BULLETIN OF MARINE SCIENCE, 69(3): 1089–1094, 2001 ALGAL COLONIZATION OF CARIBBEAN SCORPIONFISHES David L. Ballantine, J. Nelson Navarro and Dannie A. Hensley ABSTRACT Forty algal species (four Cyanophyta, 20 Rhodophyta, three Chlorophyta, three Phaeophyceae and 10 Bacillariophyceae) are reported as growing on Scorpaena grandicornis Cuvier and Scorpaena plumieri Bloch from Puerto Rico. A third scorpionfish species, Scorpaenodes tredecimspinosus (Metzelaar), did not support algal growth. Algae were principally associated with the region of the head and dorsal cirri. Presence of algae undoubtedly enhances the cryptic camouflage of these fishes. The phenomenon of algae growing on fish tissue, while unusual, is not rare. Occurrences of algae growing on some freshwater fishes are apparently mostly associated with superficial wounding. Published accounts of these incidences include that of Nigrelli et al. (1958) who indicated presence of microscopic algal filaments below the epidermis of the kissing gourami, Helostoma temmincki Cuvier (ex Kuhl and van Hasselt). The green filamentous alga Cladophora has also been shown to occur on two Oklahoma freshwater fish species, Micropterus salmoides (Lacépède) and Ictiobus bubalus (Rafinesque) (Vinyard, 1953); on carp, Cyprinus carpio Linnaeus (Edwards, 1978), and on the operculum of rainbow trout, Oncorhynchus mykiss (Walbaum) (=Salmo gairdneri Richardson) (Hoffman, 1967). These occurrences were all considered infections. Growth of two filamentous algal species on lesions over opercular bones in seawater-cultured Tilapia aurea (Steindachner) have also been seen (Miller and Ballantine, 1972). Millstein (1998) showed that sloughed skin of the sculpin, Blepsias bilobus Cuvier in Cuvier and Valenciennes contained large numbers of diatoms. However, most known occurrences of algae growing on marine fishes are limited to growth on teeth of parrotfishes. Winn and Bardach (1960) reported conspicuous growths of algae on teeth of large specimens of Scarus guacamaia Cuvier and S. vetula Bloch and Schneider (ex Parra) from Bermuda. Other records of presence of algae on teeth of Pacific parrotfishes include those of Isokawa (1956) and Tsuda et al. (1972). The latter identified twelve algal species on beaks of parrotfishes from Guam. Scorpionfishes are venomous bottom fishes which exhibit a cryptic mode of life (Böhlke and Chaplin, 1968). Their coloration and fleshy skin outgrowths mimic the surrounding habitat in such a way that they are difficult to see (Cott, 1957). Fishelson (1973: 498) stated that various stonefishes (Synanceiidae) and scorpionfishes (Scorpaenidae) are covered by a “sheet of algae, hydrozoans, diatomeans and other organisms ....” and speculated that this promotes the ability of the fish to blend with its surroundings. Grobecker (1983) also speculated that in addition to camouflage on stonefish,” Synanceia verrucosa Bloch and Schneider, presence of algae might serve as an attractant to herbivorous prey. Beyond indication of presence of filamentous algae and diatoms (Fishelson, 1973), the fouling organisms were not further identified in these studies. Nagelkerken (1980: 71) figured an individual of Scorpaena plumieri Bloch that possessed obvious algal growth; however, he did not further discuss the phenomenon. We report here species of algae colonizing three species of scorpionfishes in Caribbean western Puerto Rico. 1089 1090 BULLETIN OF MARINE SCIENCE, VOL. 69, NO. 3, 2001 METHODS AND MATERIALS Scorpionfishes were collected from coastal waters in western Puerto Rico. Specimens were either collected with a multiprong spear or were coaxed into a diver’s collecting bag. Specimens were fixed in 10% Formalin/seawater on return to the lab. Lengths of fish specimens were measured as standard lengths (SL) (Hubbs and Lagler, 1949) to the nearest mm using dial calipers. Pieces of skin were observed with a