Literature DB >> 28310597

Overgrowth in a marine epifaumal community: Competitive hierarchies and competitive networks.

Garry R Russ1.   

Abstract

The frequencies with which organisms of a species overgrew or were overgrown by organisms of other species in a marine epifaunal community were estimated. The ranking of the ability of the major taxonomic groups to overgrow others was basically hierarchical:ascidians≧sponges>bryozoans>barnacles, polychaetes, tubicolous amphipods, hydroids. In contrast, the ranking of the competitive ability of species in the community did not form a simple linear hierarchy and there was no single competitively dominant species (measured in terms of overgrowth). There were often no significant differences in the ability of species to overgrow each other within the three major taxonomic groups of sponges, ascidians and bryozoans. Such results were common also between the species of large sponges and ascidiams which dominated substrata immersed for periods longer than two years.A lack of a significant difference in the competitive ability of species was usually the result of (a) frequent formation of delay/ties or "standoffs" and (b) changes in the outcome of interactions due to change in the relative size of interacting colonies. In many two-species interactions the species which had the larger colony in a given encounter had a greater probability of winning.When the range of colony sizes of two species was similar there was often no significant difference between the competitive ability of each species. Such cases without a clearcut winner often represented a backloop in an otherwise hierarchical sequence of competitive ability, i.e. Species A beats Species B, Species B beats Species C, no significant differences in competitive ability between Species C and A. No examples of competitive networks of the form Species A beats Species B, Species B beats Species C, Species C beats Species A were found. Backloops in otherwise hierarchical sequences (no significant differences in competitive ability) occurred most frequently between species within the same major taxonomic groups and were the result of a very even balance in the generalised competitive mechanism of overgrowth.It seems probable that backloops in hierarchical sequences are more commonly due to the absence of clear competitive dominance in interactions between species (reversals in the outcome of overgrowth interactions and "standoffs"), rather than to direct backloops formed by a specialised or to a generalised competitive mechanism. Network-like arrangements of competitive ability formed by the type of processes described here are likely to contribute significantly to the high levels of species diversity observed in many marine epifaunal communities subject to low levels of physical disturbance.

Year:  1982        PMID: 28310597     DOI: 10.1007/BF00377130

Source DB:  PubMed          Journal:  Oecologia        ISSN: 0029-8549            Impact factor:   3.225


  9 in total

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Authors:  J B Jackson; L Buss
Journal:  Proc Natl Acad Sci U S A       Date:  1975-12       Impact factor: 11.205

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Authors:  L W Buss
Journal:  Proc Natl Acad Sci U S A       Date:  1980-09       Impact factor: 11.205

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Journal:  Science       Date:  1974-11-08       Impact factor: 47.728

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Journal:  Br Sci News       Date:  1949

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Authors:  J H Connell
Journal:  Science       Date:  1978-03-24       Impact factor: 47.728

6.  Spatial competition among porifera: Solution by epizoism.

Authors:  Klaus Rützler
Journal:  Oecologia       Date:  1970-06       Impact factor: 3.225

7.  Occupation of patches in the epifaunal communities on pier pilings and the bivalve Pinna bicolor at Edithburgh, South Australia.

Authors:  Alice M Kay; Michael J Keough
Journal:  Oecologia       Date:  1981-02       Impact factor: 3.225

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Journal:  Nature       Date:  1977-02-24       Impact factor: 49.962

9.  Intertidal community structure : Experimental studies on the relationship between a dominant competitor and its principal predator.

Authors:  R T Paine
Journal:  Oecologia       Date:  1974-06       Impact factor: 3.225

  9 in total
  13 in total

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Authors:  Barbara L Ignacio; Luciana M Julio; Andrea O R Junqueira; Maria A G Ferreira-Silva
Journal:  PLoS One       Date:  2010-09-29       Impact factor: 3.240

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Authors:  G J Bakus; N M Targett; B Schulte
Journal:  J Chem Ecol       Date:  1986-05       Impact factor: 2.626

3.  Natural variation of toxicity in encrusting spongeCrambe crambe (Schmidt) in relation to size and environment.

Authors:  M A Becerro; X Turon; M J Uriz
Journal:  J Chem Ecol       Date:  1995-12       Impact factor: 2.626

4.  Competitive reversals and environment-dependent resource partitioning in Erodium.

Authors:  Kevin J Rice; John W Menke
Journal:  Oecologia       Date:  1985-10       Impact factor: 3.225

5.  Small-scale association measures in epibenthic communities as a clue for allelochemical interactions.

Authors:  Xavier Turon; Mikel A Becerro; Maria J Uriz; Jaume Llopis
Journal:  Oecologia       Date:  1996-10       Impact factor: 3.225

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Authors:  Avril L Ayling
Journal:  Oecologia       Date:  1983-12       Impact factor: 3.225

7.  Competitive equivalence in a community of lichens on rock.

Authors:  Patricia M Harris
Journal:  Oecologia       Date:  1996-12       Impact factor: 3.225

8.  Spatial pattern of distribution of marine invertebrates within a subtidal community: do communities vary more among patches or plots?

Authors:  Chun-Yi Chang; Dustin J Marshall
Journal:  Ecol Evol       Date:  2016-10-22       Impact factor: 2.912

9.  Cockles, barnacles and ascidians compose a subtidal facilitation cascade with multiple hierarchical levels of foundation species.

Authors:  Eugeniy Yakovis; Anna Artemieva
Journal:  Sci Rep       Date:  2017-03-22       Impact factor: 4.379

10.  Persistence and space preemption explain species-specific founder effects on the organization of marine sessile communities.

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Journal:  Ecol Evol       Date:  2018-02-23       Impact factor: 2.912

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