Food partitioning between breeding White-tailed Kites (Elanus leucurus; Aves; Accipitridae) and Barn Owls (Tyto alba; Aves; Tytonidae) in southern Brazil.

I examined the diet of breeding White-tailed Kites (Elanus leucurus; Aves; Accipitridae) and Barn Owls (Tyto alba; Aves; Tytonidae) in an agrarian area of southern Brazil by analyzing regurgitated prey remains. The objective was to evaluate how these raptors, which differ markedly in their hunting activity periods (owls are nocturnal and kites diurnal), share their mammalian food component. 2,087 prey consumed by Barn Owls and 1,276 by White-tailed Kites were identified. They presented a high overlap of food-niches (Piankas index was 0.98). Based on the daily activity period of their main small mammal prey, a lower overlap would be expected. The crepuscular/nocturnal Mus musculus was the main prey for the diet of breeding Barn Owls (81%) and White-tailed Kites (63%). This small exotic rodent provided 63% of the small mammal biomass ingested by owls and 44% by kites. Larger native small mammals were also considered important for the diet of kites, mainly because of their biomass contribution. Although these raptors differ markedly in their hunting activity periods, Barn Owls and White-tailed Kites are very similar predators in southern Brazil, overlapping their diets.     

Wing and hindlimb myology of vultures and raptors (Accipitriformes) in relation to locomotion and foraging

Herein, we compare functional muscle properties among convergent forms of large, obligate avian scavengers. We performed quantitative analyses of all the muscle masses and cross‐sectional areas (CSA) of the wings and hindlimbs of five species from two families, Cathartidae (New World vultures; Cathartes aura and Vultur gryphus) and Accipitridae (Old World vultures and raptors; Gyps africanus, Aquila rapax, and Buteo lineatus). These species comprise two paraphyletic functional groups, raptors (Aquila and Buteo) and vultures (Gyps, Cathartes, and Vultur). Our ordination analyses based on all of the muscles of the wings, hindlimbs, and wing and hindlimb muscles combined produced patterns that appeared to be more related to phylogeny, with a hint of a functional signal in wing muscle CSA. However, when wing muscles were grouped according to their functional roles (upstroke, downstroke, and wing stabilization), the percentages of mass and CSA allocated to the upstroke and stabilizing muscles were 1.4–5% greater in the vultures than in the raptors. Conversely, when hindlimb muscles were grouped according to their roles in grasping and terrestrial locomotion, the percentages of mass and CSA allocated to grasping muscles were 5.9–14% greater in the raptors. Our results provide a baseline for future lines of inquiry aimed at understanding how muscle mass and CSA are affected differentially across locomotor modules, possibly in response to differential demands on wing and hindlimb function experienced by these disparate accipitriform clades.     

The effect of rainfall on the breeding behaviour of the Red Bishop,Euplectes orix

The behaviour and activities of 6 458 raptors (Accipitridae and Falconidae) and 1 947 Corvidae in the Karoo, South Africa, were recorded during the period January 1988 to June 2000 (n = 208 surveys) over a total distance of 90 012km. A significantly larger proportion of raptors and corvids were recorded foraging in road verges, or flying along roads than foraging or flying over rangelands. About 21% of all observations of crows feeding or foraging were associated with road-kills, whereas less than 2% of observations of feeding and foraging Accipitridae and Falconidae were associated with road-kills. The most frequent Accipitridae feeding on road-kills were Pale Chanting Goshawk (Melierax canorus), Yellow-billed Kite (Milvus migrans parasitus) and Jackal Buzzard (Buteo rufofuscus). There was no seasonal pattern in the number of crows feeding on roadkills, although there was a trend for more mammals to be killed on the roads, and thus more available food, in winter (June). It is likely that Accipitridae and Falconidae are attracted to roads by the availability of perches and the relatively productive road verges rather than the availability of road-killed animals, whereas crows may be attracted by road-kills as well.     

