Echosounding observations of coverage,height, PVI,and biomass of submerged macrophytes in the southern basin of Lake Biwa,Japan

We have developed a procedure to process echosounding data to map the distribution of submerged aquatic macrophytes in the southern basin of Lake Biwa, a water body that has a surface area of 52 km² and a mean depth of 4 m. Echosounding observations were made along 27 transect lines spaced at 500-m intervals on August 4 and September 2 and 30, 2003. Quantitative vegetation data including percent coverage, mean vegetation height, and percent vegetation infestation were directly determined using image data from the echosounder recorded digitally on videotape. Based on the image data from an echosounder, a regression model was developed for estimating biomass of submerged macrophytes. The regression model using the total echo strength as the explanatory variable could reliably estimate macrophyte biomass up to 300 g m⁻². Distribution maps of macrophyte height and biomass suggest that the recent summer decline of submerged macrophytes started earlier in shallow areas (<3 m of depth) than deep areas (>4 m) in the southern basin of Lake Biwa.     

Above- and belowground competition between two submersed macrophytes

Several studies have shown that submerged macrophytes provide a refuge for zooplankton against fish predation, whereas the role of emergent and floating-leaved species, which are often dominant in eutrophic turbid lakes, is far less investigated. Zooplankton density in open water and amongst emergent and floating-leaved vegetation was monitored in a small, eutrophic lake (Frederiksborg Slotssø) in Denmark during July–October 2006. Emergent and floating-leaved macrophytes harboured significantly higher densities of pelagic as well as plant-associated zooplankton species, compared to the open water, even during periods where the predation pressure was presumably high (during the recruitment of 0+ fish fry). Zooplankton abundance in open water and among vegetation exhibited low values in July and peaked in August. Bosmina and Ceriodaphnia dominated the zooplankton community in the littoral vegetated areas (up to 4,400 ind l^?1 among Phragmites australis and 11,000 ind l^?1 between Polygonum amphibium stands), whereas the dominant species in the pelagic were Daphnia (up to 67 ind l^?1) and Cyclops (41 ind l^?1). The zooplankton density pattern observed was probably a consequence of concomitant modifications in the predation pressure, refuge availability and concentration of cyanobacteria in the lake. It is suggested that emergent and floating-leaved macrophytes may play an important role in enhancing water clarity due to increased grazing pressure by zooplankton migrating into the plant stands. As a consequence, especially in turbid lakes, the ecological role of these functional types of vegetation, and not merely that of submerged macrophyte species, should be taken into consideration.     

Potential effects of spawning habitat changes on the segregation of northern pike (<Emphasis Type="Italic">Esox lucius</Emphasis>) and muskellunge (<Emphasis Type="Italic">E</Emphasis>. <Emphasis Type="Italic">masquinongy</Emphasis>) in the Upper St. Lawrence River

Changes in spawning habitat of northern pike (Esox lucius) may affect their segregation from and coexistence with the closely related muskellunge (E. masquinongy). We estimated the areal coverage of robust and shallow emergent vegetation in three shared-spawning bays in the Upper St. Lawrence River from aerial photographs taken from 1948 to 2003. Robust emergent vegetation (e.g., cattail) increased in coverage by 155–241% while shallow emergents (sedges) decreased by 46–96%. The loss of sedges, an important northern pike-spawning habitat, may facilitate greater spawning overlap in offshore-submersed aquatic vegetation within bay habitats used by muskellunge. Development rates and characteristics of northern pike and muskellunge eggs and larvae were compared to better understand the implications of greater spawning overlap. Northern pike eggs developed faster than muskellunge eggs at temperatures of 4.7–19°C, and adhesive eggs and the presence of adhesive papillae were present in both species. Equations were used to predict degree-day requirements for hatching and swim-up in three habitats (shallow emergents, bay, and offshore shoal) along a temperature gradient. Northern pike required more estimated degree days to reach hatching in bay and offshore shoal habitat relative to shallow emergent habitat due to cooler temperatures. Significant spawning overlap is known to occur within bay habitats, but poor success of northern pike in deep bay habitats and overall reductions in abundance are hypothesized to currently buffer muskellunge from potential negative interactions between these species. Guest editors: J. M. Farrell, C. Skov, M. Mingelbier, T. Margenau & J. E. Cooper International Pike Symposium: Merging Knowledge of Ecology, Biology, and Management for a Circumpolar Species     

