight (BW18) and shank length (SL18) at 18 weeks of age in genetics, and DB was positively correlated with BC in terms of genetics and phenotype. We also found that layers of chicken cages played a role on beak shape, which could be attributed to the difference of lightness in different cage layers. By a genome-wide association study (GWAS) for the chicken UL, we identified 9 significant candidate genes associated with UL in RIR. For the variants with low minor allele frequencies (MAF

Despite previous research on the impacts of beak treatment on laying hens, little information exists regarding how variation in beak morphology that can occur following beak treatment affects production, behavior, and welfare. Following infrared beak treatment (IRBT), variations in beak shape, such as a shovel beak (bottom beak longer than top), cracks (Cr), or bubbles (B) may occur if the IRBT equipment is damaged or if a quality control program is not followed at the hatchery. This study aimed to determine if variations in beak morphology post-IRBT impacted laying hen production or welfare. Infrared beak-treated Lohmann LSL-Lite hens (n = 80) were selected from a 56-wk-old flock and randomly assigned into 1 of 8 treatments: flush beak (control), shovel beak extending 0–1 mm (SB0-1), 1–2 mm (SB1-2), 2–3 mm (SB2-3), 3–4 mm (SB3-4), or >4 mm (SB > 4), Cr, or B. Hens were housed in individual cages for 4 wk and production (body weight, feed intake, egg production, and egg quality), and welfare (behavior and histology) parameters were evaluated. Consumption of different particle sizes was assessed by measuring feed particle size of refused feed. Data were analyzed as a one-way ANOVA, in a completely randomized design using PROC GLM (SAS 9.4). The results indicated that the beak morphologies examined had minimal effects on the production or welfare of the hens. Histological assessment did not show the presence of neuromas in the beak tissue, suggesting that the hens were not experiencing chronic pain from the IRBT procedure.

ABSTRACT: This study aimed to determine the effects of infrared beak treatment on the behavior and welfare of male and female turkeys reared to 12 wk of age. To do this, poults (236 males and 324 females) were assigned to one of 2 beak treatments: infrared beak treated on day of hatch (IR) or sham untreated control (C). Data collected included heterophil/lymphocyte (H/L) ratio, pecking force, feather cover, behavioral expression, and beak histology. Data were analyzed as a 2 × 2 factorial of beak treatment and gender, in a completely randomized design and analyzed using PROC MIXED (SAS 9.4). H/L ratio (indicative of a stress response) did not differ between treated and control poults during early life, except at 20 d of age when H/L ratio was higher for C poults than IR poults. Pecking force, measured as a method of monitoring pain, was different only at 1 wk of age, when IR poults pecked with more force than C poults. Feather cover was better in IR poults at 12 wk of age. Differences in behavior between treatments were minor over the 12-wk period. Overall, infrared beak treatment of commercial turkeys had minimal negative impacts on behavior and welfare. The results suggest that stress may be reduced in flocks that are beak treated and that the procedure itself does not cause a pain response.

ABSTRACT: Controlling injurious pecking in commercial turkeys remains a significant challenge to producers and the industry. Infrared beak treatment is an effective method of controlling injurious pecking in chickens; however, the effects of infrared beak treatment on turkey performance are still largely unknown. Two experiments were conducted to determine the impact of infrared beak treatment on the beak length and performance of turkeys raised to 12 wk of age. Experiment 1 tested both toms (n = 236) and hens (n = 324), while Experiment 2 focused on hens (n = 608). Poults for each experiment were assigned to 1 of 2 beak treatments: infrared beak treated (IR) on the day of hatch at a commercial hatchery or sham untreated control (C). Data collected included beak length, body weight, feed intake, feed efficiency, and mortality. Data were analyzed using a 1 or 2-way ANOVA, followed by Tukey's range test for mean separation when interactions were found. Results showed that beak length (Experiment 1 only) was significantly shorter in IR poults from 2 to 12 wk of age. In the same experiment, IR toms had lighter body weight than C toms, but IR hens were heavier than C hens from 2 to 4 wk of age. By 12 wk, IR poults were heavier than C poults, regardless of gender. In experiment 2, IR hens had lighter body weight from 2 to 4 wk of age. In conclusion, infrared beak treatment had minimal effects on feed intake, feed efficiency, or mortality over the 12-wk periods of both experiments.

