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D. M. BRYANT 《Ibis》1978,120(1):16-26
Nestling birds may differ in size and weight on the first day a clutch is fully hatched, mainly because eggs within clutches hatch over a period of several days. This asynchronous pattern of hatching is usually thought to facilitate brood reduction when the food supply is unpredictably restricted. The purpose of the study reported here was to examine the contribution of egg-weight, clutch-size, hatching spread, food supply and season to weight differences in newly hatched broods of the House Martin. At laying, heavy eggs had a greater moisture and dry weight content than light eggs and immediately before hatching there was a correlation between initial egg-weight and the dry weight of embryo and yolk. Heavier clutches also tended to give rise to heavier hatchlings. There was, however, no correlation of fresh egg-weight with the dry weight of embryos alone and the relative dry weight of embryos in a clutch was dependent on laying sequence. Hatching spread (the number of days between the emergence from the egg of the first and the last hatchling of the clutch) was 0.75 ± 0.46 days for clutches of two and increased with the size of the clutch up to 1.80 ± 0.79 days for clutches of five. When food was scarce during laying, hatching spread was greater. Weight difference in newly hatched broods was correlated with hatching spread and moreover in multivariate analysis was also correlated with periods of food scarcity during laying. It was concluded that all examples of weight hierarchies among hatchlings should not be considered adaptive; in some cases they may be imposed by food scarcity. This can lead to mortality of the runs even if food is plentiful. When the weight hierarchy is not adversely accentuated by food scarcity it may function as previously suggested, to allow brood reduction. Alternatively, particularly among House Martins, it may spread out the peak food needs of individual nestlings thereby spreading the demand on the adults.  相似文献   

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D. C. Seel 《Ibis》1970,112(1):1-14
Nestling survival and nestling weights in P. domesticus and P. montanus were studied in 1961 and 1963–64 at Oxford. This paper concludes a study of factors influencing the reproductive rate. Taking all losses into account, P. domesticus reared an average of 1.6 nestlings per brood (45%) and P. montanus 2.7 nestlings per brood (59%). About a third of all broods of both species failed completely to survive the nestling period. In P. domesticus these failures were most numerous in the middle part of the breeding season and are attributed to nutritional deficiencies derived from unsuitable food provided as a consequence of a seasonal food shortage, but in P. montanus complete brood failures occurred mostly in the second half of the nestling period and are attributed to predation. 43 broods of P. domesticus and one brood of P. montanus were weighed daily. Those of P. domesticus were classified as (1) successful broods—in these some nestlings died in the larger brood-sizes, apparently through starvation; (2) long-lived unsuccessful broods—in these the nestlings died at intervals and failure was attributed to nutritional deficiencies; and (3) short-lived unsuccessful broods. A slight decrease in the weights of nestlings in successful broods at the end of the nestling period is attributed to the utilization of insulating fat facilitated by the completion of the feather covering. Nestlings of both species left the nest at 88–89% of the adult weight. Taking all “successful” broods together, the percentage survival rates on nestling day 131/2 (day of hatching = day 1/2) in P. domesticus were 81–82% in b/2–3, 70% in b/4 and 56% in b/5 (a situation paralleled in this respect by P. hispaniolensis), but in P. montanus they were c. 82% in all brood-sizes. Hence, in P. domesticus b/4 probably gave rise to the largest number of nestlings reared per brood, while in P. montanus most nestlings were produced by the largest brood-size. Weighings of many broods on day 131/2 showed two trends in the weight of the nestlings: (1) in both species the weight of the nestling decreased as the number of survivors from each initial brood-size decreased; (2) between successive initial brood-sizes the weight of the nestling of P. domesticus decreased with increasing brood-size but in P. montanus there was no change. The losses in the larger broods of P. domesticus occurred mostly in the first half of the nestling period—apparently in association with the asynchronous hatching of the eggs and as a consequence of the limitation on the feeding frequency of the adults. Nestling survival was lowest in the larger broods in the middle of the breeding season and contrasted with the mid-season increase in mean clutch-size. It is suggested that in the study area there was a (possibly unnatural) shortage of food suitable for nestlings in the middle of the season. It is suggested that in P. domesticus the unexpectedly low feeding frequencies of the adults with large broods, apparently causing their low survival rates, may be an adaptation evolved to obtain the maximum amount of food in the presence of other adults which would be attracted to a food source by higher rates of activity. The breeding success calculated from data derived from the whole of this study was 35% for P. domesticus and 49% for P. montanus (2.9 and 3.9 nestlings per breeding pair per year respectively). It is suggested that the population of P. domesticus was much closer to a critical limiting factor, e.g. food supply, than that of P. montanus. This may account for the striking differences between the two species in their nestling survival rates and their nestling weights in relation to brood-size; in particular, the success of the larger broods of P. montanus may have been a temporary phenomenon.  相似文献   

