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Marine Biodiversity

, Volume 42, Issue 2, pp 289–295 | Cite as

Extreme morphological plasticity enables a free mode of life in Favia gravida at Ascension Island (South Atlantic)

  • B. W. Hoeksema
Open Access
Short Communication

Abstract

Samples of free-living corals of Favia gravida (Scleractinia: Faviidae) have been studied. They were collected from an intertidal rock pool on Ascension Island, southern Atlantic Ocean. They consist of phaceloid clusters of corallites that appear to be able to easily break apart from each other by the formation of slits inbetween them, which indicates the occurrence of asexual reproduction by fragmentation. The base of the fragments is usually tapering or conical and covered by an epitheca. Small corallites on the base of some specimens suggest that the corals also reproduce by budding. By not depending on a solid substratum for reproduction, the corals appear to be utterly adapted to a free mode of life. These traits have not been reported before from Favia, which normally consists of massive corals. The variable shape of the corals at hand indicate that they have adopted a plastic free-living growth form that appears to be confined to a rock pool habitat.

Keywords

Asexual reproduction Budding Epitheca Fragmentation Free-living Isolation Rock pool 

Introduction

The scleractinian coral family Faviidae has a long tradition regarding studies dealing with intra-specific ecophenotypic variation. These studies deal mostly with the dimensions and spacing of corallites, which appear to respond to light and sedimentation (Laborel 1969; Wijsman-Best 1974; Foster 1979, 1980; Budd 1993; Van Veghel and Bak 1993; Amaral 1994; Todd et al. 2001, 2004; Amaral and Ramos 2007; Ow and Todd 2010; Chen et al. 2011). This habitat-induced phenotypic variability has often hampered the recognition of species and also of monophyletic groups at higher taxonomic levels within the Faviidae (Fukami et al. 2004; Huang et al. 2009; Budd and Stolarski 2011). Since most Faviidae species are attached and massive, they have so far not been known to reproduce asexually by fragmentation or by budding, which are life history traits shown by corals with a free mode of life, such as free-living species in various Fungiidae clades (Hoeksema 1989, 1991, 2004; Hoeksema and Gittenberger 2010; Hoeksema and Yeemin 2011; Gittenberger et al 2011; Hoeksema and Waheed 2011) and in the Flabeliidae (Cairns 1989).

Therefore, it was a surprise that during a recent study of Atlantic Favia specimens in the coral collection of NCB Naturalis in Leiden, two lots of small unattached corals were discovered that belong to Favia gravida (Verrill, 1868). According to their label, they were collected from an intertidal rock pool on Ascension, an isolated island in the South Atlantic Ocean (Fig. 1). Two anonymous reviewers brought additional material from the same locality to my attention, which was consequently also studied. The material is described, illustrated and discussed here in the light of an extreme morphological variety within Favia, enabling it to reproduce asexually and to colonize various substrates as a free-living coral.
Fig. 1

Distribution range of Favia gravida (after Laborel 1974; Gasparini and Floeter 2001; Amaral and Ramos 2007; modified from Aronson et al. 2008 for F. fragum)

Material

The specimens were part of coral collections in natural history museums (abbreviations below).

Type specimens of Favia gravida: two syntypes (YPM 1465a, 1465b) from Brazil, Bahia State, Abrolhos Archipelago, Abrolhos Reef, coll. CF Hartt, 1867 (see also Verrill 1901, Pl. 13, Fig. 3); one syntype (YPM 4549) from Brazil, Pernambuco State, Recife, coll. CF Hartt, 1867.

Free-living specimens of F. gravida: RMNH Coel. 17339 (16 specimens) from “Ascension Island, SW Coast, Shelley Beach, Coral Pool”, 1 June 1983, coll. JC den Hartog; RMNH Coel. 23341 (two specimens) from “Ascention, Shelly Beach”, 10 November 1989, coll. JH Stock. USNM 78222 (one specimen) from “South Atlantic Ocean, Ascension Island, South Shelly Beach”, 20 November 1985, coll. JT; USNM 78223 (one specimen) from “South Atlantic Ocean, Ascension Island, South Shelly Beach”, 1 December 1985, coll. JT; USNM 89298 (≈ 80 specimens and fragments) from “Ascension Island (South Atlantic), inland tidepool at Shelly Beach, 200–300 ft from intertidal areas bottom paved with coral”, 23 May 1971, coll. RB Manning; USNM 96980 (five specimens and fragments) from “Ascension Island (South Atlantic), tidepool at Turtle Shell beach”, 25 May 1971, coll. RB Manning; USNM 96981 (one specimen from “Ascension Island (South Atlantic), North East Bay, beach and tidepools on rocky point, West of main beach”, 19 May 1971, coll. RB Manning; USNM 96983 (≈ 40 specimens and fragments) from “Ascension Island, Shelly Beach, Procaris pool”, 13 July 1976, coll. Jones, Manning, Pawson, Provenzano, Rosswater.

