Comparisons of diversity of bacterial communities associated with three sessile marine eukaryotes
By Sharon R. Longford, N. Tujula, Gregory R. Crocetti, A. Holmes, C. Holmström, S. Kjelleberg, Peter D. Steinberg, Michael W Taylor. 2007
150 citations recorded by the source corpus.
Subfields: Ecology, Oceanography
View Paper: https://www.semanticscholar.org/paper/d461e1b338f5d0836958a1707fbd118d45d7347f
How researchers see this paper
The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
In Ecology
In Oceanography
- T. Harder
- Peter D. Steinberg
- S. Kjelleberg
- A. Campbell
- J. Imhoff
- Shaun Nielsen
- Jutta Wiese
- F. Goecke
Citations in the corpus
- Chemical interactions between marine macroalgae and bacteria (2010, background): “Molecular techniques: CLO = cloning, CFISH = cytogenetic fluorescence in situ hybridization, DGGE = denaturing gradient gel electrophoresis, FISH = fluorescence in situ hybridization, IFN = immunofluorescent detection, RQT = real time quantitative PCR, RFLP = restriction fragment length polymorphism”
- Algae as an important environment for bacteria – phylogenetic relationships among new bacterial species isolated from algae (2013, background): “…(RFLP) fingerprinting, which have shown clear differences between the bacterial communities associated with algae and the surrounding seawater (Grossart et al. 2005; Staufenberger et al. 2008; Bengtsson et al. 2010; Burke et al. 2011b) or from other living surfaces (Longford et al. 2007).”
- The seaweed holobiont: understanding seaweed-bacteria interactions. (2013, background): “These limitations are exemplified by studies on the cosmopolitan green alga Ulva lactuca (also referred to as U. australis ), where DGGE-based analysis suggested the existence of a core community that is stable over space and time (Longford et al. , 2007; Tujula et al. , 2010).”
- Climate change and disease: bleaching of a chemically defended seaweed (2011, background): “Normally, the healthy, chemically defended surface of D. pulchra supports relatively specific microbial communities (Longford et al., 2007; Longford, 2008).”