Search Help Show/Hide Menu
Metadata Rubric
100%
6 / 6
View Report
NWFSC Metadata Library > EFS (Environmental and Fisheries Sciences) Divi... > Migrated from Environmental Conservation Divisi... > Oceanographic and physiological parameters rela... >

NOAA/NSF ECOHAB Heterosigma Discreete Data

Entity (ENT)  |  Northwest Fisheries Science Center (NWFSC)
GUID: gov.noaa.nmfs.inport:36787  |  Updated: August 9, 2022  |  Published / External 
Summary
Item Identification
Entity Info
Data Attributes
Catalog Details

Summary

Abstract

Over one half of the worlds fish production for human consumption currently comes from aquaculture, while wild fisheries yields are either stable or declining. Recurring threats from the raphidophyte, Heterosigma akashiwo Hada (Sournia) have caused extensive damage ($2-6 million per episode) to wild and net-penned fish of Puget Sound, Washington, and are believed to be increasing in scope and magnitude in this region, and elsewhere in the world over the past two decades. The mechanism of H. akashiwo toxicity is not well understood. The toxic activity of H. akashiwo has been attributed to the production of reactive oxygen species, brevetoxin-like compound(s), excessive mucus, or hemolytic activity; however these mechanisms are not confirmed consistently in all fish-killing events or cultured strains. The difficulty of conducting research with active, toxin-producing field populations of H. akashiwo have resulted in conflicting findings from those obtained in lab culture studies, thereby limiting the ability of fish farmers to respond to these episodic blooms. Collaborators in this project are: Vera Trainer (NWFSC), William Cochlan (San Francisco State University), Charles Trick (University of Western Ontario), and Mark Wells (University of Maine). The overall goal of this project is to identify the primary toxic element and the specific environmental factors that stimulate fish-killing H. akashiwo blooms, and thereby provide managers with the fundamental tools needed to help reduce the frequency and toxic magnitude of these harmful algal events. Studies to date have provided incomplete and conflicting observations on the mode of toxicity and the environmental stimulation of toxification. We propose a three-pronged approach to study the environmental controls of H. akashiwo growth and toxin production; laboratory culture experiments, field observations, and bottle and mesocosm manipulation experiments.The project objectives are to: 1. identify the element(s) of toxic activity (inorganic, organic, or synergistic) associated with blooms of H. akashiwo and the various cellular morphologies of this alga, 2. determine the environmental parameters that stimulate the growth success and expression of cell toxicity in the H. akashiwo populations of Puget Sound. Because previous studies have used H. akashiwo cultures with little or no toxic activity, our approach is to use a living laboratory to study H. akashiwo bloom ecology and toxicity using natural assemblages. Using a mobile lab at field sites where H. akashiwo cells are regularly found will enable us to fully characterize the toxic element(s) responsible for fish mortality, and the environmental factors influencing toxicity. Findings from annual field studies in June and two rapid response deployments during major bloom events will be confirmed using laboratory studies with fresh ( 6 mo. old) isolates. The expected results are: 1. determination of the key elements of toxicity of H. akashiwo, 2. characterization of the environmental variables that influence either the induction or depression of elements of toxic activity in H. akashiwo, 3. characterization of environmentally-induced metabolites corresponding to condition of toxin production (metabolomics) and 4. design of a strategy for realistic mitigation of H. akashiwo activities in Puget Sound, Washington. This is a stand-alone project funded for 3 years through the NOAA/NSF ECOHAB program.

