Gordon T. Taylor
Ph.D., 1983, University of Southern California
Marine microbiology, interests in microbial ecology,
biogeochemistry and marine biofouling
(Global Research Projects: 1, 2)
My research efforts have mainly focused on (i) microbial mediation of biogeochemical process (particularly carbon cycling), (ii) trophic interactions among microorganisms (bacteria, protozoans, algae and viruses), and (iii) microbial biofouling. Microbiological and chemical exchange processes across interfaces, such as oxic/anoxic, solid/water and air/water boundaries are particularly fascinating to me. I also have abiding interests in cycling of B-vitamins and other micronutrients between producers and consumers.
Microbial ecology and diagenesis of organic debris as it transits from sites of production to sites of deposition are enduring central research interests. Flux and decomposition of this material in the ocean have important implications on nutrient cycling, ocean productivity, transport of contaminants, and the ocean's capacity to sequester atmospheric carbon dioxide in its interior (the biological carbon pump). Microbiological processes are intimately linked to the fate of this carbon and are responsive to climatic changes. As founding members of the NSF-funded CARIACO Ocean Time Series Program, our research has improved understanding of current carbon cycling dynamics in the southern Caribbean Sea on the continental margin of Venezuela. For example, our studies have documented a >1°C rise in sea surface temperatures, declines in upwelling, nutrient supply, plankton productivity and pH as well as an ecosystem state change between 1995 and 2011 (Taylor et al. 2012; Astor et al. 2013). Results are also being used to better interpret ocean conditions and climate in the geologic past in order to better predict the future. To learn more about this program, visit its website or refer to some of the publications listed below.
My lab and Prof. M. Scranton's lab have focused on microbial dynamics, biogeochemistry and transformations of organic materials transported through redoxclines (transition between oxic and anoxic waters). We are particularly keen to understand processes that control carbon cycling, such as chemoautotrophic production. The reasons being that chemoautotrophic carbon fixation is quantitatively significant to the food web and processes occurring in this layer also control cycling of other globally-important elements, such as nitrogen and sulfur. In addition to our times series program, my lab with colleagues from Woods Hole Oceanographic Institution added an NSF-sponsored Metagenomics and Metatranscriptomics project in 2013 to the CARIACO core program, focusing on how genes and transcripts from Bacteria, Archaea and Protists change with the geochemical seascape. In my lab, we combine traditional microbial ecological and geochemical measurements with modern molecular techniques, such as ssu rRNA libraries, terminal restriction fragment length polymorphism (T-RFLP), fluorescent in situ hybridization (FISH), and quantitative PCR of functional genes, to unravel the interplay between chemical gradients, elemental cycling and microbial population dynamics. Beyond being intrinsically fascinating, the Cariaco Basin serves as a model for other oxygen-impoverished water columns (e.g., the Black Sea, Baltic and Mediterranean Deeps, Boundary Oxygen Minimum Zones, Gulf of Mexico "Dead Zone", Long Island Sound, and fjords), which are becoming more widespread geographically as human populations grow eutrophying their watersheds and as climate changes.
Over the years, our holy grail has been to link phylogeny to function, i.e., understand the jobs of specific microbial populations across wide-ranging geochemical seascapes. To that end, we have employed cell and taxon-specific tools, such as microautoradiography-FISH (MAR-FISH) and stable isotopic probing of nucleic acids (SIP), as well as classical cultivation approaches. Through NSF's Major Research Instrumentation funding, we have built exciting new single-cell analytical capability within SoMAS' NAno-Raman Molecular Imaging Laboratory (opened Jan 2014). NARMIL houses a novel, state-of-the-art Renishaw inVia confocal laser Raman microspectrometer coupled to a Bruker Innova Atomic Force Microscope (AFM), which permits 3-D mapping of chemical functionalities resolved to <30 nm, while coincidentally providing fluorescent, bright field and topographic images. By combining stable isotopic labeling, fluorescent phylogenetic probes and Raman mapping, we are determining identity of cells actively assimilating a particular label. By focusing the laser beam on the AFM tip, we can achieve nanometer-scale spatial resolution and greater sensitivity through the Tip-Enhanced Raman Scattering (TERS) effect. TERS enables non-destructive mapping of chemical distributions at spatial scales relevant to individual microorganisms. NARMIL provides SoMAS with a unique and powerful analytical tool with countless applications throughout the natural sciences and engineering. We are eagerly exploring new research frontiers with these novel capabilities! To learn more about our facility, please visit: http://you.stonybrook.edu/nanoraman/.
