Early Miocene coral reef-associated bryozoans from Colombia. Part I: Cyclostomata, “Anasca” and Cribrilinoidea Cheilostomata

Abstract. This is the first of two comprehensive taxonomic works on the early Miocene (ca. 23–20 Ma) bryozoan fauna associated with coral reefs from the Siamaná Formation, in the remote region of Cocinetas Basin in the La Guajira Peninsula, northern Colombia, southern Caribbean. Fifteen bryozoan species in 11 families are described, comprising two cyclostomes and 13 cheilostomes. Two cheilostome genera and seven species are new: Antropora guajirensis n. sp., Calpensia caribensis n. sp., Atoichos magnus n. gen. n. sp., Gymnophorella hadra n. gen. n. sp., Cribrilaria multicostata n. sp., Cribrilaria nixor n. sp., and Figularia bragai n. sp. Eight species are identified only at genus level and remain in open nomenclature. Of the species found, 27% have erect colonies and 73% encrusting colonies. Both types contributed to the reef framework and produced sediment. The observed bryozoan diversity was higher in the barrier reefs than in the lagoonal patch reefs.


Introduction
Within a generally high marine biodiversity (Jackson and Johnson, 2001;Buzas et al., 2002), bryozoan diversity in Cenozoic tropical latitudes was also very high . In the Caribbean, a notable increase of bryozoan species richness has been recorded since the Burdigalian (ca. 18 Ma) (Cheetham and Jackson, 1996;Cheetham et al., 1999;O'Dea et al., 2004;. However, reports of fossil bryozoans in tropical regions, especially in continental South America, remain sparse (Taylor et al., 2009;Zágoršek et al., 2014;Taylor and Waeschenbach, 2015;Ramalho et al., 2019). Diagenetic processes, which mainly affect bryozoans with aragonitic skeletons (Taylor et al., 2009), and several other factors, have undoubtedly biased against the fossil record of bryozoans in the Cenozoic tropics . In addition to the limited collection effort, small bryozoan colonies tended to be overlooked in the field and inventories are therefore largely incomplete. Consequently, taxonomic studies of bryozoan faunas from the early Miocene are generally limited not only for the Caribbean/Gulf of Mexico region (e.g., Sandberg, 1962;Cheetham et al., 1999Cheetham et al., , 2007Herrera-Cubilla and Jackson, 2014;, the western Atlantic (e.g., Zágoršek et al., 2014;Ramalho et al., 2015Ramalho et al., , 2017Ramalho et al., , 2019, or the Indo-Pacific (e.g., Li, 1990;Gopikrishna, 2005, 2007;Taylor, 2014, 2015), but also for the more thoroughly investigated Paratethys/Mediterranean Sea (e.g., Duvergier, 1920;Buge, 1973;Nikulina and Taylor, 2010;Vávra, 2012;. Despite their small size, bryozoans are a diverse group of invertebrates within marine benthic communities. Their distribution and species richness are related, in part, to the availability of hard substrata and habitat heterogeneity (Clarke and Lidgard, 2000). Coral reefs provide diverse surfaces for the settlement and growth of bryozoans, including cryptic habitats, such as caves, crevices, areas under coral colonies, rubble, and sand grains (Jackson and Winston, 1982;Choi, 1984;Ramalho et al., 2018). In addition, a high diversity of macroinvertebrates (e.g., sponges, crabs, and mollusk shells) are susceptible to colonization by bryozoans (e.g., Almeida et al., 2017;Di Martino et al., 2019). Although bryozoans are not the most abundant organisms in these tropical ecosystems in terms of biomass, their species diversity is relatively high (e.g., Santodomingo et al., 2015).
Several studies have focused on the characterization of bryozoans associated with modern coral reefs in the western central Atlantic region, and have addressed the ecological roles they play in these ecosystems (Cuffey and Kissling, 1973;Schopf, 1974;Cuffey and Fonda, 1977;Jackson and Winston, 1982;Choi, 1984;Winston, 1984Winston, , 1986Winston and Jackson, 1984;Jackson et al., 1985). However, comprehensive taxonomic studies of bryozoan faunas in ancient coral reefs remain scarce.
The most representative taxonomic works on Caribbean Miocene bryozoans were carried out by Bassler (1919, 1923) in the islands of Jamaica, Hispaniola, and Cuba, as well as in Costa Rica and the federal states of Maryland, Virginia, North Carolina, and Florida (USA); by McGuirt (1941) in Louisiana; by Scolaro (1968) and Di  in Florida; and by Cheetham et al. (1999) in the Dominican Republic and Panama. In Colombia, studies on fossil bryozoans are almost non-existent. Some work has been done on Devonian and Cretaceous samples (McNair, 1940;Jerez-Jaimes et al., 2013), and there are isolated mentions of "Sertella sp." and "Acanthodesia savartii form texturata" from the Miocene reefs in the oceanic island of Providencia (Buge in Geister, 1992).
The purpose of this paper is to: (1) describe the bryozoan species associated with shallow coral reefs in the Siamaná Formation (Aquitanian, ca. 23-20 Ma), thereby contributing to knowledge of bryozoan assemblages in the Caribbean Basin; (2) estimate the role played by bryozoans in reefs from the Siamaná Formation; and (3) identify the biogeographical patterns of the bryozoan fauna during the early Miocene in the southern Caribbean.

