Lateralisation in birds of prey: adaptive and phylogenetic considerations

Lateralisation, the different use of one or other side or appendix of the body, is basically determined by brain asymmetry which, in turn, is likely to be due to adaptive reasons. Several studies have been carried out on birds in general. However, birds of prey in particular, although they are very good candidates, have not been investigated from the sensory lateralisation point of view. In fact, many species scan for prey while perched and capture terrestrial prey with the feet, having at the same time the obvious necessity to keep their balance. This paper, therefore, investigates the existence of some sort of lateralisation in several species of both Falconiformes and Strigiformes temporarily in captivity. Attention is given to: (a) the direction of body rotation when perceiving a sound stimulus from behind the body and (b) the use of the feet when grasping a terrestrial prey. Lateralisation was found to be clearly present in both types of tests, although with some difference in its expression. In fact, almost every species tested rotated its body anti-clockwise, i.e. to the left, both in the first test and in repeated tests, with no noticeable difference between Falconiformes and Strigiformes. Also prey grasping showed a preferential use of one foot. Falconiformes preferred clearly to grasp the prey with one foot only in both the first test and in subsequent ones. Strigiformes, on the other hand, preferred using both feet, although a not insignificant proportion of individuals used one foot. Only the little owl seemed to have the tendency to prefer to use the right foot only, in a similar manner to Falconiformes. In fact, this bird is the most "diurnal" owl species among those tested, suggesting that lateralisation in footedness might be affected by adaptive constraints more than by phylogenetic similarities. Lateralisation, therefore, seems to be very widespread among birds of prey. Preferential use of the right foot also appears to be a general habit, and this is probably connected to the use of left hemisphere when manipulating food items.     

A comparison of digestive efficiency in birds of prey

Differences in how raptors hunt and what they catch are correlated with size-independent differences in length of the small intestine, the region of the digestive tract responsible for food absorption. The study examined the functional significance of these differences among ten raptor species. Dry matter apparent digestive efficiency was calculated for each species fed a diet of day-old cockerels. For Falconiformes and Strigiformes, efficiencies varied between 75% and 82%, digestive efficiency being positively correlated with intestine length.
Generalist species, with a wide prey spectrum and feeding on relatively easily caught prey and carrion, had long intestines and high digestive efficiencies. Raptors specializing on fast-moving, avian prey had short intestines and reduced digestive efficiency. The Peregrine Falco peregrinus and the Common Buzzard Buteo buteo were used as examples of specialist and generalist feeders, respectively. Rabbit and pigeon were fed to both. Buzzards digested both diets more efficiently than Peregrines. Body-mass changes were used to examine the nutritional value of the two diets to each species. Buzzards gained body-mass when eating rabbit, Peregrines lost mass. Both species gained mass when feeding on pigeon. It seems that consideration of diet quality, not just quantity, is essential in understanding raptor food requirements. Generalist raptors have high efficiencies on several diets, specialists compensate for their reduced efficiency by eating food of high nutritional quality. Various aspects of prey quality are examined.     

An improved technique for estimating pectoral muscle protein condition from body measurements of live gulls

Body measurements, which could be taken from live birds, were used to estimate total pectoral muscle protein in Lesser Black-backed Gulls Larus fuscus. The maximum cross-sectional area of the flight muscles was measured from the profile of the muscle surface over the keel, and this was used in conjunction with the length of the flight muscle to estimate muscle volume. The estimate of muscle volume was then used with fresh body weight to estimate total flight muscle protein. A highly significant correlation was found between the estimated values and actual pectoral muscle protein mass determined by carcass analysis. The model developed from the source group was then validated using a second independent sample, in which flight muscle protein was estimated from the model. Carcass analysis again demonstrated a good correlation between estimated and actual total protein. Different methods of controlling for body-size to calculate protein condition from measures of total protein were considered. The technique described here provides a simple and reliable method of estimating pectoral muscle protein condition in live gulls which could be applied to studies of body condition in other species.     

