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pdfNational Marine Fisheries Service
Endangered Species and Marine
Mammals
Parts Permits
OMB No. 0648-0084
Expires: Month Day, Year
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NATIONAL MARINE FISHERIES SERVICE (NMFS)
ENDANGERED SPECIES AND MARINE MAMMALS:
SCIENTIFIC RESEARCH AND ENHANCEMENT PERMITS
Parts Permits
TABLE OF CONTENTS
INTRODUCTION.......................................................................................................... 3
PROJECT INFORMATION ....................................................................................................................... 5
PROJECT DESCRIPTION ........................................................................................................................ 6
PROJECT SUPPLEMENTAL INFORMATION ......................................................................................... 8
PROJECT LOCATION .............................................................................................................................. 9
SAMPLE ACTIVITY INFORMATION (A.K.A. TAKE TABLES) ............................................................ 9
NATIONAL ENVIRONMENTAL POLICY ACT ..................................................................................... 10
PROJECT CONTACTS ........................................................................................................................... 11
SUBMIT APPLICATION ......................................................................................................................... 14
ADDITIONAL INFORMATION ............................................................................. 14
PAPERWORK REDUCTION ACT STATEMENT .................................................................................. 14
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Introduction
What is this permit application for?
This application is for requesting a NMFS scientific research or enhancement
permit under the Marine Mammal Protection Act (MMPA) and Endangered
Species Act (ESA) to:
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Import and export protected species parts /samples
Receive or collect parts from U.S. subsistence-hunted marine mammals
Develop and use cell lines
Salvage dead ESA-listed sturgeon or sawfish
If you are requesting any of the above, you may also include
receiving samples domestically from other U.S. permitted sources.
Protected species covered by this permit include these under NMFS jurisdiction:
cetaceans (dolphins, porpoises, and whales)
pinnipeds (seals and sea lions)
sawfishes (largetooth and smalltooth)
sturgeon (Atlantic and shortnose)
other foreign ESA-listed species.
You may request samples from the following U.S. or foreign sources:
Animals in captivity (samples taken during routine husbandry procedures
or under separate authorization)
Animals in foreign countries stranded alive or dead or that died during
rehabilitation
Animals killed during legal subsistence harvests
Animals killed incidental to legal commercial fishing operations
Samples from other authorized researchers or collections
Soft or hard parts that are sloughed, excreted, or discharged naturally.
What is this permit application NOT for?
Taking (e.g., collecting samples from or harassing) live animals in the United
States. See http://www.nmfs.noaa.gov/pr/permits/types.html.
Collecting or receiving samples from dead or live beached/stranded marine
mammals in the United States (this requires a separate authorization). Contact
http://www.nmfs.noaa.gov/pr/health/coordinators.htm.
Importing, exporting, selling, and possessing marine mammal parts taken prior to
the enactment of the MMPA (December 21, 1972) or endangered species parts
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Marine mammal parts are defined by regulation: Hard part means any bone, tooth, baleen, treated pelt, or
other part of a marine mammal that is relatively solid. Soft part means any marine mammal part that is not
a hard part; soft parts do not include urine or feces. NMFS regulates cell lines, DNA (excluding replicated
DNA), and other tissue derivatives as parts.
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that are at least 100 years old (antique under the ESA). See
http://www.nmfs.noaa.gov/pr/permits/parts_instructions.htm.
Only receiving samples from permitted U.S. researchers. See placeholder for new
website with parts information to be developed.
Obtaining a Convention on International Trade in Endangered Species of Wild
Fauna and Flora (CITES) permit. See http://www.fws.gov/international/permits/.
Urine, feces, and synthetic or replicated samples without any of the original
source part remaining (e.g., replicated DNA, RNA; synthetic proteins).
Importing samples into the United States from marine mammals:
Taken in any high seas driftnet fishery after December 31, 1992
Deliberately killed for the express purposes of fulfilling this permit
Taken illegally in the country of origin
Taken during whaling activities not approved by the International Whaling
Commission (IWC)
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Taken during whaling activities opposed by the United States
Taken in a directed cetacean fishery opposed by the United States,
including Japanese “drive fisheries.”
