Biogenic silica and diatom thanatocoenosis in surface sediments below the Peru–Chile Current: controlling mechanisms and relationship with productivity of surface waters

Abstract Based on 76 surface sediment samples collected between ca. 22° and 44°S along the Chilean coast in the southeast Pacific Ocean, we report on the north–south distribution of opal content and diatom concentration, and the quantitative and qualitative composition of the preserved diatom community. Latitudinal differences in the siliceous signal reflect the influence of two main mechanisms of surface water production: coastal upwelling off northern and central Chile till ca. 38°S, and nutrient enrichment by the input of cold, southern, non-upwelling-associated waters south of ca. 38°S. The poleward increase in biogenic opal and diatom values parallels well the north–south increase of pigment concentration in surface waters as recorded by satellites. Between 22° and 33°S, where low pigment concentrations are measured, opal content and diatom concentration are mostly low (except at 22°–23°S). In contrast, both higher opal and diatom values at 34°–38°S and 41°–42°S correspond well with higher pigment estimations. Preserved diatom populations document the present-day dominant hydrographical conditions. Nutrient enrichment of surface waters due to coastal upwelling results in intensive production of diatoms off northern and central Chile, reflected by the predominance of the richly-composed association of Chaetoceros spores north of ca. 38°S. The diatom association shows that the area between 35° and 38°S is transitional. The abrupt decrease of Chaetoceros spores south of ∼38°S off Chile coupled with the enhanced contribution of Thalassiosira spp., representatives of high-productivity, low-temperature waters, points to the presumed high nutrient supply by the iron-limited, nutrient-rich Antarctic Circumpolar Water. The contribution of benthic diatoms reflects some lateral transport from the near-shore area into deeper positions south of 38°S.

[1]  C. Lange,et al.  SEDIMENTATION PATTERNS OF DIATOMS, RADIOLARIANS, AND SILICOFLAGELLATES IN SANTA BARBARA BASIN, CALIFORNIA , 1997 .

[2]  R. Thunell,et al.  RESPONSE OF SILICEOUS MICROPLANKTON FROM THE SANTA BARBARA BASIN TO THE 1997-98 EL NINO EVENT , 2000 .

[3]  O. Pizarro,et al.  Currents in the deep ocean off Chile (30°S) , 1995 .

[4]  G. Wefer,et al.  The impact of sediment provenance on barium-based productivity estimates , 2000 .

[5]  F. Huang,et al.  Comparison of the seasonal and interannual variability of phytoplankton pigment concentrations in the Peru and California Current systems , 1994 .

[6]  Kenneth H. Brink,et al.  The global coastal ocean : regional studies and syntheses , 1998 .

[7]  O. Ulloa,et al.  Primary production and community respiration in the Humboldt Current System off Chile and associated oceanic areas , 2000 .

[8]  D. M. Nelson,et al.  Production and dissolution of biogenic silica in the ocean: Revised global estimates, comparison with regional data and relationship to biogenic sedimentation , 1995 .

[9]  D. M. Nelson,et al.  A review of the Si cycle in the modern ocean: recent progress and missing gaps in the application of biogenic opal as a paleoproductivity proxy , 2000 .

[10]  G. Wefer,et al.  Surface sediment distribution along the Chilean continental slope related to upwelling and productivity , 2000 .

[11]  G. Wefer,et al.  High concentrations of biogenic barium in Pacific sediments after Termination I—a signal of changes in productivity and deep water chemistry , 2001 .

[12]  Gerold Wefer,et al.  Use of proxies in paleoceanography : examples from the South Atlantic , 1999 .

[13]  R. R. Schmidt,et al.  Micropaleontological counting methods and techniques : an exercise on an eight metres section of the lower Pliocene of Capo Rossello, Sicily , 1978 .

[14]  G. Wefer,et al.  Temporal and spatial variability in export production in the SE Pacific Ocean: evidence from siliceous plankton fluxes and surface sediment assemblages , 2001 .

[15]  Rainer Gersonde,et al.  Diatoms and silicoflagellates , 1978 .

