Lessons on broodstock maintenance,spawning, larval rearing and juvenile production of marine gastropods of ornamental value

Research on marine gastropod breeding in India is in its infancy and scanty literature is only available. To fill the lacunae, marine gastropods of three ornamentally valued and conservation important groups such as Cyprids, Strombids and Muricids were held under captivity and studied for their broodstock maintenance, spawning behaviour, larval rearing and metamorphosis into juveniles at the Shellfish Hatchery of Central Marine Fisheries Research Institute, Tuticorin. Valuable information on the focal themes of the article was obtained for Strombids and Muricids leading to the successful life cycle closing for Lambis lambis and Chicoreus virgineus are reported earlier. In the present study, experiments were conducted on aspects such as post‐metamorphosed juvenile rearing up to 76 days post hatch for L. lambis, spawning, larval development and life cycle closing and reasonable level of juvenile production (8.8%) for Chicoreus ramosus. In addition, the primary observations on the captive breeding of Cypraea tigris with reference to its egg mass, brooding habit and early development is reported. However, while studying these groups few unanswered questions and bottle necks in their breeding nature, larval rearing and metamorphosis arose. The following account details the experiments conducted and results obtained in each of the focal themes of the paper and the constraints faced.     

Diversity of Sodium Transporter HKT1;5 in Genus Oryza

Asian cultivated rice shows allelic variation in sodium transporter, OsHKT1;5, correlating with shoot sodium exclusion (salinity tolerance). These changes map to intra/extracellularly-oriented loops that occur between four transmembrane-P loop-transmembrane (MPM) motifs in OsHKT1;5. HKT1;5 sequences from more recently evolved Oryza species (O. sativa/O. officinalis complex species) contain two expansions that involve two intracellularly oriented loops/helical regions between MPM domains, potentially governing transport characteristics, while more ancestral HKT1;5 sequences have shorter intracellular loops. We compared homology models for homoeologous OcHKT1;5-K and OcHKT1;5-L from halophytic O. coarctata to identify complementary amino acid residues in OcHKT1;5-L that potentially enhance affinity for Na⁺. Using haplotyping, we showed that Asian cultivated rice accessions only have a fraction of HKT1;5 diversity available in progenitor wild rice species (O. nivara and O. rufipogon). Progenitor HKT1;5 haplotypes can thus be used as novel potential donors for enhancing cultivated rice salinity tolerance. Within Asian rice accessions, 10 non-synonymous HKT1;5 haplotypic groups occur. More HKT1;5 haplotypic diversities occur in cultivated indica gene pool compared to japonica. Predominant Haplotypes 2 and 10 occur in mutually exclusive japonica and indica groups, corresponding to haplotypes in O. sativa salt-sensitive and salt-tolerant landraces, respectively. This distinct haplotype partitioning may have originated in separate ancestral gene pools of indica and japonica, or from different haplotypes selected during domestication. Predominance of specific HKT1;5 haplotypes within the 3 000 rice dataset may relate to eco-physiological fitness in specific geo-climatic and/or edaphic contexts.     

Maternal and burial environment determine the physical dormancy release in tropical Senna auriculata(Fabaceae) seeds

In tropical ecosystems,species with an impermeable seed coat,i.e.physical dormancy(PY),are large in number and their seed coat is considered to be an adaptive trait for species persistence and colonization.However,only little is known about their mechanisms for breaking dormancy.The objective of this study was to understand the importance of seed maturation site and burial location in determining the PY release of Senna auriculata.Freshly collected seeds of S.auriculata from Vellore and Coimbatore,Tamil Nadu,India,germinated to 11±1.5%and19±2.5%respectively and remaining seeds did not imbibe water,thus had PY.Germination of seeds from both sites following hot-water treatment for 30 s and mechanical scarification increased significantly and seeds were able to germinate at a wide-range of temperatures(5–35℃)both in light and darkness.When incubated at 15/60℃for 3 months,dormancy release for seeds collected from Coimbatore(72%)was greater than seeds matured in Vellore(53%).Following 1 year of burial at three different locations,seeds from Coimbatore germinated to higher percentage than Vellore seeds at all locations.In particular,the higher temperature sites released dormancy to greater extent than the lower temperature site.Our results suggest that summer temperatures(>60℃)prevailing in the tropics provide appropriate cues for breaking PY,but this could be greatly affected by the initial state of seeds and the burial environment.     

Survey of campylobacter, salmonella and mycoplasmas in house crows (Corvus splendens) in Malaysia

House crows (Corvus splendens) in Selangor, Malaysia were examined for the presence of Campylobacter species, Salmonella species, Mycoplasma gallisepticum and Mycoplasma synoviae by serology, culture and pcr. For the detection of Campylobacter and Salmonella species swabs were taken either from the intestine or cloaca. For the detection of mycoplasmas, swabs were taken either from the choanal cleft or trachea for culture and pcr and serum samples were tested by the rapid serum agglutination (rsa) and monoclonal antibody-blocking elisa (mbelisa) for antibodies to M gallisepticum and M synoviae. For campylobacter, 25.3 per cent of the crows were positive by culture, and the species identified were Campylobacter jejuni and Campylobacter coli. No Salmonella species were isolated. Four of 24 swabs were positive for M gallisepticum dna but none gave positive results for M synoviae dna. No M gallisepticum or M synoviae antibodies were detected by rsa but 60 per cent of the sera gave positive reactions for M gallisepticum and 13 per cent gave positive reactions for M synoviae by mbelisa.