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Smithsonian at the Poles: Contributions to International Polar

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310 SMITHSONIAN AT THE POLES / SMITH AND COMISO<br />

sp<strong>at</strong>ial scales through time. At present, <strong>the</strong> only means <strong>to</strong><br />

accomplish this on <strong>the</strong> appropri<strong>at</strong>e scales is via s<strong>at</strong>ellite<br />

oceanography.<br />

S<strong>at</strong>ellites presently have <strong>the</strong> capability <strong>to</strong> accur<strong>at</strong>ely<br />

map <strong>the</strong> distributions of ice (Comiso, 2004), sea surface<br />

temper<strong>at</strong>ure (SST; Comiso, 2000; Kwok and Comiso,<br />

2002), and pigment concentr<strong>at</strong>ions (Moore and Abbott,<br />

2000), as well as o<strong>the</strong>r parameters such as winds, b<strong>at</strong>hymetry,<br />

cloud cover, and some gas concentr<strong>at</strong>ions such<br />

as ozone (Comiso, 2009). Some measurements use visible<br />

wavelengths and refl ectance from <strong>the</strong> surface, and<br />

<strong>the</strong>refore <strong>the</strong> d<strong>at</strong>a returned are reduced in space and time<br />

because of clouds; o<strong>the</strong>rs are ei<strong>the</strong>r passively detected or<br />

use o<strong>the</strong>r wavelengths <strong>to</strong> determine <strong>the</strong> distribution of <strong>the</strong><br />

variable. In biological oceanography a major variable of<br />

interest is ocean color, which is converted in<strong>to</strong> quantit<strong>at</strong>ive<br />

estim<strong>at</strong>es of pigment (chlorophyll) concentr<strong>at</strong>ions. While<br />

<strong>the</strong> estim<strong>at</strong>es include signifi cant error terms (because of<br />

<strong>the</strong> dependence of pigment estim<strong>at</strong>es as a function of l<strong>at</strong>itude,<br />

<strong>the</strong> limit<strong>at</strong>ion of refl ectance <strong>to</strong> <strong>the</strong> optical surface<br />

layer r<strong>at</strong>her than <strong>the</strong> entire euphotic zone, and <strong>the</strong> interference<br />

in some w<strong>at</strong>ers of dissolved organic m<strong>at</strong>ter), <strong>the</strong>se<br />

estim<strong>at</strong>es remain, and will remain, <strong>the</strong> only means <strong>to</strong> obtain<br />

synoptic assessments of phy<strong>to</strong>plank<strong>to</strong>n distributions<br />

over large areas as well as <strong>the</strong>ir temporal changes over<br />

rel<strong>at</strong>ively short (e.g., days) periods.<br />

Two s<strong>at</strong>ellites have provided nearly all of <strong>the</strong> d<strong>at</strong>a in <strong>the</strong><br />

past three decades on pigment distributions in <strong>the</strong> Sou<strong>the</strong>rn<br />

Ocean. The fi rst was <strong>the</strong> Nimbus 7 s<strong>at</strong>ellite, launched<br />

in 1978, which carried <strong>the</strong> Coastal Zone Color Scanner<br />

(CZCS). While questions concerning <strong>the</strong> d<strong>at</strong>a quality and<br />

coverage from CZCS have been voiced, <strong>the</strong> d<strong>at</strong>a were used<br />

<strong>to</strong> investig<strong>at</strong>e both <strong>the</strong> large-scale distributions of pigments<br />

in rel<strong>at</strong>ion <strong>to</strong> oceanographic variables (Sullivan et al., 1993;<br />

Comiso et al., 1993) and also <strong>the</strong> specifi c processes and<br />

regions (e.g., Arrigo and McClain, 1994). However, given<br />

<strong>the</strong> orbit, <strong>the</strong> frequency of d<strong>at</strong>a collection in <strong>the</strong> Sou<strong>the</strong>rn<br />

Ocean was quite restricted, and when compounded by <strong>the</strong><br />

loss of d<strong>at</strong>a from cloud cover, <strong>the</strong> temporal frequency was<br />

far from optimal. In 1996 <strong>the</strong> ORBView-2 s<strong>at</strong>ellite was<br />

launched, which included <strong>the</strong> Sea-viewing Wide Field-ofview<br />

Sensor (SeaWiFS). This s<strong>at</strong>ellite proved <strong>to</strong> be an extremely<br />

useful <strong>to</strong>ol for biological oceanographers, as <strong>the</strong><br />

sampling frequency was much gre<strong>at</strong>er and <strong>the</strong> d<strong>at</strong>a return<br />

in polar regions was far gre<strong>at</strong>er. For example, Moore et al.<br />

