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Efficiency of carbon removal per added iron in ocean iron fertilization

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de Baar et al.: <strong>Efficiency</strong> <strong>of</strong> <strong>ocean</strong> <strong>iron</strong> <strong>fertilization</strong>279for quantification <strong>of</strong> the <strong>carbon</strong> C stocks and turnoverrates are the same or similar, hence the <strong>in</strong>herent uncerta<strong>in</strong>tieslikely are similar. On the other hand, the quantifications<strong>of</strong> the Fe supply, stocks and turnover ratesare vastly different. For the <strong>in</strong> situ ex<strong>per</strong>iments, thetotal amount <strong>of</strong> <strong>added</strong> Fe is accurately known, but thefate <strong>of</strong> this Fe is very poorly quantified due to some 60to 75% be<strong>in</strong>g lost, somehow, somewhere. Budget estimations<strong>of</strong> the fate <strong>of</strong> <strong>added</strong> Fe are difficult and onlyone budget assessment has been published (Bowie etal. 2001). For the natural <strong>fertilization</strong> ex<strong>per</strong>iments, thequantification <strong>of</strong> Fe supply from below sediments isdifficult and <strong>in</strong> KEOPS was shown to be far lower thandesirable.Ranges <strong>of</strong> estimatesThe <strong>ocean</strong>s are dynamic regions, with much variability<strong>in</strong> time and place, where day-to-day variability <strong>of</strong>the weather (w<strong>in</strong>d, <strong>in</strong>solation) is a major driver <strong>of</strong> variability<strong>of</strong> any one up<strong>per</strong> <strong>ocean</strong> plankton ecosystem. Inevery s<strong>in</strong>gle <strong>fertilization</strong> ex<strong>per</strong>iment or natural <strong>fertilization</strong>study, the complete 3D mapp<strong>in</strong>g every day <strong>of</strong>all key variables cannot be achieved with merely 1 (orat most 3) ships and their shipboard observers. Foreach ex<strong>per</strong>iment the ensu<strong>in</strong>g dataset, therefore, is verylimited <strong>in</strong> space, <strong>in</strong> time, and <strong>in</strong> a very restricted number<strong>of</strong> key variables. Thus, we are only scratch<strong>in</strong>g thesurface. Nevertheless, for each study, the overarch<strong>in</strong>gsynthesis article (e.g. Tsuda et al. 2003, 2007, Boyd etal. 2004, Coale et al. 2004, Bla<strong>in</strong> et al. 2007) very cleverlycomb<strong>in</strong>es these limited observations <strong>in</strong>to an overallcoherent <strong>in</strong>terpretation, based on the underly<strong>in</strong>gmore specific reports (e.g. Buesseler et al. 2004, Nishiokaet al. 2005, Gerr<strong>in</strong>ga et al. 2008) <strong>of</strong> that 1 study.Previously (de Baar et al. 2005, Boyd et al. 2007) and<strong>in</strong> this article, an effort has been made to comb<strong>in</strong>ethese <strong>in</strong>dividual field projects (IronEx II throughCROZEX, KEOPS) <strong>in</strong>to a synthesis, where <strong>in</strong>evitablyits conclusions carry the sum <strong>of</strong> all uncerta<strong>in</strong>ties <strong>of</strong> thes<strong>in</strong>gle studies. Moreover, the various estimates as citedhere from work by others, as well as <strong>in</strong> this article, areall based on many <strong>in</strong>evitable assumptions, as requireddue to lack <strong>of</strong> data or knowledge, where a large number<strong>of</strong> these assumptions are highly debatable, if notquestionable. In other words, due to the limiteddatasets, there is much room for alternative <strong>in</strong>terpretationsand conclusions.CONCLUSIONSThe most reliable estimate <strong>of</strong> (C:Fe) large-diatoms-optimalis to date ~23 000 for <strong>in</strong> situ large Antarctic diatomswith<strong>in</strong> the Fe-replete SOFeX-South patch. This is <strong>in</strong>good