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Grid DAP Data | Sub- set | Table DAP Data | Make A Graph | W M S | Source Data Files | Acces- sible | Title | Sum- mary | FGDC, ISO, Metadata | Back- ground Info | RSS | E | Institution | Dataset ID |
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data | graph | files | public | [Stegastes planiforms attacks by predator] - Experimental results indicating which predators were attacked by Stegastes planiforms in the Cayman Islands and the Bahamas during 2011 (Mechanisms and Consequences of Fish Biodiversity Loss on Atlantic Coral Reefs Caused by Invasive Pacific Lionfish) | F I M | background | BCO-DMO | bcodmo_dataset_653159 |
Row Type | Variable Name | Attribute Name | Data Type | Value |
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attribute | NC_GLOBAL | access_formats | String | .htmlTable,.csv,.json,.mat,.nc,.tsv,.esriCsv,.geoJson |
attribute | NC_GLOBAL | acquisition_description | String | Area of study and microhabitat assessment This study was conducted during July-August 2011, observing the behavioral response of 40 three spot damselfish:\u00a020 in the Bahamas and 20 in the Cayman Islands. Damselfish in these two locations were chosen to be studied because of their difference in timing of the lionfish invasion: lionfish were first sighted in the Bahamas in 2004 and in the Cayman Islands in 2008 (Schofield 2009). In the Bahamas, damselfish were studied at three sites in the shallow waters (sites were <4 m deep) of the Great Bahama Bank in the vicinity of Lee Stocking Island, which is part of the Exuma Cays. Study sites consisted of patch reefs composed of small coral heads and larger coral bommies surrounded by sand and seagrass beds. About 380 miles Southwest of Lee Stocking Island, damselfish behavior was observed\u00a0off of Little Cayman Island at three deeper sites (6\u201312 m deep) located along the northern side of the island, just inshore of the Bloody Bay Wall. This area is characterized by continuous stretches of reef that includes coral heads of various sizes and large coral formations. The benthic territories maintained year-round by three spot damselfish are less than 1 m2 and are easily identified by the algal gardens covering reef substrata that the damselfish cultivate (Brawley and Adey 1977). The underlying substrata of damselfish territories differed at sites both within and between the Bahamas and Cayman Islands. Since the type of habitat could potentially affect damselfish response by influencing an individual\u2019s ability to defend its territory,\u00a0the microhabitat of each damselfish territory was characterized by recording the following four habitat categories: (1) low-relief dead coral rubble (mostly Acropora cervicornis), (2) low-relief continuous reef, (3) high-relief large coral\u00a0bommies, and (4) high-relief continuous reef. Low-relief habitats lacked vertical structure, whereas\u00a0high-relief\u00a0habitats consisted of vertical structure over 1 m high, which could potentially interfere with the ability of damselfish to detect intruders. Experimental treatments and fish capture Each three spot damselfish was exposed to a series of treatments consisting of a single individual of (1) invasive lionfish, or the following native fishes, all of which are commonly found on reefs near three spot damselfish territories and are chased at varying degrees by damselfish (Thresher 1976; Robertson 1984): (2) herbivorous ocean surgeonfish (Acanthurus bahianus), a potential food competitor; (3) white grunt (Haemulon plumierii), a potential egg predator; and (4) coney grouper (Cephalopholis fulva), a mesopredator ecologically similar to lionfish and at larger sizes is a potential predator of three spot damselfish. At both study regions, 2-3 individuals were captured per fish species, which were rotated daily for experimental use based on each individual\u2019s appearance, apparent condition, and behavior. All fish were caught underwater from non-study sites using hand nets and the fish anesthetic quinaldine when needed. Body size of individual fish, ranging from 10 to 18 cm TL, was restricted to allow for ease of movement in bottles during the experiment. At these sizes, both lionfish and coney grouper were sufficiently large to pose a threat to small recruit fishes inhabiting damselfish territories (Albins 2013). Fish were maintained in flow-through aquarium tanks both prior to and between daily observational trials. Model-bottle experiment Using a model-bottle study design (Myrberg and Thresher 1974), individual fish were presented in weighted, clear-plastic gallon bottles to haphazardly located adult damselfish (7\u201311 cm total length [TL]) in order to measure the relative behavioral responses exhibited by each focal damselfish. Bottle lids were replaced with secured mesh screening to allow for flow of both water and any fish chemical cues. An empty bottle was used as a control treatment. Each treatment was introduced in random order to individual damselfish territories. All fishes inside bottles were either resting or hovering upon introduction. To measure damselfish aggression per treatment, each bottle was sequentially placed at 100, 50, and 0 cm away from the center of each territory. At each increment, damselfish behavior was observed from a distance of 3 m for 2 