Eelgrass,Zostera marina,as essential fish habitat for young‐of‐the‐year winter flounder,Pseudopleuronectes americanus (Walbaum, 1792) in Maine estuaries

Distribution and density by habitat for age‐0, young‐of‐the‐year (YOY) winter flounder, Pseudopleuronectes americanus (Walbaum, 1792), were compared for two Maine estuaries to help define essential fish habitat for this life history stage. Two estuaries (Weskeag River and Penobscot Bay) along Mid‐coast Maine were sampled monthly with daytime 1.0 m² fixed‐frame throw traps around neap low tide, May–December over two consecutive years (2003–2004). Both eelgrass and adjacent sand/mud (20–60 cm deep) were randomly sampled with equal effort (4–12 samples per month) at two sites in both the Weskeag River and Penobscot Bay. Significantly higher densities of YOY winter flounder (2–9 cm TL) occurred in eelgrass relative to sand/mud. Density increased significantly in both habitats in 2004, and was higher in Penobscot Bay relative to the Weskeag River. YOY densities compared by eelgrass coverage within throw traps were found to be significantly higher in eelgrass that exceeded 30% coverage when compared with adjacent sand/mud areas and eelgrass coverage of 10–20%. YOY occurred in all months sampled (May–December); no density differences existed by month. These results indicate that very shallow (<0.6 m) eelgrass habitat is of key importance to YOY winter flounder in Maine estuaries and should be viewed as essential fish habitat (EFH) for this species and life stage.     

Spatial distribution of four freshwater fish species in different types of artificial European water bodies

Spatial distribution of young-of-the-year (YOY) and older roach, rudd, perch and ruffe was compared in two artificial lakes with macrophytes present and absent, and a valley reservoir, using gillnets. Almost all species of interest and both age categories preferred benthic habitats. The depth distribution in benthic habitats was relatively consistent across water bodies with the highest fish densities found in the shallowest depths. In the macrophyte-rich lake, YOY roach and perch utilize the 3–6 m benthic layer the most, whereas the fish preferred the 0–3 m benthic layer in the macrophyte-poor lake and reservoir. No differences were found in the depth distribution in pelagic habitats sampled by pelagic gillnets for YOY fish between the water bodies. Older fish usually utilized the surface water layer. Macrophytes influenced the depth distribution of YOY fish in benthic habitats, where their density maximum shifted deeper in the macrophyte-rich lake when fewer macrophytes were present in the shallowest benthic depth. In lakes, YOY fish utilized a wider depth spectrum due to the deeper thermocline when compared to the reservoir. Oxygen and temperature stratification are the main factors influencing fish distribution, whereas macrophyte presence particularly influences the depth distribution of YOY fish in benthic habitats.     

Abrupt shift from clear to turbid state in a shallow eutrophic, biomanipulated lake

Monitoring data were used to assess causes behind a recent shift from a clear-water to a turbid-water state in Lake Major, a 10 ha shallow lake in Hungary. In 1999–2000, fish manipulation was conducted in this hypertrophic lake. Reduced fish stock resulted in clearing water and the development of a dense (>80% coverage) submerged vegetation in 2005. During the recent abrupt shift, which occurred in 2007, submerged vegetation subsequently declined after a two-year period of clear water and abundant vegetation. An intense decay of macrophytes within the lake produced a rapid transition between the clear- and turbid-water states. During the clear-water state in 2005–2006, the most important variables predominantly correlating with macrophyte cover were Secchi transparency, temperature and TN, while TN, temperature, Secchi depth and chlorophyll-a were the most significant variables during the turbid-water state in 2007. Nitrogen may play a significant role in the cover of submerged macrophytes when TP is moderate. We argue that several factors in concert are necessary to initiate a shift. Water temperature likely has contributed to triggering shift through inter-year-dependent changes in cover of macrophytes, with fish recruitment having key roles in the dynamics of shallow lakes. Handling editor: Luigi Naselli-Flores     

