81 FR 27332 - Methoxyfenozide; Pesticide Tolerances for Emergency Exemptions
ENVIRONMENTAL PROTECTION AGENCY Federal Register Volume 81, Issue 88 (May 6, 2016)
Federal Register Volume 81, Issue 88 (May 6, 2016)
| Page Range | 27332-27337 | |
| FR Document | 2016-09969 |
[Federal Register Volume 81, Number 88 (Friday, May 6, 2016)] [Rules and Regulations] [Pages 27332-27337] From the Federal Register Online [www.thefederalregister.org] [FR Doc No: 2016-09969] ----------------------------------------------------------------------- ENVIRONMENTAL PROTECTION AGENCY 40 CFR Part 180 [EPA-HQ-OPP-2014-0591; FRL-9945-28] Methoxyfenozide; Pesticide Tolerances for Emergency Exemptions AGENCY: Environmental Protection Agency (EPA). ACTION: Final rule. ----------------------------------------------------------------------- SUMMARY: This regulation establishes time-limited tolerances for residues of methoxyfenozide in or on rice, grain and rice, bran resulting from use of methoxyfenozide in accordance with the terms of an emergency exemption issued under section 18 of the Federal Insecticide, Fungicide, and Rodenticide Act (FIFRA). This action is in response to the California Department of Pesticide Regulation's issuance of a crisis emergency exemption under FIFRA section 18 authorizing use of the pesticide on rice, bran and rice, grain. This time-limited tolerance regulation establishes a maximum permissible level for residues of methoxyfenozide in or on these commodities. These time-limited tolerances expire on December 31, 2019. DATES: This regulation is effective May 6, 2016. Objections and requests for hearings must be received on or before July 5, 2016, and must be filed in accordance with the instructions provided in 40 CFR part 178 (see also Unit I.C. of the SUPPLEMENTARY INFORMATION). ADDRESSES: The docket for this action, identified by docket identification (ID) number EPA-HQ-OPP-2014-0591, is available at http://www.regulations.gov or at the Office of Pesticide Programs Regulatory Public Docket (OPP Docket) in the Environmental Protection Agency Docket Center (EPA/DC), West William Jefferson Clinton Bldg., Rm. 3334, 1301 Constitution Ave. NW., Washington, DC 20460-0001. The Public Reading Room is open from 8:30 a.m. to 4:30 p.m., Monday through Friday, excluding legal holidays. The telephone number for the Public Reading Room is (202) 566-1744, and the telephone number for the OPP Docket is (703) 305-5805. Please review the visitor instructions and additional information about the docket available at http://www.epa.gov/dockets. FOR FURTHER INFORMATION CONTACT: Susan Lewis, Registration Division (7505P), Office of Pesticide Programs, Environmental Protection Agency, 1200 Pennsylvania Ave. NW., Washington, DC 20460-0001; main telephone number: (703) 305-7090; email address: [email protected]. SUPPLEMENTARY INFORMATION: I. General Information A. Does this action apply to me? You may be potentially affected by this action if you are an agricultural producer, food manufacturer, or pesticide manufacturer. The following list of North American Industrial Classification System (NAICS) codes is not intended to be exhaustive, but rather provides a guide to help readers determine whether this document applies to them. Potentially affected entities may include:[emsp14]Crop production (NAICS code 111). [emsp14]Animal production (NAICS code 112). [emsp14]Food manufacturing (NAICS code 311). [emsp14]Pesticide manufacturing (NAICS code 32532). B. How can I get electronic access to other related information? You may access a frequently updated electronic version of 40 CFR part 180 through the Government Printing Office's e-CFR site at http://www.ecfr.gov/cgi-bin/text-idx?&c=ecfr&tpl=/ecfrbrowse/Title40/40tab_02.tpl. C. How can I file an objection or hearing request? Under section 408(g) of the Federal Food, Drug, and Cosmetic Act (FFDCA), 21 U.S.C. 346a, any person may file an objection to any aspect of this regulation and may also request a hearing on those [[Page 27333]] objections. You must file your objection or request a hearing on this regulation in accordance with the instructions provided in 40 CFR part 178. To ensure proper receipt by EPA, you must identify docket ID number EPA-HQ-OPP-2014-0591 in the subject line on the first page of your submission. All objections and requests for a hearing must be in writing, and must be received by the Hearing Clerk on or before July 5, 2016. Addresses for mail and hand delivery of objections and hearing requests are provided in 40 CFR 178.25(b). In addition to filing an objection or hearing request with the Hearing Clerk as described in 40 CFR part 178, please submit a copy of the filing (excluding any Confidential Business Information (CBI)) for inclusion in the public docket. Information not marked confidential pursuant to 40 CFR part 2 may be disclosed publicly by EPA without prior notice. Submit the non-CBI copy of your objection or hearing request, identified by docket ID number EPA-HQ-OPP-2014-0591, by one of the following methods: Federal eRulemaking Portal: http://www.regulations.gov. Follow the online instructions for submitting comments. Do not submit electronically any information you consider to be CBI or other information whose disclosure is restricted by statute. Mail: OPP Docket, Environmental Protection Agency Docket Center (EPA/DC), (28221T), 1200 Pennsylvania Ave. NW., Washington, DC 20460-0001. Hand Delivery: To make special arrangements for hand delivery or delivery of boxed information, please follow the instructions at http://www.epa.gov/dockets/contacts.html. Additional instructions on commenting or visiting the docket, along with more information about dockets generally, is available at http://www.epa.gov/dockets. II. Background and Statutory Findings EPA, on its own initiative, in accordance with FFDCA sections 408(e) and 408(l)(6) of, 21 U.S.C. 346a(e) and 346a(1)(6), is establishing time-limited tolerances for residues of methoxyfenozide in or on rice, bran and rice, grain at 4.0 and 0.50 parts per million (ppm), respectively. These time-limited tolerances expire on December 31, 2019. Section 408(l)(6) of FFDCA requires EPA to establish a time-limited tolerance or exemption from the requirement for a tolerance for pesticide chemical residues in food that will result from the use of a pesticide under an emergency exemption granted by EPA under FIFRA section 18. Such tolerances can be established without providing notice or period for public comment. EPA does not intend for its actions on FIFRA section 18 related time-limited tolerances to set binding precedents for the application of FFDCA section 408 and the safety standard to other tolerances and exemptions. Section 408(e) of FFDCA allows EPA to establish a tolerance or an exemption from the requirement of a tolerance on its own initiative, i.e., without having received any petition from an outside party. Section 408(b)(2)(A)(i) of FFDCA allows EPA to establish a tolerance (the legal limit for a pesticide chemical residue