The validity of the Lophophorata as a monophyletic group remains controversial. New data on the innervation of the lophophore, which is a unique feature of the lophophorates, may help clarify the status of the Lophophorata and provide new information on the early evolution of the group. In this paper, the organization of the nervous system of the lophophore is described in adults of the minute phoronid Phoronis ovalis. The lophophore nervous system includes a dorsal ganglion, a tentacular nerve ring, an inner ganglion, an inner nerve ring, and six nerves in each tentacle. The inner ganglion and inner nerve ring, which is associated with sensory cells, are described for the first time in adult phoronids. The general plan of the nervous system of the lophophore and tentacles is similar in P. ovalis and bryozoans. These new results suggest the presence of two nerve centers and two nerve rings in the last common ancestor of phoronids and bryozoans. During evolution, bryozoans may have lost the outer nerve center and outer nerve ring, whereas phoronids may have lost the inner nerve center and inner nerve ring. These morphological results evidence the lophophorates are monophyletic.
Tentacular apparatuses are known in many different diploblastic and bilaterian animals. The lophophore is specific tentacular apparatus, in which tentacles surround the mouth but not the anus. Based on their possession of a lophophore, three phyla of invertebrates have been traditionally regarded as lophophorates: phoronids, brachiopods, and bryozoans (=ectoprocts)1,2,3,4. Although the monophyly of lophophorates has been supported by anatomical and embryological data1,2,3,4,5,6 and by some molecular phylogenetic data7,8, most molecular data are inconsistent with the unity of the lophophorates9,10. Accordingly to many molecular results, the lophophorates have been divided into two unrelated clades: Brachiozoa (Phoronida + Brachiopoda) and Bryozoa10,11,12.
At the same time, bryozoans have a lot in common with phoronids. Both groups have a similar bauplan: the dorsal side of adult animals is very short but the ventral side is very long; the digestive tract is U-shaped: mouth and anus are placed closely each other13. Phoronids are sessile benthic animals living in organic tubes, which are embedded in soft or hard substrata. The ventral portion of the phoronid body is embedded in the tube, while the lophophore and associated tentacles extend into the water. When in danger, the adult phoronid strongly contacts its longitudinal muscles, causing the body length to greatly decrease and the lophophore to be pulled into the tube. Some phoronids are known to reproduce asexually, which leads to the formation of a “colony”4. Most adult bryozoans are colonial animals. Each bryozoan individual (zooid) in a colony consists of two parts: a soft polypide with the lophophore and tentacles, and a cystid, which is the firm shelter for the internal organs. When in danger, the zooid pulls the polypide with the lophophore into the cystid.
Although the general morphology of the lophophore is similar among different lophophorates, it differs in detail between and within phyla3,14,15. The lophophore has two morphological schemes. In one scheme, which is characteristic of all brachiopods, new tentacles arise at the tip of each lophophore arm. In the second scheme, which is characteristic of both phoronids and bryozoans, new tentacles arise at two points located behind the mouth. The scheme of the lophophore organization is another feature that is similar between phoronids and bryozoans.
Phoronids have six main types of lophophore organization3,15. The oval lophophore is the simplest type, and Phoronis ovalis has an oval lophophore that bears about 20 tentacles. According to molecular data, P. ovalis is regarded as the sister taxon to the remaining Phoronida16 and the oval lophophore is supposed to be the ancestral type for all phoronids3. Among bryozoans, there are four main types of lophophore. The complex horseshoe-shaped lophophore bears more than 40 tentacles and is known in some recent phylactolaemates. The simplest lophophore is round and occurs in many bryozoans. The evolution of the lophophore within bryozoans has been discussed6,17.
Innervation of the lophophore and tentacles seems to differ among different lophophorates. At the same time, some lophophoral main nerves can be regarded as homologous in all lophophorates5,6,18. According to previous results5,6, all lophophorates have three main nerve centers: the dorsal (=cerebral) ganglion, the inner lophophoral nerve ring, and the outer lophophoral nerve ring. In brachiopods, there is tendency for the inner lophophoral nerve ring to be weakly developed. This tendency was recently described in two brachiopod species, which belong to two different classes, but have the same type of the lophophore19. Juvenile phoronids have an inner lophophoral nerve ring20,21, but adult phoronids do not22,23,24. Most species of bryozoans have only the inner lophophoral nerve ring; the outer lophophoral nerve ring has been described only in Amathia gracilis 6.
