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Biological Invasions by Marine Jellyfish 247<br />

14.5 The Role of Life-Histories<br />

Studies into the ecology of invasions by hydromedusae and scyphomedusae<br />

are hampered by their complex bipartite life-history: a typically cryptic sessile,<br />

asexually reproducing polypoid stage is followed by a pelagic, sexually<br />

reproducing medusa stage. Depending upon food availability and other environmental<br />

variables, the polypoid stages of scyphozoans can asexually produce<br />

large numbers of planktonic young medusae, or remain dormant for<br />

extended periods, perhaps even years or decades. Such a life-history trait is<br />

not only important as a potential vector (Sect. 14.7), but makes monitoring for<br />

invasions all the more difficult, since polyps are typically inconspicuous<br />

members of a larger fouling community. In addition, similarly to the P. punctata<br />

invasion of the Gulf of Mexico in 2000, little warning would likely precede<br />

the sudden onset of an invasive jellyfish bloom.<br />

Lotan et al. (1992) conducted a study involving the culture and growth of<br />

the asexual polyp stage of Rhopilema nomadica. They determined that the<br />

period from planula settlement, through polyp generation, to the release of<br />

new medusae was on the order of 3–4 months. This would suggest that several<br />

cohorts of medusae could be produced from newly recruited planula larvae<br />

2–3 times per year. Likewise, Phyllorhiza punctata also has a bipartite life-history<br />

involving both medusa and polyp. Rippingale and Kelly (1995) provided<br />

laboratory measured growth rates of polyps, and they report fully grown<br />

polyps after only 2–3 days post-settlement of planula larvae. This may be of<br />

little value to the Gulf of Mexico invasive population, as this P. punctata population<br />

is entirely male (Graham et al. 2003; Bolton and Graham 2004). [Interestingly,<br />

a purported invasive population of Cassiopea andromeda sampled<br />

along fish farm canals on Oahu (Hawaii) by Hofmann and Hadfield (2002)<br />

was also entirely male, though the ecological implications of this observation<br />

were not discussed.]<br />

While the ctenophore Mnemiopsis is holoplanktonic (i.e., no sessile stage),<br />

it has its own life-history peculiarity. Mnemiopsis is a simultaneous hermaphrodite<br />

capable of an extremely high degree of fecundity (Mayer 1912; Reeve et<br />

al. 1989). This ctenophore is capable of reproduction within days of hatching<br />

(Martindale 1987), producing thousands of eggs with very little energy investment<br />

(Reeve et al. 1989). As a result, Mnemiopsis is able to very rapidly<br />

increase its population size in response to higher food concentrations<br />

(Feigenbaum and Kelly 1984; Kremer 1994). Accordingly, an initial invading<br />

population, say contained within ballast water, could be very small (theoretically,<br />

only one), but still lead to a successful invasion.

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