2014
DOI: 10.1016/j.parint.2013.11.010
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Larval stages of the bluefin tuna blood fluke Cardicola opisthorchis (Trematoda: Aporocotylidae) found from Terebella sp. (Polychaeta: Terebellidae)

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Cited by 46 publications
(22 citation statements)
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“…Other farm infrastructure such as mooring lines and chains, walkways and buoys are cleaned at much lower frequencies, occasionally only following the grow-out phase. Therefore, biofouling accumulation on these structures can be considerable (Bloecher et al 2015) and may act as a reservoir for pathogens (Sugihara et al 2014;Shirakashi and Hirano 2015), likely exacerbating biofouling recruitment to cage nets (Bloecher et al 2015).…”
Section: Net Cleaning and Exchangementioning
confidence: 99%
“…Other farm infrastructure such as mooring lines and chains, walkways and buoys are cleaned at much lower frequencies, occasionally only following the grow-out phase. Therefore, biofouling accumulation on these structures can be considerable (Bloecher et al 2015) and may act as a reservoir for pathogens (Sugihara et al 2014;Shirakashi and Hirano 2015), likely exacerbating biofouling recruitment to cage nets (Bloecher et al 2015).…”
Section: Net Cleaning and Exchangementioning
confidence: 99%
“…A total of 64terebellidpolychaetes, including 39 Terebella sp. were collected from ropes and floats attached to tuna cages at a PBTculture farm in Tsushima, Nagasaki Prefecture, Japan on February 15, 2016, the same site as Sugihara et al [7]collected infected polychaetes. Terebellidpolychaeteswere also sampledat a PBT culture farm in Kushimoto, Wakayama Prefecture, Japan on June 23, 2015 as a part of monthly samplings [6].…”
Section: Field Samplingmentioning
confidence: 99%
“…Each polychaete was flattened and examined for sporocysts in the body cavity by light microscopy in Tsushima as in Sugihara et al [8]or by stereomicroscopy in Kushimoto as in Shirakashi et al [6].When found infected, sporocystswere isolated in clean sea water and later used for morphological and molecular analyses. For sporocysts collected in Kushimoto, the 28S ribosomal DNA sequences were determined as 4 described in Shirakashi et al [6].For those collected in Tsushima, C. opisthorchis was confirmed by the sequences of the PCR products targeting the internal transcribedspacer 2 and 28S of the ribosomal DNA sequences, as described in Sugihara et al [7].The infected terebellids were fixed in 10% seawater formalin for traditional identification.…”
Section: Field Samplingmentioning
confidence: 99%
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