41 research outputs found
Seasonal and inter-annual variability in nutrient supply in relation to mixing in the Bay of Biscay
Post-print
The diagenetic formation of metal-rich layers in sapropel-containing sediments in the eastern Mediterranean
2008 Inter-laboratory Comparison Study of a Reference Material for Nutrients in Seawater
Autoclaved natural seawater collected in the North Pacific Ocean was used as a reference material for nutrients in seawater (RMNS) during an inter-laboratory comparison (I/C) study conducted in 2008. This study was a follow-up to previous studies conducted in 2003 and 2006. A set of six samples was distributed to each of 58 laboratories in 15 countries around the globe, and results were returned by 54 of those laboratories (15 countries). The homogeneities of samples used in the 2008 I/C study, based on analyses for three determinants, were improved compared to those of samples used in the 2003 and 2006 I/C studies.
Results of these I/C studies indicate that most of the participating laboratories have an analytical technique for nutrients that is sufficient to provide data of high comparability. The differences between reported concentrations from the same laboratories in the 2006 and 2008 I/C studies for the same batch of RMNS indicate that most of the laboratories have been maintaining internal comparability for two years.
Thus, with the current high level of performance in the participating laboratories, the use of a common reference material and the adaptation of an internationally accepted
nutrient scale system would increase comparability among laboratories worldwide, and
the use of a certified reference material would establish traceability.
In the 2008 I/C study we observed a problem of non-linearity of the instruments of the participating laboratories similar to that observed among the laboratories in the 2006
I/C study. This problem of non-linearity should be investigated and discussed to improve comparability for the full range of nutrient concentrations. For silicate comparability in particular, we see relatively larger consensus standard deviations than those for nitrate and phosphate
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Constraining oceanic dust deposition using surface ocean dissolved Al
We use measurements of ocean surface dissolved Al, a global Biogeochemical Elemental Cycling (BEC) ocean model, and the global Dust Entrainment and Deposition (DEAD) model to constrain dust deposition to the oceans. Our Al database contains all available measurements with best coverage in the Atlantic. Vertical profiles and seasonal data exist in limited regions. Observations show that surface dissolved Al is distributed similarly to the dust deposition predicted by DEAD and other models. There is an equatorial Atlantic Al maximum that decreases toward higher latitudes. There are high Al concentrations in the Mediterranean Sea and the Arabian Sea and low concentrations in the Pacific and the Southern Ocean. The ocean basins maintain more distinct Al profiles than Fe profiles in the upper ocean, consistent with a weaker biological influence on Al than Fe. The BEC-predicted surface dissolved Al compares relatively well with observations. The Al distribution reflects the combined effects of Al input from dust and Al removal by particle scavenging and biological uptake by diatoms. Model-observed biases suggest a southward shift of maximum dust deposition compared to current dust model predictions. DEAD appears to overestimate deposition north of 30°N in the Pacific and to underestimate deposition south of 30°N. Observed Al concentrations and the ocean model–predicted surface Al lifetime provide a semi-independent method to estimate oceanic dust deposition. This technique indicates that DEAD may overestimate dust deposition to the north equatorial Atlantic but underestimate in other Atlantic regions, the Southern Ocean, and the Arabian Sea. However, spatial variations in aerosol Al solubility may also contribute to the model-observation mismatch. Our results have implications for all dust-borne ocean nutrients including Fe and demonstrate the potential of marine geochemical data to constrain atmospheric aerosol deposition fields
Variability of alkalinity and the alkalinity-salinity relationship in the tropical and subtropical surface ocean
The variability of total alkalinity (TA) and its relationship with salinity in the tropical and subtropical surface ocean were examined using data collected in various marine environments from a ship of opportunity. In the open ocean regions of the Atlantic, Pacific, and Indian Oceans, sea surface TA variability was observed to be mainly controlled by the simple dilution or concentration (SDC) effect of precipitation and evaporation, and the measured concentrations of TA agreed well with those predicted from salinity and temperature. Non-SDC changes in alkalinity in ocean margins and inland seas were examined by comparing the salinity-normalized alkalinity with that of the open ocean end-member. Non-SDC alkalinity additions to the western North Atlantic margin, eastern North Pacific margin, and Mediterranean Sea were identified, which mainly resulted from river inputs and shelf currents. In contrast, removal of TA through formation and sedimentation of calcium carbonate was observed to be an important control in the Red Sea. The concentration of the river end-member can only be reliably derived from the y intercept of TA-S regression (TAS0) in river-dominated systems such as estuaries and river plumes. In coastal regions where other processes (evaporation, shelf currents, upwelling, calcification, etc.) are more influential, TAS0 can significantly deviate from the river water concentration and hence be an unreliable indicator of it. Negative values of TAS0 can result from non-SDC TA removal at the low salinity end (relative to the salinity of the oceanic end-member) and/or non-SDC TA addition at high salinities (as occurs in the Mediterranean Sea)