Reservoir design and operation: Effects on aquatic biota-a case study of planktonic copepods

Copepod assemblages from two cascade reservoirs were analyzed during two consecutive years. The upstream reservoir (Chavantes) is a storage system with a high water retention time (WRT of 400 days), and the downstream one (Salto Grande) is a run-of-river system with only 1. 5 days WRT. Copepod composition, richness, abundance, and diversity were correlated with the limnological variables and the hydrological and morphometric features. Standard methods were employed for zooplankton sampling and analysis (vertical 50-μm net hauls and counting under a stereomicroscope). Two hypotheses were postulated and confirmed through the data obtained: (1) compartmentalization is more pronounced in the storage reservoir and determines the differences in the copepod assemblage structure; and (2) the assemblages are more homogeneous in the run-of-river reservoir, where the abundance decreases because of the predominance of washout effects. For both reservoirs, the upstream zone is more distinctive. In addition, in the smaller reservoir the influence of the input from tributaries is stronger (turbid waters). Richness did not differ significantly among seasons, but abundance was higher in the run-of-river reservoir during summer. © 2012 Springer Science+Business Media Dordrecht.

A comunidade zooplanctônica em um canal de maré no estuário do rio Caeté, Bragança (Pará, Brasil)

Poucos são os estudos realizados sobre zooplâncton em estuários na região Bragantina do Estado do Pará. Este trabalho foi realizado em um canal de maré, denominado de Furo do Chato, próximo a localidade de Ajuruteua. Município de Bragança, no litoral do Estado do Pará, e teve por objetivo estudar a composição qualitativa e quantitativa do zooplâncton, bem como as variações sazonais em função das variáveis ambientais, Durante o período de agosto/96 a janeiro/97 foram feitas oito campanhas a cada três semanas, com obtenção de amostras a cada duas horas, durante 24 horas. O Furo do Chato é um canal de maré com forte influência costeira. Assim, a maior parte dos representantes do zooplâncton encontrados são de origem costeira. Além de componentes holoplanctônicos e meroplanctônicos, as amostras de zooplâncton no Furo do Chato apresentaram representantes da fauna bentônica. Dez filos foram identificados: Protozoa, Mollusca, Chordata, Annelida, Cnidaria, Arthropoda, Urochordata, Chaetognatha, Nematoda e Bryozoa. A classe Copepoda teve maior representatividade, tanto pela densidade, pela biomassa como Oela freqüência de ocorrência nas amostras. As categorias mais abundantes e frequentes (>40%) foram Pseudodiaptomus marshi, Acartia iilljeborgi, A. tonsa, Harpacticoida, Sagitta sp., Oiko pleura dioica, Cnidaria, lsopoda, zoeas de caranguejo, pós-larvas de camarão e alevinos de peixes. A abundâncias médias foram baixas (1,07 indiv./m³e 16,43 mg/m³). A comunidade do zooplâncton é mais abundante nos meses de transição do que no período seco A maiores abundâncias ocorreram em geral à noite e durante as marés de sizígia. Contudo, o ciclo diário de marés, a salinidade e as fases lunares não influenciaram a variabilidade do zooplâncton como um todo, mas apenas em algumas categorias isoladamente.

