Contributors | Affiliation | Role |
---|---|---|
Butler, Mark | Old Dominion University (ODU) | Principal Investigator |
Behringer, Donald | University of Florida (UF) | Co-Principal Investigator |
Paris-Limouzy, Claire B. | University of Miami Rosenstiel School of Marine and Atmospheric Science (UM-RSMAS) | Co-Principal Investigator |
Shields, Jeffery | Virginia Institute of Marine Science (VIMS) | Co-Principal Investigator |
Copley, Nancy | Woods Hole Oceanographic Institution (WHOI BCO-DMO) | BCO-DMO Data Manager |
From 1999-2014, lobsters were briefly captured in Florida Bay. Measurements taken included sex, length, molt condition, evidence of injury and disease. PaV1 virus PCR results were logged.
Related References:
Portions of these data have been reported in the following publication:
Behringer, D.C., M.J. Butler, J. Shields, and J. Moss. 2011. A review of Panulirus argus Virus 1 – a Decade after its Discovery. Diseases of Aquatic Organisms 94: 153–160.
At each permanent 25m x 25m sample location (hard-bottom habitat 1.5 – 3.0 m depth), delineated by rope border affixed to seafloor, two divers search the entire site for spiny lobsters (Panulirus argus). All lobsters sighted are collected in hand nets by divers and brought aboard the topside vessel where the data are collected & recorded. Lobsters are then returned live to the original site. Hemolymph samples are stored in labeled vials with 90% ETOH and kept in dark and on ice until return to shore where they are then stored in a -40C freezer until processed.
BCO-DMO Processing:
- added conventional header with dataset name, PI name, version date, reference information
- renamed parameters to BCO-DMO standard
- added lat/lon
- changed NA and ? to nd
- replace blanks with 0 for injuries, disease, blood sample, PCR Results; replaced other blanks with nd
File |
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longterm_survey.csv (Comma Separated Values (.csv), 208.96 KB) MD5:92925e6448415b693c569141ff2844d6 Primary data file for dataset ID 556162 |
Parameter | Description | Units |
year | year of survey | yyyy |
date | date of survey | yyyy-mm-dd |
site | survey site | unitless |
lat | latitude; north is positive | decimal degrees |
lon | longitude; east is positive | decimal degrees |
sex | sex of lobster | unitless |
length_carap | carapace length of tethered lobster | millimeters |
molt_cond | visual assessment of molt condition: I = intermolt; PR = premolt; PO = postmolt | unitless |
leg_old_new | old and new injuries number of old/new leg injuries if any | unitless |
ant_old_new | number of old/new antennae injuries if any | unitless |
other_old_new | number of old/new other injuries if any | unitless |
visible_disease_flag | signs of PaV1 infection in lobster obvious to naked eye; 0 = no; 1 = yes | unitless |
blood_sample | hemolymph sample vial label if any | unitless |
PCR_result | positive or negative PCR test for presence of PaV1 virus DNAa | unitless |
comments | comments | unitless |
Dataset-specific Instrument Name | pCR |
Generic Instrument Name | Thermal Cycler |
Generic Instrument Description | A thermal cycler or "thermocycler" is a general term for a type of laboratory apparatus, commonly used for performing polymerase chain reaction (PCR), that is capable of repeatedly altering and maintaining specific temperatures for defined periods of time. The device has a thermal block with holes where tubes with the PCR reaction mixtures can be inserted. The cycler then raises and lowers the temperature of the block in discrete, pre-programmed steps. They can also be used to facilitate other temperature-sensitive reactions, including restriction enzyme digestion or rapid diagnostics.
(adapted from http://serc.carleton.edu/microbelife/research_methods/genomics/pcr.html) |
Website | |
Platform | Lobster habitat |
Start Date | 2004-07-15 |
End Date | 2004-08-11 |
Description | Field expts with diseased lobsters |
Scientists are struck by how different terrestrial epidemiology is from that in marine ecosystems, a crucial difference being the more rapid spread of diseases in the ocean due to the presumed absence of barriers to waterborne dispersal. Yet, the movement of pathogens in the sea and its importance to disease dynamics in marine metapopulations is virtually unstudied. Marine pathogens do spread among distant host populations, as demonstrated by dramatic epizootics, but is this common or demographically relevant? Nearly all studies of marine diseases treat such events as transitory, focusing instead on local disease dynamics. This approach suggests either that small-scale phenomena normally trump the influence of large-scale pathogen connectivity or, alternatively, that the dispersal of marine pathogens by highly motile adults or free-living waterborne pathogens is simply too intractable for empirical investigation. Yet, there is another perhaps unappreciated mechanism – dispersal by infected larvae. Most marine animals have life histories that include planktonic larvae, many of which are highly dispersive. If infected by pathogens, these “larval vectors” would provide an efficient mechanism for distributing pathogens at high concentrations directly into habitats where hosts dwell. More so than passive, waterborne pathogens that are subject to rapid dilution and have no means of targeting distant hosts.
We have evidence that long-distance pathogen dispersal in the sea via infected meroplanktonic larvae may be possible. The pathogen in question is an often lethal, pathogenic virus (PaV1; Panulirus argus virus 1) that infects the Caribbean spiny lobster, Panulirus argus – a species broadly distributed throughout the Caribbean where it supports the most valuable fishery in the region. We described the PaV1 virus in 1999 and since then have studied its pathology, epidemiology, transmission, and effects on juvenile lobster populations in the Florida Keys. Like others, our focus has been on local pathogen-host dynamics, but PaV1 infections in lobsters are now confirmed in distant areas of the Caribbean (Belize, Mexico, St. Croix) in regions that are demographically linked only by dispersing larvae that spend >6 mos. in the open ocean. We recently discovered that many lobster postlarvae recruiting to coastal nurseries in Florida are infected with PaV1, providing novel evidence for pathogen connectivity among distant host populations.
Focusing on the spiny lobster-PaV1 virus association as a case study, we propose an ambitious program of laboratory, field, and modeling research whose broader implications will better our understanding of the importance of dispersal by infectious agents on the spread and maintenance of disease in marine populations. The project builds upon data and techniques developed with prior NSF sponsorship, and brings together partners in developing Caribbean nations with a multidisciplinary group of scientists with long-standing research programs in larval biology, biophysical and ecological modeling, crustacean biology, molecular biology, and the study of marine diseases.
Funding Source | Award |
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NSF Division of Ocean Sciences (NSF OCE) | |
NSF Division of Ocean Sciences (NSF OCE) |