Overview
Comprehensive Description
Biology
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Nishida, K. 1990 Phylogeny of the suborder Myliobatidoidei. Mem. Fac. Fish. Hokkaido Univ. 37(1,2) (serial no. 54):1-108. (Ref. 7444)
http://www.fishbase.org/references/FBRefSummary.php?id=7444&speccode=7376
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Distribution
Range Description
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Distribution
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Anon. (1996). FishBase 96 [CD-ROM]. ICLARM: Los Baños, Philippines. 1 cd-rom pp.
http://www.marinespecies.org/aphia.php?p=sourcedetails&id=5909
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Anon. (2000). FishBase 2000 [CD-ROM]. ICLARM: Los Baños, Laguna, Philippines. 4 cd-roms pp.
http://www.marinespecies.org/aphia.php?p=sourcedetails&id=6542
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Compagno, L.J.V. and P.R. Last 1997 Plesiobatidae. Giant stingaree. p. 1467-1468. In K.E. Carpenter and V.H. Niem (eds.) FAO species identification guide for fishery purposes. The living marine resources of the Western Central Pacific. Vol. 3. Batoid fishes, chimaeras and bony fishes. Part 1 (Elopidae to Linophrynidae). FAO, Rome. (Ref. 9914)
http://www.fishbase.org/references/FBRefSummary.php?id=9914&speccode=7376
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Physical Description
Morphology
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Compagno, L.J.V., D.A. Ebert and M.J. Smale 1989 Guide to the sharks and rays of southern Africa. New Holland (Publ.) Ltd., London. 158 p. (Ref. 5578)
http://www.fishbase.org/references/FBRefSummary.php?id=5578&speccode=5891
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Size
Max. size
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Compagno, L.J.V. 1986 Dasyatidae. p. 135-142. In M.M. Smith and P.C. Heemstra (eds.) Smiths' sea fishes. Springer-Verlag, Berlin. (Ref. 3263)
http://www.fishbase.org/references/FBRefSummary.php?id=3263&speccode=6381
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Diagnostic Description
Description
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Anon. (1996). FishBase 96 [CD-ROM]. ICLARM: Los Baños, Philippines. 1 cd-rom pp.
http://www.marinespecies.org/aphia.php?p=sourcedetails&id=5909
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Compagno, L.J.V., D.A. Ebert and M.J. Smale 1989 Guide to the sharks and rays of southern Africa. New Holland (Publ.) Ltd., London. 158 p. (Ref. 5578)
http://www.fishbase.org/references/FBRefSummary.php?id=5578&speccode=5891
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Ecology
Habitat
Habitat and Ecology
Like most other deepwater batoids, the biology of Plesiobatis daviesi is poorly known. Probably viviparous but details of reproduction unknown. Its large size and deepwater occurrence suggests a probable small litter size and long gestation period, resulting in a slow biology (L.J.V. Compagno pers. comm.). Ebert et al. (2002) report a juvenile female at 189 cm TL and an adolescent female at 201 cm TL. Smallest examined mature male was 130 cm TL (Last and Stevens 1994). Maximum size at least 200 cm TL in Australia and elsewhere reported to 270 cm TL (Last and Stevens 1994). Consistent with geographic variability in maximum size, size at maturity probably also varies regionally. Size at birth is unknown, however Compagno and Last (1999) report that a 50 cm TL freeliving individual had an umbilical scar.
Diet consists of fishes (including mesopelagic species suggesting that this species may migrate into the water column to feed), crustaceans (crabs, penaeid prawns, lobsters) and cephalopods (Compagno and Last 1999, Ebert et al. 2002).
Life history parameters
Age at maturity (years): Unknown.
Size at maturity (total length/disc width): 201 cm TL (116 cm DW) or more (Southern Africa; Ebert et al. 2002) (female); 130 cm TL or less (Australia; Last and Stevens 1994) (male).
Longevity (years): Unknown.
Maximum size (total length): At least 200 cm TL (Australia); 270 cm TL elsewhere (Last and Stevens 1994).
Size at birth: Less than 50 cm TL (Compagno and Last 1999).
Average reproductive age (years): Unknown.
Gestation time (months): Unknown.
Reproductive periodicity: Unknown.
Average annual fecundity or litter size: Unknown.
Annual rate of population increase: Unknown.
Natural mortality: Unknown.
Systems
- Marine
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Water temperature and chemistry ranges based on 6 samples.