The investigation of lophophore innervation in additional specimens from each phylum of the lophophorates may help clarify the homology of the lophophore and may provide insight into the question of lophophorates monophyly. For these reasons, the study of lophophore innervation in adult phoronids could be very useful.
This report studies the nervous system of the lophophore and tentacles in adults of the minute phoronid Phoronis ovalis. As noted earlier, these results could help answer the question on homology of lophophores within the lophophorates and decide whether the lophophorates are monophyletic.
General morphology of Phoronis ovalis
Phoronis ovalis is a very small phoronid that burrows into the shells of bivalves. The lophophore and a portion of the body are exposed in the water (Fig. 1A). The oval-shaped lophophore bears 24 tentacles (Fig. 2A–C). The tentacles surround the mouth, which is partly covered at the dorsal side by the epistome. The epistome is a linguiform epidermal fold with a compact, thick tip (Fig. 2A) and a wide base (Fig. 2B–D). The integument of live animals is transparent and has many white spots (Fig. 1B,D). The coloured digestive tract is visible through the integument (Fig. 1B,D). The lophophore is separated from the body by a circular groove (Fig. 1B,C). The bilobed anal hill is located near this groove, on the anal side of the proximal portion of the anterior body (Fig. 1C). The anus opening is at the top of this hill (Fig. 2D). The body is worm-like and divided into several parts. The anterior part of the body is one-half of the body length; it is characterized by a thick epithelium and prominent bundles of longitudinal muscles (Figs 1E and 2D). In some specimens, the proximal portion of the anterior body part is swollen (Fig. 1D). A border is evident between the anterior and posterior parts of the body: the longitudinal muscles abruptly end at this border. The posterior part of the body is characterized by a thin integument and by a lack of prominent bundles of longitudinal muscles. The coelom of the posterior part of the body contains vasoperitonal tissue (Fig. 2E). The posterior part is not divided externally. However, the distal (terminal) portion of the posterior part has a prominent muscle grid. In some specimens, the posterior part of the body forms a bulb (Fig. 1D). This is a bud resulting from asexual reproduction. The digestive tract forms a branch that penetrates this bud.
Serotonin-like immunoreactive (5ht-lir) nerve elements of the lophophore
In P. ovalis, the 5ht-lir neurites and perikarya form a net around the anterior part of the body and around the lophophore base (Fig. 3A). The main nerve elements are located in the lophophore (Fig. 3B–D). The lophophore contains four main 5ht-lir nerve elements. The first element is the inner nerve centre (inner ganglion), which is located on the oral side of the epistome. At the epistome tip, the inner ganglion is represented by a large aggregation of perikarya and neurites, which form a horseshoe-like structure (Fig. 2A). At the epistome base, the shape of the inner ganglion changes: it looks like a long row of nerve cells, which are embedded in the epithelium of the epistome (Figs 2B,C and 4A). The second 5ht-lir main nerve element is the inner nerve ring (inner lophophoral nerve), which starts from the inner nerve centre and extends around the mouth, at the base of the frontal side of the tentacles (Figs 2D and 3C,D). The third 5ht-lir main nerve element is the dorsal ganglion (=dorsal nerve plexus). It is placed on the dorsal side of the body, in the lophophoral concavity, between the youngest tentacles and the anus (Fig. 2C,D).The aggregation of perikarya, which form the dorsal ganglion, is pyramidal with a small tip (Fig. 5A) and a wide base (Fig. 5B). The dorsal ganglion gives rise to the tentacle nerve ring (outer lophophoral nerve), which is the fourth 5ht-lir main nerve element. The tentacle nerve ring passes from the dorsal ganglion by two branches (Fig. 5A,B) and extends at the base of the lophophore along the abfrontal sides of tentacles. The inner ganglion and the dorsal ganglion connect (Fig. 5D), in some cases forming a compact X-like structure that gives rise to both inner and outer lophophoral nerves (Fig. 3E).
