Vegetation, microclimate, seedling frequency, freezing tolerance, and cold acclimation were compared for seedlings of Artemisia tridentata collected from 1775, 2175, and 2575 m elevation in the eastern Sierra Nevada, California. Data were used to test the hypothesis that ecotypic differences in stress physiology are important for seedling survival along gradients from desert to montane ecosystems. The vegetation canopy cover and A. tridentata seedling frequency were greatest at 2575 m, compared to 1775 and 2175 m. Snow cover ameliorated temperatures near the soil surface for part of the winter and depth varied across elevations. Freezing tolerance was compared for seedlings maintained in growth chambers at day/night air temperatures of 25°C/15°C. The temperature at which electrolyte leakage and Photosystem II function (FV/FM) from leaves were half-maximum was approximately −13·5°C for leaves of seedlings from all three elevations. Shifting day/night air temperatures from 25°C/15°C to 15°C/5°C initiated about 1·5° of acclimation by plants from all three altitudes, with seedlings from the highest elevation exhibiting the greatest acclimation change. Measurements of ambient air and canopy temperatures at the three elevations indicated that wintertime average low temperatures were consistent with the measured degree of freezing tolerance. At small spatial scales used in this study, pollen and seed dispersal between study sites may have precluded resolution of ecotypic differences. Patterns of freezing tolerance and cold acclimation may depend on a combination of mesoclimate and microclimate temperatures, canopy cover, snow depth, and snow melt patterns. 相似文献
根据Green et al(1986)提出的三元长石温压计公式.以长石三元固溶体和矿物相平衡为基础,通过热力学推导,建立了联立方程法和迭代法两种计算三元长石温度的方法。根据联立求解可获得TAb-Or、TOr-An,TAb-An三个温度值,迭代法求解可获得TAb,TOr,TAn三个温度值。因此,一个样品可计算出6个温度数据。选择粤西地区有代表性的18个花岗岩体,按混合岩建造→深熔花岗岩建造→岩浆建造南岭系列花岗岩→岩浆建造长江系列花岗岩的顺序,进行三元长石法的温度计算,所得到的相应各建造和系列花岗岩的上限温度为755℃→766℃→865℃→970℃;下限温度为664℃→665℃→775℃→814℃,亦即上下限温度都逐渐升高,其规律性与地质和地球化学研究结果完全一致,体现了三元长石地质温度计的可靠性和准确性。 相似文献
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