Environmental ranges
Depth range (m): 185 - 769
Temperature range (°C): 5.897 - 12.730
Nitrate (umol/L): 14.004 - 30.247
Salinity (PPS): 34.122 - 34.998
Oxygen (ml/l): 2.162 - 4.384
Phosphate (umol/l): 0.998 - 2.220
Silicate (umol/l): 8.114 - 54.593
Graphical representation
Depth range (m): 185 - 769
Temperature range (°C): 5.897 - 12.730
Nitrate (umol/L): 14.004 - 30.247
Salinity (PPS): 34.122 - 34.998
Oxygen (ml/l): 2.162 - 4.384
Phosphate (umol/l): 0.998 - 2.220
Silicate (umol/l): 8.114 - 54.593
Note: this information has not been validated. Check this *note*. Your feedback is most welcome.
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From 44 to 680 meters.
Habitat: bathydemersal.
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Environment
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Mundy, B.C. 2005 Checklist of the fishes of the Hawaiian Archipelago. Bishop Museum Bulletins in Zoology. Bishop Mus. Bull. Zool. (6):1-704. (Ref. 58302)
http://www.fishbase.org/references/FBRefSummary.php?id=58302&speccode=46
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Compagno, L.J.V. and P.R. Last 1997 Plesiobatidae. Giant stingaree. p. 1467-1468. In K.E. Carpenter and V.H. Niem (eds.) FAO species identification guide for fishery purposes. The living marine resources of the Western Central Pacific. Vol. 3. Batoid fishes, chimaeras and bony fishes. Part 1 (Elopidae to Linophrynidae). FAO, Rome. (Ref. 9914)
http://www.fishbase.org/references/FBRefSummary.php?id=9914&speccode=7376
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Trophic Strategy
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Nishida, K. 1990 Phylogeny of the suborder Myliobatidoidei. Mem. Fac. Fish. Hokkaido Univ. 37(1,2) (serial no. 54):1-108. (Ref. 7444)
http://www.fishbase.org/references/FBRefSummary.php?id=7444&speccode=7376
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Molecular Biology and Genetics
Molecular Biology
Barcode data: Plesiobatis daviesi
There are 3 barcode sequences available from BOLD and GenBank. Below is a sequence of the barcode region Cytochrome oxidase subunit 1 (COI or COX1) from a member of the species. See the BOLD taxonomy browser for more complete information about this specimen and other sequences.
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Download FASTA File
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Statistics of barcoding coverage: Plesiobatis daviesi
Public Records: 3
Species: 8
Species With Barcodes: 1
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Conservation
Conservation Status
IUCN Red List Assessment
Red List Category
Red List Criteria
Version
Year Assessed
Assessor/s
Reviewer/s
Justification
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Trends
Population
Population Trend
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Threats
Threats
In Australian waters, there is minimal fishing pressure on the species? range off Western Australia and Queensland. The Commonwealth managed Western Trawl Fisheries (continental slope off Western Australia) is comprised of two small-scale demersal trawl fisheries managed by limited entry with a total of 18 permits (over a wide geographical area) (AFMA 2003a). The Commonwealth managed Coral Sea Fishery (off the Queensland continental shelf) is a small-scale fishery with a demersal line sector (nine permits) and a trawl sector (two permits). The fishery is managed by limited entry and catch and effort by these sectors is very low (most operators fish a maximum of 20 days per year) (AFMA 2003b).
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IUCN 2006 2006 IUCN red list of threatened species. www.iucnredlist.org. Downloaded July 2006.
http://www.fishbase.org/references/FBRefSummary.php?id=57073
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Management
Conservation Actions
The development and implementation of management plans (national and/or regional e.g., under the FAO International Plan of Action for the Conservation and Management of Sharks: IPOA?Sharks) are required to facilitate the conservation and sustainable management of all chondrichthyan species in the region. See Anon. (2004) for an update of progress made by nations in the range of P. daviesi.
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Relevance to Humans and Ecosystems
Benefits
Importance
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Ahmad, A., A.A. Abdul Haris Hilmi, A.C. Gambang, S. Ahemad and A.R. Solahuddin (eds.) 2004 Elasmobranch resources, utilization, trade and management in Malaysia. Marine Fishery Resources Development and Management Department, Southeast Asian Fisheries Development Center. (Ref. 53392)
http://www.fishbase.org/references/FBRefSummary.php?id=53392&speccode=7376
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Wikipedia
Deepwater stingray
The deepwater stingray or giant stingaree (Plesiobatis daviesi) is a species of stingray and the sole member of the family Plesiobatidae. It is widely distributed in the Indo-Pacific, typically over fine sediments on the upper continental slope at depths of 275–680 m (900–2,230 ft). This species reaches 2.7 m (8.9 ft) in length and 1.5 m (4.9 ft) in width. It has an oval pectoral fin disc with a long, flexible, broad-angled snout. Most of the entire latter half of its tail supports a distinctively long, slender, leaf-shaped caudal fin. Its coloration is dark above and white below, and its skin is almost completely covered by tiny dermal denticles.