Ultrastructure of the main nerve elements
The ultrastructure of the inner ganglion and the inner nerve ring is similar. Both nerve elements are formed by perikarya and neurites, which are scattered in the epithelium of the epistome (Fig. 4A). Perikarya are located between basal projections of epithelial cells and form a thick basal layer under the bodies of the epithelial cells (Fig. 4B,C). Most perikarya are large cells with electron-lucent cytoplasm and a roundish nucleus that contains a nucleolus (Fig. 4D). The cytoplasm of perikarya contains synaptic vesicles, most of which are dense-core vesicles (Fig. 4D). Neurites form a thick basal layer between the extracellular matrix and the soma of perikarya. There are two main types of neurites. One type is characterized by electron-lucent cytoplasm and the presence of mostly dense-core vesicles. The second type has electron-dense cytoplasm and contains electron-lucent synaptic vesicles and synaptic vesicles with electron-dense middles (Fig. 4D).
The dorsal ganglion is an aggregation of large perikarya, whose ultrastructure differs at different levels of the dorsal ganglion. Thus, large perikarya with electron-lucent cytoplasm and large, round nuclei (one per perikaryon) and nucleoli (one per nucleus) form the tip of the dorsal ganglion. These perikarya are surrounded by long, thin projections of epithelial cells (Fig. 5C). In the middle and basal portions of the ganglion, small cells form a layer between the soma of epithelial cells and the soma of perikarya (Fig. 5B,F). These small cells (envelope cells) have electron-dense cytoplasm and small nuclei (one per cell) with electron-dense chromatin (Fig. 5F). The middle portion of the ganglion is formed by perikarya with dense cytoplasm that contains many electron-dense granules (yolk granules) that can be recognized in semi-thin sections (Fig. 5D) and in thin sections (Fig. 5F). The cytoplasm is filled with rough endoplasmic reticulum, multi-vesicular bodies, mitochondria, and synaptic vesicles of different sizes (Fig. 5F). In some perikarya, a basal body, an additional centriole, and a short striated root are evident (Fig. 5F). The basal portion of the dorsal ganglion has a similar organization as the middle portion but does not contain yolk granules. In the dorsal ganglion, most neurites have large diameter and electron-lucent cytoplasm.
The tentacle nerve ring is formed by two types of perikarya. The ultrastructure of the first type is similar to that of perikarya of the dorsal ganglion. The perikarya of the second type are small and have electron-dense cytoplasm and small, irregularly shaped nuclei (Fig. 5E). The perikarya of the second type form long, thin projections that form an aggregation that passes between neurites of large diameter (Fig. 5E).
Innervation of tentacles
Each tentacle has several anatomical zones: one frontal zone, which faces the mouth; two laterofrontal zones; and one abfrontal zone, which is opposite to frontal zone (Fig. 6A,B). The abfrontal zone is innervated by thin neurites that are grouped into 7–8 neurite bundles (Fig. 7A,C). Neurites of the abfrontal side extend from the perikarya of the tentacular nerve ring (Fig. 7E,H). There are inter-tentacular empty spaces between neurite bundles of adjacent tentacles (Fig. 7A). Among the abfrontal neurite bundles, the two most lateral groups of neurites exhibit serotonin-like immunoreactivity (Fig. 7E,I). According to transmission electron microscopy (TEM), each abfrontal neurite bundle consists of 4–11 neurites of small diameter and with electron-dense cytoplasm (Fig. 6G). Each laterofrontal zone is innervated by a thick neurite bundle, which extends from T-like inter-tentacular nerves. Two inter-tentacular nerves emanate from the inner nerve ring, extend between adjacent tentacles at their base, fuse with each other, and give rise to the two laterofrontal nerves, which penetrate into adjacent tentacles (Fig. 7B–D). Each laterofrontal nerve consists of about 20 thin neurites with electron-dense cytoplasm and one thick neurite with electron-light cytoplasm (Fig. 6H). The frontal zone is innervated by a thick, compact neurite bundle, which extends from the inner nerve ring (Fig. 6B). The frontal neurite bundle extends from the inner nerve ring by two or three thin projections (Fig. 7C,D,G).