When should I apply?
At least 6 months before you wish to start; preferably 8 months prior.
What is the process for getting a permit?
1. Follow these instructions and contact the Permits and Conservation Division at
301-427-8401 with any questions.
2. Submit your application.
a. An assigned permit analyst will contact you and review the application.
3. Address any questions on the application. To facilitate processing, reference the
application File No. in all correspondence.
a. Once complete, we will publish a notice in the Federal Register, which
starts a mandatory 30-day public comment period.
b. Concurrently, we will send your application to subject matter experts in
partner institutions and federal and state agencies for review.
4. Address any questions received during the comment period.
a. We will then draft the permit and supporting documentation (including
National Environmental Policy Act analyses), which will be reviewed by
various NMFS offices including a legal review by General Counsel.
b. A final decision will be made by the Office Director.
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Including samples taken during scientific whaling and commercial hunts after the IWC Whaling
Moratorium of 1986.
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How do I use APPS?
Refer to Chapter 2 (“How to Use the System”) for instructions to use APPS. When
starting from your portfolio, click on the link of your file number under the “File
Number” column to take you to the application. Save your application every 20
minutes or you will lose information! An * means it is a required field.
Questions?
Contact our office at 301-427-8401.
Project Information
File Number
This number is automatically generated and cannot be changed.
*Project Title (255 characters)
Provide a concise title to include the activity, species (or taxa if multiple species),
and purpose of the study. For example:
o Receipt, import, and export of marine mammal parts to study the impact of
emerging infectious diseases on marine mammal health.
o Collection and receipt of parts from subsistence-hunted pinnipeds in the
United States for genetic and contaminant analysis.
o Salvage of dead sturgeon and sawfish for genetic identification and
opportunistic research.
*Project Status
The project status (New or Renewal) is automatically selected based on your
answers in the pre-application guide (PAG). Do not change this field.
Previous Federal or State Permit #
If applicable, enter your most recent and closely related NMFS permit number.
Otherwise leave blank. State permit numbers are not applicable.
*Permits Requested
One or more permit will be listed based on your answers in the PAG. If the
options listed are incorrect, please call the Permits Division at 301-427-8401 for
assistance.
*Where Will the Activities Occur?
One or more general locations will be listed based on your answers in the PAG.
If a location is incorrect, please call the Permits Division at 301-427-8401 for
assistance.
*Research Timeframe
Enter the desired start and end dates of the entire project in the following format:
MM/DD/YYYY. The start date must not be prior to the date you submit the
application and should be at least 6 months after the date you submit. The end
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date must be within five years of the start date because permits are issued for a
maximum five year period.
*Sampling Season/Project Duration (1,000 characters)
Describe the frequency of sample collection, import, export, or receipt. If your
research extends beyond five years, or is a continuation of previously authorized
research, discuss when the research began and when you expect it to end.
*Abstract (enter up to 2,000 characters)
The abstract must include the following information, which is published in the
Federal Register Notice of Receipt that initiates the mandatory 30-day public
comment period:
Purpose of the research.
Species (common and scientific names); if you are requesting
opportunistic samples from a large number of species under NMFS
jurisdiction, you do not need to list out all species, but rather, may indicate
taxa.
Proposed activities (e.g., import and export of samples).
Number of animals from which samples will be collected, imported,
exported, or received by species or taxa annually.
Locations (countries) from which samples will be imported or to which
they will be exported.
Requested duration of the permit (the maximum is five years).
Project Description
*Project Purpose: Hypothesis/Objectives and Justification (enter up to 64,000
characters)
Discuss how your proposed research is bona fide, including how the results of
your research:
Are likely to be accepted for publication in a refereed scientific journal;
Are likely to contribute to the basic knowledge of the species biology or
ecology. (Note: This includes, for example, parts in a properly curated,
professionally accredited scientific collection); or
Are likely to identify, evaluate, or resolve conservation problems.
