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Non-indigenous giant mud crab, Scylla serrata (Forskål, 1775) (Crustacea: Brachyura: Portunidae) in Malaysian coastal waters: a call for caution
Marine Biodiversity Records volume 10, Article number: 26 (2017)
Introduction of non-indigenous species into a well-established ecosystem can be detrimental, resulting in both ecological and economical damage. Two specimens of giant mud crab, Scylla serrata were found for the first time in two geographically distinct mud crab landing sites (Matang Mangrove Forest Reserve, Perak and Kota Marudu Mangrove Forest, Sabah) in Malaysia. Their identities were confirmed using a combination of morphological, morphometric and molecular (partial COI gene) analyses. Scylla serrata is regarded as non-indigenous species within Malaysian coastal waters as this is the first confirmed report of their occurrence in Malaysia and no established population was found in both landing sites. Accidental release or escape was considered as the possible vector for the introduction of the two specimens found in this study as frequent import of S. serrata from other countries were reported in both landing sites. Urgent intervention is needed to prevent further introduction and possible establishment of S. serrata population in Malaysian coastal waters.
A new species introduced to an ecosystem outside its native range is termed as “non-indigenous species” and can occur deliberately or accidentally by the means of humans (Holmes and Simons 1996; Manchester and Bullock 2000). If the new environment is suitable, the non-indigenous species may establish a viable population, and if it spreads fast and causes harm to either the environment, human health, economy or any other valuable resources, it will be termed as an “invasive species” (Manchester and Bullock, 2000). Aquatic ecosystems are even more susceptible to the spread of non-indigenous species due to the high reproduction rate of most aquatic organisms and rapid dispersal of propagules that is possible in water (Strayer and Dudgeon 2010; Wood et al. 2016).
The mud crab genus Scylla De Haan, 1833 (Decapoda: Portunidae) is widely distributed in the brackish and coastal mangrove area of Indo-West-Pacific region and supports important commercial, recreational and indigenous fisheries (Keenan et al. 1998; Ikhwanuddin et al. 2011). Known for their succulent meat and delicate flavour and texture, mud crabs are highly sought after in seafood restaurants, both locally and internationally. The global capture fishery production of mud crab is approximately 38,000 t in the year 2014 (FAO, 2016). Mud crabs are highly adaptable to various environments due to their ability to tolerate broad ranges of temperature (16–35 °C) and salinity (1–56 ppt) (Alberts-Hubatsch et al. 2015). They also show movement up to an average of 3.7 km for foraging purposes (Hyland et al. 1984). Mud crabs are opportunistic omnivores and feed mainly on crustaceans, molluscs and fish (Viswanathan and Raffi 2015). Thus, if introduced, either deliberate or accidental, mud crabs could potentially disrupt the balance of the local ecosystem.
There are four species of mud crab within this genus, Scylla serrata (Forskål, 1775), Scylla tranquebarica (Fabricius, 1798), Scylla olivacea (Herbst, 1796) and Scylla paramamosain (Estampador, 1949). Scylla serrata is the largest and most widespread species of genus Scylla (Keenan et al. 1998; Alberts-Hubatsch et al. 2015). Scylla serrata has been reported in most tropical and subtropical coastal regions of Indo-West-Pacific such as Bangladesh (Begum et al. 2009), India (Ali et al. 2011), Sri Lanka (Tharmine et al. 2014; Amarasekara et al. 2016), Indonesia (Roza and Hatai 1999; Nordhaus et al. 2009), Philippines (Baylon et al. 2004; Quinitio et al. 2007), Australia (Keenan et al. 1998) and around the oceanic islands of Indo-Pacific (Alberts-Hubatsch et al. 2015), except around South China Sea (Albert-Hubatsch et al. 2015; Fazhan et al. 2017). Prior to the revision of genus Scylla by Keenan et al. (1998), the species identification of mud crabs within the genus Scylla has been controversial and only one species, S. serrata, was being recognized (Stephenson and Campbell 1960). The division of genus Scylla into four distinctive species has led to the re-validation of species identification in most locations. However, since the revision of the genus Scylla (Keenan et al. 1998), S. olivacea has been the most common species in Malaysian waters, although S. paramamosain and S. tranquebarica also occur (Ikhwanuddin et al. 2011; Waiho et al. 2015; Waiho et al. 2016).