Between the bases of adjacent tentacles, there are large, inner 5ht-lir perikarya (Fig. 7E,F,I). These perikarya are flask-shaped and associated with the inner nerve ring (Fig. 3D,E). The size of inner 5ht-lir perikarya is comparable with size of multipolar 5ht-lir perikarya, which are associated with the tentacular nerve ring (Fig. 7I). According to TEM, large cells between tentacles form outer and inner rows (Fig. 6C,E). Cells of the inner row can be regarded as neuronal because their cytoplasm contains synaptic vesicles (Fig. 6F). These cells are surrounded by numerous neurites of the inner nerve ring (Fig. 6F).
In each tentacle, there are several subperitoneal neurites, which extend between the basal matrix and peritoneal cells of the coelomic lining. Subperitoneal neurites are characterized by light cytoplasm and the presence of numerous longitudinal microtubules (Fig. 6D).
Morphology of the lophophore in phoronids
In adult phoronids, there are four main types and several transitional types of lophophore3,15. The type of lophophore usually depends on body size15,25. The simplest is the oval lophophore, which is typical for the very small Phoronis ovalis and for juveniles of some species. The horseshoe-shaped lophophore is the most common type and occurs in phoronids of intermediate size. The spiral lophophore is characteristic of large phoronids. The largest phoronid Phoronopsis californica has a helicoidal lophophore, which is the most complex type.
Nervous system of the lophophore and tentacles in adult phoronids
Nervous system of the lophophore in adult phoronids has seldom been studied by modern methods. The most detailed description of the anatomy of the lophophoral nervous system was made by histological techniques22,26. The ultrastructure of the main nerve elements and nervous tracts in tentacles has been studied in several phoronid species23,24,27,28. According to all of these reports, the lophophoral nervous system in adult phoronids includes a dorsal nerve plexus (=a dorsal ganglion?), a tentacular nerve ring, and nerve tracts in tentacles (Fig. 8). The dorsal ganglion is located between the mouth and anus, on the dorsal side of the epistome, which is an epidermal fold that covers the mouth. The dorsal ganglion consists mostly of large-diameter perikarya, which apparently are motor neurons24. The tentacular nerve ring passes along the outer side of the lophophore at the tentacle bases and repeats the shape of the lophophore. The tentacular nerve ring consists mostly of transversal neurites and small-diameter perikarya, which are apparently sensory23,24. Based on histology and TEM, the tentacles are innervated by two nerve tracts, which extend along the frontal and abfrontal sides24,28,29 (Fig. 8). These nerves are thought to extend from the tentacular nerve ring22,26. The frontal and abfrontal tentacular nerve tracts develop similarly in terms of the number of bundles and number of axons per bundle28. At the same time, several large-diameter neurites occur in the frontal nerve tract24. Specific laterofrontal sensory cells are associated with the frontal nerve tract23,27.
According to recent reports concerning juvenile phoronids20,21, innervation of the lophophore in juveniles differs from the traditional scheme described above for the lophophore in adults (Fig. 8). In addition to the dorsal ganglion and the tentacular nerve ring, the oval lophophore of Phoronopsis harmeri juveniles (whose adults have the spiral type of lophophore) is innervated by the minor (=inner) nerve ring, which extends along the inner side of the lophophore20. Compared to the tentacular nerve ring, the inner nerve ring of P. harmeri juveniles is weak, consists of several neurites, and is not associated with prominent perikarya. In P. harmeri juveniles, each tentacle is innervated by six nerve tracts: one frontal, two laterofrontal, two lateroabfrontal, and one abfrontal. The frontal nerve tract extends from the inner nerve ring; the laterofrontal nerve tracts seem to be unconnected with any nerves of the lophophore. Two lateroabfrontal nerve tracts extend from the inter-tentacular nerves, which originate from the tentacular nerve ring and extend between the tentacle bases. Inter-tentacular nerves, which the juvenile inherits from the larva, are very thin20. The abfrontal nerve tract extends from both the tentacular nerve ring and the inter-tentacular nerves20.
In Phoronis ovalis adults, the nervous system of the lophophore looks more similar to that of the juveniles than adults of other phoronid species (Table 1). This similarity results from the presence of the inner nerve ring and the innervations of tentacles in P. ovalis adults. As opposed to the inner nerve ring оf juvenile P. harmeri, the inner nerve ring in P. ovalis adults is very strong, consists of many neurites, and is associated with prominent 5ht-lir perikarya. The presence of an inner ganglion seems to be a unique feature of P. ovalis adults, i.e., it has not been previously described in any phoronid.