Discuss the purpose of your project including your hypotheses and/or objectives.
If your institution is a repository, please describe previous and on-going areas of
research that your collection supports and how researchers receive access to your
collection.
Summarize published findings related to the objectives, using literature citations
from your work if you have previously held or worked under a permit, or other
published literature. Describe how your proposed study is different from, builds
upon, or duplicates past research.
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Explain how you determined your sample size. Include a power analysis or other
sample size estimation to show whether the sample size is sufficient to provide
statistically significant or otherwise robust results appropriate for your study.
For ESA-listed and MMPA-depleted species, also:
Discuss why your project must involve ESA-listed or depleted species parts.
Discuss how your project will:
contribute to the objectives identified in the species’ recovery or conservation
plan;
contribute significantly to understanding the basic biology or ecology of the
species;
contribute significantly to identifying, evaluating, or resolving conservation
problems; or
enhance the propagation or survival of the species.
*Project Description (enter up to 64,000 characters)
List the sources of your samples and all proposed activities (collection, import,
export, domestic receipt).
List the number of animals by species, life stage, and sex from which parts are
sought from which samples are sought. If you are requesting opportunistic
sample import/receipt, you may request an unlimited number of samples from a
specified number of animals, by taxa (e.g., unlimited samples from up to 100
cetaceans and 100 pinnipeds annually).
List the type of samples (e.g., blood, skin, whole carcasses) and indicate whether
you will be isolating nucleic acids or other constituent elements of the tissues, or
developing/maintaining cell lines. Note, a permit is not needed if you are only
working with synthetic or replicated samples without any of the original source
part remaining (e.g. replicated DNA or RNA; synthetic proteins).
If collecting or receiving samples from U.S. subsistence-hunted marine mammals,
or importing samples from subsistence-hunted marine mammals in foreign
countries, describe the subsistence method and whether documentation is
available to ensure the taking was conducted in a humane manner (i.e., using the
method that involves the least possible degree of pain and suffering possible).
If importing samples taken from live animals, describe how the samples were
collected including animal handling and sample collection protocols. This should
include a description of how the take was humane.
It is unlawful to import parts from an animal that was taken illegally in the
country of origin. List the authorizing government agency and authorizations or
permits obtained for the legal take of animals or parts in the country of origin. If
receiving opportunistically-available samples, documentation regarding the
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legality of the take in the country of origin must be provided with your annual
reports.
For samples received domestically from U.S. permitted researchers, include the
researcher’s name, affiliation, and permit number.
List the locations (countries and facilities/researchers) from which samples will be
imported or to which they will be exported, including listing the ports of entry for
importing samples into the United States.
Describe how samples will be preserved, transported/shipped, and stored/curated.
Describe the how samples will be analyzed and include a brief overview of the
methods that will be used including references where possible.
Project Supplemental Information
Attach a Supplemental Information File
You may attach supplemental files here.
*Status of the Affected Species (enter up to 2,000 characters)
As applicable, indicate the status of the species or stock as follows:
ESA - threatened or endangered;
MMPA - depleted or strategic; and
Convention on International Trade in Endangered Species of Wild Fauna
and Flora (CITES) - Appendix I, I, or III
Species information is available at the following web sites:
http://www.nmfs.noaa.gov/pr/species/
http://www.fws.gov/
http://www.cites.org/
Attach a References File
Attach a bibliography of references cited in this application.
*Resources Needed to Accomplish Objectives (enter up to 2,000 characters and attach
file if necessary)
Explain how your expertise, facilities, and resources are adequate to accomplish
your proposed objectives and activities.
Attach copies of any relevant formal research proposals, contracts, grant awards,
or letters of agreement that would demonstrate financial or logistical resources.
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Attach copies of any other applicable international, federal, state, or local
authorizations.