If you are interested in doing graduate work in the areas described above and in earning an advanced degree from an outstanding program, please feel free to contact me to discuss possibilities.
Selected Recent Publications
Cernadas-Martín S, Scranton MI, Astor Y, Taylor GT (2014). Aerobic and anaerobic ammonia oxidizers in the Cariaco Basin: Identification, quantification and community structure. Environ. Microb. (submitted)
Suter E, Lwiza KMM, Rose JM, Gobler C, Taylor GT (2014). Nutrient and phytoplankton regime shifts during decadal decreases in nitrogen loadings to the urbanized Long Island Sound estuary. Mar. Ecol. Prog. Ser. 497: 51-67.
Scranton MI, Taylor GT, Thunell R, Benitez-Nelson C, Muller-Karger F, Fanning K, Lorenzoni L, Montes E, Varela R, Astor Y (2014). Interannual and decadal variability in the nutrient geochemistry of the Cariaco Basin. Oceanography Magazine 27(1): 148-159.
Taylor GT, Muller-Karger F, Thunell RC, Scranton MI, Astor Y, Varela R, Troccoli-Ghinaglia L, Lorenzoni L, Fanning KA, Hameed S, Doherty O (2013). Respuesta del ecosistema Caribe Sur al cambio climático. COFA Convivencia Pesquera, www.fundatun.org, Aug-Nov. 2013, pp. 19-21.
Lopez G, Carey D, Carlton J, Cerrato R, Dam H, DiGiovanni R, Elphick C, Frisk M, Gobler C, Hice L, Howell P, Jordaan A, Lin S, Liu S, Lonsdale D, McEnroe M, McKown K, McManus G, Orson R, Peterson B, Pickerell C, Rozsa R, Siuda A, Thomas E, Taylor G, Shumway S, Talmage S, Van Patten M, Vaudrey J, Wikfors G, Yarish C, and Zajac R (2013). Biology and Ecology of Long Island Sound. Chapter 6. In: Long Island Sound: Prospects for the Urban Sea, JS Latimer, MA Tedesco, RL Swanson, C Yarish, PE Stacey, and C Garza, eds. Springer, New York. pp 285- 479.
Astor YM, Lorenzoni L, Thunell R, Varela R, Muller-Karger F, Troccoli L, Taylor GT, Scranton MI, Tappa E Rueda D (2013). Interannual variability in sea surface temperature and fCO2 changes in the Cariaco Basin, Deep-Sea Research II, 93, 33-43.
Gobler CJ, Lobanov AV, Tang Y-Z, Turanov AA, Zhang Y, Doblin M, Taylor GT, Sañudo-Wilhelmy SA, Grigoriev IV, Gladyshev VN (2013). The central role of selenium in the biochemistry and ecology of the harmful pelagophyte, Aureococcus anophagefferens J. Int. Soc. Microbial Ecology, 7, 1333-1343.
Rodriguez MJ, Madrid VM, Taylor GT, Scranton M, Chistoserdov AY (2013). Bacterial community composition in a large marine anoxic basin: a Cariaco Basin time-series survey. FEMS Microbiol. Ecol. 84, 625-639.
Muller-Karger F, Taylor GT, Astor Y, Thunell RC, Scranton MI, , Varela R, Troccoli Ghinaglia L, Lorenzoni L, Montes E, Fanning KA, & Benitez-Nelson C (2013). From Affiliated Project: The CARIACO Basin Ocean Time-Series. Land-Ocean Interactions in the Coastal Zone Inprint, ISSN 2070-2442 2013 Issue 1, pp. 5-17.
