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Smithsonian at the Poles: Contributions to International Polar

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concentr<strong>at</strong>ions are lower and <strong>the</strong> w<strong>at</strong>er column is more<br />

deeply mixed. As is typical of polar regions, <strong>the</strong> massive<br />

phy<strong>to</strong>plank<strong>to</strong>n production th<strong>at</strong> is observed during <strong>the</strong> early<br />

stages of this bloom (in <strong>the</strong> early <strong>to</strong> mid austral spring) is<br />

not accompanied by signifi cant micro- or macrozooplank<strong>to</strong>n<br />

grazing (Caron et al., 2000). The spring bloom also<br />

appears <strong>to</strong> be a period of low bacterial abundance and activity<br />

(Ducklow et al., 2001), although bacteria do bloom<br />

during <strong>the</strong> l<strong>at</strong>er stages of <strong>the</strong> algal bloom, in early <strong>to</strong> mid<br />

summer, coinciding with an increase in dissolved and particul<strong>at</strong>e<br />

organic carbon (Carlson et al., 2000).<br />

Depending on physiological and hydrodynamic fac<strong>to</strong>rs,<br />

this ecological decoupling between primary productivity<br />

and both microbial productivity and grazing may<br />

cause <strong>the</strong> phy<strong>to</strong>plank<strong>to</strong>n <strong>to</strong> sink out of <strong>the</strong> photic zone<br />

(DiTullio et al., 2000; Becquevort and Smith, 2001; Overland<br />

and Stabeno, 2004). This may lead <strong>to</strong> a signifi cant<br />

fl ux of organic m<strong>at</strong>ter <strong>to</strong> <strong>the</strong> ocean fl oor and <strong>to</strong> deepw<strong>at</strong>er<br />

CDOM production. Export of <strong>the</strong> phy<strong>to</strong>plank<strong>to</strong>n out of<br />

<strong>the</strong> photic zone may also lead <strong>to</strong> a decoupling of bloom<br />

dynamics and CDOM cycling.<br />

Here we report on sp<strong>at</strong>ial and temporal p<strong>at</strong>terns in<br />

CDOM spectra observed during <strong>the</strong> early stages of <strong>the</strong> 2005<br />

austral spring Phaeocystis antarctica bloom in <strong>the</strong> seasonal<br />

Ross Sea polynya. Our results show th<strong>at</strong> CDOM changed<br />

very little during a period when chl a concentr<strong>at</strong>ions increased<br />

more than one-hundred-fold. Implic<strong>at</strong>ions of this<br />

fi nding for CDOM cycling in <strong>the</strong> Ross Sea are discussed.<br />

METHODS<br />

ROSS SEA SITE DESCRIPTION AND SAMPLING<br />

A fi eld campaign was conducted aboard <strong>the</strong> R/V<br />

N<strong>at</strong>haniel B. Palmer in <strong>the</strong> seasonal ice-free polynya in <strong>the</strong><br />

Ross Sea, Antarctica, from 8 November <strong>to</strong> 30 November<br />

2005 (Figure 1). During this time, <strong>the</strong> surface seaw<strong>at</strong>er temper<strong>at</strong>ure<br />

was approxim<strong>at</strong>ely – 1.8°C and <strong>the</strong> phy<strong>to</strong>plank<strong>to</strong>n<br />

assemblage was domin<strong>at</strong>ed by colonial Phaeocystis<br />

antarctica. Three main hydrographic st<strong>at</strong>ions were occupied<br />

within <strong>the</strong> Ross Sea polynya for approxim<strong>at</strong>ely seven<br />

days each (i.e., R10, R13, R14). Seaw<strong>at</strong>er samples were<br />

collected from early morning hydrocasts (0400-0700 local<br />

time) directly from Niskin bottles <strong>at</strong>tached <strong>to</strong> a conductivity,<br />

temper<strong>at</strong>ure, and depth (CTD) rosette. Vertical profi les<br />

of a suite of routine measurements were obtained <strong>at</strong> each<br />

st<strong>at</strong>ion including downwelling irradiance (and coupled incident<br />

surface irradiance), chl a, and CDOM absorption<br />

spectra. Additionally, a profi le of dissolved organic carbon<br />

(DOC) was collected <strong>at</strong> one st<strong>at</strong>ion (14F).<br />

CHROMOPHORIC DISSOLVED ORGANIC MATTER CYCLING 321<br />

FIGURE 1. Loc<strong>at</strong>ions of transect sampling st<strong>at</strong>ions south of New<br />

Zealand <strong>to</strong> <strong>the</strong> Ross Sea (open circles) and <strong>the</strong> main hydrographic<br />

st<strong>at</strong>ions th<strong>at</strong> were occupied in <strong>the</strong> Ross Sea (solid black circles) during<br />

<strong>the</strong> NBP05-08 cruise. L<strong>at</strong>itude and longitude inform<strong>at</strong>ion for<br />

specifi c hydrographic st<strong>at</strong>ions (e.g., R10A and R10D) are given in<br />

fi gure captions 4, 5, 8 and 9.<br />

In addition <strong>to</strong> studying CDOM cycling in <strong>the</strong> Ross<br />

Sea, we also collected and analyzed surface w<strong>at</strong>er CDOM<br />

samples during our North-South transit from New Zealand<br />

through <strong>the</strong> Sou<strong>the</strong>rn Ocean <strong>to</strong> <strong>the</strong> Ross Sea (28 Oc<strong>to</strong>ber– 7<br />

November, 2005). Transect sampling for CDOM was conducted<br />

from �49 <strong>to</strong> �75°S. Details of <strong>the</strong> cruise track, sampling<br />

pro<strong>to</strong>cols, analyses conducted and meteoro logical and<br />

sea ice conditions for <strong>the</strong> southbound transect are presented<br />

in Kiene et al. (2007). The transect encompassed open<br />

w<strong>at</strong>ers of <strong>the</strong> Sou<strong>the</strong>rn Ocean, <strong>the</strong> nor<strong>the</strong>rn sea-ice melt<br />

zone, and ice-covered areas near <strong>the</strong> nor<strong>the</strong>rn Ross Sea.<br />

Chlorophyll a was determined fl uorometrically by employing<br />

<strong>the</strong> acidifi c<strong>at</strong>ion method described by Strickland<br />

and Parsons (1968). Briefl y, 50– 250 mL of seaw<strong>at</strong>er was fi ltered<br />

on<strong>to</strong> a 25-mm GF/C glass fi ber fi lter (Wh<strong>at</strong>man Inc.,<br />

Floram Park, New Jersey) with low vacuum. Filters were<br />

placed in 5 mL of 90% HPLC-grade ace<strong>to</strong>ne and extracted<br />

for 24 h <strong>at</strong> – 20°C. Chlorophyll fl uorescence in <strong>the</strong> ace<strong>to</strong>ne<br />

extracts was quantifi ed with a Turner Designs 10-AU fl uorometer<br />

(Sunnyvale, Calafornia) before and after 80-�L addition<br />

of 10% HCl. Dissolved organic carbon samples were

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