Radiolar Eyes of Serpulid Worms (Annelida, Serpulidae): Structures, Function, and Phototransduction.
The unusual radiolar eyes of fan worms are compelling subjects for improving our understanding of eye evolution, the emergence of new sensory systems and behaviors, and signal processing in distributed visual systems. We have previously examined the diversity of these eyes in the Sabellidae (Bok and Nilsson, 2016; Bok et al., 2016), and we now turn to the Serpulidae. Serpulids are sessile polychaetes that alongside the sabellids and fabriciids (which lack radiolar eyes) comprise the fan worms within the clade Sabellida. Serpulids live within self-secreted calcified tubes out of which they project an anterior radiolar (or branchial) crown up into the water column. This radiolar crown is bilobed and likely derived from prostomial tissue homologous to the palps of other polychaetes (Orrhage, 1980; Orrhage and Muller, 2005). Each lobe of the crown consists of a number of heavily ciliated radioles that filter food particles out of the water, passing them down to the mouth, and that contribute to respiration.
When startled, fan worms rapidly withdraw into their fortified tubes in order to safeguard their radioles from grazing predators (Rullier, 1948; Nicol, 1950). The withdrawal response is extremely rapid and can be initiated by mechanical (DeVantier et al., 1986; Pezner et al., 2017) or visual (Nicol, 1950; Smith, 1985) stimulation, which is communicated down the radiolar nerves to the brain and on to the segmental musculature via giant axons (Nicol, 1948). As an additional line of defense, and in contrast with sabellids, most serpulids modify a single radiole into a peduncle topped by an enlarged operculum, a plug with a chitinous or calcareous endplate, that stoppers the tube opening when withdrawn.
There are currently 73 recognized genera of serpulids comprising over 500 species (ten Hove and Kupriyanova, 2009; WoRMS, 2017). However, despite numerous efforts at resolving the phylogeny of the family, serpulid taxonomy is still quite confusing (Kupriyanova et al., 2006; Kupriyanova and Rouse, 2008; Kupriyanova and Nishi, 2010; Prentiss et al., 2014). Some examples of practical difficulties are given in Ben-Eliahu and ten Hove (2011; notably for Protula, Salmacina, Serpula, Spirobranchus tetraceros (Schmarda, 1861), and Vermiliopsis). Although most (sub)clades of the serpulids seem reasonably well supported and constant in mentioned papers, the affiliation of the nominal subfamily Spirorbinae and that of Salmacina/Filograna in Lehrke et al. (2007) and Kupriyanova and Rouse (2008) is distinctly different from that in Prentiss et al. (2014), admittedly based on not entirely comparable data sets. Remarkably, the former family "Sabellidae" was found to be paraphyletic, necessitating the elevation of the sabellid subfamily Fabriciinae to full family rank (Kupriyanova and Rouse, 2008; Capa et al., 2011). The three families, however, are well defined as a clade versus the outgroup genera.
Photoreceptors and eyes in serpulids
For the purposes of this report, we define ocelli and eyes as follows (after Bok et al., 2016). Photoreceptors are the fundamental light-sensitive component of a visual system. When used in visual tasks beyond slow-integrating radiance detection, these sensory cells are identifiable by extensive membranous elaborations packed with light-transducing visual pigments that increase sensitivity. When photoreceptors produce, or are coupled with, directionality-conferring screening pigments, we term the resulting structure an ocellus, the simplest configuration of an "eye." From here, evolutionary processes can add optical units to improve light capture. Furthermore, multiple ocelli can be grouped together into a compound eye, or, alternatively, multiple photoreceptors can be pooled behind a shared aperture or lens, producing a simple eye. Both of these strategies can be elaborated to accommodate higher-order visual tasks based upon image-forming vision (for reviews see Nilsson, 2009, 2013).
Polychaetes have a surprising abundance of photoreceptors, ocelli, or eyes distributed across their bodies (Purschke, 2005; Purschke et al., 2006). In general, these can be broadly grouped into four categories: cerebral, segmental, pygidial, and radiolar. Cerebral ocelli are defined here as being located in close association with the brain, within the peristomium or prostomium (excluding the radioles). They are present through development (Smith, 1984a, 1985), lost or reduced in many sedentary species, and elaborated into image-forming simple eyes in errant species such as Platynereis dumerilii (Audouin & Milne Edwards, 1834) (see Fischer, 1963) and most spectacularly in the alciopids (Wald and Rayport, 1977). Unlike sabellid fan worms, which often have well-developed segmental and pygidial ocelli (Ermak and Eakin, 1976; Dragesco-Kerneis, 1980), serpulid fan worms appear to be largely devoid of superficially obvious ocelli or eyes posterior to the collar. Notable exceptions include the genus Placostegus, which possibly has a belt of thoracic eyespots (ten Hove and Kupriyanova, 2009), and Spirobranchus nigranucha, which may have segmental eyespots on the abdomen (Smith, 1985, as Spirobranchus sp. D). Otherwise, adult serpulids typically have only simple clusters of cerebral ocelli at the base of the prostomium, closely associated with the brain. These cerebral ocelli are typically buried under obfuscating epithelial tissue and, furthermore, are often positioned below the rim of the animal's tube (Fig. 1A; Smith, 1985). Therefore, in order to avoid predation, many serpulids instead rely on radiolar eyes located on their feeding tentacles or the operculum. The radiolar eyes of fan worms were first noted in early taxonomic and anatomical works by Grube (1878), Andrews (1891), and Hesse (1899). In the 20th century, the radiolar eyes of serpulids have been mostly ignored in part due to a perceived lack of utility as a taxonomic character, especially in preserved material (Ben-Eliahu and ten Hove, 2011). However, some effort has been made to record observations regarding their presence and nature in fresh tissue (Smith, 1985; Table S1, available online).
Like sabellids (Lawrence and Krasne, 1965; Ermak and Eakin, 1976), the cerebral ocellar photoreceptors of serpulids are rhabdomeric in nature, with the elaborated photoreceptive membranes being formed from microvilli that project into a pigment cup (Figs. 1B, A1; Smith, 1984b). In contrast, the radiolar ocellar photoreceptors are ciliary, with the photoreceptive membrane being produced by stacked lamellae emerging from cilia (Fig. 1C; Smith, 1985). The radiolar ocelli are derived from epithelial cells in the outer aboral corners of the radioles (Fig. 1D), projecting their basal processes to the radiolar nerve and onto the branchial lobe of the brain.
Here we attempt to categorize the known diversity of radiolar ocelli in the Serpulidae as reported in previous anatomical and taxonomic investigations. We describe and compare new data on the fine structure of these ocelli from six serpulid species as revealed by transmission electron microscopy (TEM). Additionally, we report on phototransduction cascade components recovered from transcriptomic sequencing of the radiolar eyes of the Christmas tree worm Spirobranchus corniculatus (Grube, 1862). Finally, we report on the spectral absorbance properties of the S. corniculatus photoreceptors, as revealed by microspectrophotometry (MSP). We discuss the evolutionary and functional implications of these results among serpulids, in contrast with sabellids, and in the grander context of the evolution of visual systems.