Materials and methods
The studied material was collected in the coral reef facies of the Siamaná Formation during two expeditions to the Cocinetas Basin carried out in 2011 and 2014. The bryozoan specimens were obtained from the surfaces of coral colonies and in the attached sediment. The coral samples were collected from seven stations along transects of 10 m ( Fig. 1; Table 1). These were washed and scrubbed with a soft brush; the residual sediment was wet-sieved over mesh-sizes of 250 and 63 μm. In some cases, the sediment was gently removed from the corals with a needle and a paintbrush to preserve erect bryozoan fragments. To separate the encrusting colonies from the large coral substrates, when possible, small fragments of the corals were cut using a motor tool. Bryozoan specimens were cleaned using an ultrasonic bath for a few seconds to a few minutes, depending on the fragility of the colony. Coated and uncoated Flórez et al.-Bryozoan diversity in Colombian fossil coral reefs specimens were examined with scanning electron microscopy (SEM) at the "Centro de Instrumentación Científica, Universidad de Granada," employing FEI Quanta 400 and FEI Qemscan 650F microscopes operating at low-and high-vacuum modes using backscattered and secondary electron detectors. Measurements of zooidal characters were made from SEM images using the image-processing program ImageJ (https://imagej.nih.gov/ ij) and are given in mm, including mean (X), observed range (R), standard deviation (SD), and the number of measurements (N) (see tables for each species). The systematic paleontology section of Cheilostomatida follows the interim classification compiled by D.P. Gordon for the Treatise on Invertebrate Paleontology (2011). A list of collected specimens included in this study with catalog numbers, locality names, station numbers, type of colony, substrate, and number of specimens available is provided in Appendix 1. Descriptions and illustrations of the ascophoran-grade cheilostomes mentioned in the "Remarks" will be part of a separate work currently in preparation.
Repositories and institutional abbreviations.
Description.-Colony erect with branches circular in cross section, ∼0.46 mm in diameter. Zooids cylindrical with openings arranged in somewhat alternating whorls all around the branch, zooidal boundaries marked by narrow, thread-like, grooves. Peristomes not preserved. Frontal surface smooth, undulose, covered by moderately spaced, rounded pseudopores. Axial lumen absent. Gonozooids not observed.
Remarks. -Canu and Bassler (1920, p. 734) expanded the genus Entalophora Lamouroux, 1821 to include erect cyclostomes with cylindrical branches and zooids arranged in all directions and lacking gonozooids. However, Walter (1970) showed that species of the genus Entalophora were characterized by branches with a narrow axial lumen and subtriangular gonozooids. Based on the absence of the axial lumen, we place this poorly preserved, single branch fragment in Mecynoecia sp. indet. The lack of preserved gonozooids means that species-level identification is problematic. Mecynoecia sp. indet. was found in the sediment cemented to the scleractinian coral Goniopora hilli Vaughan, 1919. Family Oncousoeciidae Canu, 1918Genus Oncousoecia Canu, 1918 Type species.-Oncousoecia lobulata Canu, 1918 from the British Isles, Recent; by subsequent designation (Taylor and Zatoń, 2008).
Description.-Colony encrusting with large zooids, arranged in uni-to biserial alternating rows. Branches straight to slightly curved, apparently bifurcating. Zooids tubular (mean L/W = 1.66); zooidal boundaries not clearly demarcated. Zooidal surface densely perforated by rounded pseudopores, sometimes with transverse striations. Peristomes rising almost perpendicularly to the zooidal surface, with presumably circular to oval apertures. Gonozooids not observed.
Remarks.-Based on the characters of the interzooidal avicularium and autozooids, we place this specimen in Copidozoum. Other species of Copidozoum recorded in American Miocene deposits include C. parvirostris (Canu and Bassler, 1923) and C. tenuirostris (Hincks, 1880).
Etymology.-Named after the La Guajira Peninsula, in reference to the region where it was collected for the first time, plus the Latin suffix -ensis, meaning originating in.
Description.-Colony erect, articulated. Branches narrow, quadriserial, squared in cross-section. Zooids arranged in four longitudinal rows, in alternate positions with their lateral neighbors. Zooids distinct, delimited by a slender groove, all similar in size, elongate and sub-rectangular in shape. Opesia oval, occupying most of the frontal surface. Gymnocyst smooth, extended proximally and reduced laterally and distally. Cryptocyst smooth, forming a rim around the opesia. Mural rim slightly raised. Two small, elliptical avicularia placed in the proximal corners of the gymnocyst of each zooid, with a circular rootlet pore below the raised rostrum. Autozooids located at the tip of the internode tapering proximally. Ooecium not observed.
