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The influence of recruitment and post-settlement mortality on coral communities across the central Great Barrier Reef

Australian Institute of Marine Science
Australian Institute of Marine Science (AIMS) ( Contributor )
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ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Adc&rfr_id=info%3Asid%2FANDS&rft_id=http://apps.aims.gov.au/metadata/view/9aea83a2-cbb3-4b7b-94fb-b7f90359b87d&rft.title=The influence of recruitment and post-settlement mortality on coral communities across the central Great Barrier Reef&rft.identifier=http://apps.aims.gov.au/metadata/view/9aea83a2-cbb3-4b7b-94fb-b7f90359b87d&rft.publisher=Australian Institute of Marine Science (AIMS)&rft.description=Pandora Reef, Rib Reef and Myrmidon Reef, located 16.6 km, 57.6 km and 116.9 km from the coastline respectively, were chosen for a year long series of cross-shelf coral recruitment experiments, commencing in January 1981. Settling plates approximately 15 mm thick and 300-400 cm² in total surface area (sum of upper and lower surfaces) were cut from natural, uncleaned heads of the massive corals Porites and Goniastrea spp. Plates were attached to each of four pins on a galvanized steel support rack at an angle of 37-45°. Racks were then secured on the reef by attaching them to two solid steel reinforcement bars driven into the reef. On each reef, racks were placed on the exposed, windward E-SE forereef slope, with plates facing into the wave surge. To investigate natural recruitment, two racks of plates (four plates per rack) were deployed at both 3m and between 14 and 18m on each reef. One rack at each depth was retrieved after 6 months and the second after 12 months. A third rack was deployed at each depth at the end of the first 6 months and retrieved 6 months later. Transplant experiments were carried out to investigate survival of coral recruits when moved to a new environment. Two additional racks of plates (three per rack) were deployed at each depth, at each reef in January 1981. After 6 months the racks were redeployed to make all possible combinations of transplants between reefs, while maintaining original depths. A further rack of plates was deployed at each depth, at each reef in January 1981, as a control for handling. Racks were retrieved after 6 months, held onboard ship for one to several days and replaced at the same site. All transplant and control plates were retrieved within 12 months of the initiation of the experiment. After retrieval, all plates were stored frozen at -20°C until analysed. In the laboratory, plates were thawed, cleaned of sediment and debris and dried in an oven at -45°C. Each plate was then cleaned of algae and examined using a dissecting microscope. Taxonomic identification was based primarily on calical structure. Juveniles were usually identified to family, often to genus, and occasionally to species, with scanning electron microscopy (SEM) and taxonomic guides available for corals of this region. Coral spat were assessed for post-settlement mortality as follows: skeleton intact with at least remnants of tissue; coral overgrown and damaged; and complete colony mortality. Only the last category was utilized in estimating post-settlement mortality frequencies, which were calculated simply as the proportion in this state within a given taxon. Intra- and interspecific competition for space involving corals and other sessile epibiota was also assessed from the coral's perspective. Associates within 8 mm of the juvenile colony were recorded and examined for interactions and a static observation of overgrowth was taken as evidence of competition for space. A competition parameter was defined as the number of competitive wins over the total number of encounters within a taxon. Placement of settled corals or relative exposure was also assessed by differentiating between juvenile corals found on upper surfaces of the plate and those settling cryptically on the lateral or lower surface. An exposure parameter was calculated as the proportion of those juveniles in the latter state. This study was initiated to examine patterns of coral recruitment across the continental shelf in central Great Barrier Reef. The study makes use of settlement plates to look at differences in species composition of recruits, post-settlement mortality, intra- and interspecific competition for space and the placement of settled corals on the plates. An additional transplant experiment was carried out to determine the probability of survival of coral larvae if they had been transported to another location and settled successfully. During this project a taxonomic key for juvenile corals was constructed using juveniles from this and previous studies.Statement: Plates were processed according to the procedures described in: Sammarco PW (1980) Diadema and its relationship to coral spat mortality: Grazing, competition, and biological disturbance. J. Exp. Mar. Biol. Ecol. 45: 245-272. Sammarco PW (1982) Echinoid grazing as a structuring force in coral communities: Whole reef manipulations. J. Exp. Mar. Biol. Ecol. 61: 31-55. Sammarco PW and Andrews JC (1988) Localized dispersal and recruitment in Great Barrier Reef corals: The Helix Experiment. Science 239: 1422-1424. Sammarco PW and Andrews JC (1989) The Helix Experiment: Differential localized dispersal and recruitment patterns in Great Barrier Reef corals. Limnol. Oceanogr. 34: 896-912 Sammarco PW and Carleton JH (1982) Damselfish territoriality and coral community structure: Reduced grazing and effects on coral spat. Proc. 4th Int. Coral Reef Congr. 1: 525-535. Estimates of mortality may be slightly conservative due to a possible delay of several days before the skeleton of a freshly killed recruit exhibits clear signs of mortality. Bias from this source is expected to be negligible, however, because the samples integrate 6 to 12 months of mortality. The taxonomic references used in this study were: Veron JEN and Pichon M (1976) Scleractinia of eastern Australia, Part 1. Families Thamnasteriidae, Astrocoeniidae, and Pocilloporidae. Aust. Inst. Mar. Sci. Monogr. Ser. V. 1. 86 p. Veron JEN and Pichon M (1979) Scleractinia of eastern Australia, Part 3. Families Agariciidae, Siderastreidae, Fungiidae, Oculinidae, Merulinidae, Mussidae, Pectiniidae, Caryophylliidae, Dendrophylliidae. Aust. Inst. Mar. Sci. Monogr. Ser. V. 4. 422 p. Veron JEN and Pichon M (1982) Scleractinia of eastern Australia, Part 4. Family Poritidae. Aust. Inst. Mar. Sci. Monogr. Ser. V. 5. 159 p. Veron JEN, Pichon M and Wijsman-Best M (1977) Scleractinia of eastern Australia, Part 3. Families Faviidae, Trachyphylliidae. Aust. Inst. Mar. Sci. Monogr. Ser. V. 3. 233 p. Veron JEN and Wallace CC (1984) Scleractinia of eastern Australia, Part 5. Family Acroporidae. Aust. Inst. Mar. Sci. Monogr. Ser. V. 6. 485 p. Wallace CC (1978) The coral genus Acropora (Scleractinia: Astrocoeniina: Acroporidae) in the central and southern Great Barrier Reef Province. Mem. Queensl. Mus. 18: 273-319.&rft.creator=Australian Institute of Marine Science (AIMS) &rft.date=2010&rft.relation=http://data.aims.gov.au/extpubs/do/viewPub.do?articleId=8275&rft.relation=http://data.aims.gov.au/extpubs/do/viewPub.do?articleId=2980&rft.coverage=northlimit=-18.26667; southlimit=-18.26667; westlimit=147.383333; eastLimit=147.383333&rft.coverage=northlimit=-18.26667; southlimit=-18.26667; westlimit=147.383333; eastLimit=147.383333&rft.coverage=northlimit=-18.816667; southlimit=-18.816667; westlimit=146.433333; eastLimit=146.433333&rft.coverage=northlimit=-18.816667; southlimit=-18.816667; westlimit=146.433333; eastLimit=146.433333&rft.coverage=northlimit=-18.483333; southlimit=-18.483333; westlimit=146.866667; eastLimit=146.866667&rft.coverage=northlimit=-18.483333; southlimit=-18.483333; westlimit=146.866667; eastLimit=146.866667&rft_rights=Attribution-NonCommercial 3.0 Australia http://creativecommons.org/licenses/by-nc/3.0/au/&rft_rights=Format for citation of metadata sourced from Australian Institute of Marine Science (AIMS) in a list of reference is as follows: Australian Institute of Marine Science (AIMS). 2010, The influence of recruitment and post-settlement mortality on coral communities across the central Great Barrier Reef, https://apps.aims.gov.au/metadata/view/9aea83a2-cbb3-4b7b-94fb-b7f90359b87d, accessed[date-of-access].&rft_subject=Oceans&rft.type=dataset&rft.language=English Access the data

