Abstract
The inundated area of the seasonally flooded habitats in Tonle Sap Lake varies from 1314 km2 to 5343 km2. The water level varies from 2 to >5 m at the beginning of the rainy season (July–August) and reaches 8–9 m in October. In this large floodplain, fishes are strongly adapted to the seasonal flood-pulse dynamics and habitat types. The Tonle Sap Authority’s inventory in 2010–2019 listed 167 fish species, belonging to 12 orders, 35 families, and 94 genera. More than 70% of the total fish sampled were found to belong to the order of Cypriniformes, Siluriformes, and Perciformes. The relationship between species diversity and heterogeneous habitats provides useful information for better understanding of their life cycles in the Tonle Sap Lake (TSL) ecosystem, which is critically important for the conservation of their diversity and productivity. Aquaculture by cage is mostly practiced in the flooding villages. Around 6520 cages and 210 ponds have been designed for fish farming in and directly around TSL, including 650 cages for crocodile farms.
Access provided by Autonomous University of Puebla. Download chapter PDF
Similar content being viewed by others
1 The Floodplain and Its Habitats
The ecosystem of Tonle Sap Lake (TSL) serves as a complex flood regulator that is fundamental for wetlands and biodiversity of the lake itself and the wider Mekong Delta. The flood-pulse-induced bi-directional flow in the TSL system seasonally inundates the lake floodplains during the rainy season, creating heterogeneous habitats and diverse ecosystems for aquatic fauna communities (Figs. 33.1 and 33.2; see Chaps. 1–4, 31, 32, and 34). This chapter describes major aquatic fauna with their habitats and present status.
The wetland around TSL including the grassland covers approximately 2520 km2 (Legris and Blasco 1972). We conducted a study during the dry and the rainy seasons between 2018 and 2019; the results indicated that the inundated area of the seasonally flooded habitats (Fig. 33.1) varied from 1314 to 5343 km2 when the water level at the hydrological stations varied from 2 to 5 m at the beginning of the rainy season (July–August), respectively. As the seasonally flooded habitats become inundated when the water level rises, reaching 8–9 m in October, many plant species produce fruit and seeds (Arias et al. 2013).
The junction between the lake and its outlet to Tonle Sap River (TSR), called “bottle-neck,” plays a prominent role in maintaining the minimum water level in the lake necessary for the survival of the biotic communities by constituting a natural sediment trap for the inflow from Mekong River (MR, Fig. 33.2). The 11 major tributaries of TSL and their sub-basins also play a secondary role in maintaining the water level in the back swamp of TSL during the dry season (see also Chap. 8).
2 Fish
2.1 Inventory of Fish Species
Fish species in the TSL system have been well reported compared to other faunas. Campbell et al. (2006) claimed 149 fish species in TSL, whereas Nam et al. (2006) highlighted around 200 fish species, encompassing 35 families and 90 genera. Based on the inventory in 2010–2019, the Tonle Sap Authority (TSA) has listed 167 species, belonging to 12 orders, 35 families, and 94 genera. Among all the identified samples, 73% belonged to several genera including Cypriniformes (genus: Paralaubuca, Puntioplites, Labiobarbus, and Henicorhynchus), Siluriformes (genus: Mystus and Pangasius), and Perciformes (genus: Parambassis). The inventoried 167 species were classified into four categories: high consumption (commonly caught/processed by population for food), high market value, endangered species, and introduced species (Tables 33.1 and 33.2).
The knowledge of the relationship between species and habitats is necessary for better understanding of the environmental requirements of fish fauna, which are critically important for the conservation of fish fauna diversity and productivity (Chan et al. 2020), especially in a complex hydroecological system such as TSL. During the early tropical monsoon rainfalls, many fish species in MR start to disperse for spawning and longitudinally migrate to the lower floodplain habitats (e.g., TSL and flooded area) for feeding and growth. These migratory fish species access the seasonally flooded habitats to feed during the wet season (Campbell et al. 2006). During the dry season, when the water level recedes, the longitudinal migratory fishes migrate from TSL back to MR to escape from the contracting condition in the floodplain and the lake, for better water quality and deeper pools as a refuge in the dry season (Poulsen et al. 2004). By surveying the dai fishery lot (bagnet fishery, mainly located along TSR; see Chap. 48) from 2011 to 2020, we observed that genera Clupeichthys, Paralaubuca, Puntioplites, Thynnichthys, Dangila, Henichorhynchus, and Botia are the most abundant for the longitudinal migration. As these species are typically intolerant to low oxygenated water, they need the open water area of the lake where wind-induced water current oxygenates (Ngor et al. 2018).
