ALKALINE PHOSPHATASE ACTIVITIES AMONG POPULATIONS OF THE COLONY‐FORMING DIAZOTROPHIC CYANOBACTERIUM TRICHODESMIUM SPP. (CYANOBACTERIA) IN THE RED SEA

By A. Stihl, Ulrich Sommer, A. Post. 2001

100 citations recorded by the source corpus.

Subfields: Ecology, Environmental Chemistry, Oceanography

View Paper: https://www.semanticscholar.org/paper/6b28374c2e1bac8fccef05ce6dc43c54ff679f71

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In Ecology

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2. Feixue Fu
3. Jonathan P. Zehr
4. R. Foster
5. David M. Karl
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8. K. Björkman

In Environmental Chemistry

1. D. Hutchins
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In Oceanography

1. D. Hutchins
2. Feixue Fu
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4. Jonathan P. Zehr
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6. R. Foster
7. K. Björkman
8. Yaohong Zhang

Citations in the corpus

• Dynamics of community structure and phosphate status of picocyanobacterial populations in the Gulf of Aqaba, Red Sea (2005, background): “A could be explained by differences in growth rates between ecotypes (from the small ‘‘seed’’ population remaining after winter mixing) or by invasion or repopulation of Prochlorococcus originating from niches and refuges within the Gulf of Aqaba or from the main body of the Red Sea, south of the St”
• Phosphorus dynamics in cultures and natural populations of Trichodesmium spp. (2002, unknown): “The highest growth rates were observed on medium containing the highest concentration of DIP (50 µM), and growth rates were comparable between cultures grown on 3 µM DIP and 1 or 3 µM DOP (as Na-glycerolphosphate; Fig.”
• PHOSPHATE UPTAKE AND GROWTH KINETICS OF TRICHODESMIUM (CYANOBACTERIA) ISOLATES FROM THE NORTH ATLANTIC OCEAN AND THE GREAT BARRIER REEF, AUSTRALIA 1 (2005, background): “Natural populations and cultures have been shown to express alkaline phosphatase activity (Yentsch et al. 1972, Stihl et al. 2001, Dyhrman et al. 2002, Mulholland et al. 2002), suggesting Trichodesmium has the capability to use at least some portion of this DOP.”
• Phosphatase activity in the sea (2004, background): “Stihl et al. (2001) recorded in the Red Sea higher phosphatase activity per unit chlorophyll of the rare puff and bow-tie colonies of Trichodesmium compared with tuft colonies.”
• Phosphorus availability, phytoplankton community dynamics, and taxon‐specific phosphorus status in the Gulf of Aqaba, Red Sea (2006, methodology): “This confirms work of Stihl et al. (2001), which determined the bulk APA of Trichodesmium colonies (when these were found) in the gulf and suggested that they were Pi stressed.”
• Spatial and temporal distribution of Trichodesmium spp. in the stratified Gulf of Aqaba, Red Sea (2002, unknown): “High alkaline phosphatase activities among surface plankton and Trichodesmium spp. colonies from the Gulf of Aqaba measured during the same sampling period were indicative of low inorganic phosphate availability and, possibly, P-limitation (Li et al. 1998, Stihl et al. 2001).”
• Dynamics of Dissolved Organic Phosphorus (2015, background): “It also likely supplements its P requirements with DOP under field conditions, including both phosphate esters and phosphonates (Dyhrman et al., 2002, 2006; Sohm and Capone, 2006; Stihl et al., 2001; Yentsch et al., 1972).”
• Seasonality of N2 fixation and nifH gene diversity in the Gulf of Aqaba (Red Sea) (2009, background): “Enhanced alkaline phosphatase activities, the enzyme responsible for P regeneration from dissolved organic matter (DOM), have been measured in the Gulf of Aqaba and show a seasonal maximum during late summer (Stihl et al. 2001; Mackey et al. 2007).”