Reinhold Niebuhr, approaching the ethical field as a theologian rather than as a philosopher, has maintained that the Christian ethic is not single and indivisible, but that, on the contrary, it consists of what one might call an absolute ethic and a kind of interim ethic in which the notion of justice is prominent. Without commenting on Niebuhr's work I wish to put forward a view which, although more general than his, is perhaps not without a superficial resemblance to it.

The controversy between teleologists and deontologists, whether under these names or in other guises, is one of the long-standing disputes of ethics. In different branches of philosophy the perennial nature of a dispute may point to different things: in some, for example, it may properly incline one to say “a plague on both your houses” and thereafter to look for some way of disposing of the whole problem around which the philosophical problem has raged; in ethics, on the other hand, (...) root-and-branch methods of excision are to be deplored, for here a perennial issue usually draws attention to points of view which have somehow to be reconciled if the problems underlying them are to be overcome. The deontology-teleology controversy seems to me a case in point. Here, if anywhere in ethics, a reconciliation must be effected; and in the present paper my primary aim is to induce deontologists and teleologists to abandon their mutual hostility. 1 I shall attempt to carry out this mission of philosophical good will through examining the ways in which we justify imperatives. In the first section of the paper I shall say something about the controversy itself, making it clear that I consider that it has roots which it would be inconvenient to expose at this stage of the inquiry; in the second I shall study the justification of a number of typical non-moral imperatives; in the third I shall apply the findings of the second to the justification of moral imperatives; and finally, in the fourth section I shall return to the deontology-teleology controversy and attempt to elucidate how it arises, to point out the two levels on which the same dispute can be found, and to suggest a way in which the essentials of the rival views may be accepted and combined. (shrink)

?Moral Black? and Whitemail? is a study of those modes of action which involve what I propose to call ?a raising of the moral stakes?. Illustration: A wants B to do X, and B wants to do Y; so A creates a situation in which doing Y would either be morally objectionable or more objectionable than it would have been but for A's intervention. Such modes of action include all the varieties of moral blackmail as well as such practices as (...) those of returning good for evil, putting people on trust, and some kinds of non?violent resistance. I try to expose the distinguishing marks of moral blackmail, why it is thought so objectionable, and how it is related to these other practices that also involve a raising of the moral stakes. The study as a whole is intended to underline the ambiguous nature of human action. (shrink)

There appear to be a number of general things which can be said about forgiveness. If these are left sufficiently vague they seem to be applicable to all the situations in which the term is used.First, there can be no question of forgiveness unless an injury has been inflicted on somebody by a moral agent. There must be something to forgive; and the injury that is to be forgiven must be one for which a moral agent can be held responsible. (...) One cannot forgive a rock for falling on one's foot or a cougar for attacking one's child—even though a child might kick the rock and a father might shoot the cougar. (shrink)

Objectives: To study the consent process experienced by participants who are enrolled in a molecular genetic research study that aims to find new genetic mutations responsible for an apparently inherited disorder.Design: Semi-structured interviews and analysis/description of main themes.Participants: 78 members of 52 families who had been recruited to a molecular genetic study.Results: People were well informed about the goals, risks and benefits of the genetic research study but could not remember the consent process. They had mostly been recruited to take (...) part by trusted clinicians or their relatives but had little memory of, or concern about signing consent forms. Families appeared to regard the research as a continuation of their, or their relatives’, clinical care.Conclusions: Ethical review should be more flexible in its attitude to consent forms and written information sheets for some sorts of research. For rare genetic disease studies where research has been discussed fully within the clinical setting then the consent obtained at that time could suffice rather than needing extra consent at a later stage. However, clinician-researchers will need to ensure that their duty of care extends for the duration of the research and beyond. (shrink)