The current report provides the first detailed description of the innervation of tentacles in adult phoronids. The new morphological observations of P. ovalis adults are similar to our previous observations of juvenile phoronids (Table 1). The tentacles of some adult phoronids contain subperitoneal neurites (axons?)28,30. These neurites run between the peritoneal cells and the basement membrane. The subperitoneal neurites are large in diameter and have electron-lucent cytoplasm and thick, longitudinal microtubules. Fibres with a similar ultrastructure were found in the tentacles of P. ovalis adults in the current study.
Overall, the nervous system of the lophophore seems to have more elements or components in P. ovalis adults than in the adults of other phoronids. A complex (multicomponent) organization of the nervous system of the lоphophore was described in the articulate brachiopod Hemithiris psittacea 19 and was suggested to be the ancestral organization for all lophophorates.
Nervous system of the lophophore and tentacles in bryozoans
The lophophore nervous system and the innervation of tentacles in bryozoans from all taxa except the Stenolaemata has been described in many studies that used light microscopy, immunoсytochemistry combined with laser confocal microscopy, and TEM (e.g. refs17,31,32,33,34,35,36,37).
In the organization of the bryozoan nervous system, there are variations, which concern the structure of the cerebral ganglion, the innervation of tentacles, and the connections between tentaсular neurite bundles and the main nerve centers. The results were reviewed in recent papers that presented opinions about general patterns of the localization of the main nerve tracts in lophophores in all bryozoans34,36,37. All of these reports indicate that the bryozoan lophophore has a cerebral ganglion and an inner nerve ring (=circumoral nerve ring) (Fig. 8). According to recent results, ctenostome bryozoans have an outer nerve ring extending along the outer side of the lophophore6. In all bryozoans studied to date, there are large 5ht-lir perikarya associated with the circumoral nerve ring and located between tentacles at their bases. The number of perikarya is strictly established, and for each species is equivalent to the number of tentacles minus 2. These perikarya connect the circumoral nerve ring or the cerebral ganglion via prominent thick nerves. Large 5ht-lir perikarya appear to be sensory: they contact the surface of the epithelium and bear “serotonincilia”6,17. According to comparative analysis of data obtained from many species, the 5ht-lir perikarya do not form a circle and are arranged into oral and anal groups17. In most phylactolaemates, which usually have a large number of tentacles, there are many bipolar 5ht-lir perikarya scattered between the tentacles at their bases36.
Bryozoans have two to six longitudinal neurite bundles in each tentacle. Most phylactolaemates have six basiepidermal tentacular nerves: mediofrontal, medioabfrontal, one pair of lateroabfrontal, and one pair of laterofrontal36. Gymnolaemates usually have four tentacular nerves: one abfrontal, one mediofrontal, and one pair of laterofrontal35,38. Some ctenostome bryozoans have two tentacular nerves: the frontal, which originates as a result of the fusing of two laterofrontal and one frontal neurite bundles, and the abfrontal6. Accordingly to their origin, two main types of tentacular nerves can be established in bryozoans. The first type, which occurs in phylactolaemates, is characterized by the origin of all tentacular nerves from inter-tentacular (radial) nerves36. In the second type, which is common in gymnolaemates, some nerves originate from inter-tentacular nerves, and others originate directly from the circumoral nerve ring32,35,38. Many bryozoans have basiperitoneal tentacular nerves6,35,39, which do not show immunoreactivity against acetylated alpha tubulin and thereby cannot be regarded as nerve elements35.
Оrganization of the nervous system of the lophophore and tentacles in Phoronis ovalis and bryozoans
Because detailed data on early development are lacking, it is impossible to strictly establish the homology between some parts of the lophophore, including the nerve elements, in P. ovalis and bryozoans. For this reason, this report only suggests the possible homology between nerve elements of the lophophore in P. ovalis and bryozoans based on their location in respect to the same organs (mouth, tentacles, and epistome, if present) in both taxa.