Comparative gastrointestinal morphology of the Kori bustard and secretary bird

Two secretary birds and three Kori bustards were studied to determine differences between their body size and gastrointestinal morphology. Body measurements were made on captive, live birds and gastrointestinal measurements on fresh postmortem specimens. For predator species, such as the Kori bustard and secretary bird, body size is a function of their ability to capture and destroy prey. While the secretary bird was clearly the taller of the two species, superior body weight, wing length, and therefore body size was noted for the Kori bustard. The size and length of the gastrointestinal tract varied between species. The secretary bird had the shorter, less complex digestive tract, with a foregut well adapted for consumption of large quantities of flesh. The large intestine was devoid of ceca. The gastrointestinal tract of the Kori bustard was markedly different from that of the secretary bird. The foregut was less complex and the large intestine possessed large, voluminous ceca.     

Factors promoting polygyny in European birds of prey—a hypothesis

Summary Polygyny is known in at least nine (out of 36) European raptor (Accipitriformes and Falconiformes) and seven (out of 13) owl (Strigiformes) species that hunt mobile prey. The hypothesis put forward here suggests that abundant food supply and nomadic tactics of breeding dispersal are crucial factors promoting polygyny in birds of prey. The hypothesis predicts that: (1) polygyny is more common in rodent-eating birds of prey than in bird-eating ones; (2) polygyny is more frequent in good vole years than in poor ones; (3) the frequency of polygyny in vole-eating species should increase northwards in Europe, as the densities of voles in the peak phase increase in that direction; (4) the frequency of polygyny and harem size should be increased by supplementary feeding; and (5) polygyny is more common in nomadic birds of prey with annual pair bonds and weak territoriality than in resident birds of prey with longerterm pair bonds and stronger territoriality. A majority of the available data is consistent with predictions 1–3 and 5, but data on prediction 4 are scanty. Further studies on ringed birds of prey are needed to test the validity of the hypothesis.     

河南省猛禽的调查

主要论述河南省猛禽的种类、数量、分布及迁徙规律,河南省的猛禽共计41种,其中隼形目鸟类2科29种,Hao形目鸟类2科12种。     

Convergent evolution of strigiform and caprimulgiform dark-activity is supported by phylogenetic analysis using the arylalkylamine N-acetyltransferase (Aanat) gene

Alternative hypotheses propose the sister order of owls (Strigiformes) to be either day-active raptors (Falconiformes) or dark-active nightjars and allies (Caprimulgiformes). In an effort to identify molecular characters distinguishing between these hypotheses we examined a gene, arylalkylamine N-acetyltransferase (Aanat), potentially associated with the evolution of avian dark-activity. Partial Aanat coding sequences, and two introns, were obtained from the genomic DNA of 16 species: Strigiformes (four species), Falconiformes (four species), Caprimulgiformes (five species), with outgroups: Ciconiiformes (one species), Passeriformes (one species), and Apterygiformes (one species). Phylogenetic trees derived from aligned, evolutionarily conserved Aanat regions did not consistently recover clades corresponding to orders Strigiformes and Falconiformes but did place a caprimulgiform clade more distant from the strigiform and falconiform species than the latter two groups are to each other. This finding was supported by spectral analysis. The taxonomic distribution of seven intronic indels is consistent with the Aanat derived phylogenetic trees and supports conventional family-level groupings within both Strigiformes and Caprimulgiformes. The phylogenetic analyses also indicate that Caprimulgiformes is a polyphyletic grouping. In conclusion the data support, but do not conclusively prove, the proposal that Falconiformes is the sister order to Strigiformes and therefore, that the dark-activity characteristic of Strigiformes and Caprimulgiformes arose by convergent evolution.     

Null models and spatial patterns of species richness in South American birds of prey

In this paper, we used geostatistical approaches to describe bi-dimensional spatial patterns in species richness of South American birds of prey (Falconiformes and Strigiformes). They indicated strong spatial patterns both across latitude and longitude, for the two groups. These patterns were then correlated with those expected by a bi-dimensional null model constructed to take into account South America continental edges. As considerable departures from the null model were observed, there may be other ecological or evolutionary explanations for spatial patterns in species richness. Variation seems to be related to habitat heterogeneity across the continent, especially when considering differences between habitats in the central and south-eastern portion of the continent and in the Andean region. This supports previous conclusions that habitat type and heterogeneity affect species richness and abundance at different spatial scales.     

