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42 U.S.C. § 2160dFurther restrictions on exports

submitted 80 years ago by Pub. L. 102-486 to r/title-42-THE-PUBLIC-HEALTH-AND-WELFARE · 1,712 words · no verdicts yet

in plain englishAI-generated · not legal advice

The Commission generally may license highly enriched uranium for research or test reactors only when no usable lower-enriched alternative exists and the United States is developing one. Special rules govern medical-isotope exports, including review, reports, deadlines, certifications, extensions, and possible temporary suspensions.

(a) Unless subsection (b) applies, the Commission may license export of highly enriched uranium for use as fuel or a target in a nuclear research or test reactor only if it finds that (1) no lower-U-235-enriched alternative fuel or target can be used in that reactor; (2) the recipient promises to use the alternative whenever it can be used; and (3) the United States Government is actively developing such an alternative. (b)(1) Definitions. (A) \"highly enriched uranium\" means uranium with more than 20 percent U-235. (B) \"medical isotope\" includes molybdenum-99, iodine-131, xenon-133, and other radioactive materials used to produce a radiopharmaceutical for diagnosis, treatment, or research and development. (C) \"radiopharmaceutical\" means a radioactive isotope containing byproduct material combined with chemical or biological material and designed to collect temporarily in part of the body for treatment or to make a useful image for diagnosing a medical condition. (D) \"recipient country\" means Canada, Belgium, France, Germany, or the Netherlands. (b)(2) The Commission may license export, including shipment to and use by the specified intermediate and final consignees, of highly enriched uranium to a recipient country for medical-isotope production if it makes the findings in this paragraph, in addition to other chapter requirements except subsection (a). A country providing an assurance letter must have told the United States that each specified consignee must use the uranium only to make medical isotopes. The uranium may be irradiated only in a reactor in a recipient country that uses an alternative fuel or is covered by a United States agreement to convert to one when an alternative can be used. (b)(3)(A) The Commission must review whether physical-protection requirements in effect when an application is made are adequate for transportation and storage of the uranium and control of residual material after irradiation and isotope extraction. (B) If more protection is needed, including a limit on uranium per shipment, the Commission must impose it as a license condition or by another suitable method. (b)(4)(A) The Secretary must arrange for the National Academy of Sciences to study whether commercial sources not using highly enriched uranium can supply medical isotopes; current and projected domestic demand and availability; progress by the Department of Energy and others toward eliminating highly enriched uranium from reactor fuel, targets, and isotope facilities; and the possible cost difference if such systems did not use highly enriched uranium. (B) Low-enriched production is feasible if low-enriched targets have been developed and shown to work in reactors and target facilities producing significant quantities for United States needs, enough isotope is available to meet domestic needs, and the average expected total cost increase is less than 10 percent. (C) Within five years after August 8, 2005, the Secretary must report the study findings to Congress and disclose any commercial commitments to supply domestic needs without highly enriched uranium, consistently with those feasibility standards, by four years after the report. (b)(5) If the study says commercial non-highly-enriched sources are feasible but the Secretary cannot report such commitments, the Secretary must, within six years after August 8, 2005, report options for adequate domestic supplies without highly enriched uranium and within the paragraph (4)(B)(iii) cost increase. (b)(6) When non-highly-enriched commercial facilities can meet domestic needs within that cost increase without harming reliable supply, the Secretary must certify that fact to Congress. (b)(7) After that certification, the Commission must terminate by rule its review of export-license applications under this subsection. (c) Seven years after January 2, 2013, the Commission may not license export of highly enriched uranium from the United States for medical-isotope production. (d) The period may be extended by no more than six years if, no earlier than six years after January 2, 2013, the Secretary certifies to the specified House and Senate committees that the global supply of molybdenum-99 made without highly enriched uranium is insufficient for the domestic market and that exporting United States-origin highly enriched uranium is the most effective temporary way to increase that supply. (e) To permit public review and comment, the certification process under subsection (d) must be announced in the Federal Register. (f)(1) The