Schaefer Matthias
Lehrstuhl für Ökologie, Zoologisches Institut der Universität, Hegewischstr. 3, D-2300, Kiel, Germany.
Oecologia. 1976 Jun;25(2):155-174. doi: 10.1007/BF00368851.
Floronia bucculenta hibernates in the egg stage; the egg sacs are deposited on the leaves of grass tussocks without any shelter. The morphogenesis of the eggs was divided into 10 arbitrarily chosen stages, in order to test the dependence of embryonic development on temperature in the laboratory. The eggs developed slowly at 23°C, 16°, 12.5°; embryogenesis stopped after 70-45 days, when prosomal appendage rudiments began to form. At 10°, 7.5°, 5°, 0° complete embryogenesis was possible until the emergence of the first complete stage. The eggs developed most rapidly at 5° (mean developmental time 203 days). The egg development was "normal" at 5° and 0°, when compared with the timetable of the embryogenesis of the linyphiid Bathyphantes gracilis, a species which has no egg diapause. At 7.5° and 10° the embryogenesis was strongly delayed during the median phases of development (elongation of the germ band, formation of prosomal appendages); after reversion the development was accelerated (postdiapause phase). After long exposure to low temperatures (-10° to +10°) the diapause was terminated. A temperature of 0° was optimal (minimal time of exposure 8-9 weeks). The time required for embryonic development of postdiapause eggs decreased hyperbolically with increasing temperature. In the field the median phases of embryogenesis were retarded by low ambient temperatures; diapause was terminated from late December to mid-January. The spread of hatching in spring was 7-15 days.During the diapause phase the O-consumption of the eggs at 25° was depressed. It rose from 1.55 (in late diapause) to 4.21 ml/100 eggs·h at the onset of postdiapause, whereas O-utilization did not change significantly at 5° (from 0.54 to 0.61 ml/100 eggs·h just after the termination of diapause).The diapause phase was not characterized by higher resistance to cold, drought, or flooding. As compared with single eggs removed from the cocoon, the silken wall of the intact egg sac did not affect the survival of postdiapause eggs exposed to-15° (LD=28 days); it raised, however, the survival time of eggs exposed to a R.H. of 32% (at 5°) or flooding by distilled water (at 5°): from LD=37 to 68 days at drought, from LD=30 to 92 days at flooding.Diapause is important for synchronizing the life-cycle of F. bucculenta with the seasonal fluctuations of environment. The egg stage is highly tolerant to the extreme factors of the winter. Some implications of the relation of the studied spider to its habitat are discussed.
佛罗里尼亚扁蛛以卵期越冬;卵囊被产在草丛的叶子上,没有任何遮蔽物。为了在实验室中测试胚胎发育对温度的依赖性,将卵的形态发生分为10个任意选定的阶段。卵在23°C、16°C、12.5°C时发育缓慢;70 - 45天后胚胎发育停止,此时前体附肢原基开始形成。在10°C、7.5°C、5°C、0°C时,直到第一个完整阶段出现,完全胚胎发育都是可能的。卵在5°C时发育最快(平均发育时间203天)。与没有卵滞育的林姬蛛属的细纹林姬蛛的胚胎发育时间表相比,卵在5°C和0°C时的发育是“正常”的。在7.5°C和10°C时,胚胎发育在发育的中期阶段(胚带伸长、前体附肢形成)强烈延迟;恢复后发育加速(滞育后阶段)。长时间暴露在低温(-10°C至+10°C)下,滞育结束。0°C是最佳温度(最短暴露时间8 - 9周)。滞育后卵的胚胎发育所需时间随温度升高呈双曲线下降。在野外,胚胎发育的中期阶段因环境温度低而延迟;滞育从12月下旬到1月中旬结束。春季孵化的时间跨度为7 - 15天。在滞育阶段,25°C时卵的耗氧量降低。从滞育后期的1.55(ml/100个卵·小时)升至滞育后开始时的4.21 ml/100个卵·小时,而在5°C时氧利用率没有显著变化(滞育刚结束时从0.54升至0.61 ml/100个卵·小时)。滞育阶段的特点不是对寒冷、干旱或洪水有更高的抵抗力。与从茧中取出的单个卵相比,完整卵囊的丝壁不影响暴露在-15°C(致死剂量=28天)下的滞育后卵的存活;然而,它延长了暴露在32%相对湿度(5°C)或蒸馏水淹没(5°C)下的卵的存活时间:干旱时从致死剂量=37天延长到68天,水淹时从致死剂量=30天延长到92天。滞育对于使佛罗里尼亚扁蛛的生命周期与环境的季节性波动同步很重要。卵期对冬季的极端因素具有高度耐受性。讨论了所研究的蜘蛛与其栖息地关系的一些影响。