The shame system appears to be natural selection's solution to the adaptive problem of information-triggered reputational damage. Over evolutionary time, this problem would have led to a coordinated set of adaptations – the shame system – designed to minimise the spread of negative information about the self and the likelihood and costs of being socially devalued by others. This information threat theory of shame can account for much of what we know about shame and generate precise predictions. Here, we analyse the behavioural configuration that people adopt stereotypically when ashamed – slumped posture, downward head tilt, gaze avoidance, inhibition of speech – in light of shame's hypothesised function. This behavioural configuration may have differentially favoured its own replication by (a) hampering the transfer of information (e.g. diminishing audiences’ tendency to attend to or encode identifying information – shame camouflage) and/or (b) evoking less severe devaluative responses from audiences (shame display). The shame display hypothesis has received considerable attention and empirical support, whereas the shame camouflage hypothesis has to our knowledge not been advanced or tested. We elaborate on this hypothesis and suggest directions for future research on the shame pose.

Polymorphism may allow individuals to expand habitat use through morph-specific resource demands. However, the underlying mechanisms maintaining different morphotypes in nature are difficult to identify. We sampled populations of the shrimp Hippolyte obliquimanus in the macroalgae Sargassum furcatum and Galaxaura marginata to examine morph-specific distribution patterns, population structure and female reproductive output, as an initial step to understand polymorphism in this species. Two main colour morphotypes were identified: homogeneous shrimps (H), which change their colour, mostly from pink to greenish-brown tones, and striped translucent shrimps (ST), whose colour remain unaltered. Distribution of individuals between habitats was clearly morph-specific. H shrimps occupied colour-matching substrates, mainly Sargassum, where they can attain large densities, and ST individuals were evenly distributed in both algae. Brood production and size-fecundity relationships were similar between morphs and habitats, suggesting these are relatively fixed traits in the population. However, sex proportions, defined as the male to female ratio, were different between morphs and macroalgae. H shrimps were chiefly females (1:2.04) and ST shrimps mostly males (1:0.30). Given the likely polygynic pure-search mating system in H. obliquimanus, the female-biased sex ratio observed in Sargassum is apparently more advantageous than the Mendelian proportion found in Galaxaura habitat. Clustering on vegetated habitat, the female-biased H morph may be relatively cryptic and sedentary, compared with the male-biased ST morph which apparently combines a more neutral camouflage strategy to a generalized habitat use. Altogether, results suggest that selection for sex-specific traits favours the maintenance of polymorphism in H. obliquimanus.

I observed shark mackerel demonstrating multiple search and attack strategies. Strategies were categorized as three distinct types: (1) a linear search by single or groups of fish along reef features; (2) ambush from a stationary position on the seafloor; and (3) ambush from resting schools of co-occurring predators. Together these strategies were consistent with both information-sharing and producer–scrounger models of group foraging and indicate significant flexibility in individual fish foraging behaviour based on proximate conditions.

Chemical cues are so important in the recognition mechanism of social insects that most social parasites (which rely on hosts to rear their brood) have been documented as overcoming the mechanism by which colony residents recognize non-nestmates, by mimicking the odour of the usurped colony. We simulated in the laboratory the process by which the obligate social parasite, Polistes semenowi, invades nests of the host species, Polistes dominulus, in the field and analysed the epicuticular lipid layer before and after host nest usurpation. The experiment documents that P. semenowi social parasites have an epicuticular hydrocarbon pattern which is very similar to that of their host but, after entering host colonies, parasites mimic the odour of the colonies they invade, to the point that they perfectly match the hydrocarbon profile peculiar to the colony they entered. However, both before and after host nest invasion, parasites show a tendency to possess diluted recognition cues with respect to their hosts.

The chromatophores of cephalopods differ fundamentally from those of other animals: they are neuromuscular organs rather than cells and are not controlled hormonally. They constitute a unique motor system that operates upon the environment without applying any force to it. Each chromatophore organ comprises an elastic sacculus containing pigment, to which is attached a set of obliquely striated radial muscles, each with its nerves and glia. When excited the muscles contract, expanding the chromatophore; when they relax, energy stored in the elastic sacculus retracts it. The physiology and pharmacology of the chromatophore nerves and muscles of loliginid squids are discussed in detail. Attention is drawn to the multiple innervation of dorsal mantle chromatophores, of crucial importance in pattern generation. The size and density of the chromatophores varies according to habit and lifestyle. Differently coloured chromatophores are distributed precisely with respect to each other, and to reflecting structures beneath them. Some of the rules for establishing this exact arrangement have been elucidated by ontogenetic studies. The chromatophores are not innervated uniformly: specific nerve fibres innervate groups of chromatophores within the fixed, morphological array, producing ‘physiological units’ expressed as visible ‘chromatomotor fields’.

The chromatophores are controlled by a set of lobes in the brain organized hierarchically. At the highest level, the optic lobes, acting largely on visual information, select specific motor programmes (i.e. body patterns); at the lowest level, motoneurons in the chromatophore lobes execute the programmes, their activity or inactivity producing the patterning seen in the skin. In Octopus vulgaris there are over half a million neurons in the chromatophore lobes, and receptors for all the classical neurotransmitters are present, different transmitters being used to activate (or inhibit) the different colour classes of chromatophore motoneurons. A detailed understanding of the way in which the brain controls body patterning still eludes us: the entire system apparently operates without feedback, visual or proprioceptive.

The gross appearance of a cephalopod is termed its body pattern. This comprises a number of components, made up of several units, which in turn contains many elements: the chromatophores themselves and also reflecting cells and skin muscles. Neural control of the chromatophores