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Vol. 53 - Alaska Resources Library and Information Services

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Six time intervals were established to study larval hatch <strong>and</strong><br />

development (Fig. 3.17a <strong>and</strong> b).<br />

They are based on average sampling<br />

dates of cruise legs in various years, <strong>and</strong> usually span three-week<br />

intervals.<br />

The earliest zooplankton samples collected that contained<br />

red king crab larvae were prior to April 18 in 1977; the latest<br />

collections were made in August, 1982. Based on data from 1977 <strong>and</strong><br />

1978, SI larvae were abundant by mid-April <strong>and</strong> SII by late April, 1978<br />

(Fig. 3.17a).<br />

In some years, therefore, larvae hatch as early as April<br />

1 (note that 40% of all larvae were already SII in late April 1978). In<br />

other years hatching can begin a month or more later. In mid-May, 1976,<br />

virtually all larvae were still SI <strong>and</strong> in early June, 1980, 40% of<br />

larvae were SI. (During the first NAS leg from April 18 to May 7, 1983,<br />

no larvae were found along the entire NAS from Unimak Isl<strong>and</strong> to Port<br />

Heiden on the first pass.<br />

Larvae were present on the return, however,<br />

at stations revisited between May 1-6, indicating hatch began about May<br />

1). The largest interannual difference in apparent time of hatch was<br />

between the years 1976 <strong>and</strong> 1979 (Fig. 3.17a) when all larvae were SI in<br />

mid-May, 1976, but all were SIV in mid-June, 1979, indicating a very<br />

late <strong>and</strong> early hatch, respectively.<br />

Larval hatch is apparently not a synchronous event throughout the<br />

female population along the NAS as evidenced by the presence of several<br />

larval stages at most stations (Fig. 3.17a <strong>and</strong> b). Data of 1980, 1981,<br />

<strong>and</strong> 1982 show that four larval stages were present in the water column<br />

during several time intervals, although only two stages were usually<br />

dominate (Fig. 3.17b).<br />

573

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