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ABSTRACT

We conducted a field study of the ontogeny of vocal signals in the house wren Troglodytes aedon during the nestling and fledgling phases of life. We did spectrographic analyses and quantification of the developmental changes that occurred in the acoustic features of the vocalisations. Evidence of progress to adult-like vocal patterns was of two types. First, nestling calls changed into a harsh-sounding call that resembles the adult chatter call, functionally a warning call. Second, fledglings also uttered subsong, and these vocalisations were similar to notes typical of adult male song. When the vocalisations produced by developing young were broken down into their constituent vocal features, we found that the time course of development was not strictly linear. Instead of a unidirectional change through the course of nestling and fledgling life, the trajectories of the vocal features fluctuated through time and sometimes exhibited abrupt changes. These sudden shifts occurred during nestling life as well as at the time of fledging. We speculate on the possible causes of these abrupt transitions. Changes in acoustic features upon fledging appear to be linked to new social functions.  相似文献   

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Genetic and environmental (chiefly maternal) variance and covariance components were estimated for brain and body size in randombred house mice of three different ages (one, three, and five months). Heritabilities estimated from regressions of offspring on their five-month-old male parents were fairly low over all three ages, averaging about 0.2 for brain size and about 0.3 for body size. Heritability estimates from female parents were higher, however, presumably because of the influence of maternal-environmental components of variance. The total maternal impact was estimated from full-sib analyses and, for the more reliable three- and five-month ages, averaged 23% for brain size and 20% for body size. Phenotypic, genetic, and environmental correlations and regressions of brain and body size also were calculated by parent-offspring and sib-correlation techniques, the phenotypic correlations generally decreasing from about 0.4 at one month to 0.2 at three and five months. Genetic correlations of brain and body size estimated from covariances of offspring on male parents were negative whereas those from female parents were positive in sign, and this as well as positive maternal correlations was taken as evidence of the influence of maternal sources of covariance for these traits. It was concluded that, in addition to direct genetic effects, indirect genetic sources of variance and covariance mediated through the prenatal maternal environment are quite important in the determination of brain size and its association with body size.  相似文献   

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When variation in life-history characters is caused by many genes of small effect, then quantitative-genetic parameters may quantify constraints on rate and direction of microevolutionary change. I estimated heritabilities and genetic correlations for 16 life-history and morphological characters in two populations of Impatiens capensis, a partially self-pollinating herbaceous annual. The Madison population had little or no additive genetic variance for any of these characters, while the Milwaukee population had significant narrowsense heritabilities and genetic correlations for several traits, including adult size, which is highly correlated with fitness. All genetic correlations among fitness components were positive, hence there is no evidence for antagonistic pleiotropy among these traits. Dissimilarity of heritabilities in the two populations supports theoretical predictions that long-term changes in genetic variance-covariance patterns may occur when population sizes are small and selection is strong, as may occur in many plant species.  相似文献   

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The environments in which native orchids grow were examined in terms of factors which might determine the survival and reproduction of the various species. Soil tests were made for 34 species now known to be growing in Rhode Island. Soil reaction appears to be related to growth of orchids, but other factors in the environment were found to be of equal if not greater importance. These include light, moisture, temperature and destruction by animals. Fertility was not found to be limiting under the conditions observed.  相似文献   

