95-13961. Burkholderia (Pseudomonas) Cepacia Type Wisconsin; Tolerance Exemption  

  • [Federal Register Volume 60, Number 109 (Wednesday, June 7, 1995)]
    [Proposed Rules]
    [Pages 30048-30050]
    From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
    [FR Doc No: 95-13961]
    
    
    
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    ENVIRONMENTAL PROTECTION AGENCY
    40 CFR Part 180
    
    [PP 0F3885/R2142; FRL-4958-9]
    RIN 2070-AC18
    
    
    Burkholderia (Pseudomonas) Cepacia Type Wisconsin; Tolerance 
    Exemption
    
    AGENCY: Environmental Protection Agency (EPA).
    
    ACTION: Proposed rule.
    
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    SUMMARY: This document proposes that an exemption from the requirement 
    of a tolerance be established for residues of the biological pesticide 
    Burkholderia (Pseudomonas) cepacia type Wisconsin in or on all raw 
    agricultural commodities, resulting from use on plant roots or seedling 
    roots. EPA is proposing this regulation on its own initiative. The 
    proposal would amend the existing tolerance exemption for this 
    organism, which is limited to the seed treatment use.
    
    DATES: Comments identified by the docket number, [PP 0F3885/R2142], 
    must be received on or before July 7, 1995.
    
    ADDRESSES: Submit written comments by mail to: Public Response and 
    Program Resources Branch, Field Operations Division (7506C), Office of 
    Pesticide Programs, Environmental Protection Agency, 401 M St., SW., 
    Washington, DC 20460. In person, bring comments to: Public Docket, Rm. 
    1132, Crystal Mall #2, 1921 Jefferson Davis Hwy., Arlington, VA 22202. 
    Information submitted as a comment concerning this document may be 
    claimed confidential by marking any part or all of that information as 
    ``Confidential Business Information'' (CBI). Information so marked will 
    not be disclosed except in accordance with procedures as set forth in 
    40 CFR part 2. A copy of the comment that does not contain CBI must be 
    submitted for inclusion in the public record. Information not marked 
    confidential will be included in the public docket by EPA without prior 
    notice. The public docket is available for public inspection in Rm. 
    1132 at the above address, from 8 a.m. to 4:30 p.m., Monday through 
    Friday, excluding legal holidays.
        Comments and data may also be submitted electronically by sending 
    electronic mail (e-mail) to: opp-docket@epamail.epa.gov. Electronic 
    comments must be submitted as an ASCII file avoiding the use of special 
    characters and any form of encryption. Comments and data will also be 
    accepted on disks in WordPerfect in 5.1 file format or ASCII file 
    format. All comments and data in electronic form must be identified by 
    the docket number [PP 0F3885/R2142]. No Confidential Business 
    Information (CBI) should be submitted through e-mail. Electronic 
    comments on this proposed rule may be filed online at many Federal 
    Depository Libraries. Additional information on electronic submissions 
    can be found below in this document.
    
    FOR FURTHER INFORMATION CONTACT: By mail: Denise Greenway, 
    Biopesticides and Pollution Prevention Division (7501W), Environmental 
    Protection Agency, 401 M St., SW., Washington, DC 20460. Office 
    location and telephone number: Rm. CS51L6, Crystal Station #1, 2800 
    Crystal Drive, Arlington, VA 22202, (703)-308-8263; e-mail: 
    greenway.denise@epamail.epa.gov.
    