Materials and Methods
Serpulids displayed in this study were captured live at field stations: Carrie Bow Cay Field Station, Belize (administered by the Smithsonian Institution), September 2014 (Pomatostegus stellatus); Lizard Island Research Station, Queensland, Australia (administered by the Australian Museum, permit nos. SR-14-2004, SR-14-2003, SR-14-2005, SR-23-2009), March 2014 (Spirobranchus corniculatus); Estacion de Investigacion Costera (administered by the Mediterranean Institute for Advanced Studies [IMEDEA], collection permit from the Government of the Balearic Islands Ministry of Environment, Agriculture, and Fisheries), Mallorca, Spain, February 2016 (Vermiliopsis sp., Serpula sp., Protula sp.; shown in Fig. 2B-E). Additional materials were examined in the field by Harry ten Hove (see Table S1, available online, for details). Spirobranchus individuals for MSP were purchased at the live-fish store House of Tropicals in Baltimore, Maryland. The Protula sp. (Fig. 2A) was purchased from the live-fish store Bioted Marine in Kungsbacka, Sweden. All species used in electron microscopy besides Pomatostegus stellatus were wild captured by Richard Smith at a number of sites in temperate and tropical waters along the east coast of Australia. See Smith (1985) for complete details.
Photographs of live animals displayed in Figure 2 were taken with a Canon T2i DSLR and a Canon EF 100mm f/2.8L Macro IS USM lens (Canon, Melville, NY). Raw photos were post processed for brightness, contrast, and color balance using Adobe Lightroom 5 photo editing software (Adobe Systems, San Jose, CA). Light photomicroscopy on fixed material was carried out using a Nikon (SMZ25; Minato, Tokyo, Japan) stereomicroscope with the SHR Plan Apo 2x objective. Images were captured using NIS-Elements software (Nikon). Fresh material was usually photographed on compound microscopes using 20x objectives with illumination from above both sides of the samples at roughly 45[degrees]. Images were captured using a Canon T2i DSLR with a microscope ocular adaptor lens. Focal series were captured through the depth of the radiole, and they assembled into a focus-stacked image using Zerene Stacker software (Zerene Systems, Richland, WA).
Transmission electron microscopy
For P. stellatus, tissue was fixed in the field in 2% paraformaldehyde (PFA), 2.5% glutaraldehyde, 2% sucrose in 0.1 mol [l.sup.-1] Sorensen's phosphate buffer, pH 7.2, for 1 h at room temperature or overnight a 4 [degrees]C and was then stored in 0.1 mol [l.sup.-1] Sorensen's phosphate buffer for transport to the lab. Individual radioles were washed in phosphate buffer (0.1 mol [l.sup.-1]) followed by 1% osmium tetroxide in phosphate buffer for 1 h at 4 [degrees]C. Samples were washed in phosphate buffer, dehydrated on an ethanol series, infiltrated with acetone and Epon plastic (Electron Microscopy Sciences, Hatfield, PA), and embedded in Epon. Ultra-thin TEM sections (50-70 nm) were produced using a Leica (Wetzlar, Germany) Ultracut with a diamond knife and stained with 2% uranyl acetate and lead citrate (Reynolds, 1963). Sections were viewed on a JEM-1230 TEM (JEOL, Glen Ellyn, IL).
For all other species presented, refer to Smith (1985) for extensive detail. In brief, tissue was fixed in 1% osmium tetroxide in 0.1 mol [l.sup.-1] sodium cacodylate buffer at pH 7.2-7.4 for 0.5-2 h at 4 [degrees]C or ambient temperature, followed by rinsing in the same buffer. The tissue was dehydrated on an ethanol series and infiltrated and embedded in Spurr resin. Sections were cut (90-30 nm) with a diamond knife (GeFeRi, Frosinone, Italy) and collected on copper grids. Sections were stained with uranyl acetate in acidified 50% ethanol followed by Reynold's modified lead citrate. Thin sections were visualized on Philips 300, Siemens Elmiskop 102, and Philips 400 electron microscopes operating at 60, 80, and 100 kV, respectively (Philips, Amsterdam; Siemens, Munich).
Visual pigment difference spectra were obtained from 14-[micro]m transverse cryosections of Spirobranchus corniculatus radiolar eyes based on methods described previously (Cronin, 1985; Cronin and Marshall, 1989; Bok et al., 2014). The animals were dark adapted for 48 h, and the eyes were dissected and sectioned under dim red illumination. The sections were mounted between coverslips in crustacean Ringer's solution (Cavanaugh, 1956). Photobleaching was performed with maximum transmitted illumination from the tungsten source between 3 and 7 min. Pre- and post-bleach absorbance measurements were subtracted in order to obtain the difference spectra, which were fitted using the A1 visual pigment template described in Stavenga et al. (1993). Absorbance of the photostable orange screening pigment was also measured.
Total RNA was extracted from the pooled radiolar eyes of six S. corniculatus individuals collected at Lizard Island Research Station using the Nucleospin RNA XS kit (Machery-Nagel, Diiren, Germany) and quantified using a Qubit Fluorometer (ThermoFisher Scientific, Waltham, MA). Library construction and MiSeq (Illumina, San Diego, CA) sequencing of 300-bp paired-end reads was done by Molecular Research LP (Shallowater, TX), resulting in 10 million reads accessioned as BioSample SAMN0754970 in National Center for Biotechnology Information (NCBI) Bioproject PRJNA399760. Raw reads were quality checked and de novo assembled using the DNAStar software (Madison, WI) package. The resulting data set included 4.73 million reads, assembled into 8668 contigs with an average coverage of 9x and an N50 of 1540 bp. Phototransduction genes in the assembly were identified using phylogenetically informed annotation (PIA) by identifying query contigs phylogenetically placed close to landmark sequences with known functions; query contigs with long branches were not included (Speiser et al., 2014). The identities of putative phototransduction-related transcripts identified from PIA were confirmed using reciprocal BLAST searches. Expression levels were calculated as fragments per kilobase million (FPKM) using read mapping in BowTie2, version 2.2.3 (Langmead and Salzberg, 2012), run on the National Center for Genome Analysis Support (NCGAS) Mason Linux Server (Indiana University, Bloomington, FN). Opsin sequences identified from PIA were assessed in Geneious, version 10 (Kearse et al., 2012), for length, fragment overlap, and sequence similarity. The curated opsin sequences were added to the opsin amino acid alignment from Bok et al. (2017) using MAFFT (Katoh and Standley, 2014), and a new phylogeny was reconstructed using RAxML, version 8 (Stamatakis, 2006), as implemented on the CIPRES portal (Miller et al., 2010). PIA-identified S. corniculatus sequences are available on GenBank (Table Al).
