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  • 1
    ISSN: 1365-2427
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: 1. This synthesis examines 35 long-term (5–35 years, mean: 16 years) lake re-oligotrophication studies. It covers lakes ranging from shallow (mean depth 〈5 m and/or polymictic) to deep (mean depth up to 177 m), oligotrophic to hypertrophic (summer mean total phosphorus concentration from 7.5 to 3500 μg L−1 before loading reduction), subtropical to temperate (latitude: 28–65°), and lowland to upland (altitude: 0–481 m). Shallow north-temperate lakes were most abundant.2. Reduction of external total phosphorus (TP) loading resulted in lower in-lake TP concentration, lower chlorophyll a (chl a) concentration and higher Secchi depth in most lakes. Internal loading delayed the recovery, but in most lakes a new equilibrium for TP was reached after 10–15 years, which was only marginally influenced by the hydraulic retention time of the lakes. With decreasing TP concentration, the concentration of soluble reactive phosphorus (SRP) also declined substantially.3. Decreases (if any) in total nitrogen (TN) loading were lower than for TP in most lakes. As a result, the TN : TP ratio in lake water increased in 80% of the lakes. In lakes where the TN loading was reduced, the annual mean in-lake TN concentration responded rapidly. Concentrations largely followed predictions derived from an empirical model developed earlier for Danish lakes, which includes external TN loading, hydraulic retention time and mean depth as explanatory variables.4. Phytoplankton clearly responded to reduced nutrient loading, mainly reflecting declining TP concentrations. Declines in phytoplankton biomass were accompanied by shifts in community structure. In deep lakes, chrysophytes and dinophytes assumed greater importance at the expense of cyanobacteria. Diatoms, cryptophytes and chrysophytes became more dominant in shallow lakes, while no significant change was seen for cyanobacteria.5. The observed declines in phytoplankton biomass and chl a may have been further augmented by enhanced zooplankton grazing, as indicated by increases in the zooplankton : phytoplankton biomass ratio and declines in the chl a : TP ratio at a summer mean TP concentration of 〈100–150 μg L−1. This effect was strongest in shallow lakes. This implies potentially higher rates of zooplankton grazing and may be ascribed to the observed large changes in fish community structure and biomass with decreasing TP contribution. In 82% of the lakes for which data on fish are available, fish biomass declined with TP. The percentage of piscivores increased in 80% of those lakes and often a shift occurred towards dominance by fish species characteristic of less eutrophic waters.6. Data on macrophytes were available only for a small subsample of lakes. In several of those lakes, abundance, coverage, plant volume inhabited or depth distribution of submerged macrophytes increased during oligotrophication, but in others no changes were observed despite greater water clarity.7. Recovery of lakes after nutrient loading reduction may be confounded by concomitant environmental changes such as global warming. However, effects of global change are likely to run counter to reductions in nutrient loading rather than reinforcing re-oligotrophication.
    Type of Medium: Electronic Resource
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  • 2
    Publication Date: 2024-04-23
    Description: Water isotopes (δ²H and δ¹⁸O) were analyzed in samples from a range of relatively small lakes and ponds in northeastern Germany. The sampled water bodies are not connected to major river systems but are either fed by groundwater or small creeks. Water chemical parameters were determined in-situ with a portable WTW-multiparameter probe. Water samples were collected in different seasons of the years 2020, 2022 and 2023. Here, composite samples were taken from the lake centers with a Ruttner Water Sampler in 2 m intervals from the lake surface to bottom. In some cases, only a surface sample was collected from 50 cm depth using a pipette. Samples were filtered and transferred into a measurement vial. Stable isotope analysis was conducted at IGB Berlin, using a Picarro L2130-i cavity ring-down spectrometer. Measurement uncertainty was quantified to 〈0.5 ‰ for δ²H and 〈0.2 ‰ for δ¹⁸O. The data give information about the seasonal and spatial stable isotope variability at the sampled lacustrine systems.