Effects of waterfowl, large fish and periphyton on the spring growth of Potamogeton pectinatus L. in Lake Mogan, Turkey

It has been argued that waterfowl and fish may threaten growth of submerged macrophytes, especially in spring during the early growth phase when plant biomass is low. A small reduction of biomass at that time might delay growth or decrease subsequent productivity. We investigated the impact of waterfowl and large fish on the spring growth of fennel pondweed (Potamogeton pectinatusL.) by employing an exclosure experiment in the macrophyte-dominated clear-water Lake Mogan, Turkey. Birds and large fish were excluded from eight plots and both in situvegetation and macrophytes kept in pots were compared to eight open plots. Also, to investigate the effect of periphyton on plant growth it was removed from half of the pot plants. Exclusion of waterfowl and fish may decrease predation on macroinvertebrates, which in turn may affect periphyton, and macrophyte growth, why macroinvertebrates also were sampled. Waterfowl density was high (15–70 ind. of coot, Fulica atraL. ha^–1), abundance of submerged plants was also high with a surface coverage of 70–80%, and benthivorous fish were present, mainly tench, (Tinca tincaL.) and carp, (Cyprinus carpioL.). Exclusion of waterfowl and large fish did not significantly affect the spring growth of pondweed; neither plants growing in situnor kept in pots. Removal of periphyton from the plants in the pots did not favour growth. The density of macroinvertebrates was not affected by the exclusion of waterfowl and large fish, but it was positively related to aboveground biomass of fennel pondweed. We suggest that even if waterfowl and large fish are in high densities, their effect on fennel pondweed spring growth in lakes with abundant submerged vegetation, such as Lake Mogan, is low.     

Role of aquatic vegetation coverage on hypoxia and sunfish abundance in bays of a eutrophic reservoir

We studied the relation between aquatic vegetation coverage, summer dissolved oxygen and density of sunfishes (Lepomis spp.) in 10 shallow bays of a eutrophic reservoir. The bays ranged 5.2–15.7 ha in area, 0.6–1.3 m mean depth and 6–91% vegetation area coverage. Over the 10 bays mean dissolved oxygen concentration ranged 5.8–9.0 mg l^-1 in open water at least 20 m away from the vegetation, 0.8–8.1 mg l^-1 at the vegetation-water edge and 0.5–7.7 mg l^-1 in dense vegetation. Dissolved oxygen concentrations were inversely related to vegetation coverage. In open water, dissolved oxygen levels were consistently higher than 8 mg l^-1 when vegetation coverage was <20% of the bay and decreased to about 6 mg l^-1 at coverages near 80%. At the vegetation-water edge and within dense vegetation, dissolved oxygen levels dropped rapidly as vegetation coverage increased to 20% of the bay; when vegetation reached about 50% coverage, dissolved oxygen remained near 1.5 mg l^-1at the vegetation-water edge, but oxygen dropped below 1 mg l^-1in dense vegetation. Scarce vegetation harbored high Lepomis relative abundance (fish per m² of vegetation) whereas extensive vegetation harbored low relative abundance, both contributing little to absolute abundance (total fish in all vegetation); however, intermediate coverage offered a combination of mid-level fish relative abundance that together with mid-level plant coverage translated into high absolute fish abundance. We suggest this response is related to hypoxia, and where aquatic vegetation is extensive, the effect of vegetation on hypoxia and water quality in general may influence fish populations in a way similar to that often attributed to reduced foraging efficiency and increased competitive interactions.     