Radiolar eye types and arrangements
Here we report on the known diversity of radiolar eyes of serpulids as described in previous studies as well as from newly reported field observations. We have attempted to categorize serpulid radiolar eyes along similar lines to sabellids after Bok et al. (2016). In that review, we created the following categories of radiolar eyes: type S (simple ocelli), type CP (compound-paired), type CS (compound-single), and type CI (compound-inside) (Fig. 1E). Serpulids have no known analogs to type CI eyes, which in sabellids are located on the inside of the distal tips of the radioles in the genera Acromegalomma and Stylomma. However, we have created two new categories for radiolar eyes located on the operculum of serpulids: type oS (opercular-simple) and type oC (opercular-compound) (Fig. 1F). Table 1 details the types of radiolar eye arrangements found in each genus of the Serpulidae. Refer to Table S1, available online, for radiolar eye details at the species level. Usually, each species of serpulid has only a single radiolar eye arrangement type. However, in some species there is a gradient of type CP eyes diminishing distally along the radiole into type S eyes.
It should be noted that in Bok et al. (2016), we concluded that despite being derived from similar ciliary photoreceptor cells, sabellid radiolar eyes likely arose independently more than once in the family and possibly resulted from unique elaborations in essentially every genus that expresses radiolar eyes. Therefore, the radiolar eye arrangements in serpulids likely share no direct homology to those in sabellids, and the shared categorizations presented here are used out of convenience rather than to imply any evolutionary connection beyond convergence driven by similar anatomical features, developmental loci, or visually guided tasks. The similarities and differences between radiolar eyes in sabellids and serpulids will be addressed further in the "Discussion." Finally, many serpulids do not appear to possess superficially obvious radiolar eyes, but without exhaustive TEM surveys it is difficult to rule out the presence of unpigmented eyes in fresh tissue or in preserved tissue that has lost pigmentation. Indeed, it could be that unpigmented radiolar photoreceptors are widespread in fan worms.
Type S radiolar eyes are composed of single simple ocelli scattered irregularly or in pairs along both aboral corners of the radioles. Type S eyes are perhaps the most pervasive and are found in the genera Crucigera, Metavermilia, Microprotula, Pomatostegus, Protula, Spirobranchus, and Vermiliopsis. These ocelli can be very diffusely scattered on the radioles (Fig. 2A, S) or packed into dense but irregular rows along the radiolar corners (Fig. 2B, C).
Type CP radiolar eyes are paired compound eyes composed of numerous ocelli. These eyes are found distributed along the radioles as seen in some species of Protula (Fig. 2E) or at the base of each radiole as in some Serpula (Fig. 2D). These ocellar aggregations typically have fewer than a dozen facets. In Serpula jukesi (Baird, 1865) several ocelli are uniquely consolidated behind a single lens, creating a rudimentary simple eye (Fig. 3A).
Type CS radiolar eyes are single compound eyes on one aboral corner at the base of the two dorsalmost radioles. They are found exclusively in all species of Christmas tree worms (the Spirobranchus corniculatus and Spirobranchus giganteus species complexes) (Fig. 2F-N) and are composed of up to 1000 facets, by far the most numerous among serpulid radiolar eyes (Fig. 2J). In adults, these sophisticated eyes are partially shielded from many viewing angles by the twin spires of the well-developed radiolar crown that gives this group their name (Fig. 2G, H). However, when the crown is fully extended in feeding position, the eyes maintain a broad view primarily outward and upward along the dorsalmost surface of the worm's substrate. Also, when emerging from their tube, before fully extending the radiolar crown, Spirobranchus does expose its eyes to some degree (Fig. 2I). Additionally, in Spirobranchus juveniles or early adults, when the radioles are less pigmented and the spires are less developed, the eyes are much more exposed during normal crown extension (Fig. 20).
Type oS eyes are single simple ocelli scattered on the brim of the operculum and are found in some Pomatostegus (Fig. 2P-R) and Spirobranchus (Fig. 2T). In Pomatostegus stellatus (Abildgaard, 1789), the opercular ocelli appear very similar to those found scattered on the radioles (Fig. 2R, S).
Type oC eyes are compound eyes formed from numerous ocelli located on the operculum and are found in Pseudovermilia and Pyrgopolon (multiple compound eyes with 20-30 ocelli; Fig. 2U).
The structure of serpulid radiolar ocelli
Compared to sabellids, TEM studies on the ultrastructure of serpulid radiolar ocelli are much more limited in the literature (sabellid studies reviewed in Bok et al., 2016). However, the dissertation work of Smith (1985) contains previously unpublished ultrastructural descriptions of radiolar ocelli structures in five serpulid species: Spirobranchus corniculatus (as Spirobranchus giganteus (Pallas 1766); also in Smith, 1984b), Spirobranchus tetraceros, Protula sp. (as Protula tubularia (Montagu, 1803); for a discussion see Ben-Eliahu and ten Hove, 2011), Serpula jukesi, and Protula anomala (Day, 1955). Here we will describe these ocellar structures in detail for the first time and additionally present new TEM observations from Pomatostegus stellatus. Diagrammatic representations of radiolar ocelli from each of these species can be found in Figure 3A. Common features include a ciliary sensory cell invested by supporting cells that offer structural integrity to the ocellus and/or contain screening pigment granules. The supporting cells typically have apical microvilli that contribute to the cuticle and excrete lenses for the ocellus while leaving a small pore in the optical path of the sensory cell. Each sensory cell has a distal sensory segment and proximal soma that contains the nucleus, the majority of mitochondria, and other organelles. Neuronal processes extend from the base of the sensory cell soma to the radiolar nerve and presumably on to the brain. For our description of ocellar fine structures, we will focus on the major details related to the optical elements, pigment cups, and sensory cells. Readers are encouraged to refer to Smith (1985) for greater detail regarding cellular ultrastructure.
Spirobrcmchus corniculatus has by far the most sophisticated and best examined radiolar eyes among the serpulids. Their type CS eyes contain as many as 1000 facets. Each of these facets overlays a discrete ocellus unit averaging 100 [micro]m in length and constituted by a central sensory cell surrounded by usually five pigment cells (Fig. 3A). The pigment cells encapsulate the distal tip of the sensory cell, leaving only a small aperture connecting the sensory cell to the cuticle. The pigment cells project microvilli apically, excreting a cuticular lens. The distal half of the sensory cell produces a sensory cavity formed by a long tubelike invagination of its apical membrane. The distal half of the sensory cavity is filled with a matrix of microvilli from the sensory cell, resembling a rhabdom (Fig. 3B). The microvilli are well organized and are surrounded in the extracellular space by numerous perpendicularly aligned and presumably secreted membranous rodlets (Fig. 3C, D). The center of the rhabdom also produces a vertically extending filamentous column that passes through the aperture to the cuticular lens (Fig. 3B). About halfway down the sensory cavity the microvilli give way to densely folded, flattened lamellar stacks emerging from sensory cilia around the walls of the sensory cavity (Fig. 3E-G). The lamellar stacks continue nearly to the end of the sensory cavity, which terminates at the soma.
