16 results on '"Noges, T."'
Search Results
2. Scientists’ Warning to Humanity: Rapid degradation of the world's large lakes
- Author
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Jenny, J, Anneville, O, Arnaud, F, Baulaz, Y, Bouffard, D, Domaizon, I, Bocaniov, S, Chevre, N, Dittrich, M, Dorioz, J, Dunlop, E, Dur, G, Guillard, J, Guinaldo, T, Jacquet, S, Jamoneau, A, Jawed, Z, Jeppesen, E, Krantzberg, G, Lenters, J, Leoni, B, Meybeck, M, Nava, V, Noges, T, Noges, P, Patelli, M, Pebbles, V, Perga, M, Rasconi, S, Ruetz, C, Rudstam, L, Salmaso, N, Sapna, S, Straile, D, Tammeorg, O, Twiss, M, Uzarski, D, Ventela, A, Vincent, W, Wilhelm, S, Wangberg, S, Weyhenmeyer, G, Jenny J. -P., Anneville O., Arnaud F., Baulaz Y., Bouffard D., Domaizon I., Bocaniov S. A., Chevre N., Dittrich M., Dorioz J. -M., Dunlop E. S., Dur G., Guillard J., Guinaldo T., Jacquet S., Jamoneau A., Jawed Z., Jeppesen E., Krantzberg G., Lenters J., Leoni B., Meybeck M., Nava V., Noges T., Noges P., Patelli M., Pebbles V., Perga M. -E., Rasconi S., Ruetz C. R., Rudstam L., Salmaso N., Sapna S., Straile D., Tammeorg O., Twiss M. R., Uzarski D. G., Ventela A. -M., Vincent W. F., Wilhelm S. W., Wangberg S. -A., Weyhenmeyer G. A., Jenny, J, Anneville, O, Arnaud, F, Baulaz, Y, Bouffard, D, Domaizon, I, Bocaniov, S, Chevre, N, Dittrich, M, Dorioz, J, Dunlop, E, Dur, G, Guillard, J, Guinaldo, T, Jacquet, S, Jamoneau, A, Jawed, Z, Jeppesen, E, Krantzberg, G, Lenters, J, Leoni, B, Meybeck, M, Nava, V, Noges, T, Noges, P, Patelli, M, Pebbles, V, Perga, M, Rasconi, S, Ruetz, C, Rudstam, L, Salmaso, N, Sapna, S, Straile, D, Tammeorg, O, Twiss, M, Uzarski, D, Ventela, A, Vincent, W, Wilhelm, S, Wangberg, S, Weyhenmeyer, G, Jenny J. -P., Anneville O., Arnaud F., Baulaz Y., Bouffard D., Domaizon I., Bocaniov S. A., Chevre N., Dittrich M., Dorioz J. -M., Dunlop E. S., Dur G., Guillard J., Guinaldo T., Jacquet S., Jamoneau A., Jawed Z., Jeppesen E., Krantzberg G., Lenters J., Leoni B., Meybeck M., Nava V., Noges T., Noges P., Patelli M., Pebbles V., Perga M. -E., Rasconi S., Ruetz C. R., Rudstam L., Salmaso N., Sapna S., Straile D., Tammeorg O., Twiss M. R., Uzarski D. G., Ventela A. -M., Vincent W. F., Wilhelm S. W., Wangberg S. -A., and Weyhenmeyer G. A.
- Abstract
Large lakes of the world are habitats for diverse species, including endemic taxa, and are valuable resources that provide humanity with many ecosystem services. They are also sentinels of global and local change, and recent studies in limnology and paleolimnology have demonstrated disturbing evidence of their collective degradation in terms of depletion of resources (water and food), rapid warming and loss of ice, destruction of habitats and ecosystems, loss of species, and accelerating pollution. Large lakes are particularly exposed to anthropogenic and climatic stressors. The Second Warning to Humanity provides a framework to assess the dangers now threatening the world's large lake ecosystems and to evaluate pathways of sustainable development that are more respectful of their ongoing provision of services. Here we review current and emerging threats to the large lakes of the world, including iconic examples of lake management failures and successes, from which we identify priorities and approaches for future conservation efforts. The review underscores the extent of lake resource degradation, which is a result of cumulative perturbation through time by long-term human impacts combined with other emerging stressors. Decades of degradation of large lakes have resulted in major challenges for restoration and management and a legacy of ecological and economic costs for future generations. Large lakes will require more intense conservation efforts in a warmer, increasingly populated world to achieve sustainable, high-quality waters. This Warning to Humanity is also an opportunity to highlight the value of a long-term lake observatory network to monitor and report on environmental changes in large lake ecosystems.
