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März, Christian; Poulton, Simon W; Wagner, Thomas; Schnetger, Bernhard; Brumsack, Hans-Jürgen (2016): Extractions and analyses of reactive phosphorus in the Bering Sea from IODP Holes 323-U1341A and 323-U1341B [dataset]. PANGAEA, https://doi.org/10.1594/PANGAEA.857261, Supplement to: März, C et al. (2014): Phosphorus burial and diagenesis in the central Bering Sea (Bowers Ridge, IODP Site U1341): Perspectives on the marine P cycle. Chemical Geology, 363, 270-282, https://doi.org/10.1016/j.chemgeo.2013.11.004

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Abstract:
To reconstruct the cycling of reactive phosphorus (P) in the Bering Sea, a P speciation record covering the last ~ 4 Ma was generated from sediments recovered during Integrated Ocean Drilling Program (IODP) Expedition 323 at Site U1341 (Bowers Ridge). A chemical extraction procedure distinguishing between different operationally defined P fractions provides new insight into reactive P input, burial and diagenetic transformations. Reactive P mass accumulation rates (MARs) are ~ 20-110 µmol/cm2/ka, which is comparable to other open ocean locations but orders of magnitude lower than most upwelling settings. We find that authigenic carbonate fluorapatite (CFA) and opal-bound P are the dominant P fractions at Site U1341. An overall increasing contribution of CFA to total P with sediment depth is consistent with a gradual "sink switching" from more labile P fractions (fish remains, Fe oxides, organic matter) to stable authigenic CFA. However, the positive correlation of CFA with Al content implies that a significant portion of the supposedly reactive CFA is non-reactive "detrital contamination" by eolian and/or riverine CFA. In contrast to CFA, opal-bound P has rarely been studied in marine sediments. We find for the first time that opal-bound P directly correlates with excess silica contents. This P fraction was apparently available to biosiliceous phytoplankton at the time of sediment deposition and is a long-term sink for reactive P in the ocean, despite the likelihood for diagenetic re-mobilisation of this P at depth (indicated by increasing ratios of excess silica to opal-bound P). Average reactive P MARs at Site U1341 increase by ~ 25% if opal-bound P is accounted for, but decrease by ~ 25% if 50% of the extracted CFA fraction (based on the lowest CFA value at Site U1341) is assumed to be detrital. Combining our results with literature data, we present a qualitative perspective of terrestrial CFA and opal-bound P deposition in the modern ocean. Riverine CFA input has mostly been reported from continental shelves and margins draining P-rich lithologies, while eolian CFA input is found across wide ocean regions underlying the Northern Hemispheric "dust belt". Opal-bound P burial is important in the Southern Ocean, North Pacific, and likely in upwelling areas. Shifts in detrital CFA and opal-bound P deposition across ocean basins likely occurred over time, responding to changing weathering patterns, sea level, and biogenic opal deposition.
Further details:
Latimer, Jennifer C; Filippelli, Gabriel M; Hendy, Ingrid L; Newkirk, Derrick R (2006): Opal-associated particulate phosphorus: Implications for the marine P cycle. Geochimica et Cosmochimica Acta, 70(15), 3843-3854, https://doi.org/10.1016/j.gca.2006.04.033
Ruttenberg, K (1992): Development of a sequential extraction method for different forms of phosphorus in marine sediments. Limnology and Oceanography, 37(7), 1460-1482, https://doi.org/10.4319/lo.1992.37.7.1460
Schenau, S J; de Lange, Gert J (2001): Phosphorus regeneration vs. burial in sediments of the Arabian Sea. Marine Chemistry, 75(3), 201-217, https://doi.org/10.1016/S0304-4203(01)00037-8
Coverage:
Median Latitude: 54.033341 * Median Longitude: 179.008475 * South-bound Latitude: 54.033307 * West-bound Longitude: 179.008332 * North-bound Latitude: 54.033375 * East-bound Longitude: 179.008618
Minimum DEPTH, sediment/rock: 1.3 m * Maximum DEPTH, sediment/rock: 600.5 m
Event(s):
323-U1341A * Latitude: 54.033375 * Longitude: 179.008332 * Elevation: -2139.6 m * Recovery: 373.23 m * Campaign: Exp323 (Bering Sea Paleoceanography) * Basis: Joides Resolution * Method/Device: Drilling/drill rig (DRILL) * Comment: 41 cores; 359.2 m cored; 104 % recovered
323-U1341B * Latitude: 54.033307 * Longitude: 179.008618 * Elevation: -2139.6 m * Recovery: 594.98 m * Campaign: Exp323 (Bering Sea Paleoceanography) * Basis: Joides Resolution * Method/Device: Drilling/drill rig (DRILL) * Comment: 71 cores; 600 m cored; 99 % recovered
Comment:
Extraction steps according to Ruttenberg (1992; doi:10.4319/lo.1992.37.7.1460), Schenau and De Lange (2000; doi:10.1016/S0304-4203(01)00037-8) and Latimer et al. (2006; doi:10.1016/j.gca.2006.04.033).