Pomatostegus stellatus has scattered simple ocelli appearing on the radioles (type S) as well as on the opercular brim (type oS). These ocelli appear similar in the two areas but vary among themselves slightly in size and pigmentation (Fig. 2R). The general ultrastructure of the ocelli on the radioles and operculum is indistinguishable. Each ocellus is formed by a single sensory cell and up to two or four surrounding pigmented supporting cells (Fig. 3A, H). The pigment cells contribute microvilli into the optical path, secreting a granular, conical lens that lies well below the cuticle surface, which is produced by surrounding epithelia cells. There is no cuticular lens, and the cuticle surface overlying the ocelli is flush. The pigment cells are arranged in a nested, tiered configuration, with the innermost pigment cell encapsulating the sensory cavity and contributing to the proximal segment of the lens (Fig. 3H). Additional pigment cells contribute to more distal stretches of the lens, and their pigment granules become decreasingly electron dense (Fig. 31). Thus, the number of pigment cells encapsulating each ocellus may explain the differences in size and coloration. The sensory cell is unusual compared to other serpulids. The soma is located outside of the pigment sheath, through which it projects a narrow cytoplasmic channel that expands into a sensory chamber filled with whorled lamellae produced by sensory cilia (Fig. 3H, J).
Spirobrcmchus tetraceros radiolar ocelli are an example of perhaps the most rudimentary design. They occur in diffuse rows of around 10 ocelli in a type S configuration, with the greatest number of ocelli located on the dorsalmost radioles. An ocellus consists of a single sensory cell surrounded by a number of supporting cells with variable pigmentation (Fig. 3A). The apical microvilli from the supporting cells produce the cuticle as well as a cuticular lens that is flush externally and convex on its inner surface. An unpigmented supporting cell encircles the apex of the sensory cell. The sensory cell has a distal sensory segment and a proximal soma. The sensory segment is formed by an apical invagination around 12 [micro]m in depth and filled with whorled lamellae produced by sensory cilia on the sides of the cavity. In the distalmost segment of this sensory cavity the lamellae give way to a small array of microvilli. It should be noted that S. tetraceros is presently regarded to be a complex of species, and Smith (1985) reported possible specific variation in ocelli distribution, including absence of ocelli in some individuals.
Members of Protula have rows of type S diffuse single radiolar ocelli on both sides of the radioles. In addition to pigmented ocelli, Protula also has unpigmented photoreceptors that are not superficially visible and were discovered by chance during TEM investigations of the pigmented ocelli (Fig. 3A). The pigmented ocelli are composed of a sensory cell whose distal sensory cavity is surrounded by a pair of pigmented supporting cells. Uniquely in this species, the apical microvilli of the supporting cells do not produce a cuticular lens. Rather, the distal half of the sensory cell cavity contains microvilli that secrete a lens into the cavity (Fig. 3M). Below the lens, whorled and folded lamellae contributed by sensory cilia fill the sensory cavity. The Protula unpigmented photoreceptors are generally comparable to Spirobranchus tetraceros but lack pigmented supporting cells and a cuticular lens. Like S. tetraceros, the unpigmented ocellus sensory cavity is filled with whorled lamellae and a small microvillar matrix at the distal pore encircling a filamentous mass (Fig. 3K). Similar pigmented radiolar ocelli were also found in P. anomala (see Smith, 1985).
Serpulajukesi has radiolar eyes unlike any other described serpulid. Instead of having scattered single ocelli or grouping ocelli together into a compound eye, S. jukesi has radiolar eyes with four to six sensory cells and their supporting cells placed behind a single shared lens in a continuous pigment cup (Fig. 3A, L). These simple eyes occur in a pair near the base of each radiole. The lens is produced by microvillar projections from the supporting cells alone and is flush with the cuticular surface and convex internally along the margin of the pigment cup. The cluster of sensory cells lies below the lens at the bottom of the pigment cup. Each sensory cell is ensheathed by three mostly unpigmented supporting cells that also contribute to producing the lens. The sensory cells themselves are divided into a proximal soma and a larger distal sensory segment. The sensory cavity is 16 [micro]m in depth and filled with stacked and whorled lamellae contributed from sensory cilia on all sides of the cavity.
Spirobranchus corniculatus visual pigment absorbance spectra
We used MSP to measure the spectral absorbance of photoreceptors in the S. corniculatus type CS compound eye. We obtained clean post-bleach photoconversions for seven photoreceptors. The raw pre- and post-bleach difference spectra were averaged and fitted with a visual pigment template curve based on the equations of Stavenga et al. (1993). This had a wavelength of maximum absorbance ([[lambda].sub.max]) of 464 nm (Fig. 4A). The [[lambda].sub.max] range of template fits for individual scans was between 450.2 and 472.3 nm, so there is the possibility for the existence of multiple visual pigments (Fig. A2). However, it should be noted that the best fits with the strongest photoconversions all had [[lambda].sub.max] above 460 nm, making 450.2 nm a slight outlier.
This visual pigment, with [[lambda].sub.max] = 464 nm, is well suited for operating in the shallow marine habitats of S. corniculatus (Fig. 4B, thin gray lines representing idealized down-welling irradiance spectra at increasing depths). We also obtained MSP transmission spectra for the orange pigment in the S. corniculatus pigment cells (Fig. 4B, thin black line), which blocks most light below 550 nm and efficiently acts as a screening pigment for the blue-green-absorbing visual pigment in the marine habitat. We also observed that we were able to record photoconversions only from the proximal, presumably lamellar, region of the photoreceptor. We did not obtain photoconversions in the more distal segment of the photoreceptor sensory cavity that contains microvilli (see Fig. 2A-D) despite bleaching periods of up to 7 min.
Transcriptomic sequencing of Spirobranchus corniculatus radiolar eye
We used transcriptomic sequencing to identify proteins putatively involved in the phototransduction cascade in the radiolar eyes of S. corniculatus. Metazoan visual systems detect light using membrane-embedded visual pigments formed by the coupling of opsin G-protein-coupled receptors and light-sensitive chromophores. Transduction occurs when a photon is absorbed by the chromophore, causing a conformational change in the visual pigment, activating a G protein and thus propagating a cellular signal along a cascade of downstream enzymes, channel proteins, and signaling molecules.
