Mine Water and the Environment

, Volume 34, Issue 3, pp 343–351 | Cite as

An Overview of an Acidic Uranium Mine Pit Lake (Caldas, Brazil): Composition of the Zooplankton Community and Limnochemical Aspects

  • Carla R. Ferrari
  • Heliana de Azevedo
  • Maria José S. Wisniewski
  • Suzelei Rodgher
  • Cláudio Vitor Roque
  • Marcos Roberto L. Nascimento
Technical Article

Abstract

Water samples were collected quarterly for 1 year from the newly created Osamu Utsumi uranium mine pit lake, Brazil, which is affected by acid mine drainage (AMD). The water presented mean pH values of 3.8, high mean electrical conductivity values (2391 µS/cm), manganese (74 mg/L), sulfate (1413 mg/L) and uranium (3 mg/L). The density of rotifera was significantly higher than that of cladoceran. Rotifera Keratella americana, K. cochlearis and the Cladocera Bosminopsis deitersi, Bosmina sp., are being reported for the first time in samples from a uranium pit lake with AMD. Of the species registered, the order Bdelloidea was the most important in terms of density (17,500–77,778 ind/m3), since it occurred throughout the whole sampling period. The combined effect of moderately acidic pH and other potential stress factors, such as high concentrations of stable and radioactive contaminants, probably influenced the zooplankton species composition in the pit lake.

Keywords

Mine pit lake Acid mine drainage Bdelloidea 

Ein Überblick zu einem sauren Tagebausee in einer Urangrube (Caldas, Brasilien): Zusammensetzung des Zooplanktons und limnologische Aspecte

Zusammenfassung

Für ein Jahr wurden vierteljährlich Wasserproben aus dem jüngst hergestellten Tagebausee in der Osma Utsumi Urangrube (Brasilien) entnommen, der durch saure Grubenwässer (AMD) beeinträchtigt wird. Das Wasser hatte einen mittleren pH-Wert von 3,8, eine hohe mittlere elektrische Leitfähigkeit (2391 µS/cm) sowie Mangan- (74 mg/L), Sulfat- (1413 mg/L) und Urankonzentrationen (3 mg/L). Die Populationsdichte der Rotatorien war signifikant höher als die der Cladoceren. Das Vorkommen der Rotatorien Keratella Americana und K. cochlearis und der Cladoceren Bosminopsis deitersi und Bosmina sp. wurde erstmalig für saure Tagebauseen in Urangruben mit AMD-Einfluss dokumentiert. Von den registrierten Taxa war die Ordnung Bdelloidea das wichtigste hinsichtlich der Populationsdichte (17,500 bis 77,778 Ind/m³), da es während der gesamten Untersuchungszeit auftrat. Die Kombination aus moderat saurem pH und anderen potentiellen Stressfaktoren, wie z.B. hohe Konzentrationen an stabilen und radioaktiven Kontaminanten, beeinflussten wahrscheinlich die Artenzusammensetzung des Zooplanktons im Tagebausee.

Una visión global del lago del hoyo de una mina ácida de uranio (Caldas, Brasil): Composición de la comunidad zooplancton y aspectos limnoquímicos

Resumen

Muestras de aguas fueron colectadas trimestralmente durante un año en el nuevo lago del hoyo de mina de uranio Osamu Utsumi, Brasil, que es afectado por drenaje ácido de minas (AMD). El agua presentó un pH promedio de 3,8, altos valores de conductividad eléctrica (2391 µS/cm), manganeso (74 mg/L), sulfato (1413 mg/L) y uranio (3 mg/L). La densidad de rotífera fue significativamente mayor que la de cladocera. Rotifera Keratella americana, K. cochlearis y Cladocera Bosminopsis deitersi, Bosmina sp., son reportadas por primera vez en muestras de un lago de hoyo de mina de uranio afectado con AMD. De las especies registradas, el orden Bdelloidea fue el más importante en términos de densidad (17.500 a 77.778 ind/m3), ya que estuvieron presentes durante todo el período de muestreo. El efecto combinado de pH moderadamente ácido y otros factores de estrés, tales como altas concentraciones de contaminantes estables y radioactivos, probablemente influenció la composición de especies de zooplancton en el lago.