in or on a food) only if EPA determines that the tolerance is ``safe.'' Section 408(b)(2)(A)(ii) of FFDCA defines ``safe'' to mean that ``there is a reasonable certainty that no harm will result from aggregate exposure to the pesticide chemical residue, including all anticipated dietary exposures and all other exposures for which there is reliable information.'' This includes exposure through drinking water and in residential settings, but does not include occupational exposure. Section 408(b)(2)(C) of FFDCA requires EPA to give special consideration to exposure of infants and children to the pesticide chemical residue in establishing a tolerance and to ``ensure that there is a reasonable certainty that no harm will result to infants and children from aggregate exposure to the pesticide chemical residue. . . .'' Section 18 of FIFRA authorizes EPA to exempt any Federal or State agency from any provision of FIFRA, if EPA determines that ``emergency conditions exist which require such exemption.'' EPA has established regulations governing such emergency exemptions in 40 CFR part 166. III. Emergency Exemption for Methoxyfenozide on Rice, Grain and Rice, Bran and FFDCA Tolerances The California Department of Pesticide Regulation asserted that an emergency condition existed in accordance with the criteria for approval of an emergency exemption, and utilized a crisis exemption under FIFRA section 18 to allow the use of methoxyfenozide on rice to control armyworm and Western yellow striped armyworm in Butte, Glenn, Sacramento, Sutter, Yolo, and Yuba counties. The California Department of Pesticide Regulation invoked the crisis exemption provision on August 27, 2015. After having reviewed the submission and determining that the risks associated with the emergency use were reasonable in comparison to the expected benefits to the California rice growers who faced the largest outbreak of armyworms in 25 years and significant economic loss, EPA concurred on the crisis exemption. The crisis exemption expired on September 10, 2015. As part of its evaluation of the emergency exemption application, EPA assessed the potential risks presented by residues of methoxyfenozide in or on rice, bran and rice, grain. In doing so, EPA considered the safety standard in FFDCA section 408(b)(2), and EPA decided that the necessary tolerances under FFDCA section 408(l)(6) would be consistent with the safety standard and with FIFRA section 18. Consistent with the need to move quickly on the emergency exemption in order to address an urgent non-routine situation and to ensure that the resulting food is safe and lawful, EPA is issuing these tolerances without notice and opportunity for public comment as provided in FFDCA section 408(l)(6). Although these time-limited tolerances expire on December 31, 2019, under FFDCA section 408(l)(5), residues of the pesticide not in excess of the amounts specified in the tolerances remaining in or on rice, bran and rice, grain after that date will not be unlawful, provided the pesticide was applied in a manner that was lawful under FIFRA, and the residues do not exceed a level that was authorized by these time-limited tolerances at the time of that application. EPA will take action to revoke these time-limited tolerances earlier if any experience with, scientific data on, or other relevant information on this pesticide indicate that the residues are not safe. Because these time-limited tolerances are being approved under emergency conditions, EPA has not made any decisions about whether methoxyfenozide meets FIFRA's registration requirements for use on rice, grain and rice, bran or whether permanent tolerances for this use would be appropriate. Under these circumstances, EPA does not believe that these time-limited tolerance decisions serve as a basis for registration of methoxyfenozide by a State for special local needs under FIFRA section 24(c). Nor do these tolerances by themselves serve as the authority for persons in any State other than California to use this pesticide on the applicable crops under FIFRA section 18 absent the issuance of an emergency exemption applicable within that State. For additional information regarding the crisis emergency exemption for methoxyfenozide, contact the Agency's Registration Division at the address [[Page 27334]] provided under FOR FURTHER INFORMATION CONTACT. IV. Aggregate Risk Assessment and Determination of Safety Section 408(b)(2)(A)(i) of FFDCA allows EPA to establish a tolerance (the legal limit for a pesticide chemical residue in or on a food) only if EPA determines that the tolerance is ``safe.'' Section 408(b)(2)(A)(ii) of FFDCA defines ``safe'' to mean that ``there is a reasonable certainty that no harm will result from aggregate exposure to the pesticide chemical residue, including all anticipated dietary exposures and all other exposures for which there is reliable information.'' This includes exposure through drinking water and in residential settings, but does not include occupational exposure. Section 408(b)(2)(C) of FFDCA requires EPA to give special consideration to exposure of infants and children to the pesticide chemical residue in establishing a tolerance and to ``ensure that there is a reasonable certainty that no harm will result to infants and children from aggregate exposure to the pesticide chemical residue. . . .'' Consistent with the factors specified in FFDCA section 408(b)(2)(D), EPA has reviewed the available scientific data and other relevant information in support of this action. EPA has sufficient data to assess the hazards of and to make a determination on aggregate exposure expected as a result of this emergency exemption request and the time-limited tolerances for residues of methoxyfenozide on rice, bran and rice, grain at 4.0 and 0.50 ppm, respectively, measured as 3- methoxy-2-methylbenzoic acid 2-(3,5-dimethylbenzoyl)-2-(1,1- dimethylethyl)-hydrazide. EPA's assessment of exposures and risks associated with establishing time-limited tolerances follows. A. Toxicological Points of Departure/Levels of Concern Once a pesticide's toxicological profile is determined, EPA identifies toxicological points of departure (POD) and levels of concern to use in evaluating the risk posed by human exposure to the pesticide. For hazards that have a threshold below which there is no appreciable risk, the toxicological POD is used as the basis for derivation of reference values for risk assessment. PODs are developed based on a careful analysis of the doses in each toxicological study to determine the dose at which no adverse effects are observed (the NOAEL) and the lowest dose at which adverse effects of concern are identified (the LOAEL). Uncertainty/safety factors are used in conjunction with the POD to calculate a safe exposure level--generally referred to as a population-adjusted dose (PAD) or a reference dose (RfD)--and a safe margin of exposure (MOE). For non-threshold risks, the Agency assumes that any amount of exposure will lead to some degree of risk. Thus, the