CONSPECIFICITY AND INDO‐PACIFIC DISTRIBUTION OF SYMBIODINIUM GENOTYPES (DINOPHYCEAE) FROM GIANT CLAMS

By B. Baillie, C. A. Belda-Baillie, T. Maruyama. 2000

142 citations recorded by the source corpus.

Subfields: Ecology, Global and Planetary Change, Oceanography

View Paper: https://www.semanticscholar.org/paper/f214ceeb7f509a647c56351e15faa6e61a18c887

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 Global and Planetary Change

In Oceanography

Citations in the corpus

Patterns of coral–dinoflagellate associations in Acropora: significance of local availability and physiology of Symbiodinium strains and host–symbiont selectivity (2001, methodology): “Gene boundaries were determined by a comparison with Symbiodinium strain HH1A (accession number AF183575; Baillie et al. 2000).”
Diversity and community structure of symbiotic dinoflagellates from Caribbean coral reefs (2002, result): “These data also confirm findings from cultured isolates that some ITS types are widely distributed (Baillie et al. 2000; LaJeunesse and Trench 2000; LaJeunesse 2001).”
Bleaching Resistance and the Role of Algal Endosymbionts (2009, unknown): “Diversity below the level of the clade is usually assessed using the internal transcribed spacers (ITS1, ITS2) of the nrDNA (Hunter et al. 1997; Baillie et al. 2000a; LaJeunesse 2001; van Oppen et al. 2001), the rDNA 23S gene (Santos et al. 2002) or the psbA non-coding region (Moore et al. 2003) o”
Symbiodinium sp. associations in the gorgonian Pseudopterogorgia elisabethae in the Bahamas: high levels of genetic variability and population structure in symbiotic dinoflagellates (2003, background): “Mechanisms driving population differentiation of Symbiodinium sp. clade B across the Bahamas Our documentation of striking population differentiation in Symbiodinium sp. clade B across the Bahamas is surprising given the recovery of Symbiodinium spp. isolates with identical rDNA sequences, such as c”
Symbiodinium tridacnidorum sp. nov., a dinoflagellate common to Indo-Pacific giant clams, and a revised morphological description of Symbiodinium microadriaticum Freudenthal, emended Trench & Blank (2015, unknown): “…the Indo-West Pacific, have commonly identified (genetically) and cultured S. tridacnidorum from giant clams in the molluscan subfamily Tradacninae (Rowan et al., 1996; Carlos et al., 1999; Baillie et al., 2000; LaJeunesse, 2001; LaJeunesse et al., 2004a, 2004b; Weber, 2009; DeBoer et al., 2012).”
Flexibility and Specificity in Coral-Algal Symbiosis: Diversity, Ecology, and Biogeography of Symbiodinium (2003, unknown): “Symbiont Diversity in Individual Hosts In addition to within-species symbiont diversity, multiple types ofSymbiodinium within single individuals and/or colonies have been documented in a number of hosts, including scleractinian corals (Baker 1999, 2001; Baker et al. 1997; Darius et al. 1998, 2000; L”
The ecological significance of giant clams in coral reef ecosystems (2015, background): “…stomach into its mantle (Fankboner and Reid, 1990; Norton et al., 1992) provides numerous microhabitats for zooxanthellae (Norton et al., 1992) allowing multiple clades or multiple types from a single clade of symbionts to co-exist in a single host (Baillie et al., 2000; DeBoer et al., 2012).”
INVESTIGATING THE BIODIVERSITY, ECOLOGY, AND PHYLOGENY OF ENDOSYMBIOTIC DINOFLAGELLATES IN THE GENUS SYMBIODINIUM USING THE ITS REGION: IN SEARCH OF A “SPECIES” LEVEL MARKER (2001, methodology): “It was then shown that all their isolates had virtually identical ITS sequences (type A3) (Baillie et al. 2000b).”
IDENTIFICATION OF PFIESTERIA PISCICIDA (DINOPHYCEAE) AND PFIESTERIA‐LIKE ORGANISMS USING INTERNAL TRANSCRIBED SPACER‐SPECIFIC PCR ASSAYS 1 (2003, background): “As reported for other dinoflagellate species (Adachi et al. 1994, 1995, 1997, Hudson and Adlard 1996, Baillie et al. 2000), the ITS region of PLO dinoflagellates enabled us to distinguish closely related species.”
Symbiont diversity in scleractinian corals from tropical reefs and subtropical non-reef communities in Taiwan (2005, background): “…(Rowan and Powers 1991a, 1991b; Rowan and Knowlton 1995; Baker and Rowan 1997; Baker et al. 1997; Hunter et al. 1997; Rowan et al. 1997; Wiclox 1998; Carlos et al. 1999; Baillie et al. 2000; LaJeunesse 2001; Pochon et al. 2001; Toller et al. 2001a, 2001b; van Oppen et al. 2001; Santos et al. 2002).”
Closely related Symbiodinium spp. differ in relative dominance in coral reef host communities across environmental, latitudinal and biogeographic gradients (2004, background): “Some types have wide geographic distributions (Baillie et al. 2000, LaJeunesse 2001) and are found in numerous host taxa (LaJeunesse 2002).”
Multiple marker parallel tag environmental DNA sequencing reveals a highly complex eukaryotic community in marine anoxic water (2010, background): “Dinoflagellates and their close relatives are increasingly recognized as important primary producers, symbionts, parasites (of each other as well as other organisms), and heterotrophic grazers in marine systems (Baillie et al. 2000; Chambouvet et al. 2008; Gast & Caron 1996; Guillou et al. 2008; Kno”
Distributions of stress-resistant coral symbionts match environmental patterns at local but not regional scales (2009, background): “In a similar vein, internal transcribe spacer sequences and microsatellite genotypes occur over wide ranges (Baillie et al. 2000, Santos et al. 2004, van Oppen et al. 2005).”
Low symbiont diversity in southern Great Barrier Reef corals, relative to those of the Caribbean (2003, background): “The most common symbiont types from each clade (B1, C1, C3, and D1a) were found in both the Caribbean and Pacific (A3 is found in tridacnid clams from the Pacific (Baillie et al. 2000) (Fig.”