Provides substratum to other marine invertebrates to settle on, increasing the spatial heterogeneity and consequently local diversity. Fishermen collect them from reefs for use as bait. ♦
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Evolution and systematics
The name "myzostomid" comes from the Greek myzo, meaning "to suck," and stoma, meaning "mouth." Leuckart described the first myzostomid, Myzostoma parasiticum, in 1827 and 1836. Since that discovery, the phylogenetic position of myzostomids within the metazoans has been a subject of controversy. The early assignments of myzostomids to Trematoda, then to Crustacea or Stelechopoda (a taxon grouping myzostomids with Tardigrada and Pentastomida), are no longer considered valid. Because myzostomids exhibit characters such as parapodia with chaetae, trochophore-type larvae, and segmentation (although incomplete), they are now classified in textbooks and encyclopedias as a family of Poly-chaeta or as a class of Annelida (the latter classification is followed here). However, phylogenetic analyses, including that of myzostomid DNA sequences, strongly support the view that they are not annelids but a phylum closely related to the flatworms.
The class Myzostomida is divided in two orders and eight families: the order Proboscidea (Myzostomatidae); and the order Pharyngidea (Protomyzostomatidae, Asteromyzos-tomatidae, Asteriomyzostomatidae, Endomyzostomatidae, Stelechopidae, Pulvinomyzostomatidae, and Mesomyzos-tomatidae). There are about 170 species.
The body of most myzostomids consists of an anterior cylindrical introvert (also called a proboscis) and a flat, disk like trunk. The introvert is extended when the individual feeds, but it is retracted into an anteroventral pouch within the trunk most of the time. The trunk ranges in length from 0.118 in (3 mm) to 1.181 in (3 cm) for the largest species. There are usually five pairs of parapodia, located lateroven-trally in two rows; each parapodium contains a protrusible hook, some replacement hooks, and a support rod, or acicu-lum. Most species have four pairs of slitlike or disklike lat-eroventral sense organs, commonly named lateral organs, and the trunk margin often bears needlelike cirri (more than 100 in some species). In a few species, humplike cirri occur at the base of each parapodium. Two male gonopores are located at the level of the third pair of parapodia; the female gonopore opens close to the anus, posteroventrally.
When myzostomids are parasitic, their body is often highly modified. The introvert, external appendages, and sensory organs are usually reduced or have disappeared. According to the location of myzostomids in the host, their trunk may be pleated dorsally, mushroom shaped, or irregular in shape.
Myzostomids are found in all oceans from shallow waters to depths of over 9,840 ft (3,000 m). Most occur in tropical waters, but a few are found in the Arctic and Antarctic Oceans.
These marine animals live in association with echinoderms.
All myzostomids live in association with echinoderms. Most species (90% of myzostomids) are ectocommensals of crinoids, but a few are parasites of crinoids, asteroids, or ophi-uroids, infesting their gonads, coelom, integumental, or digestive systems. The association between myzostomids and echinoderms is ancient, and signs of parasitic activities, similar to those induced by extant parasitic myzostomids, are found in fossilized crinoid skeletons dating back to the Carboniferous period.
Very few myzostomids feed on host tissues or coelomic fluid, most feed on particles that they divert from the host using their introvert. Crinoids, the main hosts, are suspension feeders, catching food particles in the water column with podia on both sides of the ciliated grooves that run along their arms. When myzostomids want to feed, they insert their introvert into these ciliated grooves and suck up water and food particles into their mouth.
Most myzostomids are hermaphroditic. They are often functional simultaneous hermaphrodites, even though the male genital system develops a bit earlier than the female genital system during organogenesis. In some species, both males and females occur, and are often interpreted as the two stages of protandrous hermaphroditic species, the dwarf male apparently transforming into a female once it lives alone.
Reproduction in myzostomids takes place by the emission of spermatophores followed by the intradermic penetration of sperm cells. In ectocommensals, mating involves two mature individuals that contact each other, one individual ejecting one spermatophore that attaches to the integument of the other. Contact between the two individuals is very brief and they separate quickly after mating. Spermatophores generally attach to the back of the receiver, but they can be emitted successfully onto any body part.
Depending on the species, the emitted spermatophores may be white V-shaped, club-shaped, or ball-shaped baskets. After attachment, they pierce the integument and release all the sperm cells into it. Penetration can be observed, thanks to the presence of the white trails produced by the sper-matophore contents extending into the translucent body of the receiver. These trails appear from 10 to 30 minutes after attachment of a spermatophore, and after from one to five hours, the spermatophores are reduced to an empty matrix. Fertilization of mature oocytes is internal, and eggs are accumulated into a uterus before being laid. Division is spiral, occurring in the water column, and gives rise to free-swimming trochophore larvae.
No species of myzostomids are listed by the IUCN.
Significance to humans
No parasitic myzostomids infest humans or animals reared by humans. They have no impact on human health.
No common name
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