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AACL Bioflux, 2020, Volume 13, Issue 4.
http://www.bioflux.com.ro/aacl 1970
Short note: The fecundity and egg size of
the freshwater crab (Isolapotamon bauense Ng,
1987) from Sarawak, Borneo
1Lirong Yu Abit, 2Mohd. Zafri Hassan, 1Kamil Latif, 3Jongkar Grinang,
1Abdulla-Al-Asif
1
Department of Animal Science and Fishery, Faculty of Agriculture Science and
Technology, Universiti Putra Malaysia Bintulu Campus, 97008, Bintulu, Sarawak,
Malaysia; 2
Department of Aquaculture, Faculty of Agriculture, Universiti Putra Malaysia,
43400 UPM Serdang, Selangor, Malaysia; 3
Institute of Biodiversity and Environmental
Conservation, Universiti Malaysia Sarawak, 94300 Kota Samarahan, Sarawak, Malaysia.
Corresponding Author: Kamil Latif, Email: kamill@upm.edu.my
Abstract. The Island of Borneo harbors a high species richness of freshwater brachyurans, many of
which are endemic in the region and their existence is threatened by anthropogenic activities. Our
knowledge on the fundamental aspects which are required for species conservation assessment
is currently limited. For instance, information on fecundity of most Bornean freshwater crabs is almost
non-existent despite this being an important predictor of vulnerability to extinction. This paper describes
the fecundity and egg size of the giant freshwater crab (Isolapotamon bauense Ng, 1987)
from Kuching Division in Sarawak, Borneo. The fecundity of the crab is between 26 and 81 eggs, with
the egg diameter ranging between 3.7–4.2 mm. The macrolecithal eggs are attached to the pleopods of
the female abdominal brood pouch; they are bright orange and are comprised of two layers of
membrane, with a thicker outer layer and a thinner inner layer, encapsulating the large embryonic yolk
sac.
Key Words: brachyuran crab, Isolapotamon bauense, reproductive biology, vulnerable species,
endemic species.
Introduction. Isolapotamon bauense Ng, 1987 is the largest true freshwater crab in
Malaysia and is endemic to the Kuching-Serian region in Sarawak. In addition to the
extreme endemism, population density of the species is so low that it has acquired the
“Vulnerable” species status in the IUCN Red List of Threatened Species (Esser &
Cumberlidge 2008). Currently, not much government and non-government efforts has
been done to conserve the species, particularly due to limited information to justify
funding application.
Fecundity is often defined as the physiological reproductive potential of an
individual (Bradshaw & McMahon 2008), that serves as a key determinant to ascertain
the efficiency of population replacement, especially for decapod crustaceans (Cobo &
Okamori 2008). The brachyuran crabs represent more than 7,000 valid species from 98
families, which have colonized a wide range of aquatic systems, some taxa have even
successfully populated terrestrial habitats (Ahyong et al 2011; Ng et al 2008). Fecundity
provides valuable insights into the evolutionary and reproductive strategies of a species
(Carlos et al 2005). The recording of egg-bearing females is a useful index for
determining the reproductive cycle of a species (Knudson 1960; Valter & Claudia 2008;
Muzaffer & Ibrahim 2000). For decapod crustaceans, fecundity can be defined as the
number of eggs produced by a female (Hartnoll 2015).
Freshwater crabs are the most species-rich of all decapod crustacean groups and
show high levels of endemism (Esser & Cumberlidge 2008; Ng et al 2008). The
taxonomy and systematics of freshwater crabs has gained significant interest due to
AACL Bioflux, 2020, Volume 13, Issue 4.
http://www.bioflux.com.ro/aacl 1971
high taxa richness and endemicity (Klaus et al 2009). The freshwater crabs of Borneo
comprise more than 95 species in three families, all of which are endemic to the island
(Grinang 2016; Ng & Grinang 2018; Ng & Ng 2019). Among the three political
boundaries in Borneo, the crab fauna of Sarawak has been relatively extensively studied
for 49 species (Grinang 2016; Ng & Grinang 2018). Isolapotamon bauense is the largest
true freshwater crab in Malaysia and can attain a carapace width of more than 9 cm
(Grinang et al 2016). Anecdotal evidence from indigenous people have claimed
that Isolapotamon bauense can grow to over 10 cm in carapace width. Currently only a
few ecological characteristics of this species have been reported, which include
geographical distribution, sex ratio, growth pattern and population size (Grinang et al
2018). This crab has been harvested by the Bidayuh community as a supplementary
source of protein to their diet for millennia (Grinang et al 2017). Given the current lack
of knowledge regarding many aspects of the reproductive biology of this species, any
new information is important to reassess and evaluate the current sustainability of the
population, conservation status, as well as the potential for aquaculture.
