Time series measurements of transient tracers and tracer-derived transport in the Deep Western Boundary Current between the Labrador Sea and the subtropical Atlantic Ocean at Line W

Author Posting. © American Geophysical Union, 2016. This article is posted here by permission of American Geophysical Union for personal use, not for redistribution. The definitive version was published in Journal of Geophysical Research: Oceans 121 (2016): 8115–8138, doi:10.1002/2016JC011759.Time series measurements of the nuclear fuel reprocessing tracer 129I and the gas ventilation tracer CFC-11 were undertaken on the AR7W section in the Labrador Sea (1997–2014) and on Line W (2004–2014), located over the US continental slope off Cape Cod, to determine advection and mixing time scales for the transport of Denmark Strait Overflow Water (DSOW) within the Deep Western Boundary Current (DWBC). Tracer measurements were also conducted in 2010 over the continental rise southeast of Bermuda to intercept the equatorward flow of DSOW by interior pathways. The Labrador Sea tracer and hydrographic time series data were used as input functions in a boundary current model that employs transit time distributions to simulate the effects of mixing and advection on downstream tracer distributions. Model simulations of tracer levels in the boundary current core and adjacent interior (shoulder) region with which mixing occurs were compared with the Line W time series measurements to determine boundary current model parameters. These results indicate that DSOW is transported from the Labrador Sea to Line W via the DWBC on a time scale of 5–6 years corresponding to a mean flow velocity of 2.7 cm/s while mixing between the core and interior regions occurs with a time constant of 2.6 years. A tracer section over the southern flank of the Bermuda rise indicates that the flow of DSOW that separated from the DWBC had undergone transport through interior pathways on a time scale of 9 years with a mixing time constant of 4 years.US NSF supported this work. Grant Numbers: OCE-0241354, OCE-0726720, OCE-0926848, OCE13-328342017-05-1

USING FLUORESCENT DISSOLVED ORGANIC MATTER TO TRACE ARCTIC SURFACE FRESH WATER

Climate change affects the Arctic environment with regards to permafrost thaw, changes in the riverine runoff and subsequent export of fresh water and terrestrial material to the Arctic Ocean. In this context, the Fram Strait represents a major pathway for export to the Atlantic basin. We assess the potential of visible wavelength dissolved organic matter fluorescence (VIS-FDOM) to trace the origin of Arctic outflow waters. Oceanographic surveys were performed in the Fram Strait, as well as on the east Greenland shelf (following the East Greenland Current), in late summer 2012 and 2013. Meteoric (fmw), sea-ice melt (fsim), Atlantic (faw) and Pacific (fpw) water fractions were determined and FDOM components were identified by PARAFAC modeling. In Fram Strait and east Greenland shelf, a robust correlation between VIS-FDOM and fmw was apparent, suggesting it as a reliable tracer of polar waters. However, variability was observed in the origin of polar waters, in relation to contribution of faw and fpw, between the sampled years. VIS-FDOM traced this variability, and distinguished between the origins of the halocline waters as originating in either the Eurasian or Canada basins. The findings presented highlight the potential of designing in situ DOM fluorometers to trace the freshwater origins and decipher water mass dynamics in the region

Use of SF6 to estimate anthropogenic CO2 in the upper ocean

The highest concentrations of anthropogenic carbon (C_ant) are found in the upper layers of the world ocean. However, this is where seasonal variability of inorganic carbon and related parameters due to thermal and biological effects complicates use of back-calculation approaches for C ant . Tracer based approaches to C_ant estimation are unaffected by biological variability and have found wide application. However, slow-down, even reversal, of the atmospheric growth of chlorofluorocarbons (CFCs) restricts use of these tracers for C ant estimation for waters ventilated since the mid 1990s. Here we apply SF6, a tracer that continues to increase in the atmosphere, as a basis for the C_ant estimation, using samples collected in the midlatitude North Atlantic in 2004. C ant estimates derived from water mass transit time distributions (TTDs) calculated with SF6 are compared to those based on CFC-12. For recently ventilated waters (pCFC-12 > ∼450 ppt), the uncertainty of SF6 based estimates of C_ant is ∼6 μmol kg−1 less than that of CFC-12 based estimates. CFC-12 based estimates remain more reliable for older (deeper) water masses, as a result of the longer input history and more readily detectable concentrations of CFC-12. Historical data suggest that the near-surface saturation of CFC-12 has increased over time, in inverse proportion to its atmospheric growth rate. Use of a time-dependent saturation of CFC-12 in TTD calculations appears to provide more reliable estimation of C_ant

