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Head Morphology (head + morphology)

Distribution by Scientific Domains

Life Sciences	70%
Medical Sciences	11%

Selected Abstracts

Head morphology in perinatal dolphins: A window into phylogeny and ontogeny

JOURNAL OF MORPHOLOGY, Issue 11 2006
Michael A. Rauschmann
Abstract In this paper on the ontogenesis and evolutionary biology of odontocete cetaceans (toothed whales), we investigate the head morphology of three perinatal pantropical spotted dolphins (Stenella attenuata) with the following methods: computer-assisted tomography, magnetic resonance imaging, conventional X-ray imaging, cryo-sectioning as well as gross dissection. Comparison of these anatomical methods reveals that for a complete structural analysis, a combination of modern imaging techniques and conventional morphological methods is needed. In addition to the perinatal dolphins, we include series of microslides of fetal odontocetes (S. attenuata, common dolphin Delphinus delphis, narwhal Monodon monoceros). In contrast to other mammals, newborn cetaceans represent an extremely precocial state of development correlated to the fact that they have to swim and surface immediately after birth. Accordingly, the morphology of the perinatal dolphin head is very similar to that of the adult. Comparison with early fetal stages of dolphins shows that the ontogenetic change from the general mammalian bauplan to cetacean organization was characterized by profound morphological transformations of the relevant organ systems and roughly seems to parallel the phylogenetic transition from terrestrial ancestors to modern odontocetes. J. Morphol., 2006. © 2006 Wiley-Liss, Inc. [source]

Habitat complexity modulates phenotype expression through developmental plasticity in the threespine stickleback

BIOLOGICAL JOURNAL OF THE LINNEAN SOCIETY, Issue 2 2010
MÓNICA V. GARDUÑO-PAZ
The expression of alternative phenotypes within a single species is often considered to be the result of ontogenetic processes and specifically phenotypic plasticity responses to exposure to different environmental conditions. In fish, which have been widely used to test such questions, exposure to different diets is the most frequently described initiator of plastic responses. The effect of physical characteristics of the habitat on fish morphology has not been fully explored. In the present study, a clear effect of habitat complexity on fish shape was found. Threespine sticklebacks were exposed to two different habitat treatments, simple and complex, over a 17-week period. The exposure to the habitats resulted in the expression of very significant differences in body and head morphologies and spine position, showing that the physical environment can modulate the expression of traits through phenotypic plasticity during ontogeny. © 2010 The Linnean Society of London, Biological Journal of the Linnean Society, 2010, 100, 407,413. [source]

Sexual dimorphism of head morphology in three-spined stickleback Gasterosteus aculeatus

JOURNAL OF FISH BIOLOGY, Issue 4 2010
W. E. Aguirre
This study examined sexual dimorphism of head morphology in the ecologically diverse three-spined stickleback Gasterosteus aculeatus. Male G. aculeatus had longer heads than female G. aculeatus in all 10 anadromous, stream and lake populations examined, and head length growth rates were significantly higher in males in half of the populations sampled, indicating that differences in head size increased with body size in many populations. Despite consistently larger heads in males, there was significant variation in size-adjusted head length among populations, suggesting that the relationship between head length and body length was flexible. Inter-population differences in head length were correlated between sexes, thus population-level factors influenced head length in both sexes despite the sexual dimorphism present. Head shape variation between lake and anadromous populations was greater than that between sexes. The common divergence in head shape between sexes across populations was about twice as important as the sexual dimorphism unique to each population. Finally, much of the sexual dimorphism in head length was due to divergence in the anterior region of the head, where the primary trophic structures were found. It is unclear whether the sexual dimorphism was due to natural selection for niche divergence between sexes or sexual selection. This study improves knowledge of the magnitude, growth rate divergence, inter-population variation and location of sexual dimorphism in G. aculeatus head morphology. [source]

Head morphology in perinatal dolphins: A window into phylogeny and ontogeny

Sperm head morphology in 36 species of artiodactylans, perissodactylans, and cetaceans (Mammalia)