ban in subsections (c) and (d) cannot take effect unless the Secretaries of Energy and Health and Human Services jointly certify that enough non-highly-enriched molybdenum-99 is available for United States patients and that exporting United States-origin highly enriched uranium is unnecessary to meet patient needs. (f)(2) They must make the certification within seven years after January 2, 2013. If subsection (d) extends the period, the deadline extends by the same amount. (g) After the subsection (c) restriction takes effect, a critical shortage may suspend it for no more than 12 months if the Secretary of Energy certifies to Congress that exporting United States-origin highly enriched uranium is the only effective temporary way to supply needed molybdenum-99 and Congress enacts a joint resolution approving the suspension. (h) In this section, \"alternative nuclear reactor fuel or target\" means fuel or a target enriched to less than 20 percent U-235. \"highly enriched uranium\" means uranium enriched to 20 percent or more U-235. A fuel or target \"can be used\" if the Department of Energy's Reduced Enrichment Research and Test Reactor Program has qualified it and its use permits most ongoing and planned experiments and medical-isotope production without a large percentage increase in total reactor operating cost. \"medical isotope\" includes molybdenum-99, iodine-131, xenon-133, and other radioactive materials used to produce a radiopharmaceutical for diagnostic or therapeutic procedures or research and development."},{"id":54437,"citation":"42 U.S.C. § 2160e","summary":"This section requires the President to submit agreements with Iran's nuclear program to Congress, establishes review periods and limits on sanctions relief, and requires continuing reports and certifications. It also creates expedited procedures for legislation reinstating sanctions and defines key terms.","explanation":"(a)(1) Within five calendar days after reaching an agreement with Iran about Iran's nuclear program, the President must send the appropriate congressional committees and leaders the agreement and all related materials and annexes; the Secretary of State's verification-assessment report; and a certification. The certification must say the agreement has suitable terms, conditions, and duration for Iran's nuclear activities and identifies sanctions the United States or another nation or entity, including the United Nations, will waive, suspend, or reduce. The President must also determine that the agreement meets United States nonproliferation goals, does not endanger the common defense and security, adequately ensures that permitted Iranian nuclear activities will not harm or unreasonably risk that defense and security, and ensures those activities will not support a nuclear-related military or explosive purpose, including research or development of an explosive device. (a)(2) The Secretary of State must prepare a report assessing how well the Secretary can verify Iran's compliance; whether the agreement's safeguards, controls, and assurances adequately prevent permitted activities from supporting such military or explosive purposes; and whether the International Atomic Energy Agency can effectively carry out the required verification, including access to suspicious sites or covert-activity allegations and enough funding, personnel, and authority. The Secretary must assume Iran could use any measure not expressly prohibited to hide violations and could change or depart from standard practices to obstruct verification. The report must be unclassified but include a classified annex, prepared with the Director of National Intelligence, summarizing relevant classified information. (a)(3) The requirements for the report and certification in (a)(1)(B) and (C), and subsections (b) through (g), do not apply to an agreement described in subsection (h)(5) or the EU-Iran Joint Statement of April 2, 2015. But any agreement meeting the definition in (h)(1), and related materials concluded before or after May 22, 2015, is not covered by that exception. (b)(1) For 30 calendar days after the President sends the agreement, the Senate Foreign Relations Committee and House Foreign Affairs Committee must, as appropriate, hold hearings and briefings and obtain information to review it fully. (b)(2) The period is 60 calendar days for an agreement and all required materials sent between July 10, 2015, and September 7, 2015. (b)(3) Before and during the sending period and review period, the President may not waive, suspend, reduce, relieve, or otherwise limit statutory sanctions on Iran, or refrain from applying them under the agreement, except as paragraph (6) allows. (b)(4) If both Houses pass a joint resolution of disapproval, the same prohibition continues for 12 calendar days after passage. (b)(5) If both Houses pass it and the President vetoes it, the prohibition continues for 10 calendar days after the veto. (b)(6) These prohibitions do not cover a new deferral, waiver, or suspension under the Joint Plan of Action if it is consistent with law in effect on May 22, 2015, and is made at least 45 calendar