Effect of hemoprotozoal infections on rehabilitation of wild raptors.
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Lens extraction by phacoemulsification in two raptors.
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Some common toxicoses in raptors.
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Relay toxicity of strychnine in raptors in relation to a pigeon eradication program.
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Treatment of aspergillosis in raptors (order falconiformes) with miconazole.
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Birds of prey as limiting factors of gamebird populations in Europe: a review.
Whether predators can limit their prey has been a topic of scientific debate for decades. Traditionally it was believed that predators take only wounded, sick, old or otherwise low-quality individuals, and thus have little impact on prey populations. However, there is increasing evidence that, at least under certain circumstances, vertebrate predators may indeed limit prey numbers. This potential role of predators as limiting factors of prey populations has created conflicts between predators and human hunters, because the hunters may see predators as competitors for the same resources. A particularly acute conflict has emerged over the past few decades between gamebird hunters and birds of prey in Europe. As a part of a European-wide research project, we reviewed literature on the relationships between birds of prey and gamebirds. We start by analysing available data on the diets of 52 European raptor and owl species. There are some 32 species, mostly specialist predators feeding on small mammals, small passerine birds or insects, which never or very rarely include game animals (e.g. hares, rabbits, gamebirds) in their diet. A second group (20 species) consists of medium-sized and large raptors which prey on game, but for which the proportion in the diet varies temporally and spatially. Only three raptor species can have rather large proportions of gamebirds in their diet, and another seven species may utilise gamebirds locally to a great extent. We point out that the percentage of a given prey species in the diet of an avian predator does not necessarily reflect the impact of that predator on densities of prey populations. Next, we summarise available data on the numerical responses of avian predators to changing gamebird numbers. In half of these studies, no numerical response was found, while in the remainder a response was detected such that either raptor density or breeding success increased with density of gamebirds. Data on the functional responses of raptors were scarce. Most studies of the interaction between raptors and gamebird populations give some estimate of the predation rate (per cent of prey population taken by predator), but less often do they evaluate the subsequent reduction in the pre-harvest population or the potential limiting effect on breeding numbers. The few existing studies indicate that, under certain conditions, raptor predation may limit gamebird populations and reduce gamebird harvests. However, the number and extent of such studies are too modest to draw firm conclusions. Furthermore, their geographical bias to northern Europe, where predator-prey communities are typically simpler than in the south, precludes extrapolation to more diverse southern European ecosystems. There is an urgent need to develop further studies, particularly in southern Europe, to determine the functional and numerical responses of raptors to gamebird populations in species and environments other than those already evaluated in existing studies. Furthermore, additional field experiments are needed in which raptor and possibly also mammalian predator numbers are manipulated on a sufficiently large spatial and temporal scale. Other aspects that have been little studied are the role of predation by the non-breeding part of the raptor population, or floaters, on the breeding success and survival of gamebirds, as well as the effect of intra-guild predation. Finally there is a need for further research on practical methods to reduce raptor predation on gamebirds and thus reduce conflict between raptor conservation and gamebird management.
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Gliding flight: drag and torque of a hawk and a falcon with straight and turned heads, and a lower value for the parasite drag coefficient.
Raptors - falcons, hawks and eagles in this study - such as peregrine falcons (Falco peregrinus) that attack distant prey from high-speed dives face a paradox. Anatomical and behavioral measurements show that raptors of many species must turn their heads approximately 40 degrees to one side to see the prey straight ahead with maximum visual acuity, yet turning the head would presumably slow their diving speed by increasing aerodynamic drag. This paper investigates the aerodynamic drag part of this paradox by measuring the drag and torque on wingless model bodies of a peregrine falcon and a red-tailed hawk (Buteo jamaicensis) with straight and turned heads in a wind tunnel at a speed of 11.7 m s(-)(1). With a turned head, drag increased more than 50 %, and torque developed that tended to yaw the model towards the direction in which the head pointed. Mathematical models for the drag required to prevent yawing showed that the total drag could plausibly more than double with head-turning. Thus, the presumption about increased drag in the paradox is correct. The relationships between drag, head angle and torque developed here are prerequisites to the explanation of how a raptor could avoid the paradox by holding its head straight and flying along a spiral path that keeps its line of sight for maximum acuity pointed sideways at the prey. Although the spiral path to the prey is longer than the straight path, the raptor's higher speed can theoretically compensate for the difference in distances; and wild peregrines do indeed approach prey by flying along curved paths that resemble spirals. In addition to providing data that explain the paradox, this paper reports the lowest drag coefficients yet measured for raptor bodies (0.11 for the peregrine and 0.12 for the red-tailed hawk) when the body models with straight heads were set to pitch and yaw angles for minimum drag. These values are markedly lower than value of the parasite drag coefficient (C(D,par)) of 0.18 previously used for calculating the gliding performance of a peregrine. The accuracy with which drag coefficients measured on wingless bird bodies in a wind tunnel represent the C(D,par) of a living bird is unknown. Another method for determining C(D,par) selects values that improve the fit between speeds predicted by mathematical models and those observed in living birds. This method yields lower values for C(D,par) (0.05-0.07) than wind tunnel measurements, and the present study suggests a value of 0.1 for raptors as a compromise.
