2016
DOI: 10.3391/mbi.2016.7.1.07
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Distribution and diversity of tunicates utilizing eelgrass as substrate in the western North Atlantic between 39° and 47° north latitude (New Jersey to Newfoundland)

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Cited by 9 publications
(5 citation statements)
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“…Available space is the limiting factor in many natural and artificial benthic habitats (Sebens, ), so this could result in greater competition for space and favor species that are strong competitors. It may also favor species that are able to utilize a wide range of substrates, including eelgrass, in order to gain a release from space competition (Carman et al., ).…”
Section: Discussionmentioning
confidence: 99%
“…Available space is the limiting factor in many natural and artificial benthic habitats (Sebens, ), so this could result in greater competition for space and favor species that are strong competitors. It may also favor species that are able to utilize a wide range of substrates, including eelgrass, in order to gain a release from space competition (Carman et al., ).…”
Section: Discussionmentioning
confidence: 99%
“…Colonial ascidians such as didemnids have also been observed growing on top of seagrass leaves, impeding photosynthesis (Carman & Grunden, 2010; Wong & Vercaemer, 2012; Worcester, 1994). In fact, the larger leaves of the Fijian seagrass Syringodium isoetifolium (De los Santos et al, 2016), the Australian and Mediterranean Posidonia species (Beqiraj et al, 2008; De los Santos et al, 2016; Demers et al, 2016), and the tropical Thalassia hemprichii (Carman et al, 2016; De los Santos et al, 2016; Millar, 1962) are often fouled by colonial ascidians and also encrusting bryozoans (Wong & Vercaemer, 2012; Worcester, 1994). Conversely, in this study, all colonial specimens were attached to rocks and shells within seagrass meadows but not to the plants.…”
Section: Discussionmentioning
confidence: 99%
“…As a result of ascidian fouling, the amount of photosynthetically active radiation that reaches seagrass leaves is reduced, leading to increased shading and the detachment of shoots (Brush & Nixon, 2002; Bulthuis & Woelkerling, 1983). Moreover, non‐native opportunistic ascidians have often been observed in seagrass beds (Carman et al, 2016; Carman & Grunden, 2010; Simpson et al, 2016; Worcester, 1994), which may serve as stepping stones to access the reef from the harbors where they were introduced, further threatening the health and integrity of natural ecosystems.…”
Section: Introductionmentioning
confidence: 99%
“…These communities provide an excellent, experimentally tractable model system to test ecological theories about community assembly, physiological stress, ecosystem function, and biotic interactions in estuarine, as well as fully marine, systems (e.g., Altman & Whitlatch, 2007; Freestone et al, 2013; Osman, 1977; Stachowicz & Byrnes, 2006; Stachowicz et al, 1999). Although the species in this community dominate piers and marinas, they also establish on other invertebrates, seagrass blades, cobbles, exposed bedrock, and hard mud, and can greatly affect foundation species and estuarine functions (Aldred & Clare, 2014; Carman et al, 2016; Fitridge et al, 2012; Forrest et al, 2013; Long & Grosholz, 2015; Ruiz et al, 1999). Common non‐native sessile invertebrates in Tomales Bay include Botrylloides violaceus (colonial ascidian), Bugula nertina (arborescent bryozoan), Ciona robusta (solitary ascidian), Didemnum vexillum (colonial ascidian), and Watersipora subtorquata (encrusting bryozoan).…”
Section: Methodsmentioning
confidence: 99%