http://lod.bco-dmo.org/id/dataset/700263
eng; USA
utf8
dataset
Highest level of data collection, from a common set of sensors or instrumentation, usually within the same research project
Biological and Chemical Oceanography Data Management Office (BCO-DMO)
Unavailable
508-289-2009
WHOI MS#36
Woods Hole
MA
02543
USA
info@bco-dmo.org
http://www.bco-dmo.org
Monday - Friday 8:00am - 5:00pm
For questions regarding this resource, please contact BCO-DMO via the email address provided.
pointOfContact
2017-05-18
ISO 19115-2 Geographic Information - Metadata - Part 2: Extensions for Imagery and Gridded Data
ISO 19115-2:2009(E)
Initial hunting preferences by predator species in the Bahamas in 2013
2017-05-16
publication
2017-05-16
revision
Marine Biological Laboratory/Woods Hole Oceanographic Institution Library (MBLWHOI DLA)
2019-03-28
publication
https://doi.org/10.1575/1912/bco-dmo.700263.1
Mark Hixon
University of Hawaii
principalInvestigator
Emily Anderson
Old Dominion University
principalInvestigator
Biological and Chemical Oceanography Data Management Office (BCO-DMO)
Unavailable
508-289-2009
WHOI MS#36
Woods Hole
MA
02543
USA
info@bco-dmo.org
http://www.bco-dmo.org
Monday - Friday 8:00am - 5:00pm
For questions regarding this resource, please contact BCO-DMO via the email address provided.
publisher
Cite this dataset as: Hixon, M., Anderson, E. (2017) Initial hunting preferences by predator species in the Bahamas in 2013. Biological and Chemical Oceanography Data Management Office (BCO-DMO). (Version 1) Version Date 2017-05-16 [if applicable, indicate subset used]. doi:10.1575/1912/bco-dmo.700263.1 [access date]
Initial hunting preferences of predator species. Dataset Description: <p>Behavioral response of invasive lionfish versus native grouper when presented with two congeneric prey fishes (fairy and blackcap basslets) in aquaria.</p>
<p><strong>For related datasets, please visit the project link listed at the top of the page.</strong></p> Methods and Sampling: <p>To determine whether the preference of predators for basslets was driven by basslet species (fairy and blackcap) or basslet size (small and large: 1.7–2.5 and 3.5–5.2 cm TL, respectively) we presented pairs of basslets in cross-factored combinations of the 2 variables, resulting in the following treatments: (1) small fairy and large fairy, (2) small blackcap and large blackcap, (3) small fairy and small blackcap, (4) large fairy and large blackcap, (5) small fairy and large blackcap, and (6) large fairy and small blackcap. In addition to randomizing the order of basslet treatments presented to each predator, we also randomized the corner of the tank basslets were placed in every time a treatment was presented.</p>
<p>Once the predator and basslets were in their respective sides of the tank, we allowed them to acclimate for 20 min, after which we removed the central barrier and observed the predator’s behavior for 10 min. Observations were performed either in person (74 lionfish trials; 73 graysby trials) or filmed with a digital video camera (16 lionfish trials; 17 graysby trials) positioned outside of the tank. During each 10 min trial, we recorded (1) which basslet the predator hunted first (initial hunting preference); (2) the number of times the predator’s mouth made physical contact with each glass container (number of strikes); and (3) the amount of time the predator hunted each basslet (hunting time). We defined the hunting behavior of lionfish as occurring when an individual directly faced a basslet with flared pectoral fins and/or blew pulsed jets of water towards a basslet (Cure et al. 2012). We characterized graysby hunting behavior as occurring when an individual positioned itself near a basslet (&lt;10 cm in this experiment) while directly facing the basslet (Webster 2004).</p>
<p>At the conclusion of the 10 min trial, we separated the predator from the basslets and placed the central barrier back in the tank. A new combination of basslets were placed in the glass containers, and all fish were allowed to acclimate for 20 min before removing the barrier and observing predator response for another 10 min. This procedure was repeated until all 6 basslet treatments had been presented to each predator in random order.</p>
Funding provided by NSF Division of Ocean Sciences (NSF OCE) Award Number: OCE-1233027 Award URL: http://www.nsf.gov/awardsearch/showAward.do?AwardNumber=1233027
completed
Mark Hixon
University of Hawaii
Department of Zoology 3029 Cordley Hall
Corvallis
OR
97331-2914
USA
hixonm@science.oregonstate.edu
pointOfContact
Emily Anderson
Old Dominion University
eande005@odu.edu
pointOfContact
asNeeded
Dataset Version: 1
Unknown
predator_ID
predator_species
predator_size
bass_treatment
first_size
first_species
theme
None, User defined
sample identification
species
fish_len
treatment
brief description
featureType
BCO-DMO Standard Parameters
LSI_Reef_Surveys_09-12
service
Deployment Activity
Lee Stocking Island, Bahamas
place
Locations
otherRestrictions
otherRestrictions
Access Constraints: none. Use Constraints: Please follow guidelines at: http://www.bco-dmo.org/terms-use Distribution liability: Under no circumstances shall BCO-DMO be liable for any direct, incidental, special, consequential, indirect, or punitive damages that result from the use of, or the inability to use, the materials in this data submission. If you are dissatisfied with any materials in this data submission your sole and exclusive remedy is to discontinue use.