Air Movements↗
[Tuberculosis in raptorial birds (II). Review of the literature and suggestions for clinical diagnosis and vaccination].
Although avian tuberculosis is a common disease in raptors, the diagnosis is not often established in vivo. Mycobacterium avium, serotype 2, is the aetiological agent most commonly involved. As the disease may become apparent in a variety of clinical forms and as it is so common, routine screening for avian tuberculosis is advocated in any diseased raptor. X-ray examination should be a routine diagnostic procedure in diseased raptors. Laparoscopy is an important diagnostic tool in raptors. Laparoscopy followed by liver biopsy may be essential in the diagnosis of generalized avian tuberculosis. The usefulness of haematological examination in the diagnosis of avian tuberculosis in raptors should be studied. A diagnosis may be established by identifying acid-fast rods in a smear, followed by cultures of the organism on specific media. Of the immunological methods, tuberculination in conjunction with a rapid whole blood agglutination test would seem to be the most practical technique. However, closer examination of the practicability of the rapid whole blood agglutination test in the diagnosis of avian tuberculosis in raptors is desirable. Other immunological methods referred to in the literature are haemagglutination tests, an enzyme-labeled antibody test and a lymphocyte transformation test. Vaccination of birds against avian tuberculosis would appear to be possible, judging by the literature on the subject. Further study of this subject, however, is indicated to investigate the use of vaccinating birds of prey against this disease.
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Influence of habitat and temperature on dispersal behaviour of two pteromalid parasitoids of houseflies during an inundative release at a dairy barn.
1. About 11,000 each of Muscidifurax raptor Girault and Saunders and Urolepis rufipes (Ashmead) were released weekly for 7 weeks at a commercial dairy farm in central New York state, U.S.A. Dispersal behaviour was monitored by parasitism rates of house fly, Musca domestica L., pupae placed in sentinel bags. 2. M. raptor, which was released inside the barn, parasitized fly pupae both inside and outside, and it achieved highest rates of parasitism in indoor straw calf-bedding and in outdoor manure and silage. 3. U. rufipes, which was released outside the barn, did not attack pupae inside the barn, and its highest rates of parasitism occurred in outdoor manure and silage. 4. M. raptor appeared to be more effective than U. rufipes in parasitizing pupae located at sites where natural fly-breeding occurred. 5. Interspecific competition did not appear to explain these distribution patterns. 6. There was no significant trend in parasitism by M. raptor as a function of distance from the release station. Furthermore, high rates of parasitism near open doorways and at an outdoor site 30 m away suggests that M. raptor dispersed throughout the barn and its immediate surroundings. 7. Air temperature was positively correlated to flight activity, but not to parasitization activity in natural fly-breeding substrates.
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The TOR pathway interacts with the insulin signaling pathway to regulate C. elegans larval development, metabolism and life span.
The highly conserved target-of-rapamycin (TOR) protein kinases control cell growth in response to nutrients and growth factors. In mammals, TOR has been shown to interact with raptor to relay nutrient signals to downstream translation machinery. We report that in C. elegans, mutations in the genes encoding CeTOR and raptor result in dauer-like larval arrest, implying that CeTOR regulates dauer diapause. The daf-15 (raptor) and let-363 (CeTOR) mutants shift metabolism to accumulate fat, and raptor mutations extend adult life span. daf-15 transcription is regulated by DAF-16, a FOXO transcription factor that is in turn regulated by daf-2 insulin/IGF signaling. This is a new mechanism that regulates the TOR pathway. Thus, DAF-2 insulin/IGF signaling and nutrient signaling converge on DAF-15 (raptor) to regulate C. elegans larval development, metabolism and life span.