Habitat preferences and habitat restoration options for small‐bodied and juvenile fish species in the northern Murray–Darling Basin

Degradation of instream habitats in the northern Murray–Darling Basin has occurred through numerous stressors, including siltation, clearing of bankside vegetation, intrusion of livestock and impacts of pest species. A better understanding of habitat preferences of native fish species could help guide future instream habitat restoration actions. The habitat choices of seven native fish species, juvenile Murray Cod (Maccullochella peelii), juvenile Golden Perch (Macquaria ambigua ambigua), juvenile Silver Perch (Bidyanus bidyanus), adult Murray–Darling Rainbowfish (Melanotaenia fluviatilis), adult Olive Perchlet (Ambassis agassizii), adult Un‐specked Hardyhead (Craterocephalus stercusmuscarum fulvus) and adult carp gudgeons (Hypseleotris spp.) were tested in preference troughs to help inform potential habitat restoration actions in the Condamine catchment. Each species was given a choice between pair combinations of open sandy habitat, submerged macrophytes, emergent plants and rocky rubble. Habitat preferences varied between species. Murray Cod, Golden Perch, carp gudgeons and Olive Perchlets preferred structure over open sandy habitat, whilst juvenile Silver Perch, Un‐specked Hardyhead and Murray–Darling Rainbowfish did not avoid open sandy habitats. Juvenile Murray Cod preferred rocky rubble habitat over all other habitat choices. Use of complex rock piles to provide nursery habitat for Murray Cod populations is a potential restoration option. Introduction of rock could also benefit Golden Perch and carp gudgeons. Use of emergent plants, submerged macrophytes and rocky rubble for habitat restoration all appear to have merit for one or more species of small‐bodied fishes or juvenile stages of larger sized fishes. Rocky rubble or floating attached macrophytes could be viable restoration options in areas too turbid to establish submerged macrophytes. These habitat interventions would complement existing actions such as re‐snagging and provision of fish passage to assist with sustainable management of native fish populations.     

Biomanipulation as an Application of Food-Chain Theory: Constraints, Synthesis, and Recommendations for Temperate Lakes

The aim of this review is to identify problems, find general patterns, and extract recommendations for successful biomanipulation. An important conclusion is that the pelagic food chain from fish to algae may not be the only process affected by a biomanipulation. Instead, this process should be viewed as the “trigger” for secondary processes, such as establishment of submerged macrophytes, reduced internal loading of nutrients, and reduced resuspension of particles from the sediment. However, fish reduction also leads to a high recruitment of young-of-the-year (YOY) fish, which feed extensively on zooplankton. This expansion of YOY the first years after fish reduction is probably a major reason for less successful biomanipulations. Recent, large-scale biomanipulations have made it possible to update earlier recommendations regarding when, where, and how biomanipulation should be performed. More applicable recommendations include (1) the reduction in the biomass of planktivorous fish should be 75% or more; (2) the fish reduction should be performed efficiently and rapidly (within 1–3 years); (3) efforts should be made to reduce the number of benthic feeding fish; (4) the recruitment of YOY fish should be reduced; (5) the conditions for establishment of submerged macrophytes should be improved; and (6) the external input of nutrients (phosphorus and nitrogen) should be reduced as much as possible before the biomanipulation. Recent biomanipulations have shown that, correctly performed, the method also achieves results in large, relatively deep and eutrophic lakes, at least in a 5-year perspective. Although repeated measures may be necessary, the general conclusion is that biomanipulation is not only possible, but also a relatively inexpensive and attractive method for management of eutrophic lakes, and in particular as a follow-up measure to reduced nutrient load. Received 14 April 1998; accepted 31 August 1998     

The impact of intra- and interspecific interactions on young-of-the-year brook charr, in temperate lakes