While morphological traits are often associated with multiple functions, it remains unclear how evolution balances the selective effects of different functions. Birds' beaks function not only in foraging but also in thermoregulating and singing, among other behaviours. Studies of beak evolution abound, however, most focus on a single function. Hence, we quantified relative contributions of different functions over an evolutionary timescale. We measured beak shape using geometric morphometrics and compared this trait with foraging behaviour, climatic variables and song characteristics in a phylogenetic comparative study of an Australasian radiation of songbirds (Meliphagidae). We found that both climate and foraging behaviour were significantly correlated with the beak shape and size. However, foraging ecology had a greater effect on shape, and climate had a nearly equal effect on size. We also found that evolutionary changes in beak morphology had significant consequences for vocal performance: species with elongate-shaped beaks sang at higher frequencies, while species with large beaks sang at a slower pace. The evolution of the avian beak exemplifies how morphological traits can be an evolutionary compromise among functions, and suggests that specialization along any functional axis may increase ecological divergence or reproductive isolation along others. [ABSTRACT FROM AUTHOR]

This research examined how infrared beak treatment (IRBT), sloughing of the treated beak tissue, and the variations in beak shape that can occur post-IRBT impact the welfare and mortality of Lohmann LSL-Lite (LW) and Lohmann Brown (LB) pullets and hens. Two experiments were conducted and birds for both experiments were treated on the day of hatch. IRBT equipment settings were adjusted to create 4 specific beak shapes: shovel (SHV), step (STP), standard (STAN), and an untreated sham control (C). Experiment 1 pullets (n = 80 per strain) were reared in bioassay cages from 1 to 29 D of age (4 replicates per treatment). Data collected included time and presence of beak sloughing, pecking force, behavioral expression, and mortality. Experiment 2 pullets (n = 320 per strain) were reared in floor pens from 1 D to 18 wk of age (2 replicates per treatment) and then conventional cages from 18 to 60 wk of age (6 replicates per treatment). Data collected for Experiment 2 included behavioral expression, feather cover, comb damage, and mortality. Data were analyzed using PROC MIXED (SAS® 9.4) with Tukey's test to separate means. Differences were significant when P ≤ 0.05. IRBT and sloughing had no effect on pecking force or mortality throughout rearing. The variations in post-IRBT beak shape had minor effects on behavior. During rearing, STAN pullets were more active than C pullets but STP and STAN pullets performed less exploratory pecking. During the laying period, SHV and STP hens preened more than C hens. The IRBT treatments, regardless of beak shape, reduced feather loss, comb damage, and cannibalism-related mortality during the laying period. Overall, the results indicate that LW and LB pullets and hens can cope with the change in beak shape that occurs with IRBT, and that welfare is not negatively impacted if some variation in beak shape occurs. [ABSTRACT FROM AUTHOR]

Infrared beak treatment (IRBT) results in a change in beak shape; however, it is unclear what effect variations in post-treatment beak shape have on young pullets. Additionally, the impact of sloughing of the treated beak tissue is not fully understood. Two experiments were conducted to determine the effects of beak tissue sloughing and post-treatment beak shape on the productivity of infrared beak-treated Lohmann Brown (LB) and Lohmann LSL-Lite (LW) pullets and hens. Birds were treated on day of hatch and IRBT equipment settings were adjusted to create 4 specific beak shapes: shovel (SHV), step (STP), standard (STAN), and an untreated sham control (C). Experiment 1 pullets (n = 160) were housed in cages from 1 to 29 d of age and had access to water through chick founts or 360° nipple drinkers (2 replicate cages per treatment). Data collected included body weight (BW), feed intake (FI), feed efficiency (FE), and water disappearance (WD). Experiment 2 pullets (n = 640) were housed in floor pens from 1 d to 18 wk of age (2 replicate pens per treatment) then conventional cages during the laying period (6 replicate cages per treatment). Data collected included BW, FI, egg production, and egg quality. Data were analyzed using PROC MIXED (SAS® 9.4) and differences were significant when P ≤ 0.05. During early life, the IRBT treatments and sloughing had minor effects on FI, FE, and BW. At 4 wk of age, STAN pullets were lighter than C pullets; however, differences were no longer apparent after this age. Pullets with STP or STAN beak shapes had lower WD than C pullets when allowed access to water via nipple drinkers but this did not result in reduced growth. Throughout the laying period, SHV hens laid more saleable eggs than C hens, with no other effects on production. Overall, variations in beak shape and sloughing of the beak tissue had minimal impacts on the productivity of LW and LB pullets and hens. [ABSTRACT FROM AUTHOR]