A 30 ‐Year Time Series of Transient Tracer‐Based Estimates of Anthropogenic Carbon in the Central Labrador Sea

We use a 30-year time series (1986–2016) of dichlorodifluoromethane (CFC-12) concentrations with a refined transit time distribution (TTD) method, to estimate the temporal variation of anthropogenic carbon (Cant) in the Central Labrador Sea. We determined that the saturation of CFC-12 and sulfur hexafluroide (SF6) in newly-formed Labrador Sea Water had departed significantly from 100% and varied systematically with time. Multiple linear regression of the time-varying saturation, with the tracer's atmospheric growth rate and the wintertime mixed layer depth as independent variables, allowed reconstruction of the saturation history of CFC-12 and SF6 in wintertime surface waters, which was implemented in the TTD method. Use of the time-varying saturation for CFC-12 gave Cant concentrations ∼7 μmol kg−1 larger than estimates obtained assuming a constant saturation of 100%. The resulting Cant column inventories were ∼20% larger and displayed lower interannual variability compared to conventional TTD-based estimates. The column inventory of Cant increased at an average rate of 1.8 mol m−2 y−1 over the 30-year period. However, the accumulation rate of Cant was higher than this average in the early 1990s and since 2013, whereas inventories remained almost unchanged between 2003 and 2012. The variation in the Cant accumulation rate is shown to be linked to temporal variability in the relative layer thickness of the annually ventilated Labrador Sea Water and the underlying Deep Intermediate Water. The non-steady Cant accumulation highlights the importance of sampling frequency, especially in regions of variable deep mixing and high carbon inventories, and potential misinterpretation of Cant dynamic

Impact of an adiabatic correction technique on the simulation of CFC-12 in a model of the North Atlantic Ocean

A model of the North Atlantic Ocean is used to simulate the spreading of CFC‐12 from the Labrador Sea deep convection site. The standard version of the model fails to capture the local maximum in CFC‐12 concentration that is observed along the continental slope of the western boundary. Hydrographic data are used to apply a simple correction to the model's horizontal momentum equations. The corrected model is much more successful at capturing the nearslope maximum in CFC‐12 concentration than the uncorrected model and also exhibits a 50% increase of the deep southward export of CFC‐12 at 24°N. The difference between the two model runs is shown to be a consequence of the different paths taken by the Deep Western Boundary Current in the two model versions

Variability of USA East Coast surface total alkalinity distributions revealed by automated instrument measurements

Seawater total alkalinity (TA) is one important determinant used to monitor the ocean carbon cycle, whose spatial distributions have previously been characterized along the United States East Coast via discrete bottle samples. Using these data, several regional models for TA retrievals based on practical salinity (S) have been developed. Broad-scale seasonal or interannual variations, however, are not well resolved in these models and existing data are highly seasonally biased. This study reports findings from the first long duration deployment of a new, commercially available TA titrator aboard a research vessel and the continuous underway surface TA measurements produced. The instrument, operated on seven East Coast USA cruises during six months in 2017 and for two months in 2018 on the summertime East Coast Ocean Acidification survey (ECOA-2), collected a total of nearly 11,000 surface TA measurements. Data from these efforts, along with a newly synthesized set of more than 11,000 regional surface TA observations, are analyzed to re-examine distributions of TA and S along the United States East Coast. Overall, regional distributions of S and TA generally agreed with prior findings, but linear TA:S regressions varied markedly over time and deviated from previously developed models. This variability is likely due to a combination of biological, seasonal, and episodic influences and indicates that substantial errors of ±10–20 μmol kg−1 in TA estimation from S can be expected due to these factors. This finding has likely implications for numerical ecosystem modeling and inorganic carbon system calculations. New results presented in this paper provide refined surface TA:S relationships, present more data in space and time, and improve TA modeling uncertainty

Freshwater composition of the waters off southeast Greenland and their link to the Arctic Ocean

