Skip to main content

The Response of Benthic Foraminifera to Low-Oxygen Conditions of the Peruvian Oxygen Minimum Zone

  • Chapter
  • First Online:
Anoxia

Abstract

Recent benthic foraminifera and their distribution in surface sediments were studied on a transect through the Peruvian oxygen minimum zone (OMZ) between 10 and 12°S. The OMZ with its steep gradients of oxygen concentrations allows determinations of the oxygen-dependent changes of species compositions in a relatively small area. Our results from sediments of 13 multicorer stations from 79 to 823 m water depth demonstrate that calcareous species, especially bolivinids, dominate the assemblages throughout the OMZ. The depth distribution of several species matches distinct ranges of bottom water oxygen levels. The distribution pattern inferred a proxy which allows estimating dissolved oxygen concentrations for reconstructing oxygen levels in the geological past.

This is a preview of subscription content, log in via an institution to check access.

Access this chapter

Chapter
USD 29.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD 169.00
Price excludes VAT (USA)
  • Available as EPUB and PDF
  • Read on any device
  • Instant download
  • Own it forever
Softcover Book
USD 219.99
Price excludes VAT (USA)
  • Compact, lightweight edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info
Hardcover Book
USD 219.99
Price excludes VAT (USA)
  • Durable hardcover edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Purchases are for personal use only

Institutional subscriptions

References

  • Altenbach AV, Sarnthein M (1989) Productivity record in benthic foraminifera. In: Berger WH, Smetacek VS, Wefer G (eds) Production in the ocean: present and past. Wiley, New York, pp 255–269

    Google Scholar 

  • Bernhard JM, Alve E (1996) Survival, ATP pool, and ultrastructural characterization of benthic foraminifera from Drammensfjord (Norway): response to anoxia. Mar Micropaleontol 28:5–I7

    Article  Google Scholar 

  • Bernhard JM, Bowser SS (1999) Benthic foraminifera of dysoxic sediments: chloroplast sequestration and functional morphology. Earth-Sci Revs 46:149–165

    Article  CAS  Google Scholar 

  • Bernhard JM, Bowser SS (2008) Peroxisome Proliferation in Foraminifera Inhabiting the Chemocline: An Adaptation to Reactive Oxygen Species Exposure? J Eukaryot Microbiol 55(3):135–144

    Article  PubMed  CAS  Google Scholar 

  • Bernhard JM, Reimers CE (1991) Benthic foraminiferal population fluctuations related to anoxia: Santa Barbara Basin. Biogeochemistry 15:127–149

    Article  CAS  Google Scholar 

  • Bernhard JM, Sen Gupta BK (1999) Foraminifera of oxygen-depleted environments. In: SenGupta BK (ed) Modern foraminifera. Kluwer Academic Publishers, Great Britain, pp 201–216

    Google Scholar 

  • Bernhard JM, Sen Gupta BS, Borne PF (1997) Benthic foraminiferal proxy to estimate dysoxic bottom-water oxygen concentrations. Santa Barbara Basin, U.S. Pacific continental margin. J Foraminife Res 27:301–310

    Article  Google Scholar 

  • Bernhard JM, Buck KR, Barry JP (2001) Monterey Bay cold-seep biota: Assemblages, abundance, and ultrastructure of living foraminifera. Deep-Sea Res I 48:2233–2249

    Article  Google Scholar 

  • Bernhard JM, Bowser SS, Goldstein S (2010) An ectobiont-bearing foraminiferan, Bolivina pacifica, that inhabits microxic pore waters: cell-biological and paleoceanographic insights: Environ Microbiol 12:2107–2119

    Google Scholar 

  • Boltovskoy E, Theyer F (1970) Foraminiferos recientes de Chile Central. Revista del Museo Argentino de Ciencias Natururales. Bernard Rivadavia 2(9):280–397