Sarmento H, Romera-Castillo C, Lindh M, Pinhassi J, Montserrat Sala M, Gasol JM, Marrase´ C, Taylor GT (2013). Phytoplankton species-specific release of dissolved free amino acids and their selective consumption by bacteria. Limnol. Oceanogr. 58(3), 1123-1135.
Lorenzoni L, Taylor GT, Benitez-Nelson C, Hansell DA, Masserini R, Montes E, Fanning KA, Varela R, Astor Y, Guzmán L, Muller-Karger FE (2013). Spatial and seasonal variability of dissolved organic matter in the Cariaco Basin, Venezuela. J Geophys Res - Biogeosciences 118, 1-12, doi:10.1002/jgrg.20075.
Taylor GT (2013). Review of Marine Microbiology: Ecology and Applications, 2nd Edn. by Colin Munn, Garland Science Publ. NY and London, 2011 Quarterly Review of Biology, Univ. Chicago Press, 88(2), 144.
Muller-Karger FE, Lorenzoni L, Montes E, Taylor G, Thunell R, Scranton M, Benitez-Nelson C, Astor Y, Varela R, Troccoli L, Fanning K (2013). The CARIACO Ocean Time-Series: 18 years of international collaboration in ocean biogeochemistry and ecological research. Ocean Carbon and Biogeochemistry News 6(3), 7-12.
Orsi W, Edgcomb V, Faria J, Foissner W, Fowle WH, Hohmann T, Suarez P, Taylor C, Taylor GT, Vdacný P & Epstein SS (2012). Class Cariacotrichea, a novel ciliate taxon from the anoxic Cariaco Basin,Venezuela. Internat'l Jour System Evolutionary Microbio. 62: 1425-1433.
Podlaska A, Wakeham SG, Fanning K, Taylor GT (2012). Microbial community structure and chemoautotrophic activity in the oxygen minimum zone of the eastern tropical North Pacific. Deep-Sea Res. I, 66: 77-89.
Taylor GT, Muller-Karger F, Thunell RC, Scranton MI, Astor Y, Varela R, Troccoli-Ghinaglia L, Lorenzoni L, Fanning KA, Hameed S, Doherty O (2012). Ecosystem response to global climate change in the southern Caribbean Sea. Proc. Nat'l. Acad. Sci. (USA) 109(47): 19315-19320.
Bell SL, Allam B, McElroy A, Dove A, Taylor GT (2012). Investigation of epizootic shell disease in American lobsters (Homarus americanus) from Long Island Sound: I. Characterization of associated microbial communities. J Shellfish Res 31(2): 473-484.
Homerding M, McElroy A, Taylor G, Dove A, Allam B (2012). Investigation of epizootic shell disease in American lobsters (Homarus americanus) from Long Island Sound: II. Immune parameters in lobsters and relationships to the disease. J Shellfish Res 31(2): 495-504.
Wakeham SG, Turich C, Schubotz F, Podlaska A, Li XN, Varela R, Astor Y, Saenz J, Rush D, Sinninghe Damsté J, Summons RE, Scranton MI, Taylor GT, Hinrichs K-U (2012). Biomarkers, chemistry and microbiology show chemoautotrophy in a multilayer chemocline in the Cariaco Basin. Deep-Sea Res. 63: 133-156.
Li XN, Taylor GT, Astor Y, Varela R, Scranton MI (2012). The conundrum between chemoautotrophic production and oxidant and reductant supply: a case study from the Cariaco Basin. Deep-Sea Res. I, 61: 1-10.
Li XN, Taylor GT, Astor Y, Varela R, Scranton MI (2012). Response to comment on ‘The conundrum between chemoautotrophic production and reductant and oxidant supply: A case study from the Cariaco Basin'. Deep-Sea Res. 70:106-108.
Finiguerra MB, Escribano DF, Taylor GT (2011). Light-independent mechanisms of virion inactivation in coastal marine systems. Hydrobiologia, 665: 51-66.
Edgcomb V, Orsi W, Taylor GT, Vdacny P, Taylor C, Suarez P, Epstein S (2011). Accessing marine protists from the anoxic Cariaco Basin. J. Int Soc Microb Ecol. 5(8): 1237-1241.