Agency estimates risk in terms of the probability of an occurrence of the adverse effect expected in a lifetime. For more information on the general principles EPA uses in risk characterization and a complete description of the risk assessment process, see http://www.epa.gov/pesticides/factsheets/riskassess.htm. A summary of the toxicological endpoints for methoxyfenozide used for human risk assessment is discussed in Table 1 of Unit III B. of the final rule published in the Federal Register of August 27, 2014 (79 FR 51103) (FRL-9913-99). Further, the Agency's exposure and risk assessment for the emergency use on rice, bran and rice, grain is discussed in greater detail in ``Methoxyfenozide: Human Health Risk Assessment for the Proposed Use of the Insecticide (Associated with Section 18 Registration) on Rice in California,'' January 5, 2016 is available in the docket at the address provided under ADDRESSES. B. Exposure Assessment 1. Dietary exposure from food and feed uses. In evaluating dietary exposure to methoxyfenozide, EPA considered exposure under the time- limited tolerances established by this action as well as all existing methoxyfenozide tolerances in 40 CFR 180.544. EPA assessed dietary exposures from methoxyfenozide in food as follows: i. Acute exposure. Quantitative acute dietary exposure and risk assessments are performed for a food-use pesticide, if a toxicological study has indicated the possibility of an effect of concern occurring as a result of a 1-day or single exposure. No such effects were identified in the toxicological studies for methoxyfenozide; therefore, a quantitative acute dietary exposure assessment is unnecessary. ii. Chronic exposure. In conducting the chronic aggregate dietary (food and drinking water) exposure and risk assessment, EPA used the Dietary Exposure Evaluation Model software (Version 3.16) with the Food Commodity Intake Database (DEEM-FCID). This software includes 2003 to 2008 food consumption data from the United States Department of Agriculture's (USDA's) National Health and Nutrition Examination Survey, What We Eat in America (NHANES/WWEIA). All current and proposed uses of methoxyfenozide, were included in this assessment. As to residue levels in food, the chronic dietary assessment assumes 100% crop treated (PCT). DEEM (Version 7.81) default processing factors were used for most processed commodities that do not have individual tolerances. The only exception was a processing factor of 0.2X that was used for orange juice from a processing study. The chronic dietary assessment is highly conservative (protective); therefore, providing an upper-bound estimate of dietary exposure and risk. iii. Cancer. Based on the data referenced in Unit IV.A., EPA has concluded that methoxyfenozide should be classified as ``Not Likely to Be Carcinogenic to Humans.'' As a result, a cancer dietary exposure assessment for the purpose of assessing cancer risk is unnecessary for methoxyfenozide, and was not conducted. 2. Dietary exposure from drinking water. The residues of concern in drinking water are methoxyfenozide and the degradates, RH-117,236 and RH-131,154, which are only present at low concentrations. The Agency used screening-level water exposure models in the dietary exposure analysis and risk assessment for methoxyfenozide and its degradates in drinking water. These simulation models take into account data on the physical, chemical, and fate/transport characteristics of methoxyfenozide and its degradates. Further information regarding EPA drinking water models used in pesticide exposure assessment can be found at http://www.epa.gov/oppefed1/models/water/index.htm. Based on the FPQA Index Reservoir Screening Tool (FIRST), Screening Concentration in Ground Water (SCI-GROW), and the Pesticide Root Zone Model Ground Water (PRZM GW) models, the estimated drinking water concentrations (EDWCs) of methoxyfenozide and its degradates for chronic exposures for non-cancer assessments are estimated to be 7.57 parts per billion (ppb) for surface water and 214 ppb for ground water. Modeled estimates of drinking water concentrations were directly entered into the dietary exposure model. For chronic dietary risk assessment, the water concentration of value 214 ppb was used to assess the contribution to drinking water. 3. From non-dietary exposure. The term ``residential exposure'' is used in this document to refer to non-occupational, non-dietary exposure [[Page 27335]] (e.g., for lawn and garden pest control, indoor pest control, termiticides, and flea and tick control on pets). Methoxyfenozide is currently registered for use on ornamentals in and around home gardens, which could result in residential exposures. EPA assessed residential exposure using the following assumptions: Residential handlers were assessed for potential short-term inhalation exposures from mixing, loading, and applying methoxyfenozide. A quantitative dermal assessment for residential handlers was not conducted since there is no systemic toxicity associated with dermal exposures to methoxyfenozide. Adult post-application exposures were not quantitatively assessed since no dermal hazard was identified for methoxyfenozide and inhalation exposures are typically negligible in outdoor settings. Furthermore, the inhalation exposure assessment performed for residential handlers is representative of worse case inhalation exposures and is considered protective for post-application inhalation exposure scenarios. Post-application oral exposure to children is not expected since the extent to which young children engage in activities associated with areas where treated ornamentals are grown (or utilize these areas for prolonged periods of play) is low. Therefore, an incidental oral post- application exposure assessment was not conducted. Further information regarding EPA standard assumptions and generic inputs for residential exposures may be found at http://www.epa.gov/pesticides/trac/science/trac6a05.pdf. 4. Cumulative effects from substances with a common mechanism of toxicity. Section 408(b)(2)(D)(v) of FFDCA requires that, when considering whether to establish, modify, or revoke a tolerance, the Agency consider ``available information'' concerning the cumulative effects of a particular pesticide's residues and ``other substances that have a common mechanism of toxicity.'' EPA has not found methoxyfenozide to share a common mechanism of toxicity with any other substances, and methoxyfenozide does not appear to produce a toxic metabolite produced by other substances. For the purposes of this tolerance action, therefore, EPA has assumed that methoxyfenozide does not have a common mechanism of toxicity with other substances. For information regarding EPA's efforts to determine which chemicals have a common mechanism of toxicity and to evaluate the cumulative effects of such chemicals, see EPA's Web site at http://www.epa.gov/pesticides/cumulative. C. Safety Factor for Infants and Children 1. In general. Section 408(b)(2)(C) of FFDCA provides that EPA shall apply an additional tenfold (10X) margin of safety for infants and children in the case of threshold effects to account for prenatal and postnatal toxicity and the completeness of the database on toxicity and exposure unless EPA determines based on reliable data that a different margin of safety will be safe for infants and children. This additional margin of safety is commonly referred to as the Food Quality Protection Act Safety Factor (FQPA SF). In applying this provision, EPA either retains the default value of 10X, or uses a different additional SF when reliable data available to EPA support the choice of a different factor. 