Description

Over one half of the worlds fish production for human consumption currently comes from aquaculture, while wild fisheries yields are either stable or declining. Recurring threats from the raphidophyte, Heterosigma akashiwo Hada (Sournia) have caused extensive damage ($2-6 million per episode) to wild and net-penned fish of Puget Sound, Washington, and are believed to be increasing in scope and magnitude in this region, and elsewhere in the world over the past two decades. The mechanism of H. akashiwo toxicity is not well understood. The toxic activity of H. akashiwo has been attributed to the production of reactive oxygen species, brevetoxin-like compound(s), excessive mucus, or hemolytic activity; however these mechanisms are not confirmed consistently in all fish-killing events or cultured strains. The difficulty of conducting research with active, toxin-producing field populations of H. akashiwo have resulted in conflicting findings from those obtained in lab culture studies, thereby limiting the ability of fish farmers to respond to these episodic blooms. Collaborators in this project are: Vera Trainer (NWFSC), William Cochlan (San Francisco State University), Charles Trick (University of Western Ontario), and Mark Wells (University of Maine). The overall goal of this project is to identify the primary toxic element and the specific environmental factors that stimulate fish-killing H. akashiwo blooms, and thereby provide managers with the fundamental tools needed to help reduce the frequency and toxic magnitude of these harmful algal events. Studies to date have provided incomplete and conflicting observations on the mode of toxicity and the environmental stimulation of toxification. We propose a three-pronged approach to study the environmental controls of H. akashiwo growth and toxin production; laboratory culture experiments, field observations, and bottle and mesocosm manipulation experiments.The project objectives are to: 1. identify the element(s) of toxic activity (inorganic, organic, or synergistic) associated with blooms of H. akashiwo and the various cellular morphologies of this alga, 2. determine the environmental parameters that stimulate the growth success and expression of cell toxicity in the H. akashiwo populations of Puget Sound. Because previous studies have used H. akashiwo cultures with little or no toxic activity, our approach is to use a living laboratory to study H. akashiwo bloom ecology and toxicity using natural assemblages. Using a mobile lab at field sites where H. akashiwo cells are regularly found will enable us to fully characterize the toxic element(s) responsible for fish mortality, and the environmental factors influencing toxicity. Findings from annual field studies in June and two rapid response deployments during major bloom events will be confirmed using laboratory studies with fresh ( 6 mo. old) isolates. The expected results are: 1. determination of the key elements of toxicity of H. akashiwo, 2. characterization of the environmental variables that influence either the induction or depression of elements of toxic activity in H. akashiwo, 3. characterization of environmentally-induced metabolites corresponding to condition of toxin production (metabolomics) and 4. design of a strategy for realistic mitigation of H. akashiwo activities in Puget Sound, Washington. This is a stand-alone project funded for 3 years through the NOAA/NSF ECOHAB program.

Entity Information

Entity Type
Spreadsheet

Data Attribute / Type Description
Event
VARCHAR2 		The name of the individual cruise or event in which samples were collected for the overall project.
Event start date
DATE 		The date on which the individual cruise or event began (local time).
Event end date
DATE 		The date on which the individual cruise or event ended (local time).
Station
VARCHAR2 		The name or identification number of a given station at which samples were collected.
Sampling Date
DATE 		The date (local time) on which as sample was collected.
Sampling Start Time
DATE 		The time (local time) on the date in which a sample began to be collected.
Sampling End Time
DATE 		The time (local time) on the date in which a sample was finished being collected.
Sampling Depth (m)
NUMBER 		The depth at which a given sample was collected. Units for values are meters.
Latitude
NUMBER 		The latitude of the sampling station in decmal degrees. Units for values are decimal degrees.
Longitude
NUMBER 		The longitude of the sampling station in decimal degrees. Units for values are decimal degrees.
Station Depth (m)
NUMBER 		The water depth at a given station. Units for values are meters.
Chl-a
NUMBER 		A measurement of chlorophyll a in a seawater sample. Units for values are micrograms per Liter.
NO3 + NO2
NUMBER 		A combination of nitrate and nitrite measured in a seawater sample. Units for values are micromolar.
H2PO4
NUMBER 		A measurement of orthophosphate in a seawater sample. Units for values are micromolar.
SiO2
NUMBER 		A measurement of silicate in a seawater sample. Units for values are micromolar.
NH4
NUMBER 		a measurement of ammonium in a seawater sample. Units for values are micromolar.
Urea
NUMBER 		A measurement of urea in a seawater sample. Units for values are nanograms of nitrogen atoms per Liter.
HetCount (cells/L)
NUMBER 		The total number of Heterosigma cells counted in a given volume of water. This is a genus level enumeration and therefore includes all Heterosigma species present in the sample. Units for values are cells per Liter.
Mean FeII(nM)
NUMBER 		The mean measured value of iron II in a water sample. Units for values are nanomolar.

