Seasonal fluctuations in fecundity and hatching success in the planktonic copepod Centropages typicus

A mismatch of {small tilde}2–3 months was observed betweenreproductive rates and population abundances in the planktoniccopepod Centropages typicus, with the highest production atrelatively low female abundance and low production at high abundance,during the course of a 2 year study in 1989 and 1990 in neriticwaters of the Gulf of Naples. During this period, egg mortalitywas at times severe, with values as high as 59% in February1989. The seasonal trend in percentage hatching success didnot match seasonal fluctuations in breeding intensity, and wasnot correlated with variations in environmental variables suchas temperature and chlorophyll a. The results of experimentsusing the fluorescent dye Hoechst 33342 showed that unhatchedeggs had been fertilized and that in most cases developmenthad proceeded to an advanced stage before death of the embryo.The causes of high egg mortality are uncertain, but here wegive evidence, for the first time, that egg mortality may notonly be due to infertility caused by failure to remate.     

Torsional constant of 27-mer DNA oligomers of different sequences.

We have studied the torsional elastic constant (alpha) of short DNA (27mer) oligomers of various sequence by fluorescence polarization anysotropy (FPA) measurements. The lowest alpha values were found in samples with sequence rich in AA dinucleotides or containing the alternating d(A-T) x d(A-T) motif. The torsional rigidity of our DNA samples was compared to that calculated according to the current values of twist angle fluctuations derived for ten dinucleotide steps by recent analyses of DNA crystal structure database. The values of torsional rigidity derived from crystals are higher than our experimental ones, obtained by FPA analysis, suggesting that packing force in crystals may notably hinder the dinucleotide twist angle fluctuations that occur in solution. This behaviour is more evident for samples containing AA, TA and AT steps. In all the samples there is about a twofold change of the alpha value in the 10-40 degrees C range. An activation enthalpy (Delta H (#)) of about 17.4 kJ mol(-1), on average, was obtained for the temperature dependence of eight of the ten samples studied. A correlation with the stacking energy is discussed.     

GENESIS OF THE APYRENE PARASPERM IN THE APPLE SNAIL POMACEA CANALICULATA (GASTROPODA: AMPULLARIIDAE): AN ULTRASTRUCTURAL STUDY

The apyrene paraspermatogenesis in the freshwater gastropod Pomaceacanaliculata has been studied with electron microscopy. Matureapyrene parasperm result from a cytodifferentiation processwithout maturation division. The atypical condition is recognizedearly. Paraspermatogonia are characterized by voluminous nucleiwith irregular clusters of heterochromatin, numerous dilated cisternaeof the rough endoplasmic reticulum and small electron-dense granulesspread through the cytoplasm. As this process advances, the nucleibecome lobed and chromatin degenerates. The remnant chromatin condensesto form dense bodies which are finally excreted from the cells.At the cytoplasmic level a centriolar multiplication with the consequentflagellogenesis takes place. The axonemal microtubules run alongthe entire length of the cell and emerge from the posteriorend forming a tuft of three or more free flagella. The roughendoplasmic reticulum and the Golgi complex are involved inthe production of secretory granules, some of which are laterreleased by exocytosis. At the end of paraspermatogenesis matureapyrene parasperm are fusiform-shaped anuclear ciliated cells. (Received 20 January 2000; accepted 18 July 2000)     

Exopolysaccharide-producing strains of thermophilic lactic acid bacteria cluster into groups according to their EPS structure

AIMS: To compare galactose-negative strains of Streptococcus thermophilus and Lactobacillus delbrueckii subspecies bulgaricus isolated from fermented milk products and known to produce exopolysaccharides (EPSs). METHODS AND RESULTS: The structures of the EPSs were determined using nuclear magnetic resonance (NMR) and their genetic relationships determined using restriction endonuclease analysis (REA) and random amplification of polymorphic DNA (RAPD). Similar groupings were apparent by REA and RAPD, and each group produced an EPS with a particular subunit structure. CONCLUSION: Although none of the strains assimilated galactose, all inserted a high proportion of galactose into their EPS when grown in skimmed milk, and fell into three distinct groups. Significance and Impact of the Study: This information should help in an understanding of genetic exchanges in lactic acid bacteria.     

Parametric and Nonparametric Analyses of Repeated Ordinal Categorical Data

We compare two models for the analysis of repeated ordinal categorical data: the classical parametric model for means of scores assigned to the categories of the response variable and a nonparametric model based on relative effects derived from the marginal distribution functions of the response. An example in the field of Dentistry is used to illustrate and to compare the models. We also consider a simulation study to evaluate the type‐I error rates and the power of tests under both models in a balanced design setup. The simulation results suggest that both approaches behave similarly for equally spaced scores but may perform differently otherwise. (© 2004 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

Novel non-isotopic method for the localization of receptors in tissue sections.

We describe a novel fluorescent method for the detection of receptors for chimeric proteins in tissue sections. The technique was developed using a recombinant human insulin-like growth factor (IGF-1) chimera, bearing six additional histidine residues at the carboxy-terminal end (IGF-1-His). We demonstrated that dehydration of the tissue sections was detrimental for binding and that its prevention dramatically increased sensitivity. The specificity of IGF-1-His interaction was shown by gradual abolition of the fluorescent signal in the presence of increasing concentrations of IGF-1. Combining immunofluorescence with in situ ligand binding, we showed that IGF-1-His binding corresponded to the IGF-1 receptor (IGFR-1) distribution in human fetal kidney. Moreover, incubation of the tissue sections with an anti-IGFR-1 blocking antibody abolished IGF-1-His binding, demonstrating that the interaction was mediated by the IGFR-1. The method was also used to localize the IGFR-1 in E18 rat embryo sagittal sections. The IGF-1-His binding pattern was observed in brain, cartilage, lung, skin, heart, diaphragm, and tongue, and paralleled the previously reported IGFR-1 distribution. We believe that this new non-isotopic in situ ligand binding method will facilitate rapid and accurate localization of receptors in tissue sections.