JOURNAL OF MORPHOLOGY, Issue 2 2005
Amy Downing Meisner
Abstract Detailed descriptions of mammalian sperm morphology across a range of closely related taxa are rare. Most contributions have been generalized descriptions of a few distantly related mammalian species. These studies have emphasized a generalized ungulate sperm morphology, but have not underscored several important morphological differences in ungulate sperm, such as head shape. The present study is the first to document descriptions of sperm head morphology using cold field-emission scanning electron microscopy (FE-SEM) for a large number of closely related mammalian species. In total, the sperm of 36 species in three orders: Artiodactyla (even-toed ungulates), Cetacea (whales, porpoises, and dolphins), and Perissodactyla (odd-toed ungulates) were examined to gather new information relevant to the debate about the phylogenetic placement of cetaceans relative to terrestrial ungulates. In all species examined, the sperm heads were generally flattened and ovate in shape with a distinct apical ridge, although considerable variation in sperm head shape was detected, both within and between orders. In artiodactylans, the sperm head was uniformly flat in lateral view, whereas perissodactylan and cetacean sperm heads showed a distinct posterior thickening. In both artiodactylans and perissodactylans, the mitochondria were elongate and wound in a tight helix around the midpiece, whereas in cetaceans the mitochondria were rounded and appeared to be randomly arranged around the midpiece. Additionally, prominent ridges running along the anterior,posterior axis were observed in the postacrosomal region of the sperm head in four species of cetaceans. These ridges were not observed in any of the terrestrial ungulates examined. Pits or fenestrations were detected in the postacrosomal region in most artiodactylan species examined; these structures were not detected in perissodactylans or cetaceans. The equatorial segment of the acrosome was detected in the artiodactylan species examined, tentatively identified in perissodactylans, but not found in cetaceans. Its shape and location are described for relevant taxa. The presence of a recently reported substructure within the equatorial segment (the equatorial subsegment; Ellis et al. [2002] J Struct Biol 138:187,198) was detected in artiodactylans, and its shape is described for the species examined. © 2004 Wiley-Liss, Inc. [source]

Characteristics of Buck Semen with Regard to Ejaculate Numbers, Collection Intervals, Diluents and Preservation Periods

REPRODUCTION IN DOMESTIC ANIMALS, Issue 2 2000
M Shamsuddin
Contents To determine the number of ejaculates which can be collected within a 20-min period after the smallest number of days of sexual rest, and a good diluent to preserve semen for routine AI, five mature Black Bengal bucks were used in three experiments. In experiment 1, semen from the bucks were collected by using artificial vagina at homosexual mounts as many times as possible during 20 min. The ejaculate numbers 1, 3 and 4 (or 5 when the buck could produce it) were examined for important semen characteristics. The mean ejaculate volume, density, mass activity, sperm motility, sperm concentrations, total spermatozoa/ejaculate, proportion of spermatozoa with normal acrosome, midpiece and tail, and the proportion with normal head morphology varied between 267 and 342 µl, 4.1,4.5 (1,5 scale), 4.1,4.2 (1,5 scale), 77,79%, 4187 × 106,5064 × 106/ml, 1140 × 106,1746 × 106, 91,94% and 99%, respectively, depending on the collection number of the ejaculate. The difference between the ejaculates was significant only with respect to volume (p < 0.05). In experiment 2, semen was collected from the bucks successively during 20 min after 1, 2, 3 and 4 day intervals, and the first ejaculates were evaluated for the above-mentioned semen characteristics. Semen collected after 2 or more day intervals had significantly higher volume, sperm concentration and total spermatozoa/ejaculate (p < 0.05). In experiment 3, pools of two to three ejaculates were diluted (1 : 5; semen : diluent) in splits with glucose-citrate-egg yolk (GCEY), Tris-fructose-egg yolk (TFEY) or skim milk (SM) and preserved at +4 to +7°C. Before chilling or after 0 (15 min chilling), 1, 2, 3 and 4 days of preservation, semen was evaluated for motility and proportion of normal spermatozoa with respect to acrosome, midpiece and tail. In data pooled across the bucks, the sperm motility was better in GCEY and TFEY than in SM, and the proportion of normal spermatozoa was higher in SM than in the others (p < 0.05). However, the differences in proportion of normal spermatozoa between diluents were not significant when the data were analysed separately within preservation periods. The sperm motility consistently dropped after 1 day of preservation (p < 0.01); the motility remained 50% or more up to 4 days in TFEY, 3 days in GCEY and only 2 days in SM. The proportion of spermatozoa with normal acrosome, midpiece and tail, which was generally quite high ( 90%), decreased after 3 days of preservation (p < 0.01). We conclude that Black Bengal bucks can be collected three times during 20 min, every 3 days, and that buck semen holds good motility and proportion of normal spermatozoa up to 3 days in GCEY or TFEY at 4 to 7°C. [source]