Remarks.-The internode fragments available in our material are poorly preserved and lack ooecia, preventing species-level identification. However, they resemble Nellia tenella in the characteristic arrangement and shape of the autozooids and avicularia. The specimens from the Siamaná Formation are similar to those from the Miocene of the Dominican Republic  Winston and Cheetham (1984, fig. 2D). However, the size of the opesia in these fragments is smaller than those of the Dominican specimens, as well as the syntype (MNHN-IB-2008-4546), and other specimens from different regions and ages (Cheetham, 1963(Cheetham, , 1966Winston et al., 2014;. Although Winston and Cheetham (1984) suggested that the variation in size is not significant, and proposed to consider N. tenella as a living fossil, based on the results of the statistical analyses performed on specimens ranging from the Late Cretaceous to the Recent, certain characters, which could reveal differences between localities and periods, such as ooecium morphology, have seldom been recorded. New fossil collections and phylogenetic studies using Recent material are needed to confirm its living-fossil status or to reveal that it is a species complex. "Nellia tenella" was very common in the Miocene (Winston and Cheetham, 1984). Its Recent distribution is circumtropical to subtropical and it has been recorded on coral reefs (Winston, 1986). In the Siamaná Formation, N. cf. N. tenella was found in the sediment cemented to the scleractinian coral Goniopora hilli, co-occurring with the bryozoan Poricellaria sp. (as also observed in other fossil and recent localities and environments, e.g., intertidal rocks; Winston and Cheetham, 1984), Margaretta sp., Ditaxiporina sp., and Mecynoecia sp.   Licornia sp. indet. Figure 4.4-4.8; Table 7 Occurrence.-Early Miocene, Siamaná Formation, Arroyo Ekieps, Colombia.
Description.-Colony erect, articulated. Branches flat, elliptical in cross-section. Zooids distinct, biserial, alternately arranged, sub-rectangular in shape (mean L/W = 2.97). Opesia oval, with a raised mural rim, occupying two-thirds of the frontal surface. ?Two distal spine bases. Base of the scutum arising from the distal third of the inner side of the opesia, next to the frontal avicularium of the adjacent zooid. Gymnocyst smooth, well developed proximally, tapering laterally and distally around the opesia. Avicularia adventitious, frontal, and lateral; frontal avicularia placed proximally immediately below the rim of the opesia, monomorphic, frequent, with a proximally raised, rounded rostrum, proximolaterally directed towards the exterior; lateral avicularia smaller than frontal avicularia, located on the outer distal corner of each autozooid, triangular. Abfrontal surface smooth. Vibracular chamber trapezoidal with rhizoidal pore and straight setal groove, directed obliquely to the internodal axis, occupying two-thirds of the length of the vibracular chamber. Nodal joints crossing the proximal opesia of the outer zooids and below the opesia of the inner zooids at the bifurcation. Single axial vibraculum in the bifurcation, with straight setal groove and lacking a rhizoidal pore. Ooecium not observed. Scutum and spines not preserved.
Remarks.-We place these specimens in the genus Licornia based on the position of the joint crossings, the straight rostrum of the lateral avicularia, the oblique setal groove of the vibracular chambers, and the single axial vibraculum. The closest allied genus, Paralicornia Vieira et al., 2014, differs in having an opesia occupying only half of the total length of the zooids and a shorter setal groove.
North American Cenozoic species of Licornia include Canu and Bassler's (1920) L. cookei, L. milneri, and L. resseri, all known from the Oligocene. Licornia sp. indet. differs from these species in the morphology and size of the frontal and lateral avicularia: L. cookei has rounded lateral avicularia, L. milneri has very large and acuminate frontal avicularia, and L. resseri has very large lateral avicularia. Licornia regularis (Osburn, 1940), known in the Caribbean region from the Pleistocene to Recent, differs in having larger vibracular chambers reaching half of the total length of the zooids, frontal avicularia with triangular rostrum, lateral avicularia with serrated rostrum, and squatter zooids (Winston, 2005, p. 27, figs. 63-68). Other Recent tropical Western Atlantic species, such as L. drachi (Marcus, 1955) and L. micheli (Marcus, 1955), differ from Licornia sp. indet. in having a larger opesia that covers almost the whole frontal surface of the zooids, and lateral avicularia of variable size, sometimes as long as the opesia.
Description.-Colony encrusting, multiserial, unilaminar. Zooids separated by a suture on a raised mural rim, elongate and sub-rectangular in shape (mean L/W = 1.58), widening at about mid-length and arranged in alternating, longitudinal rows. Orifice terminal, semicircular with a straight proximal margin; opercular region slightly developed. Cryptocyst flat proximally, depressed towards the opesiular area at about two-thirds of zooidal length, and raised distally; granular surface, densely and evenly perforated with up to ∼110-120 circular pseudopores, absent in the area surrounding the opesia and between the opesia and the opesiules; pseudopores ∼5 μm in diameter. Mural rim raised and crenulated. Two elliptical opesiules, longer than wide, equal in size, located proximolaterally at about two-thirds of zooidal length, ∼0.14 mm below the opesia.
Etymology.-From the Caribbean Sea, in reference to the biogeographic region that the new species inhabited, plus the Latin suffix -ensis meaning originating in.  Remarks.-The specimens of Calpensia caribensis n. sp. found in the Siamaná Formation resemble specimens of the Recent Mediterranean Calpensia nobilis (Esper, 1797). Calpensia nobilis is commonly found in the late Miocene to the Recent of the Mediterranean (Hayward and McKinney, 2002;Moissette et al., 2007). Canu and Bassler (1923) identified specimens of Calpensia as C. impressa (Moll, 1803) in the Oligocene of the southern Caribbean, which were subsequently attributed to C. nobilis by Buge (1957). The new species is similar to Mediterranean specimens of C. nobilis in the size of the opesia and opesiules (Hayward and McKinney, 2002, p. 31, fig. 13 a-c), as well as in the mean ratios of opesia length/zooid length (0.13 vs. 0.12), and opesia width/ zooid width (0.36 vs. 0.39). However, C. caribensis n. sp. has squatter autozooids (zooid length 0.67 mm vs. 0.82 mm; zooid width 0.43 mm vs. 0.38 mm). Although Canu and Bassler (1930) and Buge (1957) reported wide variations of the size of the zooids in this species, the mean ratio of zooid length/ zooid width between our specimens and Recent material differs greatly (1.58 vs. 2.15), indicating a different zooidal shape. In addition, the Siamaná Formation specimens have a greater number of pseudopores in the cryptocyst (almost twice as many; mean of pores number 116 vs. 61). Based on these differences, as well as the spatial and temporal distance between the two populations, we introduce this new species.
