Rocky intertidal fish communities of California: temporal and spatial variation

Synopsis We examined data from our own and published collections of intertidal and shallow littoral fishes of the North American Pacific Coast with respect to temporal and spatial trends in species composition and dominance. We compared (1) recent and past intertidal collections made five and seven years apart, respectively, for two California localities, (2) intertidal collections from twelve localities in California, Oregon, and British Columbia, and (3) intertidal versus subtidal collections at one California locality. Temporal comparisons indicated substantially lower abundance of the cottid Oligocottus snyderi at two California localities during 1984, at one locality due to depressed abundance of young. Interannual differences in abundances suggested that other tidepool fish assemblages undergo significant changes as well. Geographical comparisons indicated general similarity in species composition, with cottids predominating in tidepools although several other families also were well represented (e.g., Stichaeidae, Scorpaenidae). Eel-shaped stichaeids and pholids occurred at high densities in exposed boulder fields. Both the tidepool and boulder field assemblages showed north-south changes in species abundances. Comparison of collections from the intertidal and subtidal zones at one California locality demonstrated that fishes of these habitats form two essentially distinct assemblages, with most species restricted to or concentrated in one or the other habitat.     

Environmental influences on seasonal distribution of coastal and estuarine fish assemblages at Wemindji,eastern James Bay

Synopsis The coastal fish assemblages of Wemindji, eastern James Bay, were studied in 1987 and 1988 to describe seasonal utilization of the Maquatua River estuary and the adjacent coastal waters by marine and anadromous fishes. Fish diversity was low (11 sp.) and experimental gill net catches were highly variable between sites in the estuary and coastal waters, and also seasonally at a given site. During summer, the estuarine fishes were numerically dominated by two marine species, the fourhorn sculpin,Myoxocephalus quadricornis, and the slender eelblenny,Lumpenus fabricii, and also by juvenile cisco,Coregonus artedii, and juvenile lake whitefish,C. clupeaformis. In coastal waters, three marine species were abundant: the shorthorn sculpin,M. scorpius, the arctic sculpin,M. scorpioides and the Greenland cod.Gadus ogac. In contrast with the estuary, large (> 270 mm) cisco and lake whitefish were abundant in coastal waters indicating extensive movements of these species in James Bay during the summer. Distribution patterns were influenced by a combination of physical conditions (salinity and temperature) and biological characteristics (habitat choice, migration and reproduction) depending on the season.     

Extinction, colonization, and species occupancy in tidepool fishes

Despite the increasing sophistication of ecological models with respect to the size and spatial arrangement of habitat, there is relatively little empirical documentation of how species dynamics change as a function of habitat size and the fraction of habitat occupied. In an assemblage of tidepool fishes, I used maximum-likelihood estimation to test whether models which included habitat size provided a better fit to empirical data on extinction and colonization probabilities than models that assumed constant probabilities over all habitats. I found species differences in how extinction and colonization probabilities scaled with habitat size (and hence local population size). However, there was little evidence for a relationship between extinction and colonization probabilities and the fraction of occupied tidepools, as assumed in simple metapopulation models. Instead, colonization and extinction were independent of the fraction of occupied tidepools, favoring a MacArthur-Wilson island-mainland model. When I incorporated declines in extinction probability with tidepool volume in a simple simulation model, I found that predicted occupancy could change greatly, especially when colonization was low. However, the predicted fraction of occupied patches in the simulation model changed little when I incorporated the range of values reported here for extinction and colonization and the rate at which they scale with habitat size. Quantifying extinction and colonization patterns of natural populations is fundamental to understanding how species are distributed spatially and whether metapopulation models of species occupancy provide explanatory power for field populations. Received: 14 March 1997 / Accepted: 21 September 1997