*Disposition of Tissue Samples (enter up to 2000 characters)
Indicate the disposition of any remaining samples after your project is complete.
State whether samples will be consumed in analysis, destroyed, or
exported back to facility/researcher
If applicable, list the name and location of the person or institution that
will store/curate samples. Indicate if you will retain legal custody of the
archived samples or if you wish to permanently transfer the samples once
your project is complete.
*Public Availability of Product/Publications (enter up to 800 characters)
Describe the end products of your proposed project and how they will be made
available to the public.
Project Location
On the main Project Location page, you will describe the locations of sample
collection, import, export, receipt and add information in a table on the species,
number of animals, and number of samples per animal. Select the Animal Parts
option as your general location.
Enter Location Details: Use the Location Description box (up to 255 characters)
to briefly describe the locations (e.g., World-wide import, export, and receipt of
marine mammal samples. Samples will be received and analyzed at [state your
laboratory name and city, state]).
Sample Activity Information (a.k.a. Take Tables)
The table represents annual collection, import, export, or receipt of samples for
each year of your project.
Columns you will fill out in the table include:
1) Species: Select the species – they are listed alphabetically by common name
and/or category (e.g., whale, sperm). Or, if you are requesting opportunistic
receipt of any species of marine mammal under NMFS jurisdiction, choose
Cetacean, unidentified for one row, and Pinniped, unidentified for a second
row.
2) Listing Unit/Stock: Select the applicable Listing Unit/Stock. Choose Rangewide if you are importing specimens from locations worldwide.
3) Production/Origin: Choose as applicable: Wild, Captive, Rehabilitation
facility, or All.
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4) Life Stage: Select the applicable life stage or choose All if samples from any
life stage are included.
5) Sex: Select Male and Female if samples from both sexes are included.
6) Expected Take: This represents the number of animals from which samples
will be collected, imported, exported, or received annually.
7) Takes Per Animal: This represents the maximum number of samples per
individual that will be collected, imported, exported, or received annually. If
your research is opportunistic and this number is unknown (e.g., a large
volume of samples may become available), you may enter 999999 to represent
an unlimited number of samples per individual. However, if you have a
discrete project and the number of samples is known, indicate that number.
8) Take Action: Choose Collect/Import/export/receive only
9) Observe/Collect Method: Choose Other.
10) Procedures: A separate pop-up window will appear with the following
options (hold down the Control key to select all that apply):
Collect parts from U.S. subsistence hunted animals
Import
Export
Receive domestically
Other (only chose if your activity is not listed, and briefly describe what it
means in the Details box).
11) Details: Enter up to 255 characters. Provide details for each table row to
provide clarity. For example:
Unlimited samples from up to 100 animals of each species annually if
Cetacean, unidentified or Pinniped, unidentified was chosen in the
Species column.
National Environmental Policy Act
To assist us in our required National Environmental Policy Act (NEPA) analysis,
please provide information as requested below to verify your activity may be
categorically excluded from the requirement to prepare an environmental
assessment or environmental impact statement. If you believe any of the criteria
are “not applicable” you must explain why.
1) If your activities will involve equipment or techniques that are new, untested,
or otherwise have unknown or uncertain impacts on the environment, please
discuss the degree to which they are likely to be adopted by others for similar
activities or applied more broadly.
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2) If your activities involve collecting, handling, or transporting potentially
infectious agents or pathogens (e.g., blood), or using or transporting hazardous
substances (e.g., formalin), provide a description of the protocols you will use
to ensure public health and human safety are not adversely affected, such as
by spread of zoonotic diseases or contamination of food or water supplies
from disposal of hazardous waste.
3) If you are collecting samples from U.S. subsistence-hunted animals, describe
the physical characteristics of your project location, including whether you
will be working in or near unique geographic areas such as state or National
Marine Sanctuaries, Marine Protected Areas, Parks or Wilderness Areas,
Wildlife Refuges, Wild and Scenic Rivers, designated Critical Habitat for
endangered or threatened species, Essential Fish Habitat, etc. Discuss how
your activities could impact the physical environment, such as by ingress and
egress of researchers, and measures you will take to minimize these impacts.
