全文获取类型
收费全文 | 680篇 |
免费 | 79篇 |
出版年
2021年 | 6篇 |
2018年 | 5篇 |
2017年 | 5篇 |
2016年 | 9篇 |
2015年 | 20篇 |
2014年 | 22篇 |
2013年 | 31篇 |
2012年 | 33篇 |
2011年 | 27篇 |
2010年 | 25篇 |
2009年 | 16篇 |
2008年 | 27篇 |
2007年 | 32篇 |
2006年 | 32篇 |
2005年 | 23篇 |
2004年 | 23篇 |
2003年 | 20篇 |
2002年 | 17篇 |
2001年 | 19篇 |
2000年 | 32篇 |
1999年 | 30篇 |
1998年 | 14篇 |
1997年 | 12篇 |
1996年 | 12篇 |
1995年 | 11篇 |
1994年 | 15篇 |
1993年 | 10篇 |
1992年 | 17篇 |
1991年 | 19篇 |
1990年 | 17篇 |
1989年 | 13篇 |
1988年 | 8篇 |
1987年 | 7篇 |
1986年 | 11篇 |
1985年 | 8篇 |
1984年 | 7篇 |
1983年 | 7篇 |
1982年 | 5篇 |
1981年 | 7篇 |
1980年 | 5篇 |
1978年 | 9篇 |
1976年 | 5篇 |
1974年 | 7篇 |
1972年 | 10篇 |
1971年 | 6篇 |
1970年 | 7篇 |
1969年 | 5篇 |
1968年 | 5篇 |
1967年 | 5篇 |
1966年 | 5篇 |
排序方式: 共有759条查询结果,搜索用时 46 毫秒
1.
2.
3.
4.
Peter A. Abrams 《Evolutionary ecology》1989,3(3):215-220
Summary The coevolution of competitors has been analyzed by two different types of fitness-maximization techniques; ESS methods (Lawlor and Maynard Smith, 1976), and CSS methods (Roughgarden, 1979). This paper argues that CSS methods generally do not predict the outcome of competitive coevolution. Even when there is relatively little variability within species, fitness maximization leads to an ESS rather than a CSS. A simple model is analyzed to show that ESS and CSS predictions about character displacement can differ qualitatively. Previous results of CSS analyses are discussed. 相似文献
5.
Peter A. Abrams 《Evolutionary ecology》1989,3(2):95-114
Summary Several different mechanisms that may produce decreasing functional responses are investigated using models that assume that an optimally foraging consumer is exploiting one or two resources. Decreasing functional responses are associated with situations in which there are costs to resource consumption. If the process of resource acquisition has costs, decreasing functional responses may occur when there is a single homogeneous resource. If the cost is solely a function of the amount of resource ingested, decreasing functional responses on a single resource do not occur. Both types of cost can produce decreasing functional responses when there are two resource types and a trade-off relationship between consumption of one and consumption of the other. Decreasing functional responses seem to be most likely to occur on a food that yields high benefits and costs per unit of foraging time or effort when there is an alternative resource which yields low benefits and costs. Given this type of foraging choice, the functional response is most likely to decrease when the benefits of ingestion increase at a decreasing rate, and the costs of ingestion increase at an increasing rate with amount ingested. An important and unique consequence of decreasing functional responses is the possibility of population cycles in differential equation models of consumer-resource systems with non-reproducing resources; this is illustrated with a simple comsumer-resource model. 相似文献
6.
The collapse of the Classic Maya state is investigated from an ecological perspective. Settlement and palynological data from the Maya center of Copan, Honduras, are presented which indicate that substantial clearing of the upland pine forest had occurred prior to and during the abandonment of that urban center. A comparative use- rate analysis suggests that the increased clearing of pine was primarily caused by demands for domestic fuel wood by an expanding urban population. This forest mismanagement is directly linked to accelerated erosion rates which are considered primary elements in the collapse of the Maya state. 相似文献
7.
