We combined laboratory and field studies to experimentally assess how the effects of feeding regime and time since feeding influence nitrogen (N), phosphorus (P), and the N:P ratio excreted by two common freshwater fish, bluegill (Lepomis macrochirus) and gizzard shad (Dorosoma cepedianum). In addition, for adult gizzard shad, we modelled excretion rates as a function of the nutrient content of ingested sediment detritus. For both bluegill and gizzard shad, feeding significantly increased nutrient excretion rates and altered excreted N:P ratios. For both species, excretion rates were highest immediately after feeding and declined thereafter. Because the phosphorus excretion rate decreased more rapidly after feeding than did the nitrogen excretion rate, the excreted N:P ratio increased with time since feeding. Young-of-year gizzard shad excreted more nitrogen than adults, resulting in a higher excreted N:P ratio for these small fish. For P, predictions from our model agreed well with our experiments with gizzard shad; for N, the agreement was not as strong yet was still reasonable. In summary, N:P ratios excreted by these fish differed across species, size, and time since feeding. Variation in these factors may explain discrepancies among studies that examine both trophic interactions and nutrient budgets.
Disruption to migration is a growing problem for conservation and restoration of animal populations. Anthropogenic barriers along migration paths can delay or prolong migrations, which may result in a mismatch with migration-timing adaptations. To understand the interaction of dams (as barriers along a migration path), seasonally changing environmental conditions, timing of Atlantic salmon (Salmo salar) downstream migration, and ultimate migration success, we used 10 years of river temperature and discharge data as a template upon which we simulated downstream movement of salmon. Atlantic salmon is a cool-water species whose downstream migrating smolts must complete migration before river temperatures become too warm. We found that dams had a local effect on survival as well as a survival effect that was spatially and temporally removed from the encounter with the dam. While smolts are delayed by dams, temperatures downstream can reach lethal or near-lethal temperatures; as a result, the match between completion of migration and the window of appropriate migration conditions can be disrupted. The strength of this spatially and temporally removed effect is at least comparable to the local effects of dams in determining smolt migration success in the presence of dams. We also considered smolts from different tributaries, varying in distance from the river mouth, to assess the potential importance of locally adapted migration timing on the effect of barriers. Migration-initiation temperature affected modeled smolt survival differentially across tributaries, with the success of smolts from upstream tributaries being much more variable across years than that of smolts with a shorter distance to travel. As a whole, these results point to the importance of broadening our spatial and temporal view when managing migrating populations. We must consider not only how many individuals never make it across migration barriers, but also the spatially and temporally removed consequences of delays at the barriers for those individuals that successfully navigate them.
1993. Direct and indirect effects of fish predation on the replacement of a native crayfish by an invading congener. Can. 8. Fish. Aquat. Sci. 50: 1279-1 288. In Ohio streams, the crayfish Orconectes rusticus is replacing 0. sanborni, and herein we test how predators influence this replacement. In a field survey, crayfish were scarce when fish were abundant, suggesting that predators can adversely affect these prey. In laboratory experiments, we examined underlying mechanisms for this inverse relationship; specifically, we tested how crayfish species, adult aggression, and habitat heterogeneity influenced the predator-prey interaction. in a laboratory stream, smallmouth bass (Micropterus dolornieu) ate similar numbers sf equal-sized 0. rustr'cus and 0. sanborni, but when sizes mimicked those in the field (i.e., 0. rusticus 4 mm > 0. sanborni), fewer (a. rusticus were eaten. Fish also reduced juvenile activity and behaviors whereas adult aggression increased the frequency of these risky responses. More affected by adult crayfish, 0. sanborni should suffer disproportional predation where adults and juveniles interact. Thus, fish predators should increase replacement rates and adult aggression s h o~~l d further accelerate this process. Manifested through crayfish size, both indirect and direct predator effects contribute to the replacement of 0. sanborni by 0. rusticus. Dans les cours d'eau de B'Ohio, l'kcrevisse Orconecies rusticus remplace 0. sanborni, et nous avsns examin6 la f a~o n dont la predation influe sur ce ph6nomGne. Bans une etude menee sur le terrain, les ecrevisses ktaient rares quand les poissons ktaient abondants, ce qui semble indiquer que Oes prgdateurs peuvent avoir un effet negatif sur la presence des crustac6s. Dans les experiences de laboratoire, nous avons examine les mecanismes qui sous-tendent ceKe relation inverse; plus precisement, nous avons 6tudie la falsm dont les espgces c9'6crevissesf l'agression par les adultes et l'hetkrog6n6it6 de I'habitat influent sur I'interaction entre predateurs et proies. Dans un cows d'eau artificiellement recr66 en Babsratoire, les achigans petite bouche (Micropterus dolomieu) mangeaient des nombres similaires de 0. rusticus et de 0. sanborni de taille egale, mais quand on reprsduisait ies tailles existant dam la nature 6c.