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Segment I (segment + i)
Selected AbstractsSEASONAL CYCLES OF ALLOZYME-BY-CHROMOSOMAL-INVERSION GAMETIC DISEQUILIBRIUM IN DROSOPHILA SUBOBSCURAEVOLUTION, Issue 4 2003Francisco Rodríguez-Trelles Abstract Allozyme loci are frequently found non randomly associated to the chromosomal inversions in which they are included in Drosophila. Two opposite views compete to explain strong allozyme-by-inversion gametic disequilibria: they result from natural selection or, conversely, merely represent remnants of associations accidentally established at the origin of inversions. Empirical efforts aimed at deciding between adaptive and historical scenarios have focused on the spatial distribution of disequilibria. Yet, the evolutionary significance of these associations remains uncertain. I report here the results of a time-series analysis of the seasonal variation of alleles at six allozyme loci (Acph, Lap, Pept-1, Ao, Mpi, and Xdh) in connection with the O chromosomal polymorphisms of D. subobscura. The findings were: (1) in the segment I of the O chromosome, Lap and Pept-1 allozymes changed seasonally in a cyclical fashion within the ST gene arrangement, but they changed erratically within the 3+4 gene configuration; (2) the frequencies of Lap111 and Pept-10,40 within ST dropped to their lowest values in early and late summer, respectively, when the seasonal level of the ST arrangement is lowest. Furthermore, Lap1,11 and Pept-10,40 covary with ST only within these seasons, yet in a fashion inconsistent with these alleles having a major influence on the dynamics of the inversion; (3) seasonal cycling of alleles within inversions were not detected at Acph, Ao, Mpi, and Xdh, yet these loci are nearly monomorphic at the study population, and/or their sampled series were shorter than those for Lap and Pept-1; and (4) simply monitoring allozyme frequencies separately for each inversion proved to be superior, for evidencing the seasonal cycles of the disequilibria, to the use of the D' coefficient of association. Observed seasonal cycles of allozymes within inversions likely reflect natural selection. [source] Contractile properties of the proximal urethra and bladder in female pig: Morphology and functionNEUROUROLOGY AND URODYNAMICS, Issue 1 2006J.J.M. Pel Abstract Aims To compare the contractile properties of proximal urethral and bladder muscle of the female pig. Materials and Methods In two proximal segments (I and II) of the urethra, small muscle bundles were excised to measure the force-length (maximum force) and the force-velocity (unloaded shortening velocity) relation using the stop-test. The rate of force development was calculated using phase plots. Contractile properties of urethral and bladder segments were statistically compared using the Mann,Whitney U -test. Immunohistochemical staining of whole circumference urethral cross sections was used to identify the location of smooth and striated muscle fibres. Results On isometric force development, the urethral muscle bundles revealed a fast (,0.5 sec) and a slow (,2.1 sec) time constant, whereas in bladder only a slow (,2.3 sec) component was measured. On average, isometric force was highest in bladder. The length range over which force was produced was smallest in urethral segment II, followed by urethral segment I and finally bladder. The unloaded shortening velocity was 0.15, 0.25 and 0.35 1/sec, respectively. Histological preparations showed that smooth as well as striated muscle was present in proximal urethra. In urethral muscle bundles, spontaneous contractions were measured with a frequency of 0.4 Hz. Conclusions Differences in contractility found between urethra and bladder may be ascribed to the presence of striated muscle in the proximal urethra. The regulation of tone and spontaneous contractions may be part of the continence mechanism in the female pig urinary tract. © 2005 Wiley-Liss, Inc. [source] Y-chromosome and mitochondrial DNA studies on the population structure of the Christmas Island communityAMERICAN JOURNAL OF PHYSICAL ANTHROPOLOGY, Issue 3 2005Cheryl A. Wise Abstract Christmas Island is a remote Australian territory located close to the main Indonesian island of Java. Y-chromosome and mitochondrial DNA (mtDNA) markers were used to investigate the genetic structure of the population, which comprises communities of mixed ethnic origin. Analysis of 12 Y-chromosome biallelic polymorphisms revealed a high level of gene diversity and haplotype frequencies that were consistent with source populations in southern China and Southeast Asia. mtDNA hypervariable segment I (HVS-I) sequences displayed high levels of haplotype diversity and nucleotide diversity that were comparable to various Asian populations. Genetic distances revealed extremely low mtDNA differentiation among Christmas Islanders and Asian populations. This was supported by the relatively high proportion of sequence types shared among these populations. The most common mtDNA haplogroups were M* and B, followed by D and F, which are prevalent in East/Southeast Asia. Christmas Islanders of European descent were characterized by the Eurasian haplogroup R*, and a limited degree of admixture was observed. In general, analysis of the genetic data indicated population affinities to southern Chinese (in particular from the Yunnan Province) and Southeast Asia (Thailand, Malaysia, and Cambodia), which was consistent with historical records of settlement. The combined use of these different marker systems provides a useful and appropriate model for the study of contemporary populations derived from different ethnic origins. Am J Phys Anthropol, 2005. © 2005 Wiley-Liss, Inc. [source] Multichannel