The floodplain-resident or non-migratory fish species, by contrast, spend most of their lifespans in the flooded forest (Campbell et al. 2006). The floodplain residents mostly live in the lakes and marshes or swamps on the floodplains near the permanent waterbodies and migrate to flooded areas during the flooded season. The floodplain residents such as Channa striata and Cerberus microlepis have developed their external organs to breathe the air and thus adapted to the low oxygen and harsh environmental conditions in swamps and small floodplain lakes during the dry season (Poulsen et al. 2002). C. striata and all the genera of Trichogaster occur predominantly in the northern part of the lake, where the area is predominantly covered by a flooded forest, swampy and shrubland, aquatic vegetation, and rice fields (Chan et al. 2020). The flooded forest areas are also likely important habitats to rear and forage for Pangasianodon hypophthalmus, C. striata, and Cyclocheilichthys enoplos (Chan et al. 2020) because the flooded forests typically constitute an appropriate feeding ground providing a variety of terrestrial prey (e.g., insects, frogs, and small mammals) for opportunistic predators (e.g., Phalacronotus spp. and C. striata; Poulsen et al. 2004). C. striata needs flooded vegetations for breeding and hatching (Rainboth 1996).
Aquaculture is mainly practiced on floating cages attached to houses in TSL and the ponds on non-flooded land. During 2018–2019, TSA inventoried fish farms in 12 large floating villages, i.e., Psar Chhnang, Chhnok Trou, Kampong Luong, Reang Til, Kampong Khlaeng, Kampong Phluk, Chong Khneas, Me Chrey, Prek Toal, Prey Chas, Peam Bang, and Phat Sanday. Approximately 6520 cages and 210 ponds have been designed for fish aquaculture, and 650 cages are for crocodile farms. The main fish species reared include C. striata, Channa micropeltes, Clarias spp., Pangasius spp., and Hemibagrus wyckioides. Fish aquaculture around TSL produces around 14,000 tons/year and can be sold fresh for consumption.
3 Reptiles
It has been reported that 46 species of reptiles inhabit TSL’s ecosystem (Bonheur and Lane 2002). The Tonle Sap Biosphere Reserve supports internationally significant populations of at least eight globally threatened reptile species, including the critically endangered Siamese crocodile Crocodylus siamensis; at least six species of freshwater turtle, including the endangered yellow-headed temple turtle Heosemys annandalii; and the near-threatened Burmese python Python molurus (Davidson 2006).
The majority of snakes are semi-aquatic homalopsid water snakes, previously known as homalopsines (Brooks et al. 2007; Lawson et al. 2005; Saint Girons and Pfeffer 1972). Brooks et al. (2007) reported 11 species of snake from 5 families, viz., Homalopsidae (Enhydris enhydris, Enhydris longicauda (Fig. 33.4a), Homalopsis buccata, Erpeton tentaculatum, Enhydris bocourti, and Enhydris plumbea), Colubridae (Xenochrophis piscator and Cylindrophis ruffus), Elapidae (Naja kaouthia/siamensis), Boidae (Python molurus), and Acrochordidae (Acrochordus granulatus). Most of the species are restricted to vegetated areas, with their catches higher in the flooded grassland than in other habitats, except for Erpeton tentaculatum and E. plumbea. Species such as E. enhydris and Cylindrophis ruffus were very occasionally caught in the open water of the lake. Only three individuals of Acrochordus granulatus were recorded in the open lake (Brooks et al. 2007). E. plumbea showed the highest catch per unit effort in deep water. All of the other species showed significant negative relationships between catch per unit effort and water depth.
Crocodile (Crocodylus siamensis or local name Kra peu trey) is present in both the crocodile farm and the TSL floodplain. Within the TSL basin, there has been a substantial boom in the local crocodile farm industry, and approximately 600 crocodile farms exist around TSL. Local people breed and rear the native Siamese crocodile (Crocodylus siamensis, Fig. 33.4c) and the non-native Cuban crocodile (Crocodylus rhombifer) for commercial purposes (Campbell et al. 2006).
Varanus salvator (local name: An sorng, Fig. 33.4d) lives in the flooded forests around TSL, spawning in the hole of big trees during the rainy season. Around TSL, this species has become very rare and is caught by the fisherman only in the Prek Toal Biosphere Reserve. This species has been classed in CITES Appendix II of the Convention in International Trade in Endangered Species of Wild Fauna and Flora (CITES), for trade control to avoid utilization incompatible to its survival.