compound microscope. Diatoms were identified from two of the S. plumieri specimens. Algal voucher specimens are deposited in the algal herbarium (MSM) and fish voucher specimens are deposited in the fish museum (UPRM), both of the Department of Marine Sciences, University of Puerto Rico, Mayagüez, Puerto Rico. Authority designations of algal taxa are according to Brummitt and Powell (1992). The following specimens were examined: Scorpaena grandicornis Cuvier: UPRM 3768, 12.5 cm SL, Lajas, La Parguera, 1.5 km seaward Media Luna Reef, 17 m; 2.x.1980. Scorpaena plumieri Bloch: UPRM 3774, 12.0 cm SL, Lajas, La Parguera, inshore cay seaward of Cueva Island, 1.0 m; 27.xi.1980. UPRM 3770, 13.3 cm SL, Guanica, Ballena Bay, 2.0 m, 30.xii.1980. UPRM 3769, 12.1 cm SL, ibid. 18.v.1981. UPRM 3766, 28.5 cm SL, Lajas, La Parguera, 1.5 km seaward Media Luna Reef, 17 m, 13.v.1981. UPRM 3771, 9.6 cm SL, ibid., 18.viii.1981. UPRM 3765, 16.0 cm SL, ibid.; 9.ix.1981. UPRM 3775, 24.4 cm SL, Aguadilla, Crash Boat Beach, 9.1 m, 16.iii.1981. UPRM 3767, 13.8 cm SL, Desecho Island, 9.1 m 17.x.1980. Scorpaenodes tredecimspinosus (Metzelaar): UPRM 3772, 2.7 cm SL, Lajas, La Parguera, edge of insular shelf, 21 m; 2.iv.1982. UPRM 3773, four specimens (2.2, 2.3, 2.4, 3.0 cm SL), ibid.; 16.iv.1982. RESULTS Algal species were most commonly located in the region of the head (Fig. 1) and on dorsal cirri (Fig. 2); they were less commonly found on sides of the body. Of the five individuals of S. tredecimspinosus examined, only one specimen bore detectable algae, a minute amount of the cyanophyte Microcoleus lyngbyaceus. The single specimen of S. grandicornis bore 14 species of macro algae and seven diatom species. Eight specimens of S. plumieri were examined. Of these, seven bore substantial amounts of algae, and 33 species were identified on a single specimen. ALGAL SPECIES IDENTIFIED CYANOPHYTA Calothrix crustacea Schousb. & Thur. Microcoleus lyngbyaceus (Kütz.) P. Crouan & H. Crouan Oscillatoria lutea C.Agardh Schizothrix mexicana Gomont RHODOPHYTA Aglaothamnion boergesenii (Aponte & D. L. Ballant.) L’Hardy-Halos & Rueness in Aponte, D. L. Ballant. & J. N. Norris Aglaothamnion sp. Acrochaetium sp. Antithamnionella breviramosa (E. Y. Dawson) E.M.Woll. in Womersley & A. Bailey BALLENTINE ET AL.: ALGAL COLONIZATION OF CARIBBEAN SCORPIONFISHES 1091 Figure 1. Epizoic algal growth on head region of Scorpaena plumieri. Algae appear as localized fuzzy areas (arrowheads). Scale bar = 1.0 cm. Antithamnionella sp. Asparagopsis taxiformis (Delile) Trevisan [Falkenbergia stage] Centroceras clavulatum (C. Agardh) Mont. Ceramium fastigiatum Harv. forma flaccidum H. E. Peterson in Børgesen [C. flaccidum (Kütz.) Ardiss.] Ceramium sp. Champia parvula (C. Agardh) Harv. Chondria sp. Chroodactylon ornatum (C. Agardh) Basson Crouania attenuata (C. Agardh) J.Agardh Diplothamnion jolyi C. Hoek Erythrotrichia carnea (Dillwyn) J. Agardh Griffithsia globulifera Harv. ex Kütz. Herposiphonia secunda (C. Agardh) Ambronn Heterosiphonia crispella (C. Agardh) M. J. Wynne Polysiphonia havanensis Mont. Polysiphonia sp. Sahlingia subintegra (Rosenv.) Kornmann Spyridia filamentosa (Wulfen) Harv. in Hooker Stylonema alsidii (Zanardini) K. M. Drew HETEROKONTOPHYTA (BACILLARIOPHYCEAE) Amphora sp. Cocconeis spp. Isthmia enervis Ehrenb. Licmophora ehrenbergii (Kütz.) Grunov 1092 BULLETIN OF MARINE SCIENCE, VOL. 69, NO. 3, 2001 Figure 2. Algal growth, mostly diatoms on dorsal cirrus of Scorpaena plumieri. Licmophora sp. (arrowhead) and a sporeling of Ceramium sp. (arrow) are indicated. Scale bar = 250 mm Licmophora flabellata (Carm.) C. Agardh Licmophora remulus Grunov Mastogloia binotata (Grunov) Cleve Mastogloia schmidtii Heiden Mastogloia splendida (W. Greg.) Cleve Tabularia fasciculata (C. Agardh) D. M. Williams & Round HETEROKONTOPHYTA (PHAEOPHYCEAE) Dictyota sp. Hincksia sp. Sphacelaria sp. CHLOROPHYTA Cladophora