Functional adaptation of the femoral head to voluntary exercise

THE ANATOMICAL RECORD : ADVANCES IN INTEGRATIVE ANATOMY AND EVOLUTIONARY BIOLOGY, Issue 7 2006
Jeffrey H. Plochocki
Abstract The functional adaptation of limb joints during postnatal ontogeny is necessary to maintain proper joint function. Joint form is modified primarily through differential rates of articular cartilage proliferation across articular surfaces during endochondral growth. This process is hypothesized to be mechanically regulated by the magnitude and orientation of stresses in the articular cartilage. However, the adaptation of limb joint morphology to the mechanical environment is poorly understood. We investigate the effects of voluntary exercise on femoral head morphology in 7-week-old female mice of the inbred strain C57BL/6J. The mice were divided into a control group and a group treated with voluntary access to an activity wheel for the duration of the 4-week study. Histomorphometric comparisons of chondral and osseous joint tissue of the proximal femur were made between control and exercise treatment groups. We find that exercised mice have significantly thicker articular cartilage with greater chondral tissue area and cellularity. Exercised mice also exhibit significantly greater bone tissue area and longer and flatter subchondral surfaces. No significant difference is found in the curvature of the articular cartilage or the length of the chondral articular surface between groups. These data suggest that a complex mechanistic relationship exists between joint stress and joint form. Joint tissue response to loading is multifaceted, involving both size and shape changes. Our data support the hypothesis that joint growth is ontogenetically plastic. Mechanical loading significantly influences chondral and subchondral tissue proliferation to provide greater support against increased mechanical loading. Anat Rec Part A, 288A:776,781, 2006 © 2006 Wiley-Liss, Inc. [source]

Morphological and ecological responses to a conservation translocation of powan (Coregonus lavaretus) in Scotland

AQUATIC CONSERVATION: MARINE AND FRESHWATER ECOSYSTEMS, Issue 3 2010
E. C. Etheridge
Abstract 1.The establishment of refuge populations has become a common management tool for threatened fish species in recent years, yet the effects of translocation are not fully understood in a conservation context. 2.This paper examines the hypothesis that phenotypic changes have occurred during the formation of two refuge populations of the nationally rare powan (a freshwater fish species) which were established in Loch Sloy and Carron Valley Reservoir in Scotland. 3.Significant differences in head morphology, size and growth between the founder and refuge populations and between the two refuge populations were demonstrated. These changes are probably due to a combination of founder effects, intense selection and phenotypic plasticity. These changes can undermine the rationale behind the establishment of refuge populations. 4.The results call into question the usefulness of translocation as a conservation measure; however, there are times when this is the only viable management option available. The future of translocation and the validity of establishing refuge populations for powan conservation are discussed. Copyright © 2010 John Wiley & Sons, Ltd. [source]