This short note aims at reducing the information gap about Isolapotamon
bauense by determining its egg size and estimating its fecundity. Information obtained
from this study will be used to develop propagation techniques destined for wild
population restocking programs and for aquaculture.
Material and Method
Collection of live crabs. The population density of Isolapotamon bauense is
significantly low. Only six individuals of mature non-berried females were successfully
collected from an intermittent stream in the Bau district. Crab sampling was conducted
at night along a 65 m sector of a stream, with minimal disturbance to the habitat. Bait
(dead fishes) was used to attract the crabs from the burrows and then the crabs were
caught by hand. The crabs were put temporarily in plastic buckets for transport to the
Sarawak research facility, of the academic institution of Universiti Putra Malaysia Bintulu.
Setting up of terrarium and observation. The mature Isolapotamon bauense females
were kept together at ambient room temperature in a HDPE tank (179 cm length,
119 cm width, 60 cm height) equipped with adequate aeration and submersible pump,
with overhead filter to provide circulation as well as filtration. Substrate and shelter in
the form of river gravel and river rocks protruding above the water line was provided to
mimic conditions in their natural habitat. The tank was filled to a depth of 10 cm and the
crabs were fed once a day at 6 pm with freshly chopped fish meat, at a rate of 5% body
weight per feeding. 50% water exchange was carried out each morning with any excess
food and feces being siphoned off and all the filter media rinsed.
After 7 days in captivity, one of the females spawned. A second female spawned
after 16 days in captivity and a third female spawned after 48 days in
captivity. Five eggs were gently removed with forceps from the pleopods of each female
crab and measured using a scale bar and subsequently observed and photographed
under 20X and 60X magnifications using a digital microscope. Removed eggs were fixed
in 10% formaldehyde and stored in 70% alcohol. The total number of eggs attached to
the pleopods of both carrying females was counted.
Results and Discussion
Results. Off the six non-berried mature females caught, only three individuals
successfully spawned during the 60 days study period. The first spawning female had a
carapace width of 6.6 cm and a total of 81 eggs attached to the pleopods, whereas the
second female had a carapace width of 6.1 cm and a total of 26 eggs attached to
the pleopods and the third female had a carapace width of 5.7 cm and a total of 32 eggs
attached to the pleopods (Figure 1). The third spawning female perished shortly after
spawning and the eggs, though fully formed, were lacking the thick outer membrane, as
AACL Bioflux, 2020, Volume 13, Issue 4.
http://www.bioflux.com.ro/aacl 1972
observed in the eggs of the other two females, and these eggs were not viable. The eggs
were large, with a diameter of 3.7 to 4.1 mm (Figure 2). The newly formed eggs were
composed almost entirely of the bright orange yolk. The viable bright orange eggs of the
first two females consisted of a thick outer membrane with a thinner inner membrane
forming a fluid sac encapsulating the entire yolk mass (Figure 3). Prior to spawning
crabs were observed to spend time above water and clean their abdominal pouch using
their legs. Table 1 compares the average egg diameter and fecundity between
Isolapotamon bauense and some other crab species from both freshwater and brackish
water.
Figure 1. Newly captured adult female of Isolapotamon bauense.
Figure 2. Berried Isolapotamon bauense female.
Figure 3. Newly formed (2 hours after spawning) macrolecithal egg of Isolapotamon bauense and
the egg under 60X magnification.
