Anda di halaman 1dari 3

Journal of

Applied Ichthyology
J. Appl. Ichthyol. 26 (2010), 946–948 Received: July 28, 2009
 2010 Blackwell Verlag, Berlin Accepted: February 22, 2010
ISSN 0175–8659 doi: 10.1111/j.1439-0426.2010.01516.x

Technical contribution
Species composition and length-weight relationship of fishes in the Candaba wetland
on Luzon Island, Philippines
By L. M. B. Garcia

Institute of Biology, University of the Philippines, Quezon City, Philippines

Summary is an important biological component of the Candaba wetland


The length-weight relationships or LWR (W = aLb) of 18 of ecosystem, yet no study has been published on this particular
the 21 fish species caught in 2007–2008 from the Candaba resource vital to humans as well as to wildlife.
wetland in central Luzon, Philippines are reported. These Therefore, this paper reports an inventory of fish species in
species belong to 14 families and the LWR of six species are first the Candaba wetland and describes their length-weight rela-
documented in this paper. Cyprinids comprised the greatest tionships (LWR). Because the LWR reliably predicts weight
number of species. The high significance of the LWR para- from length, it has become a useful tool to estimate standing
meters indicate that fish weight may be predicted from length, at stock biomass and yield in many fishery assessment studies
least within the range of the fish lengths recorded. This first (Martin-Smith, 1996; Gonçalves et al., 1997). Information from
reference to the LWR of fishes from the Candaba wetland this study will be useful to support fishery management and the
provides baseline data for the conservation management of fish conservation of this important wetland in the Philippines.
biota in this threatened ecological resource.

Materials and methods


Introduction Fish were obtained from several sites (San Agustin, Barangca-
Tropical wetlands are biologically productive ecosystems. Malisik, Simang, Mandili) in the town of Candaba along the
They are important ecological resources that provide beneficial backwaters and tributaries of the Pampanga River (Fig. 1).
goods and services due to the wide diversity of aquatic habitats Sampling times in 2007–2008 were limited from October until
that they support (Zedler and Kercher, 2005). In addition to June when road access to the sites was not totally flooded and
their hydrological functions (Shaffer et al., 1999), these wet- therefore considered safe. Fish specimens were caught by a
land habitats maintain a rich diversity of aquatic fowl and variety of common fishing gears employed in the area such as
fishes that are exploited to feed human settlements attracted to fyke nets (bokatot) fixed in the middle of flowing tributaries and
the wetlandsÕ high biological productivity (Reddy and Gale, catch basins (salandra) to drain floodwaters retained by earthen
1994; Gibbs, 1998; Junk et al., 2006). Considered to be levees. Fish catches were immediately sorted according to
wastelands due to the lack of understanding of their important species, and specimens covering a wide range of sizes (excluding
functions has resulted in their widespread conversion for larvae and very young juveniles which had not assumed adult
residential, industrial, and agricultural use. The Candaba body form) were randomly chosen. Total body weight of each
wetland in the Philippines is no exception; it is a palustrine specimen was measured with an electronic scale to the nearest
wetland basin on Luzon Island, retaining seasonal floodwaters 0.1 g and, when necessary, large specimens were weighed with a
overflowing from the nearby Pampanga River and its tribu- spring balance having an accuracy of 5 g and 50 g. The standard
taries. In its pristine state, the wetland covered an area of length of each specimen was likewise measured to the nearest
about 32 000 ha, stretching westward to Manila Bay from the 0.1 cm. Sex of specimens was not determined.
middle section of central Luzon Island, and had been known The LWR is described by the equation W = aLb, where W
as an important staging area for many migratory birds from is total body weight, a is the regression intercept, L is standard
the Asian mainland (DENR-PAWB, 2005). However, conver- length, and b is the regression coefficient (Froese, 2006). For
sion to rice agriculture and aquaculture has significantly each species, the parameters a, b, and r2 (coefficient of
reduced the Candaba wetland to <1% of its original area determination) was estimated by least-squares regression
(DENR-PAWB, 2005). Like many productive freshwater analysis of the logarithm-transformed LWR expression log
wetlands elsewhere in Southeast Asia (Junk et al., 2006), the W = log a + b log L with W as the dependent variable. Fish
Candaba wetland supports a seasonal fishery that coincides species (Ctenopharyngodon idella, Carassius auratus, Glossogo-
with the arrival of monsoon floodwaters. Anecdotal reports by bius biocellatus) with only a single specimen each were
local people indicate a reduction in the fishery catch as a likely excluded from the analyses.
result of un-regulated fishing and reduction in size and
alteration of the natural features of the Candaba wetland
over the years. However, attempts to conserve what remains of Results and discussion
the Candaba wetland have been hampered by the absence of A total of 2341 fish specimens were collected during the 2-year
reliable information on its biota, particularly that of fish. Fish sampling period, representing 21 species from 14 families

