Response of Gonyaulax tamarensis to the presence of a pycnocline in an artificial water column

In nature, large concentrations of the toxic bloom-forming dinoflagellate,Gonyaulax tamarensis, are frequently observed in the vicinityof the pycnocline. In the absence of a pycnocline the organismis usually recorded near the surface, where light levels aremore advantageous for photosynthesis. In this paper we examinethe swimming behaviour of G.tamarensis when exposed to varyingdegrees of stratification and investigate whether the maintenanceof a subsurface (pycnocline) population is the result of retentionof the algae by a physical barrier or active accumulation ofthe organisms at a density interface. The study indicates thatG.tamarensis cells presented with a halocline of S<{smalltilde}6–7 (occurring over a few centimeters) cross thissalinity barrier and accumulate at the highest available photonflux density ({small tilde}100 µmol m^–2 s^–1).Cells exposed to a gradient of S>{small tilde}7remain atthe halocline (pfd={small tilde}40 µmol m^–2 s^–1).However, when light above the pycnocline is attenuated by theaddition of food colour to the medium, the cells cross a haloclineof S=10 and accumulate at the highest available photon fluxdensity. In the absence of added nutrients (inorganic N andP) the organism fails to exhibit a phototactic response. Thus,the presence of a strong halocline does not represent an inpenetrablephysical barrier for G.tamarensis and the development of pycnoclinepopulations of this organism is a function of density, lightand nutrient climate.     

Improved assay for quantitating adherence of ruminal bacteria to cellulose.

A quantitative technique suitable for the determination of adherence of ruminal bacteria to cellulose was developed. This technique employs adherence of cells to cellulose disks and alleviates the problem of nonspecific cell entrapment within cellulose particles. By using this technique, it was demonstrated that the adherence of Ruminococcus flavefaciens FD1 to cellulose was inhibited by formaldehyde, methylcellulose, and carboxymethyl cellulose. Adherence was unaffected by acid hydrolysates of methylcellulose, glucose, and cellobiose.     

Regulation of nuclear binding of the avian oviduct progesterone receptor. Changes during estrogen-induced oviduct development, withdrawal, and secondary stimulation

The progesterone receptors from various stages of estrogen induced oviduct development, estrogen withdrawal, and secondary stimulation with estrogen were examined. The progesterone receptors were characterized for their biological function (i.e. capacity for nuclear translocation, nuclear binding, and effects on RNA polymerase II activity) as well as certain physical properties. The progesterone receptors from the undeveloped or partially developed oviducts (0 to 8 days of estrogen treatment) displayed little or no nuclear translocation and binding in vivo or in vitro. Similarly, progesterone showed little or no effect in vivo on RNA polymerase II activity at the early stages of development. As development progressed from 8 to 12 days of estrogen treatment, the above parameters rapidly increased to maximal levels and plateaued through day 23 of estrogen treatment. A marked decrease in these parameters occurred within 1 day of estrogen withdrawal. The reverse series of events occurred during secondary estrogen stimulation of 10-day-old withdrawn chicks. While the receptor concentrations increased rapidly to maximum values by 2 days of restimulation, receptor function did not return until day 4. Similarly, the effects of progesterone on RNA polymerase II activity reached maximal values by day 4. The progesterone receptor isolated from oviducts during development, estrogen withdrawal, and restimulation, displayed similar patterns of cell-free binding to chromatin and nucleoacidic protein as that observed in vivo supporting the nativeness of the in vitro binding assay. In contrast, the cell-free binding of these same progesterone receptor to pure DNA were not similar to the in vivo binding, i.e. no patterns (differences) in progesterone receptor binding were observed. These data support that protein DNA complexes and not pure DNA represent the native acceptor sites for oviduct progesterone receptor. Comparison of the progesterone receptor between the functional and nonfunctional states revealed no differences in the steroid affinity for the receptor, in the apparent pI of the species, or in the sedimentation of the receptor under high salt conditions. However, the nonfunctional receptors consistently displayed a deficiency in one of the two monomer molecular species (the B species) as determined by isoelectric focusing. These results suggest that both monomer species of progesterone receptor are required for biological activity. Interestingly, the 7S "aggregate" species of the progesterone receptor was constantly detected even when only one of the monomer species was present.(ABSTRACT TRUNCATED AT 400 WORDS)     