Haemosporidian blood parasites in European birds of prey and owls

Avian blood parasites have been intensively studied using morphological methods with limited information on their host specificity and species taxonomic status. Now the analysis of gene sequences, especially the mitochondrial cytochrome b gene of the avian haemosporidian species of Haemoproteus, Plasmodium, and Leucocytozoon, offers a new tool to review the parasite specificity and status. By comparing morphological and genetic techniques, we observed nearly the same overall prevalence of haemosporidian parasites by microscopy (19.8%) and polymerase chain reaction (PCR) (21.8%) analyses. However, in contrast to the single valid Leucocytozoon species (L. toddi) in the Falconiformes we detected 4 clearly distinctive strains by PCR screening. In the Strigiformes, where the only valid Leucocytozoon species is L. danilewskyi, we detected 3 genetically different strains of Leucocytozoon spp. Two strains of Haemoproteus spp. were detected in the birds of prey and owls examined, whereas the strain found in the tawny owl belonged to the morphospecies Haemoproteus noctuae. Three Plasmodium spp. strains that had already been found in Passeriformes were also detected in the birds of prey and owls examined here, supporting previous findings indicating a broad and nonspecific host spectrum bridging different bird orders.     

Morphometrics of the avian small intestine compared with that of nonflying mammals: a phylogenetic approach

Flying animals may experience a selective constraint on gut volume because the energetic cost of flight increases and maneuverability decreases with greater digesta load. The small intestine is the primary site of absorption of most nutrients (e.g., carbohydrates, proteins, fat) in both birds and mammals. Therefore, we used a phylogenetically informed approach to compare small intestine morphometric measurements of birds with those of nonflying mammals and to test for effects of diet within each clade. We also compared the fit of nonphylogenetic and phylogenetic models to test for phylogenetic signal after accounting for effects of body mass, clade, and/or diet. We provide a new MATLAB program (Regressionv2.m) that facilitates a flexible model-fitting approach in comparative studies. As compared with nonflying mammals, birds had 51% less nominal small intestine surface area (area of a smooth bore tube) and 32% less volume. For animals <365 g in body mass, birds also had significantly shorter small intestines (20%-33% shorter, depending on body mass). Diet was also a significant factor explaining variation in small intestine nominal surface area of both birds and nonflying mammals, small intestine mass of mammals, and small intestine volume of both birds and nonflying mammals. On the basis of the phylogenetic trees used in our analyses, small intestine length and nominal surface area exhibited statistically significant phylogenetic signal in birds but not in mammals. Thus, for birds, related species tended to be similar in small intestine length and nominal surface area, even after accounting for relations with body mass and diet. A reduced small intestine in birds may decrease the capacity for breakdown and active absorption of nutrients. Birds do not seem to compensate for reduced digestive and absorptive capacity via a longer gut retention time of food, but we found some evidence that birds have an increased mucosal surface area via a greater villus area, although not enough to compensate for reduced nominal surface area. We predict that without increased rate of enzyme hydrolysis and/or mediated transport and without increased passive absorption of water-soluble nutrients, birds may operate with a reduced digestive capacity, compared with that of nonflying mammals, to meet an increase in metabolic needs (i.e., a reduced spare capacity).     

Bats as prey of diurnal birds: a global perspective

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Falling Victim to Wasps in the Air: A Fate Driven by Prey Flight Morphology?

In prey-predator systems where the interacting individuals are both fliers, the flight performance of both participants heavily influences the probability of success of the predator (the prey is captured) and of the prey (the predator is avoided). While the flight morphology (an estimate of flight performance) of predatory wasps has rarely been addressed as a factor that may contribute to explain prey use, how the flight morphology of potential prey influences the output of predator-prey encounters has not been studied. Here, we hypothesized that flight morphology associated with flight ability (flight muscle mass to body mass ratio (FMR) and body mass to wing area ratio (wing loading, WL)) of Diptera affect their probability of being captured by specialized Diptera-hunting wasps (Bembix merceti and B. zonata), predicting a better manoeuvrability and acceleration capacity achieved by higher FMR and lower WL, and flight speed achieved by higher WL. In addition, wasp species with better flight morphology should be less limited by an advantageous Diptera flight morphology. Overall, the abundance of dipterans in the environment explained an important part of the observed variance in prey capture rate. However, it was not the only factor shaping prey capture. First, higher prey abundance was associated with greater capture rate for one species (B. merceti), although not for the other one. Second, the interaction observed between the environmental dipteran availability and dipteran WL for B. zonata suggests that greater dipteran WL (this probably meaning high cruising speed) decreased the probability of being captured, as long as fly abundance was high in the environment. Third, greater dipteran FMR (which likely means high manoeuvrability and acceleration capacity) helped to reduce predation by B. merceti if, again, dipterans were abundant in the environment. Wasp WL only varied with body mass but not between species, thereby hardly accounting for inter-specific differences in the wasps’ predatory patterns. However, the greater FMR of B. zonata, which implies better flight performance and greater load-lifting capacity, may explain why the capture rate in the two wasp species is affected by different factor interactions. In conclusion, although prey availability remains the primary factor shaping prey use, prey flight morphology seems to gain an additional role under conditions of abundant prey, when wasps can avoid flies with better flight ability.     