U.S. Copyright Clearance Centre Code Statement: 0175–8659/2010/2606–0946$15.00/0


Fishes of Candaba wetland, Philippines 947

120.8° East longitude 120.9°

15.2° • Mandili
Arayat

Pampanga River

North latitude
• Barangca-Malisik

Candaba • Simang
Santa Ana N

Fig. 1. Location map of sampling sites 15.1° • San Agustin


2 km
in the tributaries and backwaters of
Pampanga River in Candaba town,
central Luzon island, Philippines

Table 1
Length-weight regression parameters of fish species caught in the Candaba wetland, Philippines. Six species (bold, italics) have no LWR described
by Froese and Pauly (2010) in FishBase

Standard length
Family and species n b (95% CI) a (95% CI) r2 range (cm) Status

Anabantidae
Anabas testudineus 51 2.84 (2.68–2.99) 0.056 (0.041–0.078) 0.97 4.8–11.7 Native
Ariidae
Arius dispar 3 3.44 (3.38–3.50) 0.006 (0.005–0.007) 0.99 10.2–19.5 Native
Chanidae
Chanos chanos (juveniles) 10 2.91 (2.41–3.40) 0.021 (0.006–0.081) 0.96 12.0–19.2 Native
Channidae
Channa striata 81 2.96 (2.83–3.08) 0.018 (0.012–0.027) 0.96 12.6–41.4 Introduced
Cichlidae
Oreochromis niloticus 386 3.04 (2.98–3.09) 0.036 (0.032–0.041) 0.97 4.0–21.3 Introduced
Clariidae
Clarias batrachus 12 2.70 (2.08–3.31) 0.028 (0.004–0.191) 0.90 15.8–28.9 Introduced
Cyprinidae
Barbonymus gonionotus 572 2.98 (2.95–3.01) 0.035 (0.033–0.038) 0.98 3.9–21.1 Introduced
Cyprinus carpio 467 2.89 (2.84–2.95) 0.037 (0.031–0.043) 0.97 5.8–60.0 Introduced
Ctenopharyngodon idella 1 – – – – Introduced
Carassius auratus 1 – – – – Introduced
Labeo rohita (juveniles) 107 2.92 (2.79–3.04) 0.028 (0.020–0.038) 0.95 9.5–36.2 Introduced
Hypophthalmichthys nobilis (juveniles) 13 3.19 (2.93–3.46) 0.011 (0.005–0.026) 0.98 14.6–29.8 Introduced
Gobiidae
Glossogobius giuris (juveniles) 105 3.06 (2.99–3.13) 0.015 (0.013–0.017) 0.99 2.8–17.1 Native
G. biocellatus 1 – – – – Native
Hemiramphidae
Rhynchorhamphus georgii 19 2.32 (1.84–2.79) 0.014 (0.005–0.040) 0.86 7.1–17.0 Native
Loricariidae
Pterygloplichthys disjunctivus 128 2.56 (2.42–2.69) 0.080 (0.054–0.117) 0.91 7.7–26.5 Introduced
Megalopidae
Megalops cyprinoides (juveniles) 5 3.14 (2.04–4.28) 0.011 (0.0005–0.250) 0.96 14.4–19.5 Native
Mugilidae
Liza subviridis 3 2.75 (1.82–3.67) 0.041 (0.004–0.401) 0.99 11.1–13.2 Native
Osphronemidae
Trichogaster pectoralis 109 3.22 (3.08–3.36) 0.015 (0.011–0.021) 0.95 6.5–14.9 Introduced
T. trichopterusa 4 3.0 0.051 1.0 6.7–7.7 Introduced
Teraponidae
Leiopotherapon plumbeus 263 3.00 (2.92–3.09) 0.032 (0.027–0.037) 0.95 2.2–11.8 Native
a
Specimens had the same body weight. LWR parameters were estimated following Froese (2006); thus, b = 3 and a is geometric mean of four
specimens.
n, sample size; CI, confidence interval.