Child Items

No Child Items for this record.

Contact Information

No contact information is available for this record.

Please contact the owner organization (NWFSC) for inquiries on this record.

Item Identification

Title: NOAA/NSF ECOHAB Heterosigma Discreete Data
Short Name: NOAA/NSF ECOHAB Heterosigma Discreete Data
Status: Planned
Abstract:

Over one half of the worlds fish production for human consumption currently comes from aquaculture, while wild fisheries yields are either stable or declining. Recurring threats from the raphidophyte, Heterosigma akashiwo Hada (Sournia) have caused extensive damage ($2-6 million per episode) to wild and net-penned fish of Puget Sound, Washington, and are believed to be increasing in scope and magnitude in this region, and elsewhere in the world over the past two decades. The mechanism of H. akashiwo toxicity is not well understood. The toxic activity of H. akashiwo has been attributed to the production of reactive oxygen species, brevetoxin-like compound(s), excessive mucus, or hemolytic activity; however these mechanisms are not confirmed consistently in all fish-killing events or cultured strains. The difficulty of conducting research with active, toxin-producing field populations of H. akashiwo have resulted in conflicting findings from those obtained in lab culture studies, thereby limiting the ability of fish farmers to respond to these episodic blooms. Collaborators in this project are: Vera Trainer (NWFSC), William Cochlan (San Francisco State University), Charles Trick (University of Western Ontario), and Mark Wells (University of Maine). The overall goal of this project is to identify the primary toxic element and the specific environmental factors that stimulate fish-killing H. akashiwo blooms, and thereby provide managers with the fundamental tools needed to help reduce the frequency and toxic magnitude of these harmful algal events. Studies to date have provided incomplete and conflicting observations on the mode of toxicity and the environmental stimulation of toxification. We propose a three-pronged approach to study the environmental controls of H. akashiwo growth and toxin production; laboratory culture experiments, field observations, and bottle and mesocosm manipulation experiments.The project objectives are to: 1. identify the element(s) of toxic activity (inorganic, organic, or synergistic) associated with blooms of H. akashiwo and the various cellular morphologies of this alga, 2. determine the environmental parameters that stimulate the growth success and expression of cell toxicity in the H. akashiwo populations of Puget Sound. Because previous studies have used H. akashiwo cultures with little or no toxic activity, our approach is to use a living laboratory to study H. akashiwo bloom ecology and toxicity using natural assemblages. Using a mobile lab at field sites where H. akashiwo cells are regularly found will enable us to fully characterize the toxic element(s) responsible for fish mortality, and the environmental factors influencing toxicity. Findings from annual field studies in June and two rapid response deployments during major bloom events will be confirmed using laboratory studies with fresh ( 6 mo. old) isolates. The expected results are: 1. determination of the key elements of toxicity of H. akashiwo, 2. characterization of the environmental variables that influence either the induction or depression of elements of toxic activity in H. akashiwo, 3. characterization of environmentally-induced metabolites corresponding to condition of toxin production (metabolomics) and 4. design of a strategy for realistic mitigation of H. akashiwo activities in Puget Sound, Washington. This is a stand-alone project funded for 3 years through the NOAA/NSF ECOHAB program.