Edgcomb V, Orsi W, Bunge J, Jeon SO, Christen R, Leslin C, Holder M, Taylor GT, Suarez P, Varela R, Epstein S (2011). Protistan microbial observatory in the Cariaco Basin, Caribbean. I. Pyrosequencing vs Sanger insights into species richness. J Int Soc Microb Ecol. 5(8): 1344-1356.
Orsi W, Edgcomb V, Jeon SO, Bunge J, Taylor GT, Varela R, Epstein S (2011). Protistan microbial observatory in the Cariaco Basin, Caribbean. II. Habitat specialization. J Int Soc Microb Ecol. 5(8): 1357-1373.
Wakeham SG, Turich C, Taylor GT, Podlaska A, Scranton MI, Li XN, Varela R, Astor Y (2010). Mid-chain methoxylated fatty acids within the chemocline of the Cariaco Basin: a chemoautotrophic source? Organic Geochem. 41:498-512.
Taylor GT, Thunell RC, Varela R, Benitez-Nelson C & Scranton MI (2009). Hydrolytic ectoenzyme activity associated with suspended and sinking organic particles above and within the anoxic Cariaco Basin. Deep-Sea Res. I, 56: 1266-1283.
Panzeca C, Beck AJ, Tovar-Sanchez A, Segovio-Zavala J, Gobler CJ, Taylor GT, Sañudo-Wilhelmy SA (2009). Distributions of dissolved vitamin B12 and Co in coastal and open-ocean marine systems. Estuar. Coastal Shelf Sci. 85: 223-230.
Lin X, Scranton MI, Chistoserdov AY, Varela R, Taylor GT (2008). Spatiotemporal dynamics of bacterial populations in the anoxic Cariaco Basin. Limnol Oceanogr. 53(1): 37-51.
Panzeca C, Beck AJ, LeBlanc K, Taylor GT, Hutchins DA, Sañudo-Wilhelmy SA (2008). Potential cobalt limitation of vitamin B12 synthesis in the North Atlantic Ocean. Global Biogeochemical Cycles 22: GB2029, doi:10.1029/2007GB003124
Taylor GT & Sullivan CW (2008). Vitamin B12 and cobalt cycling among diatoms and bacteria in Antarctic sea ice microbial communities. Limnol. Oceanogr. 53: 1862-1877.
Li XN, Taylor GT, Astor Y, Scranton MI (2008). Sulfur speciation in the Cariaco Basin with reference to chemoautotrophic production. Mar. Chem. 112: 53-64.
Lin X, Scranton MI, Varela R, Chistoserdov AY, Taylor GT (2007). Compositional responses of bacterial communities to redox gradients and grazing in the anoxic Cariaco Basin. Aquat. Microb. Ecol. 47: 57-72
Gobler CJ, Norman C, Panzeca C, Taylor GT, Sañudo-Wilhelmy SA (2007). Effects of vitamins (B1, B12) and inorganic nutrient dynamics on algal blooms in Long Island estuaries. Aquat. Microb. Ecol. 49: 181-194
Edgcomb VP, Jeon S, Taylor GT, Orsi W, Leslin C, Bunge J, Epstein SS (2007). Microbial observatory in the Cariaco Basin - Dynamics of protistan diversity across time, space, and chemical gradients. J. Phycol. 43: 57-57.
Stoeck T, Hayward B, Taylor GT, Varela R, Epstein SS (2006). The multiple PCR-primer approach to access the microeukaryotic diversity in the anoxic Cariaco Basin (Caribbean Sea). Protist 157: 31-43
LeBlanc LA, Gulnick JD, Brownawell BJ, Taylor GT (2006). The influence of sediment resuspension on degradation of phenanthrene in flow-through microcosms. Marine Environ. Res. 61: 202-223
Hayes MK, Taylor GT, Astor Y, & Scranton MI (2006). Vertical distributions of thiosulfate and sulfite in the Cariaco Basin. Limnol. Oceanogr. 51: 280-287
Taylor GT, Iabichella-Armas M, Varela R, Muller-Karger F, Lin X, Scranton MI (2006). Microbial ecology of the Cariaco Basin's oxic/anoxic interface: the U.S.-Venezuelan CARIACO times series program. In: Neretin LN (ed), Past and Present Water Column Anoxia, NATO Sci Ser., Springer, Netherlands, p. 473-499.
