This review of the peripheral auditory apparatus represents an attempt to analyse critically recent developments in the field. The coverage is not exhaustive, the emphasis is on functional aspects and no attempt is made to review the anatomy of the ear. Particular emphasis is placed on three broad sections: the physiology of the middle ear, basilar membrane mechanics and the electrophysiology of the cochlea. It is in these areas that recent technical advances have led to experiments which throw doubt on traditionally held concepts. Such an advance is the application of the Mössbauer technique to the problem of middle- and inner-ear mechanics. Because of its novelty, this technique is discussed in detail. Other new methods such as laser holography are just starting to be used, as are the ion selective microelectrodes for measuring dynamic changes in endolymph concentration. After many years of slow progress there is a sudden spark of enthusiasm for peripheral auditory research, and the coming decade promises to be most exciting indeed.

In many important types of observations in biological research, the information provided by the specimens is in the form of photons-quanta of visible light, u.v., or X-rays. The process of observation becomes one of recording this information in useful form, with as high an efficiency as possible. The problem becomes particularly important when for some reason or other the total number or rate of quanta provided by the specimen is small. Examples of such limitations are included in the following: (i) Processes permitting only low-intensity illumination in order not to interfere with the biological processes under observation. (ii) Processes changing very rapidly and requiring rapid sequence recording. (iii) Processes providing only a limited number of photons per event, such as bioluminescence. (iv) Processes in which radioactive tracers are utilized, and observation of radioactivity is desirable at low specific activity or within short time intervals. (v) X-ray diffraction processes where the specimen is weakly diffracting or where the X-ray intensity must be kept low in order not to damage the specimen. (vi) Processes involving the observation of fluorescence, where the intensity is low because of limitations on the amount of tagging material.

The findings of clinical and experimental studies conducted over the past 25 years provide extensive evidence that in both laboratory animals and man memory can be modified by treatments which affect the central nervous system. Patients with head injuries may suffer from retrograde amnesia, a loss of memory for experiences which occur just prior to the onset of the injury. Findings of laboratory studies using animal subjects indicate that retrograde amnesia can be produced by a wide variety of experimental treatments.

Factors involved in genetic control of protein synthesis can be classified according to their structural and regulatory roles. The structural constitution of the genetic locus determines the ordering of amino acids in the protein primary structure while regulatory factors influence the rates of protein synthesis. The genetic scheme, proposed by Jacob & Monod (1961), groups genes according to their structural and regulatory functions. This genetic classification alone is insufficient to explain the dynamics of regulatory behaviour. Basic questions such as why cells with the same complement of genes synthesize more of one protein than another are left unanswered. The answers to such questions would shed some light on the dynamical mechanism of tissue differentiation and embryological development. Regulation of protein synthesis should be the result of a combination of structural genetic factors and dynamic biochemical processes. It will be shown in this article that the interaction of structural and dynamic factors leads to a coherent and efficient control mechanism of biosynthesis.

The great number of investigations and advanced developments in neurophysiology and psychoacoustics during recent years have extensively increased our knowledge about the frequency analysis of simple sounds in the peripheral auditory system.

New methods have facilitated quantitative measurements of the amplitude of the submicroscopic vibration of a narrow segment of the basilar membrane in anaesthetized animals at physiological sound intensities. The results of these studies have quantitatively confirmed the results of past studies by showing that the basilar membrane has a selectivity with regard to tone frequency. In addition to this, the recent studies have increased our knowledge about the finer details of vibration of the basilar membrane. At the lowest levels used in the recent investigations, i.e. about 70 dB SPL, the selectivity in the 7 kHz region of the basilar membrane was found to be greater than expected on the basis of extrapolation of older data. Moreover, the high frequency slope of the tuning curves of the basilar membrane was found to be particularly steep. The results of these recent studies, furthermore, showed that the basilar membrane vibrates in a non-linear way at intensities within the physiological range. This non-linearity results in a broadening of the selectivity curves of a narrow segment of the basilar membrane when the sound intensity is increased.

Little is known as to how the motion of the basilar membrane is transformed to excitation of the cochlear sensory cells, i.e. the haircells. The excitation may be related to displacement, spatial differentiation or other transformations of the basilar membrane motion. Recording from the interior of mammalian haircells has so far been unsuccessful, and the neural excitatory process within the haircells in the cochlea is as yet practically unknown. Studies of the haircells in the lateral line organ of fish have provided fundamental knowledge about their excitation; since they in many respects resemble those in the mammalian cochlea, the results very probably can be applied to the excitatory process in the mammalian cochlea.

In all scattering phenomena the scattering angles are inversely related to the dimensions of the scattering particles. As macromolecules are giant compared with the normally used CuKα wavelength λ = 1·54 Å, we find the scattering of the particle as a whole at Correspondingly small angles.

There are now well-established examples of carriers and pores which facilitate the transfer of ions across thin lipid membranes. In the absence of such agents, lipid bilayer membranes are extremely impermeable to the common inorganic ions. Thus, the conductance of a pure lecithin + decane or glyceryl mono-oleate + decane membrane in M/10 NaCl is less than10−9Ω −1 cm−2. However, on the addition of small lipid-soluble molecules such as valinomycin, or surface-active polypeptides such as gramicidin A, the conductance may become so high (> 10−1 ω−l cm−2) that the resistance of the membrane merges into that of the aqueous phase. This review is concerned with the extent to which we now understand how these added substances transfer ions across lipid membranes. Attention has been concentrated on the simpler systems, i.e. the lipid-soluble ions, the 1–1 carriets, a simple pore and, with some loss of simplicity, a substance which prodeces interacting pores. Only molecules of known primary structure are discussed.

Visual pigments are embedded in the disc membranes of the outer segments of vertebrate rods and cones and in the microvilli of invertebrate visual cells. The pigment molecule in both is a most fascinating aggregate of known (the ubiquitous II-cis isomer of vitamin A1 or A2-aldehyde = retinal1 or 2; Hubbard & Wald, 1952) covalently bonded to the unknown (a protein termed opsin) (Anderson, Hoffman & Hall, 1971). This conjugated molecule is called rhodopsin or dehydrorhodopsin (porphryopsin) when the prosthetic portion is retinall or 2 respectively. So sensitive is this sterically hindered, bent and twisted molecule to light that absorption of one photon can initiate its isomerization to the all trans form. This conformational change is but one (but the best known) of the factors leading to receptor membrane changes ushering in the visual impulse.

Several cases of modifications of functional properties of proteins upon specific interaction with antibodies have been reported in the last few years. The purpose of this paper is to discuss evidence that these effects may be due to conformational changes in the protein molecule.