Mechanisms and Consequences of Fish Biodiversity Loss on Atlantic Coral Reefs Caused by Invasive Pacific Lionfish
http://hixon.science.oregonstate.edu/content/highlight-lionfish-invasion
Mechanisms and Consequences of Fish Biodiversity Loss on Atlantic Coral Reefs Caused by Invasive Pacific Lionfish
<p>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.</p>
<p>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? </p>
BiodiversityLossEffects_lionfish
largerWorkCitation
project
eng; USA
oceans
Lee Stocking Island, Bahamas
2017-05-16
Three Bahamian sites: 24.8318, -076.3299; 23.8562, -076.2250; 23.7727, -076.1071; Caribbean Netherlands: 12.1599, -068.2820
0
BCO-DMO catalogue of parameters from Initial hunting preferences by predator species in the Bahamas in 2013
Biological and Chemical Oceanography Data Management Office (BCO-DMO)
Unavailable
508-289-2009
WHOI MS#36
Woods Hole
MA
02543
USA
info@bco-dmo.org
http://www.bco-dmo.org
Monday - Friday 8:00am - 5:00pm
For questions regarding this resource, please contact BCO-DMO via the email address provided.
pointOfContact
http://lod.bco-dmo.org/id/dataset-parameter/700272.rdf
Name: predator_ID
Units: unitless
Description: Identification number for each predator observed
http://lod.bco-dmo.org/id/dataset-parameter/700273.rdf
Name: predator_species
Units: unitless
Description: Species of predator; CECR = Cephalopholis cruentatus; PTVO = Pterois volitan
http://lod.bco-dmo.org/id/dataset-parameter/700274.rdf
Name: predator_size
Units: centimeters
Description: Total body length of predator
http://lod.bco-dmo.org/id/dataset-parameter/700275.rdf
Name: bass_treatment
Units: unitless
Description: Combination of basslets (fairy vs. blackcap basslets) presented to predator in aquarium tank: (1) GRLO.sm_GRLO.lg = small fairy vs. large fairy; (2) GRME.sm_GRME.lg = small blackcap vs. large blackcap; (3) GRLO.sm_GRME.lg = small fairy vs. large blackcap; (4) GRME.sm_GRLO.lg = small blackcap vs. large fairy
http://lod.bco-dmo.org/id/dataset-parameter/700276.rdf
Name: first_size
Units: unitless
Description: Size of basslet that predator initially hunted (small or large)
http://lod.bco-dmo.org/id/dataset-parameter/700277.rdf
Name: first_species
Units: unitless
Description: Species of basslet that predator initially hunted (GRLO = fairy basslet; GRME = blackcap basslet)
GB/NERC/BODC > British Oceanographic Data Centre, Natural Environment Research Council, United Kingdom
Biological and Chemical Oceanography Data Management Office (BCO-DMO)
Unavailable
508-289-2009
WHOI MS#36
Woods Hole
MA
02543
USA
info@bco-dmo.org
http://www.bco-dmo.org
Monday - Friday 8:00am - 5:00pm
For questions regarding this resource, please contact BCO-DMO via the email address provided.