Spatial,road geometric and biotic factors associated with Barn Owl mortality along an interstate highway

Highway programmes typically focus on reducing vehicle collisions with large mammals because of economic or safety reasons, while overlooking the millions of birds that die annually from traffic. We studied wildlife–vehicle collisions along an interstate highway in southern Idaho, USA, with among the highest reported rates of American Barn Owl Tyto furcata road mortality. Carcass data from systematic and ad hoc surveys conducted in 2004–2006 and 2013–2015 were used to explore the extent to which spatial, road geometric and biotic factors explained Barn Owl–vehicle collisions. Barn Owls outnumbered all other identified vertebrate species of roadkill and represented > 25% of individuals and 73.6% of road‐killed birds. At a 1‐km highway segment scale, the number of dead Barn Owls decreased with increasing numbers of human structures, cumulative length of secondary roads near the highway and width of the highway median. The number of dead Barn Owls increased with higher commercial average annual daily traffic (CAADT), small mammal abundance index and grass rather than shrubs in the roadside verge. The small mammal abundance index was also greater in roadsides with grass vs. mixed shrubs, suggesting that Barn Owls may be attracted to grassy portions of the highway with more abundant small mammals for hunting prey. When assessed at a 3‐km highway segment scale, the number of dead Barn Owls again increased, with higher CAADT as well as with greater numbers of dairy farms. At a 5‐km scale, the number of dead Barn Owls increased with a greater percentage of cropland near the highway. Although human conversion of the environment from natural shrub‐steppe to irrigated agriculture in this region of Idaho has probably enhanced habitat for Barns Owls, it simultaneously has increased risk for owl–vehicle collisions where an interstate highway traverses the altered landscape. We review some approaches for highway mitigation and suggest that reducing wildlife–vehicle collisions involving Barn Owls may contribute to the persistence of this species.     

Comparative and functional myology of the prehensile tail in new world monkeys

The caudal myology of prehensile-tailed monkeys (Cebus apella, Alouatta palliata, Alouatta seniculus, Lagothrix lagotricha, and Ateles paniscus) and nonprehensile-tailed primates (Eulemur fulvus, Aotus trivirgatus, Callithrix jacchus, Pithecia pithecia, Saimiri sciureus, Macaca fascicularis, and Cercopithecus aethiops) was examined and compared in order to identify muscular differences that correlate with osteological features diagnostic of tail prehensility. In addition, electrophysiological stimulation was carried out on different segments of the intertransversarii caudae muscle of an adult spider monkey (Ateles geoffroyi) to assess their action on the prehensile tail. Several important muscular differences characterize the prehensile tail of New World monkeys compared to the nonprehensile tail of other primates. In atelines and Cebus, the mass of extensor caudae lateralis and flexor caudae longus muscles is more uniform along the tail, and their long tendons cross a small number of vertebrae before insertion. Also, prehensile-tailed monkeys, especially atelines, are characterized by well-developed flexor and intertransversarii caudae muscles compared to nonprehensile-tailed primates. Finally, Ateles possesses a bulkier abductor caudae medialis and a more cranial origin for the first segment of intertransversarii caudae than do other prehensile-tailed platyrrhines. These myological differences between nonprehensile-tailed and prehensile-tailed primates, and among prehensile-tailed monkeys, agree with published osteological and behavioral data. Caudal myological similarities and differences found in Cebus and atelines, combined with tail-use data from the literature, support the hypothesis that prehensile tails evolved in parallel in Cebus and atelines. © 1995 Wiley-Liss, Inc.     

Predatory Functional Morphology in Raptors: Interdigital Variation in Talon Size Is Related to Prey Restraint and Immobilisation Technique

Despite the ubiquity of raptors in terrestrial ecosystems, many aspects of their predatory behaviour remain poorly understood. Surprisingly little is known about the morphology of raptor talons and how they are employed during feeding behaviour. Talon size variation among digits can be used to distinguish families of raptors and is related to different techniques of prey restraint and immobilisation. The hypertrophied talons on digits (D) I and II in Accipitridae have evolved primarily to restrain large struggling prey while they are immobilised by dismemberment. Falconidae have only modest talons on each digit and only slightly enlarged D-I and II. For immobilisation, Falconini rely more strongly on strike impact and breaking the necks of their prey, having evolved a ‘tooth’ on the beak to aid in doing so. Pandionidae have enlarged, highly recurved talons on each digit, an adaptation for piscivory, convergently seen to a lesser extent in fishing eagles. Strigiformes bear enlarged talons with comparatively low curvature on each digit, part of a suite of adaptations to increase constriction efficiency by maximising grip strength, indicative of specialisation on small prey. Restraint and immobilisation strategy change as prey increase in size. Small prey are restrained by containment within the foot and immobilised by constriction and beak attacks. Large prey are restrained by pinning under the bodyweight of the raptor, maintaining grip with the talons, and immobilised by dismemberment (Accipitridae), or severing the spinal cord (Falconini). Within all raptors, physical attributes of the feet trade off against each other to attain great strength, but it is the variable means by which this is achieved that distinguishes them ecologically. Our findings show that interdigital talon morphology varies consistently among raptor families, and that this is directly correlative with variation in their typical prey capture and restraint strategy.     

