<<

Records of the Western Australian Museum 20: 349-352 (2001). Short communication

The helleri HeckeI (): another aquarium established in the wild in Western

David L. Morgan and Howard S. Gill Division of Science and Engineering, Murdoch University, South Street, Murdoch, 6150, Australia email: [email protected]

INTRODUCTION While the green swordtail Xiphophorus helleri Considering the enormous number of fish (Poeciliidae) (Figure 1) has long been imported into imported into Western Australia each year by the Australia for use in the aquarium trade, a self­ aquarium trade (ca 600 000 individual fish/year maintaining population has not previously been from overseas destinations - this figure does not captured in the natural waterways of Western include fish imported from elsewhere in Australia) Australia. Feral populations of this have, (W. Cross, personal communication - Australian however, been found in some drainages in Quarantine and Inspection Service), it is fortunate Queensland since the 1960's as well as in New that very few species have established wild South Wales, the Northern Territory and also in the populations here. Although only a small number of drainages of Lake Eyre (McKay, 1978; Thompson, introduced aquarium species, such as tilapia 1982; Milton and Arthington ,1983; Arthington and Oreochromis mossambicus (Cichlidae), goldfish Lloyd, 1989; Kailola et al., 1999). Xiphophorus helleri, Carassius auratus (), carp Cyprinus carpio which originates from eastern drainages of central (Cyprinidae), one-spot America ( southward to northern ) caudimaculatus (Poeciliidae) and the (Miller, 1966), is a livebearing species that exhibits holbrooki (Poeciliidae), are presently , i.e. the males develop a long entrenched in Western Australian inland waters 'sword' from the lower rays of their caudal fin and (Trendall and Johnson, 1981; AlIen, 1989; Pen and their anal fin becomes modified to form a Potter, 1991; Morgan et al., 1998; Kailola et al., 1999; gonopodium (intromittent organ for internal WA Museum Records; unpublished data), the sheer fertilisation) (Constantz, 1984). Captive bred fish numbers of these and other species entering the exhibit a variety of colours but are generally an state guarantee an uncertain future. The species overall bright orange, fish from wild populations mentioned above have either been deliberately or on the other hand, are olive brown to green with a accidentally released into various waterbodies narrow lateral stripe, the male retaining the orange throughout the state and, as this paper highlights, it coloration in the sword of the caudal fin (Figure 1). is probably only a matter of time before other non­ While it is has been demonstrated that G. holbrooki native species establish self-maintaining is impacting on, and causing a decline in, the native populations in Western Australia. freshwater fish fauna of both south-western and Many not only compete with eastern Australia through both competition for native fish for food and habitat, but may also limited food resources and habitat and aggressive exhibit agonistic behaviour towards or prey on behaviour (e.g. McKay, 1978; Arthington et al., 1983; native fish, often displacing them from their Hambleton et al., 1996; Gill et al., 1999), the effects of preferred habitat or even replacing them in entire other poeciliids on the native fish fauna has systems (e.g. Arthington and Lloyd, 1989; attracted only limited research. It is known, Hutchinson, 1991; Gill et al., 1999; Kailola et al., however, that male X. helleri form long term 1999). Although Western Australia has some of the hierarchies and are to an extent territorial, spending strictest quarantine laws in the country with regard much of their time aggressively fighting with other to most imports, incoming aquarium fish, males and possibly other species (Franck and particularly those entering via eastern Australia, are Ribowski,1993). subjected to only limited checks, thereby increasing This paper reports the first finding of a self­ the risk of introducing noxious species and/or maintaining population of X. helleri in south­ diseases or parasites that may be harboured either western Australia and aims to increase the public in or on the fish or in the water in which they are awareness of the impacts associated with the release transported. of non-native species into Western Australia. It also 350 D.L. Morgan, H.S. Gill

Figure 1 Male green swordtail Xiphophorus helleri, 55 mm TL.