Variação espaço-temporal do zooplâncton no estuário do rio Quatipuru-Pará

A partir da hipótese de que a salinidade influencia fortemente a comunidade zooplanctônica, o objetivo deste trabalho é analisar a influência deste fator sobre essa comunidade no estuário do rio Quatipuru, Estado do Pará. Foram realizadas amostragens zooplanctônicas e de variáveis físicas e químicas da água ao longo do estuário, contemplando diferentes faixas de salinidade. As coletas foram realizadas em marés vazantes e enchentes. Os resultados mostraram que este estuário possui uma variação temporal de características física, química e biológica. A salinidade, em especial, sofreu variações decorrentes das mudanças de marés, bem como da variação sazonal da pluviosidade. A salinidade variou de 1,4 a 33,5 ups no período seco e de 0 a 17,9 ups no período chuvoso. Esta amplitude de salinidade possibilitou determinar para área diferentes condições hidrológicas (limnética, oligohalina, meso-polihalina e euhalina). Foram identificados 48 taxa, destacando os Copepoda como o grupo mais importante em termos quali-quantitativos, sendo adultos de Parvocalanus crassirostris, Pseudodiaptomus richardi, Acartia tonsa, Acartia lilljeborgi, Paracalanus quasimodo, Euterpina acutifrons e copepoditos os principais responsáveis pela sua dominância. Mollusca foi o segundo grupo dominante, onde véligeres de gastrópodes representaram 95% do total. A densidade total do zooplancton variou entre 993, 9 e 13254,7 Ind. m^-3 no verão e entre 944, 3 e 35908,8 Ind. m^-3 no inverno. As maiores abundância em maio e novembro foram em ocasião de maré vazante e enchente, respectivamente. Os baixos valores de diversidade e equitabilidade encontrados na faixa zero na condição de enchente mostram o predomínio de determinado grupo sobre os demais (larvas de Gastropoda). A maior diversidade e uniformidade da comunidade zooplanctônica ocorreram no verão. A comunidade zooplanctônica respondeu as variações de salinidade com espécies adaptadas aos maiores valores de salinidade na porção inferior do estuário, no verão, assim como espécies adaptadas as condições de mixohalinização na porção mais a montante, em maio. A maior abundância de copepoditos esteve associada negativamente com a salinidade, demonstrando que as espécies que estão recrutando os copepoditos são mais estuarinas verdadeiras do que costeiras. As análises de agrupamento e de componentes principais revelou grupos definidos, distribuídos em diferentes faixas de salinidade, este parâmetro sozinho explicou 56% (p=0,028) da variação da fauna no estuário do rio Quatipuru. A distribuição dos organismos, de uma maneira geral, esteve de acordo com a hipótese de que a salinidade influencia fortemente a comunidade zooplanctônica no sistema estuarino de Quatipuru - Pará.

Análise comparativa da dieta, seletividade alimentar e estrutura da ictiofauna, juvenis e espécies de pequeno porte, em lagoas marginais do reservatório de Rosana (Rio Paranapanema, SP/PR)

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)

Life history and DNA barcode of Oxyurella longicaudis (Birgei, 1910) (Cladocera, Anomopoda, Chydoridae)

Background: Cladocera is an important group of freshwater zooplankton, and the species plays an important role in energy transfer and in aquatic food webs. Oxyurella longicaudis is a Chydoridae species that has been recorded in North and South America. The aim of this study is to investigate the life cycle aspects of parthenogenetic females of O. longicaudis cultured in laboratory under controlled conditions: temperature (23 degrees C +/- 05 degrees C), photoperiod (12 h light/12 h dark), food supply, and reconstituted water.Results: Embryonic development duration (2.3 +/- 0.5 days), post-embryonic development (5.2 +/- 0.69 days), mean fecundity (two eggs female(-1) brood(-1)), total egg production (22.55 +/- 3.98 eggs), average longevity (58 days), and body growth of the species were recorded. We also report the first DNA barcode for O. longicaudis isolated in Brazil, which will allow for easy identification in future zooplankton community studies. The analysis shows a genetic divergence of around 7% between our Brazilian isolate and O. longicaudis isolates from Mexico.Conclusions: The time of embryonic and post-embryonic development of O. longicaudis was higher than that of the other species of the same family, which contributed to lower total egg production throughout its life cycle. The genetic divergence appears to be sufficient to classify the two isolates as different species.

Ecological and toxicological responses in a multistressor scenario: are monitoring programs showing the stressors or just showing stress? A case study in Brazil

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

Contribuição dos ovos de resistência de Cladocera (Crustacea: Branchiopoda) para a recolonização de ambientes lacustres temporários

Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)

Heterogeneidade espacial e temporal da comunidade zooplanctônica do sistema Cantareira, São Paulo, Brasil

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

Lipid biomarkers in surface sediments from an unusual coastal upwelling area from the SW Atlantic Ocean