min, counting the number of times the focal damselfish made physical contact with the bottle (attack rate) and tallying which aggressive behaviors each damselfish displayed: (1) contact with the mouth while hovering in place directly next to the bottle (nip); (2) contact with the caudal fin while hovering in place directly next to the bottle (butt); (3) starting from a distance, swimming with force directly towards the bottle, making contact with mouth, and then quickly swimming away from the bottle (charge); and, (4) repeatedly charging the bottle multiple times (continuous attack). These categories encompass three spot damselfish behavior known to effectively exclude intruders (Thresher 1976). Avoidance behavior by damselfish was also noted, such as entering refuge sites within their territories (Helfman 1989). Each bottle was then placed at the closest distance to the territory at which the damselfish had previously made no physical contact with the bottle, then gradually moved the bottle closer to the center of the territory until the damselfish approached the bottle and made physical contact. If the damselfish had previously attacked the bottle at 100 cm away from the territory, the bottle was placed at 150 cm where all damselfish ceased attacking the bottle, and gradually moved the bottle closer to the territory from there. This method provided a measurement of the \u201cmaximum distance of attack\u201d (sensu Myrberg and Thresher 1974) per treatment. |
attribute | NC_GLOBAL | awards_0_award_nid | String | 561016 |
attribute | NC_GLOBAL | awards_0_award_number | String | OCE-1233027 |
attribute | NC_GLOBAL | awards_0_data_url | String | http://www.nsf.gov/awardsearch/showAward.do?AwardNumber=1233027 |
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 | Attacks by Predator Treatment Lead PI: Mark Hixon Sub-Project Lead: Tye L. Kindinger Version 26 July 2016 |
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 | 2016-08-02T16:27:58Z |
attribute | NC_GLOBAL | date_modified | String | 2019-05-22T19:15:28Z |
attribute | NC_GLOBAL | defaultDataQuery | String | &time<now |
attribute | NC_GLOBAL | doi | String | 10.1575/1912/bco-dmo.653159.1 |
attribute | NC_GLOBAL | Easternmost_Easting | double | -76.0 |
attribute | NC_GLOBAL | geospatial_lat_max | double | 24.0 |
attribute | NC_GLOBAL | geospatial_lat_min | double | 19.0 |
attribute | NC_GLOBAL | geospatial_lat_units | String | degrees_north |
attribute | NC_GLOBAL | geospatial_lon_max | double | -76.0 |
attribute | NC_GLOBAL | geospatial_lon_min | double | -80.0 |
attribute | NC_GLOBAL | geospatial_lon_units | String | degrees_east |
attribute | NC_GLOBAL | infoUrl | String | https://www.bco-dmo.org/dataset/653159 |
attribute | NC_GLOBAL | institution | String | BCO-DMO |
attribute | NC_GLOBAL | keywords | String | attack, bco, bco-dmo, biological, bottle, bottle_treatment, chemical, damsel, damsel_number, data, dataset, dmo, erddap, habitat, latitude, longitude, management, number, oceanography, office, preliminary, treatment |
attribute | NC_GLOBAL | license | String | https://www.bco-dmo.org/dataset/653159/license |
attribute | NC_GLOBAL | metadata_source | String | https://www.bco-dmo.org/api/dataset/653159 |
attribute | NC_GLOBAL | Northernmost_Northing | double | 24.0 |
attribute | NC_GLOBAL | param_mapping | String | {'653159': {'lat': 'master - latitude', 'lon': 'master - longitude'}} |
attribute | NC_GLOBAL | parameter_source | String | https://www.bco-dmo.org/mapserver/dataset/653159/parameters |
attribute | NC_GLOBAL | people_0_affiliation | String | University of Hawaii |
attribute | NC_GLOBAL | people_0_person_name | String | Mark Hixon |
attribute | NC_GLOBAL | people_0_person_nid | String | 51647 |
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 | Oregon State University |
attribute | NC_GLOBAL | people_1_affiliation_acronym | String | OSU |
attribute | NC_GLOBAL | people_1_person_name | String | Tye L. Kindinger |
attribute | NC_GLOBAL | people_1_person_nid | String | 51707 |
attribute | NC_GLOBAL | people_1_role | String | Contact |
attribute | NC_GLOBAL | people_1_role_type | String | related |
attribute | NC_GLOBAL | people_2_affiliation | String | Woods Hole Oceanographic Institution |
attribute | NC_GLOBAL | people_2_affiliation_acronym | String | WHOI BCO-DMO |
attribute | NC_GLOBAL | people_2_person_name | String | Hannah Ake |
attribute | NC_GLOBAL | people_2_person_nid | String | 650173 |
attribute | NC_GLOBAL | people_2_role | String | BCO-DMO Data Manager |
attribute | NC_GLOBAL | people_2_role_type | String | related |
attribute | NC_GLOBAL | project | String | BiodiversityLossEffects_lionfish |
attribute | NC_GLOBAL | projects_0_acronym | String | BiodiversityLossEffects_lionfish |
