Publications by Year: 1999

1999
Farrell BD. Flowers and Insect Evolution. Science. 1999;283 (5399) :143.
Dobler S, Farrell BD. Host use evolution in Chrysochus milkweed beetles: evidence from behaviour, population genetics and phylogeny. Molecular Ecology. 1999;8 (8) :1297-1307.Abstract

In two sister species of leaf beetles with overlapping host associations, Chrysochus auratus and C. cobaltinus, we established diet breadth and food preference of local populations for evaluation together with genetic differentiation between populations. While C. auratus turned out to be monophagous on the same plant wherever we collected the beetles, the studied populations of C. cobaltinus fed on three different plant species in the field. Plant preference and ranking of the potential host plants significantly differed between these populations. The amount of genetic differentiation between populations was measured by a polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) assay of a 1300 bp mitochondrial DNA (mtDNA) sequence. In addition, the dominant genotypes of all populations were sequenced. No genetic differentiation between the populations of C. auratus could be detected in the RFLP assay and sequence divergence was low (= 0.3%). In C. cobaltinus, on the other hand, genetic differentiation between populations was high, revealing a lack of gene flow over a much smaller scale and a maximum of 1.3% sequence divergence. C. cobaltinus thereby has the prerequisites for host race formation on different plants from the original host spectrum. Our sequence-based phylogeny estimate allows us to reconstruct historical diet evolution in Chrysochus Starting from an original association with Asclepiadaceae, the common ancestor of C. auratus and C. cobaltinus included Apocynaceae in its diet. The strict specialization on Apocynum and the loss of acceptance of Asclepiadaceae observed in C. auratus could have resulted from a process similar to that displayed by C. cobaltinus populations.

Normark BB, Jordal BH, Farrell BD. Origin of a haplodiploid beetle lineage. Proceedings of the Royal Society B-Biological Sciences. 1999;266 (1435) :2253-2259.Abstract

The beetle family Scolytidae includes several groups having regular sib-mating and extremely female-biased sex ratios. Two such groups are known to include haplodiploid species: (i) the tribe Xyleborini and (ii) Coccotrypes and related genera within the tribe Dryocoetini. Relationships of these groups have been controversial. We analysed elongation factor 1-alpha (852 bp) and cytochrome oxidase 1 (1179 bp) sequences for 40 species. The most-parsimonious trees imply a single origin of haplodiploidy uniting Xyleborini (approximately 1200 species) and sib-mating Dryocoetini (approximately 160 species). The sister-group of the haplodiploid clade is the outcrossing genus Dryocoetes. The controversial genus Premnobius is outside the haplodiploid clade. Most haplodiploid scolytids exploit novel resources, ambrosia fungi or seeds, but a few have the ancestral habit of feeding on phloem. Thus, scolytids provide the dearest example of W. D. Hamilton's scenario for the evolution of haplodiploidy (life under bark leading to inbreeding and hence to female-biased sex ratios through haplodiploidy) and now constitute a unique opportunity to study diplo-diploid and haplodiploid sister-lineages in a shared ancestral habitat. There is some evidence of sex determination by maternally inherited endosymbiotic bacteria, which may explain the consistency with which female-biased sex ratios and close inbreeding have been maintained.

Kelley ST, Farrell BD. Phylogenetic analysis of resource use and specialization in Dendroctonus (Coleoptera : Scolytidae). Proceedings of a Workshop on Bark Beetle Genetics: Current Status of Research. 1999;466 :47-63.Abstract

In this paper, we provide a molecular phylogeny of the 19 species in the bark beetle genus Dendroctonus. These beetles collectively attack plant species in four different genera of the conifer family Pinaceae. Given substantial variation in diet breadth, in both the types and numbers of plant species utilized, we asked two general questions concerning the evolution of resource use in this group: 1) “How conservative is the evolution of host use in these insects?” and 2) “Does specialization tend to be derived (that is, a “dead-end’’)?”