A recent nationwide survey of mud crab species composition revealed two specimens of the giant mud crab, S. serrata in Malaysian waters. This study describes the species identification of S. serrata found using (i) morphological (ii) morphometrics and (iii) molecular identification methods. The confirmed identity of S. serrata in this study serves as the first report of its occurrence in Malaysian waters. The possible vector and impact of its introduction are discussed.
A bimonthly nationwide survey of mud crab species composition was conducted in Malaysian waters from April 2012 to July 2013 (Fig. 1). A total of 1325 mud crabs caught using standard crab pots were identified to species level based on Keenan et al. (1998). Interestingly, two specimens of S. serrata was found for the first time from Malaysian coastal waters. One specimen (immature female) was collected from Matang Mangrove Forest Reserve, Perak (4°45′N100°37′E) (Straits of Malacca) on 27 March, 2013 by H. Fazhan and another (mature male) was found in Kota Marudu Mangrove Forest, Sabah (6°44′N117°1′E) (Sulu Sea) (Fig. 1) on 12 May, 2013 by K. Waiho. Fishing and crabbing are commonly conducted in both estuaries by local communities. Matang Mangrove Forest Reserve was gazetted as a permanent mangrove forest reserve more than a century ago whereas Kota Marudu is protected under the jurisdiction of local forestry department.
Morphological and morphometric identification
The collected specimens were identified morphologically based on the key characters (i.e. frontal lobe spines shape and height, cheliped carpus and propodus spine, cheliped color, and polygonal patterning on pereiopods) provided by Keenan et al. (1998).
Only mature male (>95 mm carapace width, CW) was subjected to morphometric identification. The measurements of 24 body parts were taken to the nearest 0.01 mm using Vernier calipers based on Keenan et al. (1998). Five morphometric ratios used by Keenan et al. (1998) for species comparison and identification was applied in this study as well.
Additionally, validation using molecular method was conducted. Both specimens were stored in −80 °C prior DNA extraction. DNA was extracted from the muscle tissue of walking leg using GF-1 Nucleic Acid Extraction Kits (Vivantis Tech., MY). Partial cytochrome oxidase subunit I (COI) gene from the mitochondrial genome was amplified using polymerase chain reaction (PCR). The temperature profile used was: pre-denaturation at 95 °C for 10 mins, denaturation at 94 °C for 30s, annealing at 50 °C for 30s, extension at 72 °C for 45 s (30 cycles) and final extension at 70 °C for 10 mins. Standard universal primers LCO-1490 (5′-GGTCAACAAATCATAAAGATATTGG-3′) and HCO-2198 (5′-TAAACTTCAGGGTGACCAAAAAATCA-3′) were used (Folmer et al. 1994; Fazhan et al. 2016). PCR products (Fig. 2) were sent for sequencing (First BASE Lab, MY), checked for quality and subjected to BLAST (Basic Local Alignment Search Tool) analysis for comparison and identification based on deposited sequences in GenBank, NCBI (National Center for Biotechnology Information) (Altschul et al. 1997).
Order: Decapoda Latreille, 1806.
Family: Portunidae Rafinesque, 1815.
Genus: Scylla De Haan, 1833.
Scylla serrata (Forskål, 1775) (Fig. 3).