Entity Information

Entity Type: Spreadsheet
Active Version?: Yes
Schema Name: PARR
Description:

Over one half of the worlds fish production for human consumption currently comes from aquaculture, while wild fisheries yields are either stable or declining. Recurring threats from the raphidophyte, Heterosigma akashiwo Hada (Sournia) have caused extensive damage ($2-6 million per episode) to wild and net-penned fish of Puget Sound, Washington, and are believed to be increasing in scope and magnitude in this region, and elsewhere in the world over the past two decades. The mechanism of H. akashiwo toxicity is not well understood. The toxic activity of H. akashiwo has been attributed to the production of reactive oxygen species, brevetoxin-like compound(s), excessive mucus, or hemolytic activity; however these mechanisms are not confirmed consistently in all fish-killing events or cultured strains. The difficulty of conducting research with active, toxin-producing field populations of H. akashiwo have resulted in conflicting findings from those obtained in lab culture studies, thereby limiting the ability of fish farmers to respond to these episodic blooms. Collaborators in this project are: Vera Trainer (NWFSC), William Cochlan (San Francisco State University), Charles Trick (University of Western Ontario), and Mark Wells (University of Maine). The overall goal of this project is to identify the primary toxic element and the specific environmental factors that stimulate fish-killing H. akashiwo blooms, and thereby provide managers with the fundamental tools needed to help reduce the frequency and toxic magnitude of these harmful algal events. Studies to date have provided incomplete and conflicting observations on the mode of toxicity and the environmental stimulation of toxification. We propose a three-pronged approach to study the environmental controls of H. akashiwo growth and toxin production; laboratory culture experiments, field observations, and bottle and mesocosm manipulation experiments.The project objectives are to: 1. identify the element(s) of toxic activity (inorganic, organic, or synergistic) associated with blooms of H. akashiwo and the various cellular morphologies of this alga, 2. determine the environmental parameters that stimulate the growth success and expression of cell toxicity in the H. akashiwo populations of Puget Sound. Because previous studies have used H. akashiwo cultures with little or no toxic activity, our approach is to use a living laboratory to study H. akashiwo bloom ecology and toxicity using natural assemblages. Using a mobile lab at field sites where H. akashiwo cells are regularly found will enable us to fully characterize the toxic element(s) responsible for fish mortality, and the environmental factors influencing toxicity. Findings from annual field studies in June and two rapid response deployments during major bloom events will be confirmed using laboratory studies with fresh ( 6 mo. old) isolates. The expected results are: 1. determination of the key elements of toxicity of H. akashiwo, 2. characterization of the environmental variables that influence either the induction or depression of elements of toxic activity in H. akashiwo, 3. characterization of environmentally-induced metabolites corresponding to condition of toxin production (metabolomics) and 4. design of a strategy for realistic mitigation of H. akashiwo activities in Puget Sound, Washington. This is a stand-alone project funded for 3 years through the NOAA/NSF ECOHAB program.

Data Attributes

Attribute Summary

Rubric Score Primary Key? Name Type Description
100
 Event VARCHAR2 The name of the individual cruise or event in which samples were collected for the overall project.
100
 Event start date DATE The date on which the individual cruise or event began (local time).
100
 Event end date DATE The date on which the individual cruise or event ended (local time).
100
 Station VARCHAR2 The name or identification number of a given station at which samples were collected.
100
 Sampling Date DATE The date (local time) on which as sample was collected.
100
 Sampling Start Time DATE The time (local time) on the date in which a sample began to be collected.
100
 Sampling End Time DATE The time (local time) on the date in which a sample was finished being collected.
100
 Sampling Depth (m) NUMBER The depth at which a given sample was collected. Units for values are meters.
100
 Latitude NUMBER The latitude of the sampling station in decmal degrees. Units for values are decimal degrees.
100
 Longitude NUMBER The longitude of the sampling station in decimal degrees. Units for values are decimal degrees.
100
 Station Depth (m) NUMBER The water depth at a given station. Units for values are meters.
100
 Chl-a NUMBER A measurement of chlorophyll a in a seawater sample. Units for values are micrograms per Liter.
100
 NO3 + NO2 NUMBER A combination of nitrate and nitrite measured in a seawater sample. Units for values are micromolar.
100
 H2PO4 NUMBER A measurement of orthophosphate in a seawater sample. Units for values are micromolar.
100
 SiO2 NUMBER A measurement of silicate in a seawater sample. Units for values are micromolar.
100
 NH4 NUMBER a measurement of ammonium in a seawater sample. Units for values are micromolar.
100
 Urea NUMBER A measurement of urea in a seawater sample. Units for values are nanograms of nitrogen atoms per Liter.
100
 HetCount (cells/L) NUMBER The total number of Heterosigma cells counted in a given volume of water. This is a genus level enumeration and therefore includes all Heterosigma species present in the sample. Units for values are cells per Liter.
100
 Mean FeII(nM) NUMBER The mean measured value of iron II in a water sample. Units for values are nanomolar.

