The classification of scleractinian corals has changed significantly over the past 20 years since molecular techniques were applied to scleractinian systematics in the late 20th century (Stolarski and Roniewicz, 2001; Budd et al., 2010; Veron, 2013).

Recent scleractinians comprise 777 zooxanthellates and 711 azooxanthellates worldwide (Roberts et al., 2009).

The family Psammocoridae includes seven species of one genus according to the World Register of Marine Species (2014). These species are zooxanthellate (Cairns, 1999, 2007; Cairns et al., 1999; Daly et al., 2007), and are characterized by the various growth forms with cerioid arrangement, enclosed and petaloid septa, and synapticulotheca in the skeletal structures. The classification of the genus Psammocora has changed as follows (Benzoni et al., 2007). This genus was placed in the family Thamnasteriidae of the suborder Fungiida (Vaughan and Wells, 1943) or of the suborder Astrocoeniina (Wells, 1956), and was classified in the new family Psammocoridae (Chevalier and Beauvais, 1987) or the family Siderastreidae (Veron, 1995) under the suborder Fungiina. Since it was suggested that the family Siderastreidae is not monophyletic (Chen et al., 2004; Benzoni et al., 2007), the genus Psammocora has belonged to the family Psammocoridae based on a combined approach of morphological and molecular studies (Benzoni et al., 2007, 2010; Stefani et al., 2008a, 2008b).

The family Faviidae includes 126 species of 24 genera (Veron, 2000). These species are zooxanthellate (Cairns, 1999, 2007; Cairns et al., 1999; Daly et al., 2007), and are distinguished by the various growth forms, polygonal calicular shape, and paliform lobes in the skeletal structures. Oulastrea crispata is only species in the genus Oulastrea. The classification of the genus Oulastrea has changed as follows (Budd et al., 2012). This genus was placed in the subfamily Montastreinae of the family Faviidae (Wells, 1956). Then, the genus Oulastrea was considered in the family Faviidae (Veron, 2000). Recent researches from molecular studies, and micromorphological and microstructural studies indicate that the genus Oulastrea remains in the family incertae sedis (Budd et al., 2012).

One species in the genus Psammocora of the family Thamnasteriidae has been described in Korea: Psammocora profundacella (Song, 1982, 1991, 2004). No species in the genus Oulastrea of the family Faviidae has been reported in Korea. In this study, Psammocora albopicta of the family Psammocoridae and Oulastrea crispata of the family Faviidae are newly recorded from Jeju-do Island, Korea.

Specimens were collected from the subtidal zones of Chagwi- do, Gapa-do, Gangjeong, Munseom, Seopseom, Jigwi-do, Pyoseon, and Seongsan in Jeju-do Island, Korea by SCUBA diving from 1999 to 2014. The previously studied (Song, 1982, 1991, 2004) and recently collected Psammocora profundacella were also examined to describe Psammocora albopicta. These specimens were collected from the subtidal zones of Munseom, Seopseom, and Jigwi-do in Jeju-do Island, Korea by SCUBA diving from 1978 to 2014. They were dissolved in sodium hypochlorite solution (Clorox: commercial bleach) with distilled water for 24 hours to remove all soft parts, washed in distilled water, and dried to observe the skeletal structures. The figures of the coralla were photographed with a digital camera (G12; Canon Inc., Tokyo, Japan and Optio WG2; Pentax Ricoh Imaging Co. Ltd., Tokyo, Japan). The skeletal structures of the corallites were examined with a stereomicroscope (Leica S8APO; Leica Microsystems, Wetzlar, Germany), photographed with a mounted camera (Leica Microsystems), and measured with an image analyzer (LAS ver. 3.6; Leica Microsystems). A series of multi-focused images were taken and combined with an image editing program (HeliconFocus 5.3 Pro; Helicon Soft Ltd., Kharkov, Ukraine) to provide clear images of detailed skeletal structures. This study partly followed Veron (2000), and Chevalier and Beauvais (1987) for the classification of scleractinian corals. The morphological and anatomical terms were referenced from Wells (1956) and Benzoni et al. (2007). The specimens are deposited at the Ewha Womans University Natural History Museum and the Korean Coral Resource Bank in Korea.

Phylum Cnidaria Hatschek, 1888

Class Anthozoa Ehrenberg, 1834

Subclass Hexacorallia Haeckel, 1866

Order Scleractinia Bourne, 1900

1*Family Psammocoridae Chevalier and Beauvais, 1987

Diagnosis. Corallum colonial, attached. Growth form encrusting or foliose or massive or columnar or branching. Enclosed septa developed. Petaloid septa developed. Synapticulotheca present.

Genus Psammocora Dana, 1846

Diagnosis. Rows of enclosed septa developed. Series of calices usually enclosed by a common wall. Septal furcation or ramification developed. Columella styliform.

