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J W Valentine

Publications and source records attributed to J W Valentine.

At least 19 recordsLinked to original sources

Dissecting latitudinal diversity gradients: functional groups and clades of marine bivalves.

The latitudinal diversity gradient, with maximum taxonomic richness in the tropics, is widely accepted as being pervasive on land, but the existence of this pattern in the sea has been surprisingly controversial. This is partly due to Thorson's influential claim that the normal latitudinal diversity gradient occurs in marine epifauna (taxa living on the surface of the substratum) but not in infauna (burrowing or boring into the substratum), a contrast he attributed to the greater spatial and temporal environmental homogeneity of infaunal habitats. In an analysis of 930 species of north-eastern Pacific marine shelf bivalves, we found that bivalves as a whole, and both infauna and epifauna separately, show a strong latitudinal diversity gradient (measured as number of species per degree latitude) that is closely related to mean sea surface temperature (SST), even in analyses of residuals and first differences. This agrees with results for marine gastropods, but contradicts Thorson's environmental homogeneity hypothesis. The relationship between SST and diversity is consistent with a species-energy hypothesis, but the linkages from SST to diversity remain unclear. Most bivalve clades within broad functional groups conform to the general latitudinal trend, except for the deposit-feeding protobranchs. This group's non-directional pattern may be related to its mode of development, because a similar effect is seen in several other groups locked into this low-fecundity, non-feeding larval mode.

Animals↗

Fossils, molecules and embryos: new perspectives on the Cambrian explosion.

The Cambrian explosion is named for the geologically sudden appearance of numerous metazoan body plans (many of living phyla) between about 530 and 520 million years ago, only 1.7% of the duration of the fossil record of animals. Earlier indications of metazoans are found in the Neoproterozic; minute trails suggesting bilaterian activity date from about 600 million years ago. Larger and more elaborate fossil burrows appear near 543 million years ago, the beginning of the Cambrian Period. Evidence of metazoan activity in both trace and body fossils then increased during the 13 million years leading to the explosion. All living phyla may have originated by the end of the explosion. Molecular divergences among lineages leading to phyla record speciation events that have been earlier than the origins of the new body plans, which can arise many tens of millions of years after an initial branching. Various attempts to date those branchings by using molecular clocks have disagreed widely. While the timing of the evolution of the developmental systems of living metazoan body plans is still uncertain, the distribution of Hox and other developmental control genes among metazoans indicates that an extensive patterning system was in place prior to the Cambrian. However, it is likely that much genomic repatterning occurred during the Early Cambrian, involving both key control genes and regulators within their downstream cascades, as novel body plans evolved.

Animals↗

Marine latitudinal diversity gradients: tests of causal hypotheses.

Latitudinal diversity gradients are first-order expressions of diversity patterns both on land and in the oceans, although the current hypotheses that seek to explain them are based chiefly on terrestrial data. We have assembled a database of the geographic ranges of 3,916 species of marine prosobranch gastropods living on the shelves of the western Atlantic and eastern Pacific Oceans, from the tropics to the Arctic Ocean. Western Atlantic and eastern Pacific diversities are similar, and the diversity gradients are strikingly similar despite many important physical and historical differences between the oceans. This shared diversity pattern cannot be explained by: (i) latitudinal differences in species range-length (Rapoport's rule); (ii) species-area effects; or (iii) recent geologic histories. One parameter that does correlate significantly with diversity in both oceans is solar energy input, as represented by average sea surface temperature. If this correlation is causal, sea surface temperature is probably linked to diversity through some aspect of productivity. In this case, diversity is an evolutionary outcome of trophodynamic processes inherent in ecosystems, and not just a byproduct of physical geographies.

Animals↗

Cleavage patterns and the topology of the metazoan tree of life.

Several major alliances of metazoan phyla have been identified by small subunit rRNA sequence comparisons. It is possible to arrange the phyla to produce a parsimonious distribution of cleavage types, requiring only one change from a radial ancestral condition to spiral cleavage and one other to "idiosyncratic" cleavage; this arrangement is consistent with most of the recent molecular phylogenies. The cleavage shifts are correlated with changes in many of the features that once were used to distinguish Protostomia and Deuterostomia. It is hypothesized that changes in cleavage direction are causally associated with changes in blastomere fates and thus that cleavage type correlates with such features as the identity of mesoderm founder cells, which in turn can constrain the mode of origination of the eucelom. Cleavage changes may also affect the timing of cell fate specification. In a tree that emphasizes cleavage parsimony, radial cleavage, regulative development, and enterocely are ancestral within the Bilateria, and spiral or idiosyncratic cleavages, mosaic development, and schizocely are associated with a change in cleavage direction. Deuterostomy is presumably ancestral and is correlated with radial cleavage for this reason, rather than mechanistically.