AACL Bioflux, 2020, Volume 13, Issue 4.
http://www.bioflux.com.ro/aacl 1973
Table 1
Comparison of average egg diameter and fecundity between Isolapotamon bauense and
other freshwater and brackish* water crab species
References Species
Carapace
width
(cm)
Egg
diameter
(mm)
Fecundity
(eggs)
Present study Isolapotamon bauense 5.7 – 6.6 3.7 – 4.2 26 – 81
Wu et al 2010 Sinopotamon yangtsekiense - 3.5 – 4.1 70 – 100
Pace et al 1976 Potamon fluviatile - 2.5 > 200
Herlinah &
Septiningsih 2015
Scylla olivacea* 12 ± 0.5 0.0035 > 2400000
Discussion. True freshwater crabs are brachyuran crustaceans which complete their
whole life cycle in freshwater. They have evolved to adopt terrestrial, semi-terrestrial, or
freshwater modes of living and reproducing by direct development without any free-
living larval stage (Yeo et al 2008). Isolapotamon bauense belongs to the Potamidae
family, which is one of the five families of crabs composed entirely of freshwater crab
species (Klaus et al 2012). The life cycle of Isolapotamon bauense is through
direct development, which excludes any external larvae stages, as found in marine and
brackish water crab species (Mantellato and Fransozo 1999). The fecundity of an animal
is an important parameter in estimating the reproductive potential and population size of
a species accurately (Mantelatto and Fransozo 1999b). Our preliminary observation
indicated Isolapotamon bauense has a low fecundity with large egg size. The inability of
the third spawning female to successfully extrude eggs with the thick outer membrane
could possibly be due to insufficient nutrients (such as naturally occurring
micronutrients) obtained from the diet provided in this study over a longer period than
the other two females. Increased egg size causes a decrease in fecundity of crustaceans
(Steele and Steele 1991). Like other true freshwater crabs, Isolapotamon
bauense produces a small number of large yolky (macrolecithal) eggs which attach to
the female’s pleopods in the abdominal brood pouch. In all true freshwater crabs the
eggs attach to the mother’s pleopods for the entire duration of development and
hatchlings remain in the abdominal brood pouch for a period of time before being
released as miniature versions of the adult crab (Wu et al 2010; Junzeng et al 2010).
The life strategy of true freshwater crabs differs greatly from marine and brackish water
crabs in that the number of eggs produced is small and all larval stages are encapsulated
within the eggs. Parental care is a major strategy of true freshwater crabs which
differentiates them from their marine brethren (Ng 1988).
Conclusions. The current results provide valuable preliminary insight into the aspect of
fecundity and the reproductive biology of Isolapotamon bauense. This new information
on the fecundity of Isolapotamon bauense may suggest that the conservation status of
the species need to be re-assessed. Currently the only fully documented embryonic
development studies in true freshwater crabs have been done on the Chinese true
freshwater crab Sinopotamon yangtsekiense and the Mediterranean edible freshwater
crab Potamon fluviatile. The incubation period for the Mediterranean edible freshwater
crab Potamon fluviatile takes 46–47 days and 77 days for the Chinese true freshwater
crab Sinopotamon yangtsekiense. The egg diameter and general characteristics of newly
formed Isolapotamon bauense eggs were remarkably similar to Sinopotamon
yangtsekiense. It is suggested that the incubation period for Isolapotamon bauense
would also require a similarly extended incubation period. Consequently, ongoing
research will be important to validate the current findings and to document the full
embryonic development of this species to support its conservation and potential for
aquaculture.
AACL Bioflux, 2020, Volume 13, Issue 4.
http://www.bioflux.com.ro/aacl 1974
Acknowledgements. The authors would like to thank the Fundamental Research Grant
Scheme (FRGS) for funding this research (FRGS/1/2018/WAB01/UPM/02/21) and YB
Datuk Henry Jinep, as well as the people of Singai, Bau for their kind cooperation during
the sampling works.
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Received: 01 January 2020. Accepted: 31 January 2020. Published online: 25 July 2020.
Authors:
Lirong Yu Abit, Department of Animal Science and Fishery, Faculty of Agriculture Science and Technology,
Universiti Putra Malaysia Bintulu Campus, 97008, Bintulu, Sarawak, Malaysia, e-mail: kelibunga76@gmail.com
Mohd. Zafri Hassan, Department of Aquaculture, Faculty of Agriculture, Universiti Putra Malaysia, 43400
UPM Serdang, Selangor, Malaysia, e-mail: mzafri@upm.edu.my
Kamil Latif, Department of Animal Science and Fishery, Faculty of Agriculture Science and Technology,
Universiti Putra Malaysia Bintulu Campus, 97008, Bintulu, Sarawak, Malaysia, e-mail: kamill@upm.edu.my
Jongkar Grinang, Institute of Biodiversity and Environmental Conservation, Universiti Malaysia Sarawak, 94300
Kota Samarahan, Sarawak, Malaysia, e-mail: gjongkar@unimas.my
Abdulla-Al-Asif, Department of Animal Science and Fishery, Faculty of Agriculture Science and Technology,
Universiti Putra Malaysia Bintulu Campus, 97008, Bintulu, Sarawak, Malaysia, e-mail:
jessoreboyhemel@gmail.com
This is an open-access article distributed under the terms of the Creative Commons Attribution License, which
permits unrestricted use, distribution, and reproduction in any medium, provided the original author and
source are credited.