Attribute Details

Event

CC ID: 731144
Seq. Order: 1
Data Storage Type: VARCHAR2
Required: No
Primary Key: No
Status: Active
Description:

The name of the individual cruise or event in which samples were collected for the overall project.
General Data Type: VARCHAR2
Allowed Values: As provided

Event start date

CC ID: 731145
Seq. Order: 2
Data Storage Type: DATE
Required: No
Primary Key: No
Status: Active
Description:

The date on which the individual cruise or event began (local time).
General Data Type: DATE
Format Mask: mm/dd/yyyy
Allowed Values: As provided

Event end date

CC ID: 731146
Seq. Order: 3
Data Storage Type: DATE
Required: No
Primary Key: No
Status: Active
Description:

The date on which the individual cruise or event ended (local time).
General Data Type: DATE
Format Mask: mm/dd/yyyy
Allowed Values: As provided

Station

CC ID: 731147
Seq. Order: 4
Data Storage Type: VARCHAR2
Required: No
Primary Key: No
Status: Active
Description:

The name or identification number of a given station at which samples were collected.
General Data Type: VARCHAR2
Allowed Values: As provided

Sampling Date

CC ID: 731148
Seq. Order: 5
Data Storage Type: DATE
Required: No
Primary Key: No
Status: Active
Description:

The date (local time) on which as sample was collected.
General Data Type: DATE
Format Mask: mm/dd/yyyy
Allowed Values: As provided

Sampling Start Time

CC ID: 731149
Seq. Order: 6
Data Storage Type: DATE
Required: No
Primary Key: No
Status: Active
Description:

The time (local time) on the date in which a sample began to be collected.
General Data Type: DATE
Format Mask: mm/dd/yyyy hh24:mi
Allowed Values: As provided

Sampling End Time

CC ID: 731150
Seq. Order: 7
Data Storage Type: DATE
Required: No
Primary Key: No
Status: Active
Description:

The time (local time) on the date in which a sample was finished being collected.
General Data Type: DATE
Format Mask: mm/dd/yyyy hh24:mi
Allowed Values: As provided

Sampling Depth (m)

CC ID: 731151
Seq. Order: 8
Data Storage Type: NUMBER
Required: No
Primary Key: No
Status: Active
Description:

The depth at which a given sample was collected. Units for values are meters.
General Data Type: NUMBER
Unit of Measure: meters
Allowed Values: As provided

Latitude

CC ID: 731152
Seq. Order: 9
Data Storage Type: NUMBER
Required: No
Primary Key: No
Status: Active
Description:

The latitude of the sampling station in decmal degrees. Units for values are decimal degrees.
General Data Type: NUMBER
Unit of Measure: decimal degrees
Allowed Values: As provided

Longitude

CC ID: 731153
Seq. Order: 10
Data Storage Type: NUMBER
Required: No
Primary Key: No
Status: Active
Description:

