Biogenic and lithogenic silica, silicic acid, production of biogenic silica, and irradiance measurements during the Ross Sea Bloom Project 1994-1996


Autoria(s): Smith, Walker O Jr; Nelson, David M; Mathot, Sylvie
Cobertura

MEDIAN LATITUDE: -75.124738 * MEDIAN LONGITUDE: 174.199003 * SOUTH-BOUND LATITUDE: -77.213167 * WEST-BOUND LONGITUDE: 163.815000 * NORTH-BOUND LATITUDE: -66.472000 * EAST-BOUND LONGITUDE: -170.723000 * DATE/TIME START: 1994-11-13T18:09:00 * DATE/TIME END: 1996-01-14T09:20:00

Data(s)

07/03/1999

Resumo

The development of the seasonal phytoplankton bloom in the Ross Sea was studied during two cruises. The first, conducted in November-December 1994, investigated the initiation and rapid growth of the bloom, whereas the second (December 1995-January 1996) concentrated on the bloom's maximum biomass period and the subsequent decline in biomass. Central to the understanding of the controls of growth and the summer decline of the bloom is a quantitative assessment of the growth rate of phytoplankton. Growth rates were estimated over two time scales with different methods. The first estimated daily growth rates from isotropic incorporation under simulated in situ conditions, including 14C, 15N and 32Si uptake measurements combined with estimates of standing stocks of particulate organic carbon, nitrogen and biogenic silica. The second method used daily to weekly changes in biomass at selected locations, with net growth rates being estimated from changes in standing stocks of phytoplankton. In addition, growth rates were estimated in large-volume experiments under optimal irradiances. Growth rates showed distinct temporal patterns. Early in the growing season, short-term estimates suggested that growth rates of in situ assemblages were less than maximum (relative to the temperature-limited maximum) and were likely reduced due to low irradiance regimes encountered under the ice. Growth rates increased thereafter and appeared to reach their maximum as biomass approached the seasonal peak, but decreased markedly in late December. Differences between the major taxonomic groups present were also noted, especially from the isotopic tracer experiments. The haplophyte Phaeocystic antarctica was dominant in 1994 throughout the growing season, and it exhibited the greatest growth rates (mean 0.41/day) during spring. Diatom standing stocks were low early in the growing season, and growth rates averaged 0.100/day. In summer diatoms were more abundant, but their growth rates remained much lower (mean of 0.08/day) than the potential maximum. Understanding growth rate controls is essential to the development of predictive models of the carbon cycle and food webs in Antarctic waters.

Formato

application/zip, 2 datasets

Identificador

https://doi.pangaea.de/10.1594/PANGAEA.758059

doi:10.1594/PANGAEA.758059

Idioma(s)

en

Publicador

PANGAEA

Direitos

CC-BY: Creative Commons Attribution 3.0 Unported

Access constraints: unrestricted

Fonte

Supplement to: Smith, Walker O Jr; Nelson, David M; Mathot, Sylvie (1999): Phytoplankton growth rates in the Ross Sea, Antarctica, determined by independent methods: temporal variations. Journal of Plankton Research, 21(8), 1519-1536, doi:10.1093/plankt/21.8.1519

