Storm-induced open-ocean convective mixing is one of the primary processes controlling the supply of nitrate to the sunlit layer of the oligotrophic North Atlantic Subtropical Gyre (NASG). Yet, the magnitude and timing of nitrate fluxes during winter convection is poorly understood due to an absence of targeted process studies. In the northwest NASG, multiple quasi-Lagrangian studies were conducted during the boreal winters of 2004 and 2005 in an effort to sample strong winter convection. During each of the time-series studies, inventories of vertically fluxed nitrate were quantified approximately every twelve hours using the distribution of helium isotopes ([delta]�He) and nitrate in the water column. This method is known as the Helium Flux Gauge Technique (HFGT).
Large variability in surface forcing and density structure of the upper ocean was observed between the two years; however, only winter 2005 experienced convective mixing to depths greater than 150 m. In winter 2004, mild atmospheric conditions coincided with a positive phase in the winter North Atlantic Oscillation (NAO), consistent with the dominant regime experienced during the previous decade. On average 36 � 9 mmol m[-2] of fluxed nitrate was inferred by excess �He in the mixed layer of the ocean during the winter 2004 study period. This inventory of physically transported nitrate is attributed to the sampling of waters laterally advected from nearby eddy features. The sampling of multiple water masses is likely due to the inability of the drogue to persistently follow water masses efficiently. Although physical evidence indicates spatial variability within the time-series data, the length scales of convective mixing appear to be greater than those associated with spatial aliasing as a result of drogue performance. This observation provides us with increased confidence that the objectives for the present study are not compromised by spatial variability in the data.
In contrast, winter 2005 experienced a negative NAO, strong physical forcing and convective mixing to depths > 250 m. Two convectively modified water masses, most likely resulting from a single storm event, were sampled at different stages of development. These two water masses exhibit large variability in the magnitude of nitrate entrained in the convective layer from the thermocline. An average inventory of 247 � 56 mmol NO₃[-]m[-2] was entrained in the rapidly expanding convective layer of the first water mass in the first few days following the storm approach. In contrast, ongoing entrainment of nitrate was absent from the second water mass, sampled two weeks later when the depth of the surface mixed layer was consistently ~ 300 m. These results indicate that surrounding fluid is entrained into the convective layer when it is actively expanding in the vertical. On the other hand, significant fluid entrainment does not occur at the base of the plume once sinking waters have reached a level of neutral buoyancy. The persistence of elevated nitrate stocks (~ 100 mmol m[-2]) in the convective layer two to three weeks after the inferred injection event, suggests sub-optimal nitrate uptake by resident phytoplankton. Phytoplankton growth was most likely resource limited by light or a micronutrient such as iron. Despite the implied biolimitation, changes in chlorophyll-a, a proxy for phytoplankton biomass, indicate net production within the convective layer. On average, the convective layer was observed to support an inventory of 62 � 6mg chlorophyll-a m[-2], increasing at an average rate of 3.4mg m[-2] d[-1]. This inventory indicates a slow build-up of phytoplankton biomass to near bloom levels, ahead of the main spring bloom that typically follows formation of the seasonal thermocline near Bermuda. Net production in the convective layer was likely due to transient periods of increased (weak) surface stability that were observed to support high phytoplankton biomass, following the cessation of thermocline fluid entrainment.
When nitrate and excess �He in samples collected from the thermocline were regressed for the purpose of quantifying nitrate fluxes, the results showed that between 1.6 - 2.0 [mu]mol kg[-1] of dissolved nitrate was present during formation of the water mass. This suggests the source of this excess (above Redfield ratios) nitrate in the thermocline of the NASG is not local, and has ramifications for local nitrogen fixation budgets determined using geochemical approaches.
Thesis supervisors: William J. Jenkins, Senior Scientist, WHOI (United States of America); Philip W. Boyd, Senior Scientist, NIWA (New Zealand); Michael W. Lomas, Senior Scientist, BIOS (Bermuda)
| Identifer | oai:union.ndltd.org:ADTP/266445 |
| Date | January 2009 |
| Creators | Walker, Carolyn Faye, n/a |
| Publisher | University of Otago. Department of Chemistry |
| Source Sets | Australiasian Digital Theses Program |
| Language | English |
| Detected Language | English |
| Rights | http://policy01.otago.ac.nz/policies/FMPro?-db=policies.fm&-format=viewpolicy.html&-lay=viewpolicy&-sortfield=Title&Type=Academic&-recid=33025&-find), Copyright Carolyn Faye Walker |
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