The coastal upwelling off Cabo Frio (SE Brazilian coast, SEBC) represents an exception to the world`s oceans since the majority of the upwelling areas are located in eastern boundary current systems. Cabo Frio represents an interesting area for investigation due to its tight physical-biological interaction and the importance of the region as a major fishery area in the SEBC. We analyzed a suite of lipid biomarkers to apportion the main sources of organic matter in surface sediments of the continental shelf off Cabo Frio, comparing the area to non-upwelling regions off the SEBC (shelf break off Cabo Frio and continental shelf off Ubatuba). During spring and summer (the upwelling period), diatoms are probably the major sources of polyunsaturated fatty acids (PUFAs) and C-28 sterols in surface sediments from Cabo Frio continental shelf. Sediments sampled in winter showed, in contrast, lower relative abundance of PUFAs and higher stanol/stenol ratio values. In deeper regions off Cabo Frio, elevated concentrations of alkenones, 24-methylcholest-5,22E-dien-3 beta-ol and 24-ethylcholest-5-en-3 beta-ol during the spring may be produced by prymnesiophytes or cryptophytes and cyanobacteria, respectively. In Ubatuba, the C-27 and C-28 sterols are likely derived from omnivorous salps and nanoflagellates. At non-upwelling areas, despite the increase in biomarker concentrations during spring and summer, lower concentrations of PUFAs, phytol and algal sterols than in shelf areas off Cabo Frio suggest the importance of the upwelling system to the rapid transfer of organic carbon to surface sediments. Our results suggest that spatial and temporal variability in organic matter production and deposition merits consideration for constraining the carbon budgets in the coastal region off Cabo Frio. (C) 2008 Elsevier Ltd. All rights reserved.

Abundance of mesozooplankton in the western part of the Black Sea in summer 1998 during the National Monitoring Programme

The dataset is based on samples collected in the summer of 1998 in the Western Black Sea in front of Bulgaria coast. The whole dataset is composed of 69 samples (from 22 stations of National Monitoring Grid) with data of mesozooplankton species composition abundance and biomass. Samples were collected in discrete layers 0-10, 0-20, 0-50, 10-25, 25-50, 50-100 and from bottom up to the surface at depths depending on water column stratification and the thermocline depth. Zooplankton samples were collected with vertical closing Juday net,diameter - 36cm, mesh size 150 µm. Tows were performed from surface down to bottom meters depths in discrete layers. Samples were preserved by a 4% formaldehyde sea water buffered solution. Sampling volume was estimated by multiplying the mouth area with the wire length. Mesozooplankton abundance: The collected material was analysed using the method of Domov (1959). Samples were brought to volume of 25-30 ml depending upon zooplankton density and mixed intensively until all organisms were distributed randomly in the sample volume. After that 5 ml of sample was taken and poured in the counting chamber which is a rectangle form for taxomomic identification and count. Large (> 1 mm body length) and not abundant species were calculated in whole sample. Counting and measuring of organisms were made in the Dimov chamber under the stereomicroscope to the lowest taxon possible. Taxonomic identification was done at the Institute of Oceanology by Lyudmila Kamburska using the relevant taxonomic literature (Mordukhay-Boltovskoy, F.D. (Ed.). 1968, 1969,1972). Taxon-specific abundance: The collected material was analysed using the method of Domov (1959). Samples were brought to volume of 25-30 ml depending upon zooplankton density and mixed intensively until all organisms were distributed randomly in the sample volume. After that 5 ml of sample was taken and poured in the counting chamber which is a rectangle form for taxomomic identification and count. Copepods and Cladoceras were identified and enumerated; the other mesozooplankters were identified and enumerated at higher taxonomic level (commonly named as mesozooplankton groups). Large (> 1 mm body length) and not abundant species were calculated in whole sample. Counting and measuring of organisms were made in the Dimov chamber under the stereomicroscope to the lowest taxon possible. Taxonomic identification was done at the Institute of Oceanology by Lyudmila Kamburska using the relevant taxonomic literature (Mordukhay-Boltovskoy, F.D. (Ed.). 1968, 1969,1972).