In the Siamaná Formation, Calpensia caribensis n. sp. was found encrusting coralline algae covering the coral Alveopora tampae and on the basal surface of the coral Colpophyllia willoughbiensis, while small detached fragments were scattered in the sediment associated with Goniopora hilli. In our material, Calpensia caribensis n. sp. co-occurs with Copidozoum sp., Gemelliporidra sp., and Rhynchozoon sp.
Diagnosis.-As the type species by monotypy.
Etymology.-From the Greek privative prefix a-and toichos (masculine), meaning wall, alluding to the absence of a raised mural rim surrounding the autozooids.
Remarks.-We place Atoichos n. gen. in the family Onychocellidae because of its extensive cryptocyst, the bell-shaped opesia with opesiular identations, the probable presence of vicarious avicularia, and the absence of a gymnocyst and spines . Atoichos n. gen. resembles in general appearance the genus Steraechmella Lagaaij, 1952, belonging to the family Microporidae Gray, 1848, which is commonly allied with Onychocellidae . It differs in having wider opesia and, as in remaining genera of this family, in lacking a raised margin around the proximal two-thirds of the zooid. The poor preservation of the single specimen available prevents a detailed description of the morphology of the putative vicarious avicularia (i.e., opesia and rostrum), which could alternatively be narrower autozooids placed at row bifurcations where two regular zooids sometimes occupy the same width of the one preceding them in the row. However, as observed in some calloporids in the studies carried out by Cook (1968) on the Recent genus Crassimarginatella Canu, 1900 and by Cheetham et al. (2006) on the fossil genus Wilbertopora Cheetham, 1954, the morphology of avicularia is variable, some involving only slight modifications of the autozooids. In some onychocellids (e.g., Euritina Canu, 1900) interzooidal avicularia are similar to autozooids, although smaller (Taylor et al., , p. 1676, fig. 10).
Diagnosis.-Colony encrusting, multiserial, uni-to multilaminar. Zooids rhomboidal to elliptical, defined by a raised opesial margin distally and a deep groove proximolaterally. Opesia terminal, triangular to bell-shaped, as long as wide, occupying the distal third of the frontal surface; opesiular indentations shallow; proximal edge projected, straight to slightly curved. Cryptocyst extensive, granular, flat to slightly convex. Gymnocyst absent. Putative vicarious avicularia narrower than regular zooids; rounded triangular, commonly located at row bifurcations; opesia poorly preserved. Ovicells unknown.
Description.-Colony encrusting, multiserial, uni-to multilaminar. Early astogenetic stages apparently fan-shaped. Zooids distinct, elongate, rhomboidal, to elliptical (mean L/W = 1.74), separated distally by a raised opesial margin, and a fine and deep groove proximo-laterally. Opesia terminal, wide, Flórez et al.-Bryozoan diversity in Colombian fossil coral reefs triangular to bell-shaped, as long as wide; borders raised forming a lateral furrow between the opesia margin and the adjacent zooids; opesiular indentations located at the proximolateral corners, slightly constricted laterally, proximal edge projecting distally with straight to slightly concave margin. Cryptocyst granular, occupying two-thirds of the frontal surface, flat to slightly convex, narrow laterally to the opesia. Putative vicarious avicularia narrower and slightly shorter than ordinary feeding zooids, rounded triangular, commonly located at longitudinal row bifurcations; opesia poorly preserved, ?oval, occupying more than half of the frontal surface, rostrum extended but broken, observed only twice, probably rounded ( Fig. 5.4). Ovicells not observed.
Etymology.-From the Latin magnus, large, in reference to the large size of the autozooids.
Remarks.-The single colony found in the Siamaná Formation exhibits signs of dissolution. However, its morphological features are well preserved enough to allow comparisons with other genera and species in the family Onychocellidae. Atoichos magnus n. gen. n. sp. resembles species of Aechmella Bassler, 1917 andAechmellina Taylor, Marta, and. Aechmella differs in having smaller interzooidal avicularia, about half the width of the zooids with an acutely triangular rostrum, while Aechmellina differs in having frequent, small interzooidal avicularia with a pointed rostrum. Atoichos magnus n. gen. n. sp. also resembles Floridinella vicksburgica Canu and Bassler, 1917 in having a wide opesia, but differs in having kenozooids and avicularia with a triangular rostrum oriented laterally (Cook and Bock, 2001, p. 547). In the Siamaná Formation, Atoichos magnus n. gen. n. sp. was found encrusting a mollusk shell, sharing the substrate with Glabrilaria sp. indet. and a poorly preserved cyclostome.
