The ecology of rafting in the marine environment - Bedim
The ecology of rafting in the marine environment - Bedim
The ecology of rafting in the marine environment - Bedim
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RAFTING OF BENTHIC MARINE ORGANISMS<br />
Table 11 (cont<strong>in</strong>ued) Ech<strong>in</strong>odermata reported or <strong>in</strong>ferred as <strong>raft<strong>in</strong>g</strong><br />
Species Region<br />
Ectoprocta (= Bryozoa)<br />
Some <strong>of</strong> <strong>the</strong> most ubiquitous organisms on float<strong>in</strong>g plastic items are bryozoans (W<strong>in</strong>ston 1982,<br />
Stevens et al. 1996, W<strong>in</strong>ston et al. 1997, Barnes & Sanderson 2000). Barnes (2002) ranked <strong>the</strong><br />
bryozoa as <strong>the</strong> most abundant faunal group on mar<strong>in</strong>e debris. Bryozoans have been found on a<br />
variety <strong>of</strong> different float<strong>in</strong>g substrata <strong>in</strong>clud<strong>in</strong>g macroalgae (Arnaud et al. 1976, Niermann 1986,<br />
Bush<strong>in</strong>g 1994), seagrass blades (Keough & Chern<strong>of</strong>f 1987, Worcester 1994), seeds (Mason 1961),<br />
Nautilus shells (Hamada 1964, Chirat 2000), float<strong>in</strong>g corals (DeVantier 1992), plastic items (Gregory<br />
1978, W<strong>in</strong>ston 1982, Stevens et al. 1996, W<strong>in</strong>ston et al. 1997, Barnes & Sanderson 2000,<br />
Donlan & Nelson 2003) and tar balls (Shaw & Mapes 1979) (Table 12). Gregory (1978) suggested<br />
that <strong>the</strong> cosmopolitan bryozoan Membranipora tuberculata, which is also very common on float<strong>in</strong>g<br />
Sargassum <strong>in</strong> <strong>the</strong> Sargasso Sea (Smith et al. 1973, Ryland 1974), may have crossed <strong>the</strong> Tasman<br />
Sea from Australia to New Zealand via <strong>raft<strong>in</strong>g</strong> on plastic pellets. W<strong>in</strong>ston (1982) found Electra<br />
tenella to be <strong>the</strong> dom<strong>in</strong>at<strong>in</strong>g and <strong>of</strong>ten only bryozoan species on plastic debris cast up on beaches<br />
along <strong>the</strong> Atlantic coast <strong>of</strong> Florida. In benthic habitats, however, this species occurs only sparsely<br />
<strong>in</strong> that region. W<strong>in</strong>ston (1982) predicted <strong>the</strong> niche <strong>of</strong> this species to expand spatially because <strong>of</strong><br />
<strong>the</strong> capability <strong>of</strong> <strong>the</strong> animals to utilise an <strong>in</strong>creas<strong>in</strong>g amount <strong>of</strong> anthropogenic debris float<strong>in</strong>g <strong>in</strong> <strong>the</strong><br />
world’s oceans as a habitat. On natural substrata such as float<strong>in</strong>g Sargassum, Electra tenella is<br />
lack<strong>in</strong>g, which could ei<strong>the</strong>r be due to settlement preferences <strong>of</strong> this species or due to its competitive<br />
<strong>in</strong>feriority to <strong>the</strong> dom<strong>in</strong>at<strong>in</strong>g species on float<strong>in</strong>g Sargassum <strong>in</strong> <strong>the</strong> North Atlantic, Membranipora<br />
tuberculata. Similar as M. tuberculata, <strong>the</strong> erect bryozoan Bugula nerit<strong>in</strong>a can be found on a wide<br />
variety <strong>of</strong> different substrata <strong>in</strong>clud<strong>in</strong>g seagrass blades (Keough & Chern<strong>of</strong>f 1987) and plastic<br />
surfaces (Thiel et al. 2003).<br />
In <strong>the</strong> western Mediterranean, Aliani & Molcard (2003) found four species <strong>of</strong> Bryozoa on<br />
float<strong>in</strong>g debris. While colonisation frequency decreased towards higher latitudes (W<strong>in</strong>ston et al.<br />
1997, Barnes & Sanderson 2000), bryozoans were still <strong>the</strong> most common sessile organisms reported<br />
from float<strong>in</strong>g plastics <strong>in</strong> <strong>the</strong> Sou<strong>the</strong>rn Ocean (Barnes & Fraser 2003). Based on geographic evidence<br />
and a meta-analysis <strong>of</strong> British bryozoans, Watts et al. (1998) suggested that <strong>raft<strong>in</strong>g</strong> played an<br />
important role <strong>in</strong> evolution and biogeography <strong>of</strong> cheilostome bryozoans (albeit <strong>in</strong> present-day<br />
oceans transport via ships may overshadow <strong>raft<strong>in</strong>g</strong> dispersal).<br />
337<br />
Raft<strong>in</strong>g<br />
<strong>in</strong>ference<br />
Float<strong>in</strong>g<br />
substratum Reference<br />
Amphiura magellanica Sou<strong>the</strong>rn Ocean R M Fell 1953, cited <strong>in</strong> Hendler<br />
1991<br />
Amphiura sp. Tasmania R M Edgar 1987<br />
Ophiactis carnea St. Helena R M Arnaud et al. 1976<br />
Ophiactis simplex California R M Hobday 2000a<br />
Ophioplocus esmarki California R M Bush<strong>in</strong>g 1994<br />
Ophiothrix caespitosa Tasmania R M Edgar 1987<br />
Ophiothrix spiculata California R M Hobday 2000a<br />
Ophiothrix triglochis St. Helena R M Arnaud et al. 1976<br />
Notes: D = distributional <strong>in</strong>ference; G = genetic <strong>in</strong>ference; M = macroalgae; n.i. = no <strong>in</strong>formation; R = <strong>raft<strong>in</strong>g</strong>.<br />
* References refer to this species under a different name.