Carlgren’s hesitation allayed: redescription and systematics of Heteranthus verruculatus Klunzinger, 1877 (Cnidaria, Actiniaria), with a redefinition of Heteranthidae Carlgren, 1900 Author Yap, Nicholas Wei Liang Author Quek, Zheng Bin Randolph Author Tan, Ria Author Nugroho, Dharma Arif Author Lee, Jen Nie Author Lee Berumen, Michael Author Tan, Koh Siang Author Huang, Danwei text Contributions to Zoology 2021 2020-11-27 90 2 155 182 http://dx.doi.org/10.1163/18759866-bja10015 journal article 268186 10.1163/18759866-BJA10015 ef0a5d8c-febb-411a-ba02-ba847d325c93 1875-9866 8343299 Heteranthus verruculatus Klunzinger, 1877 figs. 2–10 Heteranthus verruculatus Klunzinger, 1877: 84 (original description); Carlgren, 1900: 92 ; Stephenson, 1922: 290 ; Carlgren, 1943: 31 ; Carlgren, 1949: 75 ; Cutress, 1977: 138 ; den Hartog, 1997: 358 ; Fautin et al., 2008: 52 ; Fautin, 2016: 416 Actinothrix verruculata : Andres, 1883: 509 Heteranthus verriculatus [no author]: Carlgren, 1943: 32 Heteranthus insignis Carlgren, 1943: 30 (original description); Carlgren, 1950: 440 ; Fautin, 2016: 275 NEW SYNONYMY Heteranthus sp. : González-Muñoz et al., 2015: 3 ; Brugler et al., 2018: 10 Material examined (*- observed alive by the first author) ( table S2 ). Indian Ocean. – Oman , Bar Al Hikan Peninsula ( UFM 4220 x2); Western Australia , Perth , Rottnest Island : Radar Reef ( WAM Z33600 x1; WAM Z33604 x6), Cape Vlamingh ( WAM Z33601 x3). Western Pacific Ocean. – Singapore : Cyrene Reef (ZRC.CNI.0496 x2; ZRC.CNI.0505 x8; ZRC. CNI.0506 x3; ZRC.CNI.0507 x17; ZRC.CNI.0583 x3; ZRC.CNI.1207 x8*; ZRC.CNI.1230 x>50*; ZRC.CNI.1367 x18*), Pulau Jong (ZRC.CNI.1368 x>35*), Pulau Tekukor (photograph only), RafflesLighthouse(photographonly); Indonesia (Pulau Ambon): Latuhalat (RCLA.Cni.004 x3*), Tial (RCLA.Cni.003 x4*, RCLA.Cni.008 x2*); Eastern Australia : Low Isle on Snapper Island, Great Barrier Reef (NHM 1954.6.28.23 x1), Moreton Bay (MTQ-G59967 x2; MTQ-G59968 x3; MTQ-G59391 x21; MTQ-G59392 x1), Mystic Sands, Townsville (MTQ-G59393 x5). South Pacific Ocean. – French Polynesian Islands, Mangareva, Rikitea (MNHN-IK-2019-8 x3). Nomenclatural considerations and type material examined. Both Fautin et al. (2008: 52) and Fautin (2016: 416) listed two syntypes of H. verruculatus : the first is a nearly complete polyp that is kept in Berlin(ZMB 1852),while the second is a small fragment of a syntype , kept in Stockholm (NRS 4861). Regarding the latter, it has a recent label indicating that the sample was collected by ‘ Stuhlmann’ between ‘1888– 1889,’ from ‘ East-Africa , Sansibar , Kokotoni, S of Insel Puopo. Rock.’ This recent label is almost certainly an error. Despite these two syntype lots being kept in separate museums, they are not of different individuals; the fragment present in Stockholm is from the same individual present in Berlin , therefore only one syntype specimen exists instead of two. While Carlgren’s (1900) publication dealt with material collected by Stuhlmann from East Africa, it also presented diagnoses of Heteranthidae and Heteranthus . Carlgren (1900: 92) did not report any species of the genus collected from that locality and explicitly states that, “ … Heteranthus KLUNZ. mit nur einer Spezies, H.verruculatus . Diese Spezies ist nicht in der STUHLMANN’schen Sammlung enthalten,”. In other words, Carlgren did not find Heteranthus individuals from East Africa in Stuhlmann’s collection. We infer that Carlgren’s (1900) inclusion of the diagnoses served to facilitate discussion regarding East African Phymanthus specimens, which he described in detail in his publication. Older labels within lot NRS 4861 provided further support that this fragment is part of the syntype kept in Berlin . Though faded, one label has the number “1852,” written on it, which corresponds to the catalogue number present on the old label of the Berlin specimen ( fig. 2A ). Other older labels, likely written by Carlgren himself, indicate that the fragment was from “ Röda havet ” [= Red Sea ], and “Klunz orig!”