At least six species of turtles have been confirmed in TSL (Davidson 2006). In 2018–2019, TSA inventoried different turtles in TSL through surveys in floating villages with people living there since the 1980s. As a result, seven turtle species were identified, viz., yellow-headed temple turtle Heosemys annandalii, rice-field terrapin Malayemys subtrijuga and Asiatic soft-shell turtle, Asian box turtle Cuora amboinensis, black mash turtle Siebenrockiella crassicollis, Asiatic soft-shell turtle Amyda cartilaginea, and P’dao kramoun (no scientific name available yet). The spawning period of most turtles starts from November to January when the water level in TSL recedes and in the rainy season from July to August for the Asian soft-shell turtle.
4 Mollusca and Arthropod
After fish, Mollusca are the second most important contributor to food provisioning in TSL (Rainboth 1996). According to MRC (2003), bivalves (e.g., Asian clam Corbicula spp., Fig. 33.5a) are abundant in the dry season, but people start harvesting it at the end of the rainy season, whereas gastropods (e.g., apple snails Pila spp.) are abundant in the beginning of the rainy season and in the beginning of the dry season, when floodwaters recede and the water temperature reaches its minimum in the year. The report from Ting et al. (2020) recorded 33 Crustacea and Mollusca species in TSL.
Our surveys in TSL from 2018 to 2019 found 31 species, 15 bivalves (5 families), and 16 gastropods (8 families), including three new records for Cambodia (i.e., Scaphula minuta, Novaculina siamensis, and Wattebledia siamensis), a globally invasive species such as Pomacea maculata and Limnoperna fortune, which modifies the presence and abundance of native macro-invertebrate fauna and fish diets and changes the ecological condition (Boltovskoy 2015).
Until now, the estimation of catch and trade of Gastropoda in TSL has not been assessed. The preliminary inventory by TSA on the caught snail for sale at the local markets and for export from the six provinces around the lake indicated that snails were caught by rudiment and a landing net. The period of snail collection starts in the beginning of the rainy season when the water levels rise. Five species from two families were identified, including Viviparidae [Melongirapongeasis aeruginasesaiy (local name: Ka chav), Filopaludina martensi cambodjensis (local name: Ka chav Ka’ek/Ka chav kut srouch), Mekongina phaericula (local name: Ka chav doung)] and Pilidae [Pila polita (local name: k’chorng boeng, Fig. 33.5b) and Pila scutata (k’chorng boeng krang/kut teal)].
Freshwater shrimps are dominant in the upper and the middle of TSL and near the organic substrate-rich shoreline. Their exploitation is typically practiced from December to June when the water level of TSL is between 2 and 3 m. Four main species were recorded: Macrobrachium nipponense (Kam peus), Macrobrachium lotidachylus (Kam peus), Macrobrachium ohione (Kam peus dai thom), and Neocaridina spp. (Kam peus touch/angkam) (Fig. 33.5c). The freshwater shrimp is sold fresh for consumption and processed as dried shrimp. In 2019, the estimated total annual catch of Crustacea (e.g., Crab Siamthelphusa improvisa, Fig. 33.5d) in TSL was approximately 59 tons. Different fishing gears and traps are mostly brush bundle for shrimp.
Key Points
-
TSL and its surrounding floodplains form heterogeneous habitats, including flooded forests, shrubs, grasslands, and aquatic vegetations. These provide the variety of habitat for aquatic fauna to accomplish a large part of their life cycle and support high biodiversity and productivity.
-
For fish, 167 species, belonging to 12 orders, 35 families, and 94 genera, were identified in the inventory on fish biodiversity in TSL and its floodplains in 2010–2019, approx. 75% of which belong to the order Cypriniformes, Siluriformes, and Perciformes.
-
The migratory fish species access the seasonally flooded habitats to feed and grow during the wet season, whereas the floodplain-resident or non-migratory fish species spend most of their lifespans in the flooded forests.
-
TSL is also home to at least 15 species of bivalves, 16 gastropods, 11 snake species, 7 turtle species, and other arthropod species.
References
Arias ME, Cochrane TA, Kummu M, Lauri H, Koponen J, Holtgrieve GW, Piman T. Impacts of hydropower and climate change on drivers of ecological productivity of Southeast Asia’s most important wetland. Ecol Model. 2013;272:252–63.
Boltovskoy D. Ecology and environmental impact of Limnoperna fortunei: introduction. In: Boltovskoy D, editor. Limnoperna Fortunei. Invading nature, Springer series in invasion ecology, vol. 10. Cham: Springer; 2015.
