Morphological Heterogeneity (morphological + heterogeneity)

Distribution by Scientific Domains


Selected Abstracts


A cranial base of Australopithecus robustus from the hanging remnant of Swartkrans, South Africa

AMERICAN JOURNAL OF PHYSICAL ANTHROPOLOGY, Issue 4 2006
Darryl J. de Ruiter
Abstract SKW 18, a partial hominin cranium recovered from the site of Swartkrans, South Africa, in 1968 is described. It is derived from ex situ breccia of the Hanging Remnant of Member 1, dated to approximately 1.5,1.8 Mya. Although partially encased in breccia, it was refit to the facial fragment SK 52 (Clarke 1977 The Cranium of the Swartkrans Hominid SK 847 and Its Relevance to Human Origins, Ph.D. dissertation, University of the Witwatersrand, Johannesburg), producing the composite cranium SKW 18/SK 52. Subsequent preparation revealed the most complete cranial base attributable to the species Australopithecus robustus. SKW 18 suffered weathering and slight postdepositional distortion, but retains considerable anatomical detail. The composite cranium most likely represents a large, subadult male, based on the incomplete fusion of the spheno-occipital synchondrosis; unerupted third molar; pronounced development of muscular insertions; and large teeth. Cranial base measures of SKW 18 expand the range of values previously recorded for A. robustus. SKW 18 provides information on anatomical features not previously visible in this taxon, and expands our knowledge of morphological variability recognizable in the cranial base. Morphological heterogeneity in the development of the prevertebral and nuchal muscular insertions is likely the result of sexual dimorphism in A. robustus, while differences in cranial base angles and the development of the occipital/marginal sinus drainage system cannot be attributed to size dimorphism. Am J Phys Anthropol, 2006. © 2006 Wiley-Liss, Inc. [source]


,, T-cell lymphomas: a homogeneous entity?

HISTOPATHOLOGY, Issue 4 2000
De Wolf-Peeters
,, T-cells comprise an immunologically distinct lymphoid population, characterized by specific morphological, phenotypical and functional properties. Therefore it seems reasonable to speculate that neoplasms derived from this particular T-cell subset display distinct features. Indeed, the prototype ,, T-cell lymphoma, hepatosplenic T-cell lymphoma constitutes a unique clinicopathological entitity which is intimately associated with a ,, T-cell phenotype. However, ,, T-cell lymphomas have also been described in other extranodal sites where, unlike reactive ,, T-cells and hepatosplenic ,, T-cell lymphomas, they display an important morphological heterogeneity. Moreover, these nonhepatosplenic ,, T-cell lymphomas are essentially not that different from their ,, T-cell receptor for antigen (TCR)-expressing counterparts and thus may be incorporated in the established T-cell lymphoma subclasses. However, subtle differences regarding their histopathological appearance as well as their biological behaviour indicate that further studies to determine the exact significance of TCR expression are required. Such inquiries may contribute to the general understanding of T-cell lymphomagenesis in general, which is still obscure. [source]


Magnetic activated cell sorting allows isolation of spermatogonia from adult primate testes and reveals distinct GFRa1-positive subpopulations in men

JOURNAL OF MEDICAL PRIMATOLOGY, Issue 2 2010
Kathrin Gassei
Abstract Background, Isolation of spermatogonial stem cells (SSCs) could enable in vitro approaches for exploration of spermatogonial physiology and therapeutic approaches for fertility preservation. SSC isolation from adult testes is difficult due to low cell numbers and lacking cell surface markers. Glial cell-derived neurotrophic factor family receptor alpha-1 (GFR,1) plays a crucial role for the maintenance of SSCs in rodents and is expressed in monkey spermatogonia. Methods, Magnetic activated cell sorting was employed for the enrichment of GFR,1+ spermatogonia from adult primate testes. Results, Magnetic activated cell sorting of monkey cells enriched GFR,1+ cells threefold. 11.4% of GFR,1+ cells were recovered. 42.9% of GFR,1+ cells were recovered in sorted fractions of human testicular cells, representing a fivefold enrichment. Interestingly, a high degree of morphological heterogeneity among the GFR,1+ cells from human testes was observed. Conclusions, Magnetic activated cell sorting using anti-GFR,1 antibodies provides an enrichment strategy for spermatogonia from monkey and human testes. [source]