pointOfContact
7919
https://darchive.mblwhoilibrary.org/bitstream/1912/23936/1/dataset-700263_initial-predator-preferences__v1.tsv
download
https://doi.org/10.1575/1912/bco-dmo.700263.1
download
onLine
dataset
<p>To determine whether the preference of predators for basslets was driven by basslet species (fairy and blackcap) or basslet size (small and large: 1.7–2.5 and 3.5–5.2 cm TL, respectively) we presented pairs of basslets in cross-factored combinations of the 2 variables, resulting in the following treatments: (1) small fairy and large fairy, (2) small blackcap and large blackcap, (3) small fairy and small blackcap, (4) large fairy and large blackcap, (5) small fairy and large blackcap, and (6) large fairy and small blackcap. In addition to randomizing the order of basslet treatments presented to each predator, we also randomized the corner of the tank basslets were placed in every time a treatment was presented.</p>
<p>Once the predator and basslets were in their respective sides of the tank, we allowed them to acclimate for 20 min, after which we removed the central barrier and observed the predator’s behavior for 10 min. Observations were performed either in person (74 lionfish trials; 73 graysby trials) or filmed with a digital video camera (16 lionfish trials; 17 graysby trials) positioned outside of the tank. During each 10 min trial, we recorded (1) which basslet the predator hunted first (initial hunting preference); (2) the number of times the predator’s mouth made physical contact with each glass container (number of strikes); and (3) the amount of time the predator hunted each basslet (hunting time). We defined the hunting behavior of lionfish as occurring when an individual directly faced a basslet with flared pectoral fins and/or blew pulsed jets of water towards a basslet (Cure et al. 2012). We characterized graysby hunting behavior as occurring when an individual positioned itself near a basslet (&lt;10 cm in this experiment) while directly facing the basslet (Webster 2004).</p>
<p>At the conclusion of the 10 min trial, we separated the predator from the basslets and placed the central barrier back in the tank. A new combination of basslets were placed in the glass containers, and all fish were allowed to acclimate for 20 min before removing the barrier and observing predator response for another 10 min. This procedure was repeated until all 6 basslet treatments had been presented to each predator in random order.</p>
Specified by the Principal Investigator(s)
<p>To test whether initial hunting preferences be - tween basslet species (fairy and blackcap) and bass - let sizes (small and large) significantly differed be - tween predators (lionfish and graysby) and/or among predator sizes (continuous variables), we fitted generalized estimation equations (GEEs) with binomial distributions and exchangeable correlation structures. GEEs are an extension to the generalized linear model approach that allow for correlations between observations from the same subject, thus allowing us to account for repeated measures. We fitted a full model with an interaction between predators and predator size, and then compared the model fit to that of the reduced additive model by calculating quasilikelihood values under the independence model criterion (QIC; Pan 2001). If the initial hunting preference significantly varied between predators, we then performed a post-hoc McNemar test with a continuity correction for lionfish and graysby (separately) to test whether each predator had a significant initial preference.</p>
<p><span style="font-size:14px"><strong>BCO-DMO Processing Notes:</strong></span></p>
<p><span style="font-size:14px">- reformatted column names to comply with BCO-DMO standards</span><br />
<span style="font-size:14px">- reformatted dates&nbsp;</span><br />
<span style="font-size:14px">- nd used to fill blank cells</span></p>
Specified by the Principal Investigator(s)
asNeeded
7.x-1.1
Biological and Chemical Oceanography Data Management Office (BCO-DMO)
Unavailable
508-289-2009
WHOI MS#36
Woods Hole
MA
02543
USA
info@bco-dmo.org
http://www.bco-dmo.org
Monday - Friday 8:00am - 5:00pm
For questions regarding this resource, please contact BCO-DMO via the email address provided.
pointOfContact
Deployment: LSI_Reef_Surveys_09-12
LSI_Reef_Surveys_09-12
Tropical Marine Lab at Lee Stocking Island
laboratory
LSI_Reef_Surveys_09-12
Mark Hixon
Oregon State University
Tropical Marine Lab at Lee Stocking Island
laboratory