Works matching IS 00301299 AND DT 1993 AND VI 68 AND IP 2
Results: 27
Why biologists do not think like Newtonian physicists
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- Oikos, 1993, v. 68, n. 2, p. 361
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Why are female small mammals territorial?
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- Oikos, 1993, v. 68, n. 2, p. 364, doi. 10.2307/3544853
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Using response-surface methodology to detect chaos in ecological time series
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- Oikos, 1993, v. 68, n. 2, p. 329
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There are more small than large species?
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- Oikos, 1993, v. 68, n. 2, p. 375, doi. 10.2307/3544855
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The species-pool hypothesis and plant community diversity
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- Oikos, 1993, v. 68, n. 2, p. 371, doi. 10.2307/3544854
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The role of vertebrate and invertebrate predators in a grasshopper community
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- Oikos, 1993, v. 68, n. 2, p. 193, doi. 10.2307/3544830
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Taylor's power law and the measurement of variation in the size of populations in space and time
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- Oikos, 1993, v. 68, n. 2, p. 349
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Size-dependent diel foraging periodicity of a mayfly grazer in streams with and without fish
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- Oikos, 1993, v. 68, n. 2, p. 242, doi. 10.2307/3544836
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Significant potential levels of hierarchical phenotypic selection ina woody perennial plant, Cistus ladanifer
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- Oikos, 1993, v. 68, n. 2, p. 267
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Seasonal variation in body size and offspring sex ratio in field populations of the parasite wasp, Aphidius ervi (Hymenoptera: Aphidiidae)
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- Oikos, 1993, v. 68, n. 2, p. 340, doi. 10.2307/3544848
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Responses of bank voles to odours of seven species of predators: experimental data and their relevance to natural predator-vole relationships
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- Oikos, 1993, v. 68, n. 2, p. 251
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Resource use; plant defenses, and optimal digestion in ruminants
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- Oikos, 1993, v. 68, n. 2, p. 224, doi. 10.2307/3544834
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Production of chemical defenses in relation to plant growth rate
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- Oikos, 1993, v. 68, n. 2, p. 323, doi. 10.2307/3544846
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Patch information and estimation: a cost of group foraging
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- Oikos, 1993, v. 68, n. 2, p. 258, doi. 10.2307/3544838
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Measurement of variation in the size of populations in space and time: some points of clarification
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- Oikos, 1993, v. 68, n. 2, p. 357, doi. 10.2307/3544851
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Linked populations can still be chaotic
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- Oikos, 1993, v. 68, n. 2, p. 347, doi. 10.2307/3544849
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Investment in sexual reproduction by Antarctic mosses
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- Oikos, 1993, v. 68, n. 2, p. 293, doi. 10.2307/3544842
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Insect flower visitation frequency and seed production in relation to patch size of Viscaria vulgaris (Caryophyllaceae)
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- Oikos, 1993, v. 68, n. 2, p. 283
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Fungal endophytes: out of sight but should not be out of mind
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- Oikos, 1993, v. 68, n. 2, p. 379, doi. 10.2307/3544856
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Fruit maturation in the shrub Ligustrum vulgare (Oleaceae): lack of defoliation effects
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- Oikos, 1993, v. 68, n. 2, p. 309, doi. 10.2307/3544844
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Finding confidence limits on population growth rates: Monte Carlo test of a simple analytic method
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- Oikos, 1993, v. 68, n. 2, p. 273
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Evidence for mutualistic interactions in freshwater oligochaete communities
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- Oikos, 1993, v. 68, n. 2, p. 317, doi. 10.2307/3544845
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Differential snail-size predation by snail kites and limpkins
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- Oikos, 1993, v. 68, n. 2, p. 217, doi. 10.2307/3544833
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Crossing distance effect on prezygotic performance in plants: an argument for female choice
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- Oikos, 1993, v. 68, n. 2, p. 303
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Behaviour and risk of predation in larval tree hole mosquitoes: effect of hunger and population history of predation
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- Oikos, 1993, v. 68, n. 2, p. 229, doi. 10.2307/3544835
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Ant--Homoptera interaction: do alternative sugar sources distract tending ants?
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- Oikos, 1993, v. 68, n. 2, p. 202
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Anther-smut infection in Silene dioica: variation in floral morphology and patterns of spore deposition
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- Oikos, 1993, v. 68, n. 2, p. 207
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