(Table 1). Except for the families of Cyprinidae, Gobiidae, and ids, the cyprinids with six species were by far the most
Belontiidae, each family was represented by at least one fish dominant fishes sampled. Other tropical wetlands in Southeast
species. Followed by two species of gobiids and osphronemi- Asia support a variety of cyprinids, which reflects their high
948 L. M. B. Garcia

degree of endemicity in the region (Zakaria-Ismail, 1994). The City) under Project Code Number BIO 07-2-02. Field assis-
great number of cyprinid species in the Candaba wetland and tance by James Paul Gomez, Roman Aldo Reyes, Riezel Ann
elsewhere in the Philippines are the result of species introduc- Bernal, the cooperation and assistance of municipal and village
tions in support of the governmentÕs food production pro- (barangay) officials and the local people of the municipality of
grams in previous years (Welcomme, 1981). Overall, 57% of Candaba, Pampanga are gratefully acknowledged. The author
the fish species reported in this study have been introduced is grateful for the gift of field sampling gear from IDEA WILD
into Philippine freshwater habitats; the remaining 43% are (Fort Collins, Colorado, USA).
native species. Of particular concern is the increasing presence
of the invasive sailfin catfish (Pterygoplichthys disjunctivus,
Loricariidae; local name: janitor fish) in the fishery catch of References
Candaba and other freshwater bodies on Luzon Island Chavez, J. M.; Dela Paz, R. M.; Manohar, S. K.; Pagulayan, R. C.;
(Chavez et al., 2006). The prevalence of these introduced Carrandang, J. R., 2006: New Philippine record of South
American sailfin catfishes (Pisces:Loricariidae). Zootaxa 1109,
fishes in freshwater habitats in the Philippines has threatened 57–68.
local fish diversity, apparently displacing about fourteen De Silva, S.; Abery, N. W.; Nguyen, T. T. T., 2007: Endemic
endemic cyprinids in Lake Lanao in southern Philippines freshwater finfish of Asia: distribution and conservation status.
(Nguyen and De Silva, 2006; De Silva et al., 2007). The extent Divers. Distrib., 13, 172–184.
Department of Environment and Natural Resources (DENR) –
of this threat in the Candaba wetland is unknown because of Protected Areas and Wildlife Bureau (PAWB), 2005: UNEP ⁄ GEF
the lack of baseline data on fish fauna in the study area. It is Project: reversing environmental degradation trends in the South
clear, however, that the dominance of introduced fish species is China Sea and Gulf of Thailand – Philippines national report on
a reflection of the continuing degradation of this wetland. To wetlands. DENR-PAWB, Quezon City, Philippines, pp. 104.
the authorÕs best knowledge, this is the first published report Froese, R., 2006: Cube law, condition factor, and weight-length
relationships: history, meta-analysis and recommendations.
listing the occurrence of a variety of fish species in the J. Appl. Ichthyol. 22, 241–253.
Candaba wetland. Froese, R.; Pauly, D., (Eds). 2010: FishBase. World Wide Web
The LWRs were highly significant for the 18 fish species electronic publication. Available at: http://www.fishbase.org,
sampled. The intercept a varied from 0.006 (Arius dispar) to version (accessed 29 January 2010).
Gibbs, J. P., 1998: Wetland loss and biodiversity conservation.
