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Consecutive Generations (consecutive + generation)
Selected AbstractsEscape from natural enemies during climate-driven range expansion: a case studyECOLOGICAL ENTOMOLOGY, Issue 3 2008ROSA MENÉNDEZ Abstract 1.,A major, and largely unexplored, uncertainty in projecting the impact of climate change on biodiversity is the consequence of altered interspecific interactions, for example between parasitoids and their hosts. The present study investigated parasitism in the Brown Argus butterfly, Aricia agestis; a species that has expanded northward in Britain during the last 30 years in association with climate warming. 2.,Aricia agestis larvae suffered lower mortality from parasitoids in newly colonised areas compared with long-established populations. This result was consistent over four consecutive generations (2 years) when comparing one population of each type, and also when several populations within the historical and recently colonised range of the species were compared within a single year. Thus, A. agestis appears to be partially escaping from parasitism as it expands northwards. 3.,Reduced parasitism occurred despite the fact that several of the parasitoid species associated with A. agestis were already present in the newly colonised areas, supported predominantly by an alternative host species, the Common Blue butterfly, Polyommatus icarus. 4.,As the species expand their distributions into areas of increased climatic suitability, invasion fronts may escape from natural enemies, enhancing rates of range expansion. The results suggest that the decoupling of interspecific interactions may allow some species to exploit a wider range of environments and to do so more rapidly than previously thought possible. [source] Polyploidy-Associated Genomic Instability in Arabidopsis thalianaGENESIS: THE JOURNAL OF GENETICS AND DEVELOPMENT, Issue 4 2010Yixing Wang Formation of polyploid organisms by fertilization of unreduced gametes in meiotic mutants is believed to be a common phenomenon in species evolution. However, not well understood is how species in nature generally exist as haploid and diploid organisms in a long evolutionary time while polyploidization must have repeatedly occurred via meiotic mutations. Here, we show that the ploidy increased for two consecutive generations due to unreduced but viable gametes in the Arabidopsis cyclin a1;2-2 (also named tardy asynchronousmeiosis-2) mutant, but the resultant octaploid plants produced progeny of either the same or reduced ploidy via genomic reductions during meiosis and pollen mitosis. Ploidy reductions through sexual reproduction were also observed in independently generated artificial octaploid and hexaploid Arabidopsis plants. These results demonstrate that octaploid is likely the maximal ploidy produced through sexual reproduction in Arabidopsis. The polyploidy-associated genomic instability may be a general phenomenon that constrains ploidy levels in species evolution. [source] Top down preselection using marker assisted estimates of breeding values in dairy cattleJOURNAL OF ANIMAL BREEDING AND GENETICS, Issue 5 2004Jörn Bennewitz Summary Top down preselection of young bulls before entering progeny testing has been proposed as a practicable form of marker-assisted selection (MAS), especially in dairy cattle populations with large male paternal half-sib families. Linkage phase between the superior (Q) and the inferior (q) QTL alleles of heterozygous sires (Qq at the QTL) with informative markers is established within each paternal half-sib family and may be used for selection among grand-progeny. If, additionally to sires, bulldams are also genotyped and data from consecutive generations are used, then a marker-assisted best linear unbiased prediction (MA-BLUP) model can be employed to connect the information of all generations and families of a top down design, and to select across all families. A customized ,augmented' sire model (with sires and dams of sires as random effects) is introduced for this purpose. Adapted formulae for the mixed model equations are given and their equivalence to a corresponding animal model and to a certain variant of previously proposed reduced animal models is shown. The application of the augmented sire model in MA-BLUP estimation from daughter-yield deviations and effective daughter contributions is presented. Zusammenfassung Die Top down Vorselektion von jungen Bullen vor der Nachkommenschaftsprüfung ist bekannt als eine praktikable Form der markergestützten Selektion in Milchrinderpopulationen. Die Kopplungsphasen zwischen dem günstigen (Q) und dem ungünstigen (q) Allel eines QTL heterozygoten Vaters (Qq am QTL) mit den Allelen gekoppelter genetischer Marker werden innerhalb Familien festgestellt und können zur Vorselektion von Enkeln genutzt werden. Wenn zusätzlich zu den Vätern die Mütter genotypisiert sind und Daten von mehreren Generationen vorliegen, können MA-BLUP Modelle genutzt werden, um Informationen von mehreren Familien und mehreren Generationen eines Top down Designs zusammenzuführen und um eine Vorselektion über Familien hinweg vorzunehmen. Hierfür wird ein geeignetes ,erweitertes' Vatermodell eingeführt, welches die Väter und zusätzlich die Mütter der Väter als zufällige Effekte enthält. Angepasste