We recovered three opsin contigs from the transcriptome of six S. corniculatus radiolar eyes. One of the sequences, S. corniculatus opsin 1, was a full-length transcript (375 amino acids). The remaining 2 contigs were fragments of the last 140 and 122 amino acids of the C-tail, respectively. Additionally, the smallest recovered contig was identical in amino acid sequence to the longer C-tail fragment. Therefore, we treated these two fragments as a single opsin transcript, S. corniculatus opsin 2 (Fig. 5; Table A1). Phylogenetically, opsin proteins generally fall into four major clades: [G.sub.q]-opsins, tetraopsins, c-opsins, and xenopsins (Porter et al., 2012; Ramirez et al., 2016). The two S. comiculatus opsin sequences are very similar (96.4% amino acid identity), falling out with a cluster of poorly understood opsins at the base of the c-opsin clade, which we have termed invertebrate c (InvC)-opsins. In this opsin phylogeny InvC sequences form a monophyletic clade, but it is poorly supported; and in some cases this group is recovered as a number of basally branching paraphyletic clades separated by taxa: panarthropods, echinoderms, and annelids (Bok et al., 2017). Previous transcriptomic sequencing efforts have shown that the sabellid Acromegalomma interruptum (Capa & Murray, 2009) expresses a similar InvC-opsin in its radiolar eyes (Bok et al., 2017; as Megalomma interrupta).
Figure 5B also indicates the amino acid residue present at bovine rhodopsin position 94 for each InvC-opsin. This residue has been implicated in ultraviolet spectral tuning in Platynereis dumerilii InvC-opsin 2 (Tsukamoto et al., 2017). A lysine (K) at this position shifts the visual pigment's maximum absorbance into the ultraviolet range. Spirobranchus comiculatus InvC-opsin 1 has a serine (S) residue at this position. We did not recover this sequence region from S. corniculatus InvC-opsin 2.
We also recovered a number of transcripts related to phototransduction cascade components. Notably, we recovered three G-protein alpha subunits: [G[alpha].sub.o], [G[alpha].sub.i], and [G[alpha].sub.s] (Table A1). Additionally, we recovered transcripts homologous to the G-protein beta subunit, the G-protein gamma subunit (gngt1), protein kinase C (PKC), cyclic nucleotide gated-channel alpha 1 (cnga1), regulator of G-protein-signaling 9 (RGS9), retinal degeneration B (rdgB), arrestin (arr), guanylyl cyclase (GC), and cyclic nucleotide phosphodiesterase (PDE6abc)--all of which are implicated with phototransduction in ciliary-type photoreceptor cell systems (Fain et al., 2010). Furthermore, our sequencing identified a number of transcription factors implicated in eye development (Pax6, eya, six4, so, glass, dpp), as well as two cryptochrome (cry) transcripts, which code for light-sensitive proteins usually involved in the entrainment of circadian rhythms.
Structural comparison of serpulid ocelli
Serpulid photoreceptor sensory cells appear similar across the family, suggesting a conserved origin. The photoreceptor cells always display a distal sensory segment containing the lamellae-packed sensory cavity and proximal soma. The soma is typically continuous with the sensory segment, except in Pomatostegus stellatus, where a narrow channel between enveloping pigment cells connects the sensory segment and soma (Fig. 3H). The cilia-derived lamellae in the sensory cavity are identical in structure and appearance across the family, but their packing varies between stacked, folded, and whorled configurations. Furthermore, there are a great deal of additional ultrastructural similarities among serpulid photoreceptors, discussed in detail in Smith (1985). It is likely that all serpulid branchial photoreceptors share a common origin from an epidermal ciliated sensory cell, not unlike the chemo- or mechanosensory cells found throughout the length of the radioles, also in the aboral corners (Smith, 1985). At some point one such cilium may have gained opsin photopigment expression and light sensitivity, followed by invagination of the apical surface into a sensory cavity where increasingly folded whorls of ciliary lamellae could be stacked, producing a rudimentary ocellus akin to the Protula unpigmented ocellus.
Beyond the sensory cell, however, the serpulid ocelli vary greatly, suggesting that despite apparently starting with similar radiolar photoreceptor cells, ocelli arose and elaborated more than once in the family. In general, serpulid receptors are roughly analogous to ommatidia in arthropod apposition compound eyes, with a single lens element passing light into a single sensory cavity, fully shielded by screening pigment in the supporting cells. Beyond that, the structure of radiolar ocelli vary greatly among serpulid species. The number of supporting pigment cells forming the screening pigment cup can be as many as six in Spirobranchus corniculatus to none in the Protula unpigmented receptor. Likewise, the nature and origin of the lens are inconsistent among species surveyed--though it is thought to typically be composed of glycogen orcuticular materials. In S. corniculatus, Pomatostegus stellatus, Spirobranchus tetraceros, and Serpula jukesi the lens is likely produced by excretion from microvilli on the supporting pigment cells. Among these, S. corniculatus, S. tetraceros, and S. jukesi produce a cuticular lens above the ocellus while P. stellatus creates a recessed conical lens, below the flat cuticular surface and enveloped by the pigment cup of the ocellus. The Protula pigmented ocellus also has a recessed conical lens of this nature; however, it is apparently excreted by microvilli emerging from the distal segment of the sensory cell, instead of the supporting cells.
There has been some discussion regarding the rhabdom-like microvillar region in the distal half of the Spirobranchus corniculatus sensory cavity (Fig. 3B-D). Smith (1984b, 1985) suggested that these microvilli could serve some photoreceptive function in tandem with the more distal ciliary lamellar stacks. A popular notion in current vision research is that some photoreceptors may contain multiple simultaneous phototransduction cascades, perhaps locally regulating sensitivity adaptation or performing simple chromatic comparisons (Su et at, 2006; Vocking, 2016). The rhabdomeric and ciliary membrane elaborations of the S. corniculatus sensory cavity make such a system a very attractive possibility in this case. However, we find it highly unlikely that this microvillar region serves a photoreceptive purpose for several reasons. (1) We were unable to obtain MSP photoconversions when scanning more distal regions of the sensory cavities. (2) Transcriptomic sequencing from these eyes yielded only InvC-opsins and ciliary phototransduction cascade components (Fig. 5). Rhabdomeric photoreceptors are known to achieve photoreception only via [G.sub.q]-opsins and a specialized microvillar phototransduction cascade (Fain et al., 2010), no components of which were identified by our sequencing efforts. (3) The rhabdom is not as densely packed with microvilli as we would expect from an optimized photoreceptor, as in the cerebral ocelli, for instance (Fig. A1). Much space is instead reserved for the unusual rodlets that encircle the microvilli (Fig. 3C, D).