How to cite this article:
Abit L. Y., Hassan M. Z., Latif K., Grinang J., Asif A. A., 2020 Short note: The fecundity and egg size of the
freshwater crab (Isolapotamon bauense Ng, 1987) from Sarawak, Borneo. AACL Bioflux 13(4):1970-1975.

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The fecundity and egg size of the freshwater crab (Isolapotamon bauense Ng,1987) from Sarawak, Borneo

  • 1. AACL Bioflux, 2020, Volume 13, Issue 4. http://www.bioflux.com.ro/aacl 1970 Short note: The fecundity and egg size of the freshwater crab (Isolapotamon bauense Ng, 1987) from Sarawak, Borneo 1Lirong Yu Abit, 2Mohd. Zafri Hassan, 1Kamil Latif, 3Jongkar Grinang, 1Abdulla-Al-Asif 1 Department of Animal Science and Fishery, Faculty of Agriculture Science and Technology, Universiti Putra Malaysia Bintulu Campus, 97008, Bintulu, Sarawak, Malaysia; 2 Department of Aquaculture, Faculty of Agriculture, Universiti Putra Malaysia, 43400 UPM Serdang, Selangor, Malaysia; 3 Institute of Biodiversity and Environmental Conservation, Universiti Malaysia Sarawak, 94300 Kota Samarahan, Sarawak, Malaysia. Corresponding Author: Kamil Latif, Email: kamill@upm.edu.my Abstract. The Island of Borneo harbors a high species richness of freshwater brachyurans, many of which are endemic in the region and their existence is threatened by anthropogenic activities. Our knowledge on the fundamental aspects which are required for species conservation assessment is currently limited. For instance, information on fecundity of most Bornean freshwater crabs is almost non-existent despite this being an important predictor of vulnerability to extinction. This paper describes the fecundity and egg size of the giant freshwater crab (Isolapotamon bauense Ng, 1987) from Kuching Division in Sarawak, Borneo. The fecundity of the crab is between 26 and 81 eggs, with the egg diameter ranging between 3.7–4.2 mm. The macrolecithal eggs are attached to the pleopods of the female abdominal brood pouch; they are bright orange and are comprised of two layers of membrane, with a thicker outer layer and a thinner inner layer, encapsulating the large embryonic yolk sac. Key Words: brachyuran crab, Isolapotamon bauense, reproductive biology, vulnerable species, endemic species. Introduction. Isolapotamon bauense Ng, 1987 is the largest true freshwater crab in Malaysia and is endemic to the Kuching-Serian region in Sarawak. In addition to the extreme endemism, population density of the species is so low that it has acquired the “Vulnerable” species status in the IUCN Red List of Threatened Species (Esser & Cumberlidge 2008). Currently, not much government and non-government efforts has been done to conserve the species, particularly due to limited information to justify funding application. Fecundity is often defined as the physiological reproductive potential of an individual (Bradshaw & McMahon 2008), that serves as a key determinant to ascertain the efficiency of population replacement, especially for decapod crustaceans (Cobo & Okamori 2008). The brachyuran crabs represent more than 7,000 valid species from 98 families, which have colonized a wide range of aquatic systems, some taxa have even successfully populated terrestrial habitats (Ahyong et al 2011; Ng et al 2008). Fecundity provides valuable insights into the evolutionary and reproductive strategies of a species (Carlos et al 2005). The recording of egg-bearing females is a useful index for determining the reproductive cycle of a species (Knudson 1960; Valter & Claudia 2008; Muzaffer & Ibrahim 2000). For decapod crustaceans, fecundity can be defined as the number of eggs produced by a female (Hartnoll 2015). Freshwater crabs are the most species-rich of all decapod crustacean groups and show high levels of endemism (Esser & Cumberlidge 2008; Ng et al 2008). The taxonomy and systematics of freshwater crabs has gained significant interest due to
