Carbon, nitrogen, and sulfur stable isotopes were used to characterize the food webs (i.e., sources of carbon and trophic status of consumers) in Tijuana Estuary and San Dieguito Lagoon. Producer groups were most clearly differentiated by carbon, then by sulfur, and least clearly by nitrogen isotope measurements. Consumer N isotopic enrichment suggested that there are four trophic levels in the Tijuana Estuary food web and three in San Dieguito Lagoon. A significant difference in multiple isotope ratio distributions of fishes between wetlands suggested that the food web of San Dieguito Lagoon is less complex than that of Tijuana Estuary. Associations among sources and consumers indicated that inputs from intertidal macroalgae, marsh microalgae, and Spartina foliosa provide the organic matter that supports invertebrates, fishes, and the light-footed clapper rail (Rallus longirostris levipes). These three producers occupy tidal channels, low salt marsh, and mid salt marsh habitats. The only consumer sampled that appears dependent upon primary productivity from high salt marsh habitat is the sora (Porzana carolina). Two- and three-source mixing models identified Spartina as the major organic matter source for fishes, and macroalgae for invertebrates and the light-footed clapper rail in Tijuana Estuary. In San Dieguito Lagoon, a system lacking Spartina, inputs of macroalgae and microalgae support fishes. Salicornia virginica, S. subterminalis, Monanthochloe littoralis, sewage- derived organic matter, and suspended particulate organic matter were deductively excluded as dominant, direct influences on the food web. The demonstration of a salt marsh-channel linkage in these systems affirms that these habitats should be managed as a single ecosystem and that the restoration of intertidal marshes for endangered birds and other biota is compatible with enhancement of coastal fish populations; heretofore, these have been considered to be competing objectives.
Climate is a critical driver of many fish populations, assemblages, and aquatic communities. However, direct observational studies of climate change impacts on North American inland fishes are rare. In this synthesis, we (1) summarize climate trends that may influence North American inland fish populations and assemblages, (2) compile 31 peer‐reviewed studies of documented climate change effects on North American inland fish populations and assemblages, and (3) highlight four case studies representing a variety of observed responses ranging from warmwater systems in the southwestern and southeastern United States to coldwater systems along the Pacific Coast and Canadian Shield. We conclude by identifying key data gaps and research needs to inform adaptive, ecosystem‐based approaches to managing North American inland fishes and fisheries in a changing climate.
We conducted an intensive fish survey in the tailwater reach of a large Ozark river 30 years after its impoundment and compared the recent fish assemblage with those prior to impoundment and shortly (4 years) after impoundment. Our primary objective was to assess whether relatively short‐term monitoring following dam construction can adequately quantify the long‐term effects of impoundment on downstream riverine fishes. The preimpoundment survey (1962–1963) described a fish assemblage composed of warmwater fish species, predominantly Cyprinidae, Ictaluridae, Centrarchidae, and Percidae. Yoke darter Etheostoma juliae (34%), central stoneroller Campostoma anomalum (24%), and Ozark madtom Noturus albater (7%) were the most abundant species. The postimpoundment surveys of 1965–1966 and 1968 documented immediate changes in the fish assemblage. No Ozark madtoms and only four yoke darters were collected shortly after impoundment. Central stonerollers accounted for 45–50% of the fish collected, and both short‐term postimpoundment surveys collected five species of darters (Percidae) that accounted for 41–42% of the fish collected. Thirty years after impoundment, we found that the tailwater fish assemblage was composed almost entirely of coldwater species. Ozark sculpin Cottus hypselurus and four species of introduced trout (Salmonidae) accounted for 98% of the fish assemblage by number during the 1995–1997 surveys. The rank abundance of species was negatively correlated between our survey and the preimpoundment survey but not between our survey and the short‐term postimpoundment surveys. Many species that we collected (54%) are habitat generalists, and we did not collect 77% of the fluvial‐specialist species that were present in historical collections. All postimpoundment surveys documented dramatically reduced species richness and diversity. We conclude that short‐term monitoring following impoundment is inadequate to determine the impact of dams on lotic fish assemblages and suggest long‐term postimpoundment monitoring to determine when a fish assemblage has stabilized.
We sampled fish assemblages and quantified production dynamics of brook trout Salvelinus fontinalis, brown trout Salmo trutta, and rainbow trout Oncorhynchus mykiss in 13 southeastern Minnesota streams during 1988–1990 to examine the influence of water quality on fish populations in fertile trout streams. Fish assemblages in 15 stream reaches were abundant, but low in diversity; 13 species were collected. Parameter means (ranges) over the reaches were species richness, 4.1 (1–8); density, 29,490 (1,247–110,602) fish/ha; and biomass, 253.5 (49.6–568.6) kg/ha. Means (ranges) for salmonids were annual mean density, 2,279 (343–8,096) fish/ha; annual mean biomass, 162.0 (32.5–355.5) kg/ha; and annual production, 155.6 (36.7–279.6) kg/ha. Salmonid production and mean biomass were greater during the spring‐fall interval than during fall‐spring; young cohorts (ages 0–1) contributed the greatest proportion to population biomass and production. Salmonid annual production‐to‐mean‐biomass ratio (P/B) averaged 1.06 (0.64–1.42), and means were significantly different among species (1.03 for brown trout, 1.54 for brook trout, and 1.92 for rainbow trout). A significant linear model was developed that describes P/B as an inverse function of population age structure and may be used to improve accuracy in approximations of annual production from mean biomass. Fish density, biomass, or production were not correlated with eight water quality variables describing ionic and nutrient content in these streams, but when data from other United States streams with a wide range in alkalinity were incorporated, salmonid production was strongly, positively correlated with alkalinity. The wide range in fish population and production statistics and their lack of correlation with water quality suggest that no uniform fish carrying capacity exists among these streams and that factors other than water fertility limit fish density, biomass, and productivity at this spatial scale, but the overall maximum production rate in the region may be governed by water quality.
Knowledge of individual growth and mortality rates of an introduced fish population is required to determine the success and degree of establishment as well as to predict the fish's impact on native fauna. The age and growth of flathead catfish Pylodictis olivaris have been studied extensively in the species' native and introduced ranges, and estimates have varied widely. We quantified individual growth rates and age structure of three introduced flathead catfish populations in North Carolina's Atlantic slope rivers using sagittal otoliths, determined trends in growth rates over time, compared these estimates among rivers in native and introduced ranges, and determined total mortality rates for each population. Growth was significantly faster in the Northeast Cape Fear River (NECFR) than in the Lumber and Neuse rivers. Fish in the NECFR grew to a total length of 700 mm by age 7, whereas fish in the Neuse and Lumber river populations reached this length by 8 and 10 years, respectively. The growth rates of fish in all three rivers were consistently higher than those of native riverine populations, similar to those of native reservoir populations, and slower than those of other introduced riverine populations. In general, recent cohorts (1998–2001 year‐classes) in these three rivers exhibited slower growth among all ages than did cohorts previous to the 1998 year‐class. The annual total mortality rate was similar among the three rivers, ranging from 0.16 to 0.20. These mortality estimates are considerably lower than those from the Missouri and Mississippi rivers, suggesting relatively low fishing mortality for these introduced populations. Overall, flathead catfish populations in reservoirs grow faster than those in rivers, the growth rates of introduced populations exceed those of native populations, and eastern United States populations grow faster than those in western states. Such trends constitute critical information for understanding and managing local populations.
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