Introduced parasites that alter their host's mating signal can change the evolutionary trajectory of a species through sexual selection. Darwin's Camarhynchus finches are threatened by the introduced fly Philornis downsi that is thought to have accidentally arrived on the Galapagos Islands during the 1960s. The P. downsi larvae feed on the blood and tissue of developing finches, causing on average approximately 55% in-nest mortality and enlarged naris size in survivors. Here we test if enlarged naris size is associated with song characteristics and vocal deviation in the small tree finch (Camarhynchus parvulus), the critically endangered medium tree finch (C. pauper) and the recently observed hybrid tree finch group (Camarhynchus hybrids). Male C. parvulus and C. pauper with enlarged naris size produced song with lower maximum frequency and greater vocal deviation, but there was no significant association in hybrids. Less vocal deviation predicted faster pairing success in both parental species. Finally, C. pauper males with normal naris size produced species-specific song, but male C. pauper with enlarged naris size had song that was indistinguishable from other tree finches. When parasites disrupt host mating signal, they may also facilitate hybridization. Here we show how parasite-induced naris enlargement affects vocal quality, resulting in blurred species mating signals. [ABSTRACT FROM AUTHOR]

Extensive research on avian adaptive radiations has led to a presumption that beak morphology predicts feeding ecology in birds. However, this ecomorphological relationship has only been quantified in a handful of avian lineages, where associations are of variable strength, and never at a broad macroevolutionary scale. Here, we used shape analysis and phylogenetic comparative methods to quantify the relationships among beak shape, mechanical advantage, and two measures of feeding ecology (feeding behavior and semiquantitative dietary preferences) in a broad sample of modern birds, comprising most living orders. We found a complex relationship, with most variables showing a significant relationship with feeding ecology but little explanatory power. For example, diet accounts for less than 12% of beak shape variation. Similar beak shapes are associated with disparate dietary regimes, even when accounting for diet‐feeding behavior relationships and phylogeny. Very few lineages optimize for stronger bite forces, with most birds exhibiting relatively fast, weak bites, even in large predatory taxa. The extreme morphological and behavioral flexibility of the beak in birds suggests that, far from being an exemplary feeding adaptation, avian beak diversification may have been largely contingent on trade‐offs and constraints. [ABSTRACT FROM AUTHOR]

Hybridization is increasingly recognized as a potent evolutionary force. Although additive genetic variation and novel combinations of parental genes theoretically increase the potential for hybrid species to adapt, few empirical studies have investigated the adaptive potential within a hybrid species. Here, we address whether genomic contingencies, adaptation to climate, or diet best explain divergence in beak morphology using genomically diverged island populations of the homoploid hybrid Italian sparrow Passer italiae from Crete, Corsica, and Sicily. Populations vary significantly in beak morphology both between and within islands of origin. Temperature seasonality best explains population divergence in beak size. Interestingly, beak shape along all significant dimensions of variation was best explained by annual precipitation, genomic composition, and their interaction, suggesting a role for contingencies. Moreover, beak shape similarity to a parent species correlates with proportion of the genome inherited from that species, consistent with the presence of contingencies. In conclusion, adaptation to local conditions and genomic contingencies arising from putatively independent hybridization events jointly explain beak morphology in the Italian sparrow. Hence, hybridization may induce contingencies and restrict evolution in certain directions dependent on the genetic background. [ABSTRACT FROM AUTHOR]

Variability in the shape of hard structures such as mandibles (beaks) due to stock variation or sexual dimorphism is common in cephalopods, and could prove useful in the discrimination of stocks or sexes. In this study, geometric morphometrics of upper and lower beak's shape are used to analyze the variation between sexes and stocks in Ommastrephes bartramii of the northwestern Pacific Ocean. This species is targeted by the Chinese jigging fleet during the fishing period May-October 2013. Variation in the beak's pigmentation stage was also investigated. According to our analyses, upper and lower beak shapes of O. bartramii differed significantly between eastern and western stocks of O. bartramii (MANCOVA, P < 0.01), and different allometric growths were also detected. The degree of pigmentation by pigmentation stage, changed in upper beaks between the two stocks and in lower beaks with beak size. In the western stock, only lower beak shape and pigmentation stages of upper beak shape showed significant differences between sexes, while the degree of pigmentation stage changed with different beak sizes in the lower beak. Squid stocks could be effectively identified based on the results of a principal component analysis of beak shape, but sexes could not be identified with this technique. We hypothesize that reason for these differences may be caused by the variation of feeding habits between stocks but the sharing of a similar habitat by both sexes. [ABSTRACT FROM AUTHOR]

