Molecular Systematics

Phylo-transcriptomics

My research has contributed some of the first nuclear genomic studies of cockroach phylogenetics. In Proceedings of the Royal Society B, we integrated a transcriptome-based phylogeny of cockroaches with divergence dating analysis and numerous other analyses to come to novel insights about the evolution of cockroaches and termites. This data-set demonstrated strong statistical support for previously hypothesized relationships. In particular, we demonstrated that lamproblattid cockroaches are the closest relative to the social and wood-feeding Cryptocercus cockroaches and termites.

Phenotypic Evolution

Establishing this relationship provided a basis for coming to the conclusion that wood-burrowing/feeding evolved, in part, to relieve predatory pressure on egg cases (Part B in figure to left). We also integrated this phylogenetic framework with other phenotypic data to reconstruct various aspects of cockroach evolution (panels A-F on figure to left).

In 2023, we mapped the evolution of cockroach hindwings to show extreme convergence in apical field morphology.

Divergence Dating

In this research we also spent great efforts in revising the fossil record to assess the timing of important events in the evolution of Blattodea. As a result of this massive genetic data set and a largely revised fossil record, we inferred that most events in cockroach and termite evolution occurred much earlier than previously thought−significantly bridging gaps in the fossil record. This dating analysis corroborates suspicions that abundant "cockroach-like" fossils in the Carboniferous could not have been crown-Blattodea. Furthermore, it limits the occurrence of termites to the Cretaceous period−discrediting older purported fossil evidence of termites.

Phylogenonomics of cockroaches & termites

Phylogenomic

Experimental Design

Phylogenomic

Experimental Design

In my NSF funded postdoc I am using custom designed next-gen DNA data sequenced to improve to phylogenetic inference. Although many researchers have access to millions of nucleotides of sequence data, utilizing all this data for phylogenetic inference can be problematic. Sequence data contains noise that is unevenly distributed. Signal for relationships can be rare and may only be found in a few loci. Thus, reducing datasets to their most informative elements could improve phylogenetic accuracy and precision, while also yielding shorter computation times and other practical improvements.

Modelling Evolution

Coalescent approaches to species-tree inference (which have become increasingly popular) rely strongly on gene-tree topologies. Yet, limited sequence information in single genes may be inadequate for accurate gene-tree inference. To account for this, I am applying novel models of evolution that utilize information content nested in multiple scales (i.e. nucleotide, codon, protein) to test general trends among estimated gene trees and the implications for coalescent species tree inference.

Phylogeny of Blaberoidea

In all these projects, I utilize super-family Blaberoidea as a study system. To date, the relationships among the major lineages of this group have only been investigated superficially. Investigations have shown that this clade has many problematic regions, including at least one rapid radiation and a variety of "long branch" taxa. Improving upon our understanding of their phylogeny can help resolve the pattern of evolution multiple independent switches in genital symmetry and invasions of new biogeographical zones.

Phylogenetic Support

My 2017 phylogeny of cockroaches using few loci and hundreds of species demonstrated that support for relationships in this phylogeny can only be meaningfully demonstrated using multiple approaches in parallel.

In my 2024 phylogeny of cockroaches, we implimented a new approach for mapping support on super-trees, with mixed results

Landscape Genetics

We tested the extent to which certain landscape elements were affecting population level evolution in the Rupununi savanna. We hypothesized that savannas and flood regions were isolating populations. Students in a Biotechnology class at Peddie School in Hightstown, NJ assisted with this project by collecting preliminary mitochondrial data. They showed that gene flow was abundant among populations separated by up to 8 miles of savanna or floodland — the only evidence ever demonstrating cockroach dispersal abilities.

Dataset optimization

In my 2020 paper, we explored the effect of optimizing phylogenomic data sets by removing uninformative loci. In my 2024 paper, we explored the effect of keeping all loci, even uninformative ones, and iteratively constraining the tree inference.

Genetic Barcoding

Given the highly polymorphic nature of cockroaches (age stage and sexual polymorphism) and the difficulty in using taxonomic literature, genetic barcoding provides a simple alternative to traditional identification techniques. We used genetic barcodes for age-stage and sex association in taxonomic work, morphotype definitions in our richness study, and identifications of taxa. Our identification of a novel introduction of Periplaneta japonica in NYC from genetic barcodes received wide media coverage and was featured in New York magazine.

Functional Gene Evolution

I analyzed 64 transcriptomes of cockroaches, mantises and termites to examine functional gene evolution that may have led to rapid diversifications and the evolution of eusociality in termites.

Barcode/Japonica

The Roach Brain Lab

for studying biodiversity through molecular systematics