2 highlights the need for more stringent regulations from 0.05 to 5 fish m· , while the lengths of fish at regarding the importation of exotic species for the these sites ranged from 13 to 56 mm TL, aquarium industry. respectively. The presence of large numbers of very small juveniles, and the fact that many of the males had recently spawned and that some of the females MATERIALS AND METHODS were pregnant, demonstrates that the Irwin River As part of a fish survey of the inland waters population is self maintaining. Co-occurring between and Murchison, a total of eight sites species, at the sites downstream of the weir at along a 60 km stretch of the Irwin River and its Mountain Bridge (site 4), included black bream tributaries (near Dongara ca 360 km north of Perth) (Acanthopagrus butcheri), Swan River gobies were sampled for fish during summer 1998/99 (Pseudogobius olorum) and sea mullet (Mugil (Figure 2). Fish were captured using seine nets cephalus). Although there are no data or museum comprised of 3 mm woven mesh. Fish were records available on the distribution of fish in the identified, with those species native to south­ Irwin River, it is possible that the endemic western Australia immediately returned to the freshwater , the western pygmy perch Edelia water, while all individuals of the introduced green vittata and the western minnow Galaxias occidentalis, swordtail Xiphophorus helleri were anaesthetised in were once (and still may be) in the catchment. Both benzocaine and placed into 100% ethanol. The total of these species have been found by the first author length (TL), which excludes the sword, of each fish in the which is only 10 km to the was measured to the nearest mm. south of Sand Plain Creek, a tributary of the Irwin River. Information regarding the impacts of X. helleri on RESULTS AND DISCUSSION the native fauna is unavailable, however, Xiphophorus helleri was found to occur at five of Arthington (1989) found this species in waters the six sites (i.e. sites 2-5 and 7) sampled along a 42 around Brisbane to be omnivorous, consuming km stretch of the Irwin River between the town algae, plant matter, aquatic invertebrates (e.g. bridge (site 2) and Strawberry Bridge (site 7) chironomids, oligochaetes, coleopterans, tricho­ (salinity range 0.3 - 2.4 ppt) (Figure 2). 0 X. helleri pterans, hemipterans, molluscs and other fish) and was captured at the site sampled downstream of also terrestrial invertebrates (e.g. and town bridge (i.e. site 1) which was at the mouth of arachnids). They found that the majority of guts the river (salinity = 13.7 ppt) or at the only site that examined contained, on average, large amounts (ca contained water upstream of Strawberry Bridge (i.e. 88% by volume) of amorphic, partly digested Depot Hill Rd - site 8) which was almost dry. No material which included plant fragments, fish was captured at the site sampled on Sand Plain filamentous algae and diatoms. Since the Creek (i.e. site 6), which had previously dried. The reproductive cycle of female X. helleri apparently mean densities of X. helleri at sites 2-5 and 7 ranged ceases only when water temperatures fall below Xiphophorus helleri in south-western Australia 351 tN

INDIAN OCEAN ~ L-.-I - o 8km

Figure 2 The sites sampled for green swordtails Xiphophorus helleri in the Irwin River, Western Australia.

15°C (Milton and Arthington 1983), this species is which may reach over 100 mm TL, have even been capable of reproducing for an extensive period shown to out compete and dominate the aggressive throughout most of Western Australia, with only and very successful G. holbrooki (Arthington et al., winter/ spring in the south-west recording 1986). Thus, while X. helleri is only currently found temperatures less than 15°C. In the Brisbane region in the Irwin River in Western Australia, the fact that (a latitude similar to that of the Irwin River), over it can utilise an array of food/prey types, produces 30% of females were pregnant in every month of live young, can generate very large populations in a the year except June (Milton and Arthington, 1983), short period, lacks environmental constraints and is with new recruits also appearing in these months. able to coexist with and even outcompete G. Furthermore, individuals of this species can mature holbrooki (Milton and Arthington, 1983) makes the at a small size (ca 23 and 27 mm for females and swordtail a species that should be declared a pest. males, respectively), have a higher mean fecundity While it may not be possible to eradicate this than the extremely successful G. holbrooki (ca 60 species from the Irwin River, it may be possible to versus ca 23), have a short gestation period limit future introductions through both public (between 24 and 63 days) and thus have the education and the removal of this species from potential to produce up to 12 broods per year aquarium shops. The fact that many aquarium (Milton and Arthington, 1983; Kailola et al., 1999). species are relatively hardy, easy to maintain and This species can also tolerate a wide range of reproduce readily makes them a potential threat to temperatures and salinities and is able to survive in the unique fauna of Western Australia should they oxygen deficient waters by gulping at the air-water escape or be released into the wild. It should be the interface (Arthington et al., 1986). Green swordtails, responsibility of the Fisheries Department of 352 D.L. Morgan, H.S. Gill