    SUPPLEMENTARY INFORMATION: In the Federal Register of April 3, 1991 (56 
    FR 13642), EPA issued a notice that Stine Microbial Products, 4722 
    Pflaum Rd., Madison, WI 53704, had submitted pesticide petition (PP) 
    0F3885 to EPA proposing to amend 40 CFR part 180 by establishing a 
    regulation pursuant to the Federal Food, Drug and Cosmetic Act (21 
    U.S.C. 346a and 371), to exempt from the requirement of a tolerance the 
    residues of the biological pesticide Pseudomonas cepacia type Wisconsin 
    in or on all raw agricultural commodities when applied as a seed 
    treatment for growing agricultural crops in accordance with good 
    agricultural practices. There were no comments received in response to 
    the notice.
        In the Federal Register of December 23, 1992 (57 FR 61003), an 
    exemption from the requirement of a tolerance was established for 
    residues of the biological pesticide Pseudomonas cepacia type Wisconsin 
    in or on all raw agricultural commodities when applied as a seed 
    treatment for growing agricultural crops in accordance with good 
    agricultural practices.
        Stine Microbial Products has subsequently proposed a new use site, 
    plant roots or seedling roots. Like the seed treatment use for which an 
    exemption from the requirement of a tolerance now exists (40 CFR 
    180.1115), Pseudomonas cepacia type Wisconsin applied to plant roots or 
    seedling roots will colonize the developing root system, and by 
    producing antibiotics, protect the seedling or plant from a range of 
    plant pathogenic fungi and nematodes. The Agency has determined that 
    this presents no new hazard issues and that the following originally 
    submitted data can support the registration for use as a soil, seed, or 
    seedling treatment:
        The organism is a naturally occurring biotype of the bacterial 
    species Pseudomonas cepacia which is found world wide. The original 
    isolates of Pseudomonas cepacia type Wisconsin were identified as 
    colonizers of the roots and rhizospheres of maize. Further testing 
    indicated that this biotype will colonize roots of many crop plants. 
    Pseudomonas cepacia type Wisconsin has been shown to produce 
    antibiotics which are effective against a diverse range of plant 
    pathogenic fungi. Pseudomonas cepacia type Wisconsin is not generally 
    regarded as a human or animal pathogen. Products containing this 
    organism are intended to be used for formulating other end-use products 
    or as a seed treatment (and the proposed plant root and seedling root 
    use). When applied to seeds (or plant or seedling roots), the bacteria 
    colonize the developing root system, and by producing antibiotics, 
    protect the seedling from a range of plant pathogenic fungi and 
    nematodes.
        The data submitted in the petition and other relevant material have 
    been [[Page 30049]] evaluated. The toxicological data considered in 
    support of the exemption from the requirement of a tolerance include an 
    acute oral toxicity/pathogenicity study, an acute dermal toxicity 
    study, an acute pulmonary toxicity/pathogenicity study, and an acute 
    intravenous toxicity/pathogenicity study. All studies were conducted 
    with the rat as the test animal. A review of these studies indicated 
    that the organism was not acutely toxic to test animals when 
    administered via dermal and intravenous routes. The active ingredient 
    was not infective or pathogenic to test animals when administered via 
    the oral, pulmonary, or intravenous route. No reports of 
    hypersensitivity have been recorded from personnel working with this 
    organism. All of the toxicity studies submitted are considered 
    acceptable. The toxicity data provided are sufficient to show that 
    there are no foreseeable health hazards to humans or domestic animals 
    likely to arise from the use of this organism as a seed (or seedling 
    root or plant root) treatment.
        Residue chemistry data were not required; such data are necessary 
    only if the submitted toxicity studies indicate that additional Tier II 
    or Tier III toxicology data are needed. These additional data were not 
    needed. Therefore, no residue data are required to establish an 
    exemption from the requirement of a tolerance for the biological 
    pesticide Pseudomonas cepacia type Wisconsin in or on all raw 
    agricultural commodities when applied to plant roots and seedling roots 
    or used as a seed treatment for growing agricultural crops in 
    accordance with good agricultural practices.
        Acceptable daily intake (ADI) and maximum permissible intake (MPI) 
    considerations are not relevant to this petition because the data 
    submitted demonstrated that this biological control agent is not toxic 
    to humans. No enforcement actions are expected. Therefore, the 
    requirement for an analytical method for enforcement purposes is not 
    applicable to this exemption request.
        The Agency hereby takes the initiative to amend the current 
    tolerance exemption (40 CFR 180.1115) by expanding it to include the 
    proposed use on plant roots and seedling roots. The Agency also 
    proposes that the exemption from the requirement of a tolerance be 
    further amended to update the organism name. There has been a recent 
    change in the bacterial taxonomy affecting the generic affiliation of 
    the RNA group II pseudomonads and moving them from the genus 
    Pseudomonas to the newly described genus Burkholderia. To reduce 
    confusion by completely changing the organism name, it is proposed that 
    the former genus name be inserted parenthetically after the new one, 
    Burkholderia (Pseudomonas) cepacia.
        Burkholderia (Pseudomonas) cepacia type Wisconsin is considered 
    useful for the purposes for which the exemption from the requirement of 
    a tolerance is sought. Based on the information considered, the Agency 
    concludes that the establishment of a tolerance is not necessary to 
    protect the public health. Therefore, EPA proposes that an exemption 
    from the requirement of a tolerance be established as set forth below.
        Any person who has registered or submitted an application for 
    registration of a pesticide under the Federal Insecticide, Fungicide, 
    and Rodenticide Act (FIFRA) as amended, which contains the ingredient 
    listed herein, may request within 30 days after the publication of this 
    document in the Federal Register that this rulemaking proposal be 
    referred to an Advisory Committee in accordance with section 408(e) of 
    the Federal Food, Drug, and Cosmetic Act (FFDCA).
        Interested persons are invited to submit written comments on the 
    proposed regulation. Comments must bear a notation indicating the 
    document control number, [PP 0F3885/R2142]. All written comments filed 
    in response to this petition will be available in the Public Response 
    and Program Resources Branch at the above address from 8 a.m. to 4:30 
    p.m., Monday through Friday, except legal holidays.
         A record has been established for this rulemaking under docket 
    number [PP 0F3885/R2142] (including comments and data submitted 
    electronically as described below). A public version of this record, 
    including printed, paper versions of electronic comments, which does 
    not include any information claimed as CBI, is available for inspection 
    from 8 a.m. to 4:30 p.m., Monday through Friday, excluding legal 
    holidays. The public record is located in Room 1132 of the Public 
    Response and Program Resources Branch, Field Operations Division 
    (7506C), Office of Pesticide Programs, Environmental Protection Agency, 
    Crystal Mall #2, 1921 Jefferson Davis Highway, Arlington, VA.
        Electronic comments can be sent directly to EPA at:
        opp-Docket@epamail.epa.gov
    
