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Fishery bulletin of the Fish and Wildlife Service - NOAA

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BIOLOGY OF THE ATLANTIC MACKEREL 175<br />

That each series includes truly homologous groups is indicated by several criteria,<br />

independent <strong>of</strong> <strong>the</strong> straight-line conformity. In <strong>the</strong> К series, <strong>the</strong> modes all tend<br />

toward peakedness. In <strong>the</strong> S series, <strong>the</strong>y all tend to be broad. In <strong>the</strong> Т series <strong>the</strong>y<br />

are intermediate in shape. The progress in each series is reasonably consistent <strong>and</strong><br />

<strong>the</strong> course <strong>of</strong> growth is roughly parallel in <strong>the</strong> three series; moreover, <strong>the</strong> slight departure<br />

from parallelism is in <strong>the</strong> expected direction, <strong>the</strong> later series having <strong>the</strong> higher<br />

growth rates consistent with <strong>the</strong>ir development in <strong>the</strong> warmer water to which <strong>the</strong>y<br />

are subjected. Fur<strong>the</strong>rmore, <strong>the</strong> modes are consistently present in <strong>the</strong> material from<br />

each cruise with only two exceptions, R in cruise III <strong>and</strong> S in cruise IV. The absence<br />

<strong>of</strong> S in cruise IV is plainly due to failure on that cruise to visit certain stations in <strong>the</strong><br />

sou<strong>the</strong>rly end <strong>of</strong> <strong>the</strong> spawning area, where previous cruises would lead one to expect<br />

4.0<br />

3.0<br />

(Г 2.0<br />

Ul<br />

Ш<br />

э '-о<br />

z<br />

о<br />

Î.O<br />

2.0<br />

3.0<br />

.6 .в 1.0 |.г 1.4 1.6 1.8<br />

L O Q OF LENGTH<br />

FIQUEI в.—Frequency distribution <strong>of</strong> lengths <strong>of</strong> larvae plotted logarithmically.<br />

to mid larvae <strong>of</strong> sizes appropriate for this series (fig. 13, IV). Absence <strong>of</strong> К in cruise<br />

III has no such simple explanation, <strong>and</strong> can be explained only as chance sampling<br />

fluctuation.<br />

Only one o<strong>the</strong>r reasonably sensible alternative to <strong>the</strong> series <strong>of</strong> homõlogies in figure<br />

7 is possible. According to this alternative, R <strong>of</strong> cruises I <strong>and</strong> II would be considered<br />

forerunners <strong>of</strong> <strong>the</strong> 9- <strong>and</strong> 10-mm. larvae <strong>of</strong> cruise III; S <strong>of</strong> cruise III considered <strong>the</strong><br />

forerunner, <strong>of</strong> R <strong>of</strong> cruises V <strong>and</strong> VI'; <strong>the</strong> 3- <strong>and</strong> 4-mm. larvae <strong>of</strong> cruise IV, <strong>the</strong> forerunner<br />

<strong>of</strong> S <strong>of</strong> cruise V; S <strong>of</strong> cruises V <strong>and</strong> VI, <strong>the</strong> forerunner <strong>of</strong> R <strong>of</strong> cruise VII; <strong>and</strong><br />

T <strong>of</strong> cruise VI, <strong>the</strong> forerunner <strong>of</strong> S <strong>of</strong> cruise VIII. But, this would not account for <strong>the</strong><br />

presence <strong>of</strong> such prominent modes as R <strong>of</strong> cruise IV, S <strong>of</strong> cruise VII, or T <strong>of</strong> cruise<br />

VIIÍ; <strong>and</strong> <strong>the</strong>re are o<strong>the</strong>r objections to this alternative set <strong>of</strong> homõlogies which will<br />

be considered later.

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