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Anelidos intersticiales de la costa Caribe de Colombia.

Interstitial annelids from the Caribbean Coast of Colombia

Colombia is a very diverse country, and has been ranked first in terms of species richness for some taxa such as mammals, birds, reptiles, amphibians and butterflies (Andrade, 2011). Marine biodiversity research in Colombia has been concentrated primarily on sponges, corals, mollusks, as well as some groups of crustaceans, fish, and algae (Diaz & Acero, 2003). Nevertheless, over the last decade, the training of young taxonomists has expanded investigation to other groups, such as polyclad flatworms (Quiroga, Bolanos, & Litvaitis, 2004), lophophorates (Florez-Romero, Montoya-Cadavid, Reyes-Forero, & Santodomingo, 2007), sipunculan annelids (Gomez, Ardila, & Sanjuan-Munoz, 2013), and nemerteans (Gonzalez-Cueto, Quiroga, & Norenburg, 2014). Despite all the efforts, there is still a huge gap to fulfill before we have a complete picture of the marine biodiversity of the country mainly in relation to some groups, such as those dominated by microscopic animals (e.g. meiofauna), which offer additional difficulties in collecting, handling, and identifying species (Giere, 2009; Somerfield & Warwick, 2013).

Polychaetes (phylum Annelida) are one of the most abundant and diverse components of soft bottom benthic communities (Giere, 2009). The group is represented by more than 15 000 species distributed along the entire bathymetrical gradient, from the intertidal to abyssal zone (Rouse & Pleijel, 2001). This diversity is reflected in the very different body plans, life histories, and ecological niches recorded across and within their lineages (Seaver, 2003). About 80 polychaete families have been described (Read & Fauchald, 2017), most of them represented only by macrofaunal species (larger than 0.5 mm). In contrast, several families such as Dinophilidae, Diurodrilidae, Nerillidae, Parergodrilidae, Polygordiidae, Protodrilidae, Psammodrilidae, Saccocirridae, as well as some genera within Sigalionidae (e.g. Pisione, Laubierpholoe), Hesionidae (Hesionura, Microphthalmus), and Syllidae (e.g. Miscellania, Parapionosyllis) include several lineages of exclusively meiofaunal species, which complete their life cycles amongst the sand grains, moving among them causing a minimum disturbance (Worsaae & Kristensen, 2005; Westheide, 2008). Traditionally, a common origin has been attributed to several of these families, which have been historically placed in the order Archiannelida (e.g. Hermans, 1969). However, recent morphological and phylogenetic analyses have shown that these microscopic animals have most likely evolved several times independently (Andrade et al., 2015; Struck et al., 2015).

Despite being one of the regions with the highest number of recorded species of annelids in the Caribbean, Protodrilidae is so far the only interstitial family recorded for Colombia, although only from specimens identified to the family level (Guzman-Alvis, Latting, & Ruiz, 2006). Therefore, the main goal of this survey was to identify the species of interstitial annelids inhabiting the coastal zone of the Santa Marta Region, using morphological characters visible through light microscopy. Due to their small size and the high similarity between closely related meiofaunal species, optical microscopic techniques are sometimes insufficient for an accurate species identification (Martinez, Di Domenico, Jorger, Norenburg, & Worsaae, 2013; Worsaae, Kvindebjerg, & Martinez, 2015), but provide enough information for unequivocal identification to the genus level. Consequently, this report should be considered as a first attempt to assess the diversity of interstitial annelids in the Caribbean coasts of Colombia, demanding further research with additional morphological techniques, such as electron and confocal laser scanning microscopy, combined with methods of DNA taxonomy. These methods have helped solving several species complexes, their geographic distribution, and phylogenetic relationships (Di Domenico, Martinez, Lana, & Worsaae, 2013; Martinez et al., 2013; Worsaae et al., 2015). In order to warrant the re-identification of the reported species, each of our records is supported by a short description of the main light microscopy characters based on direct examination of our specimens.