Abundance of mesozooplankton in the western part of the Black Sea in summer 2001 during the National Monitoring Programme of the Bulgarian Institute of Oceanography

The dataset is based on samples collected in the summer of 2001 in the Western Black Sea in front of Bulgaria coast (transects at c. Kaliakra and c. Galata). The whole dataset is composed of 26 samples (from 10 stations of National Monitoring Grid) with data of mesozooplankton species composition abundance and biomass. Samples were collected in discrete layers 0-10, 10-20, 10-25, 25-50, 50-75, 75-90. Zooplankton samples were collected with vertical closing Juday net,diameter - 36cm, mesh size 150 µm. Tows were performed from surface down to bottom meters depths in discrete layers. Samples were preserved by a 4% formaldehyde sea water buffered solution. Sampling volume was estimated by multiplying the mouth area with the wire length. Mesozooplankton abundance: The collected material was analysed using the method of Domov (1959). Samples were brought to volume of 25-30 ml depending upon zooplankton density and mixed intensively until all organisms were distributed randomly in the sample volume. After that 5 ml of sample was taken and poured in the counting chamber which is a rectangle form for taxomomic identification and count. Large (> 1 mm body length) and not abundant species were calculated in whole sample. Counting and measuring of organisms were made in the Dimov chamber under the stereomicroscope to the lowest taxon possible. Taxonomic identification was done at the Institute of Oceanology by Lyudmila Kamburska and Kremena Stefanova using the relevant taxonomic literature (Mordukhay-Boltovskoy, F.D. (Ed.). 1968, 1969,1972). Taxon-specific abundance: The collected material was analysed using the method of Domov (1959). Samples were brought to volume of 25-30 ml depending upon zooplankton density and mixed intensively until all organisms were distributed randomly in the sample volume. After that 5 ml of sample was taken and poured in the counting chamber which is a rectangle form for taxomomic identification and count. Copepods and Cladoceras were identified and enumerated; the other mesozooplankters were identified and enumerated at higher taxonomic level (commonly named as mesozooplankton groups). Large (> 1 mm body length) and not abundant species were calculated in whole sample. Counting and measuring of organisms were made in the Dimov chamber under the stereomicroscope to the lowest taxon possible. Taxonomic identification was done at the Institute of Oceanology by Lyudmila Kamburska and Kremena Stefanova using the relevant taxonomic literature (Mordukhay-Boltovskoy, F.D. (Ed.). 1968, 1969,1972).

Abundance of mesozooplankton in the western part of the Black Sea in summer 2002 during the National Monitoring Programme

The dataset is based on samples collected in the summer of 2002 in the Western Black Sea in front of Bulgaria coast. The whole dataset is composed of 47 samples (from 19 stations of National Monitoring Grid) with data of mesozooplankton species composition abundance and biomass. Sampling for zooplankton was performed from bottom up to the surface at depths depending on water column stratification and the thermocline depth. Zooplankton samples were collected with vertical closing Juday net,diameter - 36cm, mesh size 150 µm. Tows were performed from surface down to bottom meters depths in discrete layers. Samples were preserved by a 4% formaldehyde sea water buffered solution. Sampling volume was estimated by multiplying the mouth area with the wire length. Mesozooplankton abundance: The collected material was analysed using the method of Domov (1959). Samples were brought to volume of 25-30 ml depending upon zooplankton density and mixed intensively until all organisms were distributed randomly in the sample volume. After that 5 ml of sample was taken and poured in the counting chamber which is a rectangle form for taxomomic identification and count. Large (> 1 mm body length) and not abundant species were calculated in whole sample. Counting and measuring of organisms were made in the Dimov chamber under the stereomicroscope to the lowest taxon possible. Taxonomic identification was done at the Institute of Oceanology by Lyudmila Kamburska using the relevant taxonomic literature (Mordukhay-Boltovskoy, F.D. (Ed.). 1968, 1969,1972). Taxon-specific abundance: The collected material was analysed using the method of Domov (1959). Samples were brought to volume of 25-30 ml depending upon zooplankton density and mixed intensively until all organisms were distributed randomly in the sample volume. After that 5 ml of sample was taken and poured in the counting chamber which is a rectangle form for taxomomic identification and count. Copepods and Cladoceras were identified and enumerated; the other mesozooplankters were identified and enumerated at higher taxonomic level (commonly named as mesozooplankton groups). Large (> 1 mm body length) and not abundant species were calculated in whole sample. Counting and measuring of organisms were made in the Dimov chamber under the stereomicroscope to the lowest taxon possible. Taxonomic identification was done at the Institute of Oceanology by Lyudmila Kamburska using the relevant taxonomic literature (Mordukhay-Boltovskoy, F.D. (Ed.). 1968, 1969,1972).

