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UCREFRP
UCREFRP Catalog Number
7405
Author
Bain, M. B., ed. 1990.
Title
Workshop Synopsis,
USFW Year
Ecolog
USFW - Doc Type
U.S. Department of the Interior,
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NO
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<br />BIOLOGICAL REPORT 90(5) 11 <br /> <br />Ecology of Southeastern Stream Fishes: Geographic <br />Macro- and Micro-habitat Considerations <br /> <br />Stephen T. Ross <br /> <br />by <br /> <br />Department of Biological Sciences <br />University of Southern Mississippi <br />Hattiesburg, Mississippi 39406 <br /> <br />An understanding of natural variation in fish as- <br />semblage composition is important in developing and <br />implementing stream management plans. Over the <br />last decade, fish ecologists have worked to under- <br />stand the patterns of organization and variation in <br />communities and then to explore the mechanisms <br />responsible for these patterns. Studies of stream fish <br />assemblages necessarily emphasize current condi- <br />tions and interactions, simply because we are faced <br />with finite lifespans, careers, and budgets. While <br />human and professional mortality are facts that we <br />must deal with, our mortality-and the resulting <br />short-term view of ecological communities-has led <br />to problems of interpretation. I will identify three <br />problems confronting fish community ecologists and <br />suggest approaches to dealing with them. <br />The first problem is that ecologists often approach <br />communities with the idea that biotic processes that <br />structured such systems are still ongoing and are <br />unaltered in the particular habitat under study-the <br />fallacy of community stasis. It is important to have <br />a temporal perspective on the subjects that we study <br />as fish ecologists-namely species, assemblages, <br />river systems, populations, and microhabitats. In <br />terms of species, the age of most of the fish fauna <br />in the southeastern United States probably dates <br />from the late Miocene or early Pliocene. For in- <br />stance, ancestral suckers, minnows, and darters are <br />thought to have dispersed over a North American <br />land route (Beringia) during the early Tertiary <br />(Gilbert 1976), when such a connection between <br />Europe and America still existed. <br />Somewhat later, the modern darter (tribe Etheo- <br />stomatini) arose from an unknown percid ancestor. <br />Vicariant events, such as isolation in many small <br />streams and the disruption of highland areas, led to <br />the evolution of numerous species of Etheostoma and <br />Percina (Collette and Banarescue 1977). The min- <br />nows date from about the same age, with diversi- <br />fication of the largest genus, Notropis, probably <br /> <br />~ <br /> <br />occurring in the Mississippi Basin in the early to mid- <br />dle Pliocene (Gilbert 1964, for Luxilus). Fossil data <br />indicate that centrarchids may date from the <br />Oligocene (Gilbert 1976), and Lepomis occurred in <br />the Miocene (Swift and Wing 1968). Thus, the three <br />largest families of freshwater fishes have diverged <br />since the Miocene or Pliocene (Gilbert 1964; Collette <br />and Banarescue 1977), and therefore we are most <br />concerned with recent, Pleistocene, and Pliocene <br />geology in attempting to understand fish distribu- <br />tions and the history of interactions. <br />In dealing with the diverse fishes of the North <br />American highlands, which include the area of <br />greatest diversity of North American freshwater <br />fishes, Mayden (1987a, 1987b) concluded that these <br />faunas are older-probably much older-than the <br />Pleistocene. While actual dates of origin of individual <br />species are uncertain and will probably remain so, <br />it is evident that the organisms we are studying have <br />existed as species for 2-5 million years. <br />The message for ecologists studying stream fishes <br />is clearly that these species are carrying con- <br />siderable "historical baggage." Also, it is most <br />realistic to expect that adaptations to reduce com- <br />petition or predation should be generalized rather <br />than specific to particular species or microhabitats. <br />Many studies of fish resource partitioning attempt <br />to interpret interspecific differences in resource use <br />as due solely to local spatio-temporal interactions, <br />ignoring the evolutionary history of species. The <br />history of the southeastern fish assemblages tells us <br />that each species in an assemblage represents a long, <br />spatially integrated, and potentially independent <br />evolutionary history, and at any given point a species <br />may not even be well adapted to its environment <br />(Jaksic 1981). <br />Whether or not assemblages vary significantly <br />over time has been a major issue in the attempts to <br />understand factors responsible for maintaining com- <br />munity structure (e.g., Grossman et al. 1982; Ross <br />
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