2016
DOI: 10.1086/690090
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Effects of Embryonic Exposure to Salinity Stress or Hypoxia on Post-metamorphic Growth and Survival of the PolychaeteCapitella teleta

Abstract: Although a good number of studies have investigated the impact of larval experience on aspects of post-metamorphic performance, only a few have considered the potential impact of stresses experienced by brooded embryos. In this study we separately investigated the impact of salinity stress (as low as 10) and hypoxia (1 ml O l) experienced by brooded embryos of the deposit-feeding polychaete Capitella teleta on hatching success, metamorphosis, post-metamorphic survival, and post-metamorphic growth. Salinity red… Show more

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Cited by 10 publications
(6 citation statements)
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“…Pechenik et al . (2016) described the brood tubes of C. teleta as generally about 8–15 mm long and about 0.6–1.3 mm wide, and did not mention any peculiarity in the shape of the brood tube (like sand accumulation) as observed in Capitella sp. TF (Figure 1B).…”
Section: Discussionmentioning
confidence: 99%
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“…Pechenik et al . (2016) described the brood tubes of C. teleta as generally about 8–15 mm long and about 0.6–1.3 mm wide, and did not mention any peculiarity in the shape of the brood tube (like sand accumulation) as observed in Capitella sp. TF (Figure 1B).…”
Section: Discussionmentioning
confidence: 99%
“…It is actually unusual for larvae to survive for such a long time (14 days) inside the brood tube without the presence of the mother. Usually C. teleta females do not leave the tube until the larvae hatch (Pechenik & Cerulli, 1991; Pechenik et al ., 2016). The role of the female during the brooding period consists of ventilating the fertilized eggs by periodic body undulations to allow water circulation inside the tube (Reish et al ., 1974; Reish, 1980; Pechenik et al ., 2016).…”
Section: Discussionmentioning
confidence: 99%
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“…For many years, researchers working with marine invertebrate larvae have sometimes used Instant Ocean (Spectrum Brands, Blacksburg, VA) or some other artificial substitute for natural seawater (e.g., Red Sea Salt, Marine Biological Laboratory artificial seawater; Table 1), to avoid variation in the chemical composition or quality of natural seawater, because natural seawater was not readily available (e.g., Baloun and Morse, 1984;Pires and Hadfield, 1991;George et al, 2004;Moran and Marko, 2005;Steinberg et al, 2008;Anderson and Epifanio, 2009;Biggers et al, 2011;Pechenik et al, 2016), or to reduce costs for commercial aquaculture operations (Mallasen and Valenti, 1998). As pollution levels in coastal ecosystems increase, and as harmful algal blooms continue to increase in magnitude and frequency (Hallegraeff, 1993;De Rijcke et al, 2016), it may make sense to use artificial seawater for experiments more frequently, particularly for experiments with sensitive developmental stages and for investigating larval responses to low concentrations of chemical cues for metamorphosis (e.g., Barker, 1977;Pechenik and Gee, 1993;Pechenik et al, 1995;Biggers and Laufer, 1999;Thiyagarajan et al, 2005;Burns et al, 2014).…”
Section: Introductionmentioning
confidence: 99%
“…Crepidula fornicata (Henry, Perry, & Martindale, 2010;Perry & Henry, 2015), and the planarian species Dugesia japonica and Girardia tigrina . In recent years the marine annelid Capitella teleta has been successfully used for investigations related to evolutionary and developmental processes, and also for regeneration and environmental studies (Amiel, Henry, & Seaver, 2013;de Jong & Seaver, 2016;Meyer, Boyle, Martindale, & Seaver, 2010;Meyer, Carrillo-Baltodano, Moore, & Seaver, 2015;Pechenik, Berard, & Kerr, 2000;Pechenik et al, 2016;Seaver, 2016;Sur, Magie, Seaver, & Meyer, 2017). To further add to the importance of C. teleta as a representative annelid, functional genomic studies need to be established in this system.…”
Section: Introductionmentioning
confidence: 99%