2*Psammocora albopicta Benzoni, 2006 (Fig. 1)

Psammocora sp. nov.: Yabe et al., 1936: 61, Pl. XLV, fig. 9.

Psammocora albopicta Benzoni, 2006: 49, figs. 1-3, 4a, 5; Benzoni et al., 2010: 424, fig. D; Denis et al., 2014: 157, fig. 1. a, b, electronic supplementary material a-c.

Material examined. Korea: Jeju-do: 1 ind., Seogwipo-si, Seopseom, 4 Aug 2011, Song JI, Hwang SJ (EWZS 5739); 1 ind., Seogwipo-si, Jigwi-do, 33˚13.313′N, 126˚39.175′E, 13 Oct 2012, Song JI, Hwang SJ, 15-17 m deep (EWZS 5740); 1 ind., Seogwipo-si, Jigwi-do, 33˚13.313′N, 126˚39.175′E, 13 Oct 2012, Song JI, Hwang SJ, 15-17 m deep (KCRB 1955); 2 inds., Seogwipo-si, Jigwi-do, 33.22493˚N, 126.65 100˚E, 13 Oct 2012, S. De Palmas, V. Denis, L. Ribas Deulofeu, 5-15 m deep (JIG 35, JIG 68).

Description. Corallum colonial, attached. Growth form submassive or encrusting or plate-like, unifacial, irregularly cerioid, 15-45 mm in width, 1-10 mm in thickness. Budding intratentacular. If present, 2-4 corallites in a series (average 2.3 corallites) enclosed by indistinctive common wall. Series of corallites linear or polygonal in shape. Distance between centers of corallites 0.55-2.12 mm (average 1.27 mm). Distance between centers of corallites within a series, 0.55- 1.80 mm (average 0.99 mm). Distance between centers of corallites between series, 0.76-2.12 mm (average 1.36 mm). Corallites slightly immersed, but surface of corallum generally even or shallow. No distinctive ridges developed. 8-21 corallites in 5 5 mm (average 14.6 corallites). Calice polygonal or circular or irregular in shape, 0.68-2.19 mm (average 1.09 mm) in diameter. Calicular outlines not well defined. Fossa 0.16-0.36 mm (average 0.23 mm) in diameter. Columella single, styliform, 0.06-0.19 mm (average 0.12 mm) in diameter. Synapticulotheca weakly present. 5-8 septa reaching fossa (average 6.4 septa). Non-fused septa petaloid or lamellar in shape, 1-4 (average 2.8 septa), 0.08- 0.70 mm (average 0.44 mm) in length, 0.06-0.24 mm (average 0.14 mm) in width. Septal furcation present, twice to fourth times (average 2.5). If present, enclosed septa lamellar in shape, developed incompletely or in one or two up to three rows (average 1.7 rows). Septal upper margins roughly dentated, granulated.

Color. Dark brown in living.

Habitat. The species inhabits 5-17 m deep subtidal zones. Barnacles and tube worms live in ectosymbiosis with the corallum.

Remarks. The ecology of Psammocora albopicta was first reported from Korea (Denis et al., 2014). The ecological paper reported that typical circular white patterns on the surface of P. albopicta were occasionally observed as described in the original paper (Benzoni, 2006). Psammocora albopicta (Table 1) and P. profundacella (Table 2) of this study are described in the summary, and compared with those of previous studies (Song, 1982, 1991, 2004). The materials from previous studies (Song, 1982, 1991, 2004) and recent specimens of Psammocora profundacella in Korea were examined (Table 2). Psammocora albopicta differs from P. profundacella by the high density of corallites, short intercorallite distance, small calicular diameter of 1 mm, small fossa, and single styliform columella.

Distribution. Pacific Ocean: Korea (Jeju-do Island), Japan (Udo), Philippines, Indonesia (Misool), Australia (Point Vernon, Gneering Shoals, Cook Island, Julian Rocks, Moreton Bay); Indian Ocean: Kuwait (Kubbar Island, Umm Al-Maradem, Qit’at Benaya), Yemen (Balhaf), Saudi Arabia (Jana Island), Malaysia (Pulau Telor).

1*Family Faviidae Gregory, 1900

Diagnosis. Corallum colonial, attached. Growth form massive or encrusting in cerioid or plocoid arrangement. Budding extratentacular or intratentacular. Coenosteum present. Costae developed. Paliform lobes developed.

2*Genus Oulastrea Milne Edwards and Haime, 1848

Diagnosis. Corallum massive or encrusting, plocoid. Budding extratentacular or intratentacular. Paliform lobes before large septa. Columella papillose. Septa spiny or granulated. Coenosteum costate.

3* Oulastrea crispata (Lamarck, 1816) (Fig. 2)

Astrea crispata Lamarck, 1816: 265.