The abundance, growth, spatial distribution, and feeding habits of five allopatric brook charr, Salvelinus fontinalis, populations (young-of-the-year, 0+ juveniles; YOY) were compared with five other populations living sympatrically with white sucker, Catostomus commersoni. The study was made in oligotrophic lakes of the Laurentian Shield (Québec, Canada) during three sampling periods in 1989 (July, August and September). The abundance of YOY charr was significantly higher in allopatric than in sympatric populations (45·3 ± 3·8 vs 3·4 ± 3·8 fish/lake caught in 1773 m² of gillnets; P<0·005). The mean length of YOY charr did not differ among allopatric and sympatric populations at each sampling period; July: 60·2 ± 3·0 vs 60·0 ± 4·5 mm; August: 61·9 ± 4·5 vs 63·2 ± 4·1 mm; September: 77·9 ± 8·7 vs 77·3 ± 7·8 mm respectively. Horizontal distribution of allopatric YOY charr did not differ from that of sympatric charr, 65% of the fish being captured within the first 2 m depth and the rest between 2 and 7 m depth. In contrast, the vertical distribution of allopatric YOY charr from both communities was significantly different; 81% of allopatric charr were captured within 0·5 m from the substrate compared to 64% for sympatric charr (P<0·001). Differences in vertical distribution of the fish were related to differences in diet; allopatric charr fed mainly on benthic and large planktonic organisms whereas sympatric charr fed less on these organisms and more on terrestrial organisms. In the lake where YOY charr were most abundant, individuals were spatially segregated into two groups; one ‘littoral’, found in 0–2m depth, and one ‘profundal’, found in 3–6 m depth. Growth, condition, and feeding habits of charr from the two groups were different, especially during the last sampling period.     

Cost of predation avoidance in young-of-year lake trout (Salvelinus namaycush): growth differential in sub-optimal habitats

Selection of habitat to avoid predation may affect the diet of young-of-year (YOY) lake trout (Salvelinus namaycush). YOY lake trout may use inshore habitat to avoid predation; this habitat may be sub-optimal for growth. To test this, YOY lake trout were penned in nearshore and offshore pelagic areas of two arctic lakes. Toolik Lake had a lake trout population, the other lake, S6, did not. YOY lake trout in Toolik Lake lost weight, but those offshore lost less weight. The YOY lake trout in Lake S6 gained weight and those offshore gained more weight. The primary diet item of the YOY lake trout in both lakes during this experiment was the zooplankter Diaptomis probilofensis; it was also one of the most abundant species. However, its density inshore in Lake S6 was similar to inshore and offshore densities in Toolik Lake. The increased availability of alternative zooplankton prey in Lake S6 may account for the growth differential of YOY lake trout in Lake S6 relative to Toolik Lake. Bioenergetic modeling of YOY lake trout suggests that growth similar to that in the offshore of Lake S6 would be necessary for successful recruitment. If the reduced zooplankton availability in Toolik Lake leads to the reduced growth of YOY in the inshore and offshore pelagic areas, then these fish will be more susceptable to winter predation/starvation. For YOY lake trout to survive in Toolik Lake they most likely shift to feeding on benthic prey before the end of their first summer. Dept. of Chemical Engineering     

Colonization and succession of submerged macrophytes in shallow Lake Væng during the first five years following fish manipulation

Colonization of submerged macrophytes and changes in species composition were studied in shallow Lake Væng during the first five years (1987–91) following fish manipulation in 1986–1988 and a resultant significant improvement in lake water transparency. No submerged macrophytes were present in the lake from 1981–1986, during which time the summer mean Secchi depth ranged from 0.6 and 0.8 m. From 1987 to 1990, Secchi depth increased from 0.9 m to 1.8 m and macrophyte coverage consequently increased (1 % of the lake area in 1987, 2% in 1988, 50% in 1989, 80% in 1990 and 90% in 1991). At the same time, the macrophytes became taller, and the weedbeds more dense. The macrophytes colonized from the exposed and deeper part of the lake towards the sheltered and more shallow part of the lake, a colonization pattern that was confirmed by transplantation experiments. The delay in colonization of the shallow parts may be caused by waterfowl grazing. The vegetation was initially dominated by Potamogeton crispus L., but there was a gradual change during 1988–1989 and Elodea canadensis Michx became exclusively dominant in 1990–1991.     