Initial Deposition of Colloidal Particles on a Rough Nanofiltration Membrane

THE CANADIAN JOURNAL OF CHEMICAL ENGINEERING, Issue 5 2007
Tania Rizwan
Abstract The initial rate of colloid deposition onto semi-permeable membranes is largely controlled by the coupled influence of permeation drag and particle-membrane colloidal interactions. Recent studies show that the particle-membrane interactions are subject to immense local variations due to the inherent morphological heterogeneity (roughness) of reverse osmosis (RO) and nanofiltration (NF) membranes. This experimental investigation reports the effect of membrane roughness on the initial deposition of polystyrene latex particles on a rough NF membrane during cross flow membrane filtration under different operating pressures and solution chemistries. Atomic force microscopy was used to characterize the roughness of the membrane and observe the structure of particle deposits. At the initial stages of fouling, the AFM images show that more particles preferentially accumulate near the "peaks" than in the "valleys" of the rough NF membrane surface. Le taux initial de la déposition colloïdale sur des membranes semi-perméables est largement contrôlé par l'influence couplée entre la traînée de perméation et les interactions colloïdales membrane-particules. Des études récentes montrent que les interactions membranes-particules sont sujettes à d'immenses variations locales en raison de l'hétérogénéité morphologique inhérente (rugosité) des membranes d'osmose inverse (RO) et de nanofiltration (NF). Cette étude expérimentale décrit l'effet de la rugosité des membranes sur la déposition initiale de particules de latex de polystyrène sur une membrane NF rugueuse lors de la filtration des membranes en écoulement transversal pour différentes conditions opératoires et compositions chimiques des solutions. On a eu recours à la microscopie à force atomique pour caractériser la rugosité de la membrane et observer la structure des dépôts de particules. Aux stades initiaux du refoulement, les images AFM montrent que les particules s'accumulent préférentiellement près des «pics» plutôt que dans les «vallées» de la surface de membrane NF rugueuse. [source]


Identification of novel neuropeptides in the ventral nerve cord ganglia and their targets in an annelid worm, Eisenia fetida

THE JOURNAL OF COMPARATIVE NEUROLOGY, Issue 6 2009
Zsófia Herbert
Abstract Periviscerokinins (PVKs) and pyrokinins (PKs) are neuropeptides known in several arthropod species. Sequence homology of these peptides with the molluscan small cardioactive peptides reveals that the occurrence of PVKs and PKs is not restricted to arthropods. Our study focuses on the biochemical and immunocytochemical identification of neuropeptides with sequence homology to PVKs and PKs in the central and peripheral nervous system of the earthworm Eisenia fetida. By means of affinity chromatography, nanoflow liquid chromatography, and high accuracy mass spectrometry, six peptides, SPFPR(L/I)amide, APFPR( L/I)amide, SPLPR( L/I)amide, SFVR( L/I)amide, AFVR( L/I)amide, and SPAFVR( L/I)amide, were identified in the central nervous system with the common-XR( L/I)amide C-terminal sequence. The exact anatomical position of 13 labeled XR( I/L)amide expressing neuron groups and numerous peptide-containing fibers were determined by means of immunocytochemistry and confocal laser scanning microscopy in whole-mount preparations of ventral nerve cord ganglia. The majority of the stained neurons were interneurons with processes joining the distinct fine-fibered polysegmental tracts in the central neuropil. Some stained fibers were seen running in each segmental nerve that innervated metanephridia and body wall. Distinct groups of neurosecretory cells characterized by small round soma and short processes were also identified. Based on immunoelectron microscopy six different types of labeled cells were described showing morphological heterogeneity of earthworm peptides containing elements. Our findings confirm that the sequence of the identified earthworm neuropeptides homologous to the insect PVKs and PKs suggesting that these peptides are phylogenetically conservative molecules and are expressed in sister-groups of animals such as annelids, mollusks, and insects. J. Comp. Neurol. 514:415,432, 2009. © 2009 Wiley-Liss, Inc. [source]


