California Current Ecosystem LTER

Biogenic Silica

Title
Vertical profiles of in-situ biogenic silica (bSi) from discrete rosette bottle samples from CCE-LTER starting with cruise P1706.

Abstract
Samples are taken at discrete depths from rosette bottles in the California Current Ecosystem and measured for biogenic silica (bSi) concentration to create bSi depth profiles. Diatom community and physiology affect biogenic silica concentration. These data are being used to investigate the effects of Fe limitation on carbon and silica cycling in the CCE.

Keywords
diatoms, nutrient cycling, oceans, phytoplankton, silica, biogenic silica, bSi, silica cycling

LTER Data System Record
http://dx.doi.org/10.6073/pasta/265091f2b7435d010e69ab27b7a0aa47
Projects
California Current Ecosystem LTER

Creators
Barbeau, Katherine (kbarbeau@ucsd.edu)

Contact
CCE LTER Information Manager (ccelter.im@gmail.com)

Other Personnel
Fulton, Kayleen sampling and analysis

Data

table biogenic silica
biogenic silica concentrations at discrete depths
Rows: 448
Columns: 11
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Methods


Biogenic silica collection and analysis
In-situ bSi samples were transferred to 1 L polycarbonate bottles and filtered onto 47 mm 0.6 um polycarbonate filters, which were then dried in the oven at 60˚C for 24 hours and stored for on-shore analysis. Incubation bSi samples used 400-900 mL seawater, depending on availability, and were filtered and dried similarly. Samples were digested in 4 mL 0.2 N NaOH in HF-clean teflon tubes at 95˚C for 40 minutes and then cooled in an ice bath and neutralized with 1 mL 1 N HCl. After centrifuging 10 min at 1100 x g, 4 mL were withdrawn, diluted and measured at 810 nm for reactive silicate via the colorimetric ammonium molybdate method (Brzezinski & Nelson, 1995; Paasche, 1973; Strickland & Parsons, 1977), where a 10 mL sample was added to a 4 mL molybdate solution and allowed to stand 10 minutes before being quenched by a reducing reagent of a metol-sulfite solution, oxalic acid and sulfuric acid.