The animal in the clip is called a nemertean. The Nemertea, commonly known as ribbon worms, are a group of more than 1200 known species of mostly predatory worm-like animals. The majority of nemerteans are marine, but there are also species found in freshwater or even terrestrial environments (the clip above shows a terrestrial species). As their vernacular name suggests, the majority of ribbon worms are flattish, slender animals with little in the way of external elaborations. Most are small and unassuming, but there are exceptions: one ribbon worm species from coasts of northern Europe, Lineus longissimus, grows to estimated lengths of over 30 m and may even be the longest animal in existence*. The most characteristic feature of ribbon worms is a long proboscis that they use in capturing prey; when not being deployed, this proboscis is retracted within a cavity called the rhynchocoel that runs much of the animal's length. Other than this, nemerteans have little in the way of internal body cavities other than the gut. They do have a simple blood-vascular system consisting of a few blood vessels but no actual heart; instead, the blood just kind of sloshes back and forth as a result to the animal's body contractions as it moves.
*Some uncertainty over the exact lengths of Lineus longissimus specimens is inevitable because, despite their remarkable length, they are still only a centimetre or so wide. When you're trying to extract something like that from among a bunch of rocks, it's gonna stretch and break. Still, thirty metres is a fairly conservative estimate of its length; Wikipedia cites a supposed maximum nearly twice that. These mega-nemerteans are definitely one of those animals that make me wonder, how does this thing even exist? I mean, what is the point of being so incredibly long and slender? How does it collect enough food at the front end to nourish itself all the way to the back end? How does it not just fall apart of its own accord, let alone when subjected to any external pressure?
The relationships of nemerteans to other animals are rather uncertain, and they have generally been classified as their own independent phylum. Because of their simple body plan, many early authors compared them to flatworms, at least on a grade level, but this fell out of favour as it became accepted that the rhynchoel and blood-vascular system probably correspond to anatomical structures in more complex animals. More recent evidence from molecular and other sources has converged on a position within the Lophotrochozoa, the major animal clade that also includes molluscs, brachiopods and annelids, but their exact placement within this clade remains open to debate.
Molecular data have also influenced our understanding of relationships within the Nemertea. An influential classification of the group divided them between the Enopla, in which the proboscis is usually armed with a stabbing stylet or stylets, and the Anopla, in which the proboscis is unarmed (members of this latter group often have the proboscis branched as in the clip above; I'm guessing that in the absence of a stylet the proboscis probably works through adhesion). The two groups also differ in that Anopla always have the proboscis emerging from a separate pore to the mouth, whereas in many Enopla the mouth and proboscis pore share a common opening (Kvist et al. 2014). The Anopla were further subdivided into the Heteronemertea, which have a distinctive tissue layer called the dermis underneath the outer epidermis, and the Palaeonemertea which lack such a differentiation of skin layers. However, one need not be an expert in nemerteans to spot that the Anopla and Palaeonemertea were mostly defined by their lack of derived features (no stylets, no dermis) and so it should come as little surprise that molecular studies of the group have failed to offer resounding support for their monophyly. Instead, a number of studies have suggested that the Heteronemertea and Enopla together form a clade that Thollesson & Norenburg (2003) dubbed the Neonemertea. When they did so it was on the basis of molecular data only, but later authors have identified possible synapomorphies of the Neonemertea in features of the nervous and blood-vascular systems. One family of 'Palaeonemertea', the Hubrechtidae, has been suggested to also belong within the Neonemertea as sister-taxon to the Heteronemertea. This is of interest because the Hubrechtidae and Heteronemertea share a distinctive type of ciliated planktonic larva called a pilidium (other nemerteans either develop directly or have a creeping planula-type larva). Ciliated planktonic larvae are known a number of groups of animals, such as the veliger of molluscs, the trochophore of annelids, or the tornaria of acorn worms, and there has been a lot of discussion over the years as to whether similarities between these larvae represent a shared ancestry, or whether they might have evolved independently. In the case of nemerteans, at least, the current evidence seems to favour the latter. As for the other 'palaeonemerteans', there seems to be less of a consensus as to whether they form a single clade or a paraphyletic series relative to the Neonemertea.
As for the Enopla, it appears to form a valid clade. Previous authors divided the enoplans between the Hoplonemertea, including the majority of species, and the Bdellonemertea, including the single distinctive genus Malacobdella. The Hoplonemertea were in turn divided between the Monostilifera, in which the proboscis has a single long stylet, and the Polystilifera, in which it bears a pad of small stylets, and molecular analyses support the separation of these groups. Malacobdella (which lacks proboscis stylets but has the conjoined mouth-proboscis pore) has a sucker at the posterior end of its body, by which it lives attached to the gills of a mollusc. Malacobdella is not a parasite of the mollusc, per se: instead, it feeds on food particles drawn in by water flowing through the mollusc's gills. However, the recent analyses have indicated that Malacobdella is in fact a derived monostiliferan, and a number of recent authors have used the Hoplonemertea as an equivalent name to the old Enopla.
Also distinctive within the Hoplonemertea are two clades, the polystiliferan Pelagica and the monostiliferan Korotkevitschiidae, that have left the ocean floor and adopted a pelagic life style. Members of both these groups are gelatinous and eyeless; the Pelagica have lost further internal organs such as nephridia. The Korotkevitschiidae (which also lack a proboscis stylet) are found towards the surface of the ocean; the Pelagica are found in much deeper waters (Chernyshev 2003). The pelagic nemerteans are among the most poorly known of all ribbon worms; they are rarely encountered (about half of the 100 or so described species of Pelagica are known only from single specimens) and their relatively simple morphology makes them difficult to compare to other nemerteans. If the individual in the photograph is any indication, however, they are beautiful animals.
Chernyshev, A. V. 2003. Classification system of the higher taxa of enoplan nemerteans (Nemertea, Enopla). Russian Journal of Marine Biology 29 (Suppl. 1): S57–S65.
Kvist, S., C. E. Laumer, J. Junoy & G. Giribet. 2014. New insights into the phylogeny, systematics and DNA barcoding of Nemertea. Invertebrate Systematics 28: 287–308.
Thollesson, M., & J. L. Norenburg. 2003. Ribbon worm relationships: a phylogeny of the phylum Nemertea. Proceedings of the Royal Society of London Series B—Biological Sciences 270: 407–415.