Western Australia to identify and then prohibit Gill, H.5., Hambleton, S.J. and Morgan, D.L. (1999). Is species which, if released into the wild, are capable Gambusia holbrooki a major threat to the native of readily establishing feral populations. Future freshwater of south-western Australia? In Seret, surveys of the south-west, particularly within B. and Sire, J.-Y. (eds), Proceedings of the 5th Indo­ populated areas, will undoubtably reveal other non­ Pacific Fish Conference (Noumea, 3-8 November 1997): 79-87. Societe Francaise d' Ichtyologie and native species that have established populations as Institut de Recherche pour le Development, Paris. a result of deliberate releases. Hambleton, S., Gill, H., Morgan, D. and Potter, L (1996). Interactions of the introduced mosquitofish (Gambusia holbrooki) with native fish species in the RGC ACKNOWLEDGEMENTS Wetlands, Western Australia. Technical Report No. 33: Thanks are extended to the Natural Heritage Capel: RGC Mineral Sands Ltd, Capel. Trust, Fisheries WA, Water and Rivers Commission Hutchinson, M.J. (1991). Distribution patterns of redfin of WA and Murdoch University for funding the perch Perca fluviatilis Linnaeus and western pygmy survey of the waters between Perth and Murchison. perch Edelia vittata Castelnau in the Murray River Thank you very much to Charlotte Morgan for help system Western Australia. Records of the Western with the field work. Australian Museum 15: 295--301. Kailola, P.J., Arthington, A.H., Woodland, D.J. and Zalucki, D.J. (1999). Non-native finfish species REFERENCES recorded in Australian waters. In Arthington, A.H., Kailola, P.J., Woodland, D.J. and Zalucki, D.J. (eds). AlIen, G.R (1989). Freshwater fishes of Australia. T.F.H. Provision of baseline environmental data relevant to an Publications, Neptune City. evaluation of quarantine risk potentially associated with Arthington, AH. (1989). Diet of Gambusia afftnis holbrooki, the importation to Australia of ornamental finfish. Xiphophorus helleri, X. maculatus and reticulata Australian Quarantine and Inspection Service, (Pisces: Poeciliidae) in streams of southeastern Canberra. Queensland, Australia. Asian Fisheries Science 2: 193­ McKay, RJ. (1978). The exotic freshwater fishes of 212. Queensland. Report to the Australian National Parks Arthington, AH. and Lloyd, L.N. (1989). Introduced and Wildlife Service, Canberra. poeciliids in Australia and New Zealand. In Meffe, Miller, RR (1966). Geographical distributon of Central G.K. and Snelson, F.F. (eds), Ecology and evolution of American freshwater fishes. Copeia 1966: 773-801. livebearing fishes (Poeciliidae): 333-348. Prentice Hall, Milton, D.A and Arthington, AH. (1983). Reproductive New Jersey. biology of Gambusia afftnis holbrooki Baird and Girard, Arthington, AH., McKay, RJ. and Milton, D.A. (1986). Xiphophorus helleri (Gunther) and X. maculatus The ecology and management of exotic and endemic (Heckel) (Pisces: Poeciliidae) in Queensland, freshwater fishes in Queensland. In Hundloe, T.J.A Australia. Journal ofFish Biology 23: 23-41. (ed.), Fisheries management: theory and practice in Morgan, D.L., Gill, H.S. and Potter, Le. (1998). Queensland: 224-245. Griffiths University Press, Distribution, identification and biology of freshwater Brisbane. fishes in south-western Australia. Records of the Arthington, AH. and Marshall, CJ. (1998). Diet of the Western Australian Museum Supplement No. 56: 97 pp. exotic mosquitofish, Gambusia holbrooki, in an Pen, L.J. and Potter, LC (1991). Reproduction, growth Australian lake and potential for competition with and diet of Gambusia holbrooki (Girard) in a temperate indigenous fish species. Asian Fisheries Science 12: 1-8. Australian River. Aquatic Conservation: Marine and Arthington, AH., Milton, D.A. and McKay, RJ, (1983). Freshwater Ecosystems 1: 159-172. Effects of urban development and habitat Thompson, G. (1982). Fish collecting on a part round alterations on the distribution and abundance of Australia trip. Fishtales 13: 6-10. native and exotic freshwater fish in the Brisbane region, Queensland. Australian Journal of Ecology 8: Trendall, J.T. and Johnson, MS. (1981). Identification by 87-101. anatomy and gel electrophoresis of Phalloceros caudimaculatus (Poeliliidae), preViously mistaken for Constantz, G.D. (1984). Sperm competition in poeciliid Gambusia affinis holbrooki (Poeciliidae). Australian fishes. In Smith, RL. (ed.), Sperm competition and Journal ofMarine and Freshwater Research 32: 993-996. mating systems. 465-485. Academic Press, Orlando. Franck, D. and Ribowski, A. (1993). Dominance Manuscript received 19 August 1999; accepted 15 November hierarchies of male green swordtails (XiphopllOrus 1999. helleri) in nature. Journal ofFish Biology 43: 497-499. Guide to Authors

