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Violation in Mixing

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1.5 Determ<strong>in</strong>ation of « 45<br />

� � ÙÙ� tree amplitude, the Cabibbo-suppressed � � ÙÙ× tree amplitude results <strong>in</strong> be<strong>in</strong>g smaller by a<br />

factor of about 0.2 (the Cabibbo angle) than the � � × pengu<strong>in</strong> amplitude. On the other hand, the � � ×<br />

electroweak pengu<strong>in</strong> is also suppressed by about 0.2 relative to the � � × gluonic pengu<strong>in</strong>. Therefore, the<br />

� � × electroweak pengu<strong>in</strong> and the � � ÙÙ× tree amplitude could be comparable <strong>in</strong> magnitude. So the<br />

electroweak-pengu<strong>in</strong> contributions to � � �à could be non-negligible and an isosp<strong>in</strong> analysis would not<br />

be able to isolate the tree contribution [27].<br />

In the case of � � à � , the pengu<strong>in</strong> diagram produces the appropriate set of quarks, ×��Ù, while the<br />

tree diagram produces ×ÙÙÙ: so <strong>in</strong> pr<strong>in</strong>ciple one could th<strong>in</strong>k that there can be absolutely no tree contribution,<br />

<strong>in</strong> which case this signal would represent an unambiguous observation of a gluonic pengu<strong>in</strong> process. In<br />

reality, f<strong>in</strong>al-state <strong>in</strong>teraction could convert the ÙÙ pair <strong>in</strong> the tree diagram <strong>in</strong>to a ��: so under the assumption<br />

that f<strong>in</strong>al-state <strong>in</strong>teractions are likely to be small one can still consider � � Ã � channel a pure gluonic<br />

pengu<strong>in</strong> process. Moreover, the amplitude for the tree diagram is Ç � � , while that for the pengu<strong>in</strong> is Ç � ,<br />

so it seems even more unlikely that the tree contribution could be significant.<br />

1.5.4 Direct �È <strong>Violation</strong><br />

As already said <strong>in</strong> Sec. 1.3.1, direct �È violation can occur <strong>in</strong> processes <strong>in</strong>volv<strong>in</strong>g charged or neutral �’s.<br />

In general, though, it is difficult to convert experimental observation of an asymmetry <strong>in</strong> a specific channel<br />

<strong>in</strong>to a quantitative determ<strong>in</strong>ation of the basic parameters of the Standard Model.<br />

We can observe �È -violat<strong>in</strong>g effects by compar<strong>in</strong>g the amplitude È � � with È � � only if there<br />

are both �È violat<strong>in</strong>g and non-�È violat<strong>in</strong>g phases: one could compare � � à � with � �<br />

à � . These decays have both tree and pengu<strong>in</strong> contributions which have different weak (and presumably<br />

different strong) phases. Unfortunately it is not possible at present to calculate the strong phases and the<br />

value of the weak phase would be ambiguous.<br />

An example of what can be done with direct �È violation is the Fleischer-Mannel bound which is based on<br />

an analysis of branch<strong>in</strong>g fractions for the various charged and neutral � � � modes. The decay � �<br />

à � has both pengu<strong>in</strong> and tree contributions, while, as previously discussed, to a good approximation,<br />

� � Ã � is entirely a pengu<strong>in</strong> process. Moreover, the pengu<strong>in</strong> amplitudes for these processes should<br />

be essentially identical, s<strong>in</strong>ce the correspond<strong>in</strong>g decays differ only <strong>in</strong> the isosp<strong>in</strong> of the spectator quark. One<br />

can therefore write the decay rates as<br />

� � à � ��È �Ì � �­ � �Æ �<br />

� � à � ��È �Ì � �­ � �Æ �<br />

� � à � � � � à � ���<br />

where �È and �Ì conta<strong>in</strong> no CKM phases and Æ is the relative strong phase shift between the pengu<strong>in</strong> and<br />

tree processes. Comput<strong>in</strong>g the ratio:<br />

� � à � � �à �<br />

��È� Ö Ó× ­ Ó× Æ Ö<br />

�È VIOLATION IN THE �� SYSTEM

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