Development of rat anti-mouse interleukin 3 monoclonal antibodies which neutralize bioactivity in vitro 总被引:10,自引:0,他引:10
Several rat anti-mouse interleukin 3 (IL-3) monoclonal antibodies have been developed which inhibit the biologic activity of mouse IL-3. These antibodies were produced in rats immunized with preparations of purified, recombinant mouse IL-3, obtained from transiently transfected COS7 cell supernatant. Hybridomas secreting anti-IL-3 were selected initially either on the basis of their giving a positive signal in an indirect enzyme-linked immunosorbent assay, or for their ability to inhibit the proliferation of the IL-3-dependent mouse mast cell line, MC/9. Neutralizing rat monoclonal IgG1, IgG2a, and IgG2b antibodies have been identified; these also block IL-3-induced proliferation of the NFS-60 and IC2 cell lines. These antibodies also blocked the IL-3-induced proliferation of mouse bone marrow-derived colony-forming units-culture suggesting that the same epitopes on IL-3 influence receptor recognition for both the proliferation of factor-dependent cell lines as well as normal bone marrow cells. Fab fragments produced from certain of the IgG2a-neutralizing antibodies blocked as well as the parent IgG. Antibody cross-blocking studies identified one neutralizing antibody apparently recognizing an epitope that was spatially distinct from those recognized by the other blocking antibodies tested. The development of these neutralizing rat monoclonal antibodies to mouse IL-3 should facilitate further investigation on the role of this factor in hemopoietic regulation. 相似文献
8.
Peter A. Abrams 《Evolutionary ecology》1992,6(1):56-72
Summary When foraging has costs, it is generally adaptive for foragers to adjust their foraging effort in response to changes in the population density of their food. If effort decreases in response to increased food density, this can result in a type-2 functional response; intake rate increases in a negatively accelerated manner as prey density increases. Unlike other mechanisms for type-2 responses, adaptive foraging usually involves a timelag, because foraging behaviours do not often change instantaneously with changes in food density or risks. This paper investigates predator-prey models in which there are explicit dynamics for the rate of adaptive change. Models appropriate to both behavioural and evolutionary change are considered. Both types of change can produce cycles under similar circumstances, but under some evolutionary models there is not sufficient genetic variability for evolutionary change to produce cycles. If there is sufficient variability, the remaining conditions required for cycles are surprisingly insensitive to the nature of the adaptive process. A predator population that approaches the optimum foraging strategy very slowly usually produces cycles under similar conditions as does a very rapidly adapting population. 相似文献
9.
A pipe for administration of inhaled cocaine and its pyrolytic products in laboratory animals was developed and tested. In-vitro trials showed 30.0 +/- 5.2% (mean +/- SE) recovery of cocaine in solvent. Five non-pregnant ewes were instrumented with tracheal T-tubes and vascular catheters. After surgical recovery, ewes received three doses of cocaine (free base) in a randomized fashion; 2 mg/kg and 4 mg/kg both by inhalation, and 2 mg/kg intravenously. Arterial blood samples were collected and assayed for cocaine and its major metabolites by high performance liquid chromatography. Blood pressure and heart rate were continuously recorded. Cocaine administered by inhalation was eliminated with a half-life of 1.6 +/- 0.5 min (mean +/- SE) compared to 3.4 +/- 0.9 following intravenous administration (p less than 0.03). Likewise, clearance values were greater following inhalation, 5532 +/- 1756 ml/min/kg, than following intravenous administration, 163 +/- 20.6 ml/min/kg (p less than 0.04). Both routes of administration led to significant elevations in blood pressure, 7.5% increase after smoking vs 20% increase after intravenous administration. No correlation was found between inhalational dose of cocaine and peak plasma cocaine concentration. 相似文献
10.
Peter Abrams 《Theoretical population biology》1983,24(1):22-38
The optimal life histories are examined for models in which the average life-history strategy adopted by the population affects the costs and benefits of any individual's strategy. The situation modeled is one in which organisms can gain energy to be used in reproduction by foraging, but in doing so, they expose themselves to increased mortality; thus the proportion of time spent foraging can be used to measure reproductive effort. Simple models of a demographically homogeneous population are used to reexamine questions which have been studied previously using other models. The effects upon optimal reproductive effort of the following factors are examined: increased births per unit effort, increased mortality, and variability in population parameters. In addition, the questions of whether optimal reproductive effort maximizes population size and whether there can be multiple alternative life histories are examined. Results in most cases differ significantly from those of previous studies. No generalizations emerge regarding the effects of the three factors listed above. Optimal life histories in this model generally do not maximize population size. It is possible to have globally stable alternative life histories. It is concluded that frequency dependence will often be important in determining optimal life histories. 相似文献