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Format for citation of metadata sourced from Australian Institute of Marine Science (AIMS) in a list of reference is as follows: "Australian Institute of Marine Science (AIMS). 2010, The influence of recruitment and post-settlement mortality on coral communities across the central Great Barrier Reef, https://apps.aims.gov.au/metadata/view/9aea83a2-cbb3-4b7b-94fb-b7f90359b87d, accessed[date-of-access]".

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Brief description

Pandora Reef, Rib Reef and Myrmidon Reef, located 16.6 km, 57.6 km and 116.9 km from the coastline respectively, were chosen for a year long series of cross-shelf coral recruitment experiments, commencing in January 1981. Settling plates approximately 15 mm thick and 300-400 cm² in total surface area (sum of upper and lower surfaces) were cut from natural, uncleaned heads of the massive corals Porites and Goniastrea spp. Plates were attached to each of four pins on a galvanized steel support rack at an angle of 37-45°. Racks were then secured on the reef by attaching them to two solid steel reinforcement bars driven into the reef.

On each reef, racks were placed on the exposed, windward E-SE forereef slope, with plates facing into the wave surge. To investigate natural recruitment, two racks of plates (four plates per rack) were deployed at both 3m and between 14 and 18m on each reef. One rack at each depth was retrieved after 6 months and the second after 12 months. A third rack was deployed at each depth at the end of the first 6 months and retrieved 6 months later.

Transplant experiments were carried out to investigate survival of coral recruits when moved to a new environment. Two additional racks of plates (three per rack) were deployed at each depth, at each reef in January 1981. After 6 months the racks were redeployed to make all possible combinations of transplants between reefs, while maintaining original depths. A further rack of plates was deployed at each depth, at each reef in January 1981, as a control for handling. Racks were retrieved after 6 months, held onboard ship for one to several days and replaced at the same site. All transplant and control plates were retrieved within 12 months of the initiation of the experiment.