As indicated in Table 1, many features of the organization of the lophophore nervous system seem similar in bryozoans and P. ovalis. The most prominent similarity is the presence of a conspicuous inner nerve ring (circumoral nerve) extending around the mouth and along the frontal side of the tentacles. This nerve ring is strongly developed in both bryozoans and P. ovalis. A second similarity is that the circumoral nerve ring in both bryozoans and P. ovalis is associated with 5ht-lir perikarya, which are located between tentacles at their bases (Fig. 8). The connection between the laterofrontal tentacular nerves and the innerve nerve ring is the third similarity between the lophophore nervous system in bryozoans and P. ovalis. A fourth similarity is that both bryozoans and P. ovalis have an outer lophophoral nerve extending along the abfrontal side of the tentacles; this nerve is represented by the tentacular nerve ring in P. ovalis and by the outer nerve in some ctenostome bryozoans.
Hypothetical scenario of evolution of bryozoans from a phoronid-like ancestor
That bryozoans and phoronids may be closely related has been indicated by many authors, who have suggested that bryozoans and phoronids are sister groups that originated from protophoronids or that bryozoans developed from phoronids1,13,40,41,42,43,44,45,46,47,48,49,50. The current data also suggest that both phoronids and bryozoans originated from protophoronids. This inference is inconsistent, however, with recent molecular phylogenetic data, which indicate that bryozoans are a separate clade on the phylogenetic tree of Bilateria and that phoronids form a clade (the Brachiozoa) with brachiopods9,51. According to the molecular data, phoronids and bryozoans are not relatives, and the lophophore has been evolved twice among bilaterians: in the Brachiozoa and in the Bryozoa. On the other hand, similarities in lophophore organization and in the general body plan are consistent with the inferences that phoronids and bryozoans are closely related and that the lophophorates is monophyletic5,6,18. As noted earlier, the molecular data are inconsistent with the morphological data. At the same time, the position of the Bryozoa on the phylogenetic tree of the Bilateria is still ambiguous and apparently depends on which molecular data are used in the analysis (for a review, see ref.52). Clarification of bryozoan phylogeny will require both new morphological data and new molecular data.
Because phoronids and bryozoans have a similar body plan, which seems to be unique for these two groups, it is logical to suspect that this plan was inherited by both groups from a common ancestor. Several previous papers have suggested that the body plan of phoronids probably evolved to enable the organism to escape from danger by digging into a soft substratum20,53. This change in body plan involved the formation of a large ventral protrusion, the shortening of the dorsal side, and the appearance of a U-shaped gut. This ancestor may have given rise to two evolutionary stems: the phoronids and bryozoans. According to this hypothetical scenario, the ancestor shared many features with recent P. ovalis adults: it was small and wrapped in a chitinous envelope, had asexual reproduction, and had a simple lophophore that was innervated by two ring nerves: the inner and the outer (Fig. 9).
In the phoronid stem (Fig. 9), the lophophore increased in complexity, the body and epistome became larger, the inner nerve center and the inner nerve ring were reduced, asexual reproduction was mostly lost, and a tube formed at the base of the chitinous envelope. According to this possibility, P. ovalis seems to be the most primitive phoronid, whose organization maintains many ancestral features. The basal position of P. ovalis among other phoronids is suggested by both morphology4 and molecular phylogeny16. On the other hand, P. ovalis may retain primitive features because of its neotenic origin, which is suggested by cladistic analysis of phoronid taxonomy54.
In the bryozoan stem (Fig. 9), the protophoronid ancestor underwent simplification of the lophophore, an extreme reduction in body size and a complete reduction of the epistome (which led to the fusion of the inner and outer nerve centers), a great reduction in the outer nerve ring, a great increase in asexual reproduction, and the formation of a cystid at the base of the chitinous envelope. According to this possibility, recent bryozoa species with a “soft” chitinous cystid and with a simple lophophore with 16–20 tentacles but without an epistome should be regarded as the most primitive. Ctenostome bryozoans best fit this description. In addition, ctenostome bryozoans retained the outer nerve ring, and their cerebral ganglion has zonality, which may have resulted from the fusion of several nerve centers6. According to some data, ctenostome bryozoans appeared first in the paleontological history of bryozoans. These were burrowing, non-skeletal colonial animals, whose traces are known from marine sediments beginning with the Early Ordovician55,56. Paleontological and morphological data support the basal position of the ctenostome among bryozoans. On the other hand, most phylogenetic data indicate the basal position of fresh water phylactolaemates among bryozoans10,12,57. At the same time, phylactolaemates have several apomorphic features: for example, their horseshoe-spade lophophore developed de novo due to appearance of inner rows of tentacles17. Like the new lophophore, the epistome of phylactolaemates may have developed de novo but may also have been inherited from a phoronid-like ancestor.