Animals↗

Developmental evolution of metazoan bodyplans: the fossil evidence.

Evidence from the fossil record, developmental biology and metazoan phylogeny demonstrates that the rapid origination of major metazoan bodyplans during the late Neoproterozoic and earliest Cambrian was intimately associated with a series of innovations in developmental control mechanisms that included the Hox gene cluster. The interval between about 565 Ma (million years ago) and 530 Ma evidently includes the protostome-deuterostome branching, diversification of independent higher metazoan clades, diversification of important developmental control systems, and formation of higher metazoan bodyplans. Comparative paleontological and developmental studies will allow further tests of alternative models for the sequence of these events, illuminating the association between developmental and bodyplan evolution.

Animals↗

Eastern Pacific molluscan provinces and latitudinal diversity gradient: no evidence for "Rapoport's rule".

"Rapoport's rule," which has gained wide acceptance as a potential explanation for latitudinal and other diversity gradients, holds that mean latitudinal range of species decreases toward the equator. We analyzed latitudinal ranges of 2838 eastern Pacific marine molluscan species, a subset of which figured in the original formulation of Rapoport's rule, and failed to find the predicted trends. Instead, species diversity gradients and range magnitudes appear to vary independently, with the spatial distribution of major oceanographic barriers exerting a strong influence on latitudinal ranges. Biogeographic structure should, therefore, be an important element in the assessment of diversity patterns.

Journal Article↗

Late Precambrian bilaterians: grades and clades.

A broad variety of body plans and subplans appear during a period of perhaps 8 million years (my) within the Early Cambrian, an unequaled explosion of morphological novelty, the ancestral lineages represented chiefly or entirely by trace fossils. Evidence from the fossil record can be combined with that from molecular phylogenetic trees to suggest that the last common ancestor of (i) protostomes and deuterostomes was a roundish worm with a blood vascular system and (ii) of arthropods and annelids was similar, with a hydrostatic hemocoel; these forms are probably among trace makers of the late Precambrian. Cell-phenotype numbers in living phyla, and a model of cell-phenotype number increase, suggest an origin of metazoans near 600 my ago, followed by a passive rise in body-plan complexity. Living phyla appearing during the Cambrian explosion have a Hox/HOM gene cluster, implying its presence in the common ancestral trace makers. The explosion required a repatterning of gene expression that mediated the development of novel body plans but evidently did not require an important, abrupt increase in genomic or morphologic complexity.

Animals↗

Evolutionary dynamics of plants and animals: a comparative approach.

Patterns of longevity and rate of appearance of taxa in the fossil record indicate a different evolutionary dynamic between land plants and marine invertebrates. Among marine invertebrates, rates of taxonomic turnover declined through the Phanerozoic, with increasingly extinction-resistant, long-lived, clades coming to dominate. Among terrestrial vascular plants, rates of turnover increased through the Phanerozoic, with short-lived, extinction-prone clades coming to dominate from the Devonian to the present. Terrestrial vertebrates appear to approximate the marine invertebrate pattern more closely than the plant record. We identify two features which individually or jointly may have influenced this distinction. First, land plants continuously invaded stressful environments during their evolution, while marine invertebrates and terrestrial vertebrates did not. Second, the relative structural simplicity and indeterminate mode of plant growth vs. the relative structural complexity and determinate mode of animal growth may have influenced the timing of major clade origin in the two groups.

Adaptation, Biological↗

Bilaterians of the Precambrian-Cambrian transition and the annelid-arthropod relationship.

