TL;DR: In this paper, two methods for determination of organic carbon, inorganic carbon, and total nitrogen in sediments, sediment trap materials, and plankton are described, using an automated CHN analyzer for all elemental determinations.
Abstract: Two methods are described for determination of organic carbon, inorganic carbon, and total nitrogen in sediments, sediment trap materials, and plankton. Both methods discriminate organic and inorganic carbon by acidification, avoid losses of acid-soluble organic and inorganic matter, and utilize an automated CHN analyzer for all elemental determinations. Short-term precisions for organic carbon and total nitrogen are about ± 1% of the measured value with blank levels < 1.5 µg for each element.
TL;DR: In a series of oxic and anoxic incubation experiments, the authors examined the fate of organic matter and the alteration of its carbon and nitrogen isotopic composition during microbial degradation.
TL;DR: In this paper, the authors show that most of the organic carbon rain in the deep sea is carried by calcium carbonate, because it is denser than opal and more abundant than terrigenous material.
Abstract: [1] We compiled and standardized sediment trap data below 1000 m depth from 52 locations around the globe to infer the implications of the Armstrong et al. [2002] “ballast” model to the ratio of organic carbon to calcium carbonate in the deep sea (the rain ratio). We distinguished three forms of mineral ballast: calcium carbonate, opal, and lithogenic material. We concur with Armstrong et al. [2002] that organic carbon sinking fluxes correlate tightly with mineral fluxes. Based on the correlations seen in the trap data, we conclude that most of the organic carbon rain in the deep sea is carried by calcium carbonate, because it is denser than opal and more abundant than terrigenous material. This analysis explains the constancy of the organic carbon to calcium carbonate rain ratio in the deep sea today, and argues against large changes in the mean value of this ratio in the past. However, sediment trap data show variability in the ratio in areas of high relative calcium carbonate export (mass CaCO3/mass ratio > 0.4), unexplainable by the model, leaving open the possibility of regional variations in the rain ratio in the past.
TL;DR: In this article, the authors investigated the geographic contrasts of POC export at m/b and the supply rate of ∑CO2 to the world mesopelagic water column.
TL;DR: In this article, multiple linear regression is used to derive an algorithm suggesting that the transfer efficiency of organic carbon increases with the flux of carbonate and decreases with water depth and seasonality.
Abstract: [1] Particle fluxes measured with time series sediment traps deployed below 2000 m at 68 sites in the world ocean are combined with satellite-derived estimates of export production from the overlying water to assess the factors affecting the transfer of particulate organic matter from surface to deep water. Multiple linear regression is used to derive an algorithm suggesting that the transfer efficiency of organic carbon, defined as the settling flux of organic carbon normalized to export production, increases with the flux of carbonate and decreases with water depth and seasonality. The algorithm predicts >80% of the organic carbon transfer efficiency variability in diverse oceanic regions. The influence of the carbonate flux suggests that the ballasting effect of this biogenic mineral may be an important factor promoting export of organic carbon to the deep sea by increasing the density of settling particles. However, the lack of a similar effect for biogenic opal suggests that factors other than particle density also play a role. The adverse effect of increasing seasonality on the transfer efficiency of carbon to the deep sea is tentatively attributed to greater biodegradability of organic matter exported during bloom events. In high latitude opal-dominated regions with high f-ratios and seasonality, while a higher fraction of net production is exported, a higher fraction of the exported organic matter is remineralized before reaching bathypelagic depths. On the other hand, in warm, low latitude, carbonate-dominated regions with low f-ratios and seasonality, a higher fraction of the exported organic matter sinks to the deep sea.