Description.-Colony encrusting, multiserial, unilaminar. Zooids defined by a raised rim, sub-hexagonal, rounded distally (mean L/W = 1.32). Opesia subterminal, bell-shaped, with proximolateral indentations outlining a tongue-like process medially, occupying half to one-third of the total length of the zooid. Cryptocyst extensive, depressed, flat, and coarsely granular. Vicarious avicularia symmetrical, similar in length to autozooids, but about half of their width, rounded rhomboidal; opesia reversed pear-shaped; cryptocyst granular. Ovicellate zooids with the distal edge formed by the 'cryptocyst' of the distal zooid; fertile zooids slightly longer than non-fertile autozooids. Remarks.-Among genera of the family Onychocellidae, our specimen fits better in the genus Smittipora because of the symmetrical and rounded rostrum of its avicularia (Taylor et al., , p. 1702. Although some similarities in the general morphology of the zooid can be found also with species of the genus Floridina Jullien, 1882, this latter genus differs in having acutely triangular rostra, as well as deep opesiular indentations, resulting in a more trifoliate opesia with lateral constrictions (Taylor et al., , p. 1678. Three species of Smittipora have been described from the North American Oligocene and two from the Miocene: S. fusiformis (Canu and Bassler, 1917), S. lineata (Canu and Bassler, 1920), S. tenuis (Canu and Bassler, 1920), S. levinseni (Canu and Bassler, 1917), and S. elongata (Canu and Bassler, 1923), respectively. The Oligocene species differ from Smittipora sp. indet. in having exclusively fusiform avicularia; S. levinseni, from the early Miocene to Recent, has smaller zooids and avicularia (Di . Smittipora elongata from the late Miocene lacks proximolateral indentations and a tongue-like medial process on the opesia proximal border. Our specimen also resembles the Cretaceous species Reptolunulites zipfi Taylor and McKinney, 2006 in having a bell-shaped opesia and symmetrical vicarious avicularia, but it differs in having a longer rostrum and a higher ratio between the length of the opesia and the length of the zooid. In the Siamaná Formation, Smittipora sp. indet. was found encrusting coralline algae covering the coral Porites sp., co-occurring with the ascophoran-grade cheilostome Hippopleurifera sp. and an undetermined cheilostome.
Diagnosis.-As the type species by monotypy.
Etymology.-From the Greek gymno-, referring to the gymnocystal calcification that can form in anascan-grade bryozoans in the frontal wall between the frontal membrane and the free edges of the vertical walls, and -phor meaning carrier, alluding to the presence of a gymnocyst in this Steginoporella-like genus, plus the suffix -ella commonly used in bryozoan names.
Remarks.-Specimens of Gymnophorella n. gen. from the Siamaná Formation are similar to the fossil morphospecies "Steginoporella" cornuta (Osburn, 1950) recorded by Cheetham et al. (1999) Winston et al., 2014, p. 147, fig. 5). They all have a narrow band of gymnocyst, more developed proximally, surrounding the cryptocyst and the opesia, a pair of conspicuous tubercles placed at the distal corners of the opesia, and similar shape of the opesia and opesiular indentations. However, in the original description of S. cornuta, Osburn (1950, p. 108, pl. 12, figs. 3-6) made no mention of the presence of a gymnocyst, which is effectively absent in the holotype (SBMNH 635758, Fig. 7.1, 7.2), but present in a paratype (SBMNH 636427, Fig. 7.3, 7.4). In addition, Osburn (1950) described B-zooids, also present in "Steginoporella" cornuta from the Pliocene of Panama (Cheetham and Jackson, 2000), but these were not observed or preserved in the material from the Siamaná Formation. On the other hand, the Siamaná specimens differ from S. evelinae in having an extended gymnocyst and an evenly granular cryptocyst. The family Steginoporellidae includes to date six genera, of which only Siphonoporella Hincks, 1880 develops a narrow gymnocyst, and has no avicularia or B-zooids (e.g., S. nodosa Hincks, 1880 and S. delicatissima [Busk, 1861]). However, this genus differs from Gymnophorella n. gen. in having a lightly calcified skeleton and a very obvious polypide tube (Cook et al., 2018, p. 96). Because Steginoporella sensu stricto lacks a gymnocyst (Harmer, 1926, p. 268;Gordon, 1984, p. 56), we introduce this new genus, and we place it in the family Steginoporellidae owing to its close resemblance with those (morpho-) species of Steginoporella and Siphonoporella discussed above. However, Gymnophorella n. gen. is also similar to some members of Cymuloporidae Winston and Vieira, 2013, Electridae d'Orbigny, 1852(e.g., Pyripora magna Larwood, 1973, and Calloporidae Norman, 1903(e.g., Tylopora Lang, 1917 in having oligoserial colonies, and in the morphology of the autozooids showing a well-developed gymnocyst. It differs in having deep opesiular indentations outlining a tongue-like process medially. In addition, Cymuloporidae have colonies exclusively uniserial, and opesia occupying the distal half of the zooid total length; P. magna has a reduced cryptocyst and larger opesiae; and Tylopora spp. has ovicells, avicularia, and sometimes spines on the cryptocyst. Although the paratype of the Recent Pacific species "Steginoporella cornuta" (SBMNH 636427) exhibits some morphological differences compared to the holotype, and it is likely a new species, its description is not within the objectives of this paper.