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- 2020
3. Impacts of multiple stressors on freshwater biota across spatial scales and ecosystems
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Birk, S., Chapman, D., Carvalho, L., Spears, B.M., Andersen, H.E., Argillier, C., Auer, S., Baattrup-Pedersen, A., Banin, L., Beklioglu, M., Bondar-Kunze, E., Borja, A., Branco, P., Bucak, T., Buijse, A.D., Cardoso, A.C., Couture, R.M., Cremona, F., Zwart, D. de, Feld, C.K., Ferreira, M.T., Feuchtmayr, H., Gessner, M.O., Gieswein, A., Globevnik, L., Graeber, D., Graf, W., Gutiérrez-Cánovas, C., Hanganu, J., Iskin, U., Järvinen, M., Jeppesen, E., Kotamäki, N., Kuijper, M., Lemm, J.U., Lu, S., Solheim, A.L., Mischke, U., Moe, S.J., Noges, P., Noges, T., Ormerod, S.J., Panagopoulos, Y., Phillips, G., Posthuma, L., Pouso, S., Prudhomme, C., Rankinen, K., Rasmussen, J.J., Richardson, J., Sagouis, A., Santos, J.M., Schäfer, R.B., Schinegger, R., Schmutz, S., Schneider, S.C., Schülting, L., Segurado, P., Stefanidis, K., Sures, B., Thackeray, S.J., Turunen, J., Uyarra, M.C., Venohr, M., Ohe, P.C. von der, Willby, N., Hering, D., Birk, S., Chapman, D., Carvalho, L., Spears, B.M., Andersen, H.E., Argillier, C., Auer, S., Baattrup-Pedersen, A., Banin, L., Beklioglu, M., Bondar-Kunze, E., Borja, A., Branco, P., Bucak, T., Buijse, A.D., Cardoso, A.C., Couture, R.M., Cremona, F., Zwart, D. de, Feld, C.K., Ferreira, M.T., Feuchtmayr, H., Gessner, M.O., Gieswein, A., Globevnik, L., Graeber, D., Graf, W., Gutiérrez-Cánovas, C., Hanganu, J., Iskin, U., Järvinen, M., Jeppesen, E., Kotamäki, N., Kuijper, M., Lemm, J.U., Lu, S., Solheim, A.L., Mischke, U., Moe, S.J., Noges, P., Noges, T., Ormerod, S.J., Panagopoulos, Y., Phillips, G., Posthuma, L., Pouso, S., Prudhomme, C., Rankinen, K., Rasmussen, J.J., Richardson, J., Sagouis, A., Santos, J.M., Schäfer, R.B., Schinegger, R., Schmutz, S., Schneider, S.C., Schülting, L., Segurado, P., Stefanidis, K., Sures, B., Thackeray, S.J., Turunen, J., Uyarra, M.C., Venohr, M., Ohe, P.C. von der, Willby, N., and Hering, D.