MATERIAL AND METHODS

Study site: Samples were collected from three bays in the Santa Marta area (Magdalena, Colombia): Santa Marta Bay (11[degrees]14'32" N 74[degrees]12'58" W), Rodadero Bay (11[degrees]12'25" N - 74[degrees]13'44" W) and Taganga Bay (11[degrees]15'52" N - 74[degrees]11'29" W). Beaches within these bays were chosen based on their accessibility and their biological and economic importance within the region. All these sites belong to the Tayrona Ecoregion of the Colombian Caribbean and they are highly impacted by anthropogenic activities, because they are popular touristic destinations within the city of Santa Marta (Obando, Ochoa, De Duque, Rozo, & Villada, 2011). The three sampled sites are sheltered sandy beaches located between coastal projections formed by metamorphic and igneous rocks and dikes, in a coastal plain originated by alluvial deposits and avalanches from the rivers Manzanares, Tamaca, and Gaira (Morales & Guzman, 2011). The local tidal regime is of 0.48 m (Garcia, Palacio, & Garcia, 2011). The climate is bimodal with a dry season from December to April, and a rainy season from May to November (Arevalo-Martinez & Franco-Herrera, 2008). The area is influenced by counter-current of Panama and flow West-Northwest of the Caribbean Current (Paramo, Correa, & Nunez, 2011). Salinity and surface temperature of the sea have a high annual variability, the higher salinity and lower temperatures occur during the dry season when there is coastal upwelling and Northeast winds are more intense (Andrade, Barton, & Mooers, 2003).

Three samples were collected along each beach, separated 20-50 m apart, between May and October 2014. The sediment was collected 0.3 m below the high tide line in the swash zone, using a core made with PVC tubing (3.5 cm in diameter and 10 cm high), according to the methodology suggested by Fleeger, Thistle and Thiel (1988). Samples were anesthetized in situ using 7.4 % magnesium chloride, isotonic to sea water, and later fixed in 4 % formalin neutralized with Borax. For each sample, granulometry was determined visually.

Morphological analysis: Animals were extracted from the sediments by stirring the samples and decanting the supernatant through two sieves of 500 pm and 44 pm, respectively. The fraction retained by the finer sieve, containing the meiofaunal annelids, was inspected using a dissecting microscope Zeiss Stemi DV4. Fixed annelids were collected with micropipettes of 5-50 pL and mounted in 99% glycerin. Whole mounts were examined and photographed with a Zeiss AxioCam ERc 5s digital camera integrated on a Zeiss AxioLab1 microscope equipped with phase contrast. Images were processed using AxioVision SE64 software. All studied specimens were deposited in the Centro de Colecciones Biologicas de la Universidad del Magdalena (CBUMAG).

RESULTS

We found a total of 83 specimens belonging to five families, 10 genera, and nine species. From these records, two families (Nerillidae, Saccocirridae), eight genera (Hesionides, Microphthalmus, Neogyptis, Nerilla, Protodrilus, Pharyngocirrus, Neopetitia and Westheidesyllis), and four species (Hesiones gohari, Neogyptis mediterranea, Neopetitia amphophthalma, Westheidesyllis gesae and Syllis beneliahuae) are newly recorded from Colombia.

Taxonomy Section

Family Hesionidae Grube, 1850 Hesionides gohari

Hartmann-Schroder, 1960 (Fig. 1A, Fig. 1D)

Material examined: 19 specimens collected in coarse and medium sand: Rodadero Bay, 26 May 2014 (CBUMAG: ANN: 000081 to 00008-8, 00008-10, 00015-1); Santa Marta Bay, 27 May 2014 (CBUMAG: ANN: 00012-2, 00014-2); Taganga Bay, 28 May 2014 (CBUMAG: ANN: 00020-2 to 00020-5, 00020-7, 00020-8, 00024-6). Collectors: Ana M. Lagos and M. Victoria Leon.

Diagnosis: Hyaline body, up to 13 segments. Prostomium rounded with three antennae and two simple palps, all equal in length. Tentacular cirri filiform, thinner and longer than the dorsal cirri. Muscular pharynx extending until first chaetiger. Biramous parapodia with a dorsal cirrus longer than ventral cirrus, both filiform. Notopodia supported by one acicula and bearing 2-3 long simple chaetae with 10 spines along the margin. Neuropodia with four compound chaetae with smooth blade. Pygidium with a bilobed anal plate and two long anal cirri, wider basally.

