Growth Rate of Staghorn Coral (Acropora) on Coral Garden Program at Sempu Nature Reserve Malang

  RESEARCH JOURNAL OF LIFE SCIENCE E-ISSN : 2355-9926 DESEMBER-2015 VOLUME 02 NO. 03 http://rjls.ub.ac.id 152

  Growth Rate of Staghorn Coral (Acropora) on Coral Garden Program at Sempu Nature Reserve Malang OktiyasMuzaky Luthfi 1 ; Novita Nurmalasari 1 ; dan Alfan Jauhari 2 1 Marine Science University of Brawijaya, Jl. Veteran-Malang, 65145, Indonesia 2 Fisheries Utilization University of Brawijaya, Jl. Veteran-Malang, 65145, Indonesia E-mail :

  ABSTRACT

  Live coral cover at Sempu Nature Reserve was decrease from 50% in 2006 to 36% in 2013. Adverse human activities such as: over-fishing, recreational activities, waste disposal, deforestation, reef mining and deforestation were suggested to be main factors for declining coral reef at this area. Restoration is defined as the act of returning an ecosystem, as nearly as possible, to its original condition. Coral on SendangBiru laid on northern area of Sempu Island. Coral garden was establish in the end of 2013. Aim of this research was to know the growth (wide, number of branches, growth rate) of staghorn coral that was transplanted on steel frame at coral garden in different depth. Staghorn coral were tied on doom shaped steel in 6 m depth. The result showed thatthe average of increasing staghorn coral's area was 56.91 cm

  2

  , number of branch increase was 55 and growth rate was 5.23 cm

  2

  /month respectively.Increase of depth will influence to decrease of sunlight intensity in water will be affected on calcification rate of coral. GR of staghorn coral in Sempu was higher than other area.

  Sempu strait and Segara Anakan which has 10 wide area. During last eight years live coral cover was decrease from 50% in 2006 (Reef Check, 2006), 30% in 2013 and 22% in 2014 (Luthfi, 2014). Like as another coral in the world, coral reef in Sempu Island also under the threat came from natural or anthropogenic factors. 5 threats were suggested became threat in this area, i.e. over fishing, tourism activity, run off sedimentation, domestic waste, and coral mining.

  Over fishing lead change abundance and composition of coral fish. In normal condition herbivorous fish (Scaridae) which has a pair of protruding teeth, will eat algal in surrounding of coral. Decrease or loss the kind of fish can cause algal bloom that mean will reduce coral cover (Williams, 2001).

  Even if Sempu Island was categorized as nature reserve or restricted area, in fact many domestic tourism enjoy with their water sport activities, such as diving, snorkeling, fishing and kayaking near coral reef ecosystem. Those all activities had contribute to increase coral stress and

  RESEARCH JOURNAL OF LIFE SCIENCE E-ISSN : 2355-9926 DESEMBER-2015 VOLUME 02 NO. 03 http://rjls.ub.ac.id 153

  km. More than 300 ships passing near coral reef ecosystem per-day also disposed domestic waste into water directly. During rainy season sediment run off also load into water than change color of sediment into brown color. Sediment and nutrient had important role as coral disease trigger in coral (Luthfi, 2014). Coral disease outbreak could decline coral diversity and increase algal growth or phase shift from coral to algal dominance. Potential loss of coral reef fishes in the future become main problem for human kind (Norströmet al., 2009). The last threat was coral mining which lot of massive Porites and Goniastrea used became home foundation by local people.

METHODS 1. TIME AND STUDY SITE

  Acropora are the most abundance coral were found in Indo-Pacific area which the largest species in scleractinian coral about 140-160 species (Wallace, 2011). These coral had many life forms with life form of branching or staghorn (Veron, 2000). Dominance of Acropora coral suggested influenced by its fast growth and adaptation process. Acropora can easly found in reef flat, reef front and reef slope (Dai and Horng, 2009; Veron, 2000). Many Acroporids coral commonly found on eastern part of Sempu Island in 3-6 m depth, which had 2 types of growth rate i.e. branching and tabulate form.

  Potential degradation of coral reef in Sempu Island has been looming. Coral transplantation is one method to restoration of coral reef as original state.

  (Acroporasp) during 9 months in Sempu Island's waters.

  This research was conducted at September 2013-June 2014 at strait of Sempu Island, located on Watu Mejo 2 (08

  ⁰ 25'44.8" LS - 112 ⁰41'36.5" BT) (Picture 1). Fragment of coral Acropora (10±3 cm) were tide in edge of steel frame (

   1mm) in 6 m depth used SCUBA. We took picture every single coral fragment using Canon G 16 underwater camera (Japan) with ruler beside, these data stated as t . After 9 months We took pictures of fragment with the same method, stated as t 9 .