Palavras-Chave #Biogenic and lithogenic silica concentration (Brzezinski & Nelson 1989); Biogenic silica; Bio-Rosette; Bottle, Niskin; BRO; bSiO2; DEPTH, water; Depth water; E; Event; Irradiance; Lithogenic silica; LSi; Nathaniel B. Palmer; NBP94-06; NIS; pBSi; Production of biogenic silica; Ross Sea; RossSeaBloomProject1994; RossSeaBloomProject1995/1996; RSBP1994-111394-04; RSBP1994-111494-04; RSBP1994-111494-13; RSBP1994-111594-03; RSBP1994-111594-05; RSBP1994-111594-15; RSBP1994-111694-07; RSBP1994-111694-13; RSBP1994-111694-14; RSBP1994-111794-04; RSBP1994-111794-05; RSBP1994-111894-02; RSBP1994-111994-03; RSBP1994-111994-05; RSBP1994-112094-01; RSBP1994-112094-02; RSBP1994-112094-06; RSBP1994-112094-09; RSBP1994-112194-02; RSBP1994-112194-04; RSBP1994-112194-12; RSBP1994-112294-07; RSBP1994-112294-13; RSBP1994-112394-04; RSBP1994-112494-03; RSBP1994-112694-01; RSBP1994-112794-03; RSBP1994-112794-09; RSBP1995/1996-010196-03; RSBP1995/1996-010196-10; RSBP1995/1996-010296-07; RSBP1995/1996-010396-03; RSBP1995/1996-010396-13; RSBP1995/1996-010396-17; RSBP1995/1996-010396-20; RSBP1995/1996-010496-04; RSBP1995/1996-010596-01; RSBP1995/1996-010596-03; RSBP1995/1996-010596-14; RSBP1995/1996-010696-03; RSBP1995/1996-010696-07; RSBP1995/1996-010696-12; RSBP1995/1996-010796-02; RSBP1995/1996-010796-12; RSBP1995/1996-010796-17; RSBP1995/1996-010896-03; RSBP1995/1996-010896-11; RSBP1995/1996-010896-15; RSBP1995/1996-010996-04; RSBP1995/1996-010996-14; RSBP1995/1996-010996-16; RSBP1995/1996-011096-03; RSBP1995/1996-011096-13; RSBP1995/1996-011196-02; RSBP1995/1996-011196-11; RSBP1995/1996-011196-14; RSBP1995/1996-011296-03; RSBP1995/1996-011296-14; RSBP1995/1996-011296-20; RSBP1995/1996-011396-02; RSBP1995/1996-011396-09; RSBP1995/1996-011396-14; RSBP1995/1996-011396-20; RSBP1995/1996-011496-02; RSBP1995/1996-011496-03; RSBP1995/1996-121795-11; RSBP1995/1996-122095-01; RSBP1995/1996-122195-01; RSBP1995/1996-122195-13; RSBP1995/1996-122295-02; RSBP1995/1996-122295-03; RSBP1995/1996-122295-06; RSBP1995/1996-122295-08; RSBP1995/1996-122295-12; RSBP1995/1996-122395-01; RSBP1995/1996-122395-03; RSBP1995/1996-122395-10; RSBP1995/1996-122395-14; RSBP1995/1996-122395-16; RSBP1995/1996-122495-04; RSBP1995/1996-122495-10; RSBP1995/1996-122495-11; RSBP1995/1996-122695-01; RSBP1995/1996-122695-11; RSBP1995/1996-122695-15; RSBP1995/1996-122795-01; RSBP1995/1996-122795-05; RSBP1995/1996-122795-14; RSBP1995/1996-122795-15; RSBP1995/1996-122895-03; RSBP1995/1996-122895-06; RSBP1995/1996-122895-13; RSBP1995/1996-12295-10; RSBP1995/1996-122995-03; RSBP1995/1996-122995-06; RSBP1995/1996-123095-01; RSBP1995/1996-123095-17; RSBP1995/1996-123095-23; RSBP1995/1996-123195-04; Silicic acid uptake rate, specific; Si uptake (Brzezinski & Phillips 1997); Si uptake (Nelson & Goering, 1977); Station#10-CTD#19; Station#11-CTD#21; Station#11-CTD#22; Station#12-CTD#23; Station#13-CTD#24; Station#13-CTD#26; Station#14-CTD#26; Station#15-CTD#28; Station#15-CTD#30; Station#15-CTD#31; Station#16-CTD#29; Station#17-CTD#33; Station#17-CTD#34; Station#18-CTD#35; Station#19-CTD#37; Station#19-CTD#38; Station#1-CTD#2; Station#20-CTD#38; Station#21-CTD#40; Station#21-CTD#44; Station#21-CTD#45; Station#22-CTD#42; Station#22-CTD#43; Station#22-CTD#47; Station#22-CTD#48; Station#23-CTD#45; Station#23-CTD#49; Station#23-CTD#50; Station#24-CTD#46; Station#25-CTD#48; Station#25-CTD#53; Station#25-CTD#54; Station#26-CTD#49; Station#26-CTD#50; Station#27-CTD#58; Station#28-CTD#53; Station#2-CTD#3; Station#31-CTD#57; Station#31-CTD#64; Station#33-CTD#59; Station#33-CTD#67; Station#35-CTD#61; Station#36-CTD#62; Station#36-CTD#72; Station#37-CTD#64; Station#37-CTD#76; Station#39-CTD#67; Station#39-CTD#83; Station#3-CTD#4; Station#40-CTD#69; Station#41-CTD#71; Station#42-CTD#73; Station#43-CTD#74; Station#43-CTD#91; Station#44-CTD#76; Station#45-CTD#78; Station#45-CTD#93; Station#47-CTD#80; Station#49-CTD#83; Station#4-CTD#6; Station#54-CTD#88; Station#56-CTD#91; Station#58-CTD#93; Station#5-CTD#10; Station#5-CTD#9; Station#61-CTD#96; Station#65-CTD#101; Station#67-CTD#103; Station#68-CTD#104; Station#6-CTD#11; Station#71-CTD#108; Station#72-CTD#110; Station#73-CTD#112; Station#74-CTD#114; Station#75-CTD#115; Station#77-CTD#118; Station#79-CTD#121; Station#7-CTD#11; Station#7-CTD#13; Station#7-CTD#14; Station#81-CTD#124; Station#83-CTD#127; Station#84-CTD#129; Station#86-CTD#132; Station#88-CTD#135; Station#89-CTD#137; Station#8-CTD#15; Station#90-CTD#138; Station#91-CTD#140; Station#92-CTD#141; Station#93-CTD#143; Station#94-CTD#144; Station#95-CTD#145; Station#9-CTD#17; Station#9-CTD#18; v pSi upt rate
Tipo

Dataset