- Abstract
Contains fulltext : 228877pub.pdf (Publisher’s version ) (Closed access) Contains fulltext : 228877pos.pdf (Author’s version postprint ) (Open Access)
- Published
- 2020
4. Strength and uncertainty of phytoplankton metrics for assessing eutrophication impacts in lakes
- Author
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Carvalho, L., Poikane, S., Lyche Solheim, A., Phillips, G., Borics, G., Catalan, J., De Hoyos, C., Drakare, S., Dudley, B.J., Jarvinen, M., Laplace-Treyture, C., Maileht, K., McDonald, C., Mischke, U., Moe, J., Morabito, G., Noges, P., Noges, T., Ott, I., Pasztaleniec, A., Skjelbred, B., Thackeray, S.J., Carvalho, L., Poikane, S., Lyche Solheim, A., Phillips, G., Borics, G., Catalan, J., De Hoyos, C., Drakare, S., Dudley, B.J., Jarvinen, M., Laplace-Treyture, C., Maileht, K., McDonald, C., Mischke, U., Moe, J., Morabito, G., Noges, P., Noges, T., Ott, I., Pasztaleniec, A., Skjelbred, B., and Thackeray, S.J.
- Abstract
Phytoplankton constitutes a diverse array of short-lived organisms which derive their nutrients from the water column of lakes. These features make this community the most direct and earliest indicator of the impacts of changing nutrient conditions on lake ecosystems. It also makes them particularly suitable for measuring the success of restoration measures following reductions in nutrient loads. This paper integrates a large volume of work on a number of measures, or metrics, developed for using phytoplankton to assess the ecological status of European lakes, as required for the Water Framework Directive. It assesses the indicator strength of these metrics, specifically in relation to representing the impacts of eutrophication. It also examines how these measures vary naturally at different locations within a lake, as well as between lakes, and how much variability is associated with different replicate samples, different months within a year and between years. On the basis of this analysis, three of the strongest metrics (chlorophyll-a, phytoplankton trophic index (PTI), and cyanobacterial biovolume) are recommended for use as robust measures for assessing the ecological quality of lakes in relation to nutrient-enrichment pressures and a minimum recommended sampling frequency is provided for these three metrics.
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- 2013
5. Strength and uncertainty of phytoplankton metrics for assessing eutrophication impacts in lakes
- Author
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Carvalho, L., Poikane, S., Lyche Solheim, A., Phillips, G., Borics, G., Catalán, Jordi, de Hoyos, Caridad, Drakare, S., Dudley, B. J., Järvinen, M., Laplace-Treyture, C., Maileht, K., McDonald, C., Mischke, U., Moe, J., Morabito, G., Nõges, Peeter, Noges, T., Ott, I., Pasztaleniec, A., Skjelbred, B., Thackeray, S. J., Carvalho, L., Poikane, S., Lyche Solheim, A., Phillips, G., Borics, G., Catalán, Jordi, de Hoyos, Caridad, Drakare, S., Dudley, B. J., Järvinen, M., Laplace-Treyture, C., Maileht, K., McDonald, C., Mischke, U., Moe, J., Morabito, G., Nõges, Peeter, Noges, T., Ott, I., Pasztaleniec, A., Skjelbred, B., and Thackeray, S. J.
- Abstract
Phytoplankton constitutes a diverse array of short-lived organisms which derive their nutrients from the water column of lakes. These features make this community the most direct and earliest indicator of the impacts of changing nutrient conditions on lake ecosystems. It also makes them particularly suitable for measuring the success of restoration measures following reductions in nutrient loads. This paper integrates a large volume of work on a number of measures, or metrics, developed for using phytoplankton to assess the ecological status of European lakes, as required for the Water Framework Directive. It assesses the indicator strength of these metrics, specifically in relation to representing the impacts of eutrophication. It also examines how these measures vary naturally at different locations within a lake, as well as between lakes, and how much variability is associated with different replicate samples, different months within a year and between years. On the basis of this analysis, three of the strongest metrics (chlorophyll-a, phytoplankton trophic index (PTI), and cyanobacterial biovolume) are recommended for use as robust measures for assessing the ecological quality of lakes in relation to nutrient-enrichment pressures and a minimum recommended sampling frequency is provided for these three metrics.