Effects of the risk of competition and predation on large secondary cavity breeders

The effects of competition and risk of predation on secondary cavity breeders were examined between the 2008 and 2009 breeding seasons using an experimental design manipulating two nest entrance sizes (large entrances allowed Barn Owls (Tyto alba) to enter, while the small entrances excluded them). During the 2009 breeding season, the entrance sizes of nest boxes were exchanged, so that if during one year a nest box in a particular location had a small entrance, the second year it had a large entrance and vice versa. Barn Owls and Eurasian Kestrels (Falco tinnunculus) occupied 67.3 and 17.3%, respectively, of large entrance nest boxes. Significantly more Jackdaws (Corvus monedula), House Sparrows (Passer domesticus) and Scops Owls (Otus scops) bred in nest boxes with small than with large entrances. After nest box entrance sizes were exchanged, Barn Owls and smaller species did not breed in the same nest boxes with the new entrance size. Jackdaws probably did not breed in large entrance nest boxes due both to exploitation competition (Barn Owls and Eurasian Kestrels occupied the majority of large entrance nest boxes), and may also have avoided empty nest boxes because of the risk of interference competition; whereas smaller species may have also avoided large entrance nest boxes due to risk of predation.     

The complete mitochondrial genome of Japanese sparrowhawk (Accipiter gularis) and the phylogenetic relationships among some predatory birds

Phylogenetic relationships among raptors, especially various groups are rather complex and controversial. We determined the complete mtDNA of Japanese sparrowhawk, and estimated phylogenetic trees based on the complete mtDNA alignment of it and 36 other raptor species, to clarify raptor phylogenetics. Phylogenetic trees were also estimated using a multiple sequence alignment of 12S rRNA and 16S rRNA from 81 typical species in GenBank, to further clarify the phylogenetic relationships of several groups among the raptors. The new mtDNA is a circular molecule, 17 917 bp in length, containing the 37 typical genes, with a pseudo-control region. ATG is generally the start codon, TAA is the most frequent stop codon. All tRNAs can be folded into canonical cloverleaf secondary structures except for tRNA^{Ser (AGY)} and tRNA^{Leu (CUN)}, which are missing the “DHU” arm. Phylogenetic relationships demonstrate that raptors can be divided into four branches: Accipitriformes, Falconiformes, Strigiformes and Caprimulgiformes in this study. We suggest that Accipitriformes should to be an independent order, Accipitriformes. The results also indicate that Accipitriformes contains three clades: Accipitridae, Pandionidae and Sagittariidae. Strigiformes includes species from Tytonidae and Strigidae. Caprimulgiformes contains Aegothelidae and Caprimulgidae.     

Habitat selection by a predator of rodent pests is resilient to wildfire in a vineyard agroecosystem

Conservation of uncultivated habitats can increase the potential for ecosystem services in agroecosystems, but these lands are also susceptible to wildfires in the arid western United States. In Napa Valley, California, abundant rodent pests and an interest in integrated pest management have led wine producers to use nest boxes to attract Barn Owls (Tyto furcata) to winegrape vineyards. The viability of this practice as a method to control rodent pests depends heavily on the amount of hunting effort that Barn Owls expend in vineyards, which is known to be influenced by the amount of uncultivated land cover types surrounding the nest box. Wildfires burned nearly 60,000 ha of mainly urban and uncultivated lands surrounding Napa Valley in 2017, altering Barn Owl habitats. We compared GPS tracking data from 32 Barn Owls nesting in 24 individual nest boxes before and after the fires to analyze their hunting habitat selection. Owls with burned areas available to them after the fires had home ranges that shifted toward the fires, but selection was not strongly associated with burned areas. Though there was some spatial use of burned areas, selection of land cover types was similar for birds before and after the fires and in burned and unburned areas. The strongest selection was for areas closest to the nest box, and most recorded locations were in grassland, though selection indicated that owls used land cover types in proportion to their availability. Overall, habitat selection was resilient to changes caused by wildfires. These results are important for farmers who use nest boxes as a means of rodent control, which may be affected after dramatic disturbance events, especially as wildfires increase in the western United States.     