Oulastrea crispata: Milne Edwards and Haime, 1850: 116, Pl. 9, fig. 4; Vaughan, 1919: 453; Yabe et al., 1936: 54, Pl. 9, figs. 4a, 4b; Pl. 42, figs. 1-4; Vaughan and Wells, 1943: 122, 125; Nemenzo, 1955: Wells, 1956: F405, fig. 301 2a, 2b; Eguchi, 1968: C14, Pl. C19, figs. 3, 6; Veron, 1986: 508; 2000: 229, figs. 1-4; Nishihira and Veron, 1995: 367; Dai and Horng, 2009: 58; Chen et al., 2011: 46; Hoeksema and Vicente, 2014: 430, figs. 1-4.

Material examined. Korea: Jeju-do: 1 ind., Seogwipo-si, Munseom, 19 Nov 1999, Lee YJ, 14 m deep (EWZS 3989); 2 inds., Jeju-si, Chagwi-do, 17 Aug 2001, Song JI (EWZS 4008); 2 inds., Seogwipo-si, Seongsanpo, 18 Aug 2001, Song JI (EWZS 3992); 2 inds., Seogwipo-si, Gapa-do, 33.17315˚N, 126.27747˚E, 10 Oct 2012, S. De Palmas, V. Denis, L. Ribas Deulofeu, 5-15 m deep (GAP 49, GAP 50); 2 inds., Seogwipo-si, Seongsanilchulbong, 33.45744˚N, 126.93608˚E, 11 Oct 2012, S. De Palmas, V. Denis, L. Ribas Deulofeu, 5-15 m deep (SUN 29, SUN 30); 2 inds., Seogwipo-si, Pyoseon, 33.30598˚N, 126.77989˚E, 19 Oct 2012, S. De Palmas, V. Denis, L. Ribas Deulofeu, 5-15 m deep (PYO 3, PYO 10); 1 ind., Seogwipo-si, Gangjeongdeungdae, 33˚13′19.7″N, 126˚28′44.5″E, 28 Oct 2014, Hwang SJ, Lee WG, 16 m deep, green oral part (KCRB 1817).

Description. Corallum colonial, attached. Growth form encrusting or massive, unifacial, plocoid, 17-101 mm in width, 1-20 mm in thickness. Budding extratentacular or intratentacular. 30-39 corallites in 30 30 mm (average 35.6 corallites). Distance between centers of corallites 1.30- 7.64 mm (average 5.04 mm). Corallite 1.65 2.68-7.82 10.15 mm (average 5.07 6.25 mm) in calicular diameter. Calicular shape irregularly polygonal (tetragonal to heptagonal, usually hexagonal or pentagonal), or circular or elliptical. Calicular upper margins exserted, elevated. Fossa up to 4 mm, mostly 2 mm in depth. Columella papillose, 0.95 1.26-2.03 3.26 mm (average 1.70 2.13 mm) in diameter. Paliform lobes irregularly present before some larger septa. Theca indistinctively developed between septa. Septa alternating, hexamerously or pentamerously arranged from 13 to 56 in 3-5 cycles (average 32.3 septa in 4 incomplete cycles). Up to 61 septa developed in enlarged corallite of intratentacular budding. Septal fusion present at inner edges. In 3 cycles, pairs of S3 fused before S2. In 4 cycles, pairs of S4 fused before S3, fused S4s united with S2. S1 1.02- 2.77 mm (average 1.77 mm) in length, 0.08-0.43 mm (average 0.23 mm) in width. Size, length, width of septa irregularly variable. Septa in previous cycles larger, thicker, more exserted than those in recently formed cycles. Septal upper margins rounded, elevated. Septa imperforate, covered by spines or granules. Costae 0.10-0.27 mm (average 0.17 mm) in width. Intercostal striae 0.06-0.29 mm (average 0.18 mm) in width.

Color. Coenosarc dark brown, oral disc green, and septal upper margins white in living.

Habitat. The species inhabits 5-16 m deep subtidal zones. Tube worms, bryozoans, bivalves, hydroids, and barnacles live in ectosymbiosis with the corallum.

Remarks. Fifty-six septa per corallite in five cycles (61 septa developed in an enlarged corallite of the intratentacular budding) are observed in this study (Table 3) and compared with a maximum of 45 septa in the previous study (Hoeksema and Vicente, 2014). Extratentacular budding has been one of the main keys to identify Oulastrea crispata (Vaughan and Wells, 1943; Nemenzo, 1955; Eguchi, 1968), but intratentacular and extratentacular buddings are observed as shown in recent studies (Lam, 2000; Hoeksema and Vicente, 2014).

Distribution. Pacific Ocean: Korea (Jeju-do Island), Japan (Southern Honshu, Southern Shikoku, Southern Kyushu, Okinawa), Taiwan, Thailand, China (Hong Kong), Australia, Philippines, Malaysia (Strait of Malacca), Indonesia (Bay of Jakarta, West Papua); Indian Ocean; Atlantic Ocean: France (Corsica).