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Above forest canopies, eddy covariance (EC) measurements of mass (CO2, H2O vapor) and energy exchange, assumed to represent ecosystem fluxes, are commonly made at one point in the roughness sublayer (RSL). A spatial variability experiment, in which EC measurements were made from six towers within the RSL in a uniform pine plantation, quantified large and dynamic spatial variation in fluxes. The spatial coefficient of variation (CV) of the scalar fluxes decreased with increasing integration time, stabilizing at a minimum that was independent of further lengthening the averaging period (hereafter a ‘stable minimum’). For all three fluxes, the stable minimum (CV=9–11%) was reached at averaging times (τp) of 6–7 h during daytime, but higher stable minima (CV=46–158%) were reached at longer τp (>12 h) during nighttime. To the extent that decreasing CV of EC fluxes reflects reduction in micrometeorological sampling errors, half of the observed variability at τp=30 min is attributed to sampling errors. The remaining half (indicated by the stable minimum CV) is attributed to underlying variability in ecosystem structural properties, as determined by leaf area index, and perhaps associated ecosystem activity attributes. We further assessed the spatial variability estimates in the context of uncertainty in annual net ecosystem exchange (NEE). First, we adjusted annual NEE values obtained at our long‐term observation tower to account for the difference between this tower and the mean of all towers from this experiment; this increased NEE by up to 55 g C m?2 yr?1. Second, we combined uncertainty from gap filling and instrument error with uncertainty because of spatial variability, producing an estimate of variability in annual NEE ranging from 79 to 127 g C m?2 yr?1. This analysis demonstrated that even in such a uniform pine plantation, in some years spatial variability can contribute ~50% of the uncertainty in annual NEE estimates.  相似文献   
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1. Excretion of nitrogen (N) and phosphorus (P) is a direct and potentially important role for aquatic consumers in nutrient cycling that has recently garnered increased attention. The ecosystem‐level significance of excreted nutrients depends on a suite of abiotic and biotic factors, however, and few studies have coupled measurements of excretion with consideration of its likely importance for whole‐system nutrient fluxes. 2. We measured rates and ratios of N and P excretion by shrimps (Xiphocaris elongata and Atya spp.) in two tropical streams that differed strongly in shrimp biomass because a waterfall excluded predatory fish from one site. We also made measurements of shrimp and basal resource carbon (C), N and P content and estimated shrimp densities and ecosystem‐level N and P excretion and uptake. Finally, we used a 3‐year record of discharge and NH4‐N concentration in the high‐biomass stream to estimate temporal variation in the distance required for excretion to turn over the ambient NH4‐N pool. 3. Per cent C, N, and P body content of Xiphocaris was significantly higher than that of Atya. Only per cent P body content showed significant negative relationships with body mass. C:N of Atya increased significantly with body mass and was higher than that of Xiphocaris. N : P of Xiphocaris was significantly higher than that of Atya. 4. Excretion rates ranged from 0.16–3.80 μmol NH4‐N shrimp?1 h?1, 0.23–5.76 μmol total dissolved nitrogen (TDN) shrimp?1 h?1 and 0.002–0.186 μmol total dissolved phosphorus (TDP) shrimp?1 h?1. Body size was generally a strong predictor of excretion rates in both taxa, differing between Xiphocaris and Atya for TDP but not NH4‐N and TDN. Excretion rates showed statistically significant but weak relationships with body content stoichiometry. 5. Large between‐stream differences in shrimp biomass drove differences in total excretion by the two shrimp communities (22.3 versus 0.20 μmol NH4‐N m?2 h?1, 37.5 versus 0.26 μmol TDN m?2 h?1 and 1.1 versus 0.015 μmol TDP m?2 h?1), equivalent to 21% and 0.5% of NH4‐N uptake and 5% and <0.1% of P uptake measured in the high‐ and low‐biomass stream, respectively. Distances required for excretion to turn over the ambient NH4‐N pool varied more than a hundredfold over the 3‐year record in the high‐shrimp stream, driven by variability in discharge and NH4‐N concentration. 6. Our results underscore the importance of both biotic and abiotic factors in controlling consumer excretion and its significance for nutrient cycling in aquatic ecosystems. Differences in community‐level excretion rates were related to spatial patterns in shrimp biomass dictated by geomorphology and the presence of predators. Abiotic factors also had important effects through temporal patterns in discharge and nutrient concentrations. Future excretion studies that focus on nutrient cycling should consider both biotic and abiotic factors in assessing the significance of consumer excretion in aquatic ecosystems.  相似文献   
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In this paper, which is presented in two parts, the growth anddevelopment of the banana plant have been examined from thestandpoint of the origin of the inflorescence and the developmentof the flowers (Part A) and the structure and development ofthe fruit (Part B). First the main centres of growth in thesestructures are located and the manner of their development ispresented. Thereafter, attention is focused upon the salientevents which determine the alternative courses of developmentwith a view to designating the chemical and physiological stimulithat may be required.  相似文献   
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RAM  MANASI 《Annals of botany》1960,24(1):79-82
The development and structure of the chalazal endosperm haustoriumin Cannabis sativa are described. The endosperm is nuclear anda haustorium is formed at the chalazal end. The latter remainsfree nuclear throughout. Enucleate vesicles appear in the upperpart of the endosperm but finally they merge with the cytoplasmof the haustorium. As the embryo reaches maturity it occupiesthe whole seed cavity, the haustorium collapses and the endospermpersists only as a thin layer.  相似文献   
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SYNOPSIS. The prolific reproductive capabilities of the zebramussel, Dreissena polymorpha, have facilitated the rapid spreadand high densities of this biofouling organism since its accidentalintroduction into North America less than 10 years ago. Researchon its reproductive mechanisms and capabilities may be valuablenot only in predicting its further spread, but also in investigatingbasic mechanisms of reproduction and development and in developingnew strategies to mitigate its impact. Since zebra mussels aredioecious and fertilization occurs externally, coordinated maturation,spawning, and other mechanisms have evolved to increase theprobability of successful fertilization. The zebra mussel undergoesan annual cycle of gonadal growth and gamete maturation, culminatingin one or more spawning events in late spring or early summer.Temperature, rates of temperature change, food availability,and effects of neighboring mussels seem to be critical variablesthat determine reproductive responses. Serotonin is a biogenicamine which is implicated in spawning behavior and can reliablytrigger spawning. Serotonin is present in the gonad in neuralvaricosities that encircle groups of gametes, and specific serotonergicligands can mimic or block spawning caused by serotonin. Infemales, serotonin reinitiates meiosis causing maturation fromprophase I to metaphase I prior to spawning. Spawned oocytescontain substances that are species specific sperm chemoattractants.The sequence of binding, entry, and subsequent nuclear movementshave been observed with fluorescence and scanning microscopy.Despite their negative ecological and economic impacts, zebramussels have also provided a new and easily obtainable resourcefor studies of reproductive mechanisms.  相似文献   
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