TL;DR: The results favour the conclusion that the trochophore, if defined as a feeding larval form using opposed bands, should not be regarded as an ancestral (= plesiomorphic) type for the Spiralia, or any other large taxon such as the Polychaeta or Mollusca.
Abstract: «Trochophore» is a term used in a strict sense for larvae having an opposed-band method of feeding, involving a prototroch and metatroch. Other ciliary bands such as a telotroch and neurotroch may be present. The trochophore has been proposed to represent the ancestral larval form for a group of metazoan phyla (including all members of the Spiralia). The name trochophore is also often applied to larvae that do not conform to the above definition. A cladistic analysis of spiralian taxa (with special reference to polychaete annelids), based on a suite of adult and larval characters, is used to assess several hypotheses: (1) that the trochophore (in a strict sense) is a plesiomorphic form for the Spiralia; (2) that the strictly defined trochophore is plesiomorphic for members of the Spiralia such as the Polychaeta. The homology of each of the various separate ciliary bands of spiralian larvae, and features such as the apical tuft and protonephridia is also assessed. The results favour the conclusion that the trochophore, if defined as a feeding larval form using opposed bands, should not be regarded as an ancestral (= plesiomorphic) type for the Spiralia, or any other large taxon such as the Polychaeta or Mollusca. The evidence suggests that the various ciliary bands have differing evolutionary histories, and only the Echiura (possibly an annelid group) has members with the classical trochophore. The trochophore is re-defined as a larval form with a prototroch. This broad definition covers a wide variety of larvae, and matches the current usage more accurately than the restricted term. Features such as the neurotroch, telotroch and opposed-band feeding show convergence and reversals. The nature of the metatroch requires further investigation. The presence of a prototroch (and hence trochophore larvae) is used to identify an apomorphy-based taxon, Trochozoa, that includes the first ancestor to have evolved a prototroch and all its descendants. This minimally includes the Annelida (sensu lato), Echiura, Entoprocta, Mollusca and Sipuncula and is a less inclusive taxon than the Spiralia.
TL;DR: Striae around the contracted buccal apparatus in all 3 stages were convoluted and often had thickened margins; those in telotrochs and microgamonts had oral-aboral ectoplasmic cross-connections.
Abstract: SYNOPSIS. Sessile zooids, and mobile telotrochs and microgamonts of Carchesium polypinum (Protozoa, Ciliata, Peritrichia), were examined by scanning electron microscopy. The results were compared to earlier light and electron microscope studies in order to investigate structural changes concerned with adaptation and differentiation. Telotrochs and microgamonts always had a contracted peristome and usually had a long phalange of cilia. Striae around the contracted buccal apparatus in all 3 stages were convoluted and often had thickened margins; those in telotrochs and microgamonts had oral-aboral ectoplasmic cross-connections. Nonbuccal striae of telotrochs and microgamonts varied in structure and height differences between epiplasmic peaks and alveoli surface membranes. The number of striae were constant in all 3 stages. Pellicular pore structure did not vary in any of the stages examined and resembled parasomal sacs located near buccal structures. Fully relaxed sessile zooids had ectoplasmic ridges coursing from polykinety kinetosomes and cilia to an area in front of the ciliated portion of the haplokinety; these ridges were interpreted to be the interkinetal fibers. Telotroch bands of sessile zooids consisted of 2 or 3 parallel ectoplasmic ridges which circled the aboral region and contained structures resembling pores. Telotroch bands in telotrochs and microgamonts had 2 enlarged, parallel ectoplasmic ridges circling the aboral region; telotroch band cilia were found between these ridges. In addition, a fold-like, ectoplasmic structure extended beyond the 2 ridges and was located between the telotroch band cilia and the aboral ridge. The epiplasmic shelf surrounding the stalk in sessile zooids was enlarged in telotrochs, and cilia were seen in the scopula depression. No scopula organelle was seen in any microgamont.
TL;DR: Specimens of the marine tanaid crustacea Halmyrapseudes spaansi sampled in temporary littoral muddy patches near the mouth of the Kaw river (French Guiana, SE America), showed protozoan epibionts herein described as a new species: Cothurnia guyanensis sp.
Abstract: Specimens of the marine tanaid crustacea Halmyrapseudes spaansi , sampled in temporary littoral muddy patches near the mouth of the Kaw river (French Guiana, SE America), showed protozoan epibionts herein described as a new species: Cothurnia guyanensis sp. n. (Ciliophora, Peritrichia). These ciliates were covered by a cylindrical or bell-shaped lorica containing an oval elongated zooid with a rounded contractile vacuole located anteriorly in lateral position. The macronucleus was “S” shaped. The peristomial disk was anterior and included a polikinety and a haplokinety. The external stalk was short and broad, with 8–18 longitudinal conspicuous striations. Between the external stalk and the zooid, there were an endostyle and an mesostyle both short and broad. The striations of the external stalk were prolonged in the mesostyle. Telotroch stages were observed and described, as well as specimens with two zooids per lorica. Epibionts located on the ventral area, pereopods and antennae of the basibiont.
TL;DR: A suggestion is made that larvae at the late trochophore stage are capable of digesting food and feeding, and the structure of a M. yessoensis veliger is typical for pectinids.
Abstract: Fine structural features of Mizuhopecten yessoensis in different embryonic and larval developmental stages from oocyte to early veliger have been studied. Spermatozoa have a conical head, consisting of a short acrosome, nucleus, and 4 mitochondria in the middle piece. The flagellum is approximately 40 μm in length. Oocyte cytoplasm contains numerous yolk granules, which are gradually expended during the larval development and disappear at the early veliger stage. Gastrula has two invaginations: shell gland anlage on the dorsal side and ventral side archenteron. Prototroch of a trochophore consists of two ciliary rings. Telotroch is absent. Myoblasts containing bundles of myofilaments are found in the blastocoel of trochophore. Velum and shell begin forming at the late trochophore stage. Cells of gut epithelium form numerous microvilli, organized into a brush border structure on the surface of enterocytes. A suggestion is made that larvae at the late trochophore stage are capable of digesting food and feeding. The structure of a M. yessoensis veliger is typical for pectinids. The velar retractor muscles have cross striation with a period of 1 μm. The digestive system of an 8-day-old veliger consists of the esophagus, stomach (with subdivided gastric shield and style sac), and short intestine. The digestive gland (with no discernible loops at this stage) is a part of the stomach epithelium with two types of digestive enzyme-producing cells.
TL;DR: Zoothamnium intermedium was found attached to the exoskeleton of planktonic crustaceans, most of which were copepods Acartia clausi, and formed branching colonies that consisted of zooids characterized by a bell‐like shape and peristomial cilia that formed a single haplokinety raised above a double polykinety.
Abstract: Zoothamnium intermedium was found attached to the exoskeleton of planktonic crustaceans, most of which were copepods Acartia clausi. It formed branching colonies that consisted of zooids characterized by: 1) a bell‐like shape; 2) peristomial cilia that formed a single haplokinety raised above a double polykinety; and 3) unbranched annular striae, regularly distanced from each other by about 0.5 μm, around the zooid circumference. Fully developed colonies contained also several roundish zooids that were identified as potential motile stages. In addition to colony members, free‐swimming dimorphic individuals were also occasionally observed: one type showed long trochal cilia and a scopula with a central area containing numerous protuberances; the other was characterized by short, stumpy cilia and a scopula endowed with a central finger‐like process surrounded by a pleated wrap. These free‐swimming individuals were tentatively identified as the microgamont and telotroch stage of Zoothamnium intermed...