Gymnophorella hadra new species
Figures 7.5, 8; Table 11 Holotype.  Cryptocyst granular, unperforated, slightly concave, occupying three-quarters of the zooidal length, surrounded by a raised oval rim that is constricted in the distal opercular region. Gymnocyst relatively extensive, smooth, slightly convex, surrounding the cryptocyst and the opesia, without edges between distal and proximal zooids, more extended proximally in early astogeny. B-zooids seemingly absent. Arrangement uni-and biserial in early astogeny. Kenozooids frequent in multiserial colonies.
Description.-Colony encrusting, unilaminar, uni-to biserial in early astogeny and multiserial in the advanced stages. Bifurcation of the bi-and triserial sections at angles of ∼45°. Zooids oval to elliptical, separated laterally by a fine groove (mean L/W = 1.68). Opesia terminal, trifoliate, with large opesiular indentations proximally outlining a tongue-shaped process placed medially. Tubercles prominent, blunt, ovate to Journal of Paleontology 95(4):694-719 elliptic in cross-section, placed laterodistally on each side of the opesia. Cryptocyst extensive and granular, slightly concave, surrounded by a raised mural rim, commonly with intramural buds, occupying three-quarters of the zooid length and being distinctly constricted in the distal opercular region. Gymnocyst smooth, slightly convex, surrounding the cryptocyst and the opesia, extending continually between zooids of the same row except in some bifurcations, more extended in early astogeny and the proximal part of the zooid. Kenozooids frequent in the multiserial stages: triangular, elliptical, or similar in shape to the zooids. Polypide tube and rosette-plates not observed.
Etymology.-From the Greek hadros, meaning well developed, declined in accordance to the gender of the genus, which is feminine, in reference to the well-developed gymnocyst differentiating this genus from other Steginoporellidae.
Remarks.-The absence of B-zooids in the material found in the Siamaná Formation may be a bias related to the limited number of colonies available. For instance, in Steginoporella evelinae, the B-zooids are infrequent and similar in size and shape to the A-zooids . In the Siamaná Formation, Gymnophorella hadra n. gen. n. sp. was found growing over coral rubble of Porites sp., covered by coralline algae, and sharing the substrate with Antropora guajirensis n. sp., Cribrilaria sp., ?Hippopleurifera sp. 1, and Escharoides sp.
Avicularia adventitious, small, placed on the proximal gymnocyst of each autozooid, rostrum acute and rounded, proximolaterally directed, pivotal bar absent or not preserved. Ovicells not observed.
Remarks.-Only two broken and recrystallized fragments were found in the samples. However, the inclined zooids with the oblique opesia and slit-like opesiule, as well as the avicularia placed on the gymnocyst of each autozooid, are features diagnostic of the genus Poricellaria (Harmer, 1926, p. 313). Nine species of this genus are known worldwide; among these, only Poricellaria vernoni Cheetham, 1963 is known from North America. This species from the Oligocene of Florida differs from Poricellaria sp. indet. in having a finely perforate cryptocyst. Cheetham (1973) found a specimen of Poricellaria in the Caribbean Miocene, which he identified as P. aff. ratoniensis; subsequently, Cheetham et al. (1999) reported it as Poricellaria new species 1 (figured in NMiTA Database, 1996-2016) from the Miocene (ca. 15.7-3.9 Ma) of the Dominican Republic. Although the Siamaná material resembles the species found by Cheetham et al. (1999), even in the size of the zooids, the poor preservation and scarcity of specimens preclude any further comparison and the description of a new species. In the Siamaná Formation, Poricellaria sp. indet. was found in the sediment attached to the coral Goniopora hilli, co-occurring with the bryozoan Nellia cf. N. tenella, as is common in other fossil localities and environments (Winston and Cheetham, 1984), as well as Margaretta sp., Ditaxiporina sp., and Mecynoecia sp.
Description.-Colony unilaminar, forming extensive and irregular encrustations. Zooids oval to rhomboidal, distinctly separated by deep grooves, longer than wide (mean L/W = 1.17). Orifice transversely D-shaped, bearing five spine bases in non-ovicellate zooids and four in ovicellate zooids, proximal border thick and straight. Frontal shield extensive and convex, formed by 13-17 slender costae; first pair of costae forming a 'V'-area with a large lacuna visible in some zooids, obliterated by sediment in others; five to six intercostal pores. Gymnocyst narrow. Interzooidal avicularia frequent, large, placed on a rhombic cystid with a well-developed gymnocyst; rostrum flared at the tip with slightly narrow middle portion, oriented distally. Ovicell type A of Bishop and Househam (1987), wider than long; ooecium surface smooth and with a median umbo or keel, not punctate.
Etymology.-From the Latin multus, meaning many, and costa, meaning rib in reference to the greater number of costae that distinguish this species from other Cribrilaria spp. with flared avicularia, plus the suffix -ata, pertaining to.