Preying on crustaceans, cephalopods, and bony fishes, the deepwater stingray may hunt both on the sea floor and well above it in open water. It is probably aplacental viviparous, with the mother supplying her gestating young with histotroph ("uterine milk"). Captured rays merit caution due to their long, venomous stings. This species is taken by deepwater commercial fisheries, but in numbers too small to significantly threaten its population. Therefore, the International Union for Conservation of Nature (IUCN) has assessed it as Least Concern.
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Taxonomy and phylogeny
The first scientific description of the deepwater stingray was authored by John H. Wallace, as part of a 1967 Investigational Report from the Oceanographic Research Institute (ORI), Durban. He named the new species daviesi in honor of David H. Davies, the late Director of the ORI, and placed it in the genus Urotrygon based on its long, low caudal fin and lack of a dorsal fin. The type specimens were collected during September 1996 near the Limpopo River mouth in Mozambique: the holotype is a mature male 92 cm (36 in) across, and the paratype is an immature male 33 cm (13 in) across.[3] Other common names for this species include Davies' stingray and giant stingray.[4]
In a 1990 morphological phylogenetic study, Kiyonori Nishida concluded that the deepwater stingray and the sixgill stingray (Hexatrygon bickelli) were the most basal stingrays (suborder Myliobatoidei). Therefore, he moved this species to its own genus, Plesiobatis, and family, Plesiobatidae; the name is derived from the Greek plesio ("primitive") and batis ("ray").[5] Subsequent morphological studies have corroborated the basal position of Plesiobatis, but disagreed on its relationships to nearby taxa. John McEachran, Katherine Dunn, and Tsutomu Miyake in 1996 could not fully resolve the position of Plesiobatis, and thus assigned it provisionally to the family Hexatrygonidae.[6] McEachran and Neil Aschliman in 2004 found Plesiobatis to be the sister taxon of Urolophus, and recommended that it be placed in the family Urolophidae.[7] Until the phylogeny is better-resolved, authors have tended to preserve the family Plesiobatidae.[2][8]
Distribution and habitat
Records of the deepwater stingray come from a number of locations scattered widely in the Indo-Pacific: KwaZulu-Natal in South Africa and Mozambique, the Gulf of Mannar, the northern Andaman Islands, the South China Sea, the Ryukyu Islands and the Kyushu-Palau Ridge, northwestern Australia from the Rowley Shoals to Shark Bay, northeastern Australia from Townsville to Wooli, New Caledonia, and Hawaii.[1][9][10][11] This bottom-dwelling species generally inhabits the upper continental slope at depths of 275–680 m (900–2,230 ft), over muddy or silty substrates.[11] There is an anomalous record from only 44 m (144 ft) deep off Mozambique. It seems to be locally common in tropical Australian waters, but may be rarer elsewhere.[1]
Description
The deepwater stingray has a flabby body,[11] with enlarged pectoral fins forming a disc usually longer than it is wide. The leading margins of the disc converge at a broad angle. The snout is thin and measures over six times as long as the diameter of the orbit; the snout tip protrudes slightly from the disc. The small eyes are positioned just ahead of the spiracles, which have angular posterior rims. The large, circular nostrils are placed closed to the mouth, to which they are connected by a pair of broad grooves. Between the nostrils is a broad curtain of skin with a strongly fringed posterior margin. The wide, straight mouth contains 32–60 tooth rows in either jaw, increasing in number with age. Each tooth is small with a low, blunt cusp; in adult males the teeth at the center are sharp and backward-pointing. The five pairs of gill slits are small and placed beneath the disc.[2][10]
The pelvic fins are small and have blunt outer corners. The moderately thick tail measures 93–102% as long as the disc and lacks lateral skin folds and dorsal fins. One or two serrated stinging spines are present atop the tail, just ahead of the halfway point. The slender caudal fin originates a short distance behind the sting; it is symmetrical above and below, and terminates in a rounded leaf-like shape. The skin is densely covered by fine dermal denticles, that become sparse to absent on the pelvic fins, towards the ventral disc margin, and around the mouth. The deepwater stingray is purplish brown to blackish above; some rays also have irregular darker blotches and spots. The underside is white, with a narrow dark border along the lateral disc margins. The tail is entirely dark, and the caudal fin is black. This large species grows up to 2.7 m (8.9 ft) long, 1.5 m (4.9 ft) across, and 118 kg (260 lb) in weight off southern Africa, though it is not known to exceed 2 m (6.6 ft) long off Australia.[2][3][10]
