Ecotypic variation in phosphorus-acquisition mechanisms within marine picocyanobacteria

By Lisa R. Moore, Martin Ostrowski, David J. Scanlan, K. Feren, T. Sweetsir. 2005

192 citations recorded by the source corpus.

Subfields: Ecology, Oceanography, Pollution

View Paper: https://www.semanticscholar.org/paper/6eacb3ca8766d2605f2cc4a303fb1174713ead1e

How researchers see this paper

The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.

In Ecology

1. Sonya T. Dyhrman
2. Michael W. Lomas
3. Mak A. Saito
4. J. Komárek
5. John R. Casey
6. Lisa R. Moore
7. E. Zinser
8. Allison Coe

In Oceanography

1. Sonya T. Dyhrman
2. Michael W. Lomas
3. J. Ammerman
4. Mak A. Saito
5. E. Orchard
6. John R. Casey
7. Lisa R. Moore
8. E. Zinser

In Pollution

1. Sonya T. Dyhrman
2. E. Orchard
3. Michael W. Lomas
4. J. Ammerman
5. Mak A. Saito
6. Gene W. Tyson

Citations in the corpus

• Dissolved inorganic and organic phosphorus uptake in Trichodesmium and the microbial community: The importance of phosphorus ester in the Sargasso Sea (2010, background): “However, determining the bioavailability of DOP is a difficult question to address, as the bioavailability of DOP varies among, and sometimes within, microbial taxa (Lomas et al. 2004; Moore et al. 2005).”
• Picophytoplankton in Freshwater Ecosystems: The Importance of Small-Sized Phototrophs (2008, background): “Nevertheless, in the Mediterranean area and in the North Pacific subtropical gyre, a climate-related shift from N- to P-limited ecosystem over the past several decades has been observed (Moore et al., 2005).”
• Microbial community gene expression in ocean surface waters (2008, background): “Meanwhile, laboratory studies have described physiological differentiation among isolates (12), and field surveys have documented the distribution of ecotypes in the oceans (13).”
• Phylogeny and taxonomy of Synechococcus-like cyanobacteria (2020, background): “The reference strain upon which our designated holotype is based has been the subject of numerous papers on the ecology and biochemistry of this taxon (Moore et al. 2005; Su et al. 2006; Iancu et al. 2007; Six et al. 2007; Tai & Palenik 2009; Tetu et al. 2009; Post et al. 2011, etc.).”
• Prochlorococcus contributes to new production in the Sargasso Sea deep chlorophyll maximum (2007, background): “This is especially relevant for nitrogen and phosphorus given conclusions drawn from culture and molecular studies [Moore et al., 2002, 2005] and the importance of these elements as nutrients limiting oceanic primary production.”
• Phytoplankton taxon-specific orthophosphate (Pi) and ATP utilization in the western subtropical North Atlantic (2009, background): “For example, high-light ecotypes MED4 and MIT9312 both have an inducible APase, but vary in the magnitude of induction, while low-light ecotypes MIT9313 and SS120 lack a recognizable APase gene (phoA), and actually down regulate APase under P stress (Moore et al. 2005).”
• Microbes and the marine phosphorus cycle (2007, background): “Phosphonates were generally considered to be an unavailable form of P for phytoplankton growth until the release of the marine cyanobacterial genomes revealed genes putatively involved in phosphonate metabolism (Dyhrman et al., 2006a; Martiny et al., 2006; Moore et al., 2005).”
• Culturing the marine cyanobacterium Prochlorococcus (2007, methodology): “Of course, marine bacteria are cocultured with the isolates, as they cannot be removed by size exclusion, and need to be eliminated via other means, such as plating (Saito 2001), serial dilution (Rippka et al. 2000), and flow cytometric sorting (Moore et al. 2005).”