-A-d. 0. rusticus rnesurant 4 m m > 0. sanborni), le nombre de 0. rusticus csnssmm6es etait infkrieur. Les psissons rkduisaient ainsi I'activite des juveniles et leurs comportements, tandis que I'agression par les adultes augmentait la frequence de ces reactions A risque. Bavantage affectge par ?'action des ecrevisses adultes, 0. sanborni doit subir une praatiom dioprsportionn6e quand les adultes et les juveniles sont en interaction. Ainsi, la prbdation par les poissons dsit accentuer le rernplacement d'une espgce par I'autre, et l'agression par les adultes doit acckl6rer ee processus. Par le biais de la taille des &revisses, les effets indirects et directs de la predation contribement au rernplacement de 0. sanborni par 0. rusticus.
Many populations of anadromous herring, (e.g., alewives Alosa pseudoharengus and blueback herring A. aestivalis, collectively referred to as river herring) are in decline. To help understand the various processes influencing their relative abundance, we studied juvenile river herring populations in 11 small, coastal Massachusetts systems. We examined diel and seasonal movements, variation in patterns of abundance, and relationships between juvenile river herring numbers and seven abiotic and biotic factors (stream discharge, pond temperature, habitat availability, pond transparency, pH, food availability, and spawning stock size). Seasonally, juvenile downstream migration peaked in early summer, and most juvenile river herring emigrated between 1200 and 1600 hours. Little or no emigration occurred in late summer when stream channels were often dewatered, although several streams experienced a smaller, more variable emigration peak in the fall. In univariate regressions, stream discharge, pond volume, surface area, depth, transparency, and pH were significantly related to variation in juvenile abundance across systems. Multiple regression models that integrated discharge, volume, and transparency, as well as multivariate models that included abiotic and biotic influences, trophic effects, and system size, explained 32–82% of the variability in juvenile abundance across systems. Thus, stream discharge, pond volume, transparency, pH, trophic effects, and system size contribute to heterogeneity across systems and may influence the abundance of these fish during freshwater residence. Increased understanding of the sources of heterogeneity in movement patterns and causes of variability in abundance across systems can help to implement more effective monitoring protocols, more informed land‐use decisions, and improved management of river herring.
1. Understanding the relationship between heterogeneity and biodiversity is an active focus of ecological research. Although habitat heterogeneity is conceptually linked to biodiversity, the amount and configuration of heterogeneity that maintains biodiversity within ecosystems is not well understood, especially for an entire stream network.2. Here, we tested alternative outcomes about how habitat alterations caused by beaver dams affected native fish biodiversity. Specifically, we quantified in-stream habitat and fish assemblages above and below all beaver dams (n = 15) and selected control sites (n = 9), adjacent to beaver dams, within an entire, low-gradient stream network (Fish Brook, MA, U.S.A.). 3. Beaver dams altered habitat within streams in four ways based on upstream versus downstream differences in stream width, depth, velocity and substratum. In general, habitat heterogeneity, measured using two indices, was greater at beaver dams than control sites. 4. The diversity and abundance of fish around beaver dams were positively related to habitat heterogeneity. Faster water and the coarser substratum below beaver dams increased the amount of fluvial habitat available to native fish. This alteration can be critical for fish with life histories that depend on flowing water and hard substrata. 5. In summary, within a stream network, beaver dams maintained fish biodiversity by altering in-stream habitat and increasing habitat heterogeneity. Understanding the relationship between habitat heterogeneity and biodiversity can advance basic freshwater ecology and provide science-based support for applied aquatic conservation.