days before the President sends the agreement, report, and certification. (b)(7) In the House, \"transmittal,\" \"transmitted,\" and \"transmission\" mean delivery to the Speaker. (c)(1) Congress states that its sanctions helped bring Iran to negotiations; the negotiations are important to United States and allied security and foreign policy; this section does not require a congressional vote for the agreement to begin; the section permits congressional review and possible approval, disapproval, or no action concerning statutory sanctions relief; and Congress should have an orderly chance to consider and act on a sanctions regime that only Congress can permanently change or remove. (c)(2) United States statutory sanctions relief under an agreement or the Joint Plan of Action may be taken consistently with existing law if Congress passes a joint resolution favoring the agreement during review; may not be taken if Congress passes a joint resolution opposing it during review; and may be taken consistently with existing law if no such resolution is enacted after review. (c)(3) Such relief includes waiving, suspending, reducing, relieving, or limiting sanctions on Iran, or refraining from applying them. (d)(1) The President must keep the committees and leaders fully and currently informed about every aspect of Iran's compliance. (d)(2) Within 10 calendar days after receiving credible, accurate information about a potentially significant breach or compliance incident, the President must send it to them. (d)(3) Within 30 calendar days after that submission, the President must decide whether the incident is a material breach and, if so, whether Iran cured it, and must send the decision plus, as appropriate, a report on Iran's conduct, needed cure actions, and cure status. (d)(4) Within 180 days after entering the agreement and at least every 180 days afterward, the President must report on Iran's nuclear program and compliance, including: (A) breaches or noncompliance; (B) inspector-access delays longer than one week; (C) progress resolving IAEA concerns about possible military dimensions; (D) prohibited or otherwise weapon-advancing procurement; (E) noncompliant centrifuge research or research that could greatly shorten weapon-acquisition time if deployed; (F) prohibited diversion of uranium, carbon fiber, or other material; (G) covert nuclear, weapon-related, fissile-material, research, or development activity; (H) whether Iranian financial institutions launder money or finance terrorism, naming them when applicable; (I) ballistic-missile advances, including long-range and intercontinental programs; (J) an assessment of whether Iran directly supported, financed, planned, or carried out terrorism against the United States or a United States person, the extent of Iran's terrorism support, United States actions to stop or condemn it, its effect on United States security and citizens, and all agreement-based sanctions relief and its connection to Iran's nuclear-weapons program; and (K) whether internationally recognized human-rights violations in Iran changed, increased, or decreased from the prior 180 days. (d)(5) After submission, the State, Energy, and Defense Departments must promptly provide, upon request of a committee or leader, their views on whether the agreement's safeguards and controls adequately prevent harmful or unreasonably risky permitted activity. The President must also keep them informed of every Iran nuclear initiative or negotiation, including a new or amended agreement. (d)(6) After the review period, at least every 90 calendar days the President must decide whether he can certify that Iran is transparently, verifiably, and fully implementing the agreement and related technical agreements; has not materially breached it or has cured any breach; has not taken action, including covert action, that could significantly advance its nuclear-weapons program; and that sanctions suspension is appropriate and proportionate to Iran's specific verifiable steps ending its illicit program and is vital to United States national security. If able, he must make that certification to the committees and leaders. (d)(7) Congress states that sanctions for terrorism, human rights abuses, and ballistic missiles remain; unresolved issues include compensation for Americans held and tortured after the 1979 Tehran embassy seizure and their families, release of Americans in Iran, Iran's human-rights abuses, and worldwide terrorism support; the President should ensure the agreement does not compromise Israel's security or its right to exist; and Congress should be able to review and, if needed, change statutory sanctions for a long-term P5+1 agreement. (e)(1) If the President fails to make the 90-day certification, or determines that Iran materially breached the agreement and has not cured it, qualifying legislation introduced within 60 calendar days is entitled to the expedited process. In the House, \"submit\" means submit to the Speaker. (e)(2) \"Qualifying legislation\" is only a bill whose title is \"A bill reinstating statutory sanctions imposed with respect to Iran\" and