Ungulate community structure and ecological processes: body size, hoof area and trampling in African savannas

Oecologia ◽  
2003 ◽  
Vol 134 (4) ◽  
pp. 560-568 ◽  
Author(s):  
David H. M. Cumming ◽  
Graeme S. Cumming
2016 ◽  
Vol 73 (4) ◽  
pp. 535-546 ◽  
Author(s):  
Cindy Chu ◽  
Nigel P. Lester ◽  
Henrique C. Giacomini ◽  
Brian J. Shuter ◽  
Donald A. Jackson

Across broad geographic scales, ecological indicators for fish assemblages should represent causal ecological processes, be sensitive enough to show patterns across the landscape, and reflect underlying biotic or abiotic conditions that influence those patterns. We assessed the responses of commonly applied ecological indicators for lake fish assemblages (mean body size, catch-per-unit-effort (CPUE), and normalized length size spectrum (NLSS) slope) to regional (climate, water chemistry, and watershed stress due to human activities) and local (lake morphometry, water quality, and angling pressure) ecological and anthropogenic variables. The indicators were estimated using fish assemblage catch data acquired via a standardized gillnetting protocol implemented within 693 lakes in Ontario, Canada. To our knowledge, our study is the first size-based or catch-based indicator evaluation to include detailed observations of angling pressure on hundreds of inland lakes. Boosted regression tree models showed that CPUE of large-bodied organisms and NLSS slope best described underlying patterns in the regional and local variables. Models developed with a mix of regional and local variables performed better than models developed with regional or local variables alone. The relative influences of the variables and responses varied among indicators, but in general, ecological variables had greater influence on the indicators than anthropogenic variables. These results emphasize the complex and multiscaled nature of factors and ecological processes affecting body size, habitat-community production, and trophic dynamics in lake fish assemblages.


2014 ◽  
Vol 281 (1797) ◽  
pp. 20142103 ◽  
Author(s):  
Marlee A. Tucker ◽  
Tracey L. Rogers

Predator–prey relationships and trophic levels are indicators of community structure, and are important for monitoring ecosystem changes. Mammals colonized the marine environment on seven separate occasions, which resulted in differences in species' physiology, morphology and behaviour. It is likely that these changes have had a major effect upon predator–prey relationships and trophic position; however, the effect of environment is yet to be clarified. We compiled a dataset, based on the literature, to explore the relationship between body mass, trophic level and predator–prey ratio across terrestrial ( n = 51) and marine ( n = 56) mammals. We did not find the expected positive relationship between trophic level and body mass, but we did find that marine carnivores sit 1.3 trophic levels higher than terrestrial carnivores. Also, marine mammals are largely carnivorous and have significantly larger predator–prey ratios compared with their terrestrial counterparts. We propose that primary productivity, and its availability, is important for mammalian trophic structure and body size. Also, energy flow and community structure in the marine environment are influenced by differences in energy efficiency and increased food web stability. Enhancing our knowledge of feeding ecology in mammals has the potential to provide insights into the structure and functioning of marine and terrestrial communities.


2019 ◽  
Vol 116 (20) ◽  
pp. 9931-9940 ◽  
Author(s):  
Meng Chen ◽  
Caroline A. E. Strömberg ◽  
Gregory P. Wilson

The long-standing view that Mesozoic mammaliaforms living in dinosaur-dominated ecosystems were ecologically constrained to small size and insectivory has been challenged by astonishing fossil discoveries over the last three decades. By studying these well-preserved early mammaliaform specimens, paleontologists now agree that mammaliaforms underwent ecomorphological diversification during the Mesozoic Era. This implies that Mesozoic mammaliaform communities had ecological structure and breadth that were comparable to today’s small-bodied mammalian communities. However, this hypothesis remains untested in part because the primary focus of most studies is on individual taxa. Here, we present a study quantifying the ecological structure of Mesozoic mammaliaform communities with the aim of identifying evolutionary and ecological drivers that influenced the deep-time assembly of small-bodied mammaliaform communities. We used body size, dietary preference, and locomotor mode to establish the ecospace occupation of 98 extant, small-bodied mammalian communities from diverse biomes around the world. We calculated ecological disparity and ecological richness to measure the magnitude of ecological differences among species in a community and the number of different eco-cells occupied by species of a community, respectively. This modern dataset served as a reference for analyzing five exceptionally preserved, extinct mammaliaform communities (two Jurassic, two Cretaceous, one Eocene) from Konservat-Lagerstätten. Our results indicate that the interplay of at least three factors, namely the evolution of the tribosphenic molar, the ecological rise of angiosperms, and potential competition with other vertebrates, may have been critical in shaping the ecological structure of small-bodied mammaliaform communities through time.


1992 ◽  
Vol 8 (2) ◽  
pp. 169-179 ◽  
Author(s):  
Vojtěch Novotný

ABSTRACTThe adult Auchenorrhyncha community within the understorey of a montane tropical forest in Vietnam is described A total of 1132 specimens representing 223 morphospecies and 16 families was found in a 4300-sweep sample None of the species exceeded the 5% dominance level More than half the species are represented by single individuals within the 309 ms of vegetation Spatial community pattern is mosaic like at a scale of hundreds of metres as the similarity of 100 sweep samples does not depend on their spatial distance Areas 1 5–3 km distant from one another differ markedly in their Auchenorrhyncha communities These between-site differences exceed the intra-site community heterogeneity Population density of Auchenorrhyncha species is not correlated with their body size The Auchenorrhyncha community within a forest markedly differs from the community of an adjacent ruderal area A transitional zone between these habitats is intermediate in Auchenorrhyncha species composition


2007 ◽  
Vol 23 (4) ◽  
pp. 409-417 ◽  
Author(s):  
Steven J. Presley

Evaluation of proximate mechanisms (e.g. dispersal, immigration, competition, facilitation) that determine patterns of assemblage or community structure is an important step in the development of paradigms in ecology. Host–parasite systems are useful for such studies because host-parasite assemblages are easily defined units of study, each host individual harbours a sample from a community or assemblage, and many host species are common, providing replicate samples. I used ectoparasite assemblages from Noctilio leporinus collected from Paraguay to evaluate effects of host sex and body size on ectoparasite abundance and to determine if these assemblages exhibit a nested pattern of species co-occurrence. A total of 533 ectoparasites representing seven species and four families were collected from 28 hosts. Abundances of Paradyschiria fusca and Noctiliostrebla aitkeni responded positively to host body size. Host sex had no affect on ectoparasite abundances. Streblid bat fly assemblages from Noctilio leporinus were strongly and significantly nested. Abundances of all species of streblid were positively correlated with one another with Pearson product moment correlation coefficients between 0.424 and 0.646. Competition does not appear to affect community structure of streblids from Paraguayan Noctilio leporinus. Independent responses of species of streblid to host characteristics appear to mould assemblage structure in this system.


Author(s):  
Christian M. Ibáñez ◽  
Mauricio J. Carter ◽  
Moisés A. Aguilera ◽  
M. Cecilia Pardo‐Gandarillas ◽  
Enrico L. Rezende

Ecology ◽  
2005 ◽  
Vol 86 (6) ◽  
pp. 1407-1413 ◽  
Author(s):  
S. K. Morgan Ernest

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