  • 2. AACL Bioflux, 2020, Volume 13, Issue 4. http://www.bioflux.com.ro/aacl 1971 high taxa richness and endemicity (Klaus et al 2009). The freshwater crabs of Borneo comprise more than 95 species in three families, all of which are endemic to the island (Grinang 2016; Ng & Grinang 2018; Ng & Ng 2019). Among the three political boundaries in Borneo, the crab fauna of Sarawak has been relatively extensively studied for 49 species (Grinang 2016; Ng & Grinang 2018). Isolapotamon bauense is the largest true freshwater crab in Malaysia and can attain a carapace width of more than 9 cm (Grinang et al 2016). Anecdotal evidence from indigenous people have claimed that Isolapotamon bauense can grow to over 10 cm in carapace width. Currently only a few ecological characteristics of this species have been reported, which include geographical distribution, sex ratio, growth pattern and population size (Grinang et al 2018). This crab has been harvested by the Bidayuh community as a supplementary source of protein to their diet for millennia (Grinang et al 2017). Given the current lack of knowledge regarding many aspects of the reproductive biology of this species, any new information is important to reassess and evaluate the current sustainability of the population, conservation status, as well as the potential for aquaculture. This short note aims at reducing the information gap about Isolapotamon bauense by determining its egg size and estimating its fecundity. Information obtained from this study will be used to develop propagation techniques destined for wild population restocking programs and for aquaculture. Material and Method Collection of live crabs. The population density of Isolapotamon bauense is significantly low. Only six individuals of mature non-berried females were successfully collected from an intermittent stream in the Bau district. Crab sampling was conducted at night along a 65 m sector of a stream, with minimal disturbance to the habitat. Bait (dead fishes) was used to attract the crabs from the burrows and then the crabs were caught by hand. The crabs were put temporarily in plastic buckets for transport to the Sarawak research facility, of the academic institution of Universiti Putra Malaysia Bintulu. Setting up of terrarium and observation. The mature Isolapotamon bauense females were kept together at ambient room temperature in a HDPE tank (179 cm length, 119 cm width, 60 cm height) equipped with adequate aeration and submersible pump, with overhead filter to provide circulation as well as filtration. Substrate and shelter in the form of river gravel and river rocks protruding above the water line was provided to mimic conditions in their natural habitat. The tank was filled to a depth of 10 cm and the crabs were fed once a day at 6 pm with freshly chopped fish meat, at a rate of 5% body weight per feeding. 50% water exchange was carried out each morning with any excess food and feces being siphoned off and all the filter media rinsed. After 7 days in captivity, one of the females spawned. A second female spawned after 16 days in captivity and a third female spawned after 48 days in captivity. Five eggs were gently removed with forceps from the pleopods of each female crab and measured using a scale bar and subsequently observed and photographed under 20X and 60X magnifications using a digital microscope. Removed eggs were fixed in 10% formaldehyde and stored in 70% alcohol. The total number of eggs attached to the pleopods of both carrying females was counted. Results and Discussion Results. Off the six non-berried mature females caught, only three individuals successfully spawned during the 60 days study period. The first spawning female had a carapace width of 6.6 cm and a total of 81 eggs attached to the pleopods, whereas the second female had a carapace width of 6.1 cm and a total of 26 eggs attached to the pleopods and the third female had a carapace width of 5.7 cm and a total of 32 eggs attached to the pleopods (Figure 1). The third spawning female perished shortly after spawning and the eggs, though fully formed, were lacking the thick outer membrane, as
  • 3. AACL Bioflux, 2020, Volume 13, Issue 4. http://www.bioflux.com.ro/aacl 1972 observed in the eggs of the other two females, and these eggs were not viable. The eggs were large, with a diameter of 3.7 to 4.1 mm (Figure 2). The newly formed eggs were composed almost entirely of the bright orange yolk. The viable bright orange eggs of the first two females consisted of a thick outer membrane with a thinner inner membrane forming a fluid sac encapsulating the entire yolk mass (Figure 3). Prior to spawning crabs were observed to spend time above water and clean their abdominal pouch using their legs. Table 1 compares the average egg diameter and fecundity between Isolapotamon bauense and some other crab species from both freshwater and brackish water. Figure 1. Newly captured adult female of Isolapotamon bauense. Figure 2. Berried Isolapotamon bauense female. Figure 3. Newly formed (2 hours after spawning) macrolecithal egg of Isolapotamon bauense and the egg under 60X magnification.