whose text reinstates sanctions imposed under the law or laws inserted in the blank, when those sanctions were relieved under an agreement submitted under section 135(a) of the Atomic Energy Act of 1954, and prohibits United States action to release funds or assets or give further relief under that agreement. (e)(3) During the 60-day period, the House bill may be introduced by the majority or minority leader, and the Senate bill by the majority leader or designee or minority leader or designee. (e)(4) In the House, a committee that has not reported the bill within 10 legislative days is discharged. Beginning on the third legislative day after report or discharge, a motion to proceed is in order; points of order are waived, it cannot be moved after the House has disposed of the same motion for the same agreement, the previous question is ordered, it is not debatable, and reconsideration is unavailable. The bill is considered read, points of order against it and its consideration are waived, and the previous question runs to passage with two hours equally divided between its sponsor or designee and an opponent; reconsideration of passage is unavailable. (e)(5) In the Senate, the bill goes to Foreign Relations. If not reported within 10 session days, that committee is discharged and the bill goes to the proper calendar. A motion to proceed is in order at any time after report or discharge, even after an identical motion was rejected; points of order are waived, the motion is not debatable or postponable, reconsideration is unavailable, and the bill remains unfinished business until disposed of. Debate and related debatable motions and appeals last no more than 10 hours, equally divided between majority and minority leaders or designees. Further limiting debate is permitted and not debatable; amendments, postponement, proceeding to other business, and recommittal are not in order. The vote follows debate and one requested quorum call. Appeals about procedure are decided without debate. Debate on a veto message also lasts no more than 10 hours, equally divided and controlled by the leaders or designees. (e)(6) If one House receives the other House's qualifying bill before passing its own, the other bill is not referred to committee; the receiving House follows its normal procedure but votes on the other bill. If one House does not introduce a bill, the other House's bill receives the expedited process. A House companion received by the Senate after Senate passage is not debatable. This paragraph does not apply in the House to a qualifying revenue measure. (f) Subsection (e) is adopted as an exercise of each House's rulemaking power, is part of each House's rules only for the covered procedure, supersedes inconsistent rules, and recognizes each House's constitutional power to change its rules in the same way as any other rule. (g) This section does not change the President's authority to negotiate, enter, or implement executive agreements except for the specific implementation limits here; authorize new sanctions relief or nonapplication during the review period; revoke or end statutory sanctions; or authorize military force against Iran. (h) Definitions. \"Agreement\" means an agreement about Iran's nuclear program that includes or commits the United States to action, in any form and whether binding or not, including a joint comprehensive plan of action and every related annex, appendix, codicil, side agreement, implementing material, document, guidance, technical or other understanding, or related agreement entered into or implemented before or later. \"Appropriate congressional committees\" means the Senate Finance, Banking, Housing, and Urban Affairs, Select Intelligence, and Foreign Relations Committees and the House Ways and Means, Financial Services, Permanent Select Intelligence, and Foreign Affairs Committees. \"Appropriate congressional committees and leadership\" adds the Senate majority and minority leaders and the House Speaker, majority leader, and minority leader. This section does not define \"Iranian financial institution\" or \"United States person\"; it adopts the meanings in sections 8513b(d) and 8511 of title 22. \"Joint Plan of Action\" means the plan signed at Geneva on November 24, 2013, by Iran, France, Germany, Russia, China, the United Kingdom, and the United States, plus its related materials and agreements, including the listed 2014 technical understanding and extensions and materially identical extensions on or after May 22, 2015. \"EU-Iran Joint Statement\" means only the April 2, 2015 statement by Federica Mogherini and Javad Zarif at Lausanne. \"Material breach\" means a breach, or failure to perform a nonbinding commitment, that substantially benefits Iran's nuclear program, shortens the time Iran needs to obtain a nuclear weapon, or departs from or undermines the agreement's purpose. \"Noncompliance\" means a departure from the agreement that is not a material breach. \"P5+1 countries\" means the United States, France, Russia, China, the United Kingdom, and Germany.
the actual law source: uscode.house.gov ↗public domain
(a) In general