sp. Phaeophila dendroides (P. Crouan & H. Crouan) Batters Rhizoclonium sp. DISCUSSION A surprisingly high number of species of macroalgae are able to colonize S. plumieri and S. grandicornis. A total of 40 species of fouling algae (30 spp. macroalgae, with representatives from all major groups, and 10 spp. diatoms) were found growing on S. plumieri and S. grandicornis. An unidentified hydroid species was found as well. Not all of the macroalgal species were unidentifiable to species as they were frequently repre- BALLENTINE ET AL.: ALGAL COLONIZATION OF CARIBBEAN SCORPIONFISHES 1093 sented by sporelings. The Cyanophyta species Oscillatoria lutea and M. lyngbyaceus were present on 44.4 and 55.6% of the S. plumieri examined. Two of the Rhodophyta species, Stylonema alsidii (55.6%) and Erythrotrichia carnea (66.7%), were also commonly present on scorpionfishes. Acrochaetium sp. and Ceramium spp. were the other most common algal species present. While cover of algal growth was not quantified, the amount of algae on the scorpion fishes was inconsistent, varying from a few sparsely colonizing individuals to a conspicuous cover. Typical fish epithelial cells produce a mucopolysaccharide layer (Ellis et al., 1989) and an outer glycoprotein mucous layer (Mittal and Banerjee, 1980). Dawson (1959) stated that the normal mucous covering of fishes is inhibitory to either the growth or settlement of invading species. Hence, an injury which disrupts this covering could conceivably allow the recruitment of algal spores as is seen in the colonization of algae on freshwater fish species. Few fishes, however, have keratinized epidermal cells (Mittal and Banerjee, 1980). Fishelson (1973) indicated that the keratinized epidermal cells of stonefish were colonized by fouling organisms including algae. Fishelson (1973) also observed presence of keratinization in two Red Sea scorpionfishes; however, it was less than in the stonefish. There is some uncertainty as to whether tropical west Atlantic scorpionfishes possess keratinized epithelial cells or whether skin sloughing occurs. The possibility that skin characteristics differ on different body parts is indicated by the fact that algal colonization was extremely limited away from the head region. Skin sloughing, similar to that reported by Fishelson (1973) and Millstein (1998), may explain why one of the larger S. plumieri specimens examined was devoid of algal growth altogether. The fact that the skin of S. plumieri and S. grandicornis is typically colonized by algae undoubtedly abets the camouflage exhibited by these two species. S. tredecimspinosus may have different skin characteristics which explains its lack of being colonized by algae. ACKNOWLEDGMENTS We thank E. Williams and J. Kimmel who assisted in collecting. We also thank J. Randall for discussion of fouling on Scorpaenidae. LITERATURE CITED Böhlke, J. E. and C. C. G. Chaplin. 1968. Fishes of the Bahamas and adjacent tropical waters. Acad. Nat. Sci. Philadelphia. Livingston Publishing Co., Wynnewood, Pennsylvania. 771p. Brummitt, R. K. and C. E. 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Histozoic algal growth in fish. Copeia 4: 331–333. Tsuda, R. A., W. K. Larson and R. J. Lujan. 1972. Algal growth on beaks of live parrot fishes. Pac. Sci. 26: 20–23. Vinyard, W. C. 1953. Epizoophytic algae from mollusks, turtles, and fish in Oklahoma. Proc. Oklahoma Acad. Sci. 34: 63–65. Winn, H. E. and J. E. Bardach. 1960. Some aspects of the comparative biology of parrot fishes at Bermuda. Zoologica 45: 29–34. DATE RECEIVED: May 12, 2000. DATE ACCEPTED: June 22, 2001. ADDRESSES: (D.L.B., D.A.H.) Department of Marine Sciences, P.O. Box 9013, University of Puerto Rico, Mayagüez, Puerto Rico 00681; (J.N.N.) Biology Department, Pontifical Catholic University of Puerto Rico, Ponce, Puerto Rico 00731.
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