Extirpation of alternative prey during a small rodent crash

Summary We document two episodes, in different years, of Barn Owls (Tyto alba) preying on a winter population of Burrowing Owls (Athene cunicularia) on a southern California island. The predation in each case followed a marked shift in the diet of the Barn Owls, due to the cyclic decline of their normal small mammal prey. Heavy predation in the first year resulted in the extirpation of the Burrowing Owls on the island. Such heavy predation on alternative prey species is commonly reported in cyclic predator-prey systems, however this is the first documented case of extirpation of the alternative prey. Complete elimination of any prey species by terrestrial predators is, in fact, very rare.     

Monophyletic groups within 'higher land birds'– comparison of morphological and molecular data

The relationships within the ‘higher land birds’ and putatively related taxa are analysed in a study using 89 morphological characters and DNA sequences of three nuclear, protein‐coding genes, c‐myc, RAG‐1, and myoglobin intron II. Separate analyses of the different data sets and a ‘total evidence’ analysis in which the data sets of the morphological and molecular analyses were combined are compared. All three analyses support the hitherto disputed sister group relationship between Pici (Ramphastidae, Indicatoridae and Picidae) and Galbulae (Galbulidae and Bucconidae). Previously unrecognized osteological synapomorphies of this clade are presented. All analyses further resulted in monophyly of the taxon [Aegothelidae + (Apodidae/Hemiprocnidae + Trochilidae)]. Analysis of the morphological data and of the combined data set also supported monophyly of the taxon [Strigiformes + (Falconidae + Accipitridae)]. The morphological data further support monophyly of the taxon (Upupidae + Bucerotidae). Other placements in the three analyses received either no or only weak bootstrap support.     

Tail myology and flight behaviour: Differences between caracaras,falcons and forest falcons (Aves,Falconiformes)

Caracaras, falcons and forest falcons, which are representative of the three subfamilies of the family Falconidae, have different flight behaviour. Since, during flight, the tail works in coordination with the wings, the tail muscles could be indicative of the type of flight behaviour. The aim of this work was to describe in detail the little-known tail muscles of the Falconidae and to explore their possible association with this different behaviour, by using the muscle mass as an indicator. To this end, the tail muscles of 18 specimens representing the three subfamilies of Falconidae were dissected, weighed and their percentage to the body mass calculated. The possible differences in tail muscle mass between Falconinae and Polyborinae were explored with a Bayesian statistical approach. In all species, the muscles depressor caudae and levator caudae had the highest mass values (0.028%–0.329% and 0.120%–0.274%, respectively), in accordance with the key movements performed during flight, that is, the tail depression and elevation. The total muscle masses of Falconinae and those of Polyborinae were significantly different (p < 0.05). This difference can be related with the different flight behaviour of falcons and caracaras, that is, fast and erratic flight, respectively.     

The deep divergences of neornithine birds: a phylogenetic analysis of morphological characters

Consensus is elusive regarding the phylogenetic relationships among neornithine (crown clade) birds. The ongoing debate over their deep divergences is despite recent increases in available molecular sequence data and the publication of several larger morphological data sets. In the present study, the phylogenetic relationships among 43 neornithine higher taxa are addressed using a data set of 148 osteological and soft tissue characters, which is one of the largest to date. The Mesozoic non‐neornithine birds Apsaravis, Hesperornis, and Ichthyornis are used as outgroup taxa for this analysis. Thus, for the first time, a broad array of morphological characters (including both cranial and postcranial characters) are analyzed for an ingroup densely sampling Neornithes, with crown clade outgroups used to polarize these characters. The strict consensus cladogram of two most parsimonious trees resultant from 1000 replicate heuristic searches (random stepwise addition, tree‐bisection‐reconnection) recovered several previously identified clades; the at‐one‐time contentious clades Galloanseres (waterfowl, fowl, and allies) and Palaeognathae were supported. Most notably, our analysis recovered monophyly of Neoaves, i.e., all neognathous birds to the exclusion of the Galloanseres, although this clade was weakly supported. The recently proposed sister taxon relationship between Steatornithidae (oilbird) and Trogonidae (trogons) was recovered. The traditional taxon “Falconiformes” (Cathartidae, Sagittariidae, Accipitridae, and Falconidae) was not found to be monophyletic, as Strigiformes (owls) are placed as the sister taxon of (Falconidae + Accipitridae). Monophyly of the traditional “Gruiformes” (cranes and allies) and ”Ciconiiformes” (storks and allies) was also not recovered. The primary analysis resulted in support for a sister group relationship between Gaviidae (loons) and Podicipedidae (grebes)—foot‐propelled diving birds that share many features of the pelvis and hind limb. Exclusion of Gaviidae and reanalysis of the data set, however, recovered the sister group relationship between Phoenicopteridae (flamingos) and grebes recently proposed from molecular sequence data.     