Attached specimens of F. gravida: RMNH Coel. 17341 (8 specimens) from “Ascension Islands, Mars Bay, SW coast, exposed rocky shore with tidal pools”, 31 May 1983, coll. JC den Hartog; USNM 96368 (four specimens and fragments) from “Ascension Island (South Atlantic), Shelly Beach tidepools in flat exposed at low tide on open beach”, 23 May 1971, coll. RB Manning; USNM 96984 (one specimen) from “Ascension Island, MacArthur Point. Associated with rocks in intertidal”, 13 July 1976, coll. Jones, Manning, Pawson, Provenzano, Rosswater.

RMNH = Netherlands Centre for Biodiversity Naturalis, Leiden, The Netherlands (formerly known as Rijksmuseum van Natuurlijke Historie). YPM = Peabody Museum of Natural History, Yale University, New Haven, Connecticut, U.S.A. USNM = Smithsonian Institution, National Museum of Natural History, Washington DC, U.S.A. (formerly known as U.S. National Museum of Natural History).

Locality and habitat

Ascension is an isolated volcanic island in the South Atlantic (Fig. 1). It lies about 2,200 km east of Brazil and more than 3,000 km west of the African coast. The nearest island is St. Helena, almost 1,300 km to the southeast.

In the first record of Favia from Ascension, the corals were referred to as “irregular beds of coral (Favia)” in rock pools, one of which was called “coral pool”, on Shelley Beach near the southernmost point of the island (Chace and Manning 1972). In another publication, these authors referred to “solitary corals” and “beds of the solitary coral Favia” (Manning and Chace 1990). The corals were observed to host barnacles of the species Troglocarcinus corallicola Verrill, 1908, in rock pools, and were also at a depth of 3 m inside a bay. In a more detailed study, Price and John (1980) refer to rock pools that are lined “with coral growths (Favia sp.)” and a bottom consisting of loose marl-like sediment and sand. They present an illustration (Price and John 1980: Fig. 12) showing dense patches of coral. Abele and Felgenhauer (1985) mention that the largest coral pool is approximately 7 m long, 5 m wide, and 1 m deep.

However, F. gravida from Ascension also appears to be mentioned in much older literature, in which it was referred to as Platygyra ascensionis Ridley 1881, which apparently is a junior synonym of F. gravida (see Ridley 1881; Werner 1996). There are no records of other zooxanthellate corals from Ascension, except those mentioned in an unpublished MS thesis (Werner 1996) concerning Madracis decactis (Lyman 1859) and Siderastrea radians (Pallas, 1766).

Results

The free-living specimens of F. gravida from intertidal pools at Shelley Beach, Turtle Shell Beach, and North East Bay (RMNH Coel. 17339, 23341; USNM 78222, 78223, 89298, 96980, 96981, 96983) form a mix of loose corals and coral fragments. The largest specimens (∅ up to 13 cm) resemble phaceloid bundles of corallites, some of which show indications of potential fragmentation (Fig. 2). There are no marks of previous attachment to a substratum. Small specimens have a distinct free-living shape, showing a tapering or conical base covered by an epitheca (Fig. 3). The smallest corals consist of a single corallite (∅ ≈ 0.5 cm). Some specimens of medium size consist of two or three cones of corallites, like Siamese twins or triplets, which look as if they may easily break apart (Fig. 4). Several specimens show a large detachment scar, where they may have become separated from a clone sibling (Figs. 3, 4 and 5). Such scars are not covered by an epithecal crust. Some specimens show small polyps at their underside (∅ 0.1–2.2 mm), which may be asexually produced buds or recruits settled after local planulation (Fig. 5). F. gravida corals from other Ascension Island localities (RMNH Coel. 17341, USNM 96368, 96984) are massive and do not show signs of fragmentation. Parts of the undersides that have not been in contact with the substratum are covered by an epithecal crust.
Fig. 2