Biology and ecology
The diet of the deepwater stingray consists of cephalopods, crustaceans (including penaeid prawns, crabs, and lobsters), and bony fishes (including eels).[1][4] Its long, flexible snout is well-suited for rooting through sediment, while the presence of mesopelagic species in its diet suggest that it may also hunt well above the sea floor.[11] One recorded individual was found severely gouged by kitefin sharks (Dalatias licha), which are capable of excising plugs of flesh, cookiecutter-like, from larger animals.[2] The deepwater stingray is presumed to be similar to other stingrays in being aplacental viviparous, and having the developing embryos nourished by maternally produced histotroph ("uterine milk"). Given its large size and deepwater habits, it is probably not highly prolific, with a small litter size and a long gestation period. The young are apparently born at close to 50 cm (20 in) long, as evidenced by the capture of a free-living specimen of that size that still bore a yolk sac scar. Males and females mature sexually at 1.30–1.72 m (4.3–5.6 ft) and 1.89–2.00 m (6.2–6.6 ft) long respectively. The maximum size, and likely also the maturation size, varies between geographic regions.[1][2][10]
Human interactions
When captured, the deepwater stingray flails its powerful tail violently, and its long, venomous sting can inflict a serious injury to a fishery worker. It is caught incidentally by deepwater bottom trawls and longlines; the meat may be sold but is poorly regarded.[10][11] None of the deepwater commercial fisheries operating within its range (including those off South Africa, Taiwan, Indonesia and Australia) are extensive, and thus only small numbers of deepwater stingrays are landed. As a result, the International Union for Conservation of Nature (IUCN) has determined this species to be minimally threatened by human activity, and listed it under Least Concern. However, should deepwater fisheries expand in the future, it may be susceptible to depletion due to its probable rarity and low reproductive rate.[1]
References
- ^ a b c d e f White, W.T.; Kyne, P.M.; Holtzhausen, H. (2006). "Plesiobatis daviesi". IUCN Red List of Threatened Species. Version 2010.4. International Union for Conservation of Nature. http://www.iucnredlist.org/apps/redlist/details/60111. Retrieved July 16, 2011.
- ^ a b c d e f Last, P.R.; Stevens, J.D. (2009). Sharks and Rays of Australia (second ed.). Harvard University Press. p. 394–395. ISBN 0-674-03411-2.
- ^ a b Wallace, J.H. (1967). The batoid fishes of the east coast of southern Africa. Part 2: manta, eagle, duckbill, cownose, butterfly and sting rays. Investigational Report. Oceanographic Research Institute Durban No. 16: 1–56.
- ^ a b Froese, Rainer, and Daniel Pauly, eds. (2011). "Plesiobatis daviesi" in FishBase. April 2011 version.
- ^ Nishida, K. (December 1990). "Phylogeny of the suborder Myliobatidoidei". Memoirs of the Faculty of Fisheries Hokkaido University 37 (1/2): 1–108. http://eprints.lib.hokudai.ac.jp/dspace/bitstream/2115/21887/1/37(1_2)_P1-108.pdf.
- ^ McEachran, J.D.; Dunn, K.A.; Miyake, T. (1996). "Interrelationships within the batoid fishes (Chondrichthyes: Batoidea)". In Stiassney, M.L.J.; Parenti, L.R.; Johnson, G.D.. Interrelationships of Fishes. Academic Press. pp. 63–84. ISBN 0-12-670951-3.
- ^ McEachran, J.D.; Aschliman, N. (2004). "Phylogeny of Batoidea". In Carrier, L.C.; Musick, J.A.; Heithaus, M.R.. Biology of Sharks and Their Relatives. CRC Press. pp. 79–113. ISBN 0-8493-1514-X.
- ^ Nelson, J.S. (2006). Fishes of the World (fourth ed.). John Wiley. pp. 77–78. ISBN 0-471-25031-7.
- ^ Akhilesh, K.V.; Manjebrayakath, H.; Ganga, U.; Pillai, N.G.K.; Sebastine, M. (July-December 2009). "Morphometric characteristics of deepwater stingray Plesiobatis daviesi (Wallace, 1967) collected from the Andaman Sea". Journal of the Marine Biological Association of India 51 (2): 246–249. http://eprints.cmfri.org.in/2179/1/246-249-K._V._Akhilesh.pdf.
- ^ a b c d e Compagno, L.J.V.; Last, P.R. (1999). "Plesiobatidae. Giant stingaree". In Carpenter, K.E.; Niem, V.H.. FAO Identification Guide for Fishery Purposes. The Living Marine Resources of the Western Central Pacific. Food and Agricultural Organization of the United Nations. pp. 1467–1468. ISBN 92-5-104302-7.
- ^ a b c d e Last, P.R.; White, W.T.; Caire, J.N.; Dharmadi; Fahmi; Jensen, K.; Lim, A.P.F.; Manjaji-Matsumoto, B.M.; Naylor, G.J.P.; Pogonoski, J.J.; Stevens, J.D.; Yearsley, G.K. (2010). Sharks and Rays of Borneo. CSIRO Publishing. pp. 180–181. ISBN 978-1-921605-59-8.
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