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  • 1
    Online Resource
    Online Resource
    Oxford University Press (OUP) ; 2006
    In:  FEMS Microbiology Ecology Vol. 58, No. 3 ( 2006-12), p. 464-475
    In: FEMS Microbiology Ecology, Oxford University Press (OUP), Vol. 58, No. 3 ( 2006-12), p. 464-475
    Type of Medium: Online Resource
    ISSN: 0168-6496 , 1574-6941
    URL: Issue
    RVK:
    Language: English
    Publisher: Oxford University Press (OUP)
    Publication Date: 2006
    detail.hit.zdb_id: 1501712-6
    SSG: 12
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  • 2
    Online Resource
    Online Resource
    Wiley ; 2007
    In:  ChemInform Vol. 38, No. 20 ( 2007-05-15)
    In: ChemInform, Wiley, Vol. 38, No. 20 ( 2007-05-15)
    Type of Medium: Online Resource
    ISSN: 0931-7597 , 1522-2667
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2007
    detail.hit.zdb_id: 2110203-X
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  • 3
    Online Resource
    Online Resource
    Elsevier BV ; 2009
    In:  Deep Sea Research Part II: Topical Studies in Oceanography Vol. 56, No. 17 ( 2009-8), p. 1339-1350
    In: Deep Sea Research Part II: Topical Studies in Oceanography, Elsevier BV, Vol. 56, No. 17 ( 2009-8), p. 1339-1350
    Type of Medium: Online Resource
    ISSN: 0967-0645
    Language: English
    Publisher: Elsevier BV
    Publication Date: 2009
    detail.hit.zdb_id: 1141627-0
    detail.hit.zdb_id: 1500312-7
    SSG: 14
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  • 4
    Online Resource
    Online Resource
    American Society for Microbiology ; 2008
    In:  Applied and Environmental Microbiology Vol. 74, No. 14 ( 2008-07-15), p. 4516-4529
    In: Applied and Environmental Microbiology, American Society for Microbiology, Vol. 74, No. 14 ( 2008-07-15), p. 4516-4529
    Abstract: Marine sediments of coastal margins are important sites of carbon sequestration and nitrogen cycling. To determine the metabolic potential and structure of marine sediment microbial communities, two cores were collected each from the two stations (GMT at a depth of 200 m and GMS at 800 m) in the Gulf of Mexico, and six subsamples representing different depths were analyzed from each of these two cores using functional gene arrays containing ∼2,000 probes targeting genes involved in carbon fixation; organic carbon degradation; contaminant degradation; metal resistance; and nitrogen, sulfur, and phosphorous cycling. The geochemistry was highly variable for the sediments based on both site and depth. A total of 930 (47.1%) probes belonging to various functional gene categories showed significant hybridization with at least 1 of the 12 samples. The overall functional gene diversity of the samples from shallow depths was in general lower than those from deep depths at both stations. Also high microbial heterogeneity existed in these marine sediments. In general, the microbial community structure was more similar when the samples were spatially closer. The number of unique genes at GMT increased with depth, from 1.7% at 0.75 cm to 18.9% at 25 cm. The same trend occurred at GMS, from 1.2% at 0.25 cm to 15.2% at 16 cm. In addition, a broad diversity of geochemically important metabolic functional genes related to carbon degradation, nitrification, denitrification, nitrogen fixation, sulfur reduction, phosphorus utilization, contaminant degradation, and metal resistance were observed, implying that marine sediments could play important roles in biogeochemical cycling of carbon, nitrogen, phosphorus, sulfate, and various metals. Finally, the Mantel test revealed significant positive correlations between various specific functional genes and functional processes, and canonical correspondence analysis suggested that sediment depth, PO 4 3− , NH 4 + , Mn(II), porosity, and Si(OH) 4 might play major roles in shaping the microbial community structure in the marine sediments.
    Type of Medium: Online Resource
    ISSN: 0099-2240 , 1098-5336
    RVK:
    Language: English
    Publisher: American Society for Microbiology
    Publication Date: 2008
    detail.hit.zdb_id: 223011-2
    detail.hit.zdb_id: 1478346-0
    SSG: 12
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  • 5
    Online Resource
    Online Resource
    American Chemical Society (ACS) ; 2007
    In:  Chemical Reviews Vol. 107, No. 2 ( 2007-02-01), p. 577-589
    In: Chemical Reviews, American Chemical Society (ACS), Vol. 107, No. 2 ( 2007-02-01), p. 577-589
    Type of Medium: Online Resource
    ISSN: 0009-2665 , 1520-6890
    Language: English
    Publisher: American Chemical Society (ACS)
    Publication Date: 2007
    detail.hit.zdb_id: 2003609-7
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  • 6
    Online Resource
    Online Resource
    Wiley ; 2008
    In:  Limnology and Oceanography Vol. 53, No. 1 ( 2008-01), p. 78-88
    In: Limnology and Oceanography, Wiley, Vol. 53, No. 1 ( 2008-01), p. 78-88
    Abstract: It has been hypothesized that the planktonic community of the North Pacific subtropical gyre (NPSG) underwent a "domain shift" in the early 1980s in which phytoplankton of the domain Eukarya were supplanted by phytoplankton of the domain Bacteria, primarily Prochlorococcus . P limitation of eukaryotic phytoplankton was implicated as the causative chemical factor in the domain shift, and we sought to investigate the current nutrient limitation status of Prochlorococcus , now 2 decades since this event. We measured ribonucleic acid (RNA) synthesis rates by NPSG plankton at Station ALOHA in 33 PO 4 3‐ tracer incubations and found that RNA synthesis was the single largest biochemical sink for dissolved P, accounting for about half of the total PO 4 3‐ uptake. We also found that NH 4 + stimulated RNA synthesis but that PO 4 3‐ did not, which suggested N limitation of plankton growth. We developed a new RNA capture procedure, termed radioisotope‐based tracking of RNA synthesis by hybridization and capture (RIBOTRACE), to measure RNA synthesis rates by Prochlorococcus exclusively. Data from this procedure showed that NH 4 + stimulated RNA synthesis by Prochlorococcus and confirmed that Prochlorococcus was N limited and not P limited. Our RIBOTRACE data do not necessarily refute the domain shift hypothesis, but suggest that any critical period of P limitation required for the domain shift must have subsided and given way to the N‐limiting conditions that existed previously.