Hadrosauridae, consisting of two subfamilies (Hadrosaurinae and Lambeosaurinae), is a successful herbivorous dinosaur group that established a high taxonomic diversity and a cosmopolitan biogeographic distribution during the Late Cretaceous. While its success is often attributed to a highly specialized oral processing system, the foraging strategy of this group remains unclear. This study focuses on two critical factors in foraging strategy, food selectivity and locomotor ecology, in these hadrosaurid subfamilies. Three-dimensional beak shapes and limb segment proportions are used as the proxies for food selectivity and locomotor ecology, respectively. The beak shape analysis demonstrates trends of anteriorly acute beaks in hadrosaurines and anteriorly wide beaks in lambeosaurines. The limb segment proportion analysis shows short proximal limb segments in hadrosaurines and long proximal limb segments in lambeosaurines. These results suggest that hadrosaurines preferred selective consumption of high-quality food with energy-inefficient locomotor ecology, while lambeosaurines preferred mass consumption of low-quality food with energy-efficient locomotion and that differences in foraging strategy might have enhanced dietary niche partitioning in the subfamily level of hadrosaurids. In addition, this study tests a relationship between limb proportions and habitat environments in hadrosaurids. We demonstrate that hadrosaurids from the coastal environments have shorter forelimbs than those from the terrestrial environment. Since short forelimbs are better suited for temporal bipedalism than long forelimbs, the limb proportion difference may indicate adaptations to different feeding heights, possibly due to different regional vegetations. • Hadrosaurid beak shape and limb segment proportions differ between subfamilies. • Hadrosaurines likely preferred high quality food and had inefficient locomotion. • Lambeosaurines likely had low quality food but efficient locomotor ecology. • The ecomorphology difference likely induced niche partitioning. • Hadrosaurids from inland had longer forelimb, which may better fit quadrupedality. [ABSTRACT FROM AUTHOR]

Theory predicts that variability in size and the shape of a morphological trait should often be stable both at the intra- and interspecific level. We studied variation in beak integration among several populations of two species of the genus Passer, a hybrid species, the Italian sparrow ( Passer italiae) and one of its parents, the Spanish sparrow ( Passer hispaniolensis). We show that the general shape of the beak has been conserved in these two species and that hybrid speciation has had no major effects on beak integration. However, in young, sympatric populations, phenotypic integration between beak height and length decreased significantly, to the extent that these two dimensions apparently became independent. This displacement in phenotypic integration seems to be accompanied with changes in the distribution of phenotypic variation at the univariate level. This suggests that while beak shape may have been constrained over evolutionary time-scales and major hybridization events (i.e. the formation of the hybrid Italian sparrow), under specific selection regimes linked to secondary contact, it can evolve rapidly. [ABSTRACT FROM AUTHOR]

Background: The granivorous house sparrow Passer domesticus is thought to have developed its commensal relationship with humans with the rise of agriculture in the Middle East some 10,000 years ago, and to have expanded with the spread of agriculture in Eurasia during the last few thousand years. One subspecies, P. d. bactrianus, residing in Central Asia, has apparently maintained the ancestral ecology, however. This subspecies is not associated with human settlements; it is migratory and lives in natural grass- and wetland habitats feeding on wild grass seeds. It is well documented that the agricultural revolution was associated with an increase in grain size and changes in seed structure in cultivated cereals, the preferred food source of commensal house sparrow. Accordingly, we hypothesize that correlated changes may have occurred in beak and skull morphology as adaptive responses to the change in diet. Here, we test this hypothesis by comparing the skull shapes of 101 house sparrows from Iran, belonging to five different subspecies, including the non-commensal P. d. bactrianus, using geometric morphometrics. Results: The various commensal house sparrow subspecies share subtle but consistent skeletal features that differ significantly from those of the non-commensal P. d. bactrianus. Although there is a marked overall size allometry in the data set, the shape difference between the ecologically differentiated sparrows cannot be explained by differences in size alone. Relative to the size allometry commensal house sparrows exhibit a skull shape consistent with accelerated development (heterochrony), resulting in a more robust facial cranium and a larger, more pointed beak. Conclusion: The difference in skull shape and robustness of the beak between commensal and non-commensal house sparrows is consistent with adaptations to process the larger and rachis encapsulated seeds of domesticated cereals among human associated populations. [ABSTRACT FROM AUTHOR]