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- 2012
6. Assessing ecological quality of shallow lakes: Does knowledge of transparency suffice?
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Peeters, E.T.H.M., Franken, R.J.M., Jeppesen, E., Moss, B., Becares, E., Hansson, L.A., Romo, S., Kairesalo, T., Gross, E.M., Donk, E. van, Noges, T., Irvine, K., Kornijow, R., Scheffer, M., Peeters, E.T.H.M., Franken, R.J.M., Jeppesen, E., Moss, B., Becares, E., Hansson, L.A., Romo, S., Kairesalo, T., Gross, E.M., Donk, E. van, Noges, T., Irvine, K., Kornijow, R., and Scheffer, M.
- Abstract
Item does not contain fulltext
- Published
- 2009
7. Changes in phytoplankton species composition and functional groups
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Straile, D, Adrian, R, Jankowski, T, Järvinen, M, Maberly, S, Noges, P, Noges, T, Weyhenmeyer, Gesa, Wilhelm, S, Straile, D, Adrian, R, Jankowski, T, Järvinen, M, Maberly, S, Noges, P, Noges, T, Weyhenmeyer, Gesa, and Wilhelm, S
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- 2005
8. The role of climate in shaping zooplankton communities of shallow lakes
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Gyllström, Mikael, Hansson, Lars-Anders, Jeppesen, E, Garcia-Criado, F, Gross, E, Irvine, K, Kairesalo, T, Kornijow, R, Miracle, MR, Nykänen, M, Noges, T, Romo, S, Stephen, D, van Donk, E, Moss, B, Gyllström, Mikael, Hansson, Lars-Anders, Jeppesen, E, Garcia-Criado, F, Gross, E, Irvine, K, Kairesalo, T, Kornijow, R, Miracle, MR, Nykänen, M, Noges, T, Romo, S, Stephen, D, van Donk, E, and Moss, B
- Abstract
We analyzed data from 81 shallow European lakes, which were sampled with standardized methods, for combined effects of climatic, physical, and chemical features of food-web interactions, with a specific focus on zooplankton biomass and community structure. Multiple-regression analysis showed that total phosphorus (TP) generally was the most important predictor of zooplankton biomass and community structure. Climate was the next most important predictor and acted mainly through its effect on pelagic zooplankton taxa. Benthic and plant-associated taxa (typically almost half the total zooplankton biomass) were, however, affected mainly by macrophyte coverage. Neither climate nor TP affected the relation between small and large taxa, and we found only a weak trend with increasing TP of increasing mean crustacean body mass. Dividing the data set into three climate zones revealed a pronounced difference in response to lake productivity between cold lakes, with long periods of ice cover, and the two warmer lake types. These ‘‘ice’’ lakes differed from the others with respect to the effect of TP on chlorophyll a, the zooplankton : chlorophyll a ratio, the chlorophyll a :TP ratio, and the proportion of cyclopoids in the copepod community. Our data suggest that bottom-up forces, such as nutrient concentration, are the most important predictors of zooplankton biomass. In addition, climate contributes significantly—possibly by affecting top-down regulation by fish—and may interact with productivity in determining the zooplankton standing biomass and community composition. Hence, the present study suggests that food-web dynamics are closely linked to climatic features.
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- 2005
9. Short-term coherence
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Livingstone, D, George, DG, Järvinen, M, Noges, P, Noges, T, Weyhenmeyer, Gesa, Livingstone, D, George, DG, Järvinen, M, Noges, P, Noges, T, and Weyhenmeyer, Gesa
- Published
- 2004
10. Zooplankton -- phytoplankton interactions in lakes Vortsjarv, Peipsi(Estonia) and Yaskhan (Turkmenia)
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Noges, T.
