Publications by Year: 1998

1998
Powell JA, Mitter C, Farrell BD. Evolution of larval food preference in Lepidoptera. In: Kristensen NP Handbook of Zoology. Part 35. Insecta, Lepidoptera, Moths and Butterflies, Volume 1: Evolution, Systematics, and Biogeography. Berlin: deGruyter ; 1998. pp. 403-422.
Farrell BD. "Inordinate fondness" explained: Why are there so many beetles?. Science. 1998;281 (5376) :555-559.Abstract

The phylogeny of the Phytophaga, the Largest and oldest radiation of herbivorous beetles, was reconstructed from 115 complete DNA sequences for the 18S nuclear ribosomal subunit and from 212 morphological characters. The results of these analyses were used to interpret the role of angiosperms in beetle diversification. Jurassic fossils represent basal Lineages that are still associated with conifers and cycads. Repeated origins of angiosperm-feeding beetle Lineages are associated with enhanced rates of beetle diversification, indicating a series of adaptive radiations. Collectively, these radiations represent nearly half of the species in the order Coleoptera and a similar proportion of herbivorous insect species.

Kelley ST, Farrell BD. Is specialization a dead end? The phylogeny of host use in Dendroctonus bark beetles (Scolytidae). Evolution. 1998;52 (6) :1731-1743.Abstract

Ecological explanations for the prevalence of resource specialists are abundant, whereas phylogenetic evidence on their origins is scarce. In this paper, we provide a molecular phylogenetic study of the 19 specialist or generalist species in the bark beetle genus Dendroctonus, which collectively attack species in four different genera in the conifer family Pinaceae. Given substantial variation in diet breadth, we asked two general questions concerning the evolution of resource use in this group. How conservative is the evolution of host use in these insects? Does specialization tend to be derived (i.e., a "dead end")?To answer these questions, we estimated the phylogeny of Dendroctonus using mitochondrial DNA sequences and mapped transitions in resource use on the resulting phylogeny estimate. The evolution of affiliations with Pinus and Picea hosts in Dendroctonus was conservative among beetle species (PTP test; P < 0.012), but there was no significant correspondence between the phylogeny of these beetles and the phylogeny among their Pinaceae hosts (among genera, P = 0.28; among Pinus species, P = 0.82).Degree of specialization, as measured in the proportion of hosts used, was bimodally distributed with "generalist" species utilizing greater than or equal to 60% of the congeneric hosts within their range and six specialist species utilizing less than or equal to 40% of the available hosts. Among the generalists, we found a strong correlation between the number of hosts encountered and the number of hosts utilized (R = 0.97, P < 0.0001), whereas there was no significant correlation among the specialists (R = 0.27, P = 0.59). The evolution of specialization in Dendroctonus proved highly labile-specialists arose from generalists at least six separate times (without reversal) all in derived positions, and closer examination of some specialists revealed instances where they appear to have lost particular host species from their diet. However, evidence from the ecological literature also suggests that several Dendroctonus generalists may have increased their range of host genera within the Pinaceae.

Farrell BD, Mitter C. The timing of insect/plant diversification: might Tetraopes (Coleoptera : Cerambycidae) and Asclepias (Asclepiadaceae) have co-evolved?. Biological Journal of the Linnean Society. 1998;63 (4) :553-577.Abstract

Ehrlich and Raven's essay on coevolution has stimulated voluminous work on the mechanisms of insect/plant interaction, but few explicit tests of their model's prediction that the evolutionary success of entire insect and plant clades is governed by their putative reciprocal adaptations. This paper begins an inquiry into possible coevolutionary diversification for North American milkweeds of the genus Asclepias and one of their few major herbivores, the longhorn beetle genus Tetraopes, focusing first on the historical duration and continuity of the interaction. A phylogeny for Tetraopes and relatives, estimated from morphology and allozymes, shows evident similarity to a morphology based hostplant cladogram synthesized from the literature, though the significance of the correspondence under heuristic statistical tests depends on the treatment of one beetle species reported (without certainty) from multiple host species. Fossils and biogeography support the interpretation that cladogram correspondence reflects synchronous diversification of these two clades, hence opportunity for coevolution, rather than beetle 'host-tracking' of previously-diversified plants. Cladogram correspondence is more evident at higher than at lower levels, as expected under Ehrlich and Raven's model. An apparent phylogenetic progression in the potency and location of milkweed cardenolides: seemingly related to species diversity of both Asclepias and Tetraopes subclades, provides further suggestive evidence for that model. The phylogeography of the Tetraopes/Asclepias assemblage suggests that extant species evolved largely in their current, often quite localized biomes, facilitating potential experimental tests for hypotheses of adaptation and counteradaptation and their importance to diversification. (C) 1998 The Linnean Society of London.