A silver stain for the detection of nanogram amounts of tRNA following two-dimensional electrophoresis

Three ultrasensitive protein silver-staining methods have been compared with respect to the detection of tRNA in polyacrylamide gels. The method of Sammons (D. W. Sammons, L.D. Adams, and E.E. Nishizawa (1981) Electrophoresis 2, 135-141) has been shown to have remarkable sensitivity, with a detection limit of 0.3 ng tRNA/mm2, allowing the two-dimensional fractionation of submicrogram amounts of bulk tRNA. The application of this technique to developmental and differentiation problems and other areas where the amounts of nonradioactive tRNA available are limited is anticipated.     

Mitogenomic analysis of Montipora cactus and Anacropora matthai (cnidaria; scleractinia; acroporidae) indicates an unequal rate of mitochondrial evolution among Acroporidae corals

The complete nucleotide sequence of the mitochondrial (mt) genome was determined for specimens of the coral species Montipora cactus (Bernard 1897) and Anacropora matthai (Pillai 1973), representing two morphologically distinct genera of the family Acroporidae. These sequences were compared with the published mt genome sequence for the confamilial species, Acropora tenuis (Dana 1846). The size of the mt genome was 17,887 bp and 17,888 bp for M. cactus and A. matthai. Gene content and organization was found to be very similar among the three Acroporidae mt genomes with a group I intron occurring in the NADH dehyrogenase 5 (nad5) gene. The intergenic regions were also similar in length among the three corals. The control region located between the small ribosomal RNA (ms) and the cytochrome oxidase 3 (cox3) gene was significantly smaller in M. cactus and A. matthai (both 627 bp) than in A. tenuis (1086 bp). Only one set of repeated sequences was identified at the 3′-end of the control regions in M. cactus and A. matthai. A lack of the abundant repetitive elements which have been reported for A. tenuis, accounts for the relatively short control regions in M. cactus and A. matthai. Pairwise distances and relative rate analyses of 13 protein coding genes, the group I intron and the largest intergenic region, igr3, revealed significant differences in the rate of molecular evolution of the mt genome among the three species, with an extremely slow rate being seen between Montipora and Anacropora. It is concluded that rapid mt genome evolution is taking place in genus Acropora relative to the confamilial genera Montipora and Anacropora although all are within the relatively slow range thought to be typical of Anthozoa.     

Certain observations on Scytonema stuposum (Kuetz.) Born. (Cyanophyta,Nostocales)

Some interesting cultural observations on Scytonema stuposum (Kuetz.) Born., were recorded. It was observed that frequently one or more terminal cells of a branch get cut off but they still remain attached over the sheath of the mother filament. Even in this condition such structures continue their growth and may become a multicellular body. Later, such a structure gets detached from the mother filament and serve as a hormogonium.     

Suppressive effects of soluble histocompatibility antigens on the in vitro generation of cytotoxic T cells to D-end alloantigens

Murine histocompatibility antigens were solubilized from the spleens and lungs of C57BL/6 (H-2b) animals with hypertonic salt (3 M KC1). Aggregate-free soluble antigens were incubated with nonadherent lymph node cells from BALB/c (H-2d) mice for 18 hr prior to their use as responder cells in the mixed-lymphocyte reaction (MLR). It was found that the generation of cytotoxic cells was suppressed while the proliferative response was not affected. The observed suppression was not due to a shift in the kinetics of the generation of cytotoxicity as determined throughout a 10-day culture period. The suppression was specific in that the response in MLR to unrelated H-2f stimulator cells and the subsequent generation of cytotoxic cells were unchanged. Using various H-2 recombinant strains as target cells in the assay of cell-mediated lympholysis, suppression of cytotoxicity was observed when the D end, but not the K end, was shared with the C57BL/6 strain from which the antigens were derived.     

Temporal patterns of breeding and recruitment in Nerophis lumbriciformis(Pisces; Syngnathidae) related to seawater temperatures

The breeding season of Nerophis lumbriciformis , a cold water pipefish, was positively correlated with seawater temperatures <15·5° C, whilst recruitment occurred at the end of the upwelling season, when seawater temperature attained its maximum values. The observed alterations in seawater temperatures, with steady year‐round increases, and the consequent alteration of the upwelling regime, may have dramatic consequences in the maintenance of N. lumbriciformis populations, by reducing the breeding period and simultaneously contributing to the transport of pelagic larvae northwards due to specific sea currents that occur outside the upwelling season.     

Experimental assessment of the fecundity of Eucypris virens (Ostracoda, Crustacea) under natural sex ratios

1. The adaptive significance of the observed variations in sex ratios in non‐marine ostracods is unclear. This study quantified the fecundity of females taken from a presumed fully sexual Eucypris virens population that were experimentally combined with different proportions of males (male : female sex ratios: 1 : 1, 1 : 2, 1 : 4, 1 : 8 and 0 : 1). 2. The results yielded no indications that female fecundity is altered by short‐term variations in the proportion of males, at least not within the range of sex ratios that are common in natural ostracod populations. Complete removal of males, however, did strongly reduce hatching success of dried eggs. This suggests the need for multiple mating events during the reproductive lifetime of the female. It also emphasizes the need for a minimum number of males, although this minimum number evidently may be rather low, as we found a high number of spermatozoa in the seminal receptacles after a single mating event. 3. The sex ratio in the source population was strongly female biased (1 : 3.4; n = 514), whereas in the hatchling assemblages reared in the laboratory, males and females were found in equal proportions (1 : 1.0; n = 1516), irrespective of the prevailing sex ratio. This clear discrepancy is intriguing, and points to the importance of epigenetic factors for the determination of field sex ratios.