Detached corals of F. fragum from Ascension I. Scale bars 1 cm. Largest specimen (∅ 7.6 cm) viewed from above (a) and from aside (b, c) consisting of phaceloid clusters of corallites, which are connected at the base and show an epithecal crust. Two clusters are almost broken off at the base (arrows). d Smaller specimen (∅ 4.7 cm) showing two clusters of corallites, one of which is almost detached (arrow)

Fig. 3

Free-living corals of F. fragum from Ascension I. (∅ 1.4–4.5 cm). The base is tapering towards a point and covered by an epitheca. Scale bar 1 cm. a Smallest coral. b, c Small specimen with dead corallite. d, e Specimen showing a scar possibly indicating area with which it was attachment to a clone sibling (arrows). f Large coral still attached to dead fragment

Fig. 4

Free-living corals of F. fragum from Ascension I. (∅ 2.4–3.4 cm). They show slits at their underside, indicating potential fragmentation. All show a detachment scar at their underside (arrows). Scale bar 1 cm. a, b Smallest coral with clear fission zone. c, d Small specimen about to split in three parts. Small polyp may be a bud. e, f Large coral splitting at the base, with a small part almost loose

Fig. 5

Free-living corals of F. fragum from Ascension I. (∅ 2.2–4.1 cm). They show small polyps, possibly indicating budding. Scale bar (a–e) 1 cm. a, b Smallest coral showing detachment scar (arrows) and small polyps at underside (insert). c, d Large specimen showing small polyps (insert). e, f Dead fragment with attached bundle of corallites and a small polyp underneath (insert). f Close-up of small polyp, probably dead at the time of collecting. Scale bar 0.25 cm

Discussion

The zooxanthellate scleractinian coral Favia gravida has an amphi-Atlantic distribution from Brazil to western Africa, including the mid-oceanic islands Ascension and St. Helena, which are ca. 1,300 km apart (Fig. 1). In Brazil, the species occupies a large array of shallow-water habitats and shows much morphological variability by forming solid and dense attached colonies, which are encrusting or hemispherical with a strongly developed epitheca at their sides (Amaral and Ramos 2007). F. gravida resembles F. fragum (Esper, 1793), another species with an amphi-Atlantic range (Hoeksema et al. in press). Molecular evidence supports their status as two genetically distant species (Nunes et al. 2008, 2011). The type specimens of F. gravida are massive corals. Their calices and those of the specimens from Ascension I. fit within the morphological range of F. gravida described by Laborel (1969) and by Amaral and Ramos (2007).

Since Manning and Chace (1990) refer to the “solitary coral Favia”, and the genus Favia only includes corals composed of multiple corallites, they may have confused “solitary” with “free-living”, a term commonly associated with unattached solitary corals. Many studied samples of F. gravida corals from Ascension Island’s Shelley Beach, all corals with a free-living growth form, were indeed collected from this “coral pool” (Figs. 3, 4 and 5). Most of these were sampled by Manning, although he did not mention collecting them (Manning and Chace 1990). This case confirms the importance of natural history collections in coral reef research (Hoeksema et al. 2011). Based on the description by Manning and Chace (1990), it would not be clear how their Favia corals really looked.

Hitherto, free-living corals have not been reported for Favia. The specimens of the present study lack any clear mark of attachment to a solid substrate and display a conical base partly or completely covered by an epitheca, indicating that they must have been free-living, like the faviid Manicina areolata (Linneaus 1758) (Barnes 1972; Hoeksema 1993; Roniewicz and Stolarski 1999). Moreover, some specimens are partly phaceloid and show signs of fragmentation, a trait associated with a free mode of life (Hoeksema 1993). The phaceloid clusters of corallites in the largest corals (Fig. 2) resemble stalked mushroom corals in their anthocaulus phase before detachment (Wells 1966; Hoeksema 1989; Hoeksema and Yeemin 2011).