  • 4. AACL Bioflux, 2020, Volume 13, Issue 4. http://www.bioflux.com.ro/aacl 1973 Table 1 Comparison of average egg diameter and fecundity between Isolapotamon bauense and other freshwater and brackish* water crab species References Species Carapace width (cm) Egg diameter (mm) Fecundity (eggs) Present study Isolapotamon bauense 5.7 – 6.6 3.7 – 4.2 26 – 81 Wu et al 2010 Sinopotamon yangtsekiense - 3.5 – 4.1 70 – 100 Pace et al 1976 Potamon fluviatile - 2.5 > 200 Herlinah & Septiningsih 2015 Scylla olivacea* 12 ± 0.5 0.0035 > 2400000 Discussion. True freshwater crabs are brachyuran crustaceans which complete their whole life cycle in freshwater. They have evolved to adopt terrestrial, semi-terrestrial, or freshwater modes of living and reproducing by direct development without any free- living larval stage (Yeo et al 2008). Isolapotamon bauense belongs to the Potamidae family, which is one of the five families of crabs composed entirely of freshwater crab species (Klaus et al 2012). The life cycle of Isolapotamon bauense is through direct development, which excludes any external larvae stages, as found in marine and brackish water crab species (Mantellato and Fransozo 1999). The fecundity of an animal is an important parameter in estimating the reproductive potential and population size of a species accurately (Mantelatto and Fransozo 1999b). Our preliminary observation indicated Isolapotamon bauense has a low fecundity with large egg size. The inability of the third spawning female to successfully extrude eggs with the thick outer membrane could possibly be due to insufficient nutrients (such as naturally occurring micronutrients) obtained from the diet provided in this study over a longer period than the other two females. Increased egg size causes a decrease in fecundity of crustaceans (Steele and Steele 1991). Like other true freshwater crabs, Isolapotamon bauense produces a small number of large yolky (macrolecithal) eggs which attach to the female’s pleopods in the abdominal brood pouch. In all true freshwater crabs the eggs attach to the mother’s pleopods for the entire duration of development and hatchlings remain in the abdominal brood pouch for a period of time before being released as miniature versions of the adult crab (Wu et al 2010; Junzeng et al 2010). The life strategy of true freshwater crabs differs greatly from marine and brackish water crabs in that the number of eggs produced is small and all larval stages are encapsulated within the eggs. Parental care is a major strategy of true freshwater crabs which differentiates them from their marine brethren (Ng 1988). Conclusions. The current results provide valuable preliminary insight into the aspect of fecundity and the reproductive biology of Isolapotamon bauense. This new information on the fecundity of Isolapotamon bauense may suggest that the conservation status of the species need to be re-assessed. Currently the only fully documented embryonic development studies in true freshwater crabs have been done on the Chinese true freshwater crab Sinopotamon yangtsekiense and the Mediterranean edible freshwater crab Potamon fluviatile. The incubation period for the Mediterranean edible freshwater crab Potamon fluviatile takes 46–47 days and 77 days for the Chinese true freshwater crab Sinopotamon yangtsekiense. The egg diameter and general characteristics of newly formed Isolapotamon bauense eggs were remarkably similar to Sinopotamon yangtsekiense. It is suggested that the incubation period for Isolapotamon bauense would also require a similarly extended incubation period. Consequently, ongoing research will be important to validate the current findings and to document the full embryonic development of this species to support its conservation and potential for aquaculture.