酸性铀矿采坑湖(卡尔达斯,巴西)综述:浮游动物群落组成和湖水水化学特征影响

综述

水样取自巴西新建Osama Utsumi铀矿采坑湖的酸性矿井废水,每季度采水样一次,采样期一年。水样水化学特征:低pH值(平均3.8)、高电导率(平均值2391 µS/cm)、锰浓度74 mg/L、硫酸根浓度1413 mg/L、铀浓度3 mg/L。轮虫类动物密度远大于水蚤类动物密度。美洲龟甲轮虫、螺形龟甲轮虫、颈沟基合蚤和象鼻蚤首次在铀矿采坑湖酸性废水中检出。另外,蛭形轮虫目由于密度变化大(17,500~77,778 ind/m3)且在整个采样周期均有检出而引起关注。适度的PH值和高浓度的稳定与放射性污染物等潜在因素共同作用,影响着采坑湖中浮游动物的种类组成。

Notes

Acknowledgments

This study was funded by the State of Minas Gerais Research Aid Foundation (FAPEMIG APQ-7807-5.04/07). We also thank AL Bruschi, MB Campos, HLA Caponi, EO Lima, and LB Ronqui for their technical support.

References

  1. Antunes SC, Figueiredo D, Marques RS, Castro BB, Pereira R, Gonçalves F (2007) Evaluation of water column and sediment toxicity from abandoned uranium mine using a battery of bioassays. Sci Total Environ 374:252–259CrossRefGoogle Scholar
  2. APHA (American Public Health Assoc) (1995) Standard Methods for the Examination of Water and Wastewater, 19th edn. American Public Health Assoc, American Water Works Assoc, Water Environment Federation, WashingtonGoogle Scholar
  3. Arnott SE, Vanni MJ (1993) Zooplankton assemblages in fishless bog lakes: influence of biotic and abiotic factors. Ecology 74:2361–2380CrossRefGoogle Scholar
  4. ASTM (American Society for Testing and Materials) (1980) Annual Book of ASTM standards. PA, USA, PhiladelphiaGoogle Scholar
  5. Ayres M, Ayres MJr, Ayres DL, Santos AS (2005) BioEstat 2.0: Aplicações estatísticas na área das Ciências Biológicas e Médicas. Mamirauá, Editora Gráfica LtdaGoogle Scholar
  6. Batty LC (2005) The potential importance of mine sites for biodiversity. Mine Water Environ 24(2):101–103CrossRefGoogle Scholar
  7. Belyaeva M, Deneke R (2007) Colonization of acidic mining lakes: Cydorus sphaericus and other Cladocera within a dynamic horizontal pH gradient (pH 3-7) in Lake Senftenberger See (Germany). Hydrobiologia 594:97–108CrossRefGoogle Scholar
  8. Belyaeva M, Deneke R (2013) The biology and ecosystems of acidic pit lakes. Zooplankton. In: Geller W, Schultze M, Kleinmann R, Wolkersdorfer C (eds) acidic pit lakes. Springer, Berlin, pp 117–126. doi: 10.1007/978-3-642-29384-9 Google Scholar
  9. Campos MB, Azevedo H, Nascimento MRL, Roque CV, Rodgher S (2011) Environmental assessment of water from a uranium mine (Caldas, Minas Gerais State, Brazil) in a descommissioning operation. Environ Earth Sci 62:857–863CrossRefGoogle Scholar
  10. Carlson RE (1977) A trophic state index for lakes. Limnol Oceanogr 22:361–369CrossRefGoogle Scholar
  11. Ciszewski D, Aleksander-Kwaterczak U, Pociecha A, Szarek-Gwiazda E (2013) Small effects of a large sediment contamination with heavy metals on aquatic organisms in the vicinity of an abandoned lead and zinc mine. Environ Monit Assess 185:9825–9842CrossRefGoogle Scholar
  12. De-Melo R, Hebert PDN (1994) A taxonomic reevaluation of North American Bosminidae. Can J Zool 72:1808–1825CrossRefGoogle Scholar
  13. Deneke R (2000) Review of rotifers and crustacean in highly acidic environments of pH values ≤ 3. Hydrobiologia 433:167–172CrossRefGoogle Scholar
  14. Durán AP, Rauch J, Gaston K (2013) Global spatial coincidence between protected areas and metal mining activities. Biolog Conserv 160:272–278CrossRefGoogle Scholar