Distribution and ecology: Previously reported from the Western Central Atlantic Ocean: USA (Florida) (Vieitez et al., 2004). Southwest Atlantic Ocean: Brazil (Bahia State) (Westheide, 1974). Northeast Atlantic Ocean: France (Arcachon); Mediterranean Sea: Greece (Crete), Italy (Giglio), Spain (Mallorca) (Vieitez et al., 2004). Indian Ocean: Egypt (Hurghada) and Thailand (Phuket) (Hartmann-Schroder, 1960; Schmidt & Westheide, 1999). This species typically inhabits coarse to fine intertidal and subtidal sediments (Westheide, 1974, 1987; Capaccioni, Villora, & Torres, 1989; Jing & Baoling, 1991; Villora-Moreno, Capaccioni-Azzati, & Garcia-Carrascosa, 1991; Di Domenico, 2012).

Remarks: The specimens reported here have striated anal plate lobes as those described by Rao and Ganapati (1967), Westheide (1967) and Hulings (1971); contrasting to the specimens described by Vieitez et al. (2004) and De Leon-Gonzalez et al. (2009), which have a smooth anal plate. This difference may be an artifact produced during the fixation process (Hartmann-Schroder, 1960).

Microphthalmus cf. mahensis Westheide, 2013

(Fig. 1B, Fig. 1C, Fig. 1E)

Material examined: One specimen collected in coarse sand at the swash zone: Rodadero Bay, 26 May 2014 (CBUMAG: ANN: 00007-2). Collectors: Ana M. Lagos and M. Victoria Leon.

Diagnosis: Hyaline body, with 26 segments. Prostomium rounded with two lateral and one shorter median antenna arising from the posterior margin of the prostomium, and a pair of palps. Nuchal organs ovoid, near the base of the first pair of dorsal tentacular cirri. One pair of eyes. Segments 1-3 with a pair of cirri. Dorsal cirri of the third segment longer; remaining cirri shorter and extending perpendicularly. Pharynx tubular, papillate, without jaws. Parapodia on segment 1 without notopodial chaetae. Notopodia with three tiny simple chaetae, one pectinate chaeta and two tapered chaetae, one longer and wider than the other. Neuropodia with 3-5 falcigerous and 2-3 simple chaetae. Long dorsal notopodial cirri with a bulbous base. Pygidium short, with two dorsolateral cirri and a fimbriate anal plate.

Distribution and ecology: Exclusively reported from the Indian Ocean: Seychelles (Mahe Island) in well-sorted coarse sediments at sandy beaches, and shallow subtidal areas (Westheide, 2013).

Remarks: Only Microphthalmus stocki Hartmann-Schroder, 1980 has been reported in Caribbean (Miloslavich et al. 2010), which differs from our species by the absence of eyes and a fimbriate anal plate, as well as chaetotaxy. Our specimen fits the Microphthalmus mahensis description; nevertheless we could not observe the internal stylets of the copulatory apparatus, necessary to confirm the specific identity of the specimen (Westheide, 2013).

Neogyptis mediterranea (Pleijel, 1993)

(Fig. 1F, Fig. 1G, Fig. 1H)

Synonyms: Gyptis mediterranea Pleijel, 1993

Material examined: One specimen collected in coarse sand from the swash zone: Rodadero Bay, 26 May 2014 (CBUMAG: ANN: 00005-1) Collectors: Ana M. Lagos and M. Victoria Leon.

Diagnosis: Hyaline body with 19 segments. Prostomium trapezoidal, with three antennae, paired palps, and a pair of red eyes. Lateral antennae slightly shorter and thinner than palps. Median antenna short, inserted between eyes. Palps cylindrical, with rounded tips. Pharynx with 20-32 elongated papillae. Parapodia increasing in length towards midbody. First chaetiger without parapodia, with a simple notoaciculae. Notopodia conical with 1-2 small aciculae in subsequent segments, bearing many long simple and few serrate chaetae. Neuropodia with two aciculae and 20-40 compound chaetae. Dorsal cirri with short cirrophores from chaetiger 5. All chaetae transversally striated. Pygidium with two anal cirri and a short cylindrical appendix.

