BCO-DMO ERDDAP
Accessing BCO-DMO data |
log in
Brought to you by BCO-DMO |
Row Type | Variable Name | Attribute Name | Data Type | Value |
---|---|---|---|---|
attribute | NC_GLOBAL | access_formats | String | .htmlTable,.csv,.json,.mat,.nc,.tsv,.esriCsv,.geoJson |
attribute | NC_GLOBAL | acquisition_description | String | [Reference cited below are from Dell et al (2016) Plos One.] \nStudy site and species: \n This study was conducted between January and May in 2013 and 2015 on the\ncoral coast of Fiji\\u2019s main island, Viti Levu, in the villages of Votua\nand Vatu-o-lailai (18\\u00b012\\u201932S, 177\\u00b042\\u201900E and\n18\\u00b012\\u201913S, 177\\u00b041\\u201929E respectively; Fig 1). These villages\nare ~3km apart and each has jurisdiction over their stretch of reef flat; a\nhabitat ranging between ~1.5 and 3m deep at high tide and between ~0 and 1.5m\ndeep at low tide. In 2002, these villages established small areas (0.8km2 in\nVotua and 0.5 km2 in Vatu-o-lailai; Fig 1) as no-take MPAs [25]. Though MPA\nand non-MPA areas were initially similar in coral and macroalgal cover (33-42%\nmacroalgal cover; 3-12% coral cover [25]), MPAs now differ significantly from\nthe adjacent non-MPAs in benthic cover and fish diversity and abundance. MPAs\nnow have ~56% live coral cover on hard substrate, ~2% macroalgal cover, ~8\nfold higher biomass of herbivorous fishes, and higher recruitment of both\nfishes and corals than the non-MPAs [5,22]. Meanwhile the non-MPAs have lower\nfish biomass, 5-16% live coral cover on hard substrates and 51-92% macroalgal\ncover, the majority of which is comprised by Phaeophytes (primarily Sargassum\npolycystum C. Agardh [22]). In the MPAs, macroalgal cover is restricted to the\nshallowest, most shoreward areas (where access by herbivorous fishes appears\nlimited), whereas macroalgal cover in the non-MPAs extends throughout the\nhabitat. Thus, over distances of only a few hundred metres, there are dramatic\ndifferences in community composition that may impact the efficacy of factors\ncontrolling macroalgal populations, without the confounding factors of great\ndifferences in space or time.\n \nEffect of habitat and origin on the survival and growth of mature S.\npolycystum fronds\n \nWe used Sargassum polycystum as a study organism because it is often the most\nconspicuous macroalgal species on degraded Pacific reefs and can grow to\ndominate large areas [22,28-30]. On reefs lacking adequate herbivory, S.\npolycystum can reach 8.55 kg wet weight per square metre [28] and its odour\ncan suppress both fish and coral recruitment [5], potentially limiting reef\nrecovery. In Fiji, perennial holdfasts start regenerating in December and by\nthe end of its growing season in June, S. polycystum commonly dominates large\nexpanses of the unprotected reef flats [22,29]. Around this time it may\nreproduce sexually via spores that disperse only one to three metres [31],\nsuggesting the potential for reduced connectivity between even nearby sites.\nAfter June, S. polycystum senesces leaving the perennial rhizomes sheltered\nwithin the reef structure. Populations in our study area will have undergone\nabout 10 generations since MPA establishment, which has been shown to be\nadequate time for population differentiation among some species if selection\nis strong [24,32].\n \nThe dearth of S. polycystum in the MPAs and its high abundance in the non-MPAs\ncould be due to differing physical conditions in those locations. To\ninvestigate the role of physical conditions and to test whether S. polycystum\nin these areas was acclimatising to the different local conditions, a\nreciprocal transplant experiment was performed between the MPAs and non-MPAs\nat two villages to measure survival and growth of mature S. polycystum as a\nfunction of origin (from the MPA or non-MPA) and habitat (placed in the MPA or\nnon-MPA) when the fronds were protected from herbivory in cages.