Surviving fragments may colonize various kinds of substrates, including sand and marl. The epitheca may serve as a shield to protect the soft tissue when the coral is partly buried in the sediment. Apart from the barnacles mentioned by Manning and Chace (1990), which live on the upper side of the corals, there is no sign of epibiotic species as on the epitheca of Manicina corals (Harries and Sorauf 2010), a cleanliness indicating that they may have lived semi-buried in the substrate (Hoeksema 1993). It is also possible that the free-living corals are able to settle on the coarse marl sediment on the bottom of the rock pools from which they break apart without trace of attachment (Plusquellec et al. 1999).

The small corallites on the epitheca look like asexually produced buds, as shown by some mushroom corals (Scleractinia: Fungiidae) (Boschma 1922, 1923a, b; Hoeksema 1989, 2004), in Goniopora stokesi Milne Edwards & Haime, 1851 (Scleractinia: Poritidae) (Boschma 1923c; Rosen and Taylor 1969; Hoeksema and Waheed in press), and some fossil taxa for which they have been called “hypocorallites” (Plusquellec et al. 1999). It is not clear how they could develop on the epitheca without contact with soft tissue. This is in contrast with budding by free-living mushroom corals, which are completely surrounded by soft polyp tissue. Extra-tentacular budding on the theca is also known from azooxanthellate corals. It is called “anthoblast production” or “bud shedding”, in which the detached buds leave scars behind (Zibrowius 1985; Cairns 1988). In F. gravida, they may also be locally produced offspring coming from planula larvae that had settled on the parent corals, but, if the underside of the corals was buried in sediment, this is not likely unless the sediment was very coarse, like marl. In that case, the coral would be forming pseudo- or quasi-colonies as described for Balanophyllia generatrix Cairns and Zibrowius 1997 (Cairns and Zibrowius 1997: fig. 25 g–i).

The coral fragmentation of F. gravida resembles asexual reproduction by free-living mushroom corals, which helps them to disperse over the sea floor (Hoeksema 1989; Hoeksema and Gittenberger 2010; Hoeksema and Waheed 2011). This “sessile dispersal” may help corals to spread the risk of mortality in harsh environments (Jackson 1986).

The free-living growth form of F. gravida appears to be a result of ecophenotypic variation occurring in an unusual environment (rock pools) on Ascension Island. It has not been reported in studies dealing with F. gravida in Brazil (Verrill 1901a, b; Laborel 1969; Amaral and Ramos 2007). F. gravida specimens from Brazil and St. Helena I. deposited in museum collections (RMNH, YPM) or illustrated in publications (e.g., Correia 2011) also do not represent this ecomorph, even though some of these corals were mentioned to have occurred in tide pools (Verrill 1901b). A subspherical free-living growth form has recently been reported for the massive reef coral Madracis decactis (Scleractinia: Pocilloporidae). High densities of these corals were observed inbetween boulders on sand flats and rubble beds in subtropical water off southern Brazil (Capel et al. 2011), which indicates that a free-living F. gravida ecomorph is not unique among reef coral species that are otherwise known for their massive growth form.

Apparently, the morphological plasticity and the presence of an epitheca enable F. gravida corals to survive as free-living coral fragments. A free mode of life enables corals to colonize a wide variety of substrates, and consequently the whole corallum morphology may become affected by the environment as can be observed in Manicina (Johnson 1988; Hoeksema 1993; Sorauf and Harries 2010) and free-living Fungiidae (Hoeksema and Moka 1989; Hoeksema 1993; Gittenberger and Hoeksema 2006). By not depending on a solid substratum for reproduction, the corals are completely adapted to a free mode of life. Since, this mode of life and reproduction in Favia has not been described before, it appears to be rare and may be confined just to some rock pools on Ascension Island.

Notes

Acknowledgments

This study is dedicated to the memory of the naturalists J.C. (Koos) den Hartog (1942–2000) and J.H. Stock (1931–1997), who collected the corals (RMNH) from Ascension island that triggered the present study. I am grateful to Mr. E. Lazo Wasem (YPM), who sent the type specimens of F. gravida on loan, and to Dr. S.D. Cairns (USNM), who sent additional F. gravida material from Ascension I. on loan. I am indebted to two anonymous reviewers who provided very helpful and constructive comments on the ms.

Open Access

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Copyright information

© The Author(s) 2012

Authors and Affiliations

  1. 1.Department of Marine ZoologyNetherlands Centre for Biodiversity NaturalisLeidenThe Netherlands

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