Parameter(s):
#NameShort NameUnitPrincipal InvestigatorMethod/DeviceComment
1Event labelEventMärz, Christian
2Sample code/labelSample labelMärz, ChristianDSDP/ODP/IODP sample designation
3Sample IDSample IDMärz, Christian
4DEPTH, sediment/rockDepth sedmMärz, ChristianGeocode
5Silicon dioxideSiO2%März, ChristianX-ray fluorescence spectrometer (Philips PW2400)
6Aluminium oxideAl2O3%März, ChristianX-ray fluorescence spectrometer (Philips PW2400)
7Silicon excessSi xs%März, ChristianX-ray fluorescence spectrometer (Philips PW2400)
8PhosphorusP%März, ChristianX-ray fluorescence spectrometer (Philips PW2400)
9Phosphorus excessP xs%März, ChristianX-ray fluorescence spectrometer (Philips PW2400)
10PhosphorusP%März, ChristianX-ray fluorescence spectrometer (Philips PW2400)Step 1 for weight %: Extraction procedure = 6× 2 M NH4Cl (pH 7 with NaOH), shake for 4h; Extracted fraction = Exchangable/carbonate-bound P, amorph. Ca-phosphate, fish bones; relative standard deviations triplicate analysis = 5-13%.
11PhosphorusP%März, ChristianX-ray fluorescence spectrometer (Philips PW2400)Step 2 for weight %: Extraction procedure = 0.3 M Na-citrate/1 M NaHCO3/0.14 M Na-dithionite (pH 7.5), shake for 8 h; 1 M MgCl2 (pH 8), shake for 0.5h; Extracted fraction = Iron-bound P; relative standard deviations triplicate analysis = 1-6%.
12PhosphorusP%März, ChristianX-ray fluorescence spectrometer (Philips PW2400)Step 3 for weight %: Extraction procedure = 1 M Na-acetate (pH 4.0 with acetic acid), shake for 6 h; 2 × 1MMgCl2 (pH 8), shake for 0.5h; Extracted fraction = Carbonate fluorapatite; relative standard deviations triplicate analysis = 1-8%.
13PhosphorusP%März, ChristianX-ray fluorescence spectrometer (Philips PW2400)Step 4 for weight %: Extraction procedure = 1 M HCl, shake for 24h; 1 M MgCl2 (pH 8), shake for 0.5h; Extracted fraction = Fluorapatite; relative standard deviations triplicate analysis = 1-9%.
14PhosphorusP%März, ChristianX-ray fluorescence spectrometer (Philips PW2400)Step 5 for weight %: Extraction procedure = Ashing at 550 °C for 2 h; 1 M HCl, shake for 24 h; Extracted fraction = Organic P; relative standard deviations triplicate analysis = 8-10%.
15PhosphorusP%März, ChristianX-ray fluorescence spectrometer (Philips PW2400)Step 6 for weight %: Extraction procedure = 1.5 M NaOH, in water bath at 85 °C for 2 h, shake every 15 min.; Extracted fraction = Opal-bound P; relative standard deviations triplicate analysis = 3-5%.
16PhosphorusP%März, ChristianX-ray fluorescence spectrometer (Philips PW2400)Step 1 of total P in %: Extraction procedure = 6× 2 M NH4Cl (pH 7 with NaOH), shake for 4h; Extracted fraction = Exchangable/carbonate-bound P, amorph. Ca-phosphate, fish bones; relative standard deviations triplicate analysis = 5-13%.
17PhosphorusP%März, ChristianX-ray fluorescence spectrometer (Philips PW2400)Step 2 of total P in %: Extraction procedure = 0.3 M Na-citrate/1 M NaHCO3/0.14 M Na-dithionite (pH 7.5), shake for 8 h; 1 M MgCl2 (pH 8), shake for 0.5h; Extracted fraction = Iron-bound P; relative standard deviations triplicate analysis = 1-6%.
18PhosphorusP%März, ChristianX-ray fluorescence spectrometer (Philips PW2400)Step 3 of total P in %: Extraction procedure = 1 M Na-acetate (pH 4.0 with acetic acid), shake for 6 h; 2 × 1MMgCl2 (pH 8), shake for 0.5h; Extracted fraction = Carbonate fluorapatite; relative standard deviations triplicate analysis = 1-8%.
19PhosphorusP%März, ChristianX-ray fluorescence spectrometer (Philips PW2400)Step 4 of total P in %: Extraction procedure = 1 M HCl, shake for 24h; 1 M MgCl2 (pH 8), shake for 0.5h; Extracted fraction = Fluorapatite; relative standard deviations triplicate analysis = 1-9%.
20PhosphorusP%März, ChristianX-ray fluorescence spectrometer (Philips PW2400)Step 5 of total P in %: Extraction procedure = Ashing at 550 °C for 2 h; 1 M HCl, shake for 24 h; Extracted fraction = Organic P; relative standard deviations triplicate analysis = 8-10%.
21PhosphorusP%März, ChristianX-ray fluorescence spectrometer (Philips PW2400)Step 6 of total P in %: Extraction procedure = 1.5 M NaOH, in water bath at 85 °C for 2 h, shake every 15 min.; Extracted fraction = Opal-bound P; relative standard deviations triplicate analysis = 3-5%.
22ResidualResidual%März, ChristianX-ray fluorescence spectrometer (Philips PW2400)of total Phosphorus
23RatioRatioMärz, ChristianX-ray fluorescence spectrometer (Philips PW2400)of Silicon excess/opal-Phosphorus (Si xs/opal-P)
24Accumulation rate, phosphorus, reactiveAcc rate P reactµmol/cm2/kaMärz, ChristianCalculatedWith opal-bound P, all CFA authigenic
25Accumulation rate, phosphorus, reactiveAcc rate P reactµmol/cm2/kaMärz, ChristianCalculatedWithout opal-bound P, all CFA authigenic
26Accumulation rate, phosphorus, reactiveAcc rate P reactµmol/cm2/kaMärz, ChristianCalculatedWith opal-bound P, 50% of CFA authigenic
Size:
2740 data points

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