Identification of novel neuropeptides in the ventral nerve cord ganglia and their targets in an annelid worm, Eisenia fetida

THE JOURNAL OF COMPARATIVE NEUROLOGY, Issue 5 2009
Zsófia Herbert
Abstract Periviscerokinins (PVKs) and pyrokinins (PKs) are neuropeptides known in several arthropod species. Sequence homology of these peptides with the molluscan small cardioactive peptides reveals that the occurrence of PVKs and PKs is not restricted to arthropods. Our study focuses on the biochemical and immunocytochemical identification of neuropeptides with sequence homology to PVKs and PKs in the central and peripheral nervous system of the earthworm Eisenia fetida. By means of affinity chromatography, nanoflow liquid chromatography, and high accuracy mass spectrometry, six peptides, SPFPR(L/I)amide, APFPR(L/I)amide, SPLPR(L/I)amide, SFVR(L/I)amide, AFVR(L/I)amide, and SPAFVR(L/I)amide, were identified in the central nervous system with the common ,XR(L/I)amide C-terminal sequence. The exact anatomical position of 13 labeled XR(I/L)amide expressing neuron groups and numerous peptide-containing fibers were determined by means of immunocytochemistry and confocal laser scanning microscopy in whole-mount preparations of ventral nerve cord ganglia. The majority of the stained neurons were interneurons with processes joining the distinct fine-fibered polysegmental tracts in the central neuropil. Some stained fibers were seen running in each segmental nerve that innervated metanephridia and body wall. Distinct groups of neurosecretory cells characterized by small round soma and short processes were also identified. Based on immunoelectron microscopy six different types of labeled cells were described showing morphological heterogeneity of earthworm peptides containing elements. Our findings confirm that the sequence of the identified earthworm neuropeptides homologous to the insect PVKs and PKs suggesting that these peptides are phylogenetically conservative molecules and are expressed in sister-groups of animals such as annelids, mollusks, and insects. J. Comp. Neurol. 514:415,432, 2009. © 2009 Wiley-Liss, Inc. [source]


Identification of novel neuropeptides in the ventral nerve cord ganglia and their targets in an annelid worm, Eisenia fetida

THE JOURNAL OF COMPARATIVE NEUROLOGY, Issue 5 2009
Zsófia Herbert
Abstract Periviscerokinins (PVKs) and pyrokinins (PKs) are neuropeptides known in several arthropod species. Sequence homology of these peptides with the molluscan small cardioactive peptides reveals that the occurrence of PVKs and PKs is not restricted to arthropods. Our study focuses on the biochemical and immunocytochemical identification of neuropeptides with sequence homology to PVKs and PKs in the central and peripheral nervous system of the earthworm Eisenia fetida. By means of affinity chromatography, nanoflow liquid chromatography, and high accuracy mass spectrometry, six peptides, SPFPR(L/I)amide, APFPR(L/I)amide, SPLPR(L/I)amide, SFVR(L/I)amide, AFVR(L/I)amide, and SPAFVR(L/I)amide, were identified in the central nervous system with the common ,XR(L/I)amide C-terminal sequence. The exact anatomical position of 13 labeled XR(I/L)amide expressing neuron groups and numerous peptide-containing fibers were determined by means of immunocytochemistry and confocal laser scanning microscopy in whole-mount preparations of ventral nerve cord ganglia. The majority of the stained neurons were interneurons with processes joining the distinct fine-fibered polysegmental tracts in the central neuropil. Some stained fibers were seen running in each segmental nerve that innervated metanephridia and body wall. Distinct groups of neurosecretory cells characterized by small round soma and short processes were also identified. Based on immunoelectron microscopy six different types of labeled cells were described showing morphological heterogeneity of earthworm peptides containing elements. Our findings confirm that the sequence of the identified earthworm neuropeptides homologous to the insect PVKs and PKs suggesting that these peptides are phylogenetically conservative molecules and are expressed in sister-groups of animals such as annelids, mollusks, and insects. J. Comp. Neurol. 514:415,432, 2009. © 2009 Wiley-Liss, Inc. [source]