The carapace is oval and is 1.56 times (mature ♂) / 1.57 times (immature ♀) broader than long. There are nine (9) anterolateral spines on both sides of the carapace with straight or slightly concave outer margin, and six (6) high frontal lobe spines with concave and rounded interspaces. Cervical groves are present on the anterior of the slightly raised carapace. Overall, the carapace, walking legs and chelipeds are smooth. Two obvious spines are located at the carpus of chelipeds on distal half of the outer margin. Another two sharp spines can be found at the dorsal margin of chela (propodus), near the insertion of the dactyl. Teeth-like structures are found in between the cavity of the dactyl and the distal margin of the chela. Obvious polygonal patterning is present on chelipeds and all walking legs. The chela is greenish to brownish with bright blue coloration. The overall coloration is a mixture of light brown and green. The measurements of S. serrata collected in this study is presented in Table 1.
Resides in the coastal estuaries, coastlines and brackish mangrove forests area with tidal influence and occasional salinity reflux. Prefer muddy bottoms and seagrass beds.
Perak and Sabah, Malaysia (current study); Philippines; Indonesia; Japan; Taiwan; Bangladesh; Sri Lanka; Australia; oceanic islands of the Indo-Pacific; Maldives; Mauritius; South Africa; Africa; the Red Sea; Gulf of Aden; the Persian Gulf.
The two morphometric characters and five morphometric ratios of mature male S. serrata specimen found in this study fall within the range of S. serrata when compared with the data of four Scylla species provided by Keenan et al. (1998) (Table 2). However, they were distinct from the other three species, i.e. S. tranquebarica (frontal median spine height (FMSH)/ carapace frontal width (FW) and FMSH/ distance between frontal median spines (DFMS)), S. paramamosain (inner carpus spine (ICS)/ outer carpus spine (OCS)) and S. olivacea (ICS/OCS, FMSH/FW and FMSH/DFMS) (Table 2). This further confirms the identity of our specimen as S. serrata.
BLAST analysis of the partial COI gene sequence from both specimens confirmed their identity as S. serrata, in which the sequences of both specimens were identical to that of other S. serrata specimens found in GenBank (query cover = 100%; identity = 100%; E value = 0.0). The partial COI gene sequences of S. serrata ♂ from Sabah and ♀ from Perak were deposited into GenBank with the accession number KX249605 and KX249606, respectively [see Additional file 1].
The identity of S. serrata specimens found in the current study was successfully identified and validated using a combination of morphological, morphometric and molecular analyses. All three analyses were previously used by Keenan et al. (1998) to separate the long recognised single species (i.e. S. serrata) within the genus Scylla into four distinct species, with the addition of S. tranquebarica, S. olivacea and S. paramamosain. Similar methods were also employed by Imai and Takeda (2005) to validate the identity of a natural hybrid mud crab genus Scylla in Japan.
The discovery of S. serrata in Malaysian coastal waters is unprecedented. It was reviewed by Alberts-Hubatsch et al. (2015) that despite their wide geographical distribution, S. serrata has never been reported in Malaysian waters after the division of genus Scylla into four species. The species composition of mud crab population in Malaysian waters is predominantly made up of S. olivacea, with S. tranquebarica and S. paramamosain being frequently found in smaller numbers (Ikhwanuddin et al. 2011; Waiho et al. 2016).
Both S. serrata specimens found in this study were captured in intertidal mangrove forests. The presence of only one specimen in each location despite our extensive survey involving large number of mud crabs suggests that very few individuals were introduced and there is possibly still no viable S. serrata population in the wild. Personal communication with local fishermen revealed that some mud crab traders import mud crabs, specifically S. serrata from oversea due to their large sizes and high market price. Several traders from Perak sourced S. serrata from India and Indonesia whereas traders from Sabah imported S. serrata from the neighbouring Philippines. In addition, it was observed that local traders and fishermen frequently discard unhealthy mud crabs directly onto the ground nearby during screening before selling them off to restaurants. With most of these traders and fishermen living just nearby their mud crab fishing ground (the same sampling sites in this study), it is very likely that both S. serrata specimens found in our study were imported from oversea and accidentally released or escaped into the wild.