Fish manipulation as a lake restoration tool in shallow,eutrophic, temperate lakes 2: threshold levels,long-term stability and conclusions

In order to evaluate short-term and long-term effects of fish manipulation in shallow, eutrophic lakes, empirical studies on relationships between lake water concentration of total phosphorus (P) and the occurrence of phytoplankton, submerged macrophytes and fish in Danish lakes are combined with results from three whole-lake fish manipulation experiments. After removal of less than 80 per cent of the planktivorous fish stock a short-term trophic cascade was obtained in the nutrient regimes, where large cyanobacteria were not strongly dominant and persistent. In shallow Danish lakes cyanobacteria were the most often dominating phytoplankton class in the P-range between 200 and 1 000μg P l⁻¹. Long-term effects are suggested to be closely related to the ability of the lake to establish a permanent and wide distribution of submerged macrophytes and to create self-perpetuating increases in the ratio of piscivorous to planktivorous fish. The maximum depth at which submerged macrophytes occurred, decreased exponentially with increasing P concentration. Submerged macrophytes were absent in lakes>10 ha and with P levels above 250–300μg P l⁻¹, but still abundant in some lakes<3 ha at 650μg P l⁻¹. Lakes with high cover of submerged macrophytes showed higher transparencies than lakes with low cover aboveca. 50μg P l⁻¹. These results support the alternative stable state hypothesis (clear or turbid water stages). Planktivorous fish>10 cm numerically contributed more than 80 per cent of the total planktivorous and piscivorous fish (>10 cm) in the pelagical of lakes with concentrations above 100μg P l⁻¹. Below this threshold level the proportion of planktivores decreased markedly toca. 50 per cent at 22μg P l⁻¹. The extent of the shift in depth colonization of submerged macrophytes and fish stock composition in the three whole-lake fish manipulations follows closely the predictions from the relationships derived from the empirical study. We conclude that a long-term effect of a reduction in the density of planktivorous fish can be expected only when the external phosphorus loading is reduced to below 0.5–2.0 g m⁻² y⁻¹. This loading is equivalent to an in-lake summer concentration below 80–150μg P l⁻¹. Furthermore, fish manipulation as a restoration tool seems most efficient in shallow lakes.     

Dynamics of submerged macrophyte populations in response to biomanipulation

1. A 6‐year study (1992–97) of changes in submerged vegetation after biomanipulation was carried out in the eutrophicated Lake Finjasjön, Southern Sweden. Ten sites around the lake were revisited each year. At each site five samples of above‐ground biomass were taken at 10 cm water depth intervals. An investigation of the seed bank at the 10 sites, and a grazing experiment where birds and large fish were excluded was also conducted. 2. Between 1992 and 1996, in shallow areas (water depth < 3 m), vegetation cover increased from < 3 to 75% and above‐ground biomass from < 1 to 100 g DW m^–2. Mean outer water depth increased from 0.3 to 2.5 m. Elodea canadensis and Myriophyllum spicatum accounted for > 95% of the increase in biomass and plant cover. The following year (1997), however, cover and above‐ground biomass decreased, mainly attributable to the total disappearance of E. canadensis. Secchi depth increased after biomanipulation until 1996, but decreased again in 1997. 3. Total and mean number of submerged species increased after biomanipulation, probably as a result of the improved light climate. However, after the initial increase in species number there was a decrease during the following years, possibly attributed to competition from the rapidly expanding E. canadensis and M. spicatum. The lack of increase in species number after the disappearance of E. canadensis in 1997 implies that other factors also affected species richness. 4. A viable seed bank was not necessary for a rapid recolonization of submerged macrophytes, nor did grazing by waterfowl or fish delay the re‐colonization of submerged macrophytes. 5. Submerged macrophytes are capable of rapid recolonization if conditions improve, even in large lakes such as Finjasjön (11 km²). Species that spread by fragments will increase rapidly and probably outcompete other species. 6. The results indicate that after the initial Secchi depth increase, probably caused by high zooplankton densities, submerged vegetation further improved the light climate. The decrease in macrophyte biomass in 1997 may have caused the observed increase in phosphorus and chlorophyll a, and the decrease in Secchi depth. We suggest that nutrient competition from periphyton, attached to the macrophytes, may be an important factor in limiting phytoplankton production, although other factors (e.g. zooplankton grazing) are also of importance, especially as triggers for the shift to a clear‐water state.     