Remarks.-Two fossil species of Cribrilaria from North America, both from the early Oligocene, are known: Cribrilaria anaticula Canu and Bassler, 1920 and Cribrilaria carolinensis Gabb and Horn, 1862. They resemble Cribrilaria multicostata n. sp. in having five oral spines and large interzooidal avicularia. However, C. multicostata differs from both in having avicularia with a flared rostrum. Nine Recent Cribrilaria morphospecies are described in the literature having avicularia  (Harmelin, 2006), seven of them at species level: C. flabellifera (Kirkpatrick, 1888) and C. vaceleti (Harmelin, 2006) from the Indo-Pacific; C. arrecta Bishop andHouseham, 1987, C. atlantis (Harmelin, 2006), C. macaronensis (Harmelin, 2006), and C. mikelae (Harmelin, 2006) from the central Atlantic and Mediterranean Sea; and C. smitti (Winston, 2005) from Florida and the Caribbean. Cribrilaria multicostata n. sp. is distinguishable from all of these by having a greater number of costae, up to 17 instead of 5-12, and five oral spines instead of six or seven (except in C. mikelae, which also bears five). Cribrilaria smitti, the geographically closest congener, differs also in having the first pair of costae more pronounced, leaving a wider space between it and the orifice, where it develops a bifid median umbo. In the Siamaná Formation, Cribrilaria multicostata n. sp. was found encrusting the surface of the coral Acropora panamensis, co-occurring with the bryozoans Cribrilaria nixor n. sp., Poricella sp., Hippoporina sp., and ? Hippopleurifera sp. 2.
Description.-Colony encrusting, multiserial, unilaminar. Zooids ovate to elliptical, distinctly separated by shallow grooves (mean L/W = 1.21). Orifice semicircular, wider than long; proximal border straight, formed by a thin bar. Five oral spine bases in non-ovicellate zooids and four in ovicellate zooids. Frontal shield extensive, slightly convex to flat, formed by 17-22 slender costae, tapering at the distal end, and fusing in the middle line. Costae separated by two to five circular intercostal pores. Suboral lacuna broad, elliptic, flanked by the first pair of costae forming a 'V'. Gymnocyst very narrow. Interzooidal avicularia frequent, rostrum long and slender, cystid rhombic with a well-developed gymnocyst, oriented distally, sometimes lying on the frontal shield of the distal zooid, opesia oval. Ooecium type A and B (Bishop and Househam, 1987), longer than wide, surface smooth, not punctate, and with a median keel. Kenozooids present.
Etymology.-From the Latin nixor, meaning leaning against, and used as a name in apposition, in reference to the interzooidal avicularia that lean against the frontal shield of the distal autozooids.
Remarks.-Although a single colony is available for this species, several features (e.g., the number of costae, length of the zooids, type of ovicell budding from a kenozooid [type B], wider avicularian opesia, and long and slender rostrum) allow Cribrilaria nixor n. sp. to be distinguished from Cribrilaria multicostata n. sp. occurring in the same deposits. Cribrilaria nixor n. sp. differs from Cribrilaria anaticula and Cribrilaria carolinensis, both recorded in the early Oligocene of North America (Canu and Bassler, 1920, p. 297), in having a greater number of costae (17-22 vs. 10-12) and in the shape of the avicularian rostrum, which is duck beak-shaped in C. anaticula, or thin and channeled in C. carolinensis. In the Siamaná Formation, Cribrilaria nixor n. sp. was found encrusting the surface of the coral Acropora panamensis, co-occurring with the bryozoans C. multicostata n. sp., Poricella sp., Hippoporina sp., and ?Hippopleurifera sp. 2.

Genus Figularia Jullien, 1886
Type species.-Lepralia figularis Johnston, 1847 from Cornwall, United Kingdom, Recent; by original designation. Figure 11.1-11.5; Table 15 Holotype  Martino and Taylor, 2015 in the size of zooids, number of costae, position of the pelma, and the morphology of the ooecium. However, the latter species has putative vicarious avicularia similar to autozooids, and two lateral oral spine bases, which are diagnostic of the genus Filaguria Moyano, 1991 and absent in the Colombian material. However, in Figularia bragai n. sp. we observed a single polymorph, which can be interpreted either as a putative vicarious avicularium with spoon-shaped rostrum and complete cross-bar, or as a malformed autozooid with broken costate shield, constricted between two neighboring zooids with reversed polarity. Vicarious avicularia with a spoon-shaped rostrum have been described for several species of Figularia: the Recent species F. fissa (Hincks, 1880) and F. fissurata Canu and Bassler, 1929, and Miocene species F. rhodanica Li, 1990 (see Li, 1990, pl. 2, fig. 11), but they all differ from the new species in the number of costae, number and size of pelmata, and/or characters of the ooecium (Rosso et al., 2020).  Bassler, 1928, andFigularia contraria Lagaaij, 1963, in the number of costae and size of the zooids and opesiae; the former species has six pairs of costae, and larger zooids (1.5 mm long, 1.0 mm wide); while the latter species has 8-11, more commonly nine, costae and a distinctly smaller opesia in ovicellate zooids. The absence of a pelma and proximal and lateral gymnocyst in the species described and figured by Canu and Bassler (1920, p. 316, pl. 43, fig. 9) as ?Figularia crassicostulata (Canu and Bassler, 1920) from the late Eocene of North America suggests that this specimen does not belong to the genus Figularia (Rosso et al., 2020). In the Siamaná Formation, F. bragai n. sp. was found encrusting the underside of the coral Colpophyllia willoughbiensis as well as the lateral surface of Porites baracoaensis Vaughan, 1919 and Acropora sp., sharing the substrate with an undetermined Cribrilinidae, ?Hippopleurifera sp. 2, Gemelliporidra sp., and ?Hippomenella sp.