Abstract: Differences in song between species of birds are often the most reliable criteria by which to identify them. Thus, the study of the evolution of bird song provides biologists with a powerful insight into the nature of speciation processes. Both adaptive and nonadaptive explanations have been proposed to account for the evolution of song differences in birds. In this study, we put several of these hypotheses to a test in the genus Phylloscopus, a species-rich group of Old World leaf warblers in which song is used by males for mate attraction and territory defense. We found that song characteristics contained significant amounts of phylogenetic information, although they were more labile than morphological traits. Song frequency characteristics were more phylogenetically preserved than temporal or song structure traits. Changes in body size between species were correlated with changes in maximum and minimum frequencies and frequency bandwidth: small-bodied species had higher frequencies and wider bandwidths than large-bodied species. Beak shape was not found to limit overall frequency patterns. We used an ecomorphological correlate of habitat use, the tarsus/beak ratio, to test for song adaptation to specific habitat sound transmission characteristics. We found that species with larger tarsus/beak ratio, typically inhabiting broadleaf habitats and understory vegetation, had lower emphasized frequencies in their songs, as expected if songs are adapted to maximize sound transmission. However, this relationship did not held when controlling for common descent. Song complexity, a wide-ranging measurement encompassing temporal and structural sound complexity estimates, was best explained by breeding latitude. We interpret this relationship as a correlate of increased sexual selection by mate choice toward more Northern latitudes. We failed to find a significant role of character displacement in the evolution of song in this group: sympatric pairs of species did not show larger differences in song than allopatric pairs of species. To sum up, superimposing upon large haphazard selection of song themes, selective pressures for higher song elaboration in areas of high sexual selection, and correlative change in song brought about by natural selection of body size, would explain some of the diversity of songs that are found within the genus Phylloscopus. [Copyright &y& Elsevier]

Some adaptive radiations are notable for extreme interspecific diversification in one or a few adult traits. How and why have trait differences evolved? Natural and sexual selection often provide answers to the question of why. An answer to the question of how is to be found in the genetic control of the phenotypic traits, especially in the early stages of development, when interspecific differences first become expressed. Recent studies of the molecular genetic control of beak development in Darwin's finches have shown that a signalling molecule (BMP4) plays a key role in the development of large and deep beaks. Expression of this molecule occurs earlier (heterochrony) and at higher levels in species with deep beaks compared with species with more pointed beaks. The implication of this finding is that variation in the regulation of one or a few genes that are expressed early could be the source of evolutionarily significant variation that is subject to natural selection in speciation and adaptive radiation. This view is reinforced by parallel findings with the same signalling molecule in the development of jaw morphology in cichlid fish of the Great Lakes of Africa. Further research into regulatory mechanisms is to be expected, as well as extension to other examples of radiation such as honeycreepers in Hawaii and Anolis lizards in the Caribbean. © 2006 The Linnean Society of London, Biological Journal of the Linnean Society, 2006, 88, 17–22. [ABSTRACT FROM AUTHOR]

Events occurring at the founding of a population, and in the next few generations, are potentially of great importance for the future evolution of the population. This study reports demographic, genetic, and morphological changes that took place during and after the colonization of the small Galápagos island of Daphne Major by three male and two female large ground finches, Geospiza magnirostris, at the end of 1982. Using assignment tests with microsatellite DNA data we demonstrate heterogeneity among the immigrants. Their sources included both a near island (Santa Cruz) and a far island (Marchena). However, almost all immigrants that stayed to breed were from an intermediate island (Santiago) and its satellites. Song may have been responsible for this selectivity. Mean heterozygosity stayed roughly constant over the next 15 years while allelic diversity almost doubled, after an initial decline, as the breeding population increased to a maximum of 30 pairs. Although close inbreeding occurred, with a reduction in heterozygosity, an expected net decline in heterozygosity did not occur, for two reasons: it was counteracted by continuing gene flow from immigrants at a low rate, and inbred birds (in one cohort) were at a selective disadvantage. An abrupt step-function shift in beak shape occurred after 9 years. Thus the study provides evidence of drift and selection causing morphological and genetic divergence in the establishment of a new population and in the first few generations. [ABSTRACT FROM AUTHOR]