2. Prenatal and postnatal sensitivity. There is no evidence of qualitative or quantitative susceptibility of the developing fetus or offspring, based on the developmental and reproductive toxicity study results for methoxyfenozide. No developmental toxicity was observed in either the rat or rabbit developmental toxicity studies, and there was no evidence of offspring or reproductive toxicity in the rat two- generation reproductive toxicity study. 3. Conclusion. EPA has determined that reliable data show the safety of infants and children would be adequately protected if the FQPA SF were reduced to 1X. That decision is based on the following findings: i. The toxicity database for methoxyfenozide is complete, including studies addressing potential pre- and post-natal susceptibility, neurotoxicity, and immunotoxicity. ii. There is no evidence that methoxyfenozide is neurotoxic, and a developmental neurotoxicity study or additional uncertainty factors (UFs) to account for neurotoxicity are not required. iii. There is no residual uncertainty, and no evidence increased susceptibility in the developing or young animal. iv. The dietary exposure assessments do not underestimate potential exposure from food and drinking water, and the use pattern indicates a low potential for residential exposure. D. Aggregate Risks and Determination of Safety EPA determines whether acute and chronic dietary pesticide exposures are safe by comparing aggregate exposure estimates to the acute PAD (aPAD) and chronic PAD (cPAD). For linear cancer risks, EPA calculates the lifetime probability of acquiring cancer given the estimated aggregate exposure. Short-, intermediate-, and chronic-term risks are evaluated by comparing the estimated aggregate food, water, and residential exposure to the appropriate PODs to ensure that an adequate MOE exists. 1. Acute risk. An acute aggregate risk assessment takes into account acute exposure estimates from dietary consumption of food and drinking water. No adverse effect resulting from a single oral exposure was identified and so, there is no acute dietary endpoint of concern. Therefore, methoxyfenozide is not expected to pose an acute risk. 2. Chronic risk. Using the exposure assumptions described in this unit for chronic exposure, EPA has concluded that chronic exposure to methoxyfenozide from food and water will utilize 84% of the cPAD for children 1 to 2 years old, the population group receiving the greatest exposure. Based on the explanation regarding residential use patterns, chronic residential exposure to residues of methoxyfenozide is not expected. 3. Short-term risk. Short-term aggregate exposure takes into account short-term residential exposure plus chronic exposure to food and water (considered to be a background exposure level). Methoxyfenozide is currently registered for uses that could result in short-term residential exposure, and the Agency has determined that it is appropriate to aggregate chronic exposure through food and water with short-term residential exposures to methoxyfenozide. Using the exposure assumptions described in this unit for short- term exposures, EPA has concluded the combined short-term food, water, and residential exposures result in an aggregate MOE of 540. Because EPA's level of concern for methoxyfenozide is a MOE of 100 or below, these MOEs are not of concern. 4. Intermediate-term risk. Intermediate-term aggregate exposure takes into account intermediate-term residential exposure plus chronic exposure to food and water (considered to be a background exposure level). An intermediate-term adverse effect was identified; however, methoxyfenozide is not registered for any use patterns that would result in intermediate-term residential exposure. Intermediate-term risk is assessed based on intermediate-term residential exposure plus chronic dietary exposure. Because there is no intermediate-term residential exposure and chronic dietary exposure has [[Page 27336]] already been assessed under the appropriately protective cPAD (which is at least as protective as the POD used to assess intermediate-term risk), no further assessment of intermediate-term risk is necessary, and EPA relies on the chronic dietary risk assessment for evaluating intermediate-term risk for methoxyfenozide. 5. Aggregate cancer risk for U.S. population. Based on the lack of evidence of carcinogenicity in two adequate rodent carcinogenicity studies, methoxyfenozide is not expected to pose a cancer risk to humans. 6. Determination of safety. Based on these risk assessments, EPA concludes that there is a reasonable certainty that no harm will result to the general population, or to infants and children from aggregate exposure to methoxyfenozide residues. EPA concludes that there is reasonable certainty that no harm will result to the general population, or to infants and children, from aggregate exposure to methoxyfenozide residues because the Section 18 emergency use of methoxyfenozide on rice will result in negligible increases in dietary exposure to all subgroups relative to the safety findings reached in the August 27, 2014 Federal Register document. V. Other Considerations A. Analytical Enforcement Methodology An adequate enforcement methodology is available to enforce the tolerance expression, using high performance liquid chromatography (HPLC), with either tandem mass spectrometric detection (LC-MS/MS), or ultraviolet detection (UV). The method may be requested from: Chief, Analytical Chemistry Branch, Environmental Science Center, 701 Mapes Rd., Ft. Meade, MD 20755-5350; telephone number: (410) 305-2905; email address: [email protected]. B. International Residue Limits In making its tolerance decisions, EPA seeks to harmonize U.S. tolerances with international standards whenever possible, consistent with U.S. food safety standards and agricultural practices. EPA considers the international maximum residue limits (MRLs) established by the Codex Alimentarius Commission (Codex), as required by FFDCA section 408(b)(4). The Codex Alimentarius is a joint United Nations Food and Agriculture Organization/World Health Organization food standards program, and it is recognized as an international food safety standards-setting organization in trade agreements to which the United States is a party. EPA may establish a tolerance that is different from a Codex MRL; however, FFDCA