Other alternative vectors that has been reported to facilitate the introduction of non-indigenous marine and estuarine invertebrate species are the unintentional release of invertebrate larvae via ballast water of large cargo ships and escape from aquaculture activities (Fuller et al. 2014). Invertebrate larvae are taken on-board of large cargo ship, travel far from their natural geographical habitat and release into pristine non-native environment with the loading and discharge of ballast water. This unintentional introduction method was postulated to be one of the vector responsible for the introduction of Asian shore crab, Hemigrapsus sanguineus (De Haan, 1853), to Northwest Atlantic (Epifanio et al. 1998) and Asian tiger shrimp, Penaeus monodon Fabricius, 1798 (Fuller et al. 2014). Since their introduction, both P. monodon and H. sanguineus have successfully colonised their new introduced environment, displaced other local invertebrate species and altering biodiversity (Ruiz et al. 1997; Fuller et al. 2014). Both locations where S. serrata specimens were found (Perak and Sabah) are main shipping channels (i.e. Straits of Malacca connects Indian Ocean and the Pacific Ocean whereas Sulu Sea is situated between South China Sea and the Pacific Ocean). However, introduction of S. serrata via ballast water in the form of larvae is less likely as the number of discovered S. serrata specimens was too low. If this postulate is true, the high volume of ballast water would have introduced high number of S. serrata larvae, and subsequently resulted in the formation of a sizeable population instead of just one specimen being found in each location. However, further study is needed to determine the possibility of S. serrata larvae being transferred via ballast water. Another vector, i.e. escape from aquaculture activities is unlikely as no mud crab aquaculture activity is reported and observed in both locations. Only several small-scale fattening and soft-shell crab farming are sighted in Perak, and all sourced juvenile crabs from local fishermen.
The first record of S. serrata in Malaysian waters reported in this study may have adverse impact towards the environment and could pose as threats to the local mud crab populations. Well known for their resilience – highly tolerance to water salinity changes, ability to survive out of water and without food for a long period (Quinitio et al. 2011), released or escaped S. serrata imported from other countries could easily survive and invade the local environment. Comparatively larger in terms of average body size than the other three Scylla species (Keenan et al. 1998), S. serrata may have greater nutritional requirements and a better advantage in its competition for food compared to local species i.e. S. olivacea that are of smaller size. Once a satellite population is established, crabs such as S. serrata may spread and colonised nearby habitat effortlessly via their natural larval dispersal (Behrens Yamada and Gillespie 2008), and may pose as competitors to the local mud crab populations. In addition, the report of natural hybrid mud crab crossed between S. serrata and S. olivacea (Imai and Takeda 2005) in Japan also highlights the possible inter-species crossbreeding of the escaped S. serrata with the dominant local S. olivacea population in Malaysian waters. Ultimately, it may result in the extinction of the local inhabiting mud crab species following with the emergence of a new hybrid species (Rhymer 1996). In addition, potential invasion of S. serrata may also negatively affect other intertidal communities, especially the preys (e.g. gastropods, crabs, shrimps and mollusks) along the mud crab food chain. Thus, frequent monitoring of wild mud crab populations, strict regulations on the import of non-indigenous S. serrata and the appropriate handling procedures should be introduced and imposed in near future to prevent future possible establishment of S. serrata satellite population in Malaysian waters.
Cytochrome oxidase subunit 1
Distance between frontal median spines
Frontal median spine height
Inner carpus spine
National Center for Biotechnology Information
Outer carpus spine
Polymerase chain reaction
Alberts-Hubatsch H, Lee SY, Meynecke J-O, Diele K, Nordhaus I, Wolff M. Life-history, movement, and habitat use of Scylla serrata (Decapoda, Portunidae): current knowledge and future challenges. Hydrobiologia. 2015;763:5–21.
Ali SA, Dayal JS, Ambasankar K. Presentation and evaluation of formulated feed for mud crab Scylla serrata. Indian J Fish. 2011;58:67–73.