\n \nThe uppermost 15 centimetres of a S. polycystum frond was collected from 40\nseparate holdfasts in the MPA and 40 in the non-MPA of the villages of both\nVotua and Vatu-o-lailai. To minimise the likelihood of collecting multiple\nfronds from a single clone, the holdfasts were separated by at least two\nmetres. The lowest five centimetres of each frond were defoliated, the fronds\nwere then blotted dry with paper towels and weighed to the nearest 0.1g. The\ntop of the defoliated section was marked by piercing the thallus with a needle\nand tying a thread at this 5cm point to set a standard from which to measure\ngrowth in length. One strand of S. polycystum from the MPA and one from the\nnon-MPA were affixed 20cm apart in the centre of a 50cm piece of 3-strand\nrope. The lowest 5cm of each algal stipe was threaded through the rope to\nanchor the strand in place. Four ropes were affixed in each of five cages\n(dimensions 1m x 1m x 0.8m constructed of 1cm mesh) by the two 10cm end\nsections of each rope so that the rope\\u2019s centre, holding the algae, was\nraised a few centimetres above the substrate. Five cages were anchored at a\ndepth of ~1.2m at low tide in both each MPA and non-MPA so that cages at each\nlocation were separated by a minimum of two metres. After one month, the\nlength (from the threaded point) and mass of each frond were measured to\nassess growth.\n \nChange in length was measured in centimetres after two and four weeks. As mass\nmeasurements required removing the fronds from the water, to minimise stress\nto the organism, change in mass was measured in grams only after four weeks.\nBecause significant effects were the same in each of these data sets, only\nresults from height change at week four are reported. A mean change in length\nwas calculated separately for the MPA and non-MPA adults in each cage,\nyielding an n=5 for each location. Within each independent cage, we calculated\nthe mean growth of MPA origin fronds, the mean growth of non-MPA fronds, and\nused the difference between these values in paired t-tests run separately for\neach location testing the effect of origin on growth over the four weeks.\nThese difference scores were normally distributed. |
attribute | NC_GLOBAL | awards_0_award_nid | String | 480718 |
attribute | NC_GLOBAL | awards_0_award_number | String | OCE-0929119 |
attribute | NC_GLOBAL | awards_0_data_url | String | http://www.nsf.gov/awardsearch/showAward?AWD_ID=0929119 |
attribute | NC_GLOBAL | awards_0_funder_name | String | NSF Division of Ocean Sciences |
attribute | NC_GLOBAL | awards_0_funding_acronym | String | NSF OCE |
attribute | NC_GLOBAL | awards_0_funding_source_nid | String | 355 |
attribute | NC_GLOBAL | awards_0_program_manager | String | David L. Garrison |
attribute | NC_GLOBAL | awards_0_program_manager_nid | String | 50534 |
attribute | NC_GLOBAL | cdm_data_type | String | Other |
attribute | NC_GLOBAL | comment | String | mature growth \n Growth of mature caged Sargassum polycystum fronds from MPAs and non-MPAs when reciprocally transplanted \n These data were published in Dell et al (2016) PLOS ONE, Fig. 2 \n version: 2016-05-02 \n \n M. Hay (GA Tech) |
attribute | NC_GLOBAL | Conventions | String | COARDS, CF-1.6, ACDD-1.3 |
attribute | NC_GLOBAL | creator_email | String | info at bco-dmo.org |
attribute | NC_GLOBAL | creator_name | String | BCO-DMO |
attribute | NC_GLOBAL | creator_type | String | institution |
attribute | NC_GLOBAL | creator_url | String | https://www.bco-dmo.org/ |
attribute | NC_GLOBAL | data_source | String | extract_data_as_tsv version 2.3 19 Dec 2019 |
attribute | NC_GLOBAL | date_created | String | 2016-04-29T15:48:27Z |
attribute | NC_GLOBAL | date_modified | String | 2016-05-03T17:23:19Z |
attribute | NC_GLOBAL | defaultDataQuery | String | &time<now |
attribute | NC_GLOBAL | doi | String | 10.1575/1912/bco-dmo.644663 |
attribute | NC_GLOBAL | Easternmost_Easting | double | 177.7 |
attribute | NC_GLOBAL | geospatial_lat_max | double | -18.204 |
attribute | NC_GLOBAL | geospatial_lat_min | double | -18.208 |
attribute | NC_GLOBAL | geospatial_lat_units | String | degrees_north |
attribute | NC_GLOBAL | geospatial_lon_max | double | 177.7 |
attribute | NC_GLOBAL | geospatial_lon_min | double | 177.691 |
attribute | NC_GLOBAL | geospatial_lon_units | String | degrees_east |
