Interannual variation in the reproductive cycle of the New Zealand snapper Pagrus auratus (Bloch & Schneider) (Sparidae)

Changes in reproductive condition in the New Zealand snapper Pagrus auratus (Bloch & Schneider) were monitored in a wild population over three successive years. Recrudescence occurred in spring with spawning beginning in October and continuing for 3 to 5 months. The initiation of spawning varied by up to 3 weeks and was associated with sea surface temperatures of 15–16° C. Theconclusion of spawning was associated with temperatures of 19–21° C but showed greater interannual variation than the onset of spawning. Changes in the gonadosomatic index were accompanied by parallel changes in hepatosomatic index in females but not males, reflecting the role of the liver in vitellogenesis in females.     

Estimating gonadal development using a non-destructive measurement of ovarian length in live Tasmanian striped trumpeter, Latris lineata (Forster, 1801)

Sexually mature female striped trumpeter Latris lineata (Forster, 1801) were sampled monthly for two spawning seasons until the start of gonadal recrudescence, and then fortnightly until ovulations ceased. Oocyte size and ovarian length, measured by inserting a semi-rigid biopsy catheter to the full extent of insertion, were recorded at each sample time. Ovarian length was expressed as proportion of fork length to provide a gonad index (GI). In non-ovulating females, there was little change in GI throughout the year. However, in ovulating females, GI increased from 18.3 five months before the first spawning season to 27.6 at the peak of the season in October, decreasing to 19.1 the following May and then increasing again to a maximum of 31.1 the following October, in concert with annual changes in reproductive condition. There was a positive linear correlation between GI and oocyte size during the period of oocyte growth ( r  = 0.75, n = 302). Based on the range of GI values for each stage in oocyte development (primary, cortical alveoli, vitellogenic, maturing and hydrated), GI was 90% accurate at assessing fish as pre-vitellogenic and 83% accurate at assessing fish as undergoing final oocyte maturation. This study demonstrated that measurement of GI by catheterization provides a rapid and non-destructive method for assessing maturational status of striped trumpeter broodstock.     

The relationship of ocular morphology to feeding modes and activity periods in shallow marine teleosts from New Zealand

Synopsis Thirty one species of shallow water teleosts were captured from the NE coast of New Zealand. Ocular morphology was assessed in terms of eye size, pupil shape, theoretical sensitivity and acuity based on retinal morphology, and regional distribution of photoreceptors within the retina. Eye size was relatively or absolutely larger in carnivores than herbivores. Diurnal planktivores and nocturnal species of small body size maximise vision by having relatively large eyes. Anterior aphakic spaces were present in most of the species examined, and 25% of the species also had posterior aphakic spaces. Theoretical sensitivity was generally higher among nocturnal than diurnal species, however, a number of benthic and pelagic carnivores showed retinal specialization for enhanced sensitivity. Diurnal species displayed high spatial acuity, with maximum acuity occurring in carnivorous species. Crepuscular species had either high or low acuity, whereas that of nocturnal species was generally lower than in diurnal species. Ten species displayed regional variation in rod density, with crepuscular and nocturnal species showing streaks of high rod density in the retina. Eleven species of carnivores displayed regional variation in cone density, with highest density usually occurring in the caudal part of the retina. In most of the species with areas of high cone density, there was a forward visual axis that coincided with the location of the aphakic space, suggestive of accomodation along that axis.     

Conserved plasmid/chromosome sequences in fast- and slow-growing rhizobia that nodulate the same plant

Apart from the ability to nodulate legumes, fast-and slow-growing rhizobia have few bacteriological traits in common. Given that there is only one pathway to nodulation, DNA sequences conserved in fast- and slow-growing organisms that nodulate the same host should be strongly enriched in infectivity genes. We tested this hypothesis with seven fast-growing and five slow-growing strains that produced responses varying from fully effective nodulation through various ineffective associations to non-nodulation on four different hosts (Lotus pedunculatus, Lupinus nanus, Macroptilium atropurpureum, and Vigna unguiculata). When restriction enzyme digested total DNA from 10 of the strains was separately hybridized with nick-translated plasmid DNA isolated from 4 fast-growing strains, variable but significant homologies were found with all 10 strains. Part of this homology was shown to be associated with the nifKDH genes for nitrogenase and part with putative nodulation genes carried on pC2, a cosmid clone containing a 37 kbp region of the large sym plasmid present in the fast-growing broad-host range Rhizobium sp. strain NGR234. Analysis of the extent of homology between the plasmids of 3 fastgrowing strains (NGR234, TAL 996 and UMKL 19) able to effectively nodulate Vigna unguiculata showed them to have homologous DNA fragments totalling 47 kbp. This core homology represents less than 12% of the total coding capacity of the sym plasmid present in each of these strains.Abbreviations Sym symbiotic sequences/plasmids - nod genes required for nodulation - nod putative nod genes - nif genes required for the synthesis of the enzyme nitrogenase     

