Performance trade-off across a natural resource gradient

An important environmental factor determining both phytoplankton and zooplankton community composition is lake depth and thermal stratification. However, there is little information on how the interaction between zooplankton grazers and their phytoplankton food changes along an environmental gradient of lake depth. We contrasted resource availability for daphniid zooplankton populations living in two shallow, unstratified lakes and in two deep, stratified lakes using a novel growth bioassay. Stratified lakes had consistently lower resource richness than shallow unstratified lakes. To test whether resources were important in explaining differences in daphniid composition of shallow and deep lakes, we performed reciprocal transplant experiments. We raised daphniids typical of shallow (Ceriodaphnia reticulata) and deep (Daphnia dentifera) lakes in the resources from replicate shallow and deep lakes and monitored survival and reproduction. The two species exhibited a performance trade-off, measured by life table r and R ₀, across a gradient in natural resource richness. D. dentifera had higher relative fitness than C. reticulata when raised in the poorest resource environment from a deep lake. However, under richer resource conditions typical of shallow lakes, C. reticulata outperformed D. dentifera. We further created a gradient in natural resource quantity (by dilution) to test whether this trade-off in species relative fitness involved aspects of resource quality. No trade-off in species performance was evident across the dilution gradient, indicating that resource quality was important to the trade-off. We conclude that shifts in daphniid species composition along a gradient of lake depth involve an adaptive trade-off in ability to exploit rich versus poor resource quality. Received: 11 May 1998 / Accepted: 15 January 1999     

Salinity, depth and the structure and composition of microbial mats in continental Antarctic lakes

1. Lakes and ponds in the Larsemann Hills and Bølingen Islands (East‐Antarctica) were characterised by cyanobacteria‐dominated, benthic microbial mats. A 56‐lake dataset representing the limnological diversity among the more than 150 lakes and ponds in the region was developed to identify and quantify the abiotic conditions associated with cyanobacterial and diatom communities. 2. Limnological diversity in the lakes of the Larsemann Hills and Bølingen Islands was associated primarily with conductivity and conductivity‐related variables (concentrations of major ions and alkalinity), and variation in lake morphometry (depth, catchment and lake area). Low concentrations of pigments, phosphate, nitrogen, DOC and TOC in the water column of most lakes suggest extremely low water column productivity and hence high water clarity, and may thus contribute to the ecological success of benthic microbial mats in this region. 3. Benthic communities consisted of prostrate and sometimes finely laminated mats, flake mats, epilithic and interstitial microbial mats. Mat physiognomy and carotenoid/chlorophyll ratios were strongly related to lake depth, but not to conductivity. 4. Morphological‐taxonomic analyses revealed the presence of 26 diatom morphospecies and 33 cyanobacterial morphotypes. Mats of shallow lakes (interstitial and flake mats) and those of deeper lakes (prostrate mats) were characterised by different dominant cyanobacterial morphotypes. No relationship was found between the distribution of these morphotypes and conductivity. In contrast, variation in diatom species composition was strongly related to both lake depth and conductivity. Shallow ponds were mainly characterised by aerial diatoms (e.g. Diadesmis cf. perpusilla and Hantzschia spp.). In deep lakes, communities were dominated by Psammothidium abundans and Stauroforma inermis. Lakes with conductivities higher than ±1.5 mS cm^?1 became susceptible to freezing out of salts and hence pronounced conductivity fluctuations. In these lakes P. abundans and S. inermis were replaced by Amphora veneta. Stomatocysts were important only in shallow freshwater lakes. 5. Ice cover influenced microbial mat structure and composition both directly by physical disturbance in shallow lakes and by influencing light availability in deeper lakes, as well as indirectly by generating conductivity increases and promoting the development of seasonal anoxia. 6. The relationships between diatom species composition and conductivity, and diatom species composition and depth, were statistically significant. Transfer functions based on these data can therefore be used in paleolimnological reconstruction to infer changes in the precipitation–evaporation balance in continental Antarctic lakes.     

