Seasonal variation in direct and indirect measures of energy status was examined using estimates of glycogen, lipid and protein levels in a single cohort of male three-spined sticklebacks from an annual population collected each month over one complete year. Condition factor, somatic condition factor and hepatosomatic index (HSI) were calculated as indirect indices of energy status and the accuracy of these indirect measures as predictors of energy status was investigated. Results indicate that both condition factors were significant predictors of energy reserves (lipid, protein, glycogen and total energy), but that the proportion of variance accounted for was small. Both condition factors perform better as predictors of energy content per unit body weight. The HSI was a significant, but a weak predictor of total glycogen levels over the whole year. On a seasonal basis the relationship between HSI and energy reserves was highly variable. These indices are therefore poor predictors of energy reserves in male three-spined sticklebacks. '(', 1995 The Fisheries Sociely of the British Isles

No abstract

Wet and dry weights of tissue were measured and concentrations of glycogen, lipid and protein were estimated for the liver, gonad and carcass of male sticklebacks from an annual population collected each month over one complete year. In young-of-the-year there is one period of rapid weight gain, in all three body regions (liver, carcass and gonads) but particularly of the carcass, in the autumn and a second in spring and early summer. This is accompanied by an increase in the water content of all three body regions. The gonadosomatic index also increases sharply in spring and early summer. Young sticklebacks accumulate lipid and glycogen slowly during the autumn and winter of their first year of life and more rapidly from late winter to early summer. Thus, the period of most rapid accumulation of these reserves coincides with the time when body weight and gonad maturation are also increasing sharply. Lipid and glycogen levels fall during the reproductive season in those males that breed? so that by July they are reduced to 43% and 37% (respectively) of their peak values in May. Levels of protein increase throughout the year as the fish grow, but in breeding males by July the concentration of protein in the carcass falls to 70% of pre-breeding levels. Breeding males therefore reach the end of the reproductive season with their total energy reserves severely reduced, and consequently they suffer a very high mortality. In contrast, adult males that fail to reproduce survive beyond the breeding season. They continue to gain weight and to accumulate lipid and glycogen from August to September, but these. energy reserves fall (to levels comparable to those of post-breeding fish) in December, when these fish probably die. These results demonstrate that in male sticklebacks, growth and gonad maturation can be sustained in parallel with the accumulation of energy reserves, which are subsequently extensively depleted as a result of reproductive activities.

The aims of this study were firstly to investigate the fluoride-releasing characteristics of five commercial glass ionomer materials: Ketac Fil, Chemfil Superior, Fuji II LC, Aquacem and Vitrebond. The second aim was to assess the fluoride uptake and subsequent release from the same range of materials. In both tests, ten discs, 6 mm in diameter with a thickness of 1.5 mm, were made for each material. The initial fluoride release was assessed over a 60-day period for all materials. Each disc was immersed in 2 ml of de-ionised water within a plastic vial. The solutions were changed daily up to day 15, and thereafter every 3 and 4 days until the end of the test. All of the materials released measurable amounts of fluoride throughout the test period, with a considerable range on day 1 (15.3–155.2 ppm F). The concentration of fluoride released on the 2nd day fell sharply for all materials (range 6.3–44.3 ppm F). By day 60 all materials continued to release fluoride, albeit to a lesser extent (range 0.9–3.99 ppm F). With regard to the uptake and release of fluoride, a similar protocol was employed, although all samples were immersed in 1 litre of de-ionised water for 60 days to allow the majority of the fluoride to leach out from the materials. The ten pellets for each material were divided into two groups, five samples as control and five samples as test. Each day over a 20-day period all test samples were exposed to a 1000-ppm F solution for 2 min. Fluoride uptake/release was assessed from the 2 ml of de-ionised water in which the samples had been immersed for 24 h. The control samples continued to release small concentrations of fluoride throughout the test. The test samples, exposed to the 1000-ppm F solution, consistently released more ionic fluoride than the controls at all time points from day 1 to day 20, indicating that fluoride had been taken up and subsequently released. The values ranged at day 1 from 3.29 ( ± 0.14) for Aquacem to 7.63 ( ± 0.13) for Ketac Fil at day 1, rising to values between 869 ( ± 1.88) for Aquacem to 10.34 ( ± 1.61) for Vitrebond at day 20. This study indicates that all five glass ionomer cements take up as well as release fluoride and that the amount of fluoride released may be of profound clinical significance.

The effect of baseline lesion mineral loss on the remineralization of enamel lesions by a sodium fluoride dentifrice was studied in situ by means of an appliance carrying enamel sections. Artificial lesions of various sizes were created, by means of acidified gelatin, and were then mounted on the appliances of five volunteers. Each brushed twice daily for two min with a 1000 ppm F sodium fluoride dentifrice. Measurements of mineral content were made at baseline and at weekly intervals by microradiographic/microdensitometric techniques. Data from all five volunteers showed a linear increase in remineralization rate with increasing lesion size. Thus, in studies which compare the effects of different remineralizing formulations, care must be taken to ensure that initial lesion sizes are matched, or that the results are expressed as a percentage change in mineral content.

No abstract

No abstract

An in vitro pH-cycling experiment was carried out to investigate the effect of fluoride concentration on enamel demineralization and remineralization. Artificial caries lesions were formed in an acid-buffered solution and subjected daily to a 3-hour acid attack, a 5-min immersion in the test NaF solution (0, 1,250, 500, 1,000, 1,750 and 2,500 ppm F), and to 21 h in an artificial saliva. Changes in mineral content were assessed weekly for 5 weeks using microradiography/microdensitometry. The lesions in the control group (0 ppm F) and the 1-ppm F group demineralized. Remineralization was significantly higher in the 500-ppm F group compared to the 250-ppm F group. However, higher fluoride concentrations did not produce any further significant increase in remineralization. Laminations were apparent in lesions subjected to the 250- and 500-ppm F solutions.