section 408(b)(4) requires that EPA explain the reasons for departing from the Codex level. There are currently no established Codex or Canadian MRLs for methoxyfenozide residues in rice commodities. VI. Conclusion Therefore, time-limited tolerances are established for residues of methoxyfenozide, (3-methoxy-2-methylbenzoic acid 2-(3,5- dimethylbenzoyl)-2-(1,1-dimethylethyl)-hydrazide), in or on rice, grain at 0.50 ppm; and rice, bran at 4.0 ppm. These tolerances will expire on December 31, 2019. VII. Statutory and Executive Order Reviews This action establishes tolerances under FFDCA sections 408(e) and 408(l)(6). The Office of Management and Budget (OMB) has exempted these types of actions from review under Executive Order 12866, entitled ``Regulatory Planning and Review'' (58 FR 51735, October 4, 1993). Because this action has been exempted from review under Executive Order 12866, this action is not subject to Executive Order 13211, entitled ``Actions Concerning Regulations That Significantly Affect Energy Supply, Distribution, or Use'' (66 FR 28355, May 22, 2001) or Executive Order 13045, entitled ``Protection of Children from Environmental Health Risks and Safety Risks'' (62 FR 19885, April 23, 1997). This action does not contain any information collections subject to OMB approval under the Paperwork Reduction Act (PRA), 44 U.S.C. 3501 et seq., nor does it require any special considerations under Executive Order 12898, entitled ``Federal Actions to Address Environmental Justice in Minority Populations and Low-Income Populations'' (59 FR 7629, February 16, 1994). Since tolerances and exemptions that are established in accordance with FFDCA sections 408(e) and 408(l)(6), such as the tolerances in this final rule, do not require the issuance of a proposed rule, the requirements of the Regulatory Flexibility Act (RFA) (5 U.S.C. 601 et seq.) do not apply. This action directly regulates growers, food processors, food handlers, and food retailers, not States or tribes, nor does this action alter the relationships or distribution of power and responsibilities established by Congress in the preemption provisions of FFDCA section 408(n)(4). As such, the Agency has determined that this action will not have a substantial direct effect on States or tribal governments, on the relationship between the national government and the States or tribal governments, or on the distribution of power and responsibilities among the various levels of government or between the Federal Government and Indian tribes. Thus, the Agency has determined that Executive Order 13132, entitled ``Federalism'' (64 FR 43255, August 10, 1999) and Executive Order 13175, entitled ``Consultation and Coordination with Indian Tribal Governments'' (65 FR 67249, November 9, 2000) do not apply to this action. In addition, this action does not impose any enforceable duty or contain any unfunded mandate as described under Title II of the Unfunded Mandates Reform Act (UMRA) (2 U.S.C. 1501 et seq.). This action does not involve any technical standards that would require Agency consideration of voluntary consensus standards pursuant to section 12(d) of the National Technology Transfer and Advancement Act (NTTAA) (15 U.S.C. 272 note). VIII. Congressional Review Act Pursuant to the Congressional Review Act (5 U.S.C. 801 et seq.), EPA will submit a report containing this rule and other required information to the U.S. Senate, the U.S. House of Representatives, and the Comptroller General of the United States prior to publication of the rule in the Federal Register. This action is not a ``major rule'' as defined by 5 U.S.C. 804(2). List of Subjects in 40 CFR Part 180 Environmental protection, Administrative practice and procedure, Agricultural commodities, Pesticides and pests, Reporting and recordkeeping requirements. Dated: April 21, 2016. Daniel J. Rosenblatt, Acting Director, Registration Division, Office of Pesticide Programs. Therefore, 40 CFR chapter I is amended as follows: PART 180--[AMENDED] 0 1. The authority citation for part 180 continues to read as follows: Authority: 21 U.S.C. 321(q), 346a and 371. 0 2. In Sec. 180.544, revise paragraph (b) to read as follows: Sec. 180.544 Methoxyfenozide; tolerances for residues. * * * * * [[Page 27337]] (b) Section 18 emergency exemptions. Time-limited tolerances are established for residues of the insecticide methoxyfenozide, including its metabolites and degradates in or on the commodities listed in the table below, resulting from use of the pesticide under a Section 18 emergency exemption granted by EPA. Compliance with the tolerance levels specified in the following table is to be determined by measuring only methoxyfenozide (3-methoxy-2-methylbenzoic acid 2-(3,5- dimethylbenzoyl)-2-(1,1-dimethylethyl) hydrazide) in or on the commodity. ------------------------------------------------------------------------ Parts per Commodity million Expiration/ revocation date ------------------------------------------------------------------------ Rice, bran..................... 4.0 December 31, 2019. Rice, grain.................... 0.50 December 31, 2019. ------------------------------------------------------------------------ * * * * * [FR Doc. 2016-09969 Filed 5-5-16; 8:45 am] BILLING CODE 6560-50-P
![27332 Federal Register / Vol. 81, No. 88 / Friday, May 6, 2016 / Rules and Regulations
is published in the Federal Register. challenged later in proceedings to PART 52—APPROVAL AND
This action is not a ‘‘major rule’’ as enforce its requirements. (See section PROMULGATION OF
defined by 5 U.S.C. 804(2). 307(b)(2).) IMPLEMENTATION PLANS
Under section 307(b)(1) of the CAA, List of Subjects in 40 CFR Part 52
petitions for judicial review of this ■ 1. The authority citation for part 52
continues to read as follows:
action must be filed in the United States Environmental protection, Air
Court of Appeals for the appropriate pollution control, Incorporation by Authority: 42 U.S.C. 7401 et seq.
circuit by July 5, 2016. Filing a petition reference, Intergovernmental relations, ■ 2. In § 52.770 the table in paragraph
for reconsideration by the Administrator Reporting and recordkeeping (d) is amended by adding new entries
of this final rule does not affect the requirements, Sulfur oxides. for ‘‘A.B. Brown Generating Station’’
finality of this action for the purposes of and ‘‘Clifty Creek Generating Station’’,
Dated: April 27, 2016.
judicial review nor does it extend the to read as follows:
time within which a petition for judicial Robert A. Kaplan,
review may be filed, and shall not Acting Regional Administrator, Region 5. § 52.770 Identification of plan.
postpone the effectiveness of such rule * * * * *
or action. This action may not be 40 CFR part 52 is amended as follows: (d) * * *
EPA-APPROVED INDIANA SOURCE-SPECIFIC PROVISIONS
CO date Title SIP rule EPA approval Explanation
* * * * * * *
1/11/2016 ............... A.B. Brown Gener- N.A. 5/6/16, [insert Federal Reg- Limitation intended to support attainment designation.
ating Station. ister citation].