[16]  F. Abrantes,et al.  Coastal upwelling in the Canary Island region: spatial variability reflected by the surface sediment diatom record , 2001 .

[17]  G. Fischer,et al.  Variability in Export Production Documented by Downward Fluxes and Species Composition of Marine Planktic Diatoms: Observations from the Tropical and Equatorial Atlantic , 1999 .

[18]  G. Wefer,et al.  High resolution planktic foraminiferal record of the last 13,300 years from the upwelling area off Chile , 1999 .

[19]  E. Duursma Productivity of the ocean: Present and past: Edited by W.H. Berger, V.S. Smetacek and G. Wefer. John Wiley & Sons, Chichester, UK 1989. A Dahlem Workshop Report, Life Sciences Research Rep. 44. xiii + 471 pp. ISBN 0-471-92246-3 , 1992 .

[20]  G. Wefer,et al.  Late Quaternary precessional cycles of terrigenous sediment input off the Norte Chico, Chile (27.5°S) and palaeoclimatic implications , 1998 .

[21]  C. E. Morales,et al.  Chlorophyll-a distribution and mesoscale physical processes in upwelling and adjacent oceanic zones off northern Chile (summer–autumn 1994) , 2001, Journal of the Marine Biological Association of the United Kingdom.

[22]  C. Hensen,et al.  Oceanographic control of biogenic opal and diatoms in surface sediments of the Southwestern Atlantic , 2002 .

[23]  G. Fischer,et al.  Siliceous phytoplankton of the western equatorial Atlantic: sediment traps and surface sediments , 2000 .

[24]  G. Fischer,et al.  Seasonal productivity dynamics in the pelagic central Benguela System inferred from the flux of carbonate and silicate organisms , 2002 .

[25]  Lamy,et al.  Late Quaternary rapid climate change in northern Chile , 2000 .

[26]  G. Wefer,et al.  High-Resolution Marine Record of Climatic Change in Mid-latitude Chile during the Last 28,000 Years Based on Terrigenous Sediment Parameters , 1999, Quaternary Research.

[27]  Andrew C. Thomas,et al.  Chlorophyll variability in eastern boundary currents , 2001 .

[28]  D. DeMaster The supply and accumulation of silica in the marine environment , 1981 .

[29]  D. Hebbeln PUCK: Report and preliminary results of R/V Sonne Cruise SO156, Valparaiso (Chile) - Talcahuano (Chile). March 29 - May 14, 2001. , 2001 .

[30]  R. Schneider,et al.  An automated leaching method for the determination of opal in sediments and particulate matter , 1993 .

[31]  S. Avaria,et al.  Effects of the 1982–1983 El Niño on the marine phytoplankton off northern Chile , 1987 .

[32]  A. Thomas Seasonal Distributions of Satellite-Measured Phytoplankton Pigment Concentration Along the Chilean Coast , 1999 .

[33]  H. Schrader,et al.  Peruvian coastal upwelling: Late Quaternary productivity changes revealed by diatoms , 1991 .

[34]  G. Wefer,et al.  Offshore influence of coastal upwelling off Mauritania, NW Africa, as recorded by diatoms in sediment traps at 2195 m water depth , 1998 .

[35]  R. Simonsen,et al.  The diatom plankton of the Indian Ocean expedition of RV "Meteor" 1964- 1965 , 1974 .

[36]  G. Wefer,et al.  Terrigenous sediment supply along the Chilean continental margin: modern regional patterns of texture and composition , 1998 .

[37]  C. Tomas Identifying marine diatoms and dinoflagellates , 1996 .

[38]  Wolfgang H Berger,et al.  Ocean productivity and paleoproductivity - an overview , 1989 .

[39]  Y. Zong IMPLICATIONS OF PARALIA SULCATA ABUNDANCE IN SCOTTISH ISOLATION BASINS , 1997 .

[40]  G. Wefer,et al.  Seasonal variations of the particle flux in the Peru-Chile current at 30°S under ‘normal’ and El Niño conditions , 2000 .

[41]  Paola M. Dávila,et al.  Freshwater input into the coastal ocean and its relation with the salinity distribution off austral Chile (35–55°S) , 1999 .