The distributions of trilobite species were controlled by a combination of
habitat preferences and paleogeographic constraints, which tend to limit th
eir extent. The Lower Ordovician trilobite Carolinites genacinaca Ross, 195
1, however, had a remarkable range unequaled among polymerid trilobites; it
has been recognized on all Ordovician paleocontinents. Its distribution ha
s been explained by an epipelagic mode of life, based on evidence from func
tional morphology, analogy with modern pelagic crustaceans, and geological
occurrence. In such a case, morphological identity throughout its range mig
ht be anticipated, if all occurrences can be postulated to be members of a
single pandemic population. Rotational superimposition has been used to com
pare variation within samples drawn from Alberta, Spitsbergen, and Australi
a with a benchmark population from the western United States. All are morph
ometrically similar. By any criterion, specimens identical to the benchmark
population are found within the Alberta, Spitsbergen and Australia samples
, which represent the extremes of the species' geographic range. A lone cra
nidium from France, previously referred to Carolinites vizcainoi, may be a
juvenile of C. genacinaca or C, tasmaniensis; its differences are consisten
t with ontogeny. A :;mall number of specimens from Siberia and central Chin
a show differences in cranidial proportions from the Utah specimens that ma
y bl: the result of preservational factors and/or photographic technique, o
r may represent genuine morphological disparity; this could be clarified if
more specimens were to become available. This study suggests that C. genac
inaca was ubiquitous in the epipelagic environment in a belt that encircled
the planet between paleolatitudes of approximately 30 degrees N and 30 deg
rees S.