  • 5. AACL Bioflux, 2020, Volume 13, Issue 4. http://www.bioflux.com.ro/aacl 1974 Acknowledgements. The authors would like to thank the Fundamental Research Grant Scheme (FRGS) for funding this research (FRGS/1/2018/WAB01/UPM/02/21) and YB Datuk Henry Jinep, as well as the people of Singai, Bau for their kind cooperation during the sampling works. References Ahyong S. T., Lowry J. K., Alonso M., Bamber R. N., Boxshall G. A., Castro P., Gerken S., Karaman G. S., Goy J. W., Jones D. S., Meland K., Rogers D. C., Svavarsson J., 2011 Subphylum Crustacea Brünnich, 1772. In: Zhang Z-Q, editor. Animal biodiversity: an outline of higher-level classification and survey of taxonomic richness. Zootaxa 3148:165–191. Bradshaw C. J. A., McMahon C. R., 2008 Fecundity. In: Encyclopedia of Ecology. Jørgensen S. E., Fath B. D. (eds.), Elsevier Science, pp. 1535-1543. Carlos L., Adriano M., Mantelatto F. L. M., 2005 Fecundity and sexual maturity of the crab Macrophthalmus depressus (Brachyura: Ocypodidae) from Inhaca Island, Mozambique. African Journal of Aquatic Science 30:179-183. Cobo V. J., Okamori C. M., 2008 Fecundity of the spider crab Mithraculus forceps (Decapoda, Mithracidae) from the northeastern coast of the state of São Paulo, Brazil. Iheringia. Série Zoologia 98(1):84-87. Esser L., Cumberlidge N., 2008 Isolapotamon bauense. The IUCN Red List of Threatened Species2008:e.T134148A3910232.http://dx.doi.org/10.2305/IUCN.UK.2008.RLTS .T134148A3910232.en. Downloaded on 23 January 2019. Grinang J., 2016 Taxonomy and ecology of freshwater crabs (Crustacea: Decapoda: Brachyura) in Sarawak, Borneo. (PhD dissertation). Kota Samarahan: Universiti Malaysia Sarawak. Grinang J., Das I., Peter N., 2016 Ecological characteristics of the freshwater crab, Isolapotamon bauense in one of Wallace’s collecting sites. In: Naturalists, Explorers and Field Scientists in South-East Asia and Australasia. Topics in Biodiversity and Conservation, Springer International Publishing, pp. 127-141. Grinang J., Tyan P. S., Tuen A. A., Das I., 2017 Nutrient contents of the freshwater crab, Isolapotamon bauense from Sarawak, Malaysia (Borneo). Tropical Life Sciences Research 28(2):75–87. Grinang J., Pui Y. M., Shabrani A., Muli A., Lee C. C., 2018 Freshwater Crabs of Upper Baleh River, Sarawak. Borneo Journal of Resource Science and Technology 8:1-5. Hartnoll R. G., 2015 Post-larval life histories of Brachyura. In: Treatise on Zoology - Anatomy, Taxonomy, Biology. The Crustacea. Castro P., Davie P.J.F., Guinot D., Schram F.R., von Vaupel Klein J.C. (eds.), Brill, Leiden & Boston, pp. 375–416. Herlinah, Septiningsih E., 2015 Reproduction performances of mud crab (Scylla olivacea) broodstocks with different feeds. International Journal of Agriculture System 3: 157-168. Junzeng X., Yan L., Neil C., Huixian W., 2010 First report of developmental changes inside the eggs of the Chinese freshwater crab, Sinopotamon yangtsekiense Bott, 1967 (Potamoidea, Potamidae), with comments on its evolutionary significance. Contributions to Zoology 79:79-84. Klaus S., Brandis D., Ng P., Yeo D., Schubart C., 2009 Phylogeny and Biogeography of Asian Freshwater Crabs of the Family Gecarcinucidae (Brachyura). Crustacean Issues 509–531. Klaus S., Selvandran S., Goh J. W., Wowor D., Brandis D., Koller P., Schubart C. D., Streit B., Meier R., Ng P. K. L., Yeo D. C. J., 2012 Out of Borneo: Neogene diversification of Sundaic freshwater crabs (Crustacea: Brachyura: Gecarcinucidae: Parathelphusa). Journal of Biogeography 40(1):63–74. Knudson J. W., 1960 Reproduction life history and larval ecology of the California xanthidae the pebble crabs. Pacific Science 14:3-17.