Distribution and ecology: Previously reported in the Northeastern Atlantic Ocean: France (Banyuls-sur-Mer) (Pleijel, 1993) and Portugal (Aveiro) (Ravara & Moreira, 2013). Mediterranean Sea: Greece (Crete) (Chatzigeorgiou, Faulwetter, & Arvanitidis, 2014), Italy (Brucoli) (Pleijel, Rouse, Sundkvist, & Nygren, 2012), and Turkey (Aegean Sea) (Cinar, Dagli, & Kurt Cahin, 2014). It has been found in mud and sandy mud, down to 124 m depth (Ravara & Moreira, 2013).

Remarks: Neogyptis mediterranea resembles N. nonatoi, which had been reported in Brazilian coasts. However, our specimens is assigned to N. mediterranea due to the presence of a tapered median antenna, less than 32 pharyngeal papillae, and large eyes.

Family Nerillidae Lamarck, 1818

Nerilla cf. mediterranea Schlieper, 1925

(Fig. 1I, Fig. 1J)

Material examined: 22 specimens collected in coarse sand from the swash zone: Rodadero Bay, 26 May 2014 (CBUMAG: ANN: 00006-1, 00006-5); Taganga Bay, 28 May 2014 (CBUMAG: ANN: 00016-1 to 00016-20). Collector: Ana M. Lagos and M. Victoria Leon.

Diagnosis: Delicate and hyaline body, with nine segments. Prostomium with three annulated antennae, two short bulbous ventrolateral palps, and four red eyes, anterior pair larger than posterior one. First chaetiger with annulated cirrus, equal in length or longer than antennae, and 2-3 simple chaetae. Segments 2-9 with biramous parapodia, with 5-12 simple chaetae per rami, and filiform and smooth interramal cirri. Chaetae increasing in length towards pygidium. Last chaetiger without cirrus. Pygidium short, with two long annulated cirri.

Distribution and ecology: Previously reported in the Southwest Atlantic Ocean: Brazil (Guaruja and South Coast of Brazil) (Du Bois-Reymond Marcus, 1947; Di Domenico, 2012). Mediterranean Sea: Spain (Murcia) (Besteiro, Nunez, & Martinez, 2012), Italy (Cala Spalmadori) (Gusmao et al., 2016). This species inhabits intertidally in sandy beaches, as well as subtidally in silty sand, silty shell gravel and mud (Worsaae, 2014).

Remarks: Due to their body length and width (L: 585 gm; W: 66 [micro]m), our specimens resemble those reported in Brazil as Nerilla mediterranea (L: < 1 000 [micro]m; W: 100 [micro]m) (Du Bois-Reymond Marcus, 1947; Di Domenico, 2012). The proportions of body length and width are twice smaller than those reported for Europe (L: 2 000 [micro]m; W: 200 [micro]m) (Besteiro et al., 2012). Therefore, our identification might be taken cautiously, until further examinations are performed.

Family Protodrilidae Hatschek, 1888

Protodrilus cf. smithsoni Martinez, Di Domenico, Jorger, Norenburg & Worsaae, 2013

(Fig. 1L, Fig. 1K)

Material examined: 17 specimens collected in coarse sand from the swash zone: Taganga Bay, 28 May 2014 (CBUMAG: ANN: 00002-1 to 00002-6, 00017-1, 00017-2, 00022-1 to 00022-5, 00025-2); Rodadero Bay, 26 May 2014 (CBUMAG: ANN: 00009-1 to 00009-3). Collectors: Ana M. Lagos and M. Victoria Leon.

Diagnosis: Hyaline body, with 20-70 segments. Prostomium without antennae or eyes, bearing two filiform palps, each with internal canal, and two conspicuous terminal unpigmented prostomial receptors (previously referred to as "statocysts"). Nuchal organs densely ciliated and extending dorso-laterally between prostomium and peristomium. Salivary glands extending to segment 12. Midventral ciliary band extending from mouth to pygidium. Parapodia and chaetae absent. Pygidium with two adhesives lobes.

Distribution and ecology: Previously reported in Western Central Atlantic: Panama Bocas del Toro (Martinez et al., 2013).

Remarks: Out of the 15 described species of Protodrilus (Martinez, Di Domenico, Rouse & Worsaae, 2015), only P. smithsoni has been reported in the Caribbean from Bocas del Toro (Panama) (Martinez et al. 2013). This is therefore the first record of the genus Protodrilus in Colombia. Although our specimens fit well the description of P. smithsoni, the lack of mature males are necessary to confirm the specific identity of our specimens.