We instead propose that the rhabdomeric region of the S. corniculatus ocellus may act in some optical role. The regularity of the microvilli and their rodlets, as well as the filament column, may serve as some sort of light guide. Alternatively, the microvillar region may function as a spacer along with the pigment cup to restrict the light acceptance angle of the lamellar stacks farther down in the sensory cavity. Such a spacer would then open adaptive space where a lens could be added, as we see with the Protula pigmented ocellus (Fig. 3M). Some microvillar elaboration is found on the distalmost segment of the sensory cavity in most serpulid photoreceptors cells, besides Pomatostegus stellatus, where this was not observed. In Spirobranchus tetraceros and the unpigmented Protula ocelli, this microvillar region is diminutive but regardless appears to partially contribute to an excreted filament and perhaps some granular glycogenic material, continuous with the overlaying cuticular lens produced by the supporting cells. (Fig. 3K). The S. corniculatus rhabdom appears to be homologous to, yet highly elaborated from, these small microvillar arrays.
Function of serpulid radiolar eyes
What can serpulids see? For the majority of species surveyed, the radiolar eyes likely suffer from poor spatial resolution. Instead, they seem to have prioritized redundancy, broad coverage, and rapid, specialized processing in service to their single, robust withdrawal behavior.
Correlating form to function, we can assume the majority of serpulids are capable of little more than rudimentary shadow detection. The scattered single type S/oS ocelli and compound eyes found in most genera likely trigger a withdrawal response once a certain threshold of ocelli responding to a decrease in illumination is crossed. Though rigorous light response experiments have not been carried out in serpulids, Nicol (1950) reported that the sabellid Acromegalomma vesiculosum (Montagu, 1813) (as Branchiomma) responded most dramatically when a shadow stimulus was moving. Similar field and aquarium observations were reported by Smith (1985) for Spirobranchus corniculatus. Movement discrimination in fan worm radiolar eyes could be facilitated with little processing expense by an object gradually infringing on the field of view of increasing numbers of ocelli, until some threshold is crossed. However, in essentially every example, the poor organization and semirandom distribution of ocelli preclude the serpulids from visually guided tasks beyond shadow or motion detection. Even the paired radiolar or opercular compound eyes (type CP/oC) lack the organization or facet counts required for resolving vision. Instead, these simple compound eyes probably function similarly to the type S eyes, except with a slight advantage in shared screening pigment and a distribution of fields of view that are less likely to redundantly overlap.
Nilsson (1994) suggested that the radiolar eyes in sabellids and serpulids function as a sort of "burglar alarm," responding to decreasing illumination or a moving silhouette in the water column and triggering the rapid withdrawal response. This notion is supported by behavioral observations of sabellids by Nicol (1950), who found A. vesiculosum (as Branchiomma) responding with a withdrawal response to decreases in illumination only. Furthermore, Leutscher-Hazelhoff (1984) recorded hyperpolarizing photic responses from the radiolar photoreceptors of A. vesiculosum (as Branchiomma). It has been argued that a hyperpolarizing response is a rule for ciliary photoreceptors and the natural choice for a shadow detector, since a decrease in illumination would produce a proper depolarizing neural signal (Hartline, 1938; Fain et al., 2010). It could be that early metazoans possessed both a ciliary photoreceptor for bright-light vision and shadow detection, as well as an adaptable microvillar photoreceptor geared toward dim-light vision. Our observations of a [[lambda].sub.max] = 464 nm visual pigment in Spirobranchus corniculatus indicate that these photoreceptors appear to be closely tuned to the dominant wavelengths of light in shallow marine habitats (Fig. 4B). This further supports the notion that these fan worm photo-receptors function as a shadow or silhouette detector against the prevailing bright-illumination conditions of the shallow seas. The identification of at least two expressed InvC-opsin transcripts in S. corniculatus, along with the observed variation in measured [[lambda].sub.max], offers the intriguing possibility of multiple spectrally distinct photoreceptor types contributing to shadow detection in the variable underwater light environment.
A notable exception to the distributed and poorly organized radiolar eyes in the majority of serpulids are the type CS eyes of S. corniculatus and other Christmas tree worms, which possess at a minimum the structural sophistication required for rudimentary resolving vision. These consolidated compound eyes can contain up to 1000 well-organized facets that produce a distinct pseudopupil (Fig. 2L), suggesting the possibility for some spatial analysis. Despite their apparent sophistication, it would be easy to conclude from both the shape and position of the compound eyes that they are not well suited for advanced visual function. Unique among compound eyes, each eye is concave along the major axis, twisted inward, and buried underneath much of the branchial crown when it is deployed in feeding position. Of course, the concave eye structure might only be an economical drawback, as the atypical bean shape does not necessarily hinder the potential for spatial resolution performance. Additionally, their placement at the base of the crown keeps these major sensory organs in the safest possible location in the event of a successful predatory attack.
Field and unpublished observations (Smith, 1985) suggest that the Christmas tree worm compound eye is indeed capable of mediating more complex visual behavior than basic shadow response and the detection of conspicuous overhead motion. Worms have been observed to withdraw on the approach of fish species known to predate on them with no shadows having been cast and without displaying the same response to other fish species swimming in the same area. Further research is required to determine whether the structural sophistication of the Christmas tree worm compound eye indeed translates to advanced visual functions or is merely an odd evolutionary approach to the standard serpulid "burglar alarm."
As with serpulids, in the majority of sabellid genera the radiolar ocelli or eyes are arrayed in a manner that seems counterintuitive, scattered in the dozens or hundreds along the outside corners of every radiole. Only some species of the sabellid Acromegalomma possess an economical pair of large eyes prominently positioned on the tips of the dorsalmost radioles--offering the potential for high visual performance with full viewing angles and little redundancy. However, these eyes are more vulnerable, and the cost of their loss is high, so the distributed, redundant eye approach may be preferable for the role of shadow detection.
Serpulids also have the opportunity for an additional visual strategy in their operculum. The operculum could logically serve as a sort of periscope, emerging first from the tube and being prominently positioned once extended. Indeed, several serpulids make use of this strategy (Fig. 2Q-U; Table 1); and considering the operculum's shared ontological history with the radioles, it is unsurprising that the ocelli found on these two parts of the crown were observed to be homologous in Pomatostegus stellatus.
Evolutionary context of serpulid radiolar eyes
Our comparison of radiolar eye types throughout the serpulids suggests that they serve as a weaker phylogenetic character than in sabellids (Bok et al., 2016), where eye arrangement and ocellar structure are well conserved within genera. It should be noted that there is currently poor resolution in the phylogeny, and the taxonomy of serpulid species is confused. However, comparisons of radiolar eye arrangement with most current serpulid taxonomies clearly suggest that radiolar eyes or ocelli have been gained, lost, and elaborated multiple times within the family. Beyond this, it is difficult to make a clear assessment of radiolar eye evolution in the serpulids at this time. Interestingly, a similar plasticity is hypothesized for the ontogeny of the operculum, being derived from a radiole in the SerpulalHydroideslCrucigera clade in serpulins but a de novo development from the prostomium in spirorbins (Brinkmann and Wanninger, 2009).