4) If you are collecting samples from U.S. subsistence-hunted animals, describe
any important scientific, cultural, or historic resources (e.g., archeological
resources, animals used for subsistence, sites listed in or eligible for listing in
the National Register of Historic Places) in the project area and discuss
measures you will take to ensure your work does not cause loss or destruction
of such resources. Discuss measures you will take to ensure your project does
not adversely affect the availability or suitability of animals for subsistence
use.
5) Discuss whether your project involves activities known or suspected of
introducing or spreading invasive species, intentionally or not (e.g.,
transporting animals or tissues, use of equipment at multiple sites). Describe
measures you would take to prevent the possible introduction or spread of
non-indigenous or invasive species, including plants, animals, microbes, or
other biological agents.
Project Contacts
As the person entering the application, you will automatically be assigned the following
roles: Applicant/Permit Holder, Principal Investigator, and Primary Contact. See
Chapter 2 for directions on how to change who is assigned to these roles and the table
below.
Project
Contact
Must be named in
the permit
application
Applicant/
Permit
Holder
Responsible
Party*
(if Applicant/Holder
Able to make changes to application, Description of
request changes to the permit, and
qualifications required
submit reports; will receive automatic
emails from APPS.
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Project
Contact
Must be named in
the permit
application
Able to make changes to application, Description of
request changes to the permit, and
qualifications required
submit reports; will receive automatic
emails from APPS.
is an entity)
Principal
Investigator
Primary
Contact
CoInvestigator
Authorized
Recipients
Research
Assistants
* A Responsible Party may also be the PI or a CI if participating in the research;
therefore, the description of qualifications is required.
To prevent duplicate entries, you MUST ALWAYS search the database for the person
before entering a new contact. To facilitate the search, start with only putting the last
name in APPS search box.
A project must have a Responsible Party if the Applicant/Permit Holder is an
organization, institution, or agency. The Responsible Party or Applicant/Permit Holder is
an official who has the legal authority to bind the organization, institution, or agency and
is ultimately responsible for the activities of any individual operating under the authority
of the permit.
The Principal Investigator (PI) is the individual primarily responsible for the import,
export, and any related activities conducted under the permit. The PI must have
qualifications, knowledge and experience relevant to the activities authorized by the
permit. The PI must be on site during activities conducted under the permit unless a CoInvestigator is present to act in place of the PI. There can be only one PI on a permit.
The PI may also be the Applicant/Permit Holder and Primary Contact.
You must add Co-investigators (CIs) to the application if the PI will not always be
present during the permitted activities. CIs are individuals who are qualified and
authorized to conduct or directly supervise activities, including import/exporting
activities and laboratory analysis, conducted under a permit without the on-site
supervision of the PI.
Authorized Recipients (ARs) are persons or institutions authorized to receive samples
for the purposes of analysis or curation related to the objectives of your permit. The PI
and CIs may also be ARs. ARs should not be CIs if they are only performing the analysis
and are not overseeing the study or publishing the results (i.e., they are only providing an
analytical service).
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Include a table listing the names of the PI, CIs, and ARs, and the specific procedures they
will oversee or conduct. Attach the table on the Supplemental Information page.
Example Table Attachment: Personnel Roles
Name/Affiliation
Role
Researcher name,
PI, CI, and/or AR
Affiliation, City,
State
John Smith, Ph.D., Principal Investigator and
University A, City, Authorized Recipient
State
Jane Doe, Ph.D.,
Co-Investigator and
Laboratory B,
Authorized Recipient
City, State
John Doe, D.V.M., Co-Investigator and
Institution C, City, Authorized Recipient
State
Jane Smith,
Authorized Recipient
Laboratory D,
City, State
Activities
Specific tissues they will
import/export/receive, type of
analysis, whether supervising
Supervise and perform all
activities under the permit
Import/receive blubber and
conduct fatty acid analysis
Collect lung, heart, and muscle
samples from subsistence-hunted
animals for histology
Receive skin samples for DNA
sequencing
Qualifications and Experience
Federal Regulations require that persons authorized as the PI or CIs have qualifications
commensurate with their duties. In addition, the names of the PI and CIs are sent to the
NOAA Office of Law Enforcement to determine if any violations of the MMPA or ESA
and other environmental laws have occurred.