  Photograph taken perpendicular to the diver to get maximum angle. We also record chemical-physical oceanography (temperature, salinity, pH, Dissolved oxygen, turbidity and water current) every two months. Coral growth rate and area measured by using software Image-J (NIH, America), and number of new branching calculated manually in Marine Science Laboratory. Coral accretion rate calculated using method of Ricker(1975): Β

  = Lt- L0…… (Formula 1) where :

  β = increase of length/ height of coral fragment.

  L t = average of length/ height of coral fragmentafter month of-t.

  

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RESULT AND DISCUSSION

  Lt+1 = average length or height at t+1 1. Lt = average length or height of coral

   TRANSPLANTEDCORAL

  fragment after i Fragment coral was tied on 6 columns in ti+1 = time afteri +1 different steel row, total 18 fragments ti = time after t (Table 1). Six on the top of steel frame (A1,

  C1, E1, F1, G1 and H1), another six was placed on the middle (A2, C2, E2, F2, G2 and H2) and six on the bottom (A3, C3, E3, F3, G3 and H3). Two types of species were transplanted i.e. Acropora sp1 and Acropora sp2 which both of them are branching coral. After 2 months coral fragment tied into steel frame through cementation process except some coral (A3, E3, F1, F2, H2 and H3) that didn't run into perfect cementation.

  Coral accretion, number of branch and growth rate of Acroporasp.

  Picture 1. Study area marked by green dot where coral garden was laid. Table 1. Mean of accretion, number of branch and growth rate of coralAcroporasp.

   Coral β α

  

Code LF Species Annotation

2 2 (cm ) (cm /month) branch A1 ACB Acroporasp1

  35.00

  3.89

  23 A2 ACB Acroporasp1

  38.37

  4.26

  52

  • A3

  Lost - C1 ACB Acroporasp1

  31.21

  3.47

  48

  • C2
  • C3
  • E1 ACB Acroporasp2

  62.01 5.19 114

  • E2
  • E3

  Lost

  • F1

  Lost

  • F2

  Lost

  

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  After 9 months monitoring on Acropora growth, the survival rate of coral was 62%. Nine coral was lost or broken due to high current speed on December-February (west monsoon). Table 1 showed that coral accretion rate (β) of Acropora sp2 higher than Acropora sp1. The highest of accretion rate on Acroporasp1 was found on G1 (49.31 cm2)and the lowest on G3 (4.53 cm2).

  While the highest accretion rate on Acropora sp2 was found on H1 (121.75 cm2) and the lowest on F3 (62.01 cm2). The highest of coral growth rate (α) on Acroporasp1 was found on H1 (13.53 cm2/month) and the lowest on E1 (5.19 cm2/month). The highest amount of Acropora branch was found on E1 (114 axial corallites) and the lowest on A1 (23 axial corallites).

  Appendices. Appendix 1. Initial conditions (t ) and after 9 months transplanted (t 9 ) of branching Acropora sp.

  9 t t A1 A2

  RESEARCH JOURNAL OF LIFE SCIENCE E-ISSN : 2355-9926 DESEMBER-2015 VOLUME 02 NO. 03 http://rjls.ub.ac.id 156 t t

  9 E1 F3 G1 G2

  

RESEARCH JOURNAL OF LIFE SCIENCE E-ISSN : 2355-9926 157

DESEMBER-2015 VOLUME 02 NO. 03 http://rjls.ub.ac.id 9 t t G3 H1 2.

  3. PHYSICAL-CHEMICAL PARAMETER DISCUSSION. Coral Acropora Survival Rate.

  Water temperature in Sempu Island in

  o

  normal range 2742 - 28.41

  C, also salinity in Nine coral fragment was loss from transplantation media. September-November average of 34 ‰. Water turbidity was low because clarity of sea water maximum 6.7 m where coral transplantation had started it (100%) and current speed in moderate was transition season, from east monsoon condition about 1.1 m/s (Table 2). to west monsoon, and then during

  December to April monsoon came with

  Table 2. Water quality in Sendang Biru

  strong wind, current and high sedimentation water during research. due run off from terrestrial. Coral fragments Sept. Nov. Jan. Jun. were tied using copper wire (

  Parameter Unit

  =1 mm) into

  2013 2013 2014 2014

  RESEARCH JOURNAL OF LIFE SCIENCE E-ISSN : 2355-9926 DESEMBER-2015 VOLUME 02 NO. 03 http://rjls.ub.ac.id 158

  fragments would drift cause of strong current.

  Cementation rate was the key of success of transplantation project, where it was natural process coating of media/ substrate by using calcium carbonate (CaCO3). Cementation also intend to bind coral skeleton to substrate and to close porosity thereby function as natural adhesive (Manzello, et al., 2008). Life form also affects the speed of cementation of coral fragments on the substrate. Branching Acropora had faster cementation than tubular or foliose. Many studies also has proved branching Acropora has faster growth rate than non-Acropora (Guest et al., 2011).

  Growth Rate and Branch of Acropora.