  15. Eary LE, Castendyk DN (2013) Hardrock metal mine pit lakes: occurrence and geochemical characteristics. In: Geller W, Schultze M, Kleinmann R, Wolkersdorfer C (eds) Acidic Pit Lakes. Springer, Berlin, pp 75–106. doi: 10.1007/978-3-642-29384-9 Google Scholar
  16. Elmoor-Loureiro LMA (1997) Manual de Identificação de Cladóceros Límnicos do Brasil. Universa, Brasília, BrazilGoogle Scholar
  17. Elmoor-Loureiro LMA (2004) Morphological abnormalities in the cladoceran Ilyocryptus spinifer (Apipucos reservoir, Pernambuco State, Brazil). Braz J Biol 64:53–58CrossRefGoogle Scholar
  18. Ferrari CR (2010) Avaliação de efeitos de efluentes radioativos de mineração de urânio sobre características físicas, químicas e diversidade da comunidade zooplanctônica na Unidade de Tratamento de Minérios, na Represa das Antas e Represa Bortolan, Poços de Caldas (MG). Dissertação. Universidade de São Paulo, BrazilGoogle Scholar
  19. Friese K, Herzsprung P, Schultze M (2013) Limnochemistry of water and sediments of acidic pit lakes pit lakes from coal and lignite mining. In: Geller W, Schultze M, Kleinmann R, Wolkersdorfer C (eds) acidic pit lakes. Springer, Berlin, pp 42–57. doi: 10.1007/978-3-642-29384-9 Google Scholar
  20. Fukuma HT, De Nadai Fernandes EA, Nascimento MRL, Quinelato AL (2001) Separation and spectrophotometric determination of thorium contained in uranium concentrates. J Radioanal Nucl Ch 248:533–549CrossRefGoogle Scholar
  21. Gladyshev E, Meselson M (2008) Extreme resistance of bdelloid rotifers to ionizing radiation. P Natl Acad Sci USA 105:5139–5144CrossRefGoogle Scholar
  22. Golterman HL, Clymo RS, Ohnstad MAM (1978) Methods for Physical and Chemical Analysis of Freshwaters, 2nd edn. Blackwell Scientific Publications, OxfordGoogle Scholar
  23. Gomes HA, Nouailhetas Y, Silva NC, Mezrahi A, Almeida CEB, Rodrigues GS (2002) Biological response of Tradescantia stamen-hairs to high levels of natural radiation in the Poços de Caldas plateau. Braz Arch Biol Technol 45:301–307CrossRefGoogle Scholar
  24. Havens KE (1993) Acid and aluminum effects on osmoregulation and survival of the freshwater copepod Skistodiaptomus oregonensis. J Plankton Res 15:683–691CrossRefGoogle Scholar
  25. Holopainen IJ, Holopainen AL, Hämäläinen H, Rahkola-Sorsa M, Tkatcheva V, Viljanen M (2003) Effects of mining industry waste waters on a shallow lake ecosystem in Karelia, north-west Russia. Hydrobiologia 506–509(1–3):111–119CrossRefGoogle Scholar
  26. Hrdinka T, Sobr M, Fott J, Nedbalova L (2013) The unique environment of the most acidified permanently meromictic lake in the Czech Republic. Limnologica 43:417–426CrossRefGoogle Scholar
  27. Jak RG, Maas JL, Scholten MCT (1996) Evaluation of laboratory derived toxic effect concentrations of a mixture of metals by testing freshwater plankton communities in enclosures. Water Res 30:1215–1227CrossRefGoogle Scholar
  28. Jersabek CD, Weithoff G, Weisse T (2011) Cephalodella acidophila n. sp. (Monogononta: Nommatidae), a new rotifer species from highly acidic mining lakes. Zootaxa 2939:50–58Google Scholar
  29. Kalin M, Cao Y, Smith M, Olaveson M (2001) Development of the phytoplankton community in a pit-lake in relation to water quality changes. Water Res 35:3215–3225CrossRefGoogle Scholar