attribute | NC_GLOBAL | infoUrl | String | https://www.bco-dmo.org/dataset/643915 |
attribute | NC_GLOBAL | institution | String | BCO-DMO |
attribute | NC_GLOBAL | instruments_0_acronym | String | Scale |
attribute | NC_GLOBAL | instruments_0_dataset_instrument_nid | String | 644023 |
attribute | NC_GLOBAL | instruments_0_description | String | An instrument used to measure weight or mass. |
attribute | NC_GLOBAL | instruments_0_instrument_external_identifier | String | https://vocab.nerc.ac.uk/collection/L05/current/LAB13/ |
attribute | NC_GLOBAL | instruments_0_instrument_name | String | Scale |
attribute | NC_GLOBAL | instruments_0_instrument_nid | String | 714 |
attribute | NC_GLOBAL | keywords | String | bco, bco-dmo, biological, chemical, data, dataset, dmo, erddap, growth, latitude, longitude, management, oceanography, office, origin, preliminary, village |
attribute | NC_GLOBAL | license | String | https://www.bco-dmo.org/dataset/643915/license |
attribute | NC_GLOBAL | metadata_source | String | https://www.bco-dmo.org/api/dataset/643915 |
attribute | NC_GLOBAL | Northernmost_Northing | double | -18.204 |
attribute | NC_GLOBAL | param_mapping | String | {'643915': {'lat': 'master - latitude', 'lon': 'master - longitude'}} |
attribute | NC_GLOBAL | parameter_source | String | https://www.bco-dmo.org/mapserver/dataset/643915/parameters |
attribute | NC_GLOBAL | people_0_affiliation | String | Georgia Institute of Technology |
attribute | NC_GLOBAL | people_0_affiliation_acronym | String | Georgia Tech |
attribute | NC_GLOBAL | people_0_person_name | String | Mark Hay |
attribute | NC_GLOBAL | people_0_person_nid | String | 480720 |
attribute | NC_GLOBAL | people_0_role | String | Principal Investigator |
attribute | NC_GLOBAL | people_0_role_type | String | originator |
attribute | NC_GLOBAL | people_1_affiliation | String | Woods Hole Oceanographic Institution |
attribute | NC_GLOBAL | people_1_affiliation_acronym | String | WHOI BCO-DMO |
attribute | NC_GLOBAL | people_1_person_name | String | Nancy Copley |
attribute | NC_GLOBAL | people_1_person_nid | String | 50396 |
attribute | NC_GLOBAL | people_1_role | String | BCO-DMO Data Manager |
attribute | NC_GLOBAL | people_1_role_type | String | related |
attribute | NC_GLOBAL | project | String | Killer Seaweeds |
attribute | NC_GLOBAL | projects_0_acronym | String | Killer Seaweeds |
attribute | NC_GLOBAL | projects_0_description | String | Extracted from the NSF award abstract:\nCoral reefs are in dramatic global decline, with reefs commonly converting from species-rich and topographically-complex communities dominated by corals to species- poor and topographically-simplified communities dominated by seaweeds. These phase-shifts result in fundamental loss of ecosystem function. Despite debate about whether coral-to-algal transitions are commonly a primary cause, or simply a consequence, of coral mortality, rigorous field investigation of seaweed-coral competition has received limited attention. There is limited information on how the outcome of seaweed-coral competition varies among species or the relative importance of different competitive mechanisms in facilitating seaweed dominance. In an effort to address this topic, the PI will conduct field experiments in the tropical South Pacific (Fiji) to determine the effects of seaweeds on corals when in direct contact, which seaweeds are most damaging to corals, the role allelopathic lipids that are transferred via contact in producing these effects, the identity and surface concentrations of these metabolites, and the dynamic nature of seaweed metabolite production and coral response following contact. The herbivorous fishes most responsible for controlling allelopathic seaweeds will be identified, the roles of seaweed metabolites in allelopathy vs herbivore deterrence will be studied, and the potential for better managing and conserving critical reef herbivores so as to slow or reverse conversion of coral reef to seaweed meadows will be examined.