0.08 (P. disjunctivus). The range of values for the coefficient of
Conserv. Biol. 14, 314–317.
determination (r2) of the LWR was close to or greater than 0.9, Gonçalves, J. M. S.; Bentes, L.; Lino, P. G.; Ribeiro, J.; Canario,
demonstrating that the line-of-best fit to describe the LWR A. V. M.; Erzini, K., 1997: Weight-length relationships for
explains at least 90% of the variation in fish weight, and selected fish species of the small-scale demersal fisheries of the
therefore the LWR may be applied to any value of length to south and south-west coast of Portugal. Fish. Res., 30, 253–
256.
predict weight within the range of fish lengths sampled. The Junk, W. J.; Brown, M.; Campbell, I. C.; Finlayson, M.; Gopal, B.;
LWRs in this study do not distinguish between sexes nor Ramberg, L.; Warner, B. G., 2006: The comparative biodiversity
describe variations due to seasonal somatic and gonadal of seven globally important wetlands: a synthesis. Aquat. Sci. 68,
growth. The parameters of the LWR may therefore be viewed 400–414.
Martin-Smith, K. H., 1996: Length ⁄ weight relationships of fishes in a
as an annual average for each of the fish species, particularly
diverse tropical freshwater community, Sabah, Malaysia. J. Fish
of the six species (A. dispar, Rhynchorhamphus georgii, P. Biol. 49, 731–734.
disjunctivus, Trichogaster pectoralis, T. trichopterus, Leiopo- Nguyen, T. T. T.; De Silva, S., 2006: Freshwater finfish biodiversity
therapon plumbeus) whose LWR are reported in this paper for and conservation: an Asian perspective. Biodivers. Conserv. 15,
the first time. 3543–3568.
Reddy, K. R.; Gale, P. M., 1994: Wetland processes and water quality:
A comparison of the LWR parameters of Candaba fishes a symposium review. J. Environ. Qual. 23, 875–877.
with their conspecifics elsewhere (Froese and Pauly, 2010) Shaffer, P. W.; Kentula, M. E.; Gwin, S. E., 1999: Characterization
revealed slight differences due to one or a combination of of wetland hydrology using hydrogeomorphic classification.
factors such as variations in body size range, sample size, Wetlands 19, 490–504.
Welcomme, R. L., 1981: Register of international transfers of inland
seasonal abundance, habitat characteristics in the wild or in
fish species. Food and Agriculture Organization of the United
culture, and type of body length measured. The influence of Nations, Rome, pp. 120.
these factors on the overall status of fish stocks in the study site Zakaria-Ismail, M., 1994: Zoogeography and biodiversity of the
is open to further investigation. Nonetheless, the LWRs in the freshwater fishes of Southeast Asia. Hydrobiologia 285, 41–48.
present study are the first reported for fish species caught in the Zedler, J. B.; Kercher, S., 2005: Wetland resources: status, trends,
ecosystem, services, and restorability. Annu. Rev. Environ.
Candaba wetland, providing vital information for the conser- Resour. 30, 39–74.
vation management of this wetland resource.
AuthorÕs address: Luis Maria B. Garcia, University of the Philippines,
Institute of Biology, 1101 Diliman, Quezon City,
Philippines.
Acknowledgements E-mail: aacanthurus@gmail.com
This study was funded by the Natural Science Research
Institute of the University of the Philippines (Diliman, Quezon

Anda mungkin juga menyukai