@article { ISI:000395088600004,
	title = {Anthropogenic CO2 accumulation and uptake rates in the Pacific Ocean based on changes in the C-13/C-12 of dissolved inorganic carbon},
	journal = {GLOBAL BIOGEOCHEMICAL CYCLES},
	volume = {31},
	number = {{1}},
	year = {2017},
	month = {JAN},
	pages = {59-80},
	type = {Article},
	abstract = {The anthropogenic CO2 accumulation rate for the Pacific Ocean was estimated from the decrease in C-13 of the dissolved inorganic carbon measured on six World Ocean Circulation Experiment cruises during the 1990s and repeated during Climate Variability and Predictability in the 2000s. A mean depth-integrated anthropogenic C-13 change of -8320mdecade(-1) was estimated for the basin by using the multiple linear regression approach. The largest anthropogenic C-13 decreases occurred between 40 degrees S and 60 degrees S, whereas the smallest decreases occurred in the Southern Ocean and subpolar North Pacific. A mean anthropogenic CO2 accumulation rate of 0.410.13molCm(-2)yr(-1) (0.820.26PgCyr(-1)) was determined based on observed C-13 changes and is in agreement with previous observation- and model-based estimates. The mean dissolved inorganic carbon DIC13 inventory change of -178 +/- 43 parts per thousand molm(-2)decade(-1) was primarily the result of air-sea CO2 exchange acting on the measured air-sea C-13 disequilibrium of similar to-1.2 +/- 0.1 parts per thousand. Regional differences between the DIC13 inventory change and air-sea (CO2)-C-13 flux yielded net anthropogenic CO2 uptake rates (independent of pCO(2)) that ranged from similar to 0 to 1molm(-2)yr(-1) and basin-wide mean of 1.2 +/- 1.5PgCyr(-1). High rates of surface ocean DIC increase and C-13 decrease observed in the Drake Passage (53 degrees S-60 degrees S) support above average anthropogenic CO2 accumulation since 2005. Observed C-13 changes in the Pacific Ocean indicate that ocean transport significantly impacted the anthropogenic CO2 distribution and illustrate the utility of C-13 as a tracer to unravel the processes controlling the present and future accumulation of anth ropogenic CO2 in the ocean.},
	keywords = {anthropogenic change, C-12, C-13, CO2, Pacific Ocean},
	issn = {0886-6236},
	doi = {10.1002/2016GB005460},
	author = {Quay, P. and Sonnerup, R. and Munro, D. and Sweeney, C.}
}
@article {1878,
	title = {Oxygen and carbon isotope records of calcareous nannofossils from the west Philippine Sea during the last 190ka},
	journal = {Earth Science.Journal of China University of Geoscience},
	volume = {33},
	year = {2008},
	note = {id: 1933; NO: Source type: scholarlyjournals; Object type: Article; Copyright: GeoRef in Process, Copyright 2011, American Geosciences Institute. After editing and indexing, this record will be added to Georef.; CSAUnique: 570969-5; AccNum: 570969-5; ISSN: 1000-2383; Peer Reviewed: true},
	month = {2008},
	pages = {183-183-189},
	abstract = {The piston core Ph05-5 recovered from the West Philippine Sea(16.049 degrees N, 124.344 degrees E, water depth 3382m) was used to study the delta (super 18) O and delta (super 13) C variations of calcareous nannofossils. The delta (super 18) O values of calcareous nannofossils were obviously lower in Holocene and the last interglaciation than those in the last and the penultimate glaciation. During the last 190 ka the nannofossil delta (super 18) O values were positively correlated with those of planktonic and benthic foraminifera from the same core. But the average delta (super 18) O value of nannofossils was 0.431X10 (super -3) , higher than that of planktonic foraminifera Globigerinoides rubber, and was 0.410X10 (super -3) , lower than that of planktonic foraminifera Neogloboquadrina dutertrei. All the above three average delta (super 18) O values were much lower than those of benthic foraminifera Cibicides wullerstorfi. The change of nannofossil delta (super 13) C values showed similar trends with the absolute abundance of calcareous nannofossils in core Ph05-5, which also indicates the primary productivity variations in the West Philippine Sea. The primary productivity stayed at a stable but relatively low level at MIS 6 and MIS 5e.There was an abrupt rise at the beginning of MIS 5d for the primary productivity which retained high value until 25 ka BP. The primary productivity showed a slight decline during MIS 2 and MIS 1, but still higher than that of MIS 6 and MIS 5e.},
	keywords = {02D, 24, algae, biochemistry, C-13/C-12, carbon, Cenozoic, Foraminifera, Geochemistry, Holocene, Invertebrata, Isotope geochemistry, isotope ratios, isotopes, Last glacial maximum, microfossils, nannofossils, north pacific, Northwest Pacific, O-18/O-16, oxygen, Pacific Ocean, paleo-oceanography, Philippine Sea, Plantae, Pleistocene, productivity, Protista, Quaternary, Quaternary geology, Stable isotopes, upper Pleistocene, West Pacific},
