Planktic foraminiferal populations and test flux in the eastern North Atlantic Ocean


Autoria(s): Schiebel, Ralf; Hemleben, Christoph
Cobertura

MEDIAN LATITUDE: 45.928970 * MEDIAN LONGITUDE: -19.431226 * SOUTH-BOUND LATITUDE: 33.939867 * WEST-BOUND LONGITUDE: -22.304000 * NORTH-BOUND LATITUDE: 57.995833 * EAST-BOUND LONGITUDE: -17.757050 * DATE/TIME START: 1988-04-08T09:40:00 * DATE/TIME END: 1993-06-16T08:56:00

Data(s)

21/10/2000

Resumo

Planktic foraminiferal assemblages vary in response to seasonal fluctuations of hydrographic properties, between water masses, and after periodical changes and episodic events (e.g. reproduction, storms). Distinct annual variability of the planktic foraminiferal flux is also known from sediment trap data. In this paper we discuss the short-term impacts on interannual flux rates based on data from opening-closing net hauls obtained between the ocean surface and 500 m water depth. Data were recorded during April, May, June, and August at around 47°N, 20°W (BIOTRANS) in 1988, 1989, 1990, 1992, 1993, and during May 1989 and 1992 at 57°N, 20-22°W. Species assemblages closely resemble each other when comparing the mixed layer fauna with the fauna of the upper 100 m and the upper 500 m of the water column. In addition, species assemblages >100 µm are almost indistinguishable from assemblages that are >125 µm in test size. The standing stock of planktic foraminifers at BIOTRANS can vary by more than one order of magnitude over different years; however, species assemblages may be similar when comparing corresponding seasons. Early summer assemblages (June) are distinctly different from late summer assemblages (August). Significant variations in the species composition during spring (April/May) are independent of the mixed layer depth. Spring assemblages are characterized by high numbers of Globigerinita glutinata. In particular, day-to-day variations of the number of specimens and in species composition may have the same order of magnitude as interannual variations. This appears to be independent of the reproduction cycle. Species assemblages at 47°N and 57°N are similar during spring, although surface water temperatures and salinities differ by up to 10°C and 0.7 (PSU). We suggest that the main factors controlling the planktic foraminiferal fauna are the trophic properties in the upper ocean productive layer. Planktic foraminiferal carbonate flux as calculated from assemblages reveals large seasonal variations, a quasi-annual periodicity in flux levels, and substantial differences in timing and magnitude of peak fluxes. At the BIOTRANS station, the average annual planktic foraminiferal CaCO3 fluxes at 100 and 500 m depth are estimated to be 22.4 and 10.0 g/m**2/yr, respectively.

Formato

application/zip, 153 datasets

Identificador

https://doi.pangaea.de/10.1594/PANGAEA.728676

doi:10.1594/PANGAEA.728676

Idioma(s)

en

Publicador

PANGAEA

Direitos

CC-BY: Creative Commons Attribution 3.0 Unported

Access constraints: unrestricted

Fonte

Supplement to: Schiebel, Ralf; Hemleben, Christoph (2000): Interannual variability of planktic foraminiferal populations and test flux in the eastern North Atlantic Ocean (JGOFS). Deep Sea Research Part II: Topical Studies in Oceanography, 47(9-11), 1809-1852, doi:10.1016/S0967-0645(00)00008-4