Adaptor Proteins, Signal Transducing↗
Loss of the Mechanistic Target of Rapamycin Complex 1 Causes a Lethal Alpha-1 Antitrypsin Deficiency-Associated Liver Disease.
BACKGROUND & AIMS: SERPINA1 mutations cause retention of the otherwise secreted alpha-1 antitrypsin and lead to the proteotoxic alpha-1 antitrypsin deficiency-related liver disease. As mechanistic target of rapamycin is a key coordinator of proteostasis, we studied its role in alpha-1 antitrypsin deficiency-related liver disease. METHODS: PiZ mice overexpressing the characteristic SERPINA1 mutation were mated with rodents harboring a hepatocyte specific-ablation of the interaction partners regulatory-associated protein of mechanistic target of rapamycin or rapamycin-insensitive companion of mammalian target of rapamycin, corresponding to mechanistic target of rapamycin complexes 1 or 2, or with mice lacking mechanistic target of rapamycin. Serum proteomics, liver bulk proteomics, spatial proteomics, and metabolomics were applied to characterize molecular and metabolic alterations. RESULTS: At 2 months of age, PiZ-mTORΔhep and PiZ-RaptorΔhep but not PiZ-RictorΔhep mice showed signs of increased liver injury and mortality despite diminished hepatic alpha-1 antitrypsin accumulation. PiZ-RaptorΔhep animals displayed increased levels of the proapoptotic protein C/EBP homologous protein, but C/EBP homologous protein ablation did not rescue the phenotype. Serum proteomics revealed no signs of advanced synthetic liver failure but immature hepatocellular products. Liver bulk proteomics and small metabolite measurement demonstrated a metabolic reprogramming of PiZ-RaptorΔhep mice. Spatial proteomics revealed alterations in liver zonation with increased ammonia levels as the likely cause of death in PiZ-RaptorΔhep animals. CONCLUSIONS: In summary, in alpha-1 antitrypsin deficiency-related proteotoxic liver injury, regulatory-associated protein of mechanistic target of rapamycin preserves a liver zonation, thereby protecting from lethal metabolic dysregulation.
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An additional bone in the carpal region of raptorial birds.
In a series of 4 species of owls and 12 species of diurnal raptors, an additional bone was present bilaterally in the area of the carpus. Designating the bone as an "additional bone of the raptorial carpal region" is suggested pending appropriate embryological studies to determine the origin of the bone. Generally, the bone was present in owls and in diurnal raptors with relatively short, rounded wings, but was absent in species with longer, more tapered wings. The bone lies at the cranial edge of the carpal area near the radial carpal bone, and is fixed to the surrounding skeleton by ligaments. The tendon of the tensor patagium longus muscle has one slip that attaches to the additional bone and another that passes over its craniodorsal surface en route to insertion. Awareness of the occurrence of this bone in some raptors, but not others, is essential in clinical evaluation of wing injuries, as well as in forming a prognosis for the return to soundness, the potential for release, and, therefore, the life of an injured raptor.
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Problems of deep foveas.
Deep or convexiclivate foveas occur in some birds, including raptors, some lizards and certain deep-sea fishes. Theories on their function are reviewed. Common to raptor and deep-sea fish foveas is a radial fibre lining, dark staining so probably optically dense, adjacent to the less refractile vitreous. The foveal curvatures and size are remarkably similar in a wide taxonomic and size range of birds and fishes. Ray plotting through traced foveal outlines suggests that sharp images will be formed beneath the centre and shoulders, with the centre image enlarged enough to account for the high acuity of raptors. Deep foveas will also exaggerate eccentricity of off-centre images of a point source, such as deep-sea fishes may meet. Despite similarities in foveal shape, the receptors differ widely between species. Raptors, and notosudid fishes, have short cones. Searsid fishes have long single rods. Howella and Bajacalifornia have multiple bank rods, more in the fovea than the periphery. Those of Howella are shown to be multiple inner-outer segment complexes rather than interrupted single rods. Implications of foveal and receptor features are discussed.