The longitude of the sampling station in decimal degrees. Units for values are decimal degrees.
General Data Type: NUMBER
Unit of Measure: decimal degrees
Allowed Values: As provided

Station Depth (m)

CC ID: 731154
Seq. Order: 11
Data Storage Type: NUMBER
Required: No
Primary Key: No
Status: Active
Description:

The water depth at a given station. Units for values are meters.
General Data Type: NUMBER
Unit of Measure: meters
Allowed Values: As provided

Chl-a

CC ID: 731155
Seq. Order: 12
Data Storage Type: NUMBER
Required: No
Primary Key: No
Status: Active
Description:

A measurement of chlorophyll a in a seawater sample. Units for values are micrograms per Liter.
General Data Type: NUMBER
Unit of Measure: micrograms per Liter
Allowed Values: 0 to measured value

NO3 + NO2

CC ID: 731156
Seq. Order: 13
Data Storage Type: NUMBER
Required: No
Primary Key: No
Status: Active
Description:

A combination of nitrate and nitrite measured in a seawater sample. Units for values are micromolar.
General Data Type: NUMBER
Unit of Measure: micromolar
Allowed Values: 0 to measured value

H2PO4

CC ID: 731157
Seq. Order: 14
Data Storage Type: NUMBER
Required: No
Primary Key: No
Status: Active
Description:

A measurement of orthophosphate in a seawater sample. Units for values are micromolar.
General Data Type: NUMBER
Unit of Measure: micromolar
Allowed Values: 0 to measured value

SiO2

CC ID: 731158
Seq. Order: 15
Data Storage Type: NUMBER
Required: No
Primary Key: No
Status: Active
Description:

A measurement of silicate in a seawater sample. Units for values are micromolar.
General Data Type: NUMBER
Unit of Measure: micromolar
Allowed Values: 0 to measured value

NH4

CC ID: 731159
Seq. Order: 16
Data Storage Type: NUMBER
Required: No
Primary Key: No
Status: Active
Description:

a measurement of ammonium in a seawater sample. Units for values are micromolar.
General Data Type: NUMBER
Unit of Measure: micromolar
Allowed Values: 0 to measured value

Urea

CC ID: 731160
Seq. Order: 17
Data Storage Type: NUMBER
Required: No
Primary Key: No
Status: Active
Description:

A measurement of urea in a seawater sample. Units for values are nanograms of nitrogen atoms per Liter.
General Data Type: NUMBER
Unit of Measure: nanograms of nitrogen atoms per Liter
Allowed Values: 0 to measured value

HetCount (cells/L)

CC ID: 731161
Seq. Order: 18
Data Storage Type: NUMBER
Required: No
Primary Key: No
Status: Active
Description:

The total number of Heterosigma cells counted in a given volume of water. This is a genus level enumeration and therefore includes all Heterosigma species present in the sample. Units for values are cells per Liter.
General Data Type: NUMBER
Unit of Measure: cells per Liter
Allowed Values: less than the limit of detection to the measured value

Mean FeII(nM)

CC ID: 731162
Seq. Order: 19
Data Storage Type: NUMBER
Required: No
Primary Key: No
Status: Active
Description:

The mean measured value of iron II in a water sample. Units for values are nanomolar.
General Data Type: NUMBER
Unit of Measure: nanomolar
Allowed Values: less than the limit of detection to the measured value

Catalog Details

Catalog Item ID: 36787
GUID: gov.noaa.nmfs.inport:36787
Metadata Record Created By: Jeffrey W Cowen
Metadata Record Created: 2017-02-13 16:57+0000
Metadata Record Last Modified By: SysAdmin InPortAdmin
Metadata Record Last Modified: 2022-08-09 17:11+0000
Metadata Record Published: 2018-02-27
Owner Org: NWFSC
Metadata Publication Status: Published Externally
Do Not Publish?: N
Metadata Last Review Date: 2018-02-27
Metadata Review Frequency: 1 Year
Metadata Next Review Date: 2019-02-27