    
        Electronic comments must be submitted as an ASCII file avoiding the 
    use of special characters and any form of encryption.
        The official record for this rulemaking, as well as the public 
    version, as described above will be kept in paper form. Accordingly, 
    EPA will transfer all comments received electronically into printed, 
    paper form as they are received and will place the paper copies in the 
    official rulemaking record which will also include all comments 
    submitted directly in writing. The official rulemaking record is the 
    paper record maintained at the address in ``ADDRESSES'' at the 
    beginning of this document.
        The Office of Management and Budget has exempted this document from 
    the requirement of review pursuant to Executive Order 12866.
        Pursuant to the requirements of the Regulatory Flexibility Act 
    (Pub. L. 96-354, 94 Stat. 1164, 5 U.S.C. 601-612), the Administrator 
    has determined that regulations establishing new tolerances or raising 
    tolerance levels or establishing exemptions from tolerance requirements 
    do not have a significant economic impact on a substantial number of 
    small entities. A certification statement to this effect was published 
    in the Federal Register of May 4, 1981 (46 FR 24950).
    
    List of Subjects in 40 CFR Part 180
    
        Environmental protection, Administrative practice and procedure, 
    Agricultural commodities, Pesticides and pests, Reporting and 
    recordkeeping requirements.
    
        Dated: June 1, 1995.
    
    Janet L. Andersen,
    Acting Director, Biopesticides and Pollution Prevention Division, 
    Office of Pesticide Programs.
    
        Therefore, it is proposed that 40 CFR part 180 be amended as 
    follows:
    
    PART 180--[AMENDED]
    
        1. The authority citation for part 180 continues to read as 
    follows:
    
        Authority: 21 U.S.C. 346a and 371.
    
        2. Section 180.1115 is revised to read as follows:
    
    
    Sec. 180.1115   Burkholderia (Pseudomonas) cepacia type Wisconsin; 
    exemption from the requirement of a tolerance.
    
        The biological pesticide Burkholderia (Pseudomonas) cepacia type 
    Wisconsin is exempted from the requirement of a tolerance in or on all 
    raw agricultural commodities when applied to plant roots and seedling 
    roots, or as a seed treatment for growing agricultural crops 
    [[Page 30050]] in accordance with good agricultural practices.
    
    [FR Doc. 95-13961 Filed 6-6-95; 8:45 am]
    BILLING CODE 6560-50-F
    
    

Document Information

Published:
06/07/1995
Department:
Environmental Protection Agency
Entry Type:
Proposed Rule
Action:
Proposed rule.
Document Number:
95-13961
Dates:
Comments identified by the docket number, [PP 0F3885/R2142], must be received on or before July 7, 1995.
Pages:
30048-30050 (3 pages)
Docket Numbers:
PP 0F3885/R2142, FRL-4958-9
RINs:
2070-AC18
PDF File:
95-13961.pdf
CFR: (1)
40 CFR 180.1115