    Google Scholar 

  • den Dulk M, Reichart GJ, Memon GM, Roelofs EMP, Zachariasse WJ, van der Zwaan GJ (1998) Benthic foraminiferal response to variations in surface water productivity and oxygenation in the northern Arabian Sea. Mar Micropaleontol 35:43–66

    Article  Google Scholar 

  • Frezza V, Carboni MG (2009) Distribution of recent foraminiferal assemblages near the Ombrone River mouth (Northern Tyrrhenian Sea, Italy). Rev de micropaleontol 52:43–66

    Article  Google Scholar 

  • Geslin E, Heinz P, Jorissen F, Hemleben Ch (2004) Migratory responses of deep-sea benthic foraminifera to variable oxygen conditions: laboratory investigations. Mar Micropaleontol 53:227–243

    Article  Google Scholar 

  • Glock N, Eisenhauer A, Milker Y, Liebetrau V, Schönfeld J, Mallon J, Sommer S, Hensen C (2011) Environmental influences on the pore-density of Bolivina spissa (Cushman). J Foraminifer Res 41(1):22–32

    Article  Google Scholar 

  • Glud RN, Thamdrup B, Stahl H, Wenzhoefer F, Glud A, Nomaki H, Oguri K, Revsbech NP, Kitazato H (2009) Nitrogen cycling in a deep ocean margin sediment (Sagami Bay, Japan). Limnol Oceanogr 54(3):723–734

    Article  CAS  Google Scholar 

  • Gooday AJ (1986) Meiofaunal foraminiferans from the bathyal Porcupine Seabight (northeast Atlantic): size structure, standing stock, taxonomic composition, species diversity and vertical distribution in the sediment. Deep Sea-Res 33(10):1345–1373

    Article  Google Scholar 

  • Gooday AJ, Bernhard JM, Levin LA, Suhr SB (2000) Foraminifera in the Arabian Sea oxygen minimum zone and other oxygen deficient settings: taxonomic composition, diversity, and relation to metazoan faunas. Deep-Sea Res II 47:25–54

    Article  Google Scholar 

  • Grzymski J, Schofield OM, Falkowski PG, Bernhard JM (2002) The function of plastids in the deep-sea benthic foraminifer, Nonionella stella. Limnol Oceanogr 47(6):1569–1580

    Article  CAS  Google Scholar 

  • Jannink NT, Zachariasse WJ, van der Zwaan GJ (1998) Living (Rose bengal stained) benthic foraminifera from the Pakistan continental margin (northern Arabian Sea). Deep-Sea Res I 45:1483–1513

    Article  Google Scholar 

  • Jorissen FJ, de Stigter HC, Widmark JGV (1995) A conceptual model explaining benthic foraminiferal microhabitats. Marine Micropaleontol 26:3–15

    Article  Google Scholar 

  • Kaiho K (1994) Benthic foraminiferal dissolved-oxygen index and dissolved-oxygen levels in the modern ocean. Geology 22:719–722

    Article  CAS  Google Scholar 

  • Leutenegger S, Hansen HJ (1979) Ultrastructural and radiotracer studies of pore function in Foraminifera. Mar Biol 54:11–16

    Article  Google Scholar 

  • Levin LA, Gutiérrez D, Rathburn A, Neira C, Sellanes J, Muñoz P, Gallardo V, Salamanca M (2002) Benthic processes on the Peru margin: a transect across the oxygen minimum zone during the 1997–98 El Niño. Progr Oceanogr 53:1–27

    Article  Google Scholar 

  • Loeblich AR, Tappan H (1994) Foraminifera of the Sahul Shelf and Timor Sea, Cushman Foundation for Foraminiferal Research. Spec Publ 31:1–661

    Google Scholar 

  • Moodley L, Van der Zwaan GJ, Herman PMJ, Kempers L, Van Breugel P (1997) Differential response of benthic meiofauna to anoxia with special reference to Foraminifera (Protista: Sarcodina). Mar Ecol Prog Series 158:151–163

