Microbial Ecology Laboratory

Clam Cancer

Softshell clams (Mya arenaria) are susceptible to a form of transmissible cancer known as Bivalve Transmissible Neoplasia (BTN). This disease, which was first recognized as transmissible by Metzger et al. (2015), is thought to be passed from clam to clam through the environment and may contribute to clam mortality, while carrying no known risk to consumers of diseased clams. Our role in this project is to conduct time-series analysis of clams in Maine to estimate the prevalence of this disease in both clams and environmental water samples and to map these prevalence values to temperature and salinity. Previous work by Giersch et al. (2022) demonstrated that cancerous clam cells survived better at lower temperatures and higher salinities. Diagnosis of BTN in clams can be accomplished by microscopy when clams are carrying a high load of cancerous cells. However, a DNA-based approach (qPCR) developed by Giersch et al. (2022) has greater sensitivity than microscopy at moderate to low levels of cancer. Additionally, this qPCR method provides a means of sampling the disease in environmental DNA (eDNA) samples. This work is a collaboration with colleagues at Pacific Northwest Research Institute (PNRI), Gloucester Marine Genomics Institute (GMGI) and Bigelow Laboratory for Ocean Sciences (BLOS).

Students walking along a shoreline
Our primary study site, located in Long Cove, Harpswell, Maine
Clam hemolymph under the microscope
Clam hemolymph under the microscope, revealing a mix of cancerous and healthy cells
A HOBO salinity and temperature probe
A HOBO salinity and temperature probe that is ready to be deployed at our study site.

North Atlantic Right Whale
North Atlantic Right Whale (Eubalaena glacialis). Image ©NOAA Fisheries, used with permission.
Copepod under magnification
Copepod (Calanus finmarchicus), one of the millimeter-sized prey species thought to comprise a large proportion of the NARW diet.
Students in a lab at Bigelow
Quantitative PCR test for the presence C. finmarchicus in a NARW fecal sample relative to a C. finmarchicus reference sample extracted from the copepod specimen shown on this page.

North Atlantic Right Whale Diet

North Atlantic Right Whales (NARW) are a threatened whale species, whose ranges may be shifting in response to environmental pressures and shifting distributions of their prey – minute crustaceans known as copepods. Given their size, rarity, and endangered status, studying the diets of NARW is a difficult task. However, DNA-based methods such as quantitative PCR (qPCR) and DNA metabarcode sequencing can reveal the diets of these whales by analysis of NARW fecal samples. Archived NARW fecal samples from the New England Aquarium serve as the source material for this project, with a primary focus on testing for the ecologically important copepod, Calanus finmarchicus. We have developed a qPCR assay for C. finmarchicus and have applied it to two NARW fecal samples (to date), with one sample testing positive and the other testing negative. In addition to C. finmarchicus, we will test samples for several additional species of lipid-rich copepods. The relative proportions of the different prey species will help to inform modeling efforts that seek to predict the distributions of NARW at certain times of the year. This work is a collaboration with colleagues at the University of South Carolina (USC), the New England Aquarium (NEAQ), and Bigelow Laboratory for Ocean Sciences (BLOS).




Kelp Blue Carbon

The cultivation of sugar kelp (Saccharina latissima) represents an rapidly-expanding aquaculture sector along the coast of Maine. Sugar kelp is a fast-growing macroalgal species and its growth as a farmed ‘sea crop’ has several benefits to the marine environment. These benefits include 1) reduction of dissolved inorganic carbon (counteracting the effects of ocean acidification) and 2) conversion of this inorganic carbon into so-called ‘blue carbon’ (ocean-based) biomass (kelp tissue). A portion of the kelp biomass is harvested for food, while roughly 20% of the biomass of each plant (including the stipe and unusable blade tips) is discarded as waste. Depending on the fate of this ‘waste’, a portion could be sequestered into coastal sediments as a ‘blue carbon’ storage product. Our role in this project is to develop and test environmental DNA (eDNA) tools that will help in the quantification and verification of kelp-based blue carbon storage. There are two morphological variants of Saccharina latissima, known commonly as ‘sugar’ and ‘skinny’ kelp, with the skinny variant being the preferred aquaculture strain. The primary challenge has been designing an eDNA tool that can discriminate the genetically similar variants in marine sediments, to separate the ‘cultivated’ kelp signal from any potential ‘wild’ kelp signal - to properly account for biomass storage due to aquaculture. To date, we have focused on development of a droplet digital PCR (ddPCR) approach. This work is a collaboration among numerous Bigelow based scientists and colleagues at the Darling Marine Center, University of Maine.

Sugar kelp gametophytes undrermagnification
Sugar kelp gametophytes. Extraction of DNA from adult kelp tissues can result in the co-extraction of contaminating macromolecules, however kelp gametophytes yield DNA of higher purity that is required for DNA sequencing.
A multiplex droplet digital PCR (ddPCR) assay
A multiplex droplet digital PCR (ddPCR) assay to detect a single nucleotide polymorphism (SNP) for the two morphological variants of Saccharina latissima, known as ‘skinny’ and ‘sugar’ kelp.