Comparison of radiolar ocellar fine structure, developmental history, and expression location throughout the serpulids suggests a shared ancestry for these photoreceptors, with subsequent elaborations to the supporting cells and optical elements emerging uniquely in different species (Fig. 3). Furthermore, this ciliary photoreceptor also appears to be structurally homologous to those found in the radiolar eyes of sabellids (Bok et al., 2016). This is further supported by close opsin sequence homology between the InvC-opsins found in the sabellid Acromegalomma interruptum and the serpulid Spirobranchus corniculatus (Fig. 5). InvC-opsins are primarily found in the neural and distributed visual systems of panarthropods, echinoderms, and annelids (Fig. 5B; Bok et al., 2017), but little is understood about their function. The fan worm radiolar eye InvC-opsins are most closely related to a brain photoreceptor-expressed opsin in the errant polychaete Platynereis dumerilii, where it is likely involved only in simple illuminance assessment (Arendt et al., 2004). To our knowledge, the sabellids and serpulid radiolar eyes are the first example of InvC-opsin expression in an animal's primary visual system.
Recently, it was discovered that the InvC-opsin in P. dumerilii produces a visual pigment maximally sensitive to 383-nm ultraviolet light based on the presence of a lysine residue at bovine rhodopsin position 94 (Tsukamoto et al., 2017). In metazoan opsins, ultraviolet sensitivity is typically conferred by a lysine residue at positions 86, 89, 90, or 94 (reviewed in Cronin and Bok, 2016). Lysine is not present at position 94, or any of the other ultraviolet tuning sites in the InvC-opsins of Spirobranchus corniculatus, Acromegalomma interruptum, or any other species besides P. dumerilii (Fig. 5B). This is consistent with our measurements of a visual pigment maximally sensitive to blue-green light (464 nm) in S. corniculatus (Fig. 4).
Interestingly, 5. corniculatus expresses at least two or three opsin transcripts in the radiolar eyes, compared with the single transcript found in A. interruptum (see Bok et al., 2017, as Megalomma interrupta) (Table A1). Furthermore, while A. interruptum predominantly expresses [G[alpha].sub.o], S. corniculatus radiolar eyes have greater expression of [G[alpha].sub.i] (Table A1). Both of these G-protein alpha subunits are implicated in phototransduction in ciliary photoreceptors, but it is nonetheless interesting that the radiolar photoreceptors of sabellids and serpulids, apparently homologous in so many ways, may have seized on slightly different phototransduction machinery. Additional work is required to confirm which G-proteins are at work in the radiolar eye photoreceptors of both of these families.
Distributed visual systems are common in a number of invertebrate taxa including bivalves (Nilsson, 1994; Speiser and Johnsen, 2008a, b), chitons (Speiser et al., 2011; Li et al., 2015), starfish (Garm and Nilsson, 2014), and sea urchins (Yerramilli and Johnsen, 2010; Ullrich-Litter et al., 2011). As with the fan worms, these visual systems are mostly relevant to triggering defensive responses (Nilsson, 2013), but some may also play a role in navigation for the motile groups. These diverse distributed visual systems undoubtedly represent convergence upon a common method of detecting potential threats in the aquatic environment. It is possible that distributed visual systems represent an ideal method of producing redundant, flexible, and resilient light sensors that require minimal central processing in order to initiate a fast and robust defensive response.
We are grateful to Thomas W. Cronin for use of his micro-spectrophotometer, Eva Landgren for assistance with transmission electron microscopy preparation, and Maria Capa for assisting with some animal collection. MJB and D-EN are supported by the Knut and Alice Wallenberg Foundation and the Swedish Research Council. MJB was also supported by the John and Laurine Proud Foundation and the Australian Museum's Lizard Island Research Station. MLP is supported by National Science Foundation grants DEB 1556819 and DEB 1532382. We also thank the staff of the Carrie Bow Cay Field Station, Belize, and the Lizard Island Research Station, Australia, for assistance with field research and collection.
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Table A1 Phototransduction and eye development transcripts found in Spirobranchus corniculatus radiolar eyes Accession number Species for opsin sequence Apis mellifera AF004168 Bicyclus anynana AF484249 Camponotus abdominalis AF042788 Sepia officinalis AF000947 Drosophila melanogaster Rh1 AH001026 Drosophila melanogaster Rh2 M12896 Drosophila melanogaster Rh3 M17718 Drosophila melanogaster Rh4 AH001040 Drosophila melanogaster Rh5 U67905 Drosophila melanogaster Rh6 Z86118 Hemigrapsus sanguineus D50583 Limulus polyphenols (lateral eye) L03781 Limulus polyphemus (ocelli) L03782 Manduca sexta L78080 Mysis diluviana DQ852591 Neogonodactylus oerstedii UV1 KJ127520.1 Neogonodactylus oerstedii UV2 KJ127521.1 Procambarus clarkii S53494 Procambarus milleri AF003546 Schistocerca gregaria X80071 Vanessa cardui AF385333 Species [[lambda].sub.max] (nm) Apis mellifera 439 Bicyclus anynana 560 Camponotus abdominalis 360 Sepia officinalis 492 Drosophila melanogaster Rh1 478 Drosophila melanogaster Rh2 420 Drosophila melanogaster Rh3 345 Drosophila melanogaster Rh4 375 Drosophila melanogaster Rh5 437 Drosophila melanogaster Rh6 508 Hemigrapsus sanguineus 480 Limulus polyphenols (lateral eye) 520 Limulus polyphemus (ocelli) 530 Manduca sexta 520 Mysis diluviana 501 Neogonodactylus oerstedii UV1 334 Neogonodactylus oerstedii UV2 383 Procambarus clarkii 533 Procambarus milleri 522 Schistocerca gregaria 520 Vanessa cardui 530 Species [[lambda].sub.max] reference Apis mellifera Townson et al., 1998 Bicyclus anynana Vanhoutte et al., 2002 Camponotus abdominalis Smith et al., 1997 Sepia officinalis Brown and Brown. 1958 Drosophila melanogaster Rh1 Feiler et al., 1988 Drosophila melanogaster Rh2 Feiler et al., 1988 Drosophila melanogaster Rh3 Feiler et al., 1992 Drosophila melanogaster Rh4 Feiler et al., 1992 Drosophila melanogaster Rh5 Salcedo et al., 1999 Drosophila melanogaster Rh6 Salcedo et al., 1999 Hemigrapsus sanguineus Sakamoto et al., 1996 Limulus polyphenols (lateral eye) Hubbard and Wald, 1960 Limulus polyphemus (ocelli) Nolte and Brown, 1972 Manduca sexta White et al., 1983 Mysis diluviana Porter et al., 2007 Neogonodactylus oerstedii UV1 Bok et al., 2014 Neogonodactylus oerstedii UV2 Bok et al., 2014 Procambarus clarkii Zeiger and Goldsmith, 1994 Procambarus milleri Cronin and Goldsmith, 1982; Crandall and Cronin, 1997 Schistocerca gregaria Gartner and Towner, 1995 Vanessa cardui Briscoe et al., 2003 The de novo assembly (and raw transcriptomic sequence reads) used for phylogenetically informed annotation (PIA) identification of phototransduction contigs are available at the National Center for Biotechnology Information Sequence Read Archive under bioproject PRJNA399760, biosample SAMN07949790. FPKM, fragments per kilobase million.