Altschul SF, Madden TL, Schaffer AA, Zhang J, Zhang Z, Miller W, et al. Gapped Blast and PSI-Blast: a new generation of protein database search programs. Nucleic Acids Res. 1997;25(17):3389–402.
Amarasekara GP, Priyadarshana T, Manatunge J, Tanaka N, Gunaratne GL. Mud crab (Scylla serrata) population changes in Koggala Lagoon, Sri Lanka since construction of the groyne system. Aquat Ecosyst Health and Manag. 2016;19:83–91.
Baylon JC, Bravo ME, Maningo NC. Ingestion of Brachionus plicatilis and Artemia salina nauplii by mud crab Scylla serrata larvae. Aquac Res. 2004;35:62–70.
Begum M, Shah MMR, Mamun A-A, Alam MJ. Comparative study of mud crab (Scylla serrata) fattening practices between two different systems in Bangladesh. J Bangladesh Agric Univ. 2009;7:151–6.
Behrens Yamada S, Gillespie GE. Will the European green crab (Carcinus maenas) persist in the Pacific Northwest? ICES J Mar Sci. 2008;65:725–9.
Epifanio CE, Dittel AI, Park S, Schwalm S, Fouts A. Early life history of Hemigrapsus sanguineus, a non-indigenous crab in the Middle Atlantic Bight (USA). Mar Ecol Prog Ser. 1998;170:231–8.
FAO. Species fact sheets: Scylla serrata. Food and Agriculture Organization of the United Nations, Fisheries and Aquaculture Department. 2016. http://www.fao.org/fishery/species/2637/en. Accessed 12 January 2016.
Fazhan H, Waiho K, Shahreza MS. A simple and efficient total genomic DNA extraction method for individual zooplankton. Spring. 2016;5:2049. doi:10.1186/s40064-016-3724-x.
Fazhan H, Waiho K, Wan Norfaizza WI, Megat FH, Ikhwanuddin M. Inter-species mating among mud crab genus Scylla in captivity. Aquaculture. 2017;471:49–54.
Folmer O, Black M, Hoeh W, Lutz R, Vrijenhoek R. DNA primers for amplification of mitochondrial cytochrome c oxidase subunit I from diverse metazoan invertebrates. Mol Mar Biol Biotechnol. 1994;3(5):294–9.
Fuller PL, Knott DM, Kingsley-Smith PR, Morris JA, Buckel CA, Hunter ME, et al. Invasion of Asian tiger shrimp, Penaeus monodon Fabricius, 1798, in the western north Atlantic and Gulf of Mexico. Aquat Invasions. 2014;9:59–70.
Holmes JS, Simons JR. The Introduction and Naturalisation of Birds. London: HMSO; 1996.
Hyland SJ, Hill BJ, Lee CP. Movement within and between different habitats by the portunid crab Scylla serrata. Mar Biol. 1984;80:57–61.
Ikhwanuddin M, Azmie G, Juariah HM, Zakaria MZ, Ambak MA. Biological information and population features of mud crab, genus Scylla from mangrove areas of Sarawak. Malaysia Fish Res. 2011;108:299–306.
Imai H, Takeda M. A natural hybrid mud crab (Decapoda, Portunidae) from Japan. J Crust Biol. 2005;25:620–4.
Keenan CP, Davie P, Mann D. A revision of the genus Scylla De Haan, 1833 (Crustacea: Decapoda: Brachyura: Portunidae). Raffles Bull Zool. 1998;46:217–45.
Manchester SJ, Bullock JM. The impacts of non-native species on UK biodiversity and the effectiveness of control. J Appl Ecol. 2000;37(5):845–64.
Nordhaus I, Hadipudjana FA, Janssen R, Pamungkas J. Spatio-temporal variation of microbenthic communities in the mangrove-fringed Segara Anakan lagoon, Indonesia, affected by anthropogenic activities. Reg Environ Chang. 2009;9:291–313.
