Overwintering Growth and Development of Larval Euphausia
superba: An Interannual Comparison Under
Varying Environmental Conditions West of the Antarctic
Peninsula
Kendra L. Daly
Growth,
molting and development of larval Antarctic krill (Euphausia superba Dana)
were investigated in the vicinity of Marguerite Bay during four cruises in
austral fall and winter 2001 and 2002 as part of the U.S. Southern Ocean GLOBEC
program. Overwintering survival of
larvae has been linked to annual sea ice formation and extent, as sea ice biota
may provide food when other sources are scarce in the water column. During fall 2001, larval stages C2 - F6 were
very abundant (1 - 19 individuals m-3), with F4-F6 stages dominant
at all stations over the shelf. During
fall 2002, C2 - F4 larvae were abundant offshelf (0.01 - 110 m-3),
while all stages were scarce on the shelf.
Despite the presence of declining diatom and radiolarian blooms during
fall of both years, average chlorophyll concentrations were low (0.10 vs.0.22
µg l-1). Carbon content of
larvae in fall suggested that lipid storage was moderate (41 vs. 38 % of
DW). The median fall larval growth rate
(0.027 mm d-1) was lower and the intermolt period (19 d) longer than
summer values. The following results
suggest that larvae were food limited in winter of both years: (1) the median growth rate decreased (0.00 mm
d-1) and the intermolt period increased (40 d), (2) dry weight and
body carbon and nitrogen decreased (ca. 0.4% d-1), and (3) 88% of F6
individuals did not develop to the juvenile stage after molting. In addition, an experiment showed that some
larvae could survive starvation for a month by combusting body reserves (ca. 1%
decrease in DW and body C and N d-1), implying that a portion of the
population was resilient to the suboptimal food supply. In winter 2001, furcilia were commonly
observed near the under-surface of sea ice, but only rarely in 2002 until
mid-September. Even though sea ice
formed up to two months earlier in 2002, ice algae accessible to krill at the
ice-water interface was not an abundant food source in either year (0.05 vs.
0.07 µg chl l-1). Low gut
fluorescence values also indicate that little nutrition was derived from autotrophs in winter.
Instead, larvae were opportunistic scavengers and likely exploited all
available food sources, including microzooplankton, detritus, and sea ice
biota. In summary, larval krill
exhibited several overwintering behaviors: (1) flexible feeding, (2) flexible
morphology (i.e., delayed development), (3) flexible physiology (i.e.,
increased intermolt period, reduced growth), (4) some lipid storage, and (6)
ability to withstand starvation by combusting body C and N. Because most larvae did not shrink in length,
this measurement may not be a good indicator of the body combustion
strategy. At these high latitudes, sea
ice biota may be a more important food in spring when irradiance levels
increase than in winter. Winter survivors
during 2001 resulted in a significant recruitment to the juvenile size class
during spring.
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