. In addition, the NRS fragment corresponds to the position of the missing slice of ZMB 1852, though slightly smaller in width, with the oral disc and actinopharynx absent; presumably Carlgren had prepared histological slides from the NRS material (see Carlgren, 1950 ). This confirms that the H. verruculatus fragment numbered NRS 4861 is part of the syntype ZMB 1852. We hereby designate both ZMB 1852 and NRS 4861, previously considered as separate syntypes but now found to be of the same syntype specimen, as the lectotype for the name Heteranthus verruculatus Klunzinger, 1877 (Code Article 74), to enhance its nomenclatural objectivity. While C.B. Klunzinger described the species from more than one individual that he had collected from Egypt ( Klunzinger, 1877 ; Fautin, 2016 ), the first author was not able to locate any other syntypes at museums where Klunzinger’s specimens are now kept, or in those that O. Carlgren have visited and possibly transferred some. Should these other syntypes be found, they are the paralectotypes of H. verruculatus (Code Article 74.1.3). In this publication, all three conditions stipulating the designation of a lectotype after 1999 have been met (Code Article 74.7). Heteranthus verruculatus – Lectotype . ZMB 1852 ( fig. 2A, B ), collected by C.B. Klunzinger , no later than 1877 from the Red Sea ( Koseir ). Two pieces of a single specimen, rigid and brittle, cut transversely across at mid-column ( fig. 2B ). Distalmost column slit longitudinally, a slice of distalmost margin missing ( fig. 2B ). An oily scum layer encrusts oral disc. Both pieces dark-greenish or grey. Total length 14 mm , mid-column 13 mm wide, distalmost and proximal end 15 mm wide, respectively; NRS 4861 ( fig. 2C ) a single fragment originating from ZMB 1852. A piece of distalmost end of column, also includes part of the mid-column, dark sandy-brown in colour, in good condition. Fragment 4 mm wide. Heteranthus insignis – Holotype , NRS 4076 , collected by D.C. Dawydoff from Vietnam and given to O. Carlgren ( fig. 2D ). A single specimen, 17 mm in length, cut transversely into two pieces at mid-column, with a longitudinal cut along each. A slice of distalmost margin missing. Both pieces firm, in good condition. Both pieces cream-coloured in preservative. Natural history. Encountered during low spring tides along shallow tropical coasts, with oral disc and marginal tentacles expanded ( fig. 3A ). Sand grains and shell fragments adhere to verrucae at distalmost end ( fig. 3B ). May occur as solitary or as clonal, clustering individuals ( fig. 3C, D ), inhabiting narrow rocky crevices. Clustering type abundant in sandy seagrass meadows of Halophila ovalis , with pedal end attached to the roots of plant or coral rubble underneath. Asexual propagation via longitudinal fission frequently observed ( fig. 4A–F ;supplementary video S1).Zooxanthellate. Oral disc. When fully expanded, margin may be slightly undulate in solitary individuals; in smaller clustering ones, flat( fig.5A, B ).Outline oval to round; elongated oval during onset of longitudinal fission ( fig. 4A ). In life, light to dark-brown, may be speckled with white patches. Thin-walled, mesenterial insertions seen as radial dark lines extending from mouth to marginal tentacles in living animals, as white lines in preserved materials. Discal