Some infectious and parasitic diseases in Oklahoma raptors.

Blood films and sera samples from wild Oklahoma raptors (Strigiformes--36 birds, 3 species; Falconiformes--50 birds, 7 species) were examined for hematozoa and tested for serologic antibody response to Newcastle Disease Virus (NDV), encephalitis (EEE and WEE), ornithosis, and influenza. Twenty-nine of 36 (80.5) Strigiformes and 24 of 50 (48.0%) Falconiformes showed the presence of one or more hematozoa. Serologic testing revealed the serum of one adult male red-tailed hawk positive for antibody to NDV and one additional adult male red-tailed hawk positive for antibody to type-A influenza.     

Evolution of reversed sexual size dimorphism and role partitioning among predatory birds, with a size scaling of flight performance

To explain the adaptive significance of sex role partitioning and reversed sexual size dimorphism among raptors, owls and skuas, where females are usually larger than males, we combine several previous hypotheses with some new ideas. Owing to their structural and behavioural adaptations for prey capture, predatory birds have better prospects than other birds of defending their offspring against nest predators. This makes sex role partitioning advantageous; one parent guards the offspring while the other forages for the family. Further, among predators hunting alert prey such as vertebrates, two mates because of interference may not procur much more food than would one mate hunting alone. By contrast, two mates feeding on less alert prey may together obtain almost twice as much food as one mate hunting alone. For these reasons, partitioning of breeding labours might be adaptive only in predatory birds. An initial imbalance favours female nest guarding and male foraging: the developing eggs might be damaged if the female attacks prey; their mass might reduce her flight performance; she must visit the nest to lay; and the male feeds her before she lays (‘courtship feeding’). Increased female body size should enhance egg production, incubation, ability to tear apart prey for the young, and, in particular, offspring protection in predatory birds. Efficient foraging during the breeding period then becomes most important for the male. This imposes great demands on aerial agility in males, particularly among predators of agile prey. Flight performance decreases with increasing size in five of six aspects explored. The male must therefore not be too large in relation to the most important prey. For these reasons, he should be smaller than the female. Among predatory birds, size dimorphism increases with the proportion of birds in the diet, which may be explained as follows. Adult birds have mainly one type of predators: other predatory birds. Because almost only these specialists exploit adult birds, they carry out most of the cropping of this prey. A predator of easier prey competes with many other kinds of predators, which considerably reduce prey abundance in its territory. This is not so for predators of adult birds. Further, because birds are extremely agile, the specialized predator can hunt efficiently only within a limited size range of birds, whose flight skill it can match. Increased size dimorphism among these predators therefore should be particularly important for enlarging the combined food base of the pair. A bird specialist may consume much of the available prey in the suitable size range during the breeding period. When the predator's young are large enough to defend themselves, the female aids better by hunting than by guarding the chicks. It is advantageous among bird specialists if she hunts prey of other sizes than does the male, who has by then reduced prey abundance in his prey size class. But among predatory birds hunting easier prey the female gains little by hunting outside the male's prey spectrum, because other kinds of predators will have reduced the prey abundance outside as well as inside the male's preferred size range. Intra-pair food separation through large sexual size dimorphism therefore should be particularly advantageous among predators of birds. This may be the main reason why the degree of size dimorphism increases with the dietary proportion of birds.     

河北沧州地区猛禽初步调查

依据2001年5月至2008年3月对沧州东部沿海湿地的野外考察和沧州市野生动物救护中心的鸟类救护记录,共收录沧州地区猛禽33种,隶属于2目5科16属.其中,隼形目3科10属26种,鹗形目2科6属7种.旅鸟16种,占48.5%;冬候鸟8种,占24.2%;夏候鸟3种,占9.1%;留鸟6种,占18.2%.古北界23种,占69.7%;东洋界和广布种各5种,分别占15.2%.     

