Contents 1. Introduction 563 2. Phosphorus Occurrence in the Earth's Crust 564 3. Phosphorus Sources and Sinks in the Ocean 564 3.1. Continental Weathering 565 3.2. Anthropogenic Sources 566 3.3. Atmospheric Deposition 566 3.4. Marine Sediments 566 3.5. Seawater−Ocean Crust Interactions 567 4. Phosphorus Forms and Transformations in the Water Column 567 4.1.

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A method for preparation and analysis of the oxygen isotope composition (δ 18 O) of dissolved inorganic phosphate (DIP) has been developed and preliminary results for water samples from various locations are reported. Phosphate is extracted from seawater samples by coprecipitation with magnesium hydroxide. Phosphate is further purified through a series of precipitations and resin separation and is ultimately converted to silver phosphate. Silver phosphate samples are pyrolitically decomposed to carbon monoxide and analyzed for δ 18 O. Silver phosphate samples weighing 0.7 mg (3.5 µmol oxygen) can be analyzed routinely with an average standard deviation of about 0.3‰. There is no isotope fractionation during extraction and blanks are negligible within analytical error. Reproducibility was determined for both laboratory standards and natural samples by multiple analyses. A comparison between filtered and unfiltered natural seawater samples was also conducted and no appreciable difference was observed for the samples tested. The δ18 O values of DIP in seawater determined using this method range from 18.6‰ to 22.3‰, suggesting small but detectable natural variability in seawater. For the San Francisco Bay estuary DIP δ 18 O is more variable, ranging from 11.4‰ near the San Joaquin River to 20.1‰ near the Golden Gate Bridge, and was well correlated with salinity, phosphate concentration, and δ 18 O of water. AcknowledgmentsH.S.W. wishes to thank Henry P. Schwarcz and his laboratory at McMaster University, Hamilton, Ontario, Canada, where most of the exploratory Ce precipitation chemistry was performed.

Interpreting the vulnerability of pelagic calcifiers to ocean acidification (OA) is enhanced by an understanding of their critical thresholds and how these thresholds are modified by other climate change stressors (e.g., warming). To address this need, we undertook a three-part data synthesis for pteropods, one of the calcifying zooplankton group. We conducted the first meta-analysis and threshold analysis of literature characterizing pteropod responses to OA and warming by synthetizing dataset comprising of 2,097 datapoints. Meta-analysis revealed the extent to which responses among studies conducted on differing life stages and disparate geographies could be integrated into a common analysis. The results demonstrated reduced calcification, growth, development, and survival to OA with increased magnitude of sensitivity in the early life stages, under prolonged duration, and with the concurrent exposure of OA and warming, but not species-specific sensitivity. Second, breakpoint analyses identified OA thresholds for several endpoints: dissolution (mild and severe), calcification, egg development, shell growth, and survival. Finally, consensus by a panel of pteropod experts was used to verify thresholds and assign confidence scores for five endpoints with a sufficient signal: noise ratio to develop life-stage specific, duration-dependent thresholds. The range of aragonite saturation state from 1.5-0.9 provides a risk range from early warning to lethal impacts, thus providing a rigorous basis for vulnerability assessments to guide climate change management responses, including an evaluation of the efficacy of local pollution management. In addition, meta-analyses with OA, and warming shows increased vulnerability in two pteropod processes, i.e., shell dissolution and survival, and thus pointing toward increased threshold sensitivity under combined stressor effect.