32 research outputs found

    Responses of Functional and Taxonomic Phytoplankton Diversity to Environmental Gradients in Subtropical and Tropical Reservoirs

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    Understanding the influence of environmental conditions on biodiversity is a major task in ecology. We investigated how phytoplankton taxonomic (TD) and functional (FD) diversities vary with environmental factors in eight subtropical and tropical reservoirs. We hypothesized that i) environmental variables affect phytoplankton TD and FD; ii) FD provides better relationships to environmental changes than TD, and; iii) indices based on biomass are better related to the environment than those based on identities. The relationships between phytoplankton diversities and environmental drivers were assessed through generalized linear models. Our hypotheses were partly confirmed. TD and FD were, in fact, dependent on the environment, with higher values occurring in warmer, clearer, and more enriched systems, under lower zooplankton grazing pressure; but FD based on identities was not predicted better from environmental conditions than TD based on identities. As expected, indices based on biomass are better related to the environment than their counterpart based on identities

    Downstream transport processes modulate the effects of environmental heterogeneity on riverine phytoplankton

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    Environmental heterogeneity (EH) in space and time promotes niche-partition, which leads to high variation in biological communities, such as in algae. In streams, EH is highly related to the intensity of the water flow and may lead to community variation mainly during the low flow conditions. Despite the wide knowledge on the responses of phytoplankton communities to EH in lentic and semi-lentic systems, studies of riverine phytoplankton community variation are still scarce. Here, we first investigated the relationship between phytoplankton community variation and EH in different courses of the river and between seasons. We expected that under low or intermediate flow conditions, there is a positive correlation between community variation and EH. Alternatively, we did not expect any relationship between EH and community variation under high flow condition because stronger downstream transport would mask environmental filtering. We sampled nine sites monthly (May 2012 to April 2013) in a tropical river of Brazilian Southeast. We calculated EH from abiotic data whereas for community variation, here community distinctiveness (CD), we used Sorensen (CDSor) and Bray-Curtis (CDBray) dissimilarities. Differences in EH, CDSor and CDBray were tested at between-season and among-course levels. We found lower distinctiveness during the dry season when EH was the highest. Contrastingly, phytoplankton CD was the highest even when EH was low during the wet season. We found that this pattern raised from the increasing in individuals dispersal during the wet season, promoting mass effects. Finally, our results thus reject the first hypothesis and show a negative relationship between EH and distinctiveness. However, results support our alternative hypothesis and show that during the wet season, distinctiveness is not driven by EH. These results provide new insights into how EH drives community variation, being useful for both basic research about riverine algal communities and biomonitoring programs using phytoplankton communities as bioindicators. (C). 2019 Elsevier B.V. All rights reserved.Peer reviewe

    Phytoplankton and its biotic interactions: Colin Reynolds’ legacy to phytoplankton ecologists

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    The 18th workshop of the International Association for Phytoplankton Taxonomy and Ecology (IAP), the first ‘‘tropical’’ IAP ever, the third one outside Europe, and the first one in South America, was held in Natal, Brazil, from August 27 to September 3, 2017, and its main ecological theme was the Phytoplankton and its biotic interactions. The taxonomic topic of the workshop was chosen based on function instead of phylogeny, and to link to the ecological theme of the workshop, the taxonomic theme was therefore centered on mixotrophic microalgae

    Effect of suspended clay on growth rates of the cyanobacterium Cylindrospermopsis raciborskii

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    Recent studies have shown that sediment resuspension may lead to the collapse of C. raciborskii dominance, which suggests that clay might have a negative effect on the growth of C. raciborskii. To test the hypothesis that suspended clay creates an unfavorable environment for growth of C. raciborskii, we exposed four different strains of this species to various concentrations of the clays kaolinite and bentonite, and monitored the biomass of each strain over the course of 1-week microcosm experiments. Contrary to our hypothesis, C. raciborskii was able to grow in suspensions of both clays. While kaolinite clay caused higher turbidity than bentonite, the growth rates of all four C. raciborskii strains were higher in kaolinite than in bentonite suspensions. C. raciborskii could still grow in clay concentrations that cause turbidity far above the levels found in natural lakes. Our study suggests that the reported collapse of C. raciborskii blooms with high concentrations of suspended sediments in tropical shallow lakes is probably not caused by the effects of suspended clay on light attenuation, but rather is a consequence of cell sinking or, possibly a response to disturbance events responsible for sediment suspension

    Phosphorus transport by the largest Amazon tributary (Madeira River, Brazil) and its sensitivity to precipitation and damming

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    Originating in the Bolivian and Peruvian Andes, the Madeira River is the largest tributary of the Amazon River in terms of discharge. Andean rivers transport large quantities of nutrient-rich suspended sediments and are the main source of phosphorus (P) to the Amazon basin. Here, we show the seasonal variability in concentrations and loads of different P forms (total, particulate, dissolved, and soluble reactive P) in the Madeira River through 8 field campaigns between 2009 and 2011. At our sampling reach in Porto Velho, Brazil, the Madeira River transports similar to 177-247 Gg yr(-1) of P, mostly linked to particles (similar to 85%). Concentrations and loads of all P forms have a maximum at rising waters and a minimum at low waters. Total P concentrations were substantially higher at a given discharge at rising water than at a similar discharge at falling water. The peak of P concentrations matched the peak of rainfall in the upper basin, suggesting an influence of precipitation-driven erosion. Projected precipitation increase in the eastern slopes of the Andes could enhance sediment yield and hence the P transport in the Madeira River. Because most of the P is particulate, however, we hypothesize that the planned proliferation of hydropower dams in the Madeira basin has the potential to reduce P loads substantially, possibly counteracting any precipitation-related increases. In the long term, this could be detrimental to highly productive downstream floodplain forests that are seasonally fertilized with P-rich deposits

    Supplement 1. Data from the 83 South American lakes sampled.