The Late Proterozoic fossil record contains the remains of animals that may represent a grade of organization not found among living metazoans. These forms were segmented and large enough to require a hemocoel, yet evidently were not capable of forming penetrating burrows, which are essentially absent from contemporaneous sediments containing locally common but chiefly horizontal trace fossils. As has been noted, there is no evidence that Late Proterozoic invertebrates possessed a coelom suited for peristaltic burrowing. Therefore, the annelidan body plan had probably not appeared. It is not implausible, however, that coelomic spaces in the form of ducts or organ sacs were present in Late Proterozoic segmented forms. Uniramians, some of which employ the hemocoel hydrostatically in lobopodal locomotion, may be allied to segmented hemocoelic forms not unlike sprigginids. Coelomic spaces may have been exploited in some protoarthropod lineages to enhance pedal-wave locomotion, but probably there are no eucoelomic forms in arthropodan ancestry. Annelids may represent an early divergent branch of seriated worms, perhaps rather nemertine-like at first, that developed eucoelomic compartments only in Cambrian time. The extinct grade is most likely to have arisen from flatworm-like ancestors. Of all the proposed phylogenies examined, only that of Manton closely anticipates these interpretations of the early metazoan fossil record.

Journal Article↗

A comparative study of diversification events: the early Paleozoic versus the Mesozoic.

We compare two major long-term diversifications of marine animal families that began during periods of low diversity but produced strikingly different numbers of phyla, classes, and orders. The first is the early-Paleozoic diversification (late Vendian-Ordovician; 182 MY duration) and the other the Mesozoic phase of the post-Paleozoic diversification (183 MY duration). The earlier diversification was associated with a great burst of morphological invention producing many phyla, classes, and orders and displaying high per taxon rates of family origination. The later diversification lacked novel morphologies recognized as phyla and classes, produced fewer orders, and displayed lower per taxon rates of family appearances. The chief difference between the diversifications appears to be that the earlier one proceeded from relatively narrow portions of adaptive space, whereas the latter proceeded from species widely scattered among adaptive zones and representing a variety of body plans. This difference is believed to explain the major differences in the products of these great radiations. Our data support those models that hold that evolutionary opportunity is a major factor in the outcome of evolutionary processes.

Adaptation, Biological↗

Mass extinctions: Sensitivity of marine larval types.

Developmental types of marine invertebrates may be divided into planktotrophs, which feed on suspended food items, and nonplanktotrophs, which do not feed but are supplied with nutrients (yolk) parentally; these may represent high mortality-fecundity and low mortality-fecundity strategies, respectively. Most versions of the bolide impact hypothesis of mass extinction propose occlusion of the sun by dust or smoke and severance of planktonic food chains for months or a few years, and this should select preferentially against planktotrophs. Yet among fossil prosobranch gastropods, planktotrophs survived the end-Cretaceous extinction equally as well as nonplanktotrophs. Indirect evidence suggests that end-Permian extinctions may have selected against planktotrophs but that the effect was prolonged over millions of years.

Journal Article↗

"Hopeful monsters," transposons, and Metazoan radiation.

The appearance of many novel morphologies, frequently expressed taxonomically as new phyla, classes, or orders, occurs with such rapidity in evolutionary time that microevolutionary substitutions involving structural genes seem an implausible mechanism. It has been suggested that such novelties are produced by changes in developmental and regulatory structures and patterns rather than by an accumulation of single structural gene changes. The horizontal transmission of genetic material via RNA-based viruses between members of a population may rapidly create intrafertile sub-populations that differ markedly from their parents and form the basis of new morphological types, avoiding the usual fitness problems associated with "hopeful monsters."

Journal Article↗

Multiple origins of life.

There is some indication that life may have originated readily under primitive earth conditions. If there were multiple origins of life, the result could have been a polyphyletic biota today. Using simple stochastic models for diversification and extinction, we conclude: (i) the probability of survival of life is low unless there are multiple origins, and (ii) given survival of life and given as many as 10 independent origins of life, the odds are that all but one would have gone extinct, yielding the monophyletic biota we have now. The fact of the survival of our particular form of life does not imply that it was unique or superior.

Biological Evolution↗

Genetic variability in krill.

We have estimated genetic variability by gel electrophoresis in three species of krill, genus Euphausia (Arthropoda: Crustacea). Genetic variability is low where trophic resources are most seasonal, and high where trophic resources are most stable. Simlar trends have been found in benthic marine invertebrates. The observed trends of genetic variability do not correlate with trends in the stability of physical environment parameters.

Alleles↗