Description.-Colony encrusting, unilaminar. Zooids oval and small (mean L/W = 1.36). Orifice terminal, transversely D-shaped, bearing six to seven spine bases in non-ovicellate zooids. Gymnocyst very narrow, developed proximally and laterally. Frontal shield formed by 13-15 costal ridges, fused in the middle line without forming a median suture or umbo. Between the costae, five or six lacunae are visible. A pair of small adventitious avicularia with a triangular rostrum located on each side of the orifice of ovicellate zooids, oriented distally; rostrum small, raised at its distal end. Ooecium globular, produced by the distal kenozooid, apparently with a proximo-median umbo or keel. Kenozooids present. Ancestrula not preserved.
Remarks.-Ten species of Glabrilaria have been recognized to date. Among them, the Mediterranean Glabrilaria pedunculata (Gautier, 1956) has the oldest record, ranging from the late Miocene (Pouyet, 2000) to the Recent. In the American continent, two Recent species, Glabrilaria hirsuta Rosso in Rosso et al., 2018 andGlabrilaria polita Rosso in Rosso et al., 2018, have been recorded in the deep waters of the central West Atlantic, associated with coral fragments (Rosso et al., 2018). The Siamaná species differs from G. pedunculata and G. polita in having 6-7 (and not five) oral spine bases in non-ovicellate zooids. Although G. hirsuta also has seven oral spines, it differs from the present material in having on average a greater number of costae (13-15 vs. 14-18) and a larger ooecium. However, the Siamaná colony is too small and poorly preserved to observe the characteristic spiny ornamentation, the transversal processes of the ooecia, and/or the clustering of kenozooids typical of G. hirsuta (Rosso et al., 2018). Owing to these reasons, we prefer to keep this species in open nomenclature. In the Siamaná Formation Glabrilaria sp. indet. was found encrusting a mollusk shell, sharing the substrate with Atoichos magnus n. gen. n. sp. and a poorly preserved cyclostome.

Discussion
The majority of the bryozoan species described here are cheilostomes (87%), among which the family Cribrilinidae, with four species, is the most diverse, as already observed in shallow-and deep-water ecosystems with carbonate substrates, both fossil and Recent (Winston, 2016). The family Onychocellidae is represented by two species, while the remaining nine families are represented by only one species each. Only two species, both left in open nomenclature, are cyclostomes (13%).
The remaining species (53%) are left in open nomenclature owing to their poor preservation, the absence of diagnostic features as gonozooids or ovicells, or the scarcity of available material. Species with erect colonies were commonly found only as small branch fragments, while for those with encrusting colonies only a few autozooids were recorded.
In the assemblage, 73% of the species have encrusting colonies, 20% have erect articulated colonies, and the remaining 7% have erected rigid colonies. The dominance of encrusting forms is a typical pattern in coral reef environments, favored by the availability of hard substrates (Winston, 1986;Hamdane and Moissette, 2002;Cuffey, 2011). By contrast, taxa with freeliving colonies, which in the Caribbean region are diverse and abundant from the middle Miocene (from ca. 15 Ma) to the Recent (Cheetham and Jackson, 2000;Flórez et al., 2007;O'Dea, 2009) are absent in the material studied here. This is probably a sampling/environmental bias with the collection focused on the reef framework, whereas free-living bryozoans In the Siamaná Formation, encrusting bryozoans were found on the bases and undersurfaces of scleractinian corals (e.g., Alveopora tampae, Acropora panamensis, Colpophyllia willoughbiensis, Porites baracoaensis, Acropora sp., and Porites sp.), as well as on coralline algae that covered the coral rubble, and on mollusk shells. On the other hand, the erect articulated species were found in the sediment attached to the bases and inter-branch spaces of corals such as Goniopora (1) close-up of a non-ovicellate autozooid, showing the orifice shape, oral spine bases, and pore chamber windows, (2, 3) close-up of ovicellate zooids with paired latero-oral avicularia, (4) detail of a kenozooid. All specimens are from the Siamaná Formation, Arroyo Ekieps locality. Scale bars are (1) 0.1 mm; (2, 3) 0.15 mm; (4) 0.25 mm.
Most species were found at the locality Arroyo Ekieps (80%), whereas at Arroyo Uitpa only Antropora guajirensis n. sp., Smittipora sp. indet., and Gymnophorella hadra n. gen. n. sp. were recorded (20%). In both cases, the species were exclusive of the locality. The Arroyo Uitpa paleoenvironment was characterized by patch reefs developed in a shallow lagoon close to the shore-line, while Arroyo Ekieps was a barrier reef system (Flórez et al., 2019a, b;and unpublished data), which offered a wide variety of microhabitats enhanced by the structural complexity of the reef framework. This suggests an increase of bryozoan diversity with higher reef complexity, as has been observed in modern reefs off Andros and Eleuthera in the Bahamas (Cuffey and Fonda, 1977).
In the Siamaná Formation, cryptic encrusting bryozoan colonies contribute to the fill of cavities reinforcing the reef framework, and articulated colonies contribute to production of sediment, in accordance with the role of bryozoans in fossil and modern coral reef building in tropical shallow waters (Cuffey, 1977(Cuffey, , 2011Insalaco, 1998;Taylor and James, 2013;Ramalho et al., 2018).