Palavras-Chave #102; 111; 129; 148; 158; 164; 167; 172; 173; 176; 177; 1781; 181; 187; 188; 199; 204; 211; 219; 224; 225; 227; 228; 230; 231; 247; 25; 250; 277; 285; 286; 289; 292; 30; 301; 302; 306; 309; 311; 314; 319; 320; 322; 323; 324; 325; 327; 328; 351; 357; 367; 373; 374; 381; 389; 390; 396; 407; 430; 437; 440; 445; 45; 452; 455; 460; 463; 475; 481; 485; 487; 492; 499; 52; 553; 562; 569; 77; 80; 87; 887; 895; 896; 899; 900; 901; 92; 96; 99; Aegi Ridge; Arquipelago; Azores front; B. digitata; B. pumilio; Bear Island; Beella digitata; Berggrenia pumilio; Biotrans; C. nitida; Candeina nitida; Counting, foraminifera, live (Walton, 1952, Cushman Found Foram Res 3:56-60); Counting, foraminifera, planktic; D. anfracta; Dentagloborotalia anfracta; Depth, bottom/max; Depth, top/min; DEPTH, water; Depth bot; Depth top; Depth water; FCA97; FCA97C_MSN1339; FCA97C_MSN1340; FCA97C_MSN1343; FCA97C_MSN1344; FCA97C_MSN1345; FCA97C_MSN1346; Foraminifera, planktic indeterminata; Foram plankt indet; G. bulloides; G. calida; G. conglobatus; G. crassaformis; G. digitata; G. falconensis; G. glutinata; G. hirsuta; G. inflata; G. menardii; G. minuta; G. ruber p; G. ruber w; G. rubescens; G. sacculifer; G. scitula; G. siphonifera; G. tenella; G. theyeri; G. truncatulinoides; G. tumida; G. ungulata; G. uvula; G. vivans; Gallitellia vivans; GeoTü; GIK/IfG; Globigerina bulloides; Globigerina falconensis; Globigerinella calida; Globigerinella digitata; Globigerinella siphonifera; Globigerinita glutinata; Globigerinita minuta; Globigerinita uvula; Globigerinoides conglobatus; Globigerinoides ruber pink; Globigerinoides ruber white; Globigerinoides sacculifer; Globorotalia crassaformis; Globorotalia hirsuta; Globorotalia inflata; Globorotalia menardii; Globorotalia scitula; Globorotalia theyeri; Globorotalia truncatulinoides; Globorotalia tumida; Globorotalia ungulata; Globoturborotalita rubescens; Globoturborotalita tenella; H. digitata; H. pelagica; Hastigerina digitata; Hastigerina pelagica; Institute for Geosciences, Christian Albrechts University, Kiel; JGOFS; Joint Global Ocean Flux Study; Lofoten Basin; M10/2; M10/2_MSN218; M10/2_MSN219; M10/2_MSN229; M10/2_MSN231; M10/2_MSN232; M10/2_MSN234; M10/2_MSN238; M10/2_MSN251; M10/2_MSN261; M10/2_MSN262; M10/2_MSN265; M10/2_MSN268; M10/2_MSN284; M10/2_MSN295; M10/2_MSN297; M10/2_MSN298; M10/2_MSN315; M10/2_MSN317; M10/2_MSN319; M10/2_MSN322; M10/2_MSN332; M10/2_MSN334; M11/1; M11/1_MSN517; M11/1_MSN520; M11/1_MSN522; M11/1_MSN524; M11/1_MSN526; M11/1_MSN528; M12/3; M12/3_MSN533; M12/3_MSN535; M12/3_MSN536; M12/3_MSN538; M12/3_MSN541; M12/3_MSN543; M12/3_MSN545; M12/3_MSN547; M12/3_MSN557; M12/3_MSN558; M12/3_MSN559; M12/3_MSN560; M12/3_MSN561; M12/3_MSN562; M21/1; M21/1_MSN603; M21/1_MSN604; M21/1_MSN605; M21/1_MSN606; M21/1_MSN607; M21/1_MSN608; M21/1_MSN609; M21/1_MSN610; M21/1_MSN611; M21/1_MSN613; M21/1_MSN614; M21/1_MSN615; M21/1_MSN619; M21/1_MSN620; M21/2; M21/2_MSN624; M21/2_MSN627; M21/2_MSN628; M21/2_MSN629; M21/2_MSN638; M21/2_MSN639; M21/2_MSN640