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    <h2>File List</h2><blockquote> <p><a href="South_American_Lakes_data.txt">South_American_Lakes_data.txt</a> -- data file </p> </blockquote><h2>Description</h2><blockquote> <p>The "South American Lakes data file" contains data on 83 shallow lakes sampled in South America between November 2004 and March 2006. The following data is presented: X coordinate (Decimal degrees); Y coordinate (Decimal degrees); name (Name of the lake. Not all lakes have a name and some lakes are referred to by multiple names); climate zone (The lakes were grouped in five different categories based on the prevailing climate characteristics following the Köppen climate system (1936) digitized by Leemans and Cramer (1991): tropicali, tropical, subtropical, maritime temperate and tundra zone. The Köppen classification is based on monthly rainfall and temperature. Tropicali is an isothermal subzone in the tropics, which has a smaller annual temperature range than the tropical zone, source:<br> <a href="http://www.fao.org/WAICENT/FAOINFO/SUSTDEV/EIdirect/climate/EIsp0002.htm">http://www.fao.org/WAICENT/FAOINFO/SUSTDEV/EIdirect/climate/EIsp0002.htm</a>); average air temperature in warmest month (Celcius, source: M. New, D. Lister, M. Hulme, and I. Makin. 2002. A high-resolution data set of surface climate over global land areas. Climate Research 21. The complete paper can be freely downloaded via:<br> <a href="http://www.cru.uea.ac.uk/cru/data/tmc.htm">http://www.cru.uea.ac.uk/cru/data/tmc.htm</a>); average air temperature in coldest month (Celcius, source: M. New, D. Lister, M. Hulme, and I. Makin. 2002: A high-resolution data set of surface climate over global land areas. Climate Research 21. The complete paper can be freely downloaded via:<br> <a href="http://www.cru.uea.ac.uk/cru/data/tmc.htm">http://www.cru.uea.ac.uk/cru/data/tmc.htm</a>); soil type (Source: SOTERLAC "Soil and terrain database for Latin America and the Caribbean ", FAO: Land and Water Digital Media Series #5, scale: 1:5 million scale. Type of top soil and descriptions of the different types can be found at:<br> <a href="http://www.fao.org/AG/agl/agll/key2soil.stm">http://www.fao.org/AG/agl/agll/key2soil.stm</a>); lake area (m<sup>2</sup>, determined using landsat Orthorectified Landsat Thematic Mapper Mosaics of the year 2000. If image was cloudy images of 1990 were used. In rare cases when image deviated much from area observed in the field, all waypoints measured in the field were plotted on top of the image and a "best matching" polygon was drawn around it, of which the area was determined); average depth (Meter, the average depth of the lake was determined using depth measurements from 20 random points and 20 points along transects perpendicular to the longest axis of the lake); altitude (Meter above sea level, based on DEM from gtopo30, converted to an Arcview grid using the procedure published on herpnet.org GTOPT_DEM); conductivity (µS/cm); Total nitrogen (mg/L); Total phosphorus (mg/L); chlorophyll <i>a</i> (µg/L)</p> -- TABLE: Please see in attached file. -- </blockquote

    Coagulant plus ballast technique provides a rapid mitigation of cyanobacterial nuisance

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    Cyanobacteria blooms are a risk to environmental health and public safety due to the potent toxins certain cyanobacteria can produce. These nuisance organisms can be removed from water bodies by biomass flocculation and sedimentation. Here, we studied the efficacy of combinations of a low dose coagulant (poly-aluminium chloride—PAC—or chitosan) with different ballast compounds (red soil, bauxite, gravel, aluminium modified zeolite and lanthanum modified bentonite) to remove cyanobacterial biomass from water collected in Funil Reservoir (Brazil). We tested the effect of different cyanobacterial biomass concentrations on removal efficiency. We also examined if zeta potential was altered by treatments. Addition of low doses of PAC and chitosan (1–8 mg Al L-1) to the cyanobacterial suspensions caused flock formation, but did not settle the cyanobacteria. When those low dose coagulants were combined with ballast, effective settling in a dose-dependent way up to 99.7% removal of the flocks could be achieved without any effect on the zeta potential and thus without potential membrane damage. Removal efficacy was influenced by the cyanobacterial biomass and at higher biomass more ballast was needed to achieve good removal. The combined coagulant-ballast technique provides a promising alternative to algaecides in lakes, ponds and reservoirs
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