    Type of Medium: Online Resource
    ISSN: 0024-3590 , 1939-5590
    Language: English
    Publisher: Wiley
    Publication Date: 2008
    detail.hit.zdb_id: 2033191-5
    detail.hit.zdb_id: 412737-7
    SSG: 12
    SSG: 14
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  • 7
    Online Resource
    Online Resource
    Proceedings of the National Academy of Sciences ; 2006
    In:  Proceedings of the National Academy of Sciences Vol. 103, No. 23 ( 2006-06-06), p. 8607-8612
    In: Proceedings of the National Academy of Sciences, Proceedings of the National Academy of Sciences, Vol. 103, No. 23 ( 2006-06-06), p. 8607-8612
    Abstract: There is growing evidence that dissolved phosphorus can regulate planktonic production in the oceans’ subtropical gyres, yet there is little quantitative information about the biochemical fate of phosphorus in planktonic communities. We observed in the North Pacific Subtropical Gyre (NPSG) that the synthesis of membrane lipids accounted for 18–28% of the phosphate (PO 4 3− ) taken up by the total planktonic community. Paradoxically, Prochlorococcus , the cyanobacterium that dominates NPSG phytoplankton, primarily synthesizes sulfoquinovosyldiacylglycerol (SQDG), a lipid that contains sulfur and sugar instead of phosphate. In axenic cultures of Prochlorococcus , it was observed that 〈 1% of the total PO 4 3− uptake was incorporated into membrane lipids. Liquid chromatography/mass spectrometry of planktonic lipids in the NPSG confirmed that SQDG was the dominant membrane lipid. Furthermore, the analyses of SQDG synthesis genes from the Sargasso Sea environmental genome showed that the use of sulfolipids in subtropical gyres was confined primarily to picocyanobacteria; no sequences related to known heterotrophic bacterial SQDG lineages were found. This biochemical adaptation by Prochlorococcus must be a significant benefit to these organisms, which compete against phospholipid-rich heterotrophic bacteria for PO 4 3− . Thus, evolution of this “sulfur-for-phosphorus” strategy set the stage for the success of picocyanobacteria in oligotrophic environments and may have been a major event in Earth’s early history when the relative availability of sulfate and PO 4 3− were significantly different from today’s ocean.
    Type of Medium: Online Resource
    ISSN: 0027-8424 , 1091-6490
    RVK:
    RVK:
    Language: English
    Publisher: Proceedings of the National Academy of Sciences
    Publication Date: 2006
    detail.hit.zdb_id: 209104-5
    detail.hit.zdb_id: 1461794-8
    SSG: 11
    SSG: 12
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  • 8
    Online Resource
    Online Resource
    American Society for Microbiology ; 2006
    In:  Applied and Environmental Microbiology Vol. 72, No. 10 ( 2006-10), p. 6829-6832
    In: Applied and Environmental Microbiology, American Society for Microbiology, Vol. 72, No. 10 ( 2006-10), p. 6829-6832
    Abstract: Previously available primer sets for detecting anaerobic ammonium-oxidizing (anammox) bacteria are inefficient, resulting in a very limited database of such sequences, which limits knowledge of their ecology. To overcome this limitation, we designed a new primer set that was 100% specific in the recovery of ∼700-bp 16S rRNA gene sequences with 〉 96% homology to the “ Candidatus Scalindua” group of anammox bacteria, and we detected this group at all sites studied, including a variety of freshwater and marine sediments and permafrost soil. A second primer set was designed that exhibited greater efficiency than previous primers in recovering full-length (1,380-bp) sequences related to “ Ca . Scalindua,” “ Candidatus Brocadia,” and “ Candidatus Kuenenia.” This study provides evidence for the widespread distribution of anammox bacteria in that it detected closely related anammox 16S rRNA gene sequences in 11 geographically and biogeochemically diverse freshwater and marine sediments.
    Type of Medium: Online Resource
    ISSN: 0099-2240 , 1098-5336
    RVK:
    Language: English
    Publisher: American Society for Microbiology
    Publication Date: 2006
    detail.hit.zdb_id: 223011-2
    detail.hit.zdb_id: 1478346-0
    SSG: 12
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