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102

DENVER MUSEUM OF NATURE & SCIENCE

REPORTS

|

No. 3, July 2, 2016

Cushing

time in 2010, based on recently collected specimens

and photographic records. The species has only been

recorded from the southern coastal areas (Eastern and

Western Cape Provinces) and from the central Free

State Province to date, with the vast majority of records

associated with synanthropic urban habitats. However, a

predictive model shows that the latter localities are very

unsuitable for establishment, which we explain on the

basis of climatic conditions, while the southern coastal

areas represent highly suitable habitat.

Keywords: Introduced, Australia, synanthropic, MAXENT,

distribution

Student - oral presentation

Phylogenomics and taxonomic revision of

the tarantula genus

Aphonopelma

within

the United States

*Chris A. Hamilton

1

, Brent E. Hendrixson

2

, Jason E.

Bond

1

1

Department of Biological Sciences and Auburn

University Museum of Natural History, Auburn

University, Auburn, AL 36849, USA;

2

Department of

Biology, Millsaps College, Jackson, MS 39210, USA

chris@8legs2fangs.com

This systematic study documents the taxonomy, diver-

sity, and distribution of the tarantula spider genus

Aphonopelma

Pocock, 1901 within the United States.

By employing phylogenomic, morphological, and geo-

spatial data, we evaluated all 55 nominal species in the

United States to examine the evolutionary history of

Aphonopelma

and the group’s taxonomy by implementing

an integrative approach to species delimitation. Based on

our analyses, we now recognize only 29 distinct species in

the United States. We proposed 33 new synonymies, seven

nomina dubia, and 14 new species. Based on Anchored

Enrichment phylogenomic data (581 loci, 334,436bp), our

species tree delimits five major lineages: a monotypic group

confined to California, a western group, an eastern group, a

group primarily distributed in high-elevation areas, and a

group that comprises several miniaturized species. Multiple

species are distributed throughout two biodiversity hotspots

in the United States (i.e., California Floristic Province and

Madrean Pine-Oak Woodlands). By conducting the most

comprehensive sampling of a single theraphosid genus

to date, this research significantly broadens the scope of

prior molecular and morphological investigations, finally

bringing a modern understanding of species delimita-

tion in this dynamic and charismatic group of spiders.

Keywords: biodiversity, phylogenomics, molecular

systematics, DNA taxonomy, spider taxonomy

Oral presentation

House spider venom and silk gland

transcriptomes reveal a complex tran-

scriptional landscape

Robert A. Haney, Evelyn E. Schwager, Jessica E. Garb

Department of Biological Sciences, University of Mas-

sachusetts Lowell, Lowell, MA 01854, USA

robert.a.haney@gmail.com

The venom and silk glands of spiders are both ecologi-

cally critical, being involved in prey capture and predator

defense, and a key factor in the evolutionary success of

spiders. The application of high-throughput technolo-

gies can have an important role in understanding the

maintenance and function of these tissues, by character-

izing their transcriptomes, including the prevalence of

alternative splicing of transcripts. While the proportion of

loci with alternatively spliced transcripts and the number

of transcripts produced varies among taxa, detailed

estimates from arachnids are generally lacking. Alterna-

tive splicing augments proteome complexity through

the production of many different mRNAs (and coding

regions) from pre-mRNAs derived from individual gene

loci. The production of alternatively spliced transcripts

can play a role in development, disease, and response to

stress, as well as in defining tissue specific functions. We

have leveraged deep RNA-Seq data to identify transcripts

expressed in the venom and silk glands of the Common

House Spider (

Parasteatoda tepidariorum

), and to

identify thousands of novel splice variants of transcripts.

These new forms greatly expand the catalog of such

variants in

P. tepidarioru

m, and reveal a complex tran-

scriptional landscape, with variation in 5’ and 3’ splice

sites, skipped exons and retained introns, as well as more