2/1/2016 ................. Clifty Creek Gen- N.A. 5/6/16, [insert Federal Reg- Limitation intended to support attainment designation.
erating Station. ister citation].
* * * * * DATES: This regulation is effective May I. General Information
[FR Doc. 2016–10579 Filed 5–5–16; 8:45 am] 6, 2016. Objections and requests for
A. Does this action apply to me?
BILLING CODE 6560–50–P hearings must be received on or before
July 5, 2016, and must be filed in You may be potentially affected by
accordance with the instructions this action if you are an agricultural
ENVIRONMENTAL PROTECTION provided in 40 CFR part 178 (see also producer, food manufacturer, or
AGENCY Unit I.C. of the SUPPLEMENTARY pesticide manufacturer. The following
INFORMATION). list of North American Industrial
40 CFR Part 180 Classification System (NAICS) codes is
ADDRESSES: The docket for this action, not intended to be exhaustive, but rather
[EPA–HQ–OPP–2014–0591; FRL–9945–28] identified by docket identification (ID) provides a guide to help readers
number EPA–HQ–OPP–2014–0591, is determine whether this document
Methoxyfenozide; Pesticide Tolerances available at http://www.regulations.gov applies to them. Potentially affected
for Emergency Exemptions or at the Office of Pesticide Programs entities may include:
Regulatory Public Docket (OPP Docket) • Crop production (NAICS code 111).
AGENCY: Environmental Protection in the Environmental Protection Agency • Animal production (NAICS code
Agency (EPA). Docket Center (EPA/DC), West William 112).
ACTION: Final rule. Jefferson Clinton Bldg., Rm. 3334, 1301 • Food manufacturing (NAICS code
Constitution Ave. NW., Washington, DC 311).
SUMMARY: This regulation establishes 20460–0001. The Public Reading Room • Pesticide manufacturing (NAICS
time-limited tolerances for residues of is open from 8:30 a.m. to 4:30 p.m., code 32532).
methoxyfenozide in or on rice, grain Monday through Friday, excluding legal
and rice, bran resulting from use of holidays. The telephone number for the B. How can I get electronic access to
methoxyfenozide in accordance with Public Reading Room is (202) 566–1744, other related information?
the terms of an emergency exemption and the telephone number for the OPP You may access a frequently updated
issued under section 18 of the Federal Docket is (703) 305–5805. Please review electronic version of 40 CFR part 180
Insecticide, Fungicide, and Rodenticide the visitor instructions and additional through the Government Printing
Act (FIFRA). This action is in response information about the docket available Office’s e-CFR site at http://
to the California Department of at http://www.epa.gov/dockets. www.ecfr.gov/cgi-bin/text-
Pesticide Regulation’s issuance of a idx?&c=ecfr&tpl=/ecfrbrowse/Title40/
FOR FURTHER INFORMATION CONTACT:
crisis emergency exemption under 40tab_02.tpl.
Susan Lewis, Registration Division
FIFRA section 18 authorizing use of the
(7505P), Office of Pesticide Programs, C. How can I file an objection or hearing
pesticide on rice, bran and rice, grain.
Environmental Protection Agency, 1200
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This time-limited tolerance regulation request?
Pennsylvania Ave. NW., Washington,
establishes a maximum permissible Under section 408(g) of the Federal
DC 20460–0001; main telephone
level for residues of methoxyfenozide in Food, Drug, and Cosmetic Act (FFDCA),
number: (703) 305–7090; email address:
or on these commodities. These time- 21 U.S.C. 346a, any person may file an
RDFRNotices@epa.gov.
limited tolerances expire on December objection to any aspect of this regulation
31, 2019. SUPPLEMENTARY INFORMATION: and may also request a hearing on those
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![27336 Federal Register / Vol. 81, No. 88 / Friday, May 6, 2016 / Rules and Regulations
already been assessed under the organization in trade agreements to in the preemption provisions of FFDCA
appropriately protective cPAD (which is which the United States is a party. EPA section 408(n)(4). As such, the Agency
at least as protective as the POD used to may establish a tolerance that is has determined that this action will not
assess intermediate-term risk), no different from a Codex MRL; however, have a substantial direct effect on States
further assessment of intermediate-term FFDCA section 408(b)(4) requires that or tribal governments, on the
risk is necessary, and EPA relies on the EPA explain the reasons for departing relationship between the national
chronic dietary risk assessment for from the Codex level. government and the States or tribal
evaluating intermediate-term risk for There are currently no established governments, or on the distribution of
methoxyfenozide. Codex or Canadian MRLs for power and responsibilities among the
5. Aggregate cancer risk for U.S. methoxyfenozide residues in rice various levels of government or between
population. Based on the lack of commodities. the Federal Government and Indian
evidence of carcinogenicity in two VI. Conclusion tribes. Thus, the Agency has determined
adequate rodent carcinogenicity studies, that Executive Order 13132, entitled
methoxyfenozide is not expected to Therefore, time-limited tolerances are ‘‘Federalism’’ (64 FR 43255, August 10,
pose a cancer risk to humans. established for residues of 1999) and Executive Order 13175,
6. Determination of safety. Based on methoxyfenozide, (3-methoxy-2- entitled ‘‘Consultation and Coordination
these risk assessments, EPA concludes methylbenzoic acid 2-(3,5- with Indian Tribal Governments’’ (65 FR
that there is a reasonable certainty that dimethylbenzoyl)-2-(1,1-dimethylethyl)- 67249, November 9, 2000) do not apply
no harm will result to the general hydrazide), in or on rice, grain at 0.50 to this action. In addition, this action
population, or to infants and children ppm; and rice, bran at 4.0 ppm. These does not impose any enforceable duty or
from aggregate exposure to tolerances will expire on December 31, contain any unfunded mandate as
methoxyfenozide residues. 2019. described under Title II of the Unfunded
EPA concludes that there is VII. Statutory and Executive Order Mandates Reform Act (UMRA) (2 U.S.C.
