Jr. Waldman et H. Andreyko, VARIATION IN PATTERNS OF INTERDIGITATION AMONG SUPRANEURALS, PTERYGIOPHORES, AND VERTEBRAL ELEMENTS DIAGNOSTIC FOR STRIPED BASS AND WHITE PERCH, Copeia, (4), 1993, pp. 1097-1113
It is frequently important to discriminate between larvae of striped b
ass Morone saxatilis and white perch M. americana; however, these spec
ies are not well differentiated at the postyolk-sac stage. Previous an
alysis had indicated high discrimination potential (4-14% overlap) for
three osteological characters, interdigitation patterns between (1) s
upraneurals, pterygiophores, and interneural spaces 1 to 6 (IN 1-6); (
2) pterygiophores and interneural spaces 10 to 13 (IN 10-13); and (3)
pterygiophores and interhaemal spaces 12 to 15 (IH 12-15). However, th
e earlier study was based on only 40 striped bass and 50 white perch o
f a single year class from a limited number of tributaries to Chesapea
ke Bay. We examined variation in pattern frequencies in these three ch
aracters among an additional 463 striped bass and 517 white perch from
three major estuaries where they are reproductively sympatric-the Hud
son River, Delaware River, and Chesapeake Bay-and from selected allopa
tric populations. Among samples from the three major estuaries, we fou
nd high univariate discrimination potential for IN 10-13 (3-7% overlap
); moderate discrimination potential for IN 1-6 (14-24% overlap); and
poor discrimination potential for IH 12-15 (24-69% overlap). When all
three characters were used in conjunction to discriminate Hudson River
samples, 88.6% of striped bass and 98.0% of white perch were positive
ly identified. Much of the poorer univariate discrimination potential
for IN 1-6 and IH 12-15 in comparison with the earlier study was due t
o the many additional patterns we identified for these characters. Sig
nificant differences (P < 0.05) in pattern frequencies within each spe
cies were observed in numerous comparisons among samples from primary
populations; subpopulations within Chesapeake Bay; and year classes fr
om the Hudson River. Year class differences are almost certainly envir
onmental in origin. We hypothesize that year class differences are the
products of differential survival of subcohorts within and among year
classes; subcohorts may experience different environmental conditions
that influence the relationships among the timing of supraneural and
pterygiophore development, total pterygiophore counts, and body morpho
metry.