Family Saccocirridae Czerniavsky, 1881

Pharyngocirrus cf. gabriellae (Du Bois-Reymond Marcus, 1946)

(Fig. 2A, Fig. 2C)

Material examined: 7 specimens collected in coarse and fine sand from the swash zone: Rodadero, 26 May 2014 (CBUMAG: ANN: 00005-2); Santa Marta Bay, 27 May 2014 (CBUMAG: ANN: 00013-1 to 00013-3); Taganga Bay, 28 May 2014 (CBUMAG:ANN: 00026-2 to 00026-4). Collectors: Ana M. Lagos and M. Victoria Leon.

Diagnosis: Hyaline body, with up to 60 segments. Prostomium rounded, without antennae but with a pair of filiform annulated palps (each with 15-20 articles), and two red eyes. Muscular pharynx present. Parapodia uniramous and cylindrical, each with three types of chaetae: 1) long, slender lyrate chaeta with small median tooth, 2) bifid chaeta, 3) short and wider chaetae with notched apex. Pygidium divided in two lobes, each one with 6-10 adhesives ridges.

Distribution and ecology: Previously reported in the Southwest Atlantic Ocean: Brazil (Du Bois-Reymond Marcus, 1946; Di Domenico, 2012; Di Domenico, Martinez, Lana, & Worsaae, 2014; Di Domenico, Martinez, Amaral, Lana, & Worsaae, 2014).

Northeast Atlantic Ocean: Baltic Sea (Mastepanova, 2004). Northwest Pacific Ocean: Sea of Japan (Scarlato et al., 1967; Buzhinskaja, 1967; Sveshnikov, 1967). Most records come from coarse sediments at tidal pools and shallow areas with organic matter (Di Domenico, Martinez, Amaral, Lana, & Worsaae, 2014a; Di Domenico, Martinez, Lana, & Worsaae, 2014).

Remarks: Our specimens fit the diagnosis of Pharyngocirrus gabriellae. However, since this species is diagnosed in based of the arrangement of seminal vesicle in males and the gonads in females, mature specimens are necessary to confirm the specific identity or our material.

Family Syllidae Grube, 1850

Myrianida sp. (Fig. 2B, Fig. 2D)

Material examined: One specimen collected in coarse sand from the swash zone: Rodadero Bay, 26 May 2014 (CBUMAG: ANN: 00003-1). Collectors: Ana M. Lagos and M. Victoria Leon.

Diagnosis: Hyaline body, with 20 segments. Prostomium rounded with three antennae, fused palps and two pairs of eyes. Peristomium with two pairs of smooth cylindrical tentacular cirri. Pharynx thin curvy; trepan with 10-20 teeth. Proventricle extending to segment three. Parapodia short and conical, with flattened dorsal cirri with compound dentate and simple bayonet-shaped chaetae. Cirrophores on all chaetigers, shorter than parapodial lobes.

Distribution and ecology: Myrianida has been reported throughout the Caribbean Sea (Belize), Mediterranean Sea (France, Morocco, Croatia), Northwest (USA), Northeast (Germany) and Southeastern (South Africa) Atlantic Ocean; Northeast (USA, Japan and Philippines) and Central East (Salvador, Ecuador) Pacific Ocean; and Red Sea (Nygren, 2004). Specimens of Myrianida are commonly found in shallow water, sometimes associated with sessile invertebrates, such as bryozoans, tunicates, hydroids, sea pens, and sponges upon which they feed (Dietrich et al., 2015).

Remarks: The lack observations on fresh material prevented us to examine the coloration. Furthermore, in order to examine the denticulation of the trepan dissection is needed, leading to the destruction of our single specimen. Therefore, our specimen is identified to the genus level only.

Neopetitia amphophthalma (Siewing, 1956)

(Fig. 2E, Fig. 2G)

Synonyms: Petitia amphophthalma (Siewing, 1956)

Material examined: 12 specimens collected in coarse sand from the swash zone: Rodadero, 26 May 2014 (CBUMAG: ANN: 00006-2 to 00006-4, 00006-7, 00006-8, 000089, 00009-4, 00010-2, 00011-1); Taganga Bay, 28 May 2014 (CBUMAG: ANN: 00021-1 00027-1, 00027-3). Collectors: Ana M. Lagos and M. Victoria Leon.