Cochlear Implants: Relation of Histopathology to Performance,THE LARYNGOSCOPE, Issue 8 2006Jose N. Fayad MD Abstract Objectives: To determine the relationship of surviving neural elements to auditory function in multichannel cochlear implant temporal bones. Study Design: Case series of all 14 existing multichannel cochlear implants in our temporal bone collection. Methods: Devices included Nucleus 22 (n = 11), Nucleus 24 (n = 1), Ineraid (n = 1), and Clarion (n = 1). Morphologic evaluation of structural elements including spiral ligament, stria vascularis, hair cells, peripheral processes, and spiral ganglion cells was performed. Clinical performance data were obtained from patient charts. For eight patients, nonimplanted contralateral temporal bones were available and paired comparisons were made. Results: Despite frequent absence of hair cells and peripheral processes, all bones had at least some remaining spiral ganglion cells. Percent of normal remaining structures were unrelated to auditory performance with the implant for any of the structural elements. Ganglion cell count in segment III showed significant negative correlations to speech discrimination scores for words and sentences (Rhos = ,.687 and ,.661, P , .03 and .04) as did segment IV and total ganglion cell count with word score (Rhos = ,.632 and ,.638; P , .05). Spiral ganglion cell survival did not differ between implanted and nonimplanted ears, with the exception of segment I, which had fewer cells in the implanted ear (P , .028). Conclusions: Performance variability of cochlear implants cannot be explained on the basis of cochlear neuronal survival. Although hair cells and peripheral processes were frequently absent or greatly diminished from normal, all subjects had at least some spiral ganglion cells. And, in this series, there was an inverse relationship between survival of ganglion cells and performance. [source] Zircon U,Pb age and Hf isotope evidence for contrasting origin of bimodal protoliths for ultrahigh-pressure metamorphic rocks from the Chinese Continental Scientific Drilling projectJOURNAL OF METAMORPHIC GEOLOGY, Issue 8 2007R.-X. CHEN Abstract A combined study of zircon morphology, U,Pb ages and Hf isotopes as well as whole-rock major and trace elements was carried out for ultrahigh-pressure (UHP) eclogite and felsic gneiss from the main hole (MH) of the Chinese Continental Scientific Drilling (CCSD) project in the Sulu orogen. The results show contrasting Hf isotope compositions for bimodal UHP metaigneous rocks, pointing to contrasting origins for their protoliths (thus dual-bimodal compositions). The samples of interest were from two continuous core segments from CCSD MH at depths of 734.21,737.16 m (I) and 929.67,932.86 m (II) respectively. Zircon U,Pb dating for four samples from the two core segments yields two groups of ages at 784 ± 17 and 222 ± 3 Ma, respectively, corresponding to protolith formation during supercontinental rifting and metamorphic growth during continental collision. Although the Triassic UHP metamorphism significantly reset the zircon U,Pb system of UHP rocks, the Hf isotope compositions of igneous zircon can be used to trace their protolith origin. Contrasting types of initial Hf isotope ratios are, respectively, correlated with segments I and II, regardless of their lithochemistry. The first type shows positive ,Hf(t) values of 7.8 ± 3.1 to 6.0 ± 3.0, with young Hf model age of 1.03 and 1.11 Ga. The second type exhibits negative ,Hf(t) values of ,6.9 ± 1.6 to ,9.1 ± 1.1, with old Hf model ages of 2.11 and 2.25 Ga. It appears that the UHP rocks from the two segments have protoliths of contrasting origin. Consistent results are also obtained from their trace element compositions suggesting that mid-Neoproterozoic protoliths of bimodal UHP metaigneous rocks formed during supercontinental rifting at the northern margin of the South China Block. Thus, the first type of bimodal magmatism formed by rapid reworking of juvenile crust, whereas the second type of bimodal magmatism was principally generated by rift anatexis of Paleoproterozoic crust. Melting of orogenic lithosphere has potential to bring about bimodal magmatism with contrasting origins. Because arc,continent collision zones are the best place to accumulate both juvenile and ancient crusts, the contrasting types of bimodal magmatism are proposed to occur in an arc,continent collision orogen during the supercontinental rifting, in response to the attempted breakup of the supercontinent Rodinia at c. 780 Ma. [source] In situ splitting of a liver with middle hepatic vein anomalyLIVER TRANSPLANTATION, Issue 9 2001Alessandro Genzone MD In situ liver splitting provides a way to expand the graft pool, minimize cold ischemia time, and improve hemostasis at the cut surface of the graft. Vascular anomalies of the liver may make the splitting procedure very difficult or even impossible to perform. The in situ splitting procedure, performed on a liver with a middle hepatic vein (MHV) anomaly, is described here. The MHV drained directly into the segment III vein within the hepatic parenchyma instead of draining into the left hepatic vein to form the common trunk. In situ splitting was performed during multiorgan procurement from a 33-year-old man who died of isolated cerebral trauma. The MHV was reconstructed on the back table to secure right graft venous drainage using an iliac vein graft. The resultant right graft, segments I and IV to VIII, and left graft, segments II and III, were transplanted successfully into an adult and a child, respectively. The 2 transplant recipients are currently alive with normal hepatic function 20 months after transplantation. [source] | |||||||||||||