The effect of bacterial strain and temperature changes on the nitrogenase activity of Lotus pedunculatus root nodules

After 40 days of growth at 25°C, Lotus pedunculatus cav., cv. Maku plants infected with Rhizobium loti strain NZP2037 displayed similar relative growth rates but had twice the nodule mass and only one third the whole plant dry weight of plants infected with Bradyrhizobium sp. (Lotus) strain CC814s. In the NZP2037 symbiosis, the rate of CO₂ evolution (per g dry weight of nodulated root) was 1.6 times as high as that in the CC814s symbiosis while the rate of C₂H₂ reduction (per g dry weight of nodule) was only 48% of that in the CC814s symbiosis. Studies of the effect of short term temperature changes on the gas exchange characteristics (CO₂ and H₂ evolution, C₂H₂ reduction) of these symbioses revealed wide differences in the optima for C₂H₂ reduction. Nodules infected with NZP2037 displayed maximal C₂H₂ reduction rates [157 μmol (g dry weight nodule)^?1 h^?1] at 12°C, whereas nodules infected with CC814s were optimal at 30°C [208 μmol (g dry weight nodule)^?1 h^?1]. These short term studies suggested that differences in temperature optima for N₂ may have partially accounted for the poorer effectivity, at 25°C, of strain NZP2037 when compared with strain CC-814s. The relative efficiency [RE = 1 – (H₂ evolution/C₂H₂ reduction)] of N₂ fixation varied widely with temperature in the two symbioses, but there was a general trend toward higher RE with lower temperatures. The ratio of CO₂ evolution: C₂H₂ reduction (mol/mol) in nodulated roots infected with CC814s was constant (ca 10 CO₂/C₂H₂) between 5°C and 30°C, whereas in plants infected with NZP2037 it reached a minimal value of 3.3 CO₂/C₂H₂ at 10°C and was 19 CO₂/C₂H₂ at the growing temperature (25°C).     

Mildly acidic pH activates the extracellular molecular chaperone clusterin

Many features of the chaperone action of clusterin are similar to those of the intracellular small heat shock proteins (sHSPs) that, like clusterin, exist in solution as heterogeneous aggregates. Increased temperature induces dissociation of some sHSP aggregates and an enhanced chaperone action, suggesting that a dissociated form is the active chaperone species. We recently reported that clusterin aggregates dissociate at mildly acidic pH. To further explore the similarities between clusterin and the sHSPs, we tested the effects of temperature and pH on the structure of clusterin and its chaperone action. Our results demonstrate that increased temperature does not induce dissociation of clusterin aggregates, or other major structural changes, and has little effect on its chaperone action. However, we show that the chaperone action of clusterin is enhanced at mildly acidic pH. Clusterin is the first chaperone shown to be activated by reduced pH. This unique mode of activation appears to result from an increase in regions of solvent-exposed hydrophobicity, which is independent of any major changes in secondary or tertiary structure. We propose a model in which low pH-induced dissociation of clusterin aggregates increases the abundance of the heterodimeric chaperone-active species, which has greater hydrophobicity exposed to solution.     

Vitellogenin isolation,purification and antigenic cross-reactivity in three teleost species

Vitellogenin (Vtg) was isolated from male greenback flounder (Rhombosolea tapirina), rainbow trout (Oncorhynchus mykiss) and Atlantic salmon (Salmo salar) plasma, following induction by estradiol (E(2)) inoculation. The molecular weight of each native molecule, as determined by gel filtration, was 540, 383 and 557 kDa, respectively. With sodium dodecyl sulphate polyacrylamide gel electrophoresis under reducing conditions, Atlantic salmon and greenback flounder Vtg appeared as three major bands (approximately 159, 117, 86 kDa and 155, 104, 79 kDa, respectively), whereas rainbow trout Vtg appeared as one major band (approximately 154 kDa). Several minor bands were also present in each Vtg isolate. Polyclonal antisera, produced against only the highest molecular weight band from each species following excision from reducing gels, were reactive with all major bands in Western blots. In competition ELISA, parallel binding slopes were demonstrated between purified Vtg and plasma from vitellogenic females of the same species, but there was no reaction with plasma from untreated males. These antisera were highly species-specific and little cross-reactivity was noted, even between the two salmonid species. These data suggest that excision of bands from gels is a simple procedure for the preparation of species-specific antisera, and confirm that cross-species assays give highly variable results.