  30. Koste W (1978) Rotatoria Die Rädertiere Mitteleuropas. Überordnung Monogononta, Gebrüder Borntraeger, BerlinGoogle Scholar
  31. Kotov AA, Ishida S, Taylor DJ (2009) Revision of the genus Bosmina Baird 1845 (Cladocera: Bosminidae), based on evidence from male morphological characters and molecular phylogenies. Zool J Linn Soc Lond 156:1–51CrossRefGoogle Scholar
  32. Lefcort H, Vancura J, Lider EL (2010) 75 Years after mining ends stream insect diversity is still affected by heavy metals. Ecotoxicology 19:1416–1425CrossRefGoogle Scholar
  33. Lessmann D, Deneke R, Ender R, Hemm M, Kapfer M, Krumbeck H, Wollmann K, Nixdorf B (1999) Lake Plessa 107 (Lusatia, Germany) an extremely acidic shallow mining lake. Hydrobiologia 408(409):293–299CrossRefGoogle Scholar
  34. Locke A, Sprules WG (2000) Effects of acidic pH and phytoplankton on survival and condition of Bosmina longirostris and Daphnia pulex. Hydrobiologia 437:187–196CrossRefGoogle Scholar
  35. Luís AP, Teixeira P, Almeida SFP, Ector L, Matos JX, Ferreira da Silva EA (2009) Impact of acid mine drainage (AMD) on water quality, stream sediments and periphytic diatom communities in the surrounding stream of Aljustrel mining area (Portugal). Water Air Soil Pollut 200:147–167CrossRefGoogle Scholar
  36. Lyew D, Sheppard JD (1997) Effects of physical parameters of a gravel bed on the activity of sulphate-reducing Bacteria in the presence of acid mine drainage. J Chem Technol Biotechnol 70:223–230CrossRefGoogle Scholar
  37. Lyew D, Sheppard JD (2001) Use of conductivity to monitor the treatment of acid mine drainage by sulphate-reducing Bacteria. Water Res 35:2081–2086CrossRefGoogle Scholar
  38. Mathews T, Beaugelin-Seiller K, Garnier-Laplace J, Gilbin R, Adam C, Della-Vedova C (2009) A probabilistic assessment of the chemical and radiologicalrisks of chronic exposure to uranium in freshwater ecosystems. Environ Sci Technol 43:6684–6690CrossRefGoogle Scholar
  39. Melão MGG, Rocha O (2006) Life history, population dynamics, standing biomass and production of Bosminopsis deitersi (Cladocera) in a shallow tropical reservoir. Acta Limnol Bras 18(4):433–450Google Scholar
  40. Moser M, Weisse T (2011) The most acidified Austrian lake in comparison to a neutralized mining lake. Limnologica 41:303–315CrossRefGoogle Scholar
  41. Nascimento MRL, Fukuma HT, Hortellani MA (1988) Projeto Itataia—Controle de processo na produção de ácidos fosfórico e urânio. Poços de Caldas: INB, (Manual de Métodos e Análises Químicas), BrazilGoogle Scholar
  42. Nixdorf B, Wollmann K, Deneke R (1998) Ecological potentials for planktonic development and food web interactions in extremely acidic mining lakes in Lusatia. In: Geller W, Klapper H, Salomons W (eds) Acidic mining lakes. Springer, Berlin, pp 147–167. doi: 10.1007/978-3-642-71954-7_8 CrossRefGoogle Scholar
  43. Nixdorf B, Krumbeck H, Jander J, Beulker C (2003) Comparison of bacterial and phytoplankton productivity in extremely acidic mining lakes and eutrophic hard waters lakes. Acta Oecol 24:S281–S288CrossRefGoogle Scholar
  44. Nixdorf B, Lessmann D, Deneke R (2005) Mining lakes in a disturbed landscape: application of the EC Water Framework Directive and future management strategies. Ecol Eng 24:67–73CrossRefGoogle Scholar