Except as provided in subsection (b), the Commission may issue a license for the export of highly enriched uranium to be used as a fuel or target in a nuclear research or test reactor only if, in addition to any other requirement of this chapter, the Commission determines that—

(1)

there is no alternative nuclear reactor fuel or target enriched in the isotope 235 to a lesser percent than the proposed export, that can be used in that reactor;

(2)

the proposed recipient of that uranium has provided assurances that, whenever an alternative nuclear reactor fuel or target can be used in that reactor, it will use that alternative in lieu of highly enriched uranium; and

(3)

the United States Government is actively developing an alternative nuclear reactor fuel or target that can be used in that reactor.

(b) Medical isotope production
(1) Definitions

In this subsection:

(A) Highly enriched uranium

The term “highly enriched uranium” means uranium enriched to include concentration of U–235 above 20 percent.

(B) Medical isotope

The term “medical isotope” includes Molybdenum 99, Iodine 131, Xenon 133, and other radioactive materials used to produce a radiopharmaceutical for diagnostic, therapeutic procedures or for research and development.

(C) Radiopharmaceutical

The term “radiopharmaceutical” means a radioactive isotope that—

(i)

contains byproduct material combined with chemical or biological material; and

(ii)

is designed to accumulate temporarily in a part of the body for therapeutic purposes or for enabling the production of a useful image for use in a diagnosis of a medical condition.

(D) Recipient country

The term “recipient country” means Canada, Belgium, France, Germany, and the Netherlands.

(2) Licenses

The Commission may issue a license authorizing the export (including shipment to and use at intermediate and ultimate consignees specified in the license) to a recipient country of highly enriched uranium for medical isotope production if, in addition to any other requirements of this chapter (except subsection (a)), the Commission determines that—

(A)

a recipient country that supplies an assurance letter to the United States Government in connection with the consideration by the Commission of the export license application has informed the United States Government that any intermediate consignees and the ultimate consignee specified in the application are required to use the highly enriched uranium solely to produce medical isotopes; and

(B)

the highly enriched uranium for medical isotope production will be irradiated only in a reactor in a recipient country that—

(i)

uses an alternative nuclear reactor fuel; or

(ii)

is the subject of an agreement with the United States Government to convert to an alternative nuclear reactor fuel when alternative nuclear reactor fuel can be used in the reactor.

(3) Review of physical protection requirements
(A) In general

The Commission shall review the adequacy of physical protection requirements that, as of the date of an application under paragraph (2), are applicable to the transportation and storage of highly enriched uranium for medical isotope production or control of residual material after irradiation and extraction of medical isotopes.

(B) Imposition of additional requirements

If the Commission determines that additional physical protection requirements are necessary (including a limit on the quantity of highly enriched uranium that may be contained in a single shipment), the Commission shall impose such requirements as license conditions or through other appropriate means.

(4) First report to Congress
(A) NAS study

The Secretary shall enter into an arrangement with the National Academy of Sciences to conduct a study to determine—

(i)

the feasibility of procuring supplies of medical isotopes from commercial sources that do not use highly enriched uranium;

(ii)

the current and projected demand and availability of medical isotopes in regular current domestic use;

(iii)

the progress that is being made by the Department of Energy and others to eliminate all use of highly enriched uranium in reactor fuel, reactor targets, and medical isotope production facilities; and

(iv)

the potential cost differential in medical isotope production in the reactors and target processing facilities if the products were derived from production systems that do not involve fuels and targets with highly enriched uranium.

(B) Feasibility

For the purpose of this subsection, the use of low enriched uranium to produce medical isotopes shall be determined to be feasible if—

(i)

low enriched uranium targets have been developed and demonstrated for use in the reactors and target processing facilities that produce significant quantities of medical isotopes to serve United States needs for such isotopes;

(ii)

sufficient quantities of medical isotopes are available from low enriched uranium targets and fuel to meet United States domestic needs; and

(iii)

the average anticipated total cost increase from production of medical isotopes in such facilities without use of highly enriched uranium is less than 10 percent.

(C) Report by the Secretary

Not later than 5 years after August 8, 2005, the Secretary shall submit to Congress a report that—

(i)

contains the findings of the National Academy of Sciences made in the study under subparagraph (A); and

(ii)

discloses the existence of any commitments from commercial producers to provide domestic requirements for medical isotopes without use of highly enriched uranium consistent with the feasibility criteria described in subparagraph (B) not later than the date that is 4 years after the date of submission of the report.

(5) Second report to Congress

If the study of the National Academy of Sciences determines under paragraph (4)(A)(i) that the procurement of supplies of medical isotopes from commercial sources that do not use highly enriched uranium is feasible, but the Secretary is unable to report the existence of commitments under paragraph (4)(C)(ii), not later than the date that is 6 years after August 8, 2005, the Secretary shall submit to Congress a report that describes options for developing domestic supplies of medical isotopes in quantities that are adequate to meet domestic demand without the use of highly enriched uranium consistent with the cost increase described in paragraph (4)(B)(iii).

(6) Certification

At such time as commercial facilities that do not use highly enriched uranium are capable of meeting domestic requirements for medical isotopes, within the cost increase described in paragraph (4)(B)(iii) and without impairing the reliable supply of medical isotopes for domestic utilization, the Secretary shall submit to Congress a certification to that effect.