\nPreliminary results indicate that seaweeds may commonly damage corals via lipid- soluble allelochemicals. Such chemically-mediated interactions could kill or damage adult corals and produce the suppression of coral fecundity and recruitment noted by previous investigators and could precipitate positive feedback mechanisms making reef recovery increasingly unlikely as seaweed abundance increases. Chemically-mediated seaweed-coral competition may play a critical role in the degradation of present-day coral reefs. Increasing information on which seaweeds are most aggressive to corals and which herbivores best limit these seaweeds may prove useful in better managing reefs to facilitate resilience and possible recovery despite threats of global-scale stresses. Fiji is well positioned to rapidly use findings from this project for better management of reef resources because it has already erected >260 MPAs, Fijian villagers have already bought-in to the value of MPAs, and the Fiji Locally-Managed Marine Area (FLMMA) Network is well organized to get information to villagers in a culturally sensitive and useful manner.\nThe broader impacts of this project are far reaching. The project provides training opportunities for 2-2.5 Ph.D students and 1 undergraduate student each year in the interdisciplinary areas of marine ecology, marine conservation, and marine chemical ecology. Findings from this project will be immediately integrated into classes at Ga Tech and made available throughout Fiji via a foundation and web site that have already set-up to support marine conservation efforts in Fiji and marine education efforts both within Fiji and internationally. Business and community leaders from Atlanta (via Rotary International Service efforts) have been recruited to help organize and fund community service and outreach projects in Fiji -- several of which are likely to involve marine conservation and education based in part on these efforts there. Media outlets (National Geographic, NPR, Animal Planet, Audubon Magazine, etc.) and local Rotary clubs will be used to better disseminate these discoveries to the public.\nPUBLICATIONS PRODUCED AS A RESULT OF THIS RESEARCH\nRasher DB, Stout EP, Engel S, Kubanek J, and ME Hay. \"Macroalgal terpenes function as allelopathic agents against reef corals\", Proceedings of the National Academy of Sciences, v. 108, 2011, p. 17726.\nBeattie AJ, ME Hay, B Magnusson, R de Nys, J Smeathers, JFV Vincent. \"Ecology and bioprospecting,\" Austral Ecology, v.36, 2011, p. 341.\nRasher DB and ME Hay. \"Seaweed allelopathy degrades the resilience and function of coral reefs,\" Communicative and Integrative Biology, v.3, 2010.\nHay ME, Rasher DB. \"Corals in crisis,\" The Scientist, v.24, 2010, p. 42.\nHay ME and DB Rasher. \"Coral reefs in crisis: reversing the biotic death spiral,\" Faculty 1000 Biology Reports 2010, v.2, 2010.\nRasher DB and ME Hay. \"Chemically rich seaweeds poison corals when not controlled by herbivores\", Proceedings of the National Academy of Sciences, v.107, 2010, p. 9683. |
attribute | NC_GLOBAL | projects_0_end_date | String | 2014-08 |
attribute | NC_GLOBAL | projects_0_geolocation | String | Viti Levu, Fiji (18º13.049’S, 177º42.968’E) |
attribute | NC_GLOBAL | projects_0_name | String | Killer Seaweeds: Allelopathy against Fijian Corals |
attribute | NC_GLOBAL | projects_0_project_nid | String | 480717 |
attribute | NC_GLOBAL | projects_0_start_date | String | 2009-09 |
attribute | NC_GLOBAL | publisher_name | String | Biological and Chemical Oceanographic Data Management Office (BCO-DMO) |
attribute | NC_GLOBAL | publisher_type | String | institution |
attribute | NC_GLOBAL | sourceUrl | String | (local files) |
attribute | NC_GLOBAL | Southernmost_Northing | double | -18.208 |
attribute | NC_GLOBAL | standard_name_vocabulary | String | CF Standard Name Table v55 |