Longitudinal connectivity is a fundamental characteristic of rivers that can be disrupted by natural and anthropogenic processes. Dams are significant disruptions to streams. Over 2,000,000 low-head dams (<7.6 m high) fragment United States rivers. Despite potential adverse impacts of these ubiquitous disturbances, the spatial impacts of low-head dams on geomorphology and ecology are largely untested. Progress for research and conservation is impaired by not knowing the magnitude of low-head dam impacts. Based on the geomorphic literature, we refined a methodology that allowed us to quantify the spatial extent of low-head dam impacts (herein dam footprint), assessed variation in dam footprints across low-head dams within a river network, and identified select aspects of the context of this variation. Wetted width, depth, and substrate size distributions upstream and downstream of six low-head dams within the Upper Neosho River, Kansas, United States of America were measured. Total dam footprints averaged 7.9 km (3.0–15.3 km) or 287 wetted widths (136–437 wetted widths). Estimates included both upstream (mean: 6.7 km or 243 wetted widths) and downstream footprints (mean: 1.2 km or 44 wetted widths). Altogether the six low-head dams impacted 47.3 km (about 17%) of the mainstem in the river network. Despite differences in age, size, location, and primary function, the sizes of geomorphic footprints of individual low-head dams in the Upper Neosho river network were relatively similar. The number of upstream dams and distance to upstream dams, but not dam height, affected the spatial extent of dam footprints. In summary, ubiquitous low-head dams individually and cumulatively altered lotic ecosystems. Both characteristics of individual dams and the context of neighboring dams affected low-head dam impacts within the river network. For these reasons, low-head dams require a different, more integrative, approach for research and management than the individualistic approach that has been applied to larger dams.
Telemetry has allowed researchers to document the upstream migrations of anadromous fish in freshwater. In many anadromous alosine telemetry studies, researchers use downstream movements (''fallback'') as a behavioral field bioassay for adverse tag effects. However, these downstream movements have not been uniformly reported or interpreted. We quantified movement trajectories of radio-tagged anadromous alewives (Alosa pseudoharengus) in the Ipswich River, Massachusetts (USA) and tested blood chemistry of tagged and untagged fish held 24 h. A diverse repertoire of movements was observed, which could be quantified using (a) direction of initial movements, (b) timing, and (c) characteristics of bouts of coupled upstream and downstream movements (e.g., direction, distance, duration, and speed). Because downstream movements of individual fish were almost always made in combination with upstream movements, these should be examined together. Several of the movement patterns described here could fall under the traditional definition of ''fallback'' but were not necessarily aberrant. Because superficially similar movements could have quite different interpretations, post-tagging trajectories need more precise definitions. The set of metrics we propose here will help quantify tag effects in the field, and provide the basis for a conceptual framework that helps define the complicated behaviors seen in telemetry studies on alewives and other fish in the field.
Most anadromous fish populations remain at low levels or are in decline despite substantial investments in restoration. We explore whether a resilience perspective (i.e., a different paradigm for understanding populations, communities, and ecosystems) is a viable alternative framework for anadromous fish restoration. Many life history traits have allowed anadromous fish to thrive in unimpacted ecosystems but have become contemporary curses as anthropogenic effects increase. This contradiction creates a significant conservation challenge but also makes these fish excellent candidates for a resilience approach. A resilience approach recognizes the need to maintain life history, population, and habitat characteristics that increase the ability of a population to withstand and recover from multiple disturbances. To evaluate whether a resilience approach represents a viable strategy for anadromous fish restoration, we review four issues: (1) how resilience theory can inform anadromous fish restoration, (2) how a resilience‐based approach is fundamentally different than extant anadromous fish restoration strategies, (3) ecological characteristics that historically benefited anadromous fish persistence, and (4) examples of how human impacts harm anadromous fish and how a resilience approach might produce more successful outcomes. We close by suggesting new research and restoration directions for implementation of a resilience‐based approach.
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