Variation in stickleback head morphology associated with parasite infection

BIOLOGICAL JOURNAL OF THE LINNEAN SOCIETY, Issue 4 2009
NIELS J. DINGEMANSE
Parasites can affect host phenotypes, influencing their ecology and evolution. Host morphological changes occurring post-infection might result from pathological by-products of infection, or represent adaptations of hosts or parasites. We investigated the morphology of three-spined sticklebacks, Gasterosteus aculeatus, from a population naturally infected with Schistocephalus solidus, which grows to large sizes in their body cavity. We examined local effects of infection on trunk shape, which are imposed directly by the bulk of the growing parasite, and distant effects on head morphology. We show that trunk shape differed between infection classes, and was affected more severely in fish with heavier total parasite mass. We further show unexpected differences in head morphology. The heads of infected fish were reduced in size and differently shaped to those of non-infected fish, with infected fish having deeper heads. Importantly, both head size and shape were also affected more severely in fish with heavier total parasite mass. This latter result suggests that differences in morphology are caused by post-infection changes. Such changes may be incidental, evolutionarily neutral ,side effects' of infection. However, because head morphology affects foraging ecology, such changes are likely to have fitness consequences for hosts, and may constitute adaptations, either of hosts or of parasites. We discuss our finding in the context of the evolution of phenotypic plasticity, and suggest testable hypotheses examining the proximate mechanisms underlying these morphological effects and their potential evolutionary basis. © 2009 The Linnean Society of London, Biological Journal of the Linnean Society, 2009, 96, 759,768. [source]

Morphology and function of the head in foetal and juvenile Scolecomorphus kirkii (Amphibia: Gymnophiona: Scolecomorphidae)

BIOLOGICAL JOURNAL OF THE LINNEAN SOCIETY, Issue 3 2009
HENDRIK MÜLLER
The external and musculoskeletal morphology of the head is described for an ontogenetic series of the scolecomorphid caecilian Scolecomorphus kirkii. The rostral region of foetuses and juveniles is expanded into large, posterolaterally pointing paraoral processes that are formed by the maxilla. Extraoral teeth are present on the underside of the rostrum and laterally on the paraoral processes. In the foetuses, teeth are covered by epidermal tissue. The endoskeletal part of the foetal skull is largely cartilaginous, but all of the dermal bones, with the exception of the squamosal, are present. The foetal chondrocranium is extensively developed and shows a peculiar, posterolateral process of the nasal capsule that is connected to the trabecula cranii by a transverse bar posterior to the choana, and extends further posterior beyond the level of the posterior end of the pila antotica. Only two mm. adductor mandibulae are present, together with two pterygoideus muscles that insert onto the lower jaw. The palatoquadrate and quadrate of foetuses and juveniles, respectively, are highly mobile. It is suggested that the derived head morphology of Scolecomorphus foetuses and juveniles is an adaptation to specialized postparitive feeding. © 2009 The Linnean Society of London, Biological Journal of the Linnean Society, 2009, 96, 491,504. [source]

A comprehensive phylogeny of the bumble bees (Bombus)

BIOLOGICAL JOURNAL OF THE LINNEAN SOCIETY, Issue 1 2007
S. A. CAMERON
Bumble bees (Bombus Latreille) occupy a wide diversity of habitats, from alpine meadows to lowland tropical forest, yet they appear to be similar in morphology throughout their range, suggesting that behavioural adaptations play a more important role in colonizing diverse habitats. Notwithstanding their structural homogeneity, bumble bees exhibit striking inter- and intraspecific variation in colour pattern, purportedly the outcome of mimetic evolution. A robust phylogeny of Bombus would provide the framework for elucidating the history of their wide biogeographical distribution and the evolution of behavioural and morphological adaptations, including colour pattern. However, morphological studies of bumble bees have discovered too few phylogenetically informative characters to reconstruct a robust phylogeny. Using DNA sequence data, we report the first nearly complete species phylogeny of bumble bees, including most of the 250 known species from the 38 currently recognized subgenera. Bayesian analysis of nuclear (opsin, EF-1,, arginine kinase, PEPCK) and mitochondrial (16S) sequences results in a highly resolved and strongly supported phylogeny from base to tips, with clear-cut support for monophyly of most of the conventional morphology-based subgenera. Most subgenera fall into two distinct clades (short-faced and long-faced) associated broadly with differences in head morphology. Within the short-faced clade is a diverse New World clade, which includes nearly one-quarter of the currently recognized subgenera, many of which are restricted to higher elevations of Central and South America. The comprehensive phylogeny provides a firm foundation for reclassification and for evaluating character evolution in the bumble bees. © 2007 The Linnean Society of London, Biological Journal of the Linnean Society, 2007, 91, 161,188. [source]

