About This Project
In scientific history, aquatic isopods have been an overlooked taxa. Recently there has been a breakthrough in aquatic isopod phylogenetics that has shown that in the Eastern United States there is higher diversity than previously thought. This study aims to provide much more genetic coverage of Californian aquatic isopods to investigate the possible hidden diversity of California. Due to their highly endemic nature we hypothesize that similar diversity will be reflected in California.
Ask the Scientists
Join The DiscussionWhat is the context of this research?
In 2023 a large-scale revision of Eastern North American aquatic isopods was published by Dr. Julian "Jerry" Lewis and a team of collaborators describing 24 new species of aquatic isopod (https://www.researchgate.net/p...). Since 2023 many more have been published or are in the progress of being published with new phylogenetic and morphological data available. Although this is exciting, no such large scale investigations are being done in the West where we have interesting endemic isopod genera like Calasellus, Salmasellus, Oregonasellus, and Bowmanasellus. In California Calasellus, Bowmanasellus, and Caecidotea are currently known to exist but very little genetic work has been done. We hypothesize that there is much more diversity than we currently know about.
What is the significance of this project?
The realm of systematics is important because it includes the discipline of taxonomy and is what is used to describe new species. Aquatic isopods are threatened by a multitude of factors but nothing can be protected if it has not been investigated and doesn't have a scientific name. We will describe any new species discovered increasing our knowledge of endemic Californian species.
By understanding the distribution and phylogeography of these organisms we can also make evolutionary inferences regarding why they are distributed the way they are or how certain traits may have been advantageous to their survival.
Aquatic isopods can also be great indicator species that need certain water parameters to live. Many of these species live in groundwaters, springs, and seeps, and can be sensitive to change making them good indicator species. By having a greater baseline understanding of their distribution we can monitor their population status and secondarily monitor the water parameters.
What are the goals of the project?
The goals of this project would be to collect members of Calasellus, Bowmanasellus, and Caecidotea from as many localities (at least 20 identified survey locations) as we can during our research trip to describe any species that need description and to greater our knowledge of North American asellid evolution.
After collecting from the 20 localities across northern California, a morphological analysis, and phylogenetic analysis, we aim to describe anything that warrants description.
Budget
The funds are primarily being designated for travel to collect specimens from 20 different localities across Northern California. First I will need to fly to San Francisco from Salt Lake City in the summer (~500$). We will need to rent a car and estimated that the total travel for all trips will be around 2,500 miles (~$750 in fuel). During this trip we will be trying to save money on lodging by staying with family and camping but we will need to also stay in a hotel for a few of the nights($500). Phylogenetic sequencing will make up the remainder of our budget (750$), we will sequence 2 nuclear genes and 2 mitochondrial genes. The genes we will be sequencing are as follows: Cytochrome Oxidase 1, 16S mitochondrial rDNA, FASTKD4 nuclear, and 28S nuclear rDNA. The most comprehensive phylogeny produced of aquatic isopods to date were built on those 4 genes and we plan on utilizing those same genes to build on it.
Endorsed by
Project Timeline
I expect to start my fieldwork in July of 2026. I would like to start as soon as possible but realistically it will take time to get the proper permits after this is funded. After fieldwork we will immediately start the process of dissecting, identifying, and prepping specimens to be sent for sequencing. I have allotted 5 months for manuscript preparation because depending on the findings and what needs to be described it may take longer to write and prepare the paper.
Jan 21, 2026
Project Launched
Jul 17, 2026
Start Fieldwork around San Francisco
Jul 21, 2026
Start Fieldwork in Northern and Northeastern California
Jul 29, 2026
Return to Utah
Aug 03, 2026
Start DNA Sequencing and Morphological Analysis
Meet the Team
Team Bio
My name is Christian Furness and I did my undergraduate studies in Biology at the University of Utah. During my undergraduate career my research was focused on ants, mosquitoes, and isopods. I am now a first year PhD student studying evolutionary biology.
My primary collaborator is Dr. Julian "Jerry" Lewis. He is the current taxonomic specialist of North American aquatic isopods. We have worked together previously and hope to continue our collaborations with this project.
D. Christian Furness
My name is Christian and I am a PhD student with experience in the biological sciences both professionally and from a hobbyist perspective. I specialize in work based around invertebrate and reptile fauna. I have been involved in research projects revolving around the following taxa: ants, mosquitoes, isopods, coral, invasive lionfish, desert iguanas, and skinks. These projects gave me experience in the following: population sampling, benthic surveys, behavioral studies, biogeography, and invasive species dietary analysis. I have aided in identification of isopods in the Natural History Museum of Utah and the Bean Life Science Museum.
If you would like to find my published work you can find that on my ResearchGate (https://www.researchgate.net/p...) or Google Scholar (https://scholar.google.com/cit...) accounts.
Lab Notes
Nothing posted yet.
Additional Information
All specimens collected will be placed in 95% ethanol and stored in a cooler out of the sun to try to optimize good DNA sequencing. When the manuscript is being prepared, specimens will be deposited in a North American Museum for future reference. Specimens will be saved for CalATBI.
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