Works matching IS 00301299 AND DT 1992 AND VI 65 AND IP 2
Results: 26
Why we should stop trying to measure the cost of reproduction correctly
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- Oikos, 1992, v. 65, n. 2, p. 349, doi. 10.2307/3545031
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Tree architectures adapted to efficient light utilization: is there a basis for latitudinal gradients?
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- Oikos, 1992, v. 65, n. 2, p. 275, doi. 10.2307/3545019
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The search pattern of a parasitoid wasp, Aphelinus asychis, for its host
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- Oikos, 1992, v. 65, n. 2, p. 207
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The necessarily limited adaptation of quantitative traits: example of Talitrus saltator's primary fleeing direction
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- Oikos, 1992, v. 65, n. 2, p. 338, doi. 10.2307/3545029
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The interpretation of tests for ratio-dependence
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- Oikos, 1992, v. 65, n. 2, p. 334,3, doi. 10.2307/3545027
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The flight directionality of bumblebees: do they remember where theycame from?
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- Oikos, 1992, v. 65, n. 2, p. 321, doi. 10.2307/3545025
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The effects of reproductive phenology on larval performance traits in a three-species assemblage of central Amazonian tadpoles
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- Oikos, 1992, v. 65, n. 2, p. 307, doi. 10.2307/3545023
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The effect of fire on stimulating willow regrowth and subsequent attack by grasshoppers and elk
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- Oikos, 1992, v. 65, n. 2, p. 190
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Tail loss consequences on habitat use by the Iberian rock lizard, Lacerta monticola
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- Oikos, 1992, v. 65, n. 2, p. 328
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Snakes, water and density dependent freedoms
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- Oikos, 1992, v. 65, n. 2, p. 177, doi. 10.2307/3545007
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Sexual reproduction in Daphnia magna requires three stimuli
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- Oikos, 1992, v. 65, n. 2, p. 197
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Resources for long distance migration: intertidal exploitation of Littorina and Mytilus by knots Calidris canutus in Iceland
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- Oikos, 1992, v. 65, n. 2, p. 179
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Reinterpretation and evaluation of some simple descriptive models for weed-crop interference in terms of one-sided and two-sided competition
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- Oikos, 1992, v. 65, n. 2, p. 256, doi. 10.2307/3545017
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Productivity, disturbance and food web structure at a local spatial scale in experimental container habitats
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- Oikos, 1992, v. 65, n. 2, p. 249
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Plant species coexistence-the role of historical, evolutionary and ecological factors
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- Oikos, 1992, v. 65, n. 2, p. 314, doi. 10.2307/3545024
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Plant chemical defense and twig selection by snowshoe hare: an optical foraging perspective
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- Oikos, 1992, v. 65, n. 2, p. 295
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Plant allelochemicals, tritrophic interactions and the anomalous diversity of tropical parasitoids: the ""nasty" host hypothesis
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- Oikos, 1992, v. 65, n. 2, p. 353
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Life history patterns and opportunities for queen-worker conflict inbumblebees (Hymenoptera: Apidae)
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- Oikos, 1992, v. 65, n. 2, p. 242
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Life history allometry in mammals and squamate reptiles: taxon-leveleffects
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- Oikos, 1992, v. 65, n. 2, p. 285
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Lack of a tradeoff between constitutive and induced defenses among varieties of cotton
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- Oikos, 1992, v. 65, n. 2, p. 301
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Interpretation of adaptive plasticity in Lemna minor
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- Oikos, 1992, v. 65, n. 2, p. 233
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Fecundity allocation in herbaceous plants
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- Oikos, 1992, v. 65, n. 2, p. 225, doi. 10.2307/3545013
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Emigration of meadow voles, Microtus pennsylvanicus: the effect of sex ratio
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- Oikos, 1992, v. 65, n. 2, p. 358, doi. 10.2307/3545033
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Effect of habitat fragmentation on the bank vole, Clethrionomys glareolus, in an agricultural landscape
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- Oikos, 1992, v. 65, n. 2, p. 265
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Does morphology predict ecology? Hypothesis testing within a frewhwater stream fish assemblage
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- Oikos, 1992, v. 65, n. 2, p. 213
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Application of community matrix theory to plant competition data
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- Oikos, 1992, v. 65, n. 2, p. 343
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