Author Posting. © American Geophysical Union, 2009. This article is posted here by permission of American Geophysical Union for personal use, not for redistribution. The definitive version was published in Journal of Geophysical Research 114 (2009): C05020, doi:10.1029/2008JC004808.The freshwater composition of waters on the southeast Greenland shelf and slope are described using a set of high-resolution transects occupied in summer 2004, which included hydrographic, velocity, nutrient, and chemical tracer measurements. The nutrient and tracer data are used to quantify the fractions of Pacific Water, sea ice melt, and meteoric water present in the upper layers of the East Greenland Current (EGC) and East Greenland Coastal Current (EGCC). The EGC/EGCC system dominates the circulation of this region and strongly influences the observed distribution of the three freshwater types. Sea ice melt and meteoric water fractions are surface intensified, reflecting their sources, and generally increase southward from Denmark Strait to Cape Farewell, as well as shoreward. Significant fractions of Pacific Water are found in the subsurface layers of the EGCC, supporting the idea that this inner shelf branch is directly linked to the EGC and thus to the Arctic Ocean. A set of historical sections is examined to investigate the variability of Pacific Water content in the EGC and EGCC from 1984 to 2004 in the vicinity of Denmark Strait. The fraction of Pacific Water increased substantially in the late 1990s and subsequently declined to low levels in 2002 and 2004, mirroring the reduction in Pacific Water content reported previously at Fram Strait. This variability is found to correlate significantly with the Arctic Oscillation index, lagged by 9 years, suggesting that the Arctic Ocean circulation patterns bring varying amounts of Pacific Water to the North Atlantic via the EGC/EGCC.This work was funded by National Science Foundation grant OCE- 0450658. D. Sutherland also received support from the Woods Hole Oceanographic Institution Academic Programs Office

High export of dissolved silica from the Greenland Ice Sheet

Silica is an essential element for marine life and plays a key role in the biogeochemistry of the ocean. Glacial activity stimulates rock weathering, generating dissolved silica that is exported to coastal areas along with meltwater. The magnitude of the dissolved silica export from large glacial areas such as the Greenland Ice Sheet is presently poorly quantified and not accounted for in global budgets. Here we present data from two fjord systems adjacent to the Greenland Ice Sheet which reveal a large export of dissolved silica by glacial meltwater relative to other macronutrients. Upscaled to the entire Greenland Ice Sheet, the export of dissolved silica equals 22 ± 10 Gmol Si yr−1. When the silicate-rich meltwater mixes with upwelled deep water, either inside or outside Greenland's fjords, primary production takes place at increased silicate to nitrate ratios. This likely stimulates the growth of diatoms relative to other phytoplankton groups

Changes in the CFC inventories and formation rates of upper Labrador Sea Water, 1997-2001

Chlorofluorocarbon (component CFC-11) and hydrographic data from 1997, 1999, and 2001 are presented to track the large-scale spreading of the Upper Labrador Sea Water (ULSW) in the subpolar gyre of the North Atlantic Ocean. ULSW is CFC rich and comparatively low in salinity. It is located on top of the denser “classical” Labrador Sea Water (LSW), defined in the density range σΘ = 27.68–27.74 kg m−3. It follows spreading pathways similar to LSW and has entered the eastern North Atlantic. Despite data gaps, the CFC-11 inventories of ULSW in the subpolar North Atlantic (40°–65°N) could be estimated within 11%. The inventory increased from 6.0 ± 0.6 million moles in 1997 to 8.1 ± 0.6 million moles in 1999 and to 9.5 ± 0.6 million moles in 2001. CFC-11 inventory estimates were used to determine ULSW formation rates for different periods. For 1970–97, the mean formation rate resulted in 3.2–3.3 Sv (Sv ≡ 106 m3 s−1). To obtain this estimate, 5.0 million moles of CFC-11 located in 1997 in the ULSW in the subtropical/tropical Atlantic were added to the inventory of the subpolar North Atlantic. An estimate of the mean combined ULSW/LSW formation rate for the same period gave 7.6–8.9 Sv. For the years 1998–99, the ULSW formation rate solely based on the subpolar North Atlantic CFC-11 inventories yielded 6.9–9.2 Sv. At this time, the lack of classical LSW formation was almost compensated for by the strongly pronounced ULSW formation. Indications are presented that the convection area needed in 1998–99 to form this amount of ULSW exceeded the available area in the Labrador Sea. The Irminger Sea might be considered as an additional region favoring ULSW formation. In 2000–01, ULSW formation weakened to 3.3–4.7 Sv. Time series of layer thickness based on historical data indicate that there exists considerable variability of ULSW and classical LSW formation on decadal scales