; M21/2_MSN641; M21/2_MSN642; M21/2_MSN643; M21/2_MSN644; M21/2_MSN647; M21/2_MSN648; M21/2_MSN649; M21/2_MSN650; M21/2_MSN651; M21/2_MSN652; M21/2_MSN656; M21/2_MSN657; M21/2_MSN658; M21/3; M21/3_MSN661; M21/3_MSN662; M21/3_MSN663; M21/3_MSN671; M21/3_MSN674; M21/3_MSN675; M21/3_MSN676; M21/3_MSN687; M21/3_MSN688; M21/4; M21/4_MSN694; M21/4_MSN695; M21/4_MSN696; M21/4_MSN697; M21/4_MSN698; M21/4_MSN699; M21/4_MSN700; M21/4_MSN701; M21/4_MSN702; M21/4_MSN703; M21/4_MSN704; M21/4_MSN705; M21/4_MSN706; M21/4_MSN707; M21/4_MSN710; M21/4_MSN711; M21/4_MSN712; M21/4_MSN713; M21/4_MSN714; M21/4_MSN715; M21/4_MSN716; M21/4_MSN717; M21/4_MSN718; M21/4_MSN719; M21/4_MSN720; M21/4_MSN721; M21/4_MSN722; M21/4_MSN723; M21/4_MSN724; M21/5; M21/5_MSN728; M21/5_MSN729; M21/5_MSN730; M21/5_MSN731; M21/5_MSN732; M21/5_MSN733; M21/5_MSN734; M21/5_MSN735; M21/5_MSN736; M21/5_MSN739; M21/5_MSN740; M21/5_MSN741; M21/5_MSN742; M21/5_MSN743; M21/6; M21/6_MSN766; M21/6_MSN767; M21/6_MSN768; M21/6_MSN776; M21/6_MSN777; M21/6_MSN778; M21/6_MSN784; M21/6_MSN785; M21/6_MSN786; M21/6_MSN787; M21/6_MSN788; M21/6_MSN789; M26/1; M26/1_MSN843; M26/1_MSN844; M26/1_MSN845; M27/2; M27/2_MSN879; M27/2_MSN882; M27/2_MSN883; M27/2_MSN884; M36/2; M36/2_MSN1107; M36/6; M36/6_MSN1193; M36/6_MSN1194; M36/6_MSN1195; M36/6_MSN1196; M36/6_MSN1197; M36/6_MSN1198; M42/3; M42/3_MSN1359; M42/3_MSN1360; M42/3_MSN1361; M42/3_MSN1362; M42/3_MSN1363; M42/3_MSN1364; M42/3_MSN1365; M42/3_MSN1366; M42/3_MSN1367; M42/3_MSN1368; M42/3_MSN1369; M42/3_MSN1370; M6/7; M6/7_MSN100; M6/7_MSN116; M6/7_MSN119; M6/7_MSN125; M6/7_MSN137; M6/7_MSN140; M6/7_MSN148; M6/7_MSN150; M6/7_MSN91; M6/7_MSN95; M6/7_MSN96; Madeira Basin; Meteor (1986); MSN; Multiple opening/closing net; N. dutertrei; N. incompta; N. pachyderma; NE-Atlantik; Neogloboquadrina dutertrei; Neogloboquadrina incompta; Neogloboquadrina pachyderma; North Atlantic; Northeast Atlantic; Norwegian Sea; O. universa; Orbulina universa; P. obliquiloculata; Paleoceanography at Tübingen University; PO200F; POS200/6; POS200/6_MSN837; POS231/3; POS231/3_MSN1329; POS231/3_MSN1330; POS231/3_MSN1331; POS231/3_MSN1332; POS231/3_MSN1333; POS231/3_MSN1334; POS231/3_MSN1335; POS231/3_MSN1336; POS231/3_MSN1337; POS231/3_MSN1338; POS247; POS247/2_MSN1371; POS247/2_MSN1372; POS247/2_MSN1373; POS247/2_MSN1374; POS247/2_MSN1375; POS247/2_MSN1376; POS247/2_MSN1377; POS247/2_MSN1378; POS247/2_MSN1379; POS247/2_MSN1380; POS247/2_MSN1381; POS247/2_MSN1382; POS247/2_MSN1383; POS247/2_MSN1384; POS247/2_MSN1385; POS247/2_MSN1386; POS247/2_MSN1387; POS247/2_MSN1388; POS247/2_MSN1389; POS247/2_MSN1390; POS247/2_MSN1391; Poseidon; Pulleniatina obliquiloculata; Rockall Plateau; S. dehiscens; S. globigerum; Samp com; Sample comment; Sphaeroidinella dehiscens; Streptochilus globigerum; T. clarkei; T. compressa; T. humilis; T. iota; T. parkerae; T. quinqueloba; Tenuitella compressa; Tenuitella iota; Tenuitella parkerae; test size in µm; Turborotalita clarkei; Turborotalita humilis; Turborotalita quinqueloba
Tipo

Dataset