    Keywords: Bottle, Ruttner; Calculated; Cavity ring-down spectroscopy (CRDS), L2130-i, Picarro Inc.; Chara_Seen; Chara Lakes; Conductivity, electrical; DATE/TIME; DEPTH, water; Depth, water, bottom/maximum; Depth, water, top/minimum; Depth of Secchi Disk; Dreetzsee; Dreetzsee, Germany; Dunkelsee; Dunkelsee, Germany; Event label; Germany; Giesenschlagsee_Middle; Giesenschlagsee_North; Giesenschlagsee_South; Giesenschlagsee Middle, Germany; Giesenschlagsee North, Germany; Giesenschlagsee South, Germany; Glambecksee; Glambecksee, Germany; Gottssee; Gottssee, Germany; Gr_Bodensee; Gr_Gollinsee; Gr_Griebchensee; Gr_Kronsee; Gr_Petznicksee; Gr_Tietzen; Gr_Weisser_See; Großer Bodensee, Germany; Großer Gollinsee, Germany; Großer Griebchensee, Germany; Großer Kronsee, Germany; Großer Petznicksee, Germany; Großer Tietzen, Germany; Großer Weißer See, Germany; Hinbergsee; Hinbergsee, Germany; Kl_Peetzigsee; Kleiner Peetzigsee, Germany; Krueselinsee; Krüselinsee, Germany; lakes; Latitude of event; Longitude of event; Oxygen, dissolved; Oxygen saturation; pH; ponds; Rohrhalmgrund; Rohrhalmgrund, Germany; RWS; Sabinensee; Sabinensee, Germany; SD; Secchi disk; Temperature, water; Warnitzsee; Warnitzsee, Germany; Waschsee; Waschsee, Germany; water isotopes; WTW probe, hand-held; Wuckersee; Wuckersee, Germany; δ18O, water; δ18O, water, standard deviation; δ Deuterium, water; δ Deuterium, water, standard deviation
    Type: Dataset
    Format: text/tab-separated-values, 628 data points
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  • 3
    Publication Date: 2024-04-23
    Description: Water isotopes (δ2H and δ18O) were analyzed in samples collected in lakes associated to major riverine systems in northeastern Germany throughout 2020. The dataset is derived from water samples taken at a) lake shores (sampled in March and July 2020); b) buoys temporarily installed in deep parts of the lake (sampled monthly from March to October 2020); c) multiple spatially distributed spots in four selected lakes (in September 2020); d) the outflow of Müggelsee (sampled biweekly from March 2020 to January 2021). At shores, water was sampled with a pipette from 40-60 cm below water surface and directly transferred into a measurement vial, while at buoys a Limnos water sampler was used to obtain samples from 1 m below surface. Isotope analysis was conducted at IGB Berlin, using a Picarro L2130-i cavity ring-down spectrometer. The data give information about the seasonal isotope amplitude in the sampled lakes and about spatial isotope variability in different branches of the associated riverine systems.
    Keywords: CONNECT; Connectivity and synchronization of lake ecosystems in space and time; Dahme; GEPRIS_418096356; Havel; Influence of environmental factors onto the hydrogen isotopic signature of aquatic plants; Müritz; Spree; Ucker; δ18O; δ2H
    Type: Dataset
    Format: application/zip, 6 datasets
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  • 4
    Publication Date: 2020-09-02
    Description: Until the 1990s, herbivory on aquatic vascular plants was considered to be of minor importance, and the predominant view was that freshwater and marine macrophytes did not take part in the food web: their primary fate was the detritivorous pathway. In the last 25 years, a substantial body of evidence has developed that shows that herbivory is an important factor in the ecology of vascular macrophytes across freshwater and marine habitats. Herbivores remove on average 40–48% of plant biomass in freshwater and marine ecosystems, which is typically 5–10 times greater than reported for terrestrial ecosystems. This may be explained by the lower C:N stoichiometry found in submerged plants. Herbivores affect plant abundance and species composition by grazing and bioturbation and therewith alter the functioning of aquatic ecosystems, including biogeochemical cycling, carbon stocks and primary production, transport of nutrients and propagules across ecosystem boundaries, habitat for other organisms and the level of shoreline protection by macrophyte beds. With ongoing global environmental change, herbivore impacts are predicted to increase. There are pressing needs to improve our management of undesirable herbivore impacts on macrophytes (e.g. leading to an ecosystem collapse), and the conflicts between people associated with the impacts of charismatic mega-herbivores. While simultaneously, the long-term future of maintaining both viable herbivore populations and plant beds should be addressed, as both belong in complete ecosystems and have co-evolved in these long before the increasing influence of man. Better integration of the freshwater, marine, and terrestrial herbivory literatures would greatly benefit future research efforts.
    Type: Article , PeerReviewed
    Format: text
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