Pteropod sedimentation at AWI HAUSGARTEN central station HGIV from 2000 to 2012

Pteropods are an important component of the zooplankton community and hence of the food web in the Fram Strait. They have a calcareous (aragonite) shell and are thus sensitive in particular to the effects of the increasing CO2 concentration in the atmosphere and the associated changes of pH and temperature in the ocean. In the eastern Fram Strait, two species of thecosome pteropods occur, the cold water-adapted Limacina helicina and the subarctic boreal species Limacina retroversa. Both species were regularly observed in year-round moored sediment traps at ~ 200-300 m depth in the deep-sea long-term observatory HAUSGARTEN (79°N, 4°E). The flux of all pteropods found in the trap samples varied from < 20 to ~ 870 specimen/m**2/d in the years 2000-2009, being lower during the period 2000-2006. At the beginning of the time series, pteropods were dominated by the cold-water-adapted L. helicina, whereas the subarctic boreal L. retroversa was only occasionally found in large quantities (> 50/m**2/d). This picture completely changed after 2005/6 when L. retroversa became dominant and total pteropod numbers in the trap samples increased significantly. Concomitant to this shift in species composition, a warming event occurred in 2005/6 and persisted until the end of the study in 2009, despite a slight cooling in the upper water layer after 2007/8. Sedimentation of pteropods showed a strong seasonality, with elevated fluxes of L. helicina from August to November. Numbers of L. retroversa usually increased later, during September/October, with a maximum at the end of the season during December/January. In terms of carbonate export, aragonite shells of pteropods contributed with 11-77% to the annual total CaCO3 flux in Fram Strait. The highest share was found in the period 2007 to 2009, predominantly during sedimentation events at the end of the year. Results obtained by sediment traps occasionally installed on a benthic lander revealed that pteropods also arrive at the seafloor (~ 2550 m) almost simultaneous with their occurrence in the shallower traps. This indicates a rapid downward transport of calcareous shells, which provides food particles for the deep-sea benthos during winter when other production in the upper water column is shut down. The results of our study highlight the great importance of pteropods for the biological carbon pump as well as for the carbonate system in Fram Strait at present, and indicate modifications within the zooplankton community. The results further emphasize the importance of long-term investigation to disclose such changes.

Ice and chlorophyll a concentration and mesozooplankton characteristics during two 'On Thin Ice' cruises, northern Svalbard waters

The spatial variation in mesozooplankton biomass, abundance and species composition in relation to oceanography was studied in different climatic regimes (warm Atlantic vs. cold Arctic) in northern Svalbard waters. Relationships between the zooplankton community and various environmental factors (salinity, temperature, sampling depth, bottom depth, sea-ice concentrations, algal biomass and bloom stage) were established using multivariate statistics. Our study demonstrated that variability in the physical environment around Svalbard had measurable effect on the pelagic ecosystem. Differences in bottom depth and temperature-salinity best explained more than 40% of the horizontal variability in mesozooplankton biomass (DM/m**2) after adjusting for seasonal variability. Salinity and temperature also explained much (21% and 15%, respectively) of the variability in mesozooplankton vertical distribution (ind./m**3) in August. Algal bloom stage, chlorophyll-a biomass, and depth stratum accounted for additional 17% of the overall variability structuring vertical zooplankton distribution. Three main zooplankton communities were identified, including Atlantic species Fritillaria borealis, Oithona atlantica, Calanus finmarchicus, Themisto abyssorum and Aglantha digitale; Arctic species Calanus glacialis, Gammarus wilkitzkii, Mertensia ovum and Sagitta elegans; and deeper-water inhabitants Paraeuchaeta spp., Spinocalanus spp., Aetideopsis minor, Mormonilla minor, Scolecithricella minor, Gaetanus (Gaidius) tenuispinus, Ostracoda, Scaphocalanus brevicornis and Triconia borealis. Zooplankton biomasses in Atlantic- and Arctic-dominated water masses were similar, but biological ''hot-spots'' were associated with Arctic communities.

(Table 1) Biovolume variations of cyanobacteria and total phytoplankton in the Frederiksborg Slotsso, Denmark

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 Slotsso) 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 among Phragmites australis and 11,000 ind/l between Polygonum amphibium stands), whereas the dominant species in the pelagic were Daphnia (up to 67 ind/l) and Cyclops (41 ind/l). 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.