    Article  Google Scholar 

  • Murray J (1971) An atlas of British recent foraminiferids. Heinemann Education Books, London

    Google Scholar 

  • Narayan YR, Barnes CR, Johns MJ (2005) Taxonomy and biostratigraphy of Cenozoic foraminifers from Shell Canada wells, Tofino Basin, offshore Vancouver Island, British Columbia. Micropaleontology 51(2):101–167

    Google Scholar 

  • Neira C, Sellanes J, Levin LA, Arntz WE (2001) Meiofaunal distributions on the Peru margin: relationship to oxygen and organic matter availability. Deep-Sea Res I 48:2453–2472

    Article  CAS  Google Scholar 

  • Oberhänsli H, Heinze P, Diester-Haass L, Wefer G (1990) Upwelling off Peru during the last 430,000 yr and its relationship to the bottom-water environment, as deduced from coarse grain-size distributions and analyses of benthic foraminifers at holes 679D, 680B, and 681B, Leg 112. Proc Ocean Drilling Prog Scientific Results 112:369–390

    Google Scholar 

  • Phleger FB, Soutar A (1973) Production of benthic foraminifera in three east Pacific oxygen minima. Micropaleontology 19:110–115

    Article  Google Scholar 

  • Piña-Ochoa E, Høgslund S, Geslin E, Cedhagen T, Revsbech NP, Nielsen LP, Schweizer M, Jorissen F, Rysgaard S, Risgaard-Petersen N (2010) Widespread occurrence of nitrate storage and denitrification among Foraminifera and Gromiida. Proc Natl Acad Sci 19:1148–1153

    Article  Google Scholar 

  • Rathburn AE, Corliss BH (1994) The ecology of living (stained) deep-sea benthic foraminifera from the Sulu Sea. Paleoceanography 9(1):87–150

    Article  Google Scholar 

  • Resig JM (1981) Biogeography of benthic foraminifera of the northern Nazca plate and adjacent continental margin. Geol Soc of Am Memoir 154:619–666

    Google Scholar 

  • Resig JM (1990) Benthic foraminiferal stratigraphy and Paleoenvironments off Peru, Leg 112. Proc Ocean Drilling Prog Scientific Results 112:263–296

    Google Scholar 

  • Revsbech NP, Larsen LH, Gundersen J, Dalsgaard T, Ulloa O, Thamdrup B (2009) Determination of ultra-low oxygen concentrations in oxygen minimum zones by the STOX sensor. Limnol Oceanogr Methods 7:371–381

    Article  CAS  Google Scholar 

  • Risgaard-Petersen N, Langezaal AM, Ingvardsen S, Schmid MC, Jetten MSM, Op den Camp HJM, Derksen JWM, Piña-Ochoa E, Eriksson SP, Nielsen LP, Revsbech NP, Cedhagen T, van der Zwaan GJ (2006) Evidence for complete denitrification in a benthic foraminifer. Nature 443:93–96

    Article  PubMed  CAS  Google Scholar 

  • Schumacher S, Jorissen FJ, Dissard D, Larkin KE, Gooday AJ (2007) Live (Rose Bengal stained) and dead benthic foraminifera from the oxygen minimum zone of the Pakistan continental margin (Arabian Sea). Mar Micropaleontol 62:45–73

    Article  Google Scholar 

  • Sjoerdsma PG, van der Zwaan GJ (1992) Simulating the effect of changing organic flux and oxygen content on the distribution of benthic foraminifera. Mar Micropaleontol 19:163–180

    Article  Google Scholar 

  • van Marle LJ (1991) Eastern Indonesian, Late Cenozoic smaller benthic Foraminifera. Verh. K. Nederl. Akad. Wetensch. North Holland, Amsterdam

    Google Scholar 

  • Whittaker J (1988) Benthic Cenozoic foraminifera from Ecuador, British Museum (Natural History). Great Britain, London