- Subjects
EUTROPHICATION - Abstract
Zooplankton-phytoplankton interactions have been studied in three shallow lakes of different trophic state. In strongly eutrophic, large and very shallow Lake Vortsjarv the grazing does not play a leading role in controlling phytoplankton production and its standing stock. Small-size zooplankton can not eat filamentous blue-greens. The nutrient regeneration by zooplankton has a weak impact on phytoplankton, the latter being limited rather by underwater light than by nutrient availability. In large moderately eutrophic Lake Peipsi the presence ofconcentrated zooplankton in the experimental vessel mostly stimulated steady-state phytoplankton growth and negative grazing values were measured. Most probably the nutrients (N, P), excreted by zooplanktonin grazing chamber stimulated the growth of larger phytoplankton which dominated because of heavy grazing pressure on edible forms. In Lake Peipsi phytoplankton seems to be nutrient-limited and heavily controlled by zooplankton community. In eutrophic, macrophyte-dominated Lake Yaskhan zooplankton in grazing chamber also mainly stimulated thegrowth of phytoplankton community which seemed to be nutrient-limited because of strong competition with macrophytes. [ABSTRACT FROM AUTHOR]
- Published
- 1997
- Full Text
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11. Zooplankton of Lake Peipsi-Pihkva in 1909-1987
- Author
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Maemets, A., Noges, T., and Timm, M.
- Abstract
164 taxa were identified in the net zooplankton of the pelagial of L. Peipsi-Pihkva in 1909-1987, including 3 species of protozoans, 74 species of rotifers, 58 species of cladocerans, 28 species of copepodsand 1 mollusc. One rotifer species, Ploesoma peipsiense Maemets et Kutikova, has been described as new for science here. The zooplankton of L. Peipsi-Pihkva is remarkably rich in species including rarities in Estonia: Limnosida frontosa, Drepanothrix dentata, Bythotrephes longimanus, B. cederstroemi etc. Due to its large surface area, L. Peipsi-Pihkva provides a large scale of biotopes of a diverse trophic state and humic content, which support species with different ecologicalrequirements. Most of the aquatory of the lake has lately been mesotrophic, favouring the coexistence of indicators of oligo- and mesotrophic state and species preferring a higher trophic state. The occurrece of 10 species of the genus Bosmina including B. berolinensis, B. gibbera, B. lilljeborgi, B. thersites and B. crassicornis, sparse in Estonian lakes, is the most noteworthy feature of the zooplankton of L. Peipsi-Pihkva. The coexistence of B. coregoni and B. berolinensis, B. gibbera, B. lilljeborgi etc. which were earlier regarded as subspecies of B. c. coregoni proves that they are different species producing usually no hybrids. The species composition was subjected to certain changes during the years under consideration. Larvae of Dreissena were first found in zooplankton in 1962. The oligo-mesotrophic indicator Holopedium gibberum occurred in the lake in 1909-1964, but was lacking in later samples. [ABSTRACT FROM AUTHOR]
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- 1996
12. Primary production of Lake Peipsi-Pihkva
- Author
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Noges, P., Jastremskij, V. V., and Noges, T.
- Abstract
Primary production (PP) in Lake Peipsi-Pihkva, the tripartite borderwaterbody between Estonia and Russia, was first measured in 1965-1966. Since 1970 there exists a continuous timeseries of monthly PP measurements from May to October. Detailed investigations of the seasonaland daily dynamics as well as the vertical distribution of PP were carried out in 1985-1987. The long-term average values of integral PP (PP{sub}int{end}) in Lakes Peipsi and Pihkva were equal (0.8 g C m{sup}-2{end} d{sup}-1{end}), although the values per cubic metre (PP{sub}max{end},) differed more than twofold and characterized L. Pihkva asa eutrophic lake and L. Peipsi as a transition type between meso- and eutrophic lakes. The years from 1973 to 1980, 1987 and 1991 were oflow productivity, while in 1971, 1983, 1988 and 1990 PP peaks occurred in both lakes. In the seasonal pattern PP{sub}int{end} had peaks in May and July. In June, after the spring bloom, PP as well as the chlorophyll a (Chl) and ATP content were low. The high Chl peak in autumn was probably built up by the degradation products of chlorophyll, as neither PP nor ATP increased. Seasonal changes in integral PP in L. peipsi could be well described R{sup}2{end} = 0.91) by an empiricalmodel relating PP{sub}int{end} to PP{sub}max{end}, Secchi depth (S) and total solar radiation (Q). In mixed conditions prevailing in bothlakes, PP was inhibited in the surface layer and its maximum was located at a depth of 0.25 ... 0.5 S. The threshold total solar radiation level for the onset of inhibition was between 1200 and 2000 kJ m{sup}-2{end} h{sup}-1{end} in May and July, and decreased to less than500 kJ m{sup}-2{end} h{sup}-1{end} in October. As a rule, inhibitionstarted in the morning at a higher irradiance than necessary for keeping it up during evening hours . When compared with PP{sub}max{end} , photosynthesis in the surface layer at noon was suppressed by 56 percent in May, by 45 percent in July and by 40 percent in October. [ABSTRACT FROM AUTHOR]
- Published
- 1996
13. Phytoplankton pigments and adenosine triphosphate (ATP) in Lake Peipsi-Pihkva
- Author
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Noges, T.