Diagnosis: Hyaline and slender body, up to 22 segments. Prostomium oval, wider than long, with three antennae, a pair of palps, and two lateral eyes. Antennae smooth and filiform, median slightly longer than lateral ones. Palps not fused and biarticuled. Peristomium with two pairs of tentacular cirri similar in length and shape to antennae. Dorsal cirri longer than ventral ones. Pharynx short and slender, extending along three segments, with a single tooth at anterior end. Proventricle shorter than pharynx, extending through two segments. Ventral cirri digitiform, arising distally on parapodial lobes. Each chaetiger bearing one serrated dorsal simple chaeta and 3-6 bidentate falcigerous chaetae. Pygidium with one conical anal appendage and two lateral cirri about twice longer than the anal appendage.

Distribution and ecology: Previously reported in the Western Central Atlantic Ocean: USA (Florida) (Von Soosten, Schmidt, & Westheide, 1998), Bahamas (Hartmann-Schroder, 1958) and Cuba (Dean, 2012). Northeastern Atlantic Ocean: France (Arcachon) (Von Soosten et al., 1998), and British Isles (San Martin & Worsfold, 2015). Eastern Central Atlantic Ocean: Spain (Canary Island) (Von Soosten et al., 1998), Mediterranean Sea: Spain and Tunez (Musco & Giangrande, 2005). Black Sea: Bulgaria (Sahin & Qinar, 2012). Indian Ocean: (Walteir Coast) (Von Soosten et al., 1998). This specie has been found in coarse and medium sand, as well as sandy muddy shores (Chandrasekhara & Ganapati, 1966; Hulings, 1971; Westheide & Hass-Cordes, 2001).

Remarks: Three species of the genus Neopetitia have been described: N. amphophthalma, N. occulta (Westheide & Hass-Cordes, 2001) and N. abadensis Riera, Nunez, & Brito, 2007. Our specimens correspond well to N. amphophthalma. The species is easily distinguishable from N. abadensis by lacking an acicular chaeta in the chaetiger 11 in males (Riera et al., 2007).

Westheidesyllis gesae (Perkins, 1981)

(Fig. 2F, Fig. 2H)

Synonyms: Pionosyllis gesae Perkins, 1981.

Material examined: Two specimens collected in coarse sand from the swash zone: Santa Marta Bay, 27 May 2014 (CBUMAG: ANN: 00014-1); Taganga Bay, 28 May 2014 (CBUMAG: ANN: 00024-7). Collectors: Ana M. Lagos and M. Victoria Leon.

Diagnosis: Hyaline body, with 14 segments. Prostomium oval with three antennae, one pair of flattened palps, with rounded tip, equal or longer than the prostomium, and two pairs of eyes. Pharynx extending until chaetiger 4, bearing ten soft papillae and one median tooth. Proventricle extending along chaetigers 5-7. Parapodia long, cylindrical and truncate, each with one acicula, three bidentate falcigerous chaetae, and one pointed dorsal simple chaeta (serrated near tips on anterior chaetigers). All dorsal cirri with a short cirrophore. Chaetiger 2 without dorsal cirri. Pygidium with two anal cirri longer than the dorsal cirri.

Distribution and ecology: Previously reported in the Western Central Atlantic Ocean: Cuba (Punta Pedernales, Isla de la Juventud, Cayo Matias, Archipielago de los Canarreos), USA (Gulf of Mexico, Florida); Southeast Atlantic Ocean: Cape Verde Islands (Perkins, 1981; Uebelacker, 1984; San Martin, Lopez & Aguado, 2009). Typical from coarse and medium calcareous sand, as well as from algae (Perkins, 1981; San Martin et al., 2009).

Remarks: Specimens reported here are smaller than those reported in the original description (Perkins, 1981), and the ones recorded by Uebelacker (1984).

Syllis beneliahuae (Campoy & Alquezar, 1982)

(Fig. 2I, Fig. 2J, Fig. 2K)

Synonyms: Langerhansia beneliahui (Campoy & Alquezar, 1982), Syllis beneliahui (San Martin, 1992), Ehlersia beneliahuae (Salazar-Vallejo, 1996), Typosyllis beneliahuaei (Licher, 1999).