Direct and Indirect Impacts of Raptor Predation on Lemurs in Southeastern Madagascar

I calculated rates of predation by 2 species of diurnal raptors, Polyboroides radiatus and Accipiter henstii, on the lemur community of Ranomafana National Park, Madagascar from 2700 h of observation and 470 prey deliveries at 7 nests of each hawk species. The 2 hawks consumed 7 of 12 lemurs found in the park region, with a body mass of 63–3500 g and including diurnal and nocturnal species of all group sizes. Calculations of predation rates indicate that raptor predation is a significant cause of mortality for lemur populations relative to other causes. Minimum rates of predation by Polyboroides radiatus and Accipiter henstii on Microcebus rufus, Cheirogaleus major, Avahi laniger, Hapalemur griseus, Eulemur fulvus rufus, Eulemur rubriventer, and Varecia variegata resulted in the raptors removing of 1–21% of the population per yr, similar to other rates of predation on primates documented in the literature. Modeling of lemur populations under varying levels of raptor predation pressure that I calculated found that one may attribute 3–17% of adult, juvenile, and infant mortality for nocturnal lemurs and 2–66% of adult, juvenile, and infant mortality for diurnal lemurs to diurnal raptor predation. Raptor predation may significantly depress intrinsic growth rates and carrying capacity of Avahi laniger, Hapalemur griseus, Eulemur fulvus rufus, Eulemur rubriventer, and Varecia variegata owing to their low fecundities, long life spans, and long age to sexual maturation. Nocturnal lemurs may best avoid predation by diurnal raptors by exhibiting a solitary lifestyle and cryptic antipredator tactics, whereas, diurnal lemurs benefit less by increasing group size than by using specific antipredator tactics.     

Hawk Eyes II: Diurnal Raptors Differ in Head Movement Strategies When Scanning from Perches

Background

Relatively little is known about the degree of inter-specific variability in visual scanning strategies in species with laterally placed eyes (e.g., birds). This is relevant because many species detect prey while perching; therefore, head movement behavior may be an indicator of prey detection rate, a central parameter in foraging models. We studied head movement strategies in three diurnal raptors belonging to the Accipitridae and Falconidae families.

Methodology/Principal Findings

We used behavioral recording of individuals under field and captive conditions to calculate the rate of two types of head movements and the interval between consecutive head movements. Cooper''s Hawks had the highest rate of regular head movements, which can facilitate tracking prey items in the visually cluttered environment they inhabit (e.g., forested habitats). On the other hand, Red-tailed Hawks showed long intervals between consecutive head movements, which is consistent with prey searching in less visually obstructed environments (e.g., open habitats) and with detecting prey movement from a distance with their central foveae. Finally, American Kestrels have the highest rates of translational head movements (vertical or frontal displacements of the head keeping the bill in the same direction), which have been associated with depth perception through motion parallax. Higher translational head movement rates may be a strategy to compensate for the reduced degree of eye movement of this species.

Conclusions

Cooper''s Hawks, Red-tailed Hawks, and American Kestrels use both regular and translational head movements, but to different extents. We conclude that these diurnal raptors have species-specific strategies to gather visual information while perching. These strategies may optimize prey search and detection with different visual systems in habitat types with different degrees of visual obstruction.     