  45. Nóbrega FA, Lima HM, Leite AL (2008) Análise de múltiplas variáveis no fechamento da mina-Estudo de caso da pilha de estéril BF-4, Mina Osamu Utsumi, INB Caldas, Minas Gerais. Revista Escola de Minas Ouro Preto 61:197–202Google Scholar
  46. Nogrady T, Pourriot R (1995) Rotifera: The Notommatidae. In: Nogrady T, Dumont HJ (eds) Guides to the Identification of the macroinvertebrates of the Continental Waters of the World. SPB Academic Publications, New YorkGoogle Scholar
  47. Nogueira MG (2001) Zooplankton composition, dominance and abundance as indicators of environmental compartmentalization in Jurumirim Reservoir (Paranapanema River), São Paulo Brazil. Hydrobiologia 455:1–18CrossRefGoogle Scholar
  48. Riethmuller N, Markich SJR, Van Dam A, Parry D (2001) Effects of water hardness and alkalinity on the toxicity of uranium to a tropical freshwater hydra (Hydra viridissima). Biomarkers 6:43–51CrossRefGoogle Scholar
  49. Rocha O, Güntzel AM (1999) Branchiopoda, Cladocera. In: Ismael D, Valenti WC. Matsumura-Tundisi T, Rocha O (Org), Biodiversidade do estado de São Paulo, Brasil: síntese do conhecimento ao final do século XX, 4: Invertebrados de água doce. 1st, edit, Fapesp, São Paulo, Brazil, p 107-120Google Scholar
  50. Rodgher S, Azevedo H, Ferrari CR, Roque CV, Roqui LB, Campos MB, Nascimento MRL (2013) Evaluation of surface water quality in aquatic bodies under the influence of uranium mining (MG, Brazil). Environ Monit Assess 185:2395–2406. doi: 10.1007/s10661-012-2719-5 CrossRefGoogle Scholar
  51. Sanchez-Ortiz JR, Sarma SSS, Nandini S (2010) Comparative population growth of Ceriodaphnia dubia and Daphnia pulex (Cladocera) exposed to zinc toxicity. J Environ Sci Heal A 45(1):37–41CrossRefGoogle Scholar
  52. Saro L, Lopes Y, Chastinet CBA, Cohin-de-Pinho SJ, Moreira-Santos M, Silva EM, Ribeiro R (2011) Potential re-colonisation by cladocerans of an acidic tropical pond. Chemosphere 82:1072–1079CrossRefGoogle Scholar
  53. Sheoran AS, Sheoran V (2006) Heavy metal removal mechanism of acid mine drainage in wetlands: a critical review. Miner Eng 19:105–116CrossRefGoogle Scholar
  54. Sheppard SC, Sheppard MI, Gallerand MO, Sanipelli B (2005) Derivation of ecotoxicity thresholds for uranium. J Environ Radioact 79(1):55–83CrossRefGoogle Scholar
  55. Shiel RJ, Koste W (1992) Rotifera fron Australian inland waters. VIII. Trichocercidae (Monogononta). T Roy Soc South Aust 116:1–27Google Scholar
  56. Shiel RJ, Koste W (1993) Rotifera from Australian inland waters. IX. Gastropodidae, Synchaetidae, Asplanchinidae (Rotifera Monogononta). T Roy Soc South Aust 117:111–139Google Scholar
  57. Silva NC, Taddei MHT, Cipriani M, Fernandes EAN (2000) Radioactivity associated with sediments from the Pocos de Caldas Plateau—a Brazilian area of high level natural radiation. In: Poster Proceedings 5th international conference on high levels of natural radiation and radon areas: radiation dose and health effects, Munich, p 69Google Scholar
  58. Soucek DJ, Cherry DS, Currie RJ, Latimer HA, Trent GC (2000) Laboratory to field validation in an integrative assessment of an acid mine drainage-impacted watershed. Environ Toxicol Chem 19:1036–1043Google Scholar