Assessing lake typologies and indicator fish species for Italian natural lakes using past fish richness and assemblages

In order to establish a fish-based typology of Italian lakes and identify possible reference and indicator fish species for each lake type, we analysed historical data on fish assemblages of all Italian natural lakes >0.5 km² from the period prior to the major decline in water quality in the 1950s. General linear regression models showed the ecoregion and lake altitude being the best predictors of fish species richness. The number of species was significantly higher in the Alpine than in the Mediterranean ecoregion. Among Alpine lakes, the number of fish species increased significantly with lake volume whilst decreased with altitude. In the Mediterranean lakes, none of the selected parameters was significant. Cluster analysis of fish assemblages (presence/absence) divided the lakes of the Alpine and Mediterranean ecoregions into four and two types, respectively. Pike (Esox lucius), rudd (Scardinius erythrophthalmus) and tench (Tinca tinca) were the main indicator species for the small and mostly shallow lakes in both the Alpine (Type 1) and Mediterranean (Type 6) ecoregions, minnow (Phoxinus phoxinus) for the alpine high altitude lakes (Type 2) and landlocked shad (Alosa fallax lacustris), European whitefish (Coregonus lavaretus) and burbot (Lota lota) for the large and very deep alpine lakes (Type 4). The European whitefish was the only indicator species for the deep Mediterranean lakes (Type 5). These species and associated fish assemblages may be useful indicators in future assessments of the ecological status of Italian lakes according to the European Directives (2000/60/EC and 2008/105/EC).     

Phytoplankton assemblages and steady state in deep and shallow eutrophic lakes – an approach to differentiate the habitat properties of Oscillatoriales

Ecological conditions and phytoplankton succession in two shallow hypertrophic lakes (Langer See and Melangsee) and a dimictic, eutrophic lake (Scharmützelsee) in a lake chain in Eastern Germany were analyzed from 1999 to 2001 in order to find situations of phytoplankton steady state assemblages and variables controlling the phytoplankton composition according to Reynolds et al. (2002). Long term background data from 1993 to 2001 suggest steady state conditions in shallow lakes, whereas the deep lake exhibited irregular fluctuations between various phytoplankton stages. Since the phytoplankton composition in the shallow lakes was similar in all the 3 years, it was highly predictable. Steady state conditions dominated by different species of Oscillatoriales were detected during the summer period 1999 and 2000 in Langer See and in Melangsee (see Mischke & Nixdorf, this volume). This dominant assemblage found in both lakes (group S ₁ acc. to Reynolds et al., 2002): Planktothrix agardhii (Gom.) Anagn. et Kom., Limnothrix redekei (Van Goor) Meffert, Pseudanabaena (Lauterb.) is typical in turbid mixed layers with highly light deficient conditions, but it is also regularly dominant in the dimictic lake Scharmützelsee as observed in 1999 and 2001 (Pseudanabaena limnetica (Lemm.) Kom. The Nostocales Cylindrospermopsis raciborskii (Wolz.) Seenayya et Subba Raju and Aphanizomenon gracile (Lemmerm.) Lemmerm. were important in the shallow lakes as well as in lake Scharmützelsee. Nevertheless, the occurrence of filamentous cyanobacteria in the dimictic lake was not regular and an unpredictable change in phytoplankton development was observed in 2000. It is discussed, whether this phenomenon of regular succession in shallow hypertrophic lakes is caused by adaptation to a resilient and an extreme environment or by the pool of species that can live or survive in that environment. This was checked through comparison of the depth of the mixed layer, the mean daily irradiance within this layer and the nutrient resources. Although the nutrient resources in both types of lake are near threshold levels, indicating growth inhibition by dissolved nutrients (DIP, DIN, TIC, DSi), the under water light supply seems to be the key factor favoring the dominance of filamentous cyanobacteria belonging to the functional group S ₁.     

Copepod communities in karstic mediterranean lakes along the eastern Adriatic coast