- Subjects
ECONOMIC seasonal variations - Abstract
The material for pigment analysis was collected 1-3 times a year from Lake Peipsi-Pihkva in 1983, 1987, 1988, 1991 and 1992-1995. Concentrations of chlorophyll a, b and c (Chla, Chlb, Chlc), pheopigment (Pheo) and adenosine triphosphate (ATP) were measured biweekly in 1985-1986. The mean of all Chla values was 20.2 mg m{sup}-1{end} (median 13.3 mg m{sup}-1{end} ) indicating the eutrophic state of the lake. Average Chlb, Chlc, Pheo and carotenoid (Car) contents were 3.7 mg m{sup}-3{end} , 4.1 mg m{sup}-3{end} 3 3.0 mg m{sup}- 3{end} and 4.8 mg m{sup}-3{end} , respectively. The average Chlb/Chla ratio was 22.9 percent, Chlc/Chla 23.4 percent, Pheo/Chla 38 percent, Car/Chla 37 percent and ATP/Chla 3 percent, the medians being 14.3, 13.6, 17.5, 39.4 and 1.9 percent, respectively. The proportion of Chla in phytoplankton biomass was 0.41 percent, median 0.32 percent. There were no significant differences in temperature, oxygen concentration, Chla, and ATP between the surface and bottom water; the lake was polymictic during the vegetation period. The Chla concentration had its first peak in May followed by a decrease in June and July. In late summer Chla increased again achieving its seasonal maximum in late autumn. The ATP concentration was the highest during spring and early summer, decreasing drastically in autumn together with the decline of primary production. ATP/Chla was the highest during the "clear water period" in June and early July, which coincided also with the high proportion of Chla in phytoplankton biomass. The highest Chla occurred in November (average 37.2 mg m{sup}- 3{end}) when Secchi transparency was the lowest (1.05 m). Concentrations of Chlb, Chlc and carotenoids were the highestin August, that of Pheo in June. Concentrations of Chla and other pigments were the lowest in the northern part of Lake Peipsi (mean 14.7mg m{sup}-3{end}, median 12.5 mg m{sup}-3{end} ) and the highest in the southern part of Lake Pihkva (mean 47.9 mg m{sup}- 3{end}, median16 [ABSTRACT FROM AUTHOR]
- Published
- 1996
14. General description of Lake Peipsi-Pihkva
- Author
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Laugaste, R., Lokk, S., Maemets, A., Jaani, A., Timm, T., Virro, T., Haberman, J., Noges, P., Starast, H., Pihu, E., and Noges, T.