(1999) were able <strong>to</strong> detect a short-lived bloom in <strong>the</strong> Pacifi c<br />

sec<strong>to</strong>r of <strong>the</strong> Sou<strong>the</strong>rn Ocean th<strong>at</strong> was only infrequently<br />

sampled by ships. Dierssen et al. (2002) assessed <strong>the</strong> variability<br />

of productivity in <strong>the</strong> West Antarctic Peninsula region<br />

and found (based on a model) th<strong>at</strong> pigment concentr<strong>at</strong>ions<br />

were <strong>the</strong> dominant variable cre<strong>at</strong>ing vari<strong>at</strong>ions in space and<br />

time. Smith and Comiso (2008) assessed <strong>the</strong> productivity of<br />

<strong>the</strong> entire Sou<strong>the</strong>rn Ocean and found th<strong>at</strong> <strong>the</strong> “hot spots”<br />

of production were limited <strong>to</strong> continental shelf regions,<br />

and suggested th<strong>at</strong> this was a result of low iron concentr<strong>at</strong>ions<br />

coupled with deeper mixing in <strong>the</strong> offshore regions.<br />

The interaction of low iron and low irradiance (Sunda and<br />

Huntsman, 1997; Boyd and Abraham, 2001) gives rise <strong>to</strong> a<br />

large sp<strong>at</strong>ial limit<strong>at</strong>ion over broad areas.<br />

It is <strong>the</strong> purpose of this manuscript <strong>to</strong> look <strong>at</strong> <strong>the</strong><br />

scales of variability in <strong>the</strong> Sou<strong>the</strong>rn Ocean as a whole and<br />

<strong>to</strong> determine where such vari<strong>at</strong>ions are large by using primary<br />

production derived from SeaWiFS ocean color and<br />

advanced very high resolution radiometer (AVHRR) SST<br />

d<strong>at</strong>a in conjunction with a bio-optical model. We also will<br />

compare <strong>the</strong> modeled productivity with observed values,<br />

where those d<strong>at</strong>a are available <strong>to</strong> test <strong>the</strong> robustness of <strong>the</strong><br />

model. Finally, some aspects of <strong>the</strong> temporal p<strong>at</strong>terns of<br />

productivity in <strong>the</strong> Sou<strong>the</strong>rn Ocean are reviewed.<br />

MATERIALS AND METHODS<br />

Primary productivity was estim<strong>at</strong>ed using various d<strong>at</strong>a<br />

derived from s<strong>at</strong>ellites and a bio-optical model. The model<br />

was a vertically generalized production model (Behrenfeld<br />

and Falkowski, 1997b), in which primary productivity<br />

(PPeu, in units of mg C m �2 d �1 ) was estim<strong>at</strong>ed from <strong>the</strong><br />

following equ<strong>at</strong>ion:<br />

eu<br />

B<br />

opt<br />

o<br />

o<br />

PP = 0. 66125 × P<br />

E<br />

C × Z × D<br />

E + 41 .<br />

S<strong>at</strong> eu Irr<br />

B<br />

where Popt is <strong>the</strong> optimal r<strong>at</strong>e of pho<strong>to</strong>syn<strong>the</strong>sis within<br />

<strong>the</strong> w<strong>at</strong>er column (mg C (mg chl) �1 h�1 ) and is a function<br />

of temper<strong>at</strong>ure, Eo is <strong>the</strong> surface daily pho<strong>to</strong>syn<strong>the</strong>tically<br />

active radi<strong>at</strong>ion (PAR, mol pho<strong>to</strong>ns m�2 d�1 ), Cs<strong>at</strong> is <strong>the</strong><br />

surface chlorophyll concentr<strong>at</strong>ion (mg chl m�3 ) determined<br />

by s<strong>at</strong>ellite, Zeu is <strong>the</strong> depth of <strong>the</strong> euphotic zone<br />

B<br />

(m), and DIrr is <strong>the</strong> pho<strong>to</strong>period (h). Popt was estim<strong>at</strong>ed<br />

from sea surface temper<strong>at</strong>ures by <strong>the</strong> polynomial equ<strong>at</strong>ion<br />

B<br />

of Behrenfeld and Falkowski (1997b), and all Popt values<br />

<strong>at</strong> temper<strong>at</strong>ures less than �1.0ºC were set <strong>to</strong> 1.13.<br />

Temper<strong>at</strong>ure, PAR, ice concentr<strong>at</strong>ions, and chlorophyll<br />

concentr<strong>at</strong>ions were derived from different s<strong>at</strong>ellite<br />

d<strong>at</strong>a sets. Different s<strong>at</strong>ellite d<strong>at</strong>a were mapped <strong>to</strong> <strong>the</strong><br />

same grid as described below. We arbitrarily defi ned <strong>the</strong><br />

Sou<strong>the</strong>rn Ocean roughly as <strong>the</strong> region impacted by seasonal<br />

ice movements and hence set <strong>the</strong> nor<strong>the</strong>rn bound-

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