  Coral growth rate also be characterized by increasing of mass of coral skeletal and increasing number of polyp (Soong and Chen, 2003). Skeletal extension due to increase of strontium (Sr) and calcium (Ca) in fasiculi during day time and center of calcification (COCs) occur at night. During night time micron sized crystals would be deposited on axial coralit of coral. Collection of crystals coalesce into a bundle to form new fasciculi. Skeletal extension faster during day than night time (Allison and Finch, 2004).

  This research showed that coral where on the upper frame had faster growth rate than below. Light is the main factor of coral

  Increasing branch in coral Acropora became successfully of coral transplantation. Branch is an extension of axial coraliteneither radial coralite. In macro size axial coralite form a long rod also called as synapticulae. Contrary with massive coral that have solid structure of skeletal, branching Acropora has wider and sturdy, so this is the reason why Acroporid has faster growth rate than massive coral (Nothdurft and Webb, 2007).

  Aside as former new brach in Acropora, axial coralite also have a role as nutrient translocation for main branching of Acropora (Gladfelter, 1983). Acropora coral growth rate would be reduced if nutrients (nitrite and phosphate) high in the waters. Nutrient excess water will cause reduced fecundity coral, inhibition of fertilization, embryo development and disrupt the process of attachment of coral planulae (Renegarand Riegl, 2005).

  CONCLUSIONS

  The average of coral growth rate Acroporasp in Sempu Nature Reserve was 5.23 cm2/month. Intensity of light, nutrient and depth of water have important role for coral growth rate. Coral reef in Sempu Island Nature Reserve face many threats which came from natural as well as anthropogenic.

  Coral garden initiation is simple idea for bigger step of coral conservation in the future.

  Sakai, K. (1998). Delayed maturation in the

  Eakin, C. M., Glynn, P. W., & Langdon,

  Acroporacervicornis. Mar Ecol Prog Ser, 293, 69-76.

  Renegar, D. A., & Riegl, B. M. (2005). Effect of nutrient enrichment and elevated CO2 partial pressure on growth rate of Atlantic scleractinian coral

  Nybakken, J. W. 1992. Biologi Laut: Suatu Pendekatan Ekologis. Terjemahan. PT Gramedia Pustaka Utama. Jakarta.

  Microstructure of common reef- building coral genera Acropora, Pocillopora, Goniastrea and Porites: constraints on spatial resolution in geochemical sampling. Facies, 53,1

  Folke, C. (2009). Alternative states on coral reefs: beyond coral-macroalgal phase shifts. Mar EcolProgSer, 376, 295-306. Nothdurft, L. D., and Webb, G. E., 2007.

  Scleractinian corals from Rutland Island, Andaman. IJBS, 3(155). Norström, A. V., Nyström, M., Lokrantz, J., &

  C. (2008). Poorly cemented coral reefs of the eastern tropical Pacific: Possible insights into reef development in a high-CO2 world. Proceedings of the National Academy of Sciences, 105 (30), 10450-10455. Mondal, T. (2010). New record of Nine

  Kabupaten Malang, Jawa Timur Prosiding PIT XI ISOI 2014, 1 (1). Manzello, D. P., Kleypas, J. A., Budd, D. A.,

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  Hartini, S., and Takaku, G. (2012). Macrochelid mites (Acari: Mesostigmata: Macrochelidae) in Sempu Island, East Java, Indonesia. Journal of the Acarological Society of Japan, 21 (1).

  Restoration Ecology, 19(2), 234-242. Harriott, V. J., & Fisk, D. A. (1988). Coral transplantation as a reef management option. In Proc 6th int coral Reef Symp (Vol. 2, pp. 375-379). Chicago

  Franco, C., & Gomez, E. D. (2011). How Quickly do Fragments of Coral “Self‐ Attach” after Transplantation?.

  Scleractinian coral species survive and recover from decalcification. Science, 315(5820), 1811-1811. Gladfelter, E. H. 1983. Circulation of fluids in the gastrovascular system of the reef coral Acroporacervicornis. Biological Bulletin 165: 619

  1). 國立臺灣大學出版中心. Fine, M., and Tchernov, D. (2007).

  Allison, N., and Finch, A. A. (2004). High‐ resolution Sr/Ca records in modern Poriteslobata corals: Effects of skeletal extension rate and architecture. Geochemistry, Geophysics, Geosystems, 5(5). Dai, C. F., andHorng, S. (2009). Scleractinia Fauna of Taiwan: Complex group (Vol.

  REFFERENCES

  Education (Number: 023.04.2.414989/2014, December 5, 2013) of Republic of Indonesia.

  • –636 Guest, J. R., Dizon, R. M., Edwards, A. J.,
  • – 26.

  

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DESEMBER-2015 VOLUME 02 NO. 03 http://rjls.ub.ac.id

  nursery. Restoration Ecology, 11 (1), Veron, J. E. N. (2000). Corals of the World, 62-71. vol. 1

  • –3. Australian Institute of Marine Supriharyono. 2000. Pengelolaan Ekosistem Science, Townsville.

  Terumbu Karang. Penerbit Djambatan. Jakarta. 108 hal.

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