Quinitio ET, de la Cruz JJ, Equia MRR, Parado-Estepa FD, Pates G, Lavilla-Pitogo CR. Domestication of the mud crab Scylla serrata. Aquacult Int. 2011;19:237–50.
Quinitio ET, Pedro JD, Parado-Estepa FD. Ovarian maturation stages of the mud crab Scylla serrata. Aquac Res. 2007;38:1434–41.
Rhymer JM. Extinction by hybridization and introgression. Annu Rev Ecol Evol Syst. 1996;27:83–109.
Roza D, Hatai K. Pathogenicity of fungi isolated from the larvae of the mangrove crab, Scylla serrata, in Indonesia. Mycoscience. 1999;40:427–31.
Ruiz GM, Carlton JT, Grosholz ED, Hines AH. Global invasions of marine and estuarine habitats by non-indigenous species: mechanisms, extent, and consequences. Amer Zool. 1997;37:621–32.
Stephenson W, Campbell B. The Australian Portunids (Crustacea: Portunidae) IV. Remaining genera. Aust J Mar Freshw Res. 1960;11:73–122.
Strayer DL, Dudgeon D. Freshwater biodiversity conservation: recent progress and future challenges. J N Am Benthos Sci. 2010;29:344–58.
Tharmine N, Edrisinghe U, Sivashanthini K. The status of diversity and species composition of crabs in cavanthurai coastal area in Jaffna Peninsula of Sri Lanka. Trop Agric Res. 2014;25:595–601.
Viswanathan C, Raffi SM. The natural diet of the mud crab Scylla olivacea (Herbst, 1896) in Pichavaram mangroves. India Saudi J Biol Sci. 2015;22(6):698–705.
Waiho K, Fazhan H, Baylon JC, Wan Norfaizza WI, Ikhwanuddin M. Use of abdomen looseness as an indicator of sexual maturity in male mud crab Scylla spp. J Shellfish Res. 2016;35(4):1027–35.
Waiho K, Fazhan H, Ikhwanuddin M. Size distribution, length-weight relationship and size at the onset of sexual maturity of the orange mud crab, Scylla olivacea in Malaysian waters. Mar Biol Res. 2016;12(7):726–38.
Waiho K, Mustaqim M, Fazhan H, Wan Norfaizza WI, Megat FH, Ikhwanuddin M. Mating behaviour of the orange mud crab, Scylla olivacea: The effect of sex ratio and stocking density on mating success. Aquac Rep. 2015;2:50–7.
Wood KA, Hayes RB, England J, Grey J. Invasive crayfish impacts on native fish diet and growth vary with fish life stage. Aquat Sci. 2016; doi:10.1007/s00027-016-0483-2.
We are grateful to Institute of Tropical Aquaculture, Universiti Malaysia Terengganu, Malaysia for providing us the facilities and equipment needed.
This study was partially funded by the Malaysia’s Ministry of Higher Education under the Niche Research Grant Scheme (NRGS) (Vot. No. 53131).
Availability of data and materials
The genetic data supporting the results of this study are available in GenBank under the accession numbers KX249605 (male S. serrata) and KX249606 (female S. serrata).
Ethics approval and consent to participate
All sampling sites are commercial fishing grounds and no special approval is needed. The work was approved by the Ethics Committee of Institute of Tropical Aquaculture, Universiti Malaysia Terengganu.
Consent for publication
The authors declare that they have no competing interests.
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Fazhan, H., Waiho, K. & Ikhwanuddin, M. Non-indigenous giant mud crab, Scylla serrata (Forskål, 1775) (Crustacea: Brachyura: Portunidae) in Malaysian coastal waters: a call for caution. Mar Biodivers Rec 10, 26 (2017). https://doi.org/10.1186/s41200-017-0128-8
- Giant mud crab
- Non-indigenous species
- Scylla serrata
- Species identification
- Partial COI gene