reasonable certainty that no harm will Reviews 1501 et seq.).
result to the general population, or to This action establishes tolerances This action does not involve any
infants and children, from aggregate under FFDCA sections 408(e) and technical standards that would require
exposure to methoxyfenozide residues 408(l)(6). The Office of Management and Agency consideration of voluntary
because the Section 18 emergency use of Budget (OMB) has exempted these types consensus standards pursuant to section
methoxyfenozide on rice will result in of actions from review under Executive 12(d) of the National Technology
negligible increases in dietary exposure Order 12866, entitled ‘‘Regulatory Transfer and Advancement Act
to all subgroups relative to the safety Planning and Review’’ (58 FR 51735, (NTTAA) (15 U.S.C. 272 note).
findings reached in the August 27, 2014 October 4, 1993). Because this action VIII. Congressional Review Act
Federal Register document. has been exempted from review under Pursuant to the Congressional Review
V. Other Considerations Executive Order 12866, this action is Act (5 U.S.C. 801 et seq.), EPA will
not subject to Executive Order 13211, submit a report containing this rule and
A. Analytical Enforcement Methodology entitled ‘‘Actions Concerning other required information to the U.S.
An adequate enforcement Regulations That Significantly Affect Senate, the U.S. House of
methodology is available to enforce the Energy Supply, Distribution, or Use’’ (66 Representatives, and the Comptroller
tolerance expression, using high FR 28355, May 22, 2001) or Executive General of the United States prior to
performance liquid chromatography Order 13045, entitled ‘‘Protection of publication of the rule in the Federal
(HPLC), with either tandem mass Children from Environmental Health Register. This action is not a ‘‘major
spectrometric detection (LC–MS/MS), or Risks and Safety Risks’’ (62 FR 19885, rule’’ as defined by 5 U.S.C. 804(2).
ultraviolet detection (UV). April 23, 1997). This action does not
The method may be requested from: contain any information collections List of Subjects in 40 CFR Part 180
Chief, Analytical Chemistry Branch, subject to OMB approval under the Environmental protection,
Environmental Science Center, 701 Paperwork Reduction Act (PRA), 44 Administrative practice and procedure,
Mapes Rd., Ft. Meade, MD 20755–5350; U.S.C. 3501 et seq., nor does it require Agricultural commodities, Pesticides
telephone number: (410) 305–2905; any special considerations under and pests, Reporting and recordkeeping
email address: residuemethods@ Executive Order 12898, entitled requirements.
epa.gov. ‘‘Federal Actions to Address
Dated: April 21, 2016.
Environmental Justice in Minority
B. International Residue Limits Daniel J. Rosenblatt,
Populations and Low-Income
In making its tolerance decisions, EPA Populations’’ (59 FR 7629, February 16, Acting Director, Registration Division, Office
seeks to harmonize U.S. tolerances with of Pesticide Programs.
1994).
international standards whenever Since tolerances and exemptions that Therefore, 40 CFR chapter I is
possible, consistent with U.S. food are established in accordance with amended as follows:
safety standards and agricultural FFDCA sections 408(e) and 408(l)(6),
practices. EPA considers the such as the tolerances in this final rule, PART 180—[AMENDED]
international maximum residue limits do not require the issuance of a
(MRLs) established by the Codex proposed rule, the requirements of the ■ 1. The authority citation for part 180
Alimentarius Commission (Codex), as Regulatory Flexibility Act (RFA) (5 continues to read as follows:
required by FFDCA section 408(b)(4). U.S.C. 601 et seq.) do not apply. Authority: 21 U.S.C. 321(q), 346a and 371.
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The Codex Alimentarius is a joint This action directly regulates growers, ■ 2. In § 180.544, revise paragraph (b) to
United Nations Food and Agriculture food processors, food handlers, and food read as follows:
Organization/World Health retailers, not States or tribes, nor does
Organization food standards program, this action alter the relationships or § 180.544 Methoxyfenozide; tolerances for
and it is recognized as an international distribution of power and residues.
food safety standards-setting responsibilities established by Congress * * * * *
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![Federal Register / Vol. 81, No. 88 / Friday, May 6, 2016 / Rules and Regulations 27337
(b) Section 18 emergency exemptions. Monday through Friday, excluding legal hearing requests are provided in 40 CFR
Time-limited tolerances are established holidays. The telephone number for the 178.25(b).
for residues of the insecticide Public Reading Room is (202) 566–1744, In addition to filing an objection or
methoxyfenozide, including its and the telephone number for the OPP hearing request with the Hearing Clerk
metabolites and degradates in or on the Docket is (703) 305–5805. Please review as described in 40 CFR part 178, please
commodities listed in the table below, the visitor instructions and additional submit a copy of the filing (excluding
resulting from use of the pesticide under information about the docket available any Confidential Business Information
a Section 18 emergency exemption at http://www.epa.gov/dockets. (CBI)) for inclusion in the public docket.
granted by EPA. Compliance with the FOR FURTHER INFORMATION CONTACT: Information not marked confidential
tolerance levels specified in the Susan Lewis, Registration Division pursuant to 40 CFR part 2 may be
following table is to be determined by (7505P), Office of Pesticide Programs, disclosed publicly by EPA without prior
measuring only methoxyfenozide (3- Environmental Protection Agency, 1200 notice. Submit the non-CBI copy of your
methoxy-2-methylbenzoic acid 2-(3,5- Pennsylvania Ave. NW., Washington, objection or hearing request, identified
dimethylbenzoyl)-2-(1,1-dimethylethyl) DC 20460–0001; main telephone by docket ID number EPA–HQ–OPP–
hydrazide) in or on the commodity. number: (703) 305–7090; email address: 2015–0035, by one of the following
RDFRNotices@epa.gov. methods:
Com- Parts per Expiration/ • Federal eRulemaking Portal: http://
SUPPLEMENTARY INFORMATION:
modity million revocation date www.regulations.gov. Follow the online
I. General Information instructions for submitting comments.
Rice, bran 4.0 December 31, Do not submit electronically any
2019. A. Does this action apply to me? information you consider to be CBI or
Rice, 0.50 December 31,
You may be potentially affected by other information whose disclosure is
grain. 2019.
