Temporal and spatial variation in stocks of autotrophic and heterotrophic microbes in the upper water column of the central Arctic Ocean
By E. Sherr, B. Sherr, P. Wheeler, Karen D. Thompson. 2003
226 citations recorded by the source corpus.
Subfields: Ecology, Environmental Chemistry, Oceanography
View Paper: https://www.semanticscholar.org/paper/1e9d9ee925edae13dff2655b2f8792167b050b58
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In Ecology
In Environmental Chemistry
- Warwick F. Vincent
- E. Sherr
- B. Sherr
- Sylvia Bonilla
- C. Pedrós-Alió
- S. Falk‐Petersen
- Geir Johnsen
- Michel Gosselin
In Oceanography
- Ø. Varpe
- S. Falk‐Petersen
- Malin Daase
- E. Sherr
- Lena Seuthe
- B. Sherr
- Kriss Rokkan Iversen
- Jørgen Berge
Citations in the corpus
- Seasonal microbial processes in a high-latitude fjord (Kongsfjorden, Svalbard): I. Heterotrophic bacteria, picoplankton and nanoflagellates (2011, background): “2000b), the central Arctic Ocean (Sherr et al. 2003), and southeastern Beaufort Sea (Terrado et al.”
- Protist entrapment in newly formed sea ice in the Coastal Arctic Ocean (2008, background): “2–2 μm) and nanoalgal (2– 20 μm) cells at different periods of the year (e.g., Gosselin et al., 1997; Lovejoy et al., 2002, 2006; Sherr et al., 2003).”
- In the dark: A review of ecosystem processes during the Arctic polar night (2015, background): “These bacterial losses seem to be balanced by low but persistent bacterial activity and growth during winter (Sherr et al., 2003; Alonso-Saez et al., 2008; Belzile et al., 2008; Garneau et al., 2008; Vaqué et al., 2008; Forest et al., 2011).”
- DISTRIBUTION, PHYLOGENY, AND GROWTH OF COLD‐ADAPTED PICOPRASINOPHYTES IN ARCTIC SEAS 1 (2007, background): “However, these two isolates were genetically distinct from each other, and Šlapeta et al. (2006) suggested that clade E may represent an ancient, isolated lineage that diverged from other micromonads ~60 million years ago.”
- Microbial processes in a high-latitude fjord (Kongsfjorden, Svalbard): II. Ciliates and dinoflagellates (2011, background): “In the central Arctic, for example, Sherr et al. (2003) found the protozoan biomass to increase along with phytoplankton during spring and summer, indicating strong bottom-up control, while Rysgaard et al. (1999) reported strong topdown control by copepods in an ice-covered northeast Greenlandic…”
- Variations of the abundance and nucleic acid content of heterotrophic bacteria in Beaufort Shelf waters during winter and spring (2008, background): “70×10 mL in June–September 1998 (Sherr et al., 2003) or 3.”
- Community respiration/production and bacterial activity in the upper water column of the central Arctic Ocean (2003, methodology): “Bacterial abundances in this zone doubled during the same time period ( Sherr et al., 2003 ).”
- Water masses and biogeography of picoeukaryote assemblages in a cold hydrographically complex system (2008, background): “In these perennially cold waters picoeukaryotes are vital to the ecosystem; they dominate the photosynthetic biomass for much of the year (Sherr et al. 2003; Lovejoy et al. 2007) and show both abundant and diverse heterotrophic populations (Lovejoy et al.”
- Late summer phytoplankton distribution along a 3500 km transect in Canadian Arctic waters: strong numerical dominance by picoeukaryotes (2009, background): “In late summer, nanophytoplankton biomass dominated over microphytoplankton in northern BB. Similarly, Sherr et al. (2003) reported that nanophytoplankton dominated the carbon biomass over microphytoplankton in winter (November–”
- Synechococcus in the Atlantic Gateway to the Arctic Ocean (2016, background): “, 2015) in contrast to cold adapted eukaryotic picophytoplankton that occur in high abundances both in Arctic (Sherr et al., 2003; Lovejoy et al., 2007; Tremblay et al., 2009; Zhang et al., 2015) and in Antarctic waters (Doolittle et al.”