agreement with the diffusion limitation (de Baaret al. unpubl. data) <strong>of</strong> the rate <strong>of</strong> growth <strong>of</strong> largeAntarctic diatoms <strong>in</strong> shipboard and laboratory ex<strong>per</strong>iments<strong>of</strong> <strong>in</strong>cubations <strong>of</strong> s<strong>in</strong>gle species diatoms <strong>in</strong> filteredultraclean natural Antarctic seawater (Timmermanset al. 2004). In the Fe-limited, suboptimal growthconditions <strong>of</strong> the open Antarctic Ocean, large diatomssurvive at very low, but likely <strong>per</strong>sistent, rates <strong>of</strong>growth and may have lower suboptimal <strong>in</strong>tracellularC:Fe ratio values, from ~160 000 at out-patch stations<strong>of</strong> SOFeX-South to ~227 000 <strong>in</strong> the ambient 0.09 nM Fesurface waters <strong>of</strong> Kerguelen Plateau.In the artificial Fe <strong>fertilization</strong> ex<strong>per</strong>iments, the 4estimates thus far <strong>of</strong> (C:Fe) gas-flux-efficiency range from 100to 1000 (Table 3). In the <strong>per</strong>iod after observation shipshave left, this efficiency may either <strong>in</strong>crease ordecrease, due to either cont<strong>in</strong>ued net community productionor a shift to f<strong>in</strong>al net community respiration,respectively.The estimates <strong>of</strong> <strong>carbon</strong> export efficiency at 100 mdepth range from 650 (SERIES) to 6648 (SOFeX-South)with an extrapolated value at 250 m <strong>of</strong> ~3300 forSOFeX-South (Tables 3 & 5). For EIFEX the export efficiencyat 150 m depth is estimated at ~2780 (Table 5).For these artificial <strong>fertilization</strong>s the ~75% immediateloss <strong>of</strong> <strong>added</strong> Fe may be corrected for by a factor<strong>of</strong> ~4 when assum<strong>in</strong>g future or natural <strong>fertilization</strong> asa more stable Fe-organic complex. This would<strong>in</strong>crease the CO 2 drawdown efficiency <strong>in</strong> the 400 to4000 range and the various export efficiency estimatesto a range from ~2600 (SERIES) to ~26 600(SOFeX-South), or even ~100 000 when <strong>in</strong>clud<strong>in</strong>g thehigh estimate <strong>of</strong> SEEDS II based on an assumed verylarge 1000 km 2 patch size.For the artificial <strong>in</strong> situ Fe <strong>fertilization</strong> ex<strong>per</strong>iments,at least the amount <strong>of</strong> <strong>added</strong> Fe is accurately known,such that the uncerta<strong>in</strong>ty <strong>in</strong> the above estimations <strong>of</strong>C:Fe efficiency is due solely to uncerta<strong>in</strong>ty <strong>in</strong> theassessment <strong>of</strong> the C budgets. For natural Fe <strong>fertilization</strong>sthe supply <strong>of</strong> Fe also must be derived from fieldobservations, such that the derived supply <strong>of</strong> Fe has anuncerta<strong>in</strong>ty equal or larger than the uncerta<strong>in</strong>ty <strong>in</strong> theparallel estimation <strong>of</strong> the C budget. Therefore, the(C:Fe) export-efficiency <strong>of</strong> natural <strong>fertilization</strong>s has an <strong>in</strong>herentlylarger uncerta<strong>in</strong>ty than that <strong>of</strong> the artificial <strong>fertilization</strong>ex<strong>per</strong>iments.In the natural Fe <strong>fertilization</strong> at the Crozet Plateauthe (C:Fe) export-efficiency at 100 m depth was reported tobe ~17 200, with<strong>in</strong> reported up<strong>per</strong> and lower estimates<strong>of</strong> ~60 400 and ~5400, respectively (Pollard et al. 2008).In the natural Fe <strong>fertilization</strong> at the Kerguelen Plateau,the derived (C:Fe) export-efficiency at either 100 m or 200 mdepth ranged from ~8050 to ~526 000, largely depend<strong>in</strong>gon the assumed or <strong>in</strong>voked Fe supply term.

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