Material examined: One specimen collected in coarse sand from the swash zone: Taganga Bay, 28 May 2014 (CBUMAG: ANN: 00001-1) Collectors: Ana M. Lagos and M. Victoria Leon.

Diagnosis: Hyaline body, with 60 segments. Prostomium bearing a median antenna with 23 articles, two lateral antennae with 15 articles, long triangular palps, and four eyes. Pharynx extending until chaetigers 11-12, with smooth papillae and a large distal tooth. Proventricle extending backwards from the chaetiger 12 to 19. All parapodia with dorsal articulated and ventral unarticuled cirri. Anterior parapodia with 6-8 falciger chaetae. Posterior parapodia with 4-5 chaetae. Aciculae in posterior parapodia with a stout end, and an apical tooth. Pygidium with anal cirri with 12-13 articles.

Distribution and ecology: Previously reported from the Western Central Atlantic: Cuba (San Martin, 1992), Costa Rica (Dean, 2017) and Mexico (Cozumel) (Fauchald, Granados-Barba, & Solis-Weiss, 2009). Southwest Atlantic Ocean: Brazil (Rio de Janeiro) (Omena & Creed, 2004). Mediterranean Sea: Italy, Croatia (Musco & Giangrande, 2005) and Turkey (Sea of Marmara, Aegean Sea, and Levantine Sea) (Qinar et al., 2014). Eastern Central Atlantic Ocean: Spain (Canary Islands) (San Martin, 2003; Martinez, Palmero, Brito, Nunez, & Worsaae, 2009). Eastern Central Pacific Ocean: Panama (Coiba island) (Capa, San Martin & Lopez, 2001). This species is common in hard substrates such as coral rubble, calcareous algae and anchialine caves.

Remarks: The morphology of the specimens found in this survey fit well with the description of those reported by Nunez, San Martin & Brito (1992), Capa et al. (2001), and San Martin (2003).

DISCUSSION

This study increases the number of polychaete known in Colombia from 298 (Londono-Mesa, 2017) to 302 species (without including species referred to as cf), recorded from three beaches at the Santa Marta area. Santa Marta belongs to the Tayrona Ecoregion (Diaz & Gomez, 2000), which is listed among the ten coastal areas with the greatest diversity of marine species in the Caribbean Sea (Miloslavich et al., 2010). There are about 144 species of polychaetes reported in this ecoregion (Baez & Ardila, 2003), which represents about the 50% of the species recorded in the Caribbean coasts of Colombia and about the 12% of the polychaetes registered in the Caribbean sea. This contribution adds eight genera and nine species to this list and indicates that is likely that this number will increase with more studies on the group giving the comparatively low number of beaches and habitats surveyed. Neogyptis mediterranea is a new record for the entire Caribbean Sea.

Many of the meiofaunal species that we report have a broad distribution area and have been previously recorded from other areas in the Caribbean Sea or even at different oceans. Similar patterns have been found in reef fish (Rocha, 2003; Floeter et al., 2008; and Luiz et al., 2012) and ascidians (Nobrega, Sole-Cava, & Russo, 2004), and have been explained by the existence of dispersal stages that allow the gene flow among distant populations. Whereas, those represent macrofaunal species, similar explanations can be proposed for those interstitial annelids, with pelagic feeding larvae, such as Saccocirridae or Protodrilidae (Di Domenico et al., 2014b). However, most interstitial annelids are direct developers, and therefore their dispersal across oceanic distances is improbable (Von Soosten et al., 1998; Schmidt & Westheide, 2000). For those species, these broad distribution ranges might be related to their small size according to the ubiquity theorem, which proposes that the proportions of local species richness to the global species pool is negatively related to the body size (Fenchel & Finlay, 2004; Curini-Galleti et al., 2012). However, diagnostic features in many interstitial annelids are difficult to investigate under light microscopy, often demanding more integrative microscopical studies and, the inclusion of molecular analyses (Martinez et al., 2013). Therefore, it is also likely that the apparently broad distribution range exhibited by many of the species here recorded are in fact an artifact of the lack of such studies, which might reveal that several of these taxa represent in fact complexes of species (Westheide, 1971; Westheide & Rieger, 1987; Von Soosten et al., 1998). Cosmopolitan complexes of cryptic species have been already shown for several species of meiofaunal metazoans without larvae such as nemerteans (Leasi, Andrade, & Norenburg, 2016), gastrotrichs (Leasi & Todaro, 2009), nemertodermatids (Meyer-Wachsmuth, Curini-Galletti, & Jondelius, 2014) and annelids such as Hesionides gohari (Westheide, 1974; Schmidt & Westheide, 1999), Microphthalmus listensis (Westheide & Rieger, 1987), Nerilla antennata, (Goodrich, 1912; Schmidt & Westheide, 1997/98), and Petitia amphophtalma (Westheide & Hass-Cordes, 2001; Westheide & Schmidt, 2003). Nevertheless, real cosmopolitan species also exist, as seems to be the case of Hesionides arenaria (Schmidt & Westheide, 2000). This indicates that the dispersal capability of some meiofaunal species might have been underestimated, as it suggested for some hoplonemerteans (Andrade, Norenburg, & Solferini, 2011), although the mechanisms remain unknown.