After retrieval, all plates were stored frozen at -20°C until analysed. In the laboratory, plates were thawed, cleaned of sediment and debris and dried in an oven at -45°C. Each plate was then cleaned of algae and examined using a dissecting microscope. Taxonomic identification was based primarily on calical structure. Juveniles were usually identified to family, often to genus, and occasionally to species, with scanning electron microscopy (SEM) and taxonomic guides available for corals of this region.

Coral spat were assessed for post-settlement mortality as follows: skeleton intact with at least remnants of tissue; coral overgrown and damaged; and complete colony mortality. Only the last category was utilized in estimating post-settlement mortality frequencies, which were calculated simply as the proportion in this state within a given taxon.

Intra- and interspecific competition for space involving corals and other sessile epibiota was also assessed from the coral's perspective. Associates within 8 mm of the juvenile colony were recorded and examined for interactions and a static observation of overgrowth was taken as evidence of competition for space. A competition parameter was defined as the number of competitive wins over the total number of encounters within a taxon.

Placement of settled corals or relative exposure was also assessed by differentiating between juvenile corals found on upper surfaces of the plate and those settling cryptically on the lateral or lower surface. An exposure parameter was calculated as the proportion of those juveniles in the latter state.

This study was initiated to examine patterns of coral recruitment across the continental shelf in central Great Barrier Reef. The study makes use of settlement plates to look at differences in species composition of recruits, post-settlement mortality, intra- and interspecific competition for space and the placement of settled corals on the plates. An additional transplant experiment was carried out to determine the probability of survival of coral larvae if they had been transported to another location and settled successfully.

During this project a taxonomic key for juvenile corals was constructed using juveniles from this and previous studies.

Notes

Sammarco, Paul W, Dr (Principal Investigator)

Lineage

Statement: Plates were processed according to the procedures described in:
Sammarco PW (1980) Diadema and its relationship to coral spat mortality: Grazing, competition, and biological disturbance. J. Exp. Mar. Biol. Ecol. 45: 245-272.

Sammarco PW (1982) Echinoid grazing as a structuring force in coral communities: Whole reef manipulations. J. Exp. Mar. Biol. Ecol. 61: 31-55.

Sammarco PW and Andrews JC (1988) Localized dispersal and recruitment in Great Barrier Reef corals: The Helix Experiment. Science 239: 1422-1424.

Sammarco PW and Andrews JC (1989) The Helix Experiment: Differential localized dispersal and recruitment patterns in Great Barrier Reef corals. Limnol. Oceanogr. 34: 896-912

Sammarco PW and Carleton JH (1982) Damselfish territoriality and coral community structure: Reduced grazing and effects on coral spat. Proc. 4th Int. Coral Reef Congr. 1: 525-535.

Estimates of mortality may be slightly conservative due to a possible delay of several days before the skeleton of a freshly killed recruit exhibits clear signs of mortality. Bias from this source is expected to be negligible, however, because the samples integrate 6 to 12 months of mortality.

The taxonomic references used in this study were:

Veron JEN and Pichon M (1976) Scleractinia of eastern Australia, Part 1. Families Thamnasteriidae, Astrocoeniidae, and Pocilloporidae. Aust. Inst. Mar. Sci. Monogr. Ser. V. 1. 86 p.

Veron JEN and Pichon M (1979) Scleractinia of eastern Australia, Part 3. Families Agariciidae, Siderastreidae, Fungiidae, Oculinidae, Merulinidae, Mussidae, Pectiniidae, Caryophylliidae, Dendrophylliidae. Aust. Inst. Mar. Sci. Monogr. Ser. V. 4. 422 p.

Veron JEN and Pichon M (1982) Scleractinia of eastern Australia, Part 4. Family Poritidae. Aust. Inst. Mar. Sci. Monogr. Ser. V. 5. 159 p.

Veron JEN, Pichon M and Wijsman-Best M (1977) Scleractinia of eastern Australia, Part 3. Families Faviidae, Trachyphylliidae. Aust. Inst. Mar. Sci. Monogr. Ser. V. 3. 233 p.

Veron JEN and Wallace CC (1984) Scleractinia of eastern Australia, Part 5. Family Acroporidae. Aust. Inst. Mar. Sci. Monogr. Ser. V. 6. 485 p.

Wallace CC (1978) The coral genus Acropora (Scleractinia: Astrocoeniina: Acroporidae) in the central and southern Great Barrier Reef Province. Mem. Queensl. Mus. 18: 273-319.

Modified: 20190815

Data time period: 1981-01-01 to 1982-01-31

Click to explore relationships graph

147.383333,-18.26667

147.383333,-18.26667

146.433333,-18.816667

146.433333,-18.816667

146.866667,-18.483333

146.866667,-18.483333

text: northlimit=-18.26667; southlimit=-18.26667; westlimit=147.383333; eastLimit=147.383333

text: northlimit=-18.816667; southlimit=-18.816667; westlimit=146.433333; eastLimit=146.433333

text: northlimit=-18.483333; southlimit=-18.483333; westlimit=146.866667; eastLimit=146.866667

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