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The Arabidopsis Mei2 homologue AML1 binds AtRaptor1B, the plant homologue of a major regulator of eukaryotic cell growth.
BACKGROUND: TOR, the target of the antibiotic rapamycin in both yeast and mammalian cells, is a potent cell growth regulator in all eukaryotes. It acts through the phosphorylation of downstream effectors that are recruited to it by the binding partner Raptor. In Arabidopsis, Raptor activity is essential for postembryonic growth. Though comparative studies suggest potential downstream effectors, no Raptor binding partners have been described in plants. RESULTS: AtRaptor1B, a plant Raptor homologue, binds the AML1 (Arabidopsis Mei2-like 1) protein in a yeast two-hybrid assay. This interaction is mediated by the N-terminal 219 residues of AML1, and marks AML1 as a candidate AtTOR kinase substrate in plants. The AML1 N-terminus additionally carries transcriptional activation domain activity. Plants homozygous for insertion alleles at the AML1 locus, as well as plants homozygous for insertion alleles at all five loci in the AML gene family, bolt earlier than wild-type plants. CONCLUSION: AML1 interacts with AtRaptor1B, homologue of a protein that recruits substrates for phosphorylation by the major cell-growth regulator TOR. Identification of AML1 as a putative downstream effector of TOR gives valuable insights into the plant-specific mode of action of this critical growth regulator.
Alleles↗
Parasitization by pteromalid wasps (Hymenoptera) of freeze-killed house fly (Diptera: Muscidae) puparia at varying depths in media.
Three laboratory experiments were performed to assess parasitization of freeze-killed house fly puparia, buried 0 to 6 cm in media, by Muscidifurax raptor Girault & Saunders, Muscidifurax raptorellus Kogan & Legner, Muscidifurax zaraptor Kogan & Legner, Trichomalopsis sarcophagae (Gahan) and Urolepis rufipes (Ashmead) (Hymenoptera: Pteromalidae). Virtually no parasitization occurred at depths greater than 1 cm in large arenas (988 cm2) with densities of 0.3 puparia and 0.008 female parasitoids per cm2. Parasitization was observed at depths as great as 4 cm for three of five species in small arenas (3 cm2) with densities of 6.4 puparia and 1.0 female per cm2. Combined across experiments, M. raptor achieved the highest level of parasitization, followed by M. zaraptor, M. raptorellus, U. rufipes, and T. sarcophagae. The greatest number of F1 females was produced by the gregarious species T. sarcophagae (834 female female) and M. raptorellus (708 female female), and then by the solitary species M. raptor (530 female female), M. zaraptor (365 female female) and U. rufipes (163 female female). High parasitization by M. raptor and high production of offspring by T. sarcophagae identify these species as being particularly attractive as biological control agents.
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Nest-Site Selection by black sparrowhawks Accipiter melanoleucus: implications for managing exotic pulpwood and sawlog forests in South Africa.
This study provides timber growers with silvicultural guidelines for establishing and maintaining nest-tree habitat for native black sparrowhawks (Accipiter melanoleucus) in commercial planted forests in South Africa. In this country, exotic eucalypts and pines are planted principally for pulpwood and sawlog production. Nineteen nests were sampled in indigenous forests and 58 nests in exotic forests. Although mean nest heights differed between indigenous and exotic trees, in all trees, nests were positioned, on average, at 64% of tree height. Black sparrowhawks nested near stand edges, probably seeking a compromise between nesting adjacent to open hunting habitat and selecting an insulated tree from within the forest. Black sparrowhawks nested in tall trees ( X- = 18-33 m for different tree species classes) with a large diameter (>60 cm). Unfortunately, the South African pulpwood and sawlog industry employ short rotations (<16 years) and high tree densities (>700 trees/ha) that do not allow the trees to attain the characteristics suitable for black sparrowhawk nesting sites. Eucalypt and pine nest stands must be of 25 x 25 m minimum size and incorporate 10 trees at minimum heights of 21 and 18 m and diameters of 37 and 35 cm, respectively. If such nest-tree stands are set aside as islands in a sea of commercial forests, and black sparrowhawks and other forest raptors nest in them, timber growers will improve the tree-nesting raptor diversity of planted forests. If, however, these raptors prey upon species of conservation importance, the management recommendations could be reversed to limit the potential for predation.
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