Bonheur N, Lane DB. Natural resource management for human security in Cambodia’s Tonle Sap Biosphere Reserve. Environ Sci Pol. 2002;5:33–41.
Brooks ES, Allison HE, Reynold DJ. Vulnerability of Cambodian water snakes: Initial assessment of the impact of hunting at Tonle Sap Lake. Biol Conserv. 2007;139:401–14.
Campbell I, Poole C, Giesen W, Valbo-Jorgensen J. Species diversity and ecology of Tonle Sap Great Lake, Cambodia. Aquat Sci. 2006;68(3):355–73.
Chan B, Brosse S, Hogan ZS, Ngor BP. Influence of local habitat and climatic factors on the distribution of fish species in the Tonle Sap Lake. Water. 2020;12(3):786.
Davidson PJA. Biodiversity of the Tonle Sap Biosphere Reserve, 2005 status review; 2006.
Froese R, Pauly D, eds. FishBase. World Wide Web electronic publication. www.fishbase.org, version (06/2021); 2021.
IUCN. The IUCN Red List of Threatened Species. Version 2021-1.https://www.iucnredlist.org. ISSN 2307-8235; 2021.
Lawson R, Slowinski JB, Crother BI, Burbrink FT. Phylogeny of the Colubroidea (Serpentes): new evidence from mitochondrial and nuclear genes molecular. Phylogenet Evol. 2005;37:581–601.
Legris P, Blasco F. Notice de la carte: Cambodge International du Tapis Vegetal. Extrait des travaux de la Section Scientifique et Technique de l’Institute Francaise de Pondichery, Toulous: hors serie no 1, Toulouse, France; 1972.
MRC. State of the Basin Report 2003. Phnom Penh: Mekong River Commission; 2003.
Nam S, Vann LS, Baran E, Authur R.. An Evaluation of Fish Species and Genetic Diversity of the Tonle Sap Great Lake, Cambodia. Keynote speech at the International Workshop and Training on Fish Diversity of the Mekong River. Tohoku University, Sendai, Japan; 2006.
Ngor PB, Grenouillet G, Phem S, So N, Lek S. Spatial and temporal variation in fish community structure and diversity in the largest tropical flood-pulse system of South-East Asia. Ecol Freshw Fish. 2018;27:1087–100.
Poulsen AF, Ouch P, Viravong S, Suntornratana U, Nguyen TT. Fish Migrations of the Lower Mekong River Basin: Implications for Development, Planning and Environmental Management; Mekong River Commission: Phnom Penh, Cambodia, 2002; p. 62. ISSN 1683-1489.
Poulsen AF, Hortle KG, Chan S, Chhuon CK, Viravong S, Bouakhamvongsa K, Suntornratana U, Yoorong N, Nguyen TT, Tran BQ. Distribution and Ecology of Some Important Riverine Fish Species of the Mekong River Basin; Mekong River Commission: Phnom Penh, Cambodia; 2004. Vol. 89. ISSN 1683-1489.
Rainboth WJ. FAO species identification field guide for fisheries purposes. Fishes of the Cambodian Mekong. Room, Food and Agriculture Organisation of the United Nations; 1996. p. 265.
Saint Girons H, Pfeffer P. Notes sur l’ecologie des serpents du Cambodge Zoologische Mededelingen. Leiden: Rijkmuseum van Natiirlijke Historie; 1972. p. 65–86.
Ting HN, Ekgachai J, Chirasak S, Chhuoy S, Pin K, Arthit P, Warut S, Ruttapon S, Hogan ZS, Ngor PB. Annotated checklist of freshwater molluscs from the largest freshwater lake in Southeast Asia. Zookeys. 2020;958:107–41.
Author information
Authors and Affiliations
Corresponding author
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 2022 The Author(s), under exclusive license to Springer Nature Singapore Pte Ltd.
About this chapter
Cite this chapter
Puy, L. (2022). Aquatic Fauna and Aquaculture. In: Yoshimura, C., Khanal, R., Sovannara, U. (eds) Water and Life in Tonle Sap Lake. Springer, Singapore. https://doi.org/10.1007/978-981-16-6632-2_33
Download citation
DOI: https://doi.org/10.1007/978-981-16-6632-2_33
Published:
Publisher Name: Springer, Singapore
Print ISBN: 978-981-16-6631-5
Online ISBN: 978-981-16-6632-2
eBook Packages: Earth and Environmental ScienceEarth and Environmental Science (R0)