Craig is temporarily a post-doctoral fellow at the Monterey Bay Aquarium Research Institute who is looking for a permanent position. He spends most of his time balancing his overwhelming geekdom with normalcy so he can function in the real world. Luckily his wife likes his geekiness.
Peter Etnoyer is a Graduate Research Associate at the Harte Research Institute for Gulf of Mexico Studies, Texas A&M University-Corpus Christi. He studies deep corals and ocean fronts, and he loves to be on the water.
Kevin Zelnio is a Graduate Student Researcher at Penn State studying the ecology of hydrothermal vent and methane seep communities. He raises awareness of the plight of the spineless through folk music.
Fig. 1. A circular representation of the R. magnifica genome. The innermost circle highlights genes of special interest: cbb (Calvin-Benson-Bassham cycle, red), sox (sulfur oxidation, green), dsr (dissimilatory sulfite reductase, blue), and rnf (NADH dehydrogenase). The second and third circles show GC skew and %G+C, respectively. The distribution of genes is depicted on the two outer rings (fourth and fifth, forward and reverse, respectively) colored by role category. [View Larger Version of this Image (273K JPEG file)]
The Calyptogena magnifica (Bivalvia: Vesicomyidae) symbiont, Candidatus Ruthia magnifica, is the first intracellular sulfur-oxidizing endosymbiont to have its genome sequenced, revealing a suite of metabolic capabilities. The genome encodes major chemoautotrophic pathways as well as pathways for biosynthesis of vitamins, cofactors, and all 20 amino acids required by the clam.
![[View Larger Version of this Image (273K JPEG file)]](http://www.sciencemag.org/content/vol315/issue5814/images/large/315_998_F1.jpeg){kind=link}