    Google Scholar 

  • Zheng S-Y, Zhaoxian F (2001) Granuloreticulosa: foraminifera, agglutinated foraminifera, Fauna Sinica: Invertebrata: 26. Science Press, Beijing

    Google Scholar 

Download references

Acknowledgements

We thank Dr. S. Sommer and S. Kriwanek for providing us with the calibrated oxygen data and Dr. C. Hensen for providing the Corg and [NO3] data. A. Bleyer, B. Domeyer and R. Ebbinghaus are gratefully acknowledged for the analytical work onboard. Very special thanks go to Dr. M. E. Perez for supporting us with taxonomy and also for fruitful discussions and for providing us access to the foraminiferal collection at the National History Museum, London. This study was financially supported by the DFG through the Sonderforschungsbereich 754: “Climate – Biogeochemistry Interactions in the Tropical Ocean.”

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Jürgen Mallon .

Editor information

Editors and Affiliations

Appendices

Appendix 1: Faunal Reference List

Species

References

Angulogerina angulosa (Williamson, 1858)

Loeblich and Tappan (1994): p. 487, pl. 250, figs. 13–20.

Bolivina alata (Seguenza, 1862)

van Marle (1991): p. 305, pl. 17, figs. 1–2.

Bolivina costata (d’Orbigny, 1839)

Resig (1981): p. 647, pl. 1, fig. 1.

Bolivina interjuncta (Cushman, 1926)

Boltovskoy and Theyer (1970): p. 304, pl. 1, figs. 8, 9.

Bolivina plicata (d’Orbigny, 1839)

Resig (1981): p. 647, pl. 1, figs. 3, 4.

Bolivina seminuda (Cushman, 1911)

Resig (1981): p. 655, pl. 5, fig. 14.

Bolivina serrata (Natland, 1938)

Whittaker (1988): p. 100, pl. 13, figs. 1–3.

Bolivina spissa (Cushman, 1926)

Resig (1981): p. 647, pl. 1, fig. 7.

Bolivina minuta (Natland, 1938)

Resig (1981): p. 647, pl. 1, fig. 9.

Cancris carmenensis (Natland, 1950)

Resig (1981): p. 649, pl. 2, fig. 9–11.

Cassidulina crassa (d’Orbigny, 1839)

van Marle (1991): p. 289, pl. 9, figs. 13–15.

Cyclammina cancellata (Brady, 1879)

Zheng (2001): pl. 52, figs. 3–6.

Fursenkoina fusiformis (Williamson, 1858)

Murray (1971): p. 184, pl. 77, figs. 1–5.

Globobulimina pacifica (Cushman, 1927)

Loeblich and Tappan (1994): p. 480, pl. 243, figs. 13–16.

Nonionella stella (Cushman & Moyer, 1930)

Narayan et al. (2005): p. 147, pl. 4, fig. 23.

Uvigerina peregrina (Cushman, 1923)

Frezza and Carboni (2009): p. 56, pl. 2, fig. 15.

Valvulineria glabra (Cushman, 1927)

Loeblich and Tappan (1994): p. 505, pl. 268, figs. 1–3.

Appendix 2: Supplementary Data

Supplementary data to this article can be found online at: http://doi.pangaea.de/10.1594/PANGAEA.757092

Rights and permissions

Reprints and permissions

Copyright information

© 2012 Springer Science+Business Media B.V.

About this chapter

Cite this chapter

Mallon, J., Glock, N., Schönfeld, J. (2012). The Response of Benthic Foraminifera to Low-Oxygen Conditions of the Peruvian Oxygen Minimum Zone. In: Altenbach, A., Bernhard, J., Seckbach, J. (eds) Anoxia. Cellular Origin, Life in Extreme Habitats and Astrobiology, vol 21. Springer, Dordrecht. https://doi.org/10.1007/978-94-007-1896-8_16

Download citation

Publish with us

Policies and ethics