	isbn = {1000-2383, 1000-2383},
	author = {Jingtao, Zhao and Li, Tiegang and Chang, Fengming and Li, Jun}
}
@article {2120,
	title = {In situ calcium carbonate dissolution in the Pacific Ocean},
	journal = {Global Biogeochemical Cycles},
	volume = {16},
	year = {2002},
	note = {649rqTimes Cited:86
Cited References Count:60
},
	month = {Dec 31},
	abstract = {Over the past several years researchers have been working to synthesize the WOCE/JGOFS global CO(2) survey data to better understand carbon cycling processes in the oceans. The Pacific Ocean data set has over 35,000 sample locations with at least two carbon parameters, oxygen, nutrients, CFC tracers, and hydrographic parameters. In this paper we estimate the in situ CaCO(3) dissolution rates in the Pacific Ocean water column. Calcium carbonate dissolution rates ranging from 0.01-1.1 mumol kg(-1) yr(-1) are observed in intermediate and deepwater beginning near the aragonite saturation horizon. In the North Pacific Intermediate Water between 400 and 800 m, CaCO(3) dissolution rates are more than 7 times faster than observed in middle and deep water depths (average=0.051 m mol kg(-1) yr(-1)). The total amount of CaCO(3) that is dissolved within the Pacific is determined by integrating excess alkalinity throughout the water column. The total inventory of CaCO(3) added by particle dissolution in the Pacific Ocean, north of 40degreesS, is 157 Pg C. This amounts to an average dissolution rate of approximately 0.31 Pg C yr(-1). This estimate is approximately 74\% of the export production of CaCO(3) estimated for the Pacific Ocean. These estimates should be considered to be upper limits for in situ carbonate dissolution in the Pacific Ocean, since a portion of the alkalinity increase results from inputs from sediments.},
	keywords = {anthropogenic co(2), anthropogenic co2, aragonite saturation, atmospheric carbon, caco(3) dissolution, calcite saturation, carbonate lysocline, chemical lysocline, coccolithophore emiliania-huxleyi, indian-ocean, north pacific, organic-matter, Pacific Ocean, panama basin, particulate matter},
	isbn = {0886-6236},
	doi = {10.1029/2002GB001866},
	author = {Feely, R. A. and Sabine, C. L. and Lee, K. and Millero, F. J. and Lamb, M. F. and Greeley, D. and Bullister, J. L. and Key, R. M. and Peng, T. H. and Kozyr, A. and Ono, T. and Wong, C. S.}
}
@conference {1758,
	title = {Progress of the NOSAMS facility WOCE (super 14) C data analysis},
	volume = {38},
	year = {1996},
	note = {id: 2242; Source type: conferencepapers\&proceedings; Object type: Article; Object type: Conference Paper; Copyright: GeoRef, Copyright 2007, American Geological Institute.; CSAUnique: 1999-071631; AccNum: 1999-071631; ISSN: 0033-8222; CODEN: RACAAT},
	month = {1996},
	pages = {123},
	publisher = {University of Arizona, Department of Geosciences, Tucson, AZ, United States (USA)},
	organization = {University of Arizona, Department of Geosciences, Tucson, AZ, United States (USA)},
	address = {United States (USA)},
	keywords = {02D, 07, accelerator mass spectroscopy, C-14, carbon, Isotope geochemistry, isotopes, mass spectroscopy, Oceanography, Pacific Ocean, progress report, radioactive isotopes, report, sea water, spectroscopy},
	author = {von Reden, K. F. and McNichol, A. P. and Schneider, Robert J.}
}
@conference {1794,
	title = {Stable and radio-carbon isotope measurements in the Pacific Ocean; contributions from NOSAMS},
	volume = {77},
	year = {1996},
	note = {id: 2240; Source type: conferencepapers\&proceedings; Object type: Article; Object type: Conference Paper; Copyright: GeoRef, Copyright 2007, American Geological Institute.; CSAUnique: 1997-047916; AccNum: 1997-047916; ISSN: 0096-3941; CODEN: EOSTAJ},
	month = {1996},
	pages = {79},
	publisher = {American Geophysical Union, Washington, DC, United States (USA)},
	organization = {American Geophysical Union, Washington, DC, United States (USA)},
	address = {United States (USA)},
	keywords = {02D, 07, accelerator mass spectroscopy, C-13/C-12, C-14, carbon, chemical analysis, geochemical indicators, high-resolution methods, Isotope geochemistry, isotope ratios, isotopes, marine geology, mass spectroscopy, National Ocean Sciences Accelerator Mass Spectrometry, NOSAMS, Oceanography, Pacific Ocean, radioactive isotopes, radioactive tracers, sampling, sea water, spectroscopy, Stable isotopes, tracers, Woods Hole Oceanographic Institution},
	author = {McNichol, A. P. and von Reden, K. F. and Schneider, R. J. and Key, R. M. and Jones, G. A.}
}