(7) Sunset provision

After the Secretary submits a certification under paragraph (6), the Commission shall, by rule, terminate its review of export license applications under this subsection.

(c) Medical production license sunset

Effective 7 years after January 2, 2013, the Commission may not issue a license for the export of highly enriched uranium from the United States for the purposes of medical isotope production.

(d) Medical production license extension

The period referred to in subsection (c) may be extended for no more than 6 years if, no earlier than 6 years after January 2, 2013, the Secretary of Energy certifies to the Committee on Energy and Commerce of the House of Representatives and the Committee on Energy and Natural Resources of the Senate that—

(1)

there is insufficient global supply of molybdenum-99 produced without the use of highly enriched uranium available to satisfy the domestic United States market; and

(2)

the export of United States-origin highly enriched uranium for the purposes of medical isotope production is the most effective temporary means to increase the supply of molybdenum-99 to the domestic United States market.

(e) Public notice

To ensure public review and comment, the development of the certification described in subsection (d) shall be carried out through announcement in the Federal Register.

(f) Joint certification
(1) In general

In accordance with paragraph (2), the ban on the export of highly enriched uranium for purposes of medical isotope production referred to in subsections (c) and (d) shall not go into effect unless the Secretary of Energy and the Secretary of Health and Human Services have jointly certified that—

(A)

there is a sufficient supply of molybdenum-99 produced without the use of highly enriched uranium available to meet the needs of patients in the United States; and

(B)

it is not necessary to export United States-origin highly enriched uranium for the purposes of medical isotope production in order to meet United States patient needs.

(2) Time of certification

The joint certification under paragraph (1) shall be made not later than 7 years after January 2, 2013, except that, if the period referred to in subsection (c) is extended under subsection (d), the 7-year deadline under this paragraph shall be extended by a period equal to the period of such extension under subsection (d).

(g) Suspension of medical production license

At any time after the restriction of export licenses provided for in subsection (c) becomes effective, if there is a critical shortage in the supply of molybdenum-99 available to satisfy the domestic United States medical isotope needs, the restriction of export licenses may be suspended for a period of no more than 12 months, if—

(1)

the Secretary of Energy certifies to the Congress that the export of United States-origin highly enriched uranium for the purposes of medical isotope production is the only effective temporary means to increase the supply of molybdenum-99 necessary to meet United States medical isotope needs during that period; and

(2)

the Congress enacts a Joint Resolution approving the temporary suspension of the restriction of export licenses.

(h) Definitions

As used in this section—

(1)

the term “alternative nuclear reactor fuel or target” means a nuclear reactor fuel or target which is enriched to less than 20 percent in the isotope U–235;

(2)

the term “highly enriched uranium” means uranium enriched to 20 percent or more in the isotope U–235;

(3)

a fuel or target “can be used” in a nuclear research or test reactor if—

(A)

the fuel or target has been qualified by the Reduced Enrichment Research and Test Reactor Program of the Department of Energy; and

(B)

use of the fuel or target will permit the large majority of ongoing and planned experiments and medical isotope production to be conducted in the reactor without a large percentage increase in the total cost of operating the reactor; and

(4)

the term “medical isotope” includes molybdenum-99, iodine-131, xenon-133, and other radioactive materials used to produce a radiopharmaceutical for diagnostic or therapeutic procedures or for research and development.

Source credit: (Aug. 1, 1946, ch. 724, title I, § 134, as added Pub. L. 102–486, title IX, § 903(a)(1), Oct. 24, 1992, 106 Stat. 2944; Pub. L. 109–58, title VI, § 630, Aug. 8, 2005, 119 Stat. 785; Pub. L. 112–239, div. C, title XXXI, § 3174, Jan. 2, 2013, 126 Stat. 2214.)

history & why it existsrecord from the source credit
  • 1946Enacted · Pub. L. 102-486 · 106 Stat. 2944
  • 2005Amended · Pub. L. 109-58 · 119 Stat. 785
  • 2013Amended · Pub. L. 112-239 · 126 Stat. 2214

A history note hasn’t been published yet. The record shows enactment by Pub. L. 102-486 on 1946-08-01.

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