The copepod communities of karstic lakes along the eastern Adriatic coast were studied. Lakes were divided in several groups according to their morphology (deep, shallow, barrage and reservoirs), production (oligotrophic, mesotophic and eutrophic), and salinity of water: freshwater and brackish. Copidodiaptomus steueri, Eucyclops serrulatusand Macrocyclops albidus belong to the group that inhabited most of the lakes under the study, regardless of lake type. The shallow karstic lakes are usually inhabited by Thermocyclops dybowskii, T. oithonoides, Cyclops vicinus and Eudiaptomus padanus etruscus in freshwater biotopes, and Calanipedia aquaedulcis and Copidodiaptomus steueri in brackish biotopes. The last two species can also be found in deep karstic lakes with brackish water (Bacina lakes in the Neretva River delta). Species like Cyclops abyssorumcan be found in most deep freshwater lakes. Some Calanoida were recorded in only one lake, like Eudiaptomus transsylvanicusin the deep Lake Vrana on the island of Cres, or Eudiaptomus hadzici in the barrage Lake Visovac. Production of the lakes, expressed as copepod biomass, depends on lake trophy, and in some lakes also on hydrology and salinity. Most of the meso-eutrophic lakes in the study area had Calanoida dominating, while Cyclopoida dominated in some oligotrophic and eutrophic lakes as well.     

Increased risk of cyanobacterial blooms in northern high‐latitude lakes through climate warming and phosphorus enrichment

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Long‐term limnological changes in the Ecuadorian páramo: Comparing the ecological responses to climate warming of shallow waterbodies versus deep lakes

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Global co-occurrence of methanogenic archaea and methanotrophic bacteria in Microcystis aggregates

Global warming and eutrophication contribute to the worldwide increase in cyanobacterial blooms, and the level of cyanobacterial biomass is strongly associated with rises in methane emissions from surface lake waters. Hence, methane-metabolizing microorganisms may be important for modulating carbon flow in cyanobacterial blooms. Here, we surveyed methanogenic and methanotrophic communities associated with floating Microcystis aggregates in 10 lakes spanning four continents, through sequencing of 16S rRNA and functional marker genes. Methanogenic archaea (mainly Methanoregula and Methanosaeta) were detectable in 5 of the 10 lakes and constituted the majority (~50%–90%) of the archaeal community in these lakes. Three of the 10 lakes contained relatively more abundant methanotrophs than the other seven lakes, with the methanotrophic genera Methyloparacoccus, Crenothrix, and an uncultured species related to Methylobacter dominating and nearly exclusively found in each of those three lakes. These three are among the five lakes in which methanogens were observed. Operational taxonomic unit (OTU) richness and abundance of methanotrophs were strongly positively correlated with those of methanogens, suggesting that their activities may be coupled. These Microcystis-aggregate-associated methanotrophs may be responsible for a hitherto overlooked sink for methane in surface freshwaters, and their co-occurrence with methanogens sheds light on the methane cycle in cyanobacterial aggregates.     

Modelling lake cyanobacterial blooms: Disentangling the climate‐driven impacts of changing mixed depth and water temperature

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Submerged macrophytes as indicators of the ecological quality of lakes

1. We analysed submerged macrophyte communities from 300 Danish lakes to determine the efficacy of different species, maximum colonisation depth (C_max) of plants as well as coverage and plant volume inhabited (PVI) as indicators of eutrophication. 2. Most species occurred at a wide range of phosphorus and chlorophyll a (Chla) concentrations, but some species of isoetids (Lobelia, Isoëtes) and Potamogeton (Potamogeton gramineus, Potamogeton alpinus and Potamogeton filiformis) were mainly found at low nutrient concentrations and hence may be considered as indicators of nutrient poor conditions. However, species typically found in nutrient‐rich conditions, such as Elodea canadensis and Potamogeton pectinatus, were also found at total phosphorus (TP) <0.02 mg P L^?1 and Chla <5 μg L^?1 and therefore cannot be considered as reliable indicators of eutrophic conditions. 3. Submerged macrophyte coverage, PVI and the C_max were negatively correlated with TP and Chla. However, variability among lakes was high and no clear thresholds were observed. At TP between 0.03 and 0.07 mg P L^?1 plant coverage in shallow lakes ranged from nearly 0 to 100%, whilst at concentrations between 0.10 and 0.20 mg P L^?1 only 29% of the lakes had coverage >10%. C_max was found to be a useful indicator only in deep lakes with unvegetated areas in the deeper part, whereas the use of coverage was restricted to shallow lakes or shallow areas of deep lakes. 4. Overall, submerged macrophytes responded clearly to eutrophication, but the metrics investigated here showed no well‐defined thresholds. We developed a simple index based on species richness, presence of indicator species, coverage and C_max, which might be used to track major changes in macrophyte communities and for lake classification.