Materials and Methods
Sampling of animals and light microscopy
Specimens of Phoronis ovalis Wright, 1956 are embedded into shells of bivalve Pecten sp., which were collected in Onezhskiy Bay, White Sea in July 2016 by SCUBA diving at 3–10 m depth. Animals were extracted from the shells and photographed in the laboratory using a Leica M165C (Leica, Germany) stereomicroscope equipped with a Leica DFC420 digital camera.
Whole animals were fixed in a 4% paraformaldehyde solution in filtered sea water and washed in phosphate buffer (pH 7.4) (Fisher Scientific, Pittsburgh, PA, USA) with Triton X-100 (1%) (Fisher Scientific) (PBT) for a total of 24 h. Nonspecific binding sites were blocked with 12% normal donkey serum (Jackson ImmunoResearch, Newmarket, Suffolk, UK) in PBT overnight at 4 °C. The specimens were then transferred into primary antibody, which was a mixture of anti-α-Tubulin-mouse (1:600) and anti-serotonin-rabbit (1:1100) (ImmunoStar, Hudson, WI, USA) in PBT, and incubated for 24 h at 4 °C with rotation. Specimens were washed in PBT and were then exposed to the secondary antibody, which was 532-Alexa-Rabbit (1:1000) and 635-Alexa-Mouse (1:1000) (Invitrogen, Grand Island, NY, USA) in PBT, for 24 h at 4 °C. After washing in phosphate buffer specimens were embedded in Murray Clear. Specimens were viewed with a Nikon Eclipse Ti confocal microscope (Moscow State University, Moscow, Russia). Z-projections were done using Image J version 1.43 software. Three-dimensional reconstructions were produced in Amira version 5.2.2 software (Thermo Fisher Scientific, MA, USA). Z-projections and TEM micrographs were processed in Adobe Photoshop CS3(Adobe World Headquarters, San Jose, California, USA).
Transmission electron microscopy (TEM)
For TEM, the animals were fixed in 2.5% glutaraldehyde in phosphate buffer saline and were postfixed for 2 h in 1% osmium tetroxide in the same buffer saline. After the specimens were washed with the same buffer saline, they were transferred through an ethanol series and stored in 70% ethanol at 4 °C. Further preparation included dehydration in an ethanol series and acetone, and embedding in Spurr resin (Sigma). Semithin and thin sections were cut with a Leica UC-6 ultratome (Leica, Germany), then were stained with methylene blue, observed with a Zeiss Axioplan2 microscope, and photographed with an AxioCam HRm camera. Ultrathin sections were stained in uranyl acetate followed by lead nitrate and were examined with JEM-1011 JEOL and JEM-100 B-1 JEOL transmission electron microscopes (JEOL, Akishima, Japan).
Scanning electron microscopy (SEM)
Scanning electron microscopy (SEM) For SEM, the animals were fixed in 2.5% glutaraldehyde in phosphate buffer (PBS) Fixed animals had been washed in PBS and then dehydrated in ethanol followed by an acetone series were critical point dried and then sputter coated with platinum-palladium alloy.Specimens were examined with a CamScan S2 scanning electron microscope.
Data availability statement
The data sets analyzed during the this study are available from the author in response to requests
The field sampling did not involve endangered or protected species. The use of phoronids in the laboratory does not raise any ethical issues.
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Author is very grateful to Andrei Ostrovsky (Saint-Petersburg University, Russia), who is the greatest specialist in bryozoan's morphology and development and who is always eager to help with any questions of bryozoan’s biology. Author is also very grateful to Glafira Kolbasova and Alaxander Tzetlin (Moscow State University, Russia) who collected animals. This research was supported in part by several grants. The Russian Foundation for Basic Research provided support for the collection of material (#15-29-02601) and for the TEM studies (# 17-04-00586). The Russian Science Foundation provided support for the cytochemical investigations (#14-04-00262) and for the 3D reconstructions (#14-50-00029). The research was performed at the User Facilities Center of M.V. Lomonosov Moscow State University with financial support from the Ministry of Education and Science of the Russian Federation.