The retinal nerve fiber layer and the optic nerve head morphology after glaucoma surgery

ACTA OPHTHALMOLOGICA, Issue 2009
T GRACNER
Purpose To detect and quantify changes in the retinal nerve fiber layer (RNFL) and the optic nerve head (ONH) morphology after glaucoma surgery. Methods 13 eyes of 13 patients with open-angle glaucoma in which goniotrephining with scleral flap without intraoperative antimetabolites for progressive glaucoma damage was done were included in this prospective study. Before and 6 months after the surgery: the intraocular pressure (IOP) was measured, the thicknes of the RNFL was measured with a scanning laser polarimeter (GDx VCC), the confocal scanning laser ophthalmoscopy measurements of ONH with Heidelberg retina tomograph (HRT 3) were performed and the visual field was tested with Humphrey Field Analyser. Results The mean IOP before surgery was 24.5 ? 2.3 mmHg decreasing 6 months after to a mean of 13.9 ? 3.0 mmHg (p<0.05). The RNFL measurements with GDx VCC revealed no differences between the mean TSNIT Avarage (p=0.383), mean Superior Avarage (p=0.756) and mean Inferior Avarage (p=0.269) before and after surgery. The ONH measurements with HRT 3 revealed postoperatively a significant increase in the mean Rim Area, Rim Volume and Cup Shape Measure, whereas Cup Area, Cup Volume and Linear Cup/Disc Ratio decreased (p<0.05). There were no differences between the mean Height Variation Contour (p=0.678) and Mean RNFL Thickness (p=0.064) before and after surgery. Preoperatively the mean value of the Mean Deviation on automated perimetry was ,18.82 ? 8.5 dB improving 6 months postoperatively to a mean of ,16.63 ? 7.9 dB (p<0.05). Conclusion Our study demonstrated the beneficial effect of IOP reduction obtained with glaucoma surgery on visual field indices and ONH parameters evaluated by HRT 3. [source]

On the head morphology of Tetraphalerus, the phylogeny of Archostemata and the basal branching events in Coleoptera

CLADISTICS, Issue 3 2008
Rolf G. Beutel
Internal and external features of Tetraphalerus bruchi were studied using X-ray microtomography (µ-CT) and other techniques, and head structures were described in detail. µ-Ct is highly efficient for the assessment of anatomical data. A data matrix with 90 morphological characters of recent and fossil beetles was analyzed with different approaches (parsimony, Bayesian analysis). The results of the parsimony analysis resulted in the following branching pattern: (,Tshekardocoleidae + (,Permocupedidae, ,Rhombocoleidae + (,Triadocupedidae + ((Adephaga + (Myxophaga + Polyphaga))) + Archostemata s.str. [including Jurodidae]))). Sikhotealinia is placed as sister group of ,Jurodes (Jurodidae), and Jurodidae as sister group of the remaining Archostemata (Bayesian analysis) or of a clade comprising Micromalthidae, Crowsoniellidae, ,Ademosynidae, ,Schizophoridae and ,Catiniidae. The monophyly of Ommatidae and Cupedidae is well supported and Priacma is placed as the sister group of all other Cupedidae. Important events in the early evolution of Coleoptera are the shortening of the elytra and the transformation of the elytral venation (Coleoptera excluding ,Tshekardocoleidae), the formation of a closed subelytral space (Coleoptera excluding ,Tshekardocoleidae and ,Permocupedidae), the reduction of two apical antennomeres, and the loss of the broad prothoracic postcoxal bridge (Coleoptera excluding ,Tshekardocoleidae, ,Permocupedidae and ,Rhombocoleidae). Plesiomorphic features preserved in extant Archostemata are the tuberculate cuticle, the elytral pattern with parallel longitudinal ribs and window punctures, a mesoventrite with a transverse ridge, triangular mesocoxae with a distinct meron, and the exposed metatrochantin. The fossils included in the analyses do not only contribute to the reconstruction of character evolution but also influence the branching pattern. An understanding of the major evolutionary events in Coleoptera would not be possible without considering the rich fossil record of Permian and Mesozoic beetles. © The Willi Hennig Society 2007. [source]