Abundance,size, and feeding success of larval shortnose suckers and Lost River suckers from different habitats of the littoral zone of Upper Klamath Lake

We examined near-shore habitat use by larval shortnose and Lost River suckers in the lower Williamson River and Upper Klamath Lake of south-central Oregon. Emergent macrophytes Scirpus, Sparganium and Polygonum supported significantly more, larger, and better-fed larvae than submergent macrophytes, woody vegetation, or open water. Abundance, size, and gut fullness were similar for sucker larvae collected from different emergent macropytes. During the larval period, there was no evidence of density dependant effects or habitat shifts. Ranked catch per unit effort data indicated potential predators also were more likely to use emergent macrophytes, but ordination indicated larvae and potential predators were differentially distributed along a vegetation structure-water depth gradient with larvae in shallow vegetated areas. Between-habitat differences appeared to be due to larval sucker selection for, or better survival in, emergent macrophytes, rather than differential access or exclusion from other habitats. The importance of emergent macrophytes appears to be related to increased foraging success and reduced predation. Because larvae in emergent macrophytes have a size and gut fullness advantage, the amount of emergent habitat could affect early survival. However, interannual differences in recruitment to the adult population may or may not be dependent on larval dynamics. Our results suggest larval sucker access to emergent macrophytes may be necessary, but perhaps not sufficient, for promoting good year class formation.     

Floating-leaved and emergent vegetation as habitat for fishes in a eutrophic temperate lake without submerged vegetation

Although submerged vegetation is considered to be the most suitable refuge against predators and form of foraging habitat for small fishes, submerged plants are often scarce or lacking in turbid eutrophic lakes. To evaluate emergent (Zizania latifolia) and floating-leaved (Nelumbo nucifera) vegetation as refuge areas against predators and as foraging habitats for small fishes, we investigated the fauna, abundance, and size distribution of the fish community as well as the abundance of possible prey for small fishes in beds of each vegetation type in a eutrophic shallow lake: Lake Teganuma in Japan. The leaves and stems of N. nucifera occupied an area 4.2 times larger than that of Z. latifolia. The high coverage of the water surface with plants most likely induced the hypoxia found in the N. nucifera bed. The diversity of small fishes was greater in the Z. latifolia bed with piscivorous fish than in the N. nucifera bed without piscivorous fish. The diversity of fish species in the vegetation was enhanced when there was an increased diversity of possible food sources rather than an absence of predators. Some aquatic insects of the same species had a much lower δ¹³C signature at hypoxic locations than at less hypoxic locations in the N. nucifera bed. Such site differences within a bed were not observed in the organisms caught in the Z. latifolia bed. The insects in hypoxic zones with a δ¹³C signature lower than ?30 ‰ were more depleted in ¹³C than the surface sediment or attached algae, suggesting that the larvae in the hypoxic zones incorporated the organic materials generated by methane-oxidizing bacteria. We can therefore conclude that floating-leaved vegetation, especially a N. nucifera bed, is not suitable as a replacement for submerged vegetation because of its potential to induce hypoxia, which can decrease the diversity of the fish fauna.     

