Oecologia, Год журнала: 1977, Номер 29(3), С. 233 - 247
Опубликована: Янв. 1, 1977
Язык: Английский
Oecologia, Год журнала: 1977, Номер 29(3), С. 233 - 247
Опубликована: Янв. 1, 1977
Язык: Английский
The American Naturalist, Год журнала: 1979, Номер 113(1), С. 81 - 101
Опубликована: Янв. 1, 1979
A new hypothesis, based on differences in the rates at which populations of competing species approach competitive equilibrium (reduction or exclusion some species), is proposed to explain patterns diversity. The hypothesis assumes that most communities exist a state nonequilibrium where prevented by periodic population reductions and environmental fluctuations. When prevented, dynamic balance may be established between rate displacement frequency reduction, results stable level Under conditions infrequent reductions, an increase growth competitors generally decreased This model clarifies underlying pattern variation diversity points out common elements previous hypotheses. Rather than arguing either competition, predation, productivity control diversity, it demonstrates all these contribute same basic mechanism. In doing so, not only explains correlations other hypotheses with but also exceptions could explain. applied variations both latitudinal gradient within specific regions.
Язык: Английский
Процитировано
3392Proceedings of the National Academy of Sciences, Год журнала: 1973, Номер 70(12), С. 3590 - 3593
Опубликована: Дек. 1, 1973
Very precise data on the dynamics of a competitive system two species Drosophila have been obtained. By curvilinear regression approach, analytical models competition fitted. statistical and biological criteria simplicity, reality, generality, accuracy, best these has chosen. This model represents an extension Lotka-Volterra competition; it adds fourth parameter that controls degree nonlinearity in intraspecific growth regulation. It similar logistic population growth.
Язык: Английский
Процитировано
556Theoretical Population Biology, Год журнала: 1973, Номер 4(3), С. 331 - 356
Опубликована: Сен. 1, 1973
Язык: Английский
Процитировано
401Theoretical Population Biology, Год журнала: 1976, Номер 9(2), С. 202 - 221
Опубликована: Апрель 1, 1976
Язык: Английский
Процитировано
305Journal of Theoretical Biology, Год журнала: 1975, Номер 50(1), С. 185 - 201
Опубликована: Март 1, 1975
Язык: Английский
Процитировано
298Journal of Theoretical Biology, Год журнала: 1989, Номер 136(1), С. 57 - 66
Опубликована: Янв. 1, 1989
Язык: Английский
Процитировано
243Science, Год журнала: 1975, Номер 189(4205), С. 808 - 810
Опубликована: Сен. 5, 1975
In a central New Hampshire forest, three co-occurring tree species were found to occupy different positions on reproductive strategy gradient. These differences, in part, described separate niches for the species. The three-species complex is hypothesized form dynamic climax overstory characterized by cyclical replacement of one dominant another.
Язык: Английский
Процитировано
242Nature, Год журнала: 1984, Номер 310(5975), С. 310 - 312
Опубликована: Июль 1, 1984
Язык: Английский
Процитировано
152Austral Ecology, Год журнала: 1979, Номер 4(2), С. 145 - 164
Опубликована: Июнь 1, 1979
Many species of honeyeaters and other nectar-feeding birds occur in most habitats South Australia. They frequently feed on nectar the same plants. A succession plants provide for throughout year. Nectar is abundant winter early spring least summer autumn. There more per flower flowers spring. often depleted by honeyeaters, sometimes visitors (silvereyes, lorikeets insects) between December May. It at times reduced to a level which it uneconomical some exploit. are seasonal movements into areas out these when becomes scarce. Breeding coincides with peak abundance nectar. Diversity probably maintained an interaction two types competition, exploitation interference. The larger use richest sources aggressively exclude smaller (interference) whereas can poorer because their energy requirements less (exploitation).
Язык: Английский
Процитировано
143Journal of Animal Ecology, Год журнала: 1979, Номер 48(3), С. 899 - 899
Опубликована: Окт. 1, 1979
SUMMARY (1) Models of competition in divided or heterogeneous environments are reviewed. (2) A model a environment is presented. The coefficients, a, reduced by term, 0, which measures the amount overlap between species. (3) Actual values 0 presented for two Drosophila communities. (4) depends on degree aggregation competing species and their densities. outcome must, then, be density dependent. (5) Low improve stability multi-species community allow more
Язык: Английский
Процитировано
143