attribute | NC_GLOBAL | summary | String | Raw data on the growth of mature Sargassum polycystum fronds originated from\nmarine protected and non-protected areas (MPAs and non-MPAs, respectively) in\nFiji, reciprocally transplanted between these areas and protected by cages.\nGrowth was measured as the difference between the final (30 days) and initial\nfrond length, measured from a standard point established using a thread when\nthe experiment was set. Details in Dell et al. 2016 Plos One.\n \nRelated Reference: \n Dell, C., Longo, G.O., Hay, M.E. (2016) Positive feedbacks enhance\nmacroalgal resilience on Degraded Coral Reefs. Plos One.\n \nRelated Datasets: \n[Sargassum recruit-sized survival - figure 3](\\\\http://www.bco-\ndmo.org/dataset/644035\\\\) \n[Sargassum mature growth conspecific - figure 4](\\\\http://www.bco-\ndmo.org/dataset/644062\\\\) \n[Sargassum recruit-sized growth and survival with conspecifics - figures 5 and\n6](\\\\https://www.bco-dmo.org/dataset/644080\\\\) |
attribute | NC_GLOBAL | title | String | [Sargassum mature growth - figure 2] - Growth of mature caged Sargassum polycystum fronds from MPAs and non-MPAs when reciprocally transplanted (Killer Seaweeds: Allelopathy against Fijian Corals) |
attribute | NC_GLOBAL | version | String | 1 |
attribute | NC_GLOBAL | Westernmost_Easting | double | 177.691 |
attribute | NC_GLOBAL | xml_source | String | osprey2erddap.update_xml() v1.3 |
variable | latitude | double | ||
attribute | latitude | _CoordinateAxisType | String | Lat |
attribute | latitude | _FillValue | double | NaN |
attribute | latitude | actual_range | double | -18.208, -18.204 |
attribute | latitude | axis | String | Y |
attribute | latitude | bcodmo_name | String | latitude |
attribute | latitude | colorBarMaximum | double | 90.0 |
attribute | latitude | colorBarMinimum | double | -90.0 |
attribute | latitude | description | String | latitude; north is positive |
attribute | latitude | ioos_category | String | Location |
attribute | latitude | long_name | String | Latitude |
attribute | latitude | nerc_identifier | String | https://vocab.nerc.ac.uk/collection/P09/current/LATX/ |
attribute | latitude | standard_name | String | latitude |
attribute | latitude | units | String | degrees_north |
variable | longitude | double | ||
attribute | longitude | _CoordinateAxisType | String | Lon |
attribute | longitude | _FillValue | double | NaN |
attribute | longitude | actual_range | double | 177.691, 177.7 |
attribute | longitude | axis | String | X |
attribute | longitude | bcodmo_name | String | longitude |
attribute | longitude | colorBarMaximum | double | 180.0 |
attribute | longitude | colorBarMinimum | double | -180.0 |
attribute | longitude | description | String | longitude; east is positive |
attribute | longitude | ioos_category | String | Location |
attribute | longitude | long_name | String | Longitude |
attribute | longitude | nerc_identifier | String | https://vocab.nerc.ac.uk/collection/P09/current/LONX/ |
attribute | longitude | standard_name | String | longitude |
attribute | longitude | units | String | degrees_east |
variable | village | String | ||
attribute | village | bcodmo_name | String | site |
attribute | village | description | String | village name: VLL = Vatu-o-lailai; VOT = Votua |
attribute | village | long_name | String | Village |
attribute | village | units | String | unitless |
variable | location | String | ||
attribute | location | bcodmo_name | String | site |
attribute | location | description | String | where Sargassum fronds were transplanted to: MPA = marine protected area; NON-MPA = non-protected area |
attribute | location | long_name | String | Location |
attribute | location | units | String | unitless |
variable | origin | String | ||
attribute | origin | bcodmo_name | String | site |
attribute | origin | description | String | where Sargassum fronds were collected for the transplant: MPA = marine protected area; NON-MPA = non-protected area |
attribute | origin | long_name | String | Origin |
attribute | origin | units | String | unitless |
variable | growth | float | ||
attribute | growth | _FillValue | float | NaN |
attribute | growth | actual_range | float | 4.2, 35.7 |
attribute | growth | bcodmo_name | String | growth |
attribute | growth | description | String | difference between the final (30 days) and initial frond length; measured from a standard point established when the experiment was set using a thread |
attribute | growth | long_name | String | Growth |
attribute | growth | units | String | cm |