Individual based simulations of population dynamics require the availability of growth models with adequate complexity. For this purpose a simple-to-use model (non-linear multiple regression approach) is presented describing somatic growth and reproduction of Daphnia as a function of time, temperature and food quantity. The model showed a good agreement with published observations of somatic growth (r2 = 0.954, n = 88) and egg production (r2 = 0.898, n = 35). Temperature is the main determinant of initial somatic growth and food concentration is the main determinant of maximal body length and clutch size. An individual based simulation was used to demonstrate the simultaneous effects of food and temperature on the population level. Evidently, both temperature and food supply affected the population growth rate but at food concentrations above approximately 0.4 mg Cl−1Scenedesmus acutus temperature appeared as the main determinant of population growth.
Four simulation examples are given to show the wide applicability of the model: (1) analysis of the correlation between population birth rate and somatic growth rate, (2) contribution of egg development time and delayed somatic growth to temperature-effects on population growth, (3) comparison of population birth rate in simulations with constant vs. decreasing size at maturity with declining food concentrations and (4) costs of diel vertical migration. Due to its plausible behaviour over a broad range of temperature (2–20 °C) and food conditions (0.1–4 mg Cl−1) the model can be used as a module for more detailed simulations of Daphnia population dynamics under realistic environmental conditions. 相似文献
From April 1997 to June 1998 Nemurella pictetii populations were regularly sampled in two springstreams at 220 and 850 m a.s.l., respectively, in Hesse (Germany), at approximately 51°N. Random samples of larvae were taken at three week intervals during the vegetation period, and once a month during winter. Sex, instar, body length, head capsule width and wing pad length of all larvae were recorded. Temperatures were recorded every hour, temporal patterns of temperature agreed closely between sites. Mean winter lows were 3.9 °C at both sites, the mean summer high was 11.9 °C at the lower site, as opposed to 9.6 °C at the mountain site.At both sites, adult emergence started in May. At the mountain site, recruitment started in late July and continued into autumn. There was cohort splitting in the young generation. Some individuals grew rapidly until October–November, but last instar larvae first appeared in March the next year. 1600 degree-days above 0 °C were accumulated during complete development. At the lower site, recruitment began in early July, and cohort splitting also occurred. Fast growing summer recruits emerged as adults in late August, having accumulated only 700 degree-days (above 0 °C). Their offspring hatched in November-December and emerged the next spring, having accumulated also only 700 degree-days. However, only part of the population was bivoltine. Many of the summer recruits grew more slowly and accumulated close to 1900 degree days until they emerged the next spring, together with the offspring of their own fast-growing siblings. Dependence of growth rate on temperature could not be estimated and appears to vary with daylength. For example, 3–6 °C support growth and development provided daylength exceeds 10 hrs of light, or is rising.At both sites and in all cohorts individuals emerging earliest were larger than later emerging ones. The size decline is significantly correlated with number of days after the winter solstice. For the first time it is shown that the decline does not occur shortly before adult emergence but actually takes place several instars before the last. Size differences are then carried on, and amplified, during subsequent molts, until adulthood. The literature presently relates seasonal size declines of insects to high or rising temperatures experienced by larvae approaching adulthood. Our data show that, at least in Nemurella, this explanation fails. On average, females were distinctly larger than males. Differences in mean last instar size were noticed also between sites and years. They remain presently unexplained. The mean sex ratio in both populations was close to 1:1. 相似文献
This paper investigates the refuge potential of (1) upwelling areas, (2) coral areas at medium depth, and (3) offshore bank and island reefs in a scenario of increased global warming, and thus increased sea surface temperature (SST) and increased solar UV radiation. (1) Observations on coral health and water temperature in the subtropical Atlantic (Eleuthera and Cat Island, Bahamas) and Indian Ocean (Sodwana Bay, South Africa) suggest a link between cool water delivered by upwelling and coral health. After the 1998 bleaching event, caused by strong SST anomalies, coral health and recovery from the previous year's bleaching was significantly better on the narrow southern Cat Island shelf (70% of corals healthy) where the presence of cold water was observed, which was attributed to small-scale upwelling, than on the wide northern Eleuthera shelf (44% of corals healthy), where downwelling of hot bank waters was believed to have damaged corals. In South Africa, regular, short-term upwelling events in five summers reduced SST to well below bleaching level. (2) In the northern Red Sea (Safaga Bay) and in South Africa (Sodwana Bay), wide areas with either coral frameworks or non-framework communities exist. Calculations show that if the top 10 m (20 m) of the ocean became inhospitable to corals, still 50.4% (17.5%) of the coral area would remain intact in the Red Sea and 99% (40%) in South Africa. (3) Offshore bank and island reefs investigated in the Turks, Caicos, and Mouchoir Banks and Grand and Little Cayman showed high rates of mortality and coral diseases. The most remote sites (Mouchoir Bank) were not the healthiest. Refuge areas appear to exist in (1) and (2), but in (3) only if vigorous water-circulation is encountered. 相似文献