- Subjects
FRESHWATER biology ,LIMNOLOGY - Abstract
Lake Peipsi-Pihkva (3555 km{sup}2{end} , mean depth 8.3 m), consisting of three parts, (L. Peipsi, L. Pihkva, L. Lammijarv) is located onthe border of Estonia and Russia. L. Peipsi belongs to unstratified eutrophic lakes with mesotrophic features, L. Lammijarv has some dyseutrophic features, while L. Pihkva is strongly eutrophic. The total annual nutrient load is 15.57 tons N km{sup}-2{end} and 327 kgP km{sup}-2{end} with 74 percent of N and 39 percent of P originating from agriculture. The mean concentrations of total N and P in the lake are 876 mg m{sup}-3{end} -3 and 46 mg m{sup}-3{end} , respectively, both being the highest in L. Pihkva and the lowest in the northern part of L. Peipsi. Average pH is 8.14 and Secchi disk transparency 1.63 m. Diatoms and blue-green algae prevail in phytoplankton biomass. The blue-greens Gloeotrichia echinulata and Aphanizomenon flos-aquae dominatein summer causing the water-blooms. The concentration of Chla was the lowest in the northern part of L. Peipsi (mean 14.7 mg m{sup}-3{end} ) and the highest in the southern part of L. Pihkva (mean 47.9 mg m{sup}-3{end} , median 16.3 mg m{sup}-3{end} ). An increase of Chla and decrease of Secchi depth could be noticed in 1983-1988, while in 1988-1994 the tendency was opposite. The long-term average primary production is 0.8 g C m{sup}-2{end} d{sup}-1{end} . Zooplankton is remarkably rich in species, the average biomass in the vegetative period being 2-3 g m{sup}-3{end} and production 22 g C m{sup}- 2{end}. The role of rotifers in production is 53 percent followed by that of cladocerans (30 percent), copepods (16 percent) and Dreissena polymorpha larvae (1 percent). The total count of bacteria is 1-9 million cells perml. Chironomus plumosus and Potamothrix hammoniensis are dominating in the profundal. The average abundance of macrozoobenthos (without big molluscs) 2617 ind. m{sup}-2{end} , and their biomass 12.34 g m{sup}-2{end} are considered to be the highest among the large lakes of Nort [ABSTRACT FROM AUTHOR]
- Published
- 1996
15. Scientists’ Warning to Humanity:Rapid degradation of the world's large lakes
- Author
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Jenny, Jean-Philippe, Anneville, Orlane, Arnaud, Fabien, Baulaz, Yoann, Bouffard, Damien, Domaizon, Isabelle, Bocaniov, Serghei A., Chevre, Nathalie, Dittrich, Maria, Dorioz, Jean-Marcel, Dunlop, Erin S., Dur, Gael, Guillard, Jean, Guinaldo, Thibault, Jacquet, Stephan, Jamoneau, Aurelien, Jawed, Zobia, Jeppesen, Erik, Krantzberg, Gail, Lenters, John, Leoni, Barbara, Meybeck, Michel, Nava, Veronica, Noges, Tiina, Noges, Peeter, Patelli, Martina, Pebbles, Victoria, Perga, Marie-Elodie, Rasconi, Serena, Ruetz, Carl R., Rudstam, Lars, Salmaso, Nico, Sapna, Sharma, Straile, Dietmar, Tammeorg, Olga, Twiss, Michael R., Uzarski, Donald G., Ventela, Anne-Mari, Vincent, Warwick F., Wilhelm, Steven W., Wangberg, Sten-Ake, Weyhenmeyer, Gesa A., Jenny, J, Anneville, O, Arnaud, F, Baulaz, Y, Bouffard, D, Domaizon, I, Bocaniov, S, Chevre, N, Dittrich, M, Dorioz, J, Dunlop, E, Dur, G, Guillard, J, Guinaldo, T, Jacquet, S, Jamoneau, A, Jawed, Z, Jeppesen, E, Krantzberg, G, Lenters, J, Leoni, B, Meybeck, M, Nava, V, Noges, T, Noges, P, Patelli, M, Pebbles, V, Perga, M, Rasconi, S, Ruetz, C, Rudstam, L, Salmaso, N, Sapna, S, Straile, D, Tammeorg, O, Twiss, M, Uzarski, D, Ventela, A, Vincent, W, Wilhelm, S, Wangberg, S, Weyhenmeyer, G, and Faculty of Biological and Environmental Sciences
- Subjects
MICROPLASTIC POLLUTION ,CLIMATE-CHANGE ,SEA-LAMPREY ,Large lakes ,Second Warning to Humanity, Large lakes, Global change, Biodiversity loss, Ecosystem services, Eutrophication ,Eutrophication ,ENDOCRINE DISRUPTORS ,PERSONAL CARE PRODUCTS ,ACIPENSER-FULVESCENS ,Biodiversity loss, Ecosystem services, Eutrophication, Global change, Large lakes, Second Warning to Humanity ,FRESH-WATER ECOSYSTEMS ,Second Warning to Humanity ,Biodiversity loss ,Ecosystem services ,SPATIAL-DISTRIBUTION ,LAURENTIAN GREAT-LAKES ,Global change ,LONG-TERM TRENDS ,1172 Environmental sciences - Abstract