tentacles present, papilliform ( fig. 5C, D ). Area immediately around mouth without discal tentacles ( fig. 5D ), arranged in radial rows from mid-way extending towards marginal tentacles. Radial rows of discal tentacle both endocoelic and exocoelic, numerous. In solitary individuals, discal tentacles conspicuous and densely arranged, clustering type less conspicuous and less dense ( fig. 5D ), becoming obscure when preserved. Central mouth flat, edges tinged brown, white or pink in life, cream-white in preserved specimens. Marginal tentacles. Numerous, numbers variable; in solitary individuals that exhibit a regular symmetry (i.e., mesenteries arranged symmetrically) typically 96, arranged in five cycles (e.g., RCLA.Cni.008). One per endo/exocoel; innermost cycles endocoelic, outermost exocoelic. Innermost cycle longer than outermost, longest length approximately ¾ radius of oral disc. Simple, conical, without ramified protuberances in life, some individuals slightly inflated at mid-tentacle ( figs. 3A, C , 5A ). Tip blunt, without perforation in live individuals; after preservation may appear perforated due to tentacle retraction (e.g., NHM 1954.6.28.23; fig. 5C ). Wide at base, narrow toward tip. Colour in life greenishbrown, some with light horizontal cross bands along oral face ( fig. 5A, D ). Base coloured white to dark brown, tip with white specks in life, cream-white in preserved specimens. Column. Distalmost end flared slightly outwards when expanded. Distal margin with marginal projections, both endo/exocoelic. Larger marginal projections, endocoelic; smaller: exocoelic. In solitary individuals, marginal projections densely covered with conspicuous, papillae-like verrucae ( fig. 6A– C ) that may be less dense or inconspicuous in clustering individuals (e.g., ZRC.CNI.1207, MTQG59393; fig. 6D ). Longitudinal rows of round verrucae extend proximally from marginal projections, smaller near distalmost end, increasing in size proximally towards mid-column. Verrucae very conspicuous in solitary individuals, edges thickened and slightly raised, middle depressed ( fig. 6E ); less conspicuous in clustering polyps ( fig. 6F ). Longitudinal verrucae rows both endo/ exocoelic. Endocoelic rows longer, up to 20 verrucae per row; exocoelic: shorter, up to four in each row; shell fragments, coral rubble and/or sand grains may adhere to the verrucae. Column wall thin, mesenterial insertions can be seen through as faint light lines extending from distal to proximal end. From mid-column to proximal end of column smooth, without cinclides. Fosse present, shallow. In life, light-brown with greenishtinge to cream-white with reddish orange/ pink splotches, distalmost end dark grey ( fig. 6E–F ). In preserved specimens, column entirely cream-white; distalmost end grey in recently preserved materials. FIGURE 3 Living specimens of Heteranthus verruculatus . A. an expanded individual (RCLA.Cni.003), camouflaged with the sand that it is buried in, Tial, Pulau Ambon, Indonesia. Photograph by NWL Yap. B. a partially contracted individual (RCLA.Cni.003) extending from a rocky crevice, with sand grains and shell fragments still densely attached to distalmost end, at Tial, Pulau Ambon, Indonesia. Photograph by NWL Yap.C. an expanded smaller individual with tentacles extended, encountered in a bed of Zoanthus at Pulau Tekukor, Singapore, in situ. Photograph by KS Loh, with permission. D. a population of densely packed clustering individuals (ZRC.CNI.1207), encountered in a Halophila ovalis meadow at Cyrene Reef, Singapore. Photograph by NWL Yap. Abbreviation: z, Zoanthus sp. Scale bar = 5 mm. FIGURE 4 A clustering Heteranthus verruculatus (ZRC.CNI.1230) undergoing longitudinal fission. A, B. lateral stretching, with pedal-end extending the widest. Both column and pedal-ends inflate and deflate (arrowed) as the sea anemone pulls itself in opposite directions. C, D. column cleaved; continued stretching of actinopharynx that eventually splits, with distalmost end remaining (arrowed). E, F. pulling and splitting of the distalmost end of column where sphincter muscles are. Duration of observation is denoted at the top right-hand corner of each panel, time rendered in hours, minutes, and seconds (i.e., hh:mm:ss). Scale bar = 2 mm. Video screen capture by NWL Yap. For full video, refer to supplementary video S1. Pedal disc. Adheres readily to surfaces when animal is alive. Outline: oval, may be flat or inflated. Limbus slightly scalloped. Thin-walled, mesenterial insertions seen as light lines. Diameter may be equal or greater than oral disc. Internal anatomy. Anatomy typically arranged regularly in solitary individuals (e.g.,RCLA.Cni.008); irregular in clustering individuals (e.g., NRS 4076, WAM Z33601). Actinopharynx pleated longitudinally, extends proximally to mid-column; white in life, cream-colored in preserved specimens. Marginal and oral stomata present. Usually two siphonoglyphs in solitary individuals, symmetrical; clustering individuals with supernumerary siphonoglyphs (i.e., three siphonoglyphs in WAM Z33604) or may be entirely absent, asymmetrical. Mesenteries numerous, number of pairs variable in clustering individuals ( fig. 7A, B ). In solitary individuals, mesenteries typically arranged in up to four cycles (i.e., 6 + 6 + 12 + 24 pairs), symmetrical. Mesentery pairs in first two cycles complete, those of third cycle incomplete, all with filaments and gametogenic tissue, if present ( fig. 7C ). Mesentery pairs in fourth cycle incomplete, without retractor muscle or filaments. Retractor muscles strong, diffuse, always humped along its edge but less pronounced in clustering individuals. Parietobasiliar muscles poorly developed, retractor pennon reduced or absent; if present, extends away from mesentery ( fig. 7A–C ). Directives attached to a siphonoglyph each, if present. Sphincter muscle below fosse, form variable among specimens. Typically strong, conspicuous and circumscribed, or restricted or with a few folds ( fig. 8A–C ). FIGURE 5 Oral disc appearance of Heteranthus verruculatus . A. an expanded solitary individual (RCLA.Cni.008) with a crenulated, oval oral disc. B. an expanded clustering polyp (ZRC.CNI.1207) with a round, flat oral disc. In both A and B, innermost cycle of marginal tentacles is longer than outermost. C. dense arrangement of discal tentacles of a solitary individual from the Great Barrier Reef (NHM 1954.6.28.23). D. discal tentacles of a clustering polyp (ZRC.CNI.1230) with a sparse distribution of tentacles (arrowed). Abbreviations: a, actinopharynx; dt, discal tentacles; m, mouth; mt, marginal tentacles. Scale bar = 2 mm. Photographs by NWL Yap. Cnidom Spirocysts, basitrichs, microbasic amastigophores, and microbasic p -mastigophores ( table 2 ; fig. 9 ). Distribution ( fig. 10 ). Type localities : Egypt , Koseir (of H. verruculatus ; Klunzinger, 1877 ); Vietnam , Poulo Condore [= Côn SƠn Island , Vung Tau] (of H. insignis ; Carlgren, 1943 ). Published records : Eastern Australia , Great Barrier Reef ( Carlgren, 1950 ), Moreton Bay and Townsville ( Fautin et al., 2008 ); Indonesia ( den Hartog, 1997 : locality not specified); Hawaii, Oahu, Kaneohne Bay ( Cutress, 1977 ); Western Australia ( Fautin et al., 2008 : locality not specified). New records : French Polynesian Islands, Mangareva, Rikitea; Oman , Bar Al Hikman Peninsula; Singapore .