Tawny Owl Strix aluco as an indicator of Barn Owl Tyto alba breeding biology and the effect of winter severity on Barn Owl reproduction

In the temperate zone, food availability and winter weather place serious constraints on European Barn Owl Tyto alba populations. Using data collected over 22 years in a Swiss population, we analysed the influence of early pre‐breeding food conditions and winter severity on between‐year variations in population size and reproductive performance. To estimate pre‐breeding food conditions, we attempted a novel approach based on an index that combines Tawny Owl Strix aluco reproductive parameters and the occurrence of wood mice Apodemus sp. in their diet. Tawny Owls breed earlier in the season than Barn Owls and are strongly dependent on the abundance of wood mice for breeding. This index was strongly positively associated with the number of breeding pairs and early breeding in the Barn Owl. Winter severity, measured by snow cover and low temperatures, had a pronounced negative influence on the size of the breeding population and clutch size. Food conditions early in the breeding season and winter severity differentially affect the Barn Owl life cycle. We were able to use aspects of the ecology and demography of the Tawny Owl as an indicator of the quality of the environment for a related species of similar ecology, in this case the Barn Owl.     

Evolution of nocturnality in bats: Potential competitors and predators during their early history

Despite their taxonomic and ecological diversity, modern bats (Order Chiroptera) are almost exclusively nocturnal. This behaviour is too ubiquitous to be explained by common patterns of temporal variation in availability of their diverse food sources or by the risk of hyperthermia when flying during the day. Other explanations for bat nocturnality include competition and increased predation risk from birds during the day. In the early and mid Eocene, the known bat fauna consisted of several insectivorous species of sizes similar to those of the modern European assemblage. This fauna was contemporaneous with several species of predatory birds, including owls (Strigiformes), hawks (Accipitridae), falcons (Falconidae) and rollers (Coraciiformes), which were the same size as modern predators on bats. Predation risk could therefore have been a significant factor preventing the early bats from becoming diurnal. Competition from aerial insectivorous birds, however, was less likely to have been significant for bats during the early Eocene, since very few such groups, mainly small Aegialornithidae, were present, with most of the major groups of aerial insectivores evolving later.     

FIRST ANNUAL REPORT ON THE RHODESIAN ORNITHOLOGICAL SOCIETY'S NEST RECORD SCHEME FOR THE YEAR ENDED 30 JUNE, 1956

MENDELSOHN, J. M. 1989. Habitat preferences, population size, food and breeding of six owl species in the Springbok Flats, South Africa. Ostrich 60:183-190.

Information on the habitat preferences, population size, food and breeding of Barn, Grass, Whitefaced, Marsh, Pearlspotted and Spotted Eagle Owls was obtained in a 6900-ha area in the Springbok Flats, South Africa. Seventy-two per cent of the area consisted of cultivated fields not usually used by owls. Hunting, roosting and nesting requirements were largely met in 1930 ha of verges, farmyards and patches of wood land ant grassland, here was an estimated total population of 303 owls in the area, giving an overall density of 22,7 ho/owl for the whole area or 6.4 ha/owl for those areas used by owls. These high densities were attributed to an abundance of Mastomys natalensis, the most important prey item for all except Pearlspotted Owls. Rates of predation on M. natalensis varied in relation to their population density, as indicated by rodent trapping results. Marsh Owls ate more insects in summer than at other times. Barn and Marsh Owls usuall laid in March-April and August-September, while other species started breeding in July-October. de timing of breeding of some owls may be related to changes in rates of recruitment of juvenile M. natalensis. Most Marsh Owl nests were placed on the southwestern sides of grass clumps or shrubs.     

Die mechanik der syndactylen zehen von macropus und anderen beuteltieren und ihre verwendung als putzorgan