Size and structure of the bird genome--I. DNA content of 48 species of Neognathae

The nuclear DNA content was evaluated in 48 species of Neognathae birds belonging to 13 orders, namely Anseriformes, Charadriiformes, Columbiformes, Ciconiiformes, Falconiformes, Galliformes, Gruiformes, Passeriformes, Pelicaniformes, Phoenicopteriformes, Piciformes, Psittaciformes and Strigiformes. The DNA content, expressed in pg/nucleus, ranges from 2.81 to 4.97. The genome size variability within and among families is discussed on the basis of the Hinegardner's (1976) model of genome evolution.     

社鼠和褐家鼠消化道长度和重量的季节变化

测定了浙江金华的社鼠和褐家鼠消化道长度和重量的季节变化。野生社鼠消化道各器官无论长度不审重量都有明显季差异,在寒冷的冬季具有相对较大的小肠、大肠、盲肠、雄性社鼠的消化道长度在秋季由于食物条件的改善而明显下降,但雌性社鼠由于在秋季仍有繁殖负担,其消化道长度下降不明显,而家栖的褐家鼠只有总消化道、小肠和大肠的长度有季节差异,冬、春季高于夏、秋季。消化道形态季节变化与温度、食物条件和繁殖有关。     

基于CHD基因序列的18种猛禽鸟类系统发育关系

对18个猛禽CHD基因的一段内含子序列进行比较和分析.CHD-W和CHD-Z基因的多态性存在差异,CHD-W基因不适合种间系统发生学的研究.通过对CHD-Z基因扩增序列构建的NJ和ML树显示:隼科与其他猛禽物种关系较远;鹰科鸟类与鸮形目鸟类亲缘关系较近;在白腹鹞的分类地位上与传统形态学分类不一致;长耳鸮、领角鸮、花彩角鸮、西部鸣角鸮的分类地位存在分歧.鸮形目和隼形目鸟类的CHD-W基因大小有明显区别,支持形态学分类结果,与CHD-Z序列分析结果明显不同.     

Does prey capture induce area-restricted search? A fine-scale study using GPS in a marine predator, the wandering albatross

In a patchy environment, predators are expected to increase turning rate and start an area-restricted search (ARS) when prey have been encountered, but few empirical data exist for large predators. By using GPS loggers with devices measuring prey capture, we studied how a marine predator adjusts foraging movements at various scales in relation to prey capture. Wandering albatrosses use two tactics, sit and wait and foraging in flight, the former tactic being three times less efficient than the latter. During flight foraging, birds caught large isolated prey and used ARS at scales varying from 5 to 90 km, with large-scale ARS being used only by young animals. Birds did not show strong responses to prey capture at a large scale, few ARS events occurred after prey capture, and birds did not have high rates of prey capture in ARS. Only at small scales did birds increase sinuosity after prey captures for a limited time period, and this occurred only after they had caught a large prey item within an ARS zone. When this species searches over a large scale, the most effective search rule was to follow a nearly straight path. ARS may be used to restrict search to a particular environment where prey capture is more predictable and profitable.     

Fin-tail coordination during escape and predatory behavior in larval zebrafish

Larval zebrafish innately perform a suite of behaviors that are tightly linked to their evolutionary past, notably escape from threatening stimuli and pursuit and capture of prey. These behaviors have been carefully examined in the past, but mostly with regard to the movements of the trunk and tail of the larvae. Here, we employ kinematics analyses to describe the movements of the pectoral fins during escape and predatory behavior. In accord with previous studies, we find roles for the pectoral fins in slow swimming and immediately after striking prey. We find novel roles for the pectoral fins in long-latency, but not in short-latency C-bends. We also observe fin movements that occur during orienting J-turns and S-starts that drive high-velocity predatory strikes. Finally, we find that the use of pectoral fins following a predatory strike is scaled to the velocity of the strike, supporting a role for the fins in braking. The implications of these results for central control of coordinated movements are discussed, and we hope that these results will provide baselines for future analyses of cross-body coordination using mutants, morphants, and transgenic approaches.