Works matching IS 00301299 AND DT 1997 AND VI 80 AND IP 3
Results: 28
The relationship between local and regional species richness: comparing biotas with different evolutionary histories
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- Oikos, 1997, v. 80, n. 3, p. 583
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The effect of density on size frequency distributions in chalk grassland bryophyte populations
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- Oikos, 1997, v. 80, n. 3, p. 533
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Seasonal dynamics of Daphnia and algae explained as a periodically forced predator-prey system
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- Oikos, 1997, v. 80, n. 3, p. 519, doi. 10.2307/3546625
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Root exudation of organic acids: importance to nutrient availability and the calcifuge and calcicole behaviour of plants
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- Oikos, 1997, v. 80, n. 3, p. 459
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Risk of grazing and flower number in a perennial plant
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- Oikos, 1997, v. 80, n. 3, p. 428
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On the implications of species-area relationships for endemism, spatial turnover, and food web patterns
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- Oikos, 1997, v. 80, n. 3, p. 417, doi. 10.2307/3546614
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Response of galling insects to natural browsing by mammals in Alaska
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- Oikos, 1997, v. 80, n. 3, p. 481
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Nitrogen partitioning between resorption and decomposition pathways: a trade-off between nitrogen use efficiency and litter decomposibility?
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- Oikos, 1997, v. 80, n. 3, p. 603, doi. 10.2307/3546636
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Resource allocation among clonal shoots of the fire-tolerant shrub Gaylussacia baccata
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- Oikos, 1997, v. 80, n. 3, p. 509, doi. 10.2307/3546624
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Population dynamics in sessile organisms: some general results fromthree seemingly different theory-lineages
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- Oikos, 1997, v. 80, n. 3, p. 588
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On the relationship between shade tolerance and shade avoidance strategies in woodland plants
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- Oikos, 1997, v. 80, n. 3, p. 575
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Protective polymorphism in populations of computer-simulated moth-like prey
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- Oikos, 1997, v. 80, n. 3, p. 565
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Primary productivity and trophic dynamics investigated in a North Derbyshire, UK, dale
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- Oikos, 1997, v. 80, n. 3, p. 499
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Natural selection and sexual dimorphism: sex-biased sparrowhawk predation favours crypsis in female chaffinches
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- Oikos, 1997, v. 80, n. 3, p. 540
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Metapopulation extinction and genetic variation in dispersal-relatedtraits
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- Oikos, 1997, v. 80, n. 3, p. 448, doi. 10.2307/3546617
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Long-term studies of the medionigra polymorphism in the moth Panaxiadominula: a critique
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- Oikos, 1997, v. 80, n. 3, p. 613
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Ecosystem catalysis: soil urease activity and grazing in the Serengeti ecosystem
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- Oikos, 1997, v. 80, n. 3, p. 467, doi. 10.2307/3546619
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Does immigration "rescue" populations from extinction? Implications regarding movement corridors and the conservation of mammals
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- Oikos, 1997, v. 80, n. 3, p. 618, doi. 10.2307/3546639
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Do global patterns of habitat use and migration strategies co-evolvewith relative investments in immunocompetence due to spatial variation in parasite pressure:
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- Oikos, 1997, v. 80, n. 3, p. 623, doi. 10.2307/3546640
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Competition and herbivory in establishing grassland communities: implications for plant biomass, species diversity and soil microbial activity
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- Oikos, 1997, v. 80, n. 3, p. 470, doi. 10.2307/3546620
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Community nestedness and the proper way to assess statistical significance by Monte-Carlo tests: some comments on Worthen and Rohde's (1996) paper
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- Oikos, 1997, v. 80, n. 3, p. 572, doi. 10.2307/3546631
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Barnacle recruitment and population dynamics predicted from coastal upwelling
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- Oikos, 1997, v. 80, n. 3, p. 487
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Asymmetry of population cycles: abundance--growth representation ofhidden causes of ecological dynamics
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- Oikos, 1997, v. 80, n. 3, p. 435
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Assembling ecological communities in time and space
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- Oikos, 1997, v. 80, n. 3, p. 549
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Are mixed populations of plant species more productive than pure stands?
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- Oikos, 1997, v. 80, n. 3, p. 595, doi. 10.2307/3546635
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Are "comparative methods" always necessary?
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- Oikos, 1997, v. 80, n. 3, p. 607
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An analysis of substrate selection by postlarval lobsters, Homarus americanus, using a dynamic optimization model
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- Oikos, 1997, v. 80, n. 3, p. 554
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An "audience effect" for ecological terminology: use and misuse of jargon
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- Oikos, 1997, v. 80, n. 3, p. 632
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