Subject Matter: Manuscripts: Reviews, observations and results of research into The original and two copies of manuscripts and all branches of natural science and human studies figures should be submitted to the Editors, c/­ will be considered for publication However, Publications Department, Western Australian emphasis is placed on studies pertaining to Western Museum, Francis Street, Perth, Western Australia Australia. Longer papers will be considered for 6000. They must be in double-spaced typescript on publication as a Supplement to the Records of the A4 sheets. All margins should be at least 30 mm Western Australian Museum. Short communications wide. Tables plus heading and legends to should not normally exceed three typed pages and illustrations should be typed on separate pages. The this category of paper is intended to accommodate desired position for insertion of tables and observations, results or new records of significance, illustrations in the text should be indicated in that otherwise might not get into the literature, or pencil. Tables should be numbered consecutively, for which there IS a particular urgency for have headings which make them understandable publication. All material must be original and not without reference to the text, and be referred to in have been published elsewhere. the text. High quality illustrations are required to size Presentation: (16.8 cm x 25.2 cm) or no larger than 32 cm x 40 Authors are advised to follow the layout and style cm with sans serif lettering suitable for reduction to in the most recent issue of the Records of the size. Photographs must be good quality black and Western Australian Museum including headings, white prints, not exceeding 16.8 cm x 25.2 cm. tables, illustrations and references. Scale must be indicated on illustrations. All maps, The title should be concise, informative and line drawings, photographs and graphs, should be contain key words necessary for retrieval by numbered in sequence and referred to as Figure/s in modem searching techniques. An abridged title (not the text and captions. Each must have a brief, fully exceeding 50 letter spaces) should be included for explanatory caption. On acceptance a computer disk use as a running head. containing all corrections should be sent with An abstract must be given in full length papers amended manuscript. The disk should be marked but not short communications, summarizing the with program (e.g. Word, WordPerfect, etc). scope of the work and principal findings. It should In papers dealing with historical subjects normally not exceed 2% of the paper and should be references may be cited as footnotes. In all other suitable for reprinting in reference periodicals. papers references must be cited in the text by author The International System of units should be used. and date and all must be listed alphabetically at the Numbers should be spelled out from one to nine end of the paper. The names of journals are to be in descriptive text; figures used for 10 or more. For given in full. associated groups, figures should be used consistently, e.g. 5 to 10, not five to 10. Processing: Spelling should follow the Concise Oxford Papers and short communications are reviewed Dictionary. by at least two referees and acceptance or rejection Systematic papers must conform with the is then decided by the editors. International Codes of Botanical and Zoological The senior author is sent one set of page proofs Nomenclature and, as far as possible, with their which must be returned promptly. recommendations. The senior author will receive fifty free offprints Synonymies should be given in the short form of the paper. Additional offprints can be ordered at (taxon, author, date, page) and the full reference page proof stage. cited at the end of the paper. All citations, including those associated with scientific names, must be included in the references. Records ofthe Western Australian Museu111 Volulne 20 Part 3 2001

CONTENTS

J.B. Hutchins Biodiversity of shallow reef fish assemblages in Western Australia using a rapid censusing technique 247

I. Abbott The Bilby Macrotis lagotis (Marsupialia: Peramelidae) in south-western Australia: original range limits, subsequent decline, and presumed regional extinction 271

P.E. Bock and P.L. Cook A review of Australian Siphonicytara Busk (Bryozoa: Cheilostomatida) 307

M.Zabka Salticidae (Archnida: Araneae) from the Oriental, Australian and Pacific regions, XIV. The Adoxotoma Simon 323 T. Karanovic, G.L. Pesce and W.F. Humphreys Copepods from ground waters of Western Australia, V. Phyllopodopsyllus wellsi sp. novo (Crustacea: Copepoda: Harpacticoida) with a key to world 333

M.S. Harvey Notes on the spider genus Symphytognatha (Araneae: Symphytognathidae) in Western Australia 345

SHORT COMMUNICATION

D.L. Morgan and H.S. Gill The green swordtail Xiphophorus helleri Heckel (Poeciliidae): another aquarium fish established in the wild in Western Australia 349