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The temperature requirement for growth and the upper survival temperatures (USTs) of 15 Antarctic red algal species collected on King George Island (South Shetland Islands) and Signy Island (South Orkney Islands) were determined. Two groups with different temperature requirements were identified. 1) A “eurythermal” group includes Rhodymenia subantarctica, Phyllophora ahnfeltioides, Gymnogongrus antarcticus, and Rhodochorton purpureum, growing between 0° and 10°C with optimum values at (0°) 5°(l0°)C. The USTs of these species and of Porphyra endiviifolium, Delesseria lancifolia, and Bangia atropurpurea were between 22° and 16°C. These species survived temperatures in a similar range as most endemic Arctic or Arctic/cold-temperate species but exhibited a lower temperature demand for growth, suggesting an earlier contact with low temperatures than Arctic species. 2) A stenothermal group includes Pantoneura plocamioides, Myriogramme mangini, Ballia callitricha, Phyllophora antarctica, Gigartina skottsbergii, Georgiella confluens, and Plocamium cartilagineum growing at 0° or ≤5°C with optimum values at 0° or 5°C. The USTs of these species and of Phycodrys austrogeorgica were between 14° and 7°C. The species of this group must have had an even earlier contact with the Antarctic cold-water environment than species of the “eurythermal” group. Gigartina skottsbergii, Georgiella confluens, Plocamium cartilagineum, and Pantoneura plocamioides were probably exposed longer to low temperatures than the other species of this group or Antarctic green and brown algae because they show the lowest temperature requirements so far determined in seaweeds. The results are discussed in the context of present local temperature regimes at the localities where the isolates were collected. Moreover, an attempt was made to explain the geographic distribution of individual species by the temperature requirements determined in this study. Only a few of the distribution limits are determined by temperature growth and/or survival characteristics. In many species (Rhodymenia subantarctica, Ballia callitricha, Gigartina skottsbergii, Bangia atropurpurea, Rhodochorton purpureum, and Plocamium cartilagineum), the development of temperature ecotypes is evident.  相似文献   

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This study was designed to investigate whether the larval development of an anuran amphibian could be modified by raising the animals in continuous light or darkness instead of under conditions of diurnal illumination, and to quantify the effects of these treatments at various intervals during this period of development.
Larvae of the frog, Rana pipiens , were raised through metamorphosis under conditions of constant light, constant darkness, or diurnal lighting. As measured by stages of development, body weight, tail length and body length at 20-day intervals, no significant differences in growth rate or metamorphic change were observed until near the middle of the prometamorphic period, which began at approximately the 50th day of development. After midmetamorphosis, a significant acceleration in the measured parameters was seen for the animals raised in conditions of constant light in comparison with those in constant darkness. Those with diurnal lighting were intermediate.
These results suggested that light, or its absence, can respectively stimulate or retard amphibian metamorphosis in late larval stages after the hypothalamo-hypophyseal-thyroid axis has matured. Neither continuous light nor continuous darkness during larval development prevented the transformation from tadpole to frog.  相似文献   

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郭畹华  庆宏 《动物学报》1995,41(3):314-321
中脑黑质是中缝核5-HT神经元最早期的靶组织之一。为了分析神经元对其靶细胞的作用是受某种特异性蛋白或神经营养因子的影响,本文用中缝核提取液作用于体外培养的中脑黑质神经元,证明了该提取液能促进中脑黑质神经元的存活和生长,其活性部分是分子量大于30kD的组份,经SDS-聚丙烯酰胺梯度凝胶电泳,呈现一条主带,分子量在43kD左右。  相似文献   

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中华鲟仔鱼初次摄食时间与存活及生长的关系   总被引:16,自引:0,他引:16  
研究了延迟投饵对中华鲟开口仔鱼存活及生长的影响。初次开口摄食在11—12日龄,13日龄卵黄基本吸收完毕,营养完全依靠外界供给。12日龄后,延迟投喂时间在1—10天的范围内,仔鱼成活率在46.67—73.33%之间,各组间无显著差异;延迟投喂时间为11d,成活率下降至13.3%;延迟投喂时间为12d,成活率为0。此外,延迟投喂时间在8d(20日龄)之内,42日龄后测量,仔鱼体长和体重与对照组无明显差异;延迟投喂超过9d,则体长和体重的指标明显低于对照组。仔鱼不摄食可以存活的最长时间是42日龄,但延迟投喂12天(24日龄)以上即发生不可逆转饥饿,故其饥饿的不可逆点(PNR)是24日龄。  相似文献   

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