  • 6. AACL Bioflux, 2020, Volume 13, Issue 4. http://www.bioflux.com.ro/aacl 1975 Mantelatto F. L. M., Fransozo A., 1999 Characterization of the physical and chemical parameters of Ubatuba Bay, northern coast of São Paulo State, Brazil. Revista Brasileira de Biologia 59:23-31. Mantellato F. L. M., Fransozo A., 1999 Reproductive biology and molting cycle of the crab Callinectes ornatus (Crustacea, Portunidae) in the Ubatuba Region, São Paulo, Brazil. Crustaceana 72:63–76. Muzaffer H., Ibrahim T., 2000 The relationship between egg size and female size in freshwater crayfish, Astacus leptodactylus. Aquaculture International 8:95-98. Ng P. K. L., Guinot D., Davie P., 2008 Systema brachyuorum: part I. An annotated checklist of extant brachyuran crabs of the World. Raffles Bulletin of Zoology 17: 1–286. Ng P. K. L., 1987 Freshwater crabs of the genus Isolapotamon Bott, 1968 from Sarawak, Borneo (Crustacea, Decapoda, Brachyura, Potamidae) (new series). Sarawak Museum Journal 37:139–153. Ng P. K. L., Ng P. Y. C., 2019 A new species of semiterrestrial vampire crab (Crustacea: Decapoda: Brachyura: Sesarmidae) from Brunei Darussalam, Borneo. Zootaxa 4614 (3): 529-540. Ng P. K. L., 1988 The freshwater crabs of Peninsular Malaysia and Singapore. — Department of Zoology, University of Singapore, Shinglee Press, Singapore. pp. i–viii, 1–156 Ng P. K. L., Grinang J., 2018 A new species of highland vampire crab (Crustacea: Brachyura: Sesarmidae: Geosesarma) from Serian, Sarawak. Zootaxa 4508 (4):569–575. Pace F., Harris R. R., Jaccarini V., 1976 The embryonic development of the Mediterranean freshwater crab Potamon edulis (= P. fluviatile) (Crustacea, Decapoda, Potamidae). Journal of Zoology 180 (1):93-106. Steele D. H., Steele V. J., 1991 Morphological and environmental restraints on egg production in amphipods. In: Crustacean Egg Production. Wenner A., Kuris A. (eds.) Crustacean Issues, A.A. Balkema, P.O. Box 1675, 3000 BR Rotterdam, pp. 157-170. Valter C., Claudia M. O., 2008 Fecundity of the spider crab Mithraculus forceps (Decapoda, Mithracidae) from the northeastern coast of the state of São Paulo, Brazil. Iheringia. Série Zoologia 98(1):84-87. Wu H. X., Xue J. X., Cumberlidge N., 2010 An extra embryonic phase in the true freshwater crab Sinopotamon yangtsekiense Bott, 1967 (Decapoda, Potamidae). Chinese Journal of Oceanology and Limnology 28:725-730. Yeo D. C. J., Ng P. K. L., Cumberlidge N., Magalhães C., Daniels S. R., Campos M. R., 2008 Global diversity of crabs (Crustacea: Decapoda: Brachyura) in freshwater. Hydrobiologia 595:275- 286. Received: 01 January 2020. Accepted: 31 January 2020. Published online: 25 July 2020. Authors: Lirong Yu Abit, Department of Animal Science and Fishery, Faculty of Agriculture Science and Technology, Universiti Putra Malaysia Bintulu Campus, 97008, Bintulu, Sarawak, Malaysia, e-mail: kelibunga76@gmail.com Mohd. Zafri Hassan, Department of Aquaculture, Faculty of Agriculture, Universiti Putra Malaysia, 43400 UPM Serdang, Selangor, Malaysia, e-mail: mzafri@upm.edu.my Kamil Latif, Department of Animal Science and Fishery, Faculty of Agriculture Science and Technology, Universiti Putra Malaysia Bintulu Campus, 97008, Bintulu, Sarawak, Malaysia, e-mail: kamill@upm.edu.my Jongkar Grinang, Institute of Biodiversity and Environmental Conservation, Universiti Malaysia Sarawak, 94300 Kota Samarahan, Sarawak, Malaysia, e-mail: gjongkar@unimas.my Abdulla-Al-Asif, Department of Animal Science and Fishery, Faculty of Agriculture Science and Technology, Universiti Putra Malaysia Bintulu Campus, 97008, Bintulu, Sarawak, Malaysia, e-mail: jessoreboyhemel@gmail.com This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. How to cite this article: Abit L. Y., Hassan M. Z., Latif K., Grinang J., Asif A. A., 2020 Short note: The fecundity and egg size of the freshwater crab (Isolapotamon bauense Ng, 1987) from Sarawak, Borneo. AACL Bioflux 13(4):1970-1975.