Large lakes of the world are habitats for diverse species, including endemic taxa, and are valuable resources that provide humanity with many ecosystem services. They are also sentinels of global and local change, and recent studies in limnology and paleolimnology have demonstrated disturbing evidence of their collective degradation in terms of depletion of resources (water and food), rapid warming and loss of ice, destruction of habitats and ecosystems, loss of species, and accelerating pollution. Large lakes are particularly exposed to anthropogenic and climatic stressors. The Second Warning to Humanity provides a framework to assess the dangers now threatening the world's large lake ecosystems and to evaluate pathways of sustainable development that are more respectful of their ongoing provision of services. Here we review current and emerging threats to the large lakes of the world, including iconic examples of lake management failures and successes, from which we identify priorities and approaches for future conservation efforts. The review underscores the extent of lake resource degradation, which is a result of cumulative perturbation through time by long-term human impacts combined with other emerging stressors. Decades of degradation of large lakes have resulted in major challenges for restoration and management and a legacy of ecological and economic costs for future generations. Large lakes will require more intense conservation efforts in a warmer, increasingly populated world to achieve sustainable, high-quality waters. This Warning to Humanity is also an opportunity to highlight the value of a long-term lake observatory network to monitor and report on environmental changes in large lake ecosystems. (C) 2020 The Authors. Published by Elsevier B.V. on behalf of International Association for Great Lakes Research.
- Published
- 2020
16. A global database of lake surface temperatures collected by in situ and satellite methods from 1985-2009.
- Author
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Sharma S, Gray DK, Read JS, O'Reilly CM, Schneider P, Qudrat A, Gries C, Stefanoff S, Hampton SE, Hook S, Lenters JD, Livingstone DM, McIntyre PB, Adrian R, Allan MG, Anneville O, Arvola L, Austin J, Bailey J, Baron JS, Brookes J, Chen Y, Daly R, Dokulil M, Dong B, Ewing K, de Eyto E, Hamilton D, Havens K, Haydon S, Hetzenauer H, Heneberry J, Hetherington AL, Higgins SN, Hixson E, Izmest'eva LR, Jones BM, Kangur K, Kasprzak P, Köster O, Kraemer BM, Kumagai M, Kuusisto E, Leshkevich G, May L, MacIntyre S, Müller-Navarra D, Naumenko M, Noges P, Noges T, Niederhauser P, North RP, Paterson AM, Plisnier PD, Rigosi A, Rimmer A, Rogora M, Rudstam L, Rusak JA, Salmaso N, Samal NR, Schindler DE, Schladow G, Schmidt SR, Schultz T, Silow EA, Straile D, Teubner K, Verburg P, Voutilainen A, Watkinson A, Weyhenmeyer GA, Williamson CE, and Woo KH
- Abstract
Global environmental change has influenced lake surface temperatures, a key driver of ecosystem structure and function. Recent studies have suggested significant warming of water temperatures in individual lakes across many different regions around the world. However, the spatial and temporal coherence associated with the magnitude of these trends remains unclear. Thus, a global data set of water temperature is required to understand and synthesize global, long-term trends in surface water temperatures of inland bodies of water. We assembled a database of summer lake surface temperatures for 291 lakes collected in situ and/or by satellites for the period 1985-2009. In addition, corresponding climatic drivers (air temperatures, solar radiation, and cloud cover) and geomorphometric characteristics (latitude, longitude, elevation, lake surface area, maximum depth, mean depth, and volume) that influence lake surface temperatures were compiled for each lake. This unique dataset offers an invaluable baseline perspective on global-scale lake thermal conditions as environmental change continues.
- Published
- 2015
- Full Text
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