this action if you are an agricultural restricted by statute.
producer, food manufacturer, or • Mail: OPP Docket, Environmental
* * * * *
[FR Doc. 2016–09969 Filed 5–5–16; 8:45 am] pesticide manufacturer. The following Protection Agency Docket Center (EPA/
list of North American Industrial DC), (28221T), 1200 Pennsylvania Ave.,
BILLING CODE 6560–50–P
Classification System (NAICS) codes is NW., Washington, DC 20460–0001.
not intended to be exhaustive, but rather • Hand Delivery: To make special
ENVIRONMENTAL PROTECTION provides a guide to help readers arrangements for hand delivery or
AGENCY determine whether this document delivery of boxed information, please
applies to them. Potentially affected follow the instructions at http://
40 CFR Part 180 entities may include: www.epa.gov/dockets/contacts.html.
• Crop production (NAICS code 111). Additional instructions on
[EPA–HQ–OPP–2015–0035; FRL–9945–68] • Animal production (NAICS code commenting or visiting the docket,
112). along with more information about
Clethodim; Pesticide Tolerances
• Food manufacturing (NAICS code dockets generally, is available at http://
AGENCY: Environmental Protection 311). www.epa.gov/dockets.
Agency (EPA). • Pesticide manufacturing (NAICS II. Summary of Petitioned-for Tolerance
ACTION: Final rule. code 32532).
In the Federal Register of Wednesday,
B. How can I get electronic access to May 20, 2015 (80 FR 28925) (FRL–9927–
SUMMARY: This regulation establishes other related information?
tolerances for residues of clethodim in 39), EPA issued a document pursuant to
or on multiple commodities which are You may access a frequently updated FFDCA section 408(d)(3), 21 U.S.C.
identified and discussed later in this electronic version of EPA’s tolerance 346a(d)(3), announcing the filing of a
document. Interregional Research regulations at 40 CFR part 180 through pesticide petition (PP 4E8334) by
Project Number 4 (IR–4) requested these the Government Printing Office’s e-CFR Interregional Research Project Number 4
tolerances under the Federal Food, site at http://www.ecfr.gov/cgi-bin/text- (IR–4), 500 College Road East, Suite 201
Drug, and Cosmetic Act (FFDCA). idx?&c=ecfr&tpl=/ecfrbrowse/Title40/ W, Princeton, NJ 08540. The petition
40tab_02.tpl. requested that 40 CFR 180.458 be
DATES: This regulation is effective May
amended by establishing tolerances for
6, 2016. Objections and requests for C. How can I file an objection or hearing residues of the herbicide clethodim, 2-
hearings must be received on or before request? [(1E)-1-[[[(2E)-3-chloro-2-
July 5, 2016, and must be filed in Under FFDCA section 408(g), 21 propenyl]oxy]imino]propyl]-5-[2-
accordance with the instructions U.S.C. 346a, any person may file an (ethylthio)propyl]-3-hydroxy-2-
provided in 40 CFR part 178 (see also objection to any aspect of this regulation cyclohexen-1-one, and its metabolites
Unit I.C. of the SUPPLEMENTARY and may also request a hearing on those containing the 5-(2-
INFORMATION).
objections. You must file your objection ethylthiopropyl)cyclohexene-3-one and
ADDRESSES: The docket for this action, or request a hearing on this regulation 5-(2-ethylthiopropyl)-5-
identified by docket identification (ID) in accordance with the instructions hydroxycyclohexene-3-one moieties and
number EPA–HQ–OPP–2015–0035, is provided in 40 CFR part 178. To ensure their sulphoxides and sulphones,
available at http://www.regulations.gov proper receipt by EPA, you must calculated as the stoichiometric
or at the Office of Pesticide Programs identify docket ID number EPA–HQ– equivalent of clethodim, in or on stevia
Regulatory Public Docket (OPP Docket) OPP–2015–0035 in the subject line on at 12 parts per million (ppm); pome fruit
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in the Environmental Protection Agency the first page of your submission. All group 11–10 at 0.2 ppm; stone fruit
Docket Center (EPA/DC), West William objections and requests for a hearing group 12–12 at 0.2 ppm; bulb onion
Jefferson Clinton Bldg., Rm. 3334, 1301 must be in writing, and must be subgroup 3–07A at 0.2 ppm; low
Constitution Ave. NW., Washington, DC received by the Hearing Clerk on or growing berry subgroup 13–07G, except
20460–0001. The Public Reading Room before July 5, 2016. Addresses for mail cranberry at 3.0 ppm; rapeseed
is open from 8:30 a.m. to 4:30 p.m., and hand delivery of objections and subgroup 20A, except flax 0.5 ppm;
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Document Created: 2016-05-06 00:29:54
Document Modified: 2016-05-06 00:29:54
| Category | Regulatory Information | |
| Collection | Federal Register | |
| sudoc Class | AE 2.7: GS 4.107: AE 2.106: | |
| Publisher | Office of the Federal Register, National Archives and Records Administration | |
| Section | Rules and Regulations | |
| Action | Final rule. | |
| Dates | This regulation is effective May 6, 2016. Objections and requests for hearings must be received on or before July 5, 2016, and must be filed in accordance with the instructions provided in 40 CFR part 178 (see also Unit I.C. of the SUPPLEMENTARY INFORMATION). | |
| Contact | Susan Lewis, Registration Division (7505P), Office of Pesticide Programs, Environmental Protection Agency, 1200 Pennsylvania Ave. NW., Washington, DC 20460-0001; main telephone | |
| FR Citation | 81 FR 27332 | |
| CFR Associated | Environmental Protection; Administrative Practice and Procedure; Agricultural Commodities; Pesticides and Pests and Reporting and Recordkeeping Requirements |
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