Effects of aquatic vegetation type on denitrification

In a microcosm ¹⁵N enrichment experiment we tested the effect of floating vegetation (Lemna sp.) and submerged vegetation (Elodea nuttallii) on denitrification rates, and compared it to systems without macrophytes. Oxygen concentration, and thus photosynthesis, plays an important role in regulating denitrification rates and therefore the experiments were performed under dark as well as under light conditions. Denitrification rates differed widely between treatments, ranging from 2.8 to 20.9 ??mol N m^?2 h^?1, and were strongly affected by the type of macrophytes present. These differences may be explained by the effects of macrophytes on oxygen conditions. Highest denitrification rates were observed under a closed mat of floating macrophytes where oxygen concentrations were low. In the light, denitrification was inhibited by oxygen from photosynthesis by submerged macrophytes, and by benthic algae in the systems without macrophytes. However, in microcosms with floating vegetation there was no effect of light, as the closed mat of floating plants caused permanently dark conditions in the water column. Nitrate removal was dominated by plant uptake rather than denitrification, and did not differ between systems with submerged or floating plants.     

Influence of submerged vegetation and fish abundance on water clarity in peri-urban eutrophic ponds

Despite the presence of high nutrient concentrations, most ponds located around Brussels (Belgium) show a considerable variation in turbidity. The importance of submerged macrophytes in maintaining the clear-water state requires identification of the main factors determining macrophyte abundance and diversity in ponds and small lakes. In this study, the inter-relationships between submerged macrophyte cover, fish abundance and turbidity were investigated in 13 eutrophic peri-urban ponds. Along a turbidity gradient, vegetation switched from dominance by Stoneworts (Chara and Nitella spp.) in the clearest ponds, to dominance by Potamogeton pectinatus in ponds with a slightly lower water transparency. Despite the presence of both P. pectinatus and Stoneworts in each of the vegetated ponds, only one became dominant. Only a very low abundance (around 20%) of submerged vegetation was found in ponds of intermediate turbidity, while macrophytes were absent in turbid ponds. Multi- and univariate analysis showed a marked difference in chemical, physical and biological properties between ponds deliberately used for fish stocking and ponds that were not. Macrophyte cover was significantly negatively correlated with turbidity and plankti-benthivorous fish abundance. No such correlation was observed with piscivorous fish abundance, except for pike that were associated with a charophyte vegetation in the study ponds. The strong relationship found between fish abundance and turbidity, its negative effect on submerged vegetation cover, and the importance of submerged vegetation in controlling phytoplankton abundance, should be taken into account when selecting ponds for fish stocking. It also suggests that the study ponds have a good potential for ecological quality restoration by biomanipulation.     

Species richness,composition, and abundance of fish larvae and juveniles inhabiting natural and developed shorelines of a glacial Iowa lake

Synopsis Young-of-the-year fish communities in naturally vegetated sites were compared with those inhabiting nearby sites where lakeshore development (i.e., construction of homes, boat docks, and beaches) reduced nearshore macrophyte species richness and abundance. The study was conducted in a 2266 hectare, glacially formed, eutrophic lake in northwestern Iowa during the summers of 1987 and 1988. Study sites were divided into 3 depth zones, and fishes were collected by seining (0–1 m), plexiglass traps (1–2 m), and a nonclosing Tucker trawl (2–3 m). Species richness and total fish abundance were consistently greater in natural than in developed sites in both nearshore (0–1 m) and intermediate (1–2 m) depth zones, but differed little between natural and developed sites in the offshore (2–3 m) depth zone. Nearly 50% of the species sampled, including yellow perch Perca flavescens and bluegill Lepomis macrochirus, inhabited limnetic areas as larvae before migrating inshore as juveniles. Eighteen of the 20 fish species collected as juveniles were in greater abundance in natural than in developed sites. Smallmouth bass Micropterus dolomieui was the only game species consistently found in equal or greater abundance in developed sites. Within all sites, juvenile fishes were generally most abundant where macrophyte abundance and species richness were greatest. Findings from this study demonstrate the importance of nearshore aquatic vegetation to fishes during their first summer of life. If nearshore vegetation beds of lakes continue to be regarded as a nuisance and indiscriminately removed, important fish nursery habitat will be lost. The short-term result will likely be reduced year-class strength of vegetation-dependent species. More importantly, the long-term effects will be changes in fish community richness and composition which will, in turn, alter the lake's fishery.