In conclusion, this report represents a first step towards unravelling the diversity of interstitial annelids in Colombia, but we acknowledge the need for further studies, including more detailed morphological (e.g. scanning electron microscopy) and molecular analyses, in order to more accurately describe the diversity of interstitial annelids in our region.

ACKNOWLEDGMENTS

We thank Guillermo San Martin and Maikon Di Domenico for their kind help and advices; Marcela Bolanos and Joseph Dunn for the revision of the manuscript. This work was financial supported by Departamento de Ciencia, Tecnologia e Innovacion (COLCIENCIAS) (grant number 566-2012 and 617-2013). This work is in the framework of the Master thesis project "Meiofauna intermareal de la region de Santa Marta, Colombia", Universidad Nacional de Colombia, Sede Caribe. This is Scientific Contribution No. 10 from the Centro de Colecciones Biologicas de la Universidad del Magdalena and No. 469 Universidad Nacional de Colombia, Instituto de Estudios en Ciencias del Mar CECIMAR (Sede Caribe), Programa de Posgrado en Ciencias--Biologia, Linea Biologia Marina.

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Ana Milena Lagos (1,2), M. Victoria Leon (2), Sigmer Y Quiroga (3) & Alejandro Martinez (4)

(1.) Universidad Nacional de Colombia, Sede Caribe, Calle 25 No. 2-55 Santa Marta D.T.C.H., Colombia / Grupo de investigacion MIKU, Universidad del Magdalena, Carrera 32 No. 22-08, Santa Marta D.T.C.H., Colombia; anamilagos@gmail.com

(2.) Grupo de investigacion MIKU, Universidad del Magdalena, Carrera 32 No. 22- 08, Santa Marta D.T.C.H., Colombia; mvleon0221@gmail.com

(3.) Universidad del Magdalena. Facultad de Ciencias Basicas, Programa de Biologia Carrera 32 No 22-08, Santa Marta D.T.C.H., Colombia; yamuruk@gmail.com

(4.) Institute of Ecosystems Study, Italian National Research Council, Largo Tonolli 50, 38922, Verbania, Italy; amartinez.ull@gmail.com

Received 15-VIII-2017. Corrected 10-I-2018. Accepted 06-II-2018.

Caption: Fig. 1. Hesionides gohari: A. Dorsal view, D. Parapodium. Microphthalmus mahensi: B. Dorsal view, C. Detail of prostomium, E. Parapodium. Neogyptis mediterranea: F. Dorsal view, G-H. Parapodium. Nerilla mediterranea: I. Dorsal view, J. Detail of prostomium. Protodrilus cf. smithsoni: L. Dorsal view, K. Detail of prostomium.

Caption: Fig. 2. Pharyngocirrus cf. gabriellae: A. Dorsal view, C. Detail of the chaetae. Myrianida sp.: B. Dorsal view, D. Parapodium. Neopetitia amphophthalma: E. Dorsal view, G. Parapodium. Westheidesyllis gesae: F. Dorsal view, H. Parapodium. Syllis benelihuae: I. Anterior region, J. Detail of the pharynx, K. Parapodium.
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