A seasonal study of the significance of N2 fixation by Trichodesmium spp. at the Bermuda Atlantic Time-series Study (BATS) site
By K. Orcutt, F. Lipschultz, K. Gundersen, R. Arimoto, Anthony F. Michaels, A. Knap, J. Gallon. 2001
230 citations recorded by the source corpus.
Subfields: Ecology, Oceanography
View Paper: https://www.semanticscholar.org/paper/8221db608f9668c38ebef04df84bf3bce29494ba
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In Ecology
- M. Mulholland
- D. Hutchins
- Michael J. Follows
- S. Dutkiewicz
- Sonya T. Dyhrman
- Feixue Fu
- Philip W. Boyd
- D. Capone
In Oceanography
- M. Mulholland
- D. Hutchins
- Sonya T. Dyhrman
- Michael J. Follows
- S. Dutkiewicz
- D. Capone
- Fanny M. Monteiro
- David M. Karl
Citations in the corpus
- The fate of nitrogen fixed by diazotrophs in the ocean (2007, methodology): “At BATS, Sheridan et al. (2002) report that bacteria were enriched on average 401 and 1709 times onTrichodesmium puffs and tufts, respectively.”
- Modeling the distribution of Trichodesmium and nitrogen fixation in the Atlantic Ocean (2004, background): “Trichodesmium appears to have a very flexible phosphorus requirement [Krauk, 2001], and readily grows [Carpenter and Romans, 1991; Orcutt et al., 2001] in waters where the ambient phosphorus concentrations are extremely low (e.g., in the Sargasso Sea [Wu et al., 2000]).”
- Burrowing deeper into benthic nitrogen cycling: the impact of bioturbation on nitrogen fixation coupled to sulfate reduction (2010, unknown): “For instance, the marine cyanobacteria Trichodesmium spp. exhibit ratios closer to 3:1 as determined by direct 15N2 comparisons (Orcutt et al. 2001, Capone et al. 2005) and with particulate organic nitrogen (PON) accumulation in cultures of Trichodesmium spp. (Mulholland & Capone 2001).”
- Occurrence of benthic microbial nitrogen fixation coupled to sulfate reduction in the seasonally hypoxic Eckernförde Bay, Baltic Sea (2012, background): “N2 fixation rates were calculated from the linear portion of the NA results using a conversion factor of 3 C2H4 : 1 N2, which is based on previous direct15N2 comparisons in seagrass habitats (Patriquin and Knowles, 1972; O’Donohue et al., 1991) and with the marine cyanobacteria Trichodesmium(Orcutt ”
- A REVISED ESTIMATE OF THE IRON USE EFFICIENCY OF NITROGEN FIXATION, WITH SPECIAL REFERENCE TO THE MARINE CYANOBACTERIUM TRICHODESMIUM SPP. (CYANOPHYTA) 1 (2003, background): “However, in Trichodesmium field and laboratory populations (Mulholland and Capone 2001, Orcutt et al. 2001) 1 mol N2 fixation requires a net investment of only 6 mol reducing equivalents, as evidenced by a mean 15N2 fixation:C2H2 reduction ratio of about 3.”
- Iron requirements for dinitrogen‐ and ammonium‐supported growth in cultures of Trichodesmium (IMS 101): Comparison with nitrogen fixation rates and iron: carbon ratios of field populations (2003, unknown): “An acetylene reduction : N2 fixation ratio of 3 : 1 was assumed, based on mean ratios of 15N2 fixation : C2H2 reduction from both field and lab populations of Trichodesmium (Mulholland and Capone 2001; Orcutt et al. 2001).”
- Nitrogen fixation by Trichodesmium spp.: An important source of new nitrogen to the tropical and subtropical North Atlantic Ocean (2005, unknown): “Hood et al. [2001] exploited the BATS data set, including observations of Trichodesmium abundance [Orcutt et al., 2001] in a one-dimensional model.”
- Distribution of diverse nitrogen fixers in the global ocean (2010, background): “Trichodesmium biomass varies between about 2 × 10−5 mmolP l−1 in the late Spring to about 13 × 10−5 mmolP l−1 in the late summer, consistent with time‐series observations [Orcutt et al., 2001].”
- Nitrogen fixation and release of fixed nitrogen by Trichodesmium spp. in the Gulf of Mexico (2006, methodology): “Rates of uptake were calculated based on the equations of Montoya et al. (1996) and Orcutt et al. (2001) using a mixing model N uptake ~ atom % PONð Þfinal { atom % PONð Þinitial atom % enrichment N source pool { atom % PONð Þinitial | time | PON½ ð1Þ C uptake ~ atom % POCð Þfinal{ atom % POCð…”
- Biomass and primary productivity of the cyanobacterium Trichodesmium spp. in the tropical N Atlantic ocean (2004, background): “Orcutt et al. (2001) recently reported on the distribution of Trichodesmium biomass at the Bermuda Atlantic Time Series (BATS) station, finding an average of 16% of trichomes in colonies.”
- The effect of growth rate, phosphorus concentration, and temperature on N2 fixation, carbon fixation, and nitrogen release in continuous cultures of Trichodesmium IMS101 (2005, methodology): “Similarly, Orcutt et al. (2001) reported an average ratio of about 3 : 1, with considerable variance around that mean, for a multiyear study at the Bermuda Atlantic Time Series (BATS) station.”
- Polyphosphate in Trichodesmium from the low‐phosphorus Sargasso Sea (2010, background): “…this could result in elevated polyP, the phosphocline ranged from 160 to 300 m on this transect, which is deeper than Trichodesmium is likely to migrate (White et al. 2006a), and is deeper than Trichodesmium is typically observed in this region (Orcutt et al. 2001; Davis and McGillicuddy 2006).”
- Dissolved inorganic and organic phosphorus uptake in Trichodesmium and the microbial community: The importance of phosphorus ester in the Sargasso Sea (2010, background): “Phosphorus (P) has increasingly been identified as a limiting nutrient in the ocean gyres, particularly in the Sargasso Sea region of the North Atlantic (Wu et al. 2000; Maranon et al. 2003).”
- Phosphate availability and the ultimate control of new nitrogen input by nitrogen fixation in the tropical Pacific Ocean (2007, background): “Atmospheric input of dust, which is highly enriched in Fe relative to other nutrients, plays a significant role in the distribution of Trichodesmium (Orcutt et al., 2001) and on the decoupling between N-P-Fe-Si biogeochemical cycles in the ocean (Karl, 2002).”