Scranton MI, Taylor GT, Astor Y & Muller-Karger F (2006). Temporal variability in the nutrient chemistry of the Cariaco Basin. In: Neretin LN (ed), Past and Present Water Column Anoxia, NATO Sci Ser., Springer, Netherlands, p. 139-160.
Sañudo-Wilhelmy, SA, Okbamichael M, Gobler CJ, Taylor GT (2006). Regulation of phytoplankton dynamics by vitamin B12. Geophys. Res. Lett., 33, L04604, doi:10.1029/2005GL025046
Lin X, Wakeham SG, Putnam IF, Astor YM, Scranton MI, Taylor GT (2006). Vertical distributions of prokaryotic assemblages in the anoxic Cariaco Basin and Black Sea compared using fluorescent in situ hybridization (FISH). Appl. Environ. Microbiol. 72(4): 2679-2690
Taylor GT, Gobler CJ & Sañudo-Wilhelmy SA (2006). Speciation and concentrations of dissolved nitrogen as determinants of brown tide (Aureococcus anophagefferens) bloom initiation. Mar Ecol Prog Ser. 312: 67-83
Lonsdale DJ, Greenfield DI, Hillebrand EM, Taylor GT (2006). Comparison of planktonic community composition and trophic structure in two Long Island, NY estuaries. J Plankton Res 28: 891-905
Panzeca C, Tovar-Sanchez A, Agustí S, Reche I, Duarte CM, Taylor GT, Sañudo-Wilhelmy SA (2006). B vitamin as regulators of phytoplankton dynamics. EOS, 87(52): 593-596
Ho, T-Y, Taylor GT, Astor Y, Varela R, Muller-Karger F, Scranton MI (2004). Vertical and temporal variability of redox zonation in the water column of the Cariaco Basin: implications for organic oxidation pathways. Mar. Chem. 86: 89-104.
Taylor GT, Way J, Yu Y, Scranton MI (2003). Patterns of hydrolytic ectoenzyme activity among bacterioplankton communities in the lower Hudson River and Western Long Island Sound estuaries. Mar. Ecol. Prog. Ser. 263:1-15.
Taylor GT, Hein C, Iabichella M (2003). Temporal variations in viral distributions in the anoxic Cariaco Basin. Aquatic Microbial Ecology, 30: 103-116.
Taylor GT, Way J, Scranton MI (2003). Transport and planktonic cycling of organic carbon in the highly urbanized Hudson River estuary. Limnol. Oceanogr. 48: 1779-1795.
Stoeck T, Taylor GT ,Epstein S (2003). Novel eukaryotes from a permanently anoxic Cariaco Basin (Caribbean Sea). Appl. Environ. Microbiol. 69: 5656-5663.
Madrid VM, Taylor GT, Scranton MI, Chistoserdov AY (2001). Phylogenetic diversity of Bacterial and Archaeal communities in the anoxic zone of the Cariaco Basin. Appl. Environ. Microbiol. 67: 1663-1674.
Muller-Karger F, Varela R, Thunell R, Scranton M, Bohrer R, Taylor G, Capelo J, Astor Y, Tappa E, Ho T-Y, Walsh JJ (2001). Annual cycle of primary production in the Cariaco Basin: Response to upwelling and implications for vertical export. J. Geophys. Res. 106: 4527-4542.
Anderson TH, Taylor GT (2001). Nutrient pulses, plankton blooms and hypoxia in western Long Island Sound. Estuaries, 24: 228-243.
Taylor GT, Scranton MI, Iabichella M, Ho T-Y, Thunell RC, Muller-Karger F, Varela R (2001). Chemoautotrophy in the redox transition zone of the Cariaco Basin: A significant midwater source of organic carbon production. Limnol. Oceanogr. 46: 148-163.