S. Creasey et al., THE POPULATION BIOLOGY AND GENETICS OF THE DEEP-SEA SPIDER CRAB, ENCEPHALOIDES-ARMSTRONGI WOOD-MASON 1891 (DECAPODA, MAJIDAE), Philosophical transactions-Royal Society of London. Biological sciences, 352(1351), 1997, pp. 365-379
Numerous specimens of the majid spider crab, Encephaloides armstrongi,
were sampled from six stations (populations), between 150 and 650 m d
epth, on the continental slope off the coast of Oman. This extended th
e known geographic and bathymetric range of E. armstrongi, which is no
w known to occur along the continental margins of. the northern Indian
Ocean from the western coast of Burma to the coast of Oman. This band
-like distribution is contiguous to the oxygen minimum zone in this re
gion. The biology and generics of populations of Encephaloides armstro
ngi separated by depth were studied. The overall sex ratio of the E. a
rmstrongi sampled was male-biased (p < 0.01; 3.3 males: 1 female; S-o
= 0.538). However, sex ratio varied both between populations (p < 0.01
) and between size classes of crabs. Size frequency analysis indicated
that the male and female crabs consisted of at least two instars, one
between 6 and 16 mm carapace length and one between 16 and 29 mm cara
pace length, which probably represented the terminal (pubertal) moult
for most individuals. Accumulation of female crabs in the terminal ins
tar probably caused the variation of sex ratio with size classes. Some
male crabs grew to a larger size (up to 38 mm carapace length), possi
bly as a result of maturity at later instars. Length frequency distrib
ution was significantly different between sexes (one-way ANOVA p < 0.0
01). Within sexes, length frequency distributions varied between diffe
rent populations. In both male and female Encephaloides armstrongi the
individuals from a single population located at 150 m depth were sign
ificantly smaller than individuals at all other stations and were cons
idered to represent a juvenile cohort. For female crabs no other signi
ficant differences were detected in length frequency between populatio
ns from 300 m to 650 m depth. Significant differences in length freque
ncy were detected between male crabs from populations between 300 and
650 m depth. Horizontal starch gel electrophoresis was used to detect
six enzyme systems coding for eight loci for individuals sampled from
each population of Encephaloides armstrongi. Genetic identity (I) valu
es between populations of E. armstrongi (I = 0.98-1.00) were within th
e normal range for conspecific populations. Observed heterozygosity (H
-o = 0.080-0.146) was lower than expected heterozygosity (H-e = 0.111-
0.160): but in the normal range detected for eukaryotic organisms. F-s
tatistics were used to analyse between population (F-ST) and within po
pulation (F-IS) genetic structure. For both male and female E. armstro
ngi significant genetic differentiation was detected between the popul
ation located at 150 m depth and all other populations. Analyses of F-
IS and F-ST, excluding the 150 m population indicated that for female
E. armstrongi there was no significant structuring within or between p
opulations. For male E. armstrongi significant heterozygote deficienci
es were detected within populations and significant genetic differenti
ation between populations. The most likely explanations for the observ
ations of the present study are: the population of Encephaloides armst
rongi located at 150 m depth represented a juvenile cohort that is gen
etically distinct from deeper populations; female E. armstrongi formed
a single population between 300 m and 650 m depth in the sampling are
a; male E. armstrongi were from two or more genetically distinct popul
ations which are represented by different numbers of individuals at st
ations between 300 m and 650 m depth. This caused the observed signifi
cant differences in morphology (size distribution) and allele frequenc
ies of male populations. It is likely that E. armstrongi exhibits gend
er-biased dispersal and that the crabs collected between 300 m and 650
m depth formed spawning aggregations. This also explains the bias in
ses ratio of individuals sampled in the present study.