Ohne ZusammenfassungErklärung der abkürzungen Astr. Astragalus - C I–III Cuneiforme I–III. - Ca. Calcaneus. - cd.m.Sp. caudales, mediales Sprunggelenksband. - C.l. Caput laterale gastrocnemii. - C.m. Caput mediale gastrocnemii. - Cp.f. Caput fibulae. - cr.m.Sp. craniales, mediales Sprunggelenksband. - C.t. Crista tibiae. - D.I–V Digitus I–V. - d.m.S. Dorso-mediales Seitenband. - Fib. Fibula. - Gfl. C III Gelenkfläche mit dem Cuneiforme III. - Gfl.Cale. Gelenkfläche mit dem Calcaneus. - Gefl.Cb. Gelenkfläche mit dem Cuboid. - Gfl.Mt. IV Gelenkfläche mit dem Metatarsale IV. - l.S. laterales Seitenband. - M.add. V Muse. adductor digiti V. - M.e.h.l. Musc. extensor hallucis longus. - M.e.l. Musc. extensor longus digitorum. - M.e.l. IV Musc. extensor longus digiti IV. - M.e.l. II–V Musc. extensor longus digitorum II–V. - M.e.l. II, III Musc. extensor longus digitorum II, III. - M.fl.br. II–V Musc. flexor brevis digiti II–V. - M.fl.d.p.prof. Muse. flexor digitorum pedis profundus. - M.l. Margo lateralis tibiae. - Mm.l. Musculi lumbricales. - M.p.l. Musc. peronaeus longus. - M.p. IV Musc. peronaeus digiti IV. - M.p. V Musc. peronaeus digiti V. - M.p.t. Musc. peronaeus tertius. - M.pl. Muse. plantaris (= Musc. fl. dig. ped. sublimis). - M.pl.l. lateraler Abzweig der Plantarissehne. - M.popl. Musc. popliteus. - M.s. Muse. soleus. - M.t.a. Muse. tibialis anticus. - M.t.p. Musc. tibialis posticus. - M.tric.sur.C.l. Musc. triceps surae, Caput laterale. - M.tric.sur.C.m. Musc. tricepssurae, Caput mediate. - Mt I-Mt V Metatarsale I–V. - Mt.Ph.Gk. Metatarso-Phalangealgelenk. - N. Naviculare. - o.l. Sp. oberes laterales Sprunggelenksband. - Ph. I-Ph. III Phalanx I–III. - pl.m.S. plantares mediales Seitenband. - Ssb.Mt.Ph. Gk. Sesambeine des Metatarso-Phalangealgelenkes. - S.t.p. Sehne des Musc. tibialis posticus. - u.l.Sp. unteres laterales Sprunggelenksband. - U.M.p. IV Ürsprungszone des Muse. paronaeus IV. - I–V Strahlen des Fußskelettes.     

Studies on the tendinous compartments of the extensor muscles on the back of the human hand and their tendon sheaths. I

In 47 dissected right and left hands of adults of both sexes, kept in a moist condition, significant practical-clinical investigations of the transitional zone between forearm and hand were undertaken. In particular it was sought to determine the characteristic sizes of the extensor retinaculum, the osteofibrous tunnels, the insertion tendons of the hand and finger extensor muscles, and their tendon sheaths. Together with the palmar carpal ligament, the 2 to 3 cm wide extensor retinaculum annularly surrounds the whole circumference of the carpus. It extends obliquely from radial-proximal to ulnar-distal and conducts the extensor tendons over the carpal articulations. According to recent studies, it is divided into a superficial and a deep fibrous layer. From the undermost surface, vertical and oblique septa run to the plane of the forearm and carpal bones. They separate the fibrous portion of the 6 tendinous compartments of the dorsum manus. In 8.5% of cases, an accessory and completely independent tunnel of the extensor pollicis brevis muscle exists in the material investigated, and in 2.2% of cases, there is an additional tunnel for the extensor carpi radialis muscle. Hence, one occasionally finds 8 separate osteofibrous gliding compartments for the extensor muscles in the dorsal hand region. The longest tunnel belongs, as a rule, to the extensor digiti minimi muscle, whilst the widest pertains to the extensor digitorum muscle. Within the tunnel and also proximal and distal to it, the extensor tendons are surrounded by synovial sheaths. Because of its wide encroachment on the dorsum of the hand, the insertion tendon of the extensor digiti minimi muscle possesses the longest tendon sheath, measuring 68.8 mm. The next longest sheath, that of the extensor pollicis longus muscle, which measures 56.2 mm, begins further proximal to the gap of the radiocarpal articulation. In 12.8% of cases, there are divided sheaths of the abductor pollicis longus and of the extensor pollicis brevis muscle. The tendon sheath of both extensor carpi radiales muscles is frequently divided into 2 compartments which, in 2/3 of cases, communicate. The compartment of the extensor carpi radialis brevis muscle, in 91.5% of cases, shares a window-like opening with the roof of the synovial vagina of the extensor pollicis longus muscle. The tendon sheath of the long extensor muscles of the fingers originates 5 mm proximal to the forearm border of the extensor retinaculum and has a communal recess. The IVth tendon sheath opens distally and splays out in a glove-like manner to some distal recesses.(ABSTRACT TRUNCATED AT 400 WORDS)