  59. Soucek DJ, Cherry DS, Zipper CE (2001) Aluminum-dominated acute toxicity to the cladoceran Ceriodaphnia dubia in neutral waters downstram of an acid mine drainage discharge. Can J Fish Aquat Sci 58:2396–2404CrossRefGoogle Scholar
  60. Turner PN (1987) Keratella rotifers found in Brazil, and a survey of Keratella rotifers from the Neotropics. Amazoniana 2:223–236Google Scholar
  61. Van Damme PA, Hammel C, Ayala A, Bervorts L (2008) Macroinvertebrate community response to acid mine drainage in rivers of the High Andes (Bolivia). Environ Pollut 156:1061–1068CrossRefGoogle Scholar
  62. Veiga LHS, Sachet I, Melo V, Magalhães MH, Amaral ECS (2000) Brazilian areas of high background radiation. Are levels really high? In: Poster Proceedings 5th international conference on high levels of natural radiation and radon areas: radiation dose and health effects, Munich, p 62Google Scholar
  63. Viayev RM (2010) An overview of the rotifers of the family Nommatidae (Rotifera: Monogononta: Ploima) from Ira. Caspian J Env Sci 8:127–139Google Scholar
  64. Weithoff G (2005) On the ecology of the rotifer Cephalodella hoodii from an extremely acidic lake. Freshwater Biol 50:1464–1473CrossRefGoogle Scholar
  65. Wendt-Potthoff K (2013) The biology and ecosystems of acidic pit lakes. In: Geller W, Schultze M, Kleinmann R, Wolkersdorfer C (eds) Acidic pit lakes. Springer, Berlin, p 107Google Scholar
  66. Woelfl S, Whitton BA (2000) Sampling, preservation and quantification of biological samples from highly acidic environments (pH ≤ 3). Hydrobiologia 433:173–180CrossRefGoogle Scholar
  67. Wollmann K, Deneke R, Nixdorf B, Packroff G (2000) Dynamics of planktonic food webs in three mining lakes across a pH gradient (pH 2-4). Hydrobiologia 433:3–14CrossRefGoogle Scholar
  68. World Health Organization (WHO) (2004) Manganese and its Compounds: Environmental Aspects Concise International Chemical Assessment Document 63. World Health Org, GenevaGoogle Scholar
  69. Xi Y, Jin H, Xie P, Huang X (2002) Morphological variation of Keratella cochlearis (Rotatoria) in a shallow, eutrophic subtropical Chinese Lake. J Freshwater Ecol 17:447–454CrossRefGoogle Scholar
  70. Zanata LH, Espíndola ELG, Rocha O, Pereira RHG (2008) Morphological abnormalities in Cladocera (Branchiopoda) in a cascade of reservoirs in the middle and lower Tietê river (São Paulo, Brazil). Braz J Biol 68(3):681–682CrossRefGoogle Scholar

Copyright information

© Springer-Verlag Berlin Heidelberg 2015

Authors and Affiliations

  • Carla R. Ferrari
    • 1
  • Heliana de Azevedo
    • 1
  • Maria José S. Wisniewski
    • 2
  • Suzelei Rodgher
    • 3
  • Cláudio Vitor Roque
    • 1
  • Marcos Roberto L. Nascimento
    • 4
  1. 1.Radioecology Laboratory/Poços de Caldas LaboratoryBrazilian Nuclear Energy CommissionPoços de CaldasBrazil
  2. 2.Limnology Laboratory, Biology DepartmentAlfenas Federal UniversityAlfenasBrazil
  3. 3.Environmental Engineering DepartmentUniversity Estadual PaulistaSão José dos CamposBrazil
  4. 4.Chemical Analyzes Laboratory/Poços de Caldas LaboratoryBrazilian Nuclear Energy CommissionPoços de CaldasBrazil

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