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Cytological observations were systematically employed for detecting cellular morphogenesis and chromosomal behavior of apogamous development of new sporophytes from individually cultured male gametophytes of Pyropia haitanensis. The results showed that the apical parts of premature male gametophytes initially underwent obvious apogamy, which primarily appeared in the functionally specialized spermatangial mother cells (SSMCs) that would not develop into highly differentiated spermatangia but change their developmental fate and become brownish red in color. These brownish red spermatangial mother cells (SMCs) were released accompanying the spermatia dissociated from mature spermatangia and then rarely formed circular carpospore-like cells (CLCs) and carpospore-like germlings (CLGs) that eventually developed into normal apogamous sporophytic conchocelis. Chromosome counts indicated that spermatangia and spermatia were haploid (n = 5), whereas SSMCs, CLCs, and CLGs were diploid (2n = 10). Furthermore, filamentous conchocelis and conchosporangial branch cells of apogamous sporophytes were diploid and no haploid, aneuploid, and polyploid were observed, suggesting that spontaneous chromosome doubling occurred in the process of apogamy and initiated rarely SSMCs rather than released spermatia. Moreover, pit connections were observed in the whole development of apogamous sporophytes like in heterozygous sporophytes. Mitotic chromosomal behaviors appeared during the first two divisions of conchospores that normally grew into haploid tetrads and developed into unisexual male gametophytes with the characteristics of apogamy in the aging cultures.

The genus Dunaliella comprises 28 species defined primarily by morphological and physiological criteria, which vary considerably depending on growth conditions. Concomitantly, the taxonomic status of various species is uncertain. To confirm the taxonomic identity and to better understand the relationship within Dunaliella, seven taxa ( D. salina, D. bardawil, D. tertiolecta, D. parva, D. viridis, D. lateralis, D. peircei) were compared using RFLP analysis of the nuclear rDNA repeats, specifically the internal transcribed spacer regions, including the 5.8S rRNA gene. Volvox aureus was used as an outgroup. A single ITS PCR amplification product was obtained for each taxon. An ITS fragment of ca. 640 bp was present in all the taxa within the subgenus Dunaliella, except for D. salina CCMP 1303 (ca. 540 bp) and D. lateralis (subgenus Pascheria) (ca. 600 bp). A cluster analysis based on the presence or absence of bands generated by digestion of the PCR product with 8 restriction endonucleases (DpnI, HhaI, EcoRI, PvuII, TaqI, HaeIII, MspI, StyI) revealed no correlation between the genetic relationship inferred from the ITS-RFLP data and the morpho-physiological attributes used for taxonomy. In addition, differences in morphology, physiology and in the length and restriction fragment patterns of the ITS region of D. salina CCMP 1303 suggest that this strain does not belong to Dunaliella.

Studies on microalgae species and strain selection have demonstrated the potential of a broad range of algal species suitable for large-scale mass production, but provided little data on the reliability and productivity of the cultures under outdoor conditions over a long period. Long-term studies as part of the development of large-scale microalgae mass production are essential at small scale to minimise expenditure in scaling-up and large-scale operations. The current study describes the long-term semi-continuous culture of 4 wild-type isolates of euryhaline Tetraselmis sp. grown in 1 m2 raceway ponds outdoors in 7% (w/w NaCl) saline water enriched with N and P without any additional carbon source under the environmental conditions in Perth, Western Australia. The long-term investigation indicated that Tetraselmis MUR-231 was not able to grow outdoors, while Tetraselmis strains MUR-167, MUR-230 and MUR-233 grew outdoors over long periods. Tetraselmis MUR-167 was cultured for over 16 months outdoors before terminated due to cell clump formation and heavy biofilm development on the pond walls, whereas Tetraselmis strains MUR-230 and MUR-233 were cultured in semi-continuous culture over 20 months. The latter two strains grew at high solar irradiance with daily maximum values of 58890 W m−2 and temperatures ranging from about 40 to 0 °C. Both strains had a similar average specific growth rate of 0.19 day−1 over the experimental period. Maximum biomass productivities were 9.11 g m−2 day−1 and 9.99 g m−2 day−1 for Tetraselmis MUR-230 and MUR-233, respectively. The maximum total lipid productivity of 4.30 g m−2 day−1 of Tetraselmis MUR-230 was slightly higher than Tetraselmis MUR-233 (4.05 g m−2 day−1). These results clearly indicate the potential of these two Tetraselmis strains for commercial application, such as a high lipid yielding feedstock under minimal culture management conditions in arid and semi-arid coastal regions such as northern Western Australia.

Physiological responses of the euryhaline red drum, Sciaenops ocellatus, to chloride salt addition, low salinity, and high sulfate concentration were measured. Survival was increased by addition of calcium chloride (CaCl2) or magnesium chloride (MgCl2) to dilute artificial seawater (0.2 ppt salinity). Although survival and routine metabolic rates were greater in MgCl2 treatments, growth and feed efficiency were greater in CaCl2 treatments. Marginal metabolic scope increased when CaCl2 or MgCl2 were added to dilute artificial seawater. There was a strong positive linear relationship (p=0.0001, r=0.91) between fish survival and salinity of artificial seawater dilutions over the salinity range 0.1 to 3.0 ppt. Monovalent ion concentrations in red drum plasma varied; whereas, divalent ion concentrations were relatively constant. Survival and growth were not affected by high sulfate concentrations (2000 mg l-1) in 3.0 ppt artificial seawater supplemented with either sodium sulfate or magnesium sulfate. Routine metabolic rate and marginal metabolic scope of red drum exposed to high sulfate concentrations were slightly, but not significantly, lower than those of red drum in 3 ppt artificial seawater.

The influence of habitat structure on reef-fish communities at Bar Reef Marine Sanctuary, Sri Lanka, was investigated. The relationship between habitat characteristics and the distribution and abundance of 135 species of fishes was examined on two reef types: coral and sandstone reefs. Results suggested that the reef-fish communities were strongly influenced by various aspects of reef structure. However, relationships between habitat variables and fish communities structure, varied between the two reef types. Fish species diversity was correlated with a number of habitat variables on the sandstone reefs, although structural complexity seemed to play the dominant role. There were no correlations between habitat structure and fish diversity on the coral reefs. Total abundance was not related to any one habitat parameter on either reef type. However, abundances of some species, families and trophic groups were correlated with habitat features. These specific correlations were commonly related to food or shelter availability. For example, coral feeders were correlated with live coral cover, and pomacentrid species, which used branching corals for protection, showed a significant relationship with the density of Acropora colonies. This shows that a summary statistic such as total abundance may hide important information. Effects of habitat structure on the distribution patterns of the fish communities was further investigated using multi-dimensional scaling ordination (MDS) and the RELATE-procedure. With the MDS ordinations for both habitat and fish-community composition it was possible to show that the multivariate pattern between the two ecological components was clearly correlated.

The efficiency of 9:1 acetone-water, DMSO and boiling 9:1 ethanol-water in extracting chlorophyll and carotenoid pigments from benthic cyanobacterial mats from Antarctica for HPLC (high performance liquid chromatography) analysis was examined. Considerable breakdown of chlorophylla was observed after 5 min extraction in boiling ethanol and 2 h extraction in DMSO. Over 50% of the chlorophylla was degraded to chlorophyllidea and there was substantial loss of carotenoids after a 15 h exposure of ground cells to cold 9:1 acetone-water. Mild sonication of ground mat material in 9:1 acetone-water followed by a 4 h extraction at 4 ° C was found to minimise chlorophylla breakdown and dramatically improved the extraction efficiency of chlorophylla, myxoxanthophyll and -carotene.