Formeln für die gemischten Modell Gleichungen werden beschrieben. Die Gleichheit dieses erweiterten Vatermodells mit einem entsprechenden Tiermodell und mit einer Variante des reduzierten Tiermodells wird gezeigt. Die Anwendung des erweiterten Vatermodells zur MA-BLUP Schätzung mit daughter yield deviations und effective daughter contributions ist beschrieben. [source] Rising trends of gastric cancer and peptic ulcer in the 19th centuryALIMENTARY PHARMACOLOGY & THERAPEUTICS, Issue 7 2010A. Sonnenberg Aliment Pharmacol Ther 2010; 32: 901,907 Summary Background, The risk of dying from gastric cancer appears to have increased among consecutive generations born during the 19th century. Aim, To follow the time trends of hospitalization for gastric cancer and test whether they confirm such increase. Methods, Inpatient records of the last two centuries from four hospitals in Scotland and three US hospitals were analysed. Proportional rates of hospitalization for gastric cancer, gastric ulcer and duodenal ulcer were calculated during consecutive 5-year periods. Results, The data from all seven cities revealed strikingly similar patterns. No hospital admissions for gastric cancer or peptic ulcer were recorded prior to 1800. Hospital admissions for gastric cancer increased in an exponential fashion throughout the 19th and the beginning of the 20th century. In a majority of cities, the rise in hospitalization for gastric cancer preceded a similar rise in hospitalization for gastric ulcer. Hospitalization for these two latter diagnoses clearly preceded hospitalization for duodenal ulcer by 20,40 years. Conclusions, The occurrence of gastric cancer, gastric ulcer and duodenal ulcer markedly increased during the 19th century. Improvements in hygiene may have resulted in the decline of infections by other gastrointestinal organisms that had previously kept concomitant infection by Helicobacter pylori suppressed. [source] Phenotypic characterization of DYT13 primary torsion dystonia,MOVEMENT DISORDERS, Issue 2 2004Anna Rita Bentivoglio MD Abstract We describe the phenotype of DYT13 primary torsion dystonia (PTD) in a family first examined in 1994. A complete neurological evaluation was performed on all available family members: 8 individuals were definitely affected by dystonia. The family was re-evaluated in March 2000: at that time, 3 more individuals had developed symptoms of dystonia. Inheritance of PTD was autosomal dominant, with affected individuals spanning three consecutive generations and male-to-male transmission. Age at onset ranged from 5 to 43 years. Onset occurred either in the craniocervical region or in upper limbs. Progression was mild, and the disease course was benign in most affected individuals; generalization occurred only in 2 cases. We did not find anticipation of age at onset or of disease severity through generations. Most subjects presented with jerky, myoclonic-like dystonic movements of the neck or shoulders. DYT13-PTD is an autosomal dominant disease, with incomplete penetrance (58%). Clinical presentation and age at onset were more variable than in DYT1-PTD, and the neck was involved in most of those affected. Moreover, the individuals with generalised dystonia were not severely disabled and were able to lead independent lives. To date, this is the only family with DYT13-PTD. © 2003 Movement Disorder Society [source] Inheritance and reliability of random amplified polymorphic DNA-markers in two consecutive generations of common carp (Cyprinus carpio L.)AQUACULTURE RESEARCH, Issue 2 2010Noel D Novelo Abstract Random amplified polymorphic DNA (RAPD) markers have been used in a variety of genetic studies in fisheries and aquaculture. Most population studies are performed without preliminary data demonstrating the Mendelian inheritance and reproducibility of RAPD markers. In this study, the inheritance and reproducibility of RAPD markers was examined in two consecutive generations of common carp, Cyprinus carpio L. Variability and segregation of RAPD markers were investigated in one F1 progeny and three F2 progenies. Seventy-four RAPD markers were generated by five primers using DNA extracted from the initial ornamental (koi) common carp female and wild-type colour common carp male. Fifty-five of these RAPD markers were transmitted to the F1 progeny and the inheritance patterns were analysed. Twenty RAPD markers were fully reproducible and demonstrated dominant simple Mendelian inheritance patterns in two consecutive generations. Twenty-four RAPD markers were not reproducible in all progenies. Thirteen markers displayed inheritance ratios in the progenies that did not fit simple Mendelian inheritance patterns. Non-reproducibility of RAPD markers and distorted ratios may be caused by the absence of amplification, poor amplification or by the appearance of artefact bands. Random amplified polymorphic DNA markers with poor reproducibility and non-Mendelian inheritance can lead to misinterpretations of data in population studies, resulting in errors in the estimation of genetic diversity within and between individual populations. Therefore, it is recommended to first identify the set of reproducible RAPD markers that demonstrate Mendelian inheritance before application of the RAPD technique in population studies. [source] | |||||||||||||