Genome analysis and gene expression profiling of neuroblastoma and ganglioneuroblastoma reveal differences between neuroblastic and Schwannian stromal cells

THE JOURNAL OF PATHOLOGY, Issue 3 2005
Simona Coco
Abstract Neuroblastic tumours are a group of paediatric cancers with marked morphological heterogeneity. Neuroblastoma (Schwannian stroma-poor) (NB-SP) is composed of undifferentiated neuroblasts. Ganglioneuroblastoma intermixed (Schwannian stroma-rich) (GNBi-SR) is predominantly composed of Schwannian stromal (SS) and neuroblastic (Nb) cells. There are contrasting reports suggesting that SS cells are non-neoplastic. In the present study, laser capture microdissection (LCM) was employed to isolate SS and Nb cells. Chromosome 1p36 deletion and MYCN gene amplification were found to be associated in two out of seven NB-SPs, whereas no abnormalities were observed in five GNBi-SRs. In some cases, loss of heterozygosity (LOH) at 1p36 loci was detected in Nb cells but not in the bulk tumour by LCM; furthermore, LOH was also identified in both SS and tumour tissue of a GNBi-SR. DNA gain and loss studied by comparative genomic hybridization were observed at several chromosome regions in NB-SP but in few regions of GNBi-SR. Finally, gene expression profiles studied using an oligo-microarray technique displayed two distinct signatures: in the first, 32 genes were expressed in NB-SP and in the second, 14 genes were expressed in GNBi-SR. The results show that NB-SP is composed of different morphologically indistinguishable malignant cell clones harbouring cryptic mutations that are detectable only after LCM. The degree of DNA imbalance is higher in NB-SP than in GNBi-SR. However, when the analysis of chromosome 1p36 is performed at the level of microdissection, LOH is also observed in SS cells. These data provide supportive evidence that SS cells have a less aggressive phenotype and play a role in tumour maturation. Copyright © 2005 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd. [source]


Mixed stream channel morphologies: implications for fish community diversity

AQUATIC CONSERVATION: MARINE AND FRESHWATER ECOSYSTEMS, Issue 2 2009
Christina M. Cianfrani
Abstract 1.Stream classification systems are widely used in stream management and restoration. Whereas the principal morphological types of these classification systems are increasingly recognized for their ecological connections, the roles of intermediate and mixed morphologies are still poorly understood, yet may be biologically significant. 2.Twenty-five stream reaches in north-western Vermont were classified by channel morphology to determine whether fish community diversity differed among pool-riffle, mixed (i.e. pool-riffle/cascade, pool-riffle/other) and forced pool-riffle stream morphological groups. Stream reach surveys included cross-sectional surveys, longitudinal profiles, bed substrate characterization, and fish surveys. 3.Three fish community diversity measures were calculated: (1) species richness (S); (2) Shannon,Weaver Index (H,); and (3) Simpson's Index (1/D). Multivariate analysis of covariance (MANCOVA) followed by analysis of variance (ANOVA) were used to explore potential differences in fish diversity among stream morphological groups. Fish diversity was significantly different for all three community diversity measures (P,0.05), with pool-riffle/cascade morphology consistently exhibiting the greatest fish diversity and forced pool-riffle the lowest. 4.These results suggest that fish community diversity is significantly associated with distinct channel morphologies. Generally, pool-riffle/cascade and pool-riffle/other stream morphological groups supported habitats that fostered greater species diversity than more homogeneous and uniform pool-riffle reaches. The observed patterns of diversity are likely to be the result of habitat patches created by variations in flow and other physical characteristics in reaches of mixed morphologies. 5.These results support fish sampling schemes that incorporate morphological heterogeneity, such as proportional-distance designation. Sampling strategies that focus on homogeneous reaches may underestimate diversity, and misrepresent stream condition when fish community data are used in indices of biological integrity (IBIs). Reaches of mixed stream morphologies should be recognized as areas of biological importance in stream and catchment management and in conservation efforts. Copyright © 2008 John Wiley & Sons, Ltd. [source]