Host-symbiont specificity during onset of symbiosis between the dinoflagellates Symbiodinium spp. and planula larvae of the scleractinian coral Fungia scutaria
By V. Weis, W. Reynolds, Melissa L Deboer, D. Krupp. Coral reefs, 2001
172 citations recorded by the source corpus.
Subfields: Biotechnology, Ecology
View Paper: https://www.semanticscholar.org/paper/589543917e3b1d813240bc818ea7bad24051fcdd
How researchers see this paper
The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
In Biotechnology
In Ecology
- A. Baker
- O. Hoegh‐Guldberg
- W. Fitt
- Gregory W. Schmidt
- Todd C. LaJeunesse
- D. Thornhill
- R. Buddemeier
- D. Fautin
Citations in the corpus
- Assessing the ‘deep reef refugia’ hypothesis: focus on Caribbean reefs (2010, background): “Despite the fact that Caribbean reefs were hit somewhat harder hit by disease compared to their Indo-Pacific counterparts ( Weil 2004 ), they have been less impacted by predatory species (e.g., Acanthaster planci and Drupella outbreaks; Colgan 1987; DeVantier and Deacon 1990; Turner 1994).”
- High diversity and host specificity observed among symbiotic dinoflagellates in reef coral communities from Hawaii (2004, background): “This symbiont when compared against types C15, Cld, and C31, originating from P. compressa, P. damicornis , and M. capitata respectively, infects with greater success and achieves higher growth rates in Fungia scutaria larvae (Weis et al. 2001; Rodriguez-Lanetty et al. 2004).”
- The Adaptive Hypothesis of Bleaching (2004, background): “Selectivity in these partnerships, however, may exist (Weis et al. 2001), and by analogy with other symbioses, it is likely that certain combinations of hosts and symbionts are impossible.”
- The distribution of dimethylsulfoniopropionate in tropical Pacific coral reef invertebrates (2006, background): “In some species they are obtained maternally, whereas in others they are acquired in later freeliving planktonic or sessile stages (e.g., Hirose et al. 2000; Coffroth et al. 2001; Weis et al. 2001; Schwarz et al. 2002; Pasternak et al. 2004).”
- Mangrove-Exported Nutrient Incorporation by Sessile Coral Reef Invertebrates (2009, unknown): “trophic position) were assigned as 0.5& (for example, France and Peters 1997; Vander Zanden and Rasmussen 2001; McCutchan and others 2003).”
- An Overview on Marine Sponge-Symbiotic Bacteria as Unexhausted Sources for Natural Product Discovery (2017, background): “These symbiotic relationships provide support and protection to the microbial symbionts and the host organism [43], as well as provide nutritional requirements for both the symbiont and the host [44–47].”
- Distinct ITS types of Symbiodinium in clade C correlate with cnidarian/dinoflagellate specificity during onset of symbiosis (2004, methodology): “RodriguezLanetty et al. (2003) showed, by algal infection experiments with aposymbiotic hosts, that the anemone Heteractis sp. established a successful association only with Clade C Symbiodinium, at least among the endosymbionts (Clades C and F ) occurring in the study area.”
- Flexibility and Specificity in Coral-Algal Symbiosis: Diversity, Ecology, and Biogeography of Symbiodinium (2003, unknown): “Studies of scleractinian corals have also demonstrated the capacity for diverse symbionts to be acquired during early ontogeny (Schwarz et al. 1999, Van Oppen 2001), but some symbionts may still be favored over others (Weis et al. 2001).”