The permit applicant is therefore required to submit the following information about the
qualifications and experience of the PI and all CIs to demonstrate they have qualifications
commensurate with their duties as stipulated in the Personnel Table. **If sufficient
experience is not provided, the various personnel will not be authorized to conduct the
proposed activities. A CV may be submitted IF it is up to date and contains all relevant
information.
1) Contact information - All documentation submitted will be publicly available.
DO NOT include personal information (e.g., social security number, date of birth,
nationality, or home phone/ address-unless it is also the business phone/address).
Name (first middle last)
Business phone, e-mail, and mailing address
2) Relevant education and training
Degree, major, name of institution, year received
Applicable certificates or licenses, year received
Other relevant training or certification, year received
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3) Relevant experience
Job title, affiliation/location, and dates with detailed description of when
and how the individual obtained experience in the proposed methods they
will be conducting and/or supervising, including how many years they
have been performing or supervising the activities (including specific
sample analysis, tissue handling, etc.)
Whether and to what extent they have performed them without supervision or
have supervised the proposed activities
4) List of grants awarded demonstrating available resources relevant to the
proposed activities or history of securing resources for similar work
5) Annotated publication history relevant to the activities being conducted
under the permit
Submit Application
See Chapter 2 for how to submit your application and check on its status.
Additional Information
Under section 104(c) of the MMPA and section 10(a)(1)(A) of the ESA, persons may be
authorized to take marine mammals and threatened and endangered species, respectively,
for purposes of scientific research or enhancing the survival of the species. Interested
persons are required to submit an application in accordance with the Acts and the
implementing regulations at 50 CFR part 216, subpart D, and 50 CFR part 222. These
instructions for applying for a research or enhancement permit are drawn from, but do not
substitute for, ESA regulations and MMPA regulations. These regulations are available
at the following web site: http://www.gpo.gov/. MMPA section 104 is available at:
http://www.nmfs.noaa.gov/pr/pdfs/laws/mmpa104.pdf. ESA section 10(a)(1)(A) is
available at: http://www.nmfs.noaa.gov/pr/pdfs/laws/esa_section10.pdf.
Paperwork Reduction Act Statement
The information requested in this application is required and is used to determine whether
the activities described in the application are consistent with the purposes and policies of
the Acts and their implementing regulations.
Public reporting burden for this collection of information is estimated to average 20
hours per response (i.e., filling out the above application), including the time for
reviewing instructions, searching existing data sources, gathering and maintaining the
data needed, and completing and reviewing the collection of information. Send comments
regarding this burden estimate or any other aspect of this collection of information,
including suggestions for reducing this burden, to the Chief, Permits and Conservation
Division, Office of Protected Resources, F/PR1, NOAA/National Marine Fisheries
Service, 1315 East-West Highway, Silver Spring, MD 20910.
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All permit documentation, including the application, permit and amendments, reports,
inventory information, and any other associated documents are considered public
information and as such, are subject to the Freedom of Information Act.
Notwithstanding any other provision of the law, no person is required to respond to, nor
shall any person be subject to a penalty for failure to comply with, a collection of
information subject to the requirements of the Paperwork Reduction Act, unless that
collection of information displays a currently valid OMB Control Number.
OMB No. 0648-0084, Expires: Month Day, Year
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File Type | application/pdf |
File Title | Microsoft Word - Parts Instructions_new 2016 |
Author | amy.sloan |
File Modified | 2016-08-15 |
File Created | 2016-08-15 |