MICHAEL J. BOK (1, *), MEGAN L. PORTER (2), HARRY A. TEN HOVE (3), RICHARD SMITH (4, [deagger]), AND DAN-ERIC NILSSON (1)
(1) Lund Vision Group, Department of Biology, Lund University, Solvegatan 35, 22362 Lund, Sweden; (2) Department of Biology, University of Hawai'i at Manoa, Honolulu, Hawai'i 96822; (3) Naturalis Biodiversity Center, P.O. Box 9517, 2300 RA Leiden, The Netherlands; and Department of Marine Biology, James Cook University, Townsville, Queensland 4811, Australia
Received 28 April 2017; Accepted 5 September 2017; Published online 30 October 2017.
(*) To whom correspondence should be addressed. Present address: School of Biological Sciences, University of Bristol, Bristol BS8 1TH, United Kingdom. E-mail: email@example.com.
([deagger]) Present address: Blue Planet Productions, 6 Melbourne Street, Fairlight 2094, Australia.
Abbreviations: MSP, microspectrophotometry; PIA, phylogenetically informed annotation; TEM, transmission electron microscopy.
Online enhancements: supplemental table.
Table 1 Radiolar eyes in serpulid genera Genus Eye type Apomatus CP Crucigera S, CS Dasynema CP Janita ? Metavermilia S Microprotula S Paraprotis CP Pomatostegus S, oS Protula CP, S Pseudovermilia oC Pyrgopolon oC Semivermilia oS Serpula CP Spiraserpula S Spirobranchus CS S CP oS Turbocavus CP, S Vermiliopsis s Genus Comments Apomatus Paired compound eyes along radiole aboral coiners in some species Crucigera Randomly distributed ocelli on aboral corners of radioles in some species; occasionally a single compound eye near the base of each radiole Dasynema Multiple paired compound eyes with up to 11 ocelli each along radiole aboral corners Janita Stalked eyes at the base of pinnules Metavermilia Paired single ocelli along radioles in some species Microprotula Paired, probably single, ocelli along radioles in some species Paraprotis Paired compound eyes with only two or three ocelli each along the radiole aboral corners Pomatostegus Randomly distributed ocelli on both comers of the radioles and on the rim of the operculum Protula Paired compound eyes or scattered single ocelli along the outside of radiole aboral corners in many species Pseudovermilia None in some species; in others numerous lenses in the wedge-shaped zone at the ventral edge of the opercular bulb Pyrgopolon Compound eyes on the opercular brim in Pyrgopolon ctenactis (Morch, 1863) Semivermilia A single red ocellus at the base of the opercular ampulla in Semivermilia pomatostegoides (Zibrowius, 1969) Serpula Paired clusters on the base of radioles in some species; Serpula jukesi consolidates multiple ocelli behind a shared lens Spiraserpula Contradictory observations in fresh material, from up to six single eyespots in the base of lateral radioles (not the most dorsal or ventral) or red spots without lenses Spirobranchus Spirobranchus corniculatus and Spirobranchus giganteus complexes (Christmas tree worms) with large single compound eyes at the internal base of each dorsal radiole Spirobranchus tetraceros complex with paired or irregular single ocelli along radiole aboral corners Spirobranchus kraussii (Baird, 1865) with paired compound ocelli spaced along radiole aboral corners Spirobranchus corrugatus (Straughan, 1967) with scattered red ocelli on the opercular rim Turbocavus Radioles with evenly spaced single ocelli and/or ocellar clusters in Turbocavus secretus Prentiss, Vasileiadou, Faulwetter, Arvanitidis & ten Hove, 2014 Vermiliopsis Randomly distributed ocelli on both aboral corners of radioles Genus References Apomatus Fauvel, 1927; ten Hove and Pantus, 1985 Crucigera This study Dasynema Grube, 1878 (in Andrews, 1891); Imajima and ten Hove, 1984 Janita Fauvel, 1927 (as Omphalopoma); Rioja, 1931 (as Omphalopomopsis) Metavermilia This study Microprotula Uchida, 1978 Paraprotis Uchida, 1978 Pomatostegus Smith, 1985; this study Protula Claparede, 1868 (in Andrews, 1891); Radl, 1912; Pixell, 1913; Fauvel, 1927, 1953; Monro, 1933; Imajima and Hartman, 1964; Pillai, 1971; Uchida, 1978 (as Paraprotula); Vine and Bailey-Brock, 1984; Smith, 1985; this study Pseudovermilia This study Pyrgopolon ten Hove and Kupriyanova, 2009 Semivermilia Vine and Bailey-Brock, 1984 Serpula Smith, 1985 (S. jukesi); this study Spiraserpula This study Spirobranchus Smith, 1985; this study Smith, 1985; this study Pillai, 1971; Mak, 1982; Smith, 1985 (as Pomatoleios kraussii) Vine and Bailey-Brock, 1984; Smith, 1985 (both as Spirobranchus sp.); Kupriyanova et al., 2015; this study Turbocavus Prentiss et at, 2014 Vermiliopsis Pixell, 1913; Iroso, 1921 (partially under other synonymic names); Fauvel, 1927; Pillai, 1971; Smith, 1985; this study Eye types: S, single simple ocelli; CP, compound-paired; CS, compound-single; oS, opercular simple; oC, opercular compound. Radiolar eyes not reported in Bathyditrupa, Bathyvermilia, Chitinopoma, Chitinopomoides, Ditrupa, Ficopomatus, Filograna, Filogranula, Filogranella, Floriprotis, Galeolaria, Hyalopomarus, Hydroides, Josephella, Laminatubus, Marifugia, Neomicrorbis, Omphalopomopsis, Paumotella, Placostegus, Protis, Pseudochitinopoma, Rhodopsis, Salmacina, Spirorbinae, Spirodiscus, Tanturia, and Vitreotubus.
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|Author:||Bok, Michael J.; Porter, Megan L.; Hove, Harry A. Ten; Smith, Richard; Nilsson, Dan-Eric|
|Publication:||The Biological Bulletin|
|Date:||Aug 1, 2017|
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