attribute | NC_GLOBAL | projects_0_description | String | The Pacific red lionfish (Pterois volitans), a popular aquarium fish, was introduced to the Atlantic Ocean in the vicinity of Florida in the late 20th century. Voraciously consuming small native coral-reef fishes, including the juveniles of fisheries and ecologically important species, the invader has undergone a population explosion that now ranges from the U.S. southeastern seaboard to the Gulf of Mexico and across the greater Caribbean region. The PI's past research determined that invasive lionfish (1) have escaped their natural enemies in the Pacific (lionfish are much less abundant in their native range); (2) are not yet controlled by Atlantic predators, competitors, or parasites; (3) have strong negative effects on populations of native Atlantic fishes; and (4) locally reduce the diversity (number of species) of native fishes. The lionfish invasion has been recognized as one of the major conservation threats worldwide. The Bahamas support the highest abundances of invasive lionfish globally. This system thus provides an unprecedented opportunity to understand the direct and indirect effects of a major invader on a diverse community, as well as the underlying causative mechanisms. The PI will focus on five related questions: (1) How does long-term predation by lionfish alter the structure of native reef-fish communities? (2) How does lionfish predation destabilize native prey population dynamics, possibly causing local extinctions? (3) Is there a lionfish-herbivore-seaweed trophic cascade on invaded reefs? (4) How do lionfish modify cleaning mutualisms on invaded reefs? (5) Are lionfish reaching densities where natural population limits are evident? |
attribute | NC_GLOBAL | projects_0_end_date | String | 2016-07 |
attribute | NC_GLOBAL | projects_0_geolocation | String | Three Bahamian sites: 24.8318, -076.3299; 23.8562, -076.2250; 23.7727, -076.1071; Caribbean Netherlands: 12.1599, -068.2820 |
attribute | NC_GLOBAL | projects_0_name | String | Mechanisms and Consequences of Fish Biodiversity Loss on Atlantic Coral Reefs Caused by Invasive Pacific Lionfish |
attribute | NC_GLOBAL | projects_0_project_nid | String | 561017 |
attribute | NC_GLOBAL | projects_0_project_website | String | http://hixon.science.oregonstate.edu/content/highlight-lionfish-invasion |
attribute | NC_GLOBAL | projects_0_start_date | String | 2012-08 |
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 | 19.0 |
attribute | NC_GLOBAL | standard_name_vocabulary | String | CF Standard Name Table v55 |
attribute | NC_GLOBAL | summary | String | Experimental results indicating which predators were attacked by Stegastes planiforms in the Cayman Islands and the Bahamas during 2011 |
attribute | NC_GLOBAL | title | String | [Stegastes planiforms attacks by predator] - Experimental results indicating which predators were attacked by Stegastes planiforms in the Cayman Islands and the Bahamas during 2011 (Mechanisms and Consequences of Fish Biodiversity Loss on Atlantic Coral Reefs Caused by Invasive Pacific Lionfish) |
attribute | NC_GLOBAL | version | String | 1 |
attribute | NC_GLOBAL | Westernmost_Easting | double | -80.0 |
attribute | NC_GLOBAL | xml_source | String | osprey2erddap.update_xml() v1.3 |
variable | location | String | ||
attribute | location | bcodmo_name | String | site |
attribute | location | description | String | location of sampling |
attribute | location | long_name | String | Location |
attribute | location | units | String | unitless |
variable | latitude | double | ||
attribute | latitude | _CoordinateAxisType | String | Lat |
attribute | latitude | _FillValue | double | NaN |
attribute | latitude | actual_range | double | 19.0, 24.0 |
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 |
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 | -80.0, -76.0 |
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 |
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 | bottle_treatment | String | ||
attribute | bottle_treatment | bcodmo_name | String | treatment |
attribute | bottle_treatment | description | String | type of predator fish within the bottle that was introduced to damselfish |
attribute | bottle_treatment | long_name | String | Bottle Treatment |
attribute | bottle_treatment | units | String | unitless |
variable | habitat | String | ||
attribute | habitat | bcodmo_name | String | site_descrip |
attribute | habitat | description | String | microhabitats where damselfish territories were located; Bahamas: dead coral rubble and coral bommies; Cayman Islands: high and low relief of continuous reef |
attribute | habitat | long_name | String | Habitat |
attribute | habitat | units | String | unitless |
variable | damsel_number | byte | ||
attribute | damsel_number | _FillValue | byte | 127 |
attribute | damsel_number | actual_range | byte | 1, 40 |
attribute | damsel_number | bcodmo_name | String | sample |
attribute | damsel_number | colorBarMaximum | double | 100.0 |
attribute | damsel_number | colorBarMinimum | double | 0.0 |
attribute | damsel_number | description | String | damselfish id number; 1-20 |
attribute | damsel_number | long_name | String | Damsel Number |
attribute | damsel_number | nerc_identifier | String | https://vocab.nerc.ac.uk/collection/P02/current/ACYC/ |
attribute | damsel_number | units | String | unitless |
variable | attack | byte | ||
attribute | attack | _FillValue | byte | 127 |
attribute | attack | actual_range | byte | 0, 1 |
attribute | attack | bcodmo_name | String | unknown |
attribute | attack | description | String | indication of whether or not bottle was attacked; 1=Yes 0=No |
attribute | attack | long_name | String | Attack |
attribute | attack | units | String | unitless |
The information in the table above is also available in other file formats (.csv, .htmlTable, .itx, .json, .jsonlCSV1, .jsonlCSV, .jsonlKVP, .mat, .nc, .nccsv, .tsv, .xhtml) via a RESTful web service.