Small scale preparation of skeletal muscle mitochondria, criteria of integrity, and assays with reference to tissue function

Mitochondria prepared in small scale from skeletal muscle were studied with respiration measurements and low temperature spectroscopy. The method of preparation was developed for 25–100 mg tissue with pigeon breast muscle as model organ. The yield was 40%. Data collected during the developmental work were used to evaluate criteria of mitochondrial quality. The cytochrome c conservation, i.e. cytochrome c per mitochondrial quantity in the preparation relative to that in the tissue, is a most useful test parameter. It is bounded between 0–100%. Proportionality between the state 3 rate and the cytochrome c conservation was not rejected by statistical tests. The respiratory control ratio (RCR) was also highly correlated to the cytochrome c conservation. These correlations might be extrapolated to 100% conservation to give hypothetical tissue values. The cause for the correlations is discussed. The P/O ratio showed only weak dependence on the cytochrome c conservation and the state 4 rate s howed no dependence. Other, rather insensitive test parameters are also discussed. The pigeon breast muscle mitochondria isolated by the final method showed cytochrome c conservation of 73 ± 9% (n = 16). They are compared with pig biceps femoris mitochondria prepared by the same method. The two types of mitochondria show many similarities. Some differences may be explained by a different amount of inner mitochondrial membrane relative to mitochondrial protein. The pig tissue contains ten times less mitochondrial protein than the pigeon tissue does. (Mol Cell Biochem 174: 55–60, 1997)     

Temporal occurrence of planktotrophic bivalve larvae identified morphologically and by single step nested multiplex PCR

We report the application of a recently developed molecularmethod, single step nested multiplex PCR (SSNM-PCR) assay andmicroscopy to identify and investigate temporal patterns ofbivalve larvae in a Danish estuary, Isefjord. All samples werecollected during the SUSTAINEX program from June to November2001. Using the molecular assay, larvae could be categorizedinto six groups: the blue mussel, Mytilus edulis, Ensis spp.,species of the Myoidae superfamily (Mya spp.), the common cockle(Cardiidae family), members of the Abra and Macoma genera ofthe Tellinoidae superfamily and members of the surf clam genera,Spisula spp. A seventh group was composed of unknown larvae.Greater resolution was possible by microscopy, but only forrelatively large and intact individuals (>150–200 µm).The molecular approach was capable of differentiating betweenlarvae regardless of shell size. Where it was possible to directlycompare identifications based on both methods, concordance washigh for M. edulis, Macoma balthica/Abra alba and E. americanus,whereas identification of Myoidae spp. and Cardiids was lessconsistent. Over the course of the study, two patterns of larvaloccurrence were observed. Larvae from species known to exhibita protracted annual spawning period (M. edulis, Myoidae spp.,Mysella bidentata and Cardiids) were present in the water columnthroughout the sampling period, whereas larvae of Abra alba,Barnea candida, E. americanus, Macoma balthica, Musculus marmoratusScrobicularia plana and Tapes pullastra appeared at clearlydefined periods.     

Sex, seasonal, and stress-related variations in elasmobranch corticosterone concentrations.

Serum corticosterone was previously studied in numerous elasmobranch fishes (sharks, skates and rays), but the role of this steroid, widespread throughout many taxa, has yet to be defined. The goal of this study was to test whether corticosterone varied in response to acute and chronic capture stress, and across the reproductive cycle in the bonnethead shark, Sphyrna tiburo, and Atlantic stingray, Dasyatis sabina. Serum corticosterone in S. tiburo increased following capture and again 24 h post-capture, possibly caused by interference with 1alpha-hydroxycorticosterone, the primary stress hormone in elasmobranchs. Higher serum concentrations in males compared to females were observed in both species. Variations in corticosterone also occurred during the reproductive cycle in both species. Consistent with other taxa, elevations in male bonnethead sharks and stingrays coincided with peak testicular development and mating. Elevations in female bonnethead sharks occurred from the time of mating through sperm storage into early gestation. In contrast, corticosterone levels in female stingrays were low during their protracted mating season, but elevated through late gestation and parturition. These results indicate that corticosterone has a limited role, if any, in acute and chronic stress associated with capture in S. tiburo, but likely has physiological functions associated with its glucocorticoid properties across the reproductive cycle of both species.