Sampling Atriplex bladders: a comparison of methods

Abstract. A major objection to the convenient sampling of Chenopodiacean bladders by brushing in aqueous solutions is the suspected leakage of ions from the leaf blade. To overcome this problem, a new method of sampling bladder hair is described, which also achieves rapid and quantitative separation and, at the same time, yields bladder samples of undoubtedly high purity. Leakage is stopped by the aid of liquid nitrogen. Comparison of this method to removal of bladders by brushing in aquenous solutions effectively confirm the validity of the customary method beyond dispute.     

Prenatal diagnosis of Pallister-Killian syndrome and literature review

Pallister-Killian syndrome (PKS) is a rare sporadic genetic disorder usually caused by mosaicism of an extra isochromosome of 12p (i(12p)). This retrospective study analysed the prenatal ultrasound manifestations and molecular and cytogenetic results of five PKS foetuses. Samples of amniotic fluid and/or cord blood, skin biopsy and placenta were collected. Conventional karyotyping and single nucleotide polymorphism array (SNP array) were performed on all the amniotic fluid or cord blood samples. Copy number variants sequencing (CNV-seq) and fluorescence in situ hybridization (FISH) were also used for the validation for one foetus. All the five foetuses were from pregnancies with advanced parental age. Two foetuses involved structural abnormalities and one foetus had only soft markers, all of which included increased nuchal translucency. The rest two foetuses had normal ultrasounds in the second trimester, which has rarely been reported before. The karyotype revealed typical i(12p) in four cases and a small supernumerary marker chromosome consisting of 12p and 20p in the remaining one case. The proportion of cells with i(12p) ranged from 0 to 100% in cultural cells, while SNP array results suggested 2−4 copies of 12p. For one foetus, metaphase FISH showed normal results, but the interphase FISH suggested cell lines with two, three and four copies of 12p in the amniotic fluid. Advanced parental age may be an important risk factor for PKS, and there were no typical ultrasound manifestations related to PKS. A combination of karyotype analysis and molecular diagnosis is an effective method for the diagnosis of PKS.     

Farms,pastures and woodlands: the fine‐scale distribution of Palearctic Culicoides spp. biting midges along an agro‐ecological gradient

The spatial epidemiology of Bluetongue virus (BTV) at the landscape level relates to the fine‐scale distribution and dispersal capacities of its vectors, midges belonging to the genus Culicoides Latreille (Diptera: Ceratopogonidae). Although many previous researches have carried out Culicoides sampling on farms, little is known of the fine‐scale distribution of Culicoides in the landscape immediately surrounding farms. The aim of this study was to gain a better understanding of Culicoides populations at increasing distances from typical dairy farms in north‐west Europe, through the use of eight Onderstepoort‐type black‐light traps positioned along linear transects departing from farms, going through pastures and entering woodlands. A total of 16 902 Culicoides were collected in autumn 2008 and spring 2009. The majority were females, of which more than 97% were recognized as potential vectors. In pastures, we found decreasing numbers of female Culicoides as a function of the distance to the farm. This pattern was modelled by leptokurtic models, with parameters depending on season and species. By contrast, the low number of male Culicoides caught were homogeneously distributed along the transects. When transects entered woodlands, we found a higher abundance of Culicoides than expected considering the distance of the sampling sites to the farm, although this varied according to species.     

Chromosomal and cell size analysis of cold tolerant maize

Summary C-band number, guard cell length, and chloroplast number per guard cell were determined for eight maize populations. These populations consisted of maize selected for cold tolerance at the University of Nebraska as well as the original unselected populations. The genome size of these populations had previously been determined. C-band number fluctuated concertedly with the changes in genome size indicating that deletions and additions of constitutive heterochromatin occurred during selection, resulting in altered genome sizes. Guard cell size of all the cold tolerant populations was greater than the cell size of the respective nonselected populations. Chloroplast number per guard cell was also higher in all the cold tolerant populations than in their parental populations, but the increases were not statistically significant. The results indicate that changes in genome size that occurred during selection for cold tolerance are the result of changes in amounts of C-band heterochromatin and that the selection process results in an increase in cell size in the cold tolerant populations.     

The Hemiptera (Insecta) communities of tropical rain forest in Sulawesi

The structure and composition of Hemiptera communities of tropical rain forest in Dumoga-Bone National Park, Sulawesi, Indonesia were investigated over a 1-year period. The aim was to investigate the extent to which insect samples, obtained using six different techniques, were representative of the whole community, and to explore temporal and spatial variation in Hemiptera community composition. Sampling techniques employed were Rothamsted light trapping, canopy fogging, malaise trapping at both ground and canopy level, flight interception trapping and yellow water pan trapping. Overlap between faunas collected using different techniques was surprisingly low emphasizing the limitations of using any single method to sample and thereby describe the Hemiptera community. Differences were observed at the species, family and suborder levels. Similarly, there were major differences in faunal composition between sites and diversity appeared to peak at elevations between 600–1000 m. Seasonal changes were also significant but generally lower than between methods or sites. Results are discussed in relation to factors such as food availability and host specialization and the efficacy of each sampling method is reviewed in relation to the biology of the different Hemiptera groups and the composition of the samples obtained.     

Evolution of erect helical colony form in the Bryozoa: phylogenetic, functional, and ecological factors

Erect helical colony forms have evolved at least six separate times within the Bryozoa, but only among those in which branches are composed of a single layer of feeding zooids. The four best known genera with helical colony forms evolved independently, and each occupied different benthic marine environments, achieved different growth habits, and utilized different aspects of an array of functional potentials resulting from the radially symmetrical colonies. Examination of the distribution of these four genera ( Archimedes , Bugula , Crisidmonea , and Retiflustra ) within a theoretical morphospace of hypothetical helical colony form reveals that each occupies its own characteristic region of morphospace, broadly overlapping in some dimensions but separated in others. The genera differ markedly in the branching densities within their filtration-sheet whorls, reflecting their phylogenetic legacies rather than constructional or functional constraints associated with helical growth. In contrast, all tend toward helices in which the radiating whorls of the unilaminate branches are held at an average of 50–60° to the central axis of the colony, and this may reflect a common functional optimum associated with the cilia-driven, auto-generated currents within the helix. The region of morphospace characterized by high values of surface area – i.e. helical geometries with branches orientated at very low angles to the central axis, and with very closely spaced whorls along the axis – is entirely empty of bryozoans, and these geometries apparently represent functionally unrealistic colony forms.  © 2003 The Linnean Society of London, Biological Journal of the Linnean Society , 2003, 80 , 235–260.     

Comparisons of tests for aneuploidy

The fundamental problems that face us in the development of suitable assay systems for the detection of potentially aneugenic (aneuploidy-inducing) chemicals include: (a) the diversity of cellular targets and mechanisms where perturbations of structure and function may give rise to changes in chromosome number, and (b) the phylogenetic differences that exist between species in their mechanism and kinetics of cell division and their metabolic profiles. A diverse range of assay systems have been developed, which have been shown to have potential for use in the detection of either changes in chromosome number or of perturbations of the events which may be causal in the induction of aneuploidy.

Chromosome number changes may be detected cytologically by karyotypic analysis, or by the use of specialised strains in which aneuploid progeny may be observed due to phenotypic differences with aneuploid parental cells or whole organisms. Techniques for the detection of cellular target modifications range from in vitro studies of tubulin polymerisation to observations of the behaviour of various cellular organelles and their fidelity of action during the division cycle.

The diversity of mechanisms which may give rise to aneuploidy and the qualitative relevance of events observed in experimental organisms compared to man make it unlikely that the detection and risk assessment of the aneugenic activity of chemicals will be possible using a single assay system. Optimal screening and assessment procedures will thus be dependent upon the selection of an appropriate battery of predictive tests for the measurement of the potentially damaging effects of aneuploidy induction.