{"id":102,"date":"2015-03-14T00:20:29","date_gmt":"2015-03-14T07:20:29","guid":{"rendered":"http:\/\/faculty.washington.edu\/bjbecker\/?p=102"},"modified":"2022-03-24T12:15:45","modified_gmt":"2022-03-24T19:15:45","slug":"doping-oysters-and-stealing-their-embryos","status":"publish","type":"post","link":"http:\/\/faculty.washington.edu\/bjbecker\/2015\/03\/doping-oysters-and-stealing-their-embryos\/","title":{"rendered":"Doping oysters and stealing their embryos"},"content":{"rendered":"
\"PSRF<\/a>
Puget Sound Restoration Fund hatchery at Manchester Environmental Laboratory<\/figcaption><\/figure>\n

One of the things I love about being a marine biologist is sometimes I will pause and consider the absurdity of what I am doing at that moment. This week’s example was our trip to the Puget Sound Restoration Fund<\/a>‘s hatchery in Manchester, where\u00a0we learned how to dope native\u00a0oysters and steal\u00a0their embryos.<\/p>\n

\"Listening\"<\/a>
Jake explaining to Megan, Michelle, Hank, and Brian.<\/figcaption><\/figure>\n

Why on earth would we do that to oysters?\u00a0We are beginning our Washington Sea Grant-<\/a>funded\u00a0project to track native oyster larvae to inform the restoration efforts of PSRF. In order to do this work, we will need to sample the shelled larvae\u00a0that are reared for a week or so within the shell of the adult mother oyster from dozens of sites around Puget Sound. Our past work has shown that only a few of the adults are holding larvae, or “brooding” at any one time, on the order of 10-15%. And we will need to find and sample twenty animals from each site. Until recently, we collected these samples by sacrificing the\u00a0oysters, shucking them open and looking for the larvae. You can quickly see that we’d need to kill 200 or so adults from each of our many sites to get to that number, amounting to thousands of Olympia oysters, a\u00a0State Candidate <\/a>for the Washington Species of Concern list.<\/p>\n

\"Zip<\/a>
What you see when there are embryos or larvae in there.<\/figcaption><\/figure>\n

Luckily, a student named Kate Jackson, working with the Roberts Lab <\/a>at UW School of Aquatic and Fishery Sciences, has refined a method to anesthetize the oysters, causing them to open their shells enough to wash the larvae out harmlessly. This technique was used extensively by Jake Heare<\/a>, a graduate student in that lab, who was gracious enough to meet us in Manchester to teach us the technique.<\/p>\n

\"embryos\"<\/a>
What the embryos looked like under a dissecting microscope.<\/figcaption><\/figure>\n

Members of our team got together to learn how it’s done. Essentially, the oysters are soaked in Epsom salts for some time, causing them to get very, very mellow. Then we look inside the gaping shell, or use a cable tie to gently sample the inside of the mantle cavity, the fleshy part inside of the shell. If embryos or larvae are there, we will see a creamy goo on the tip of the cable tie. Then a gentle stream of water is all that is needed to remove the babies. A few minutes later, the adult oysters will recover and go back to their usual tight-shelled style. Jake has done quite a bit of testing and has found no ill effects on the adults after recovery.<\/p>\n

After years of talking and writing about our project, it was great to finally get our hands wet and work on the nitty-gritty details of our methods. It’s the small things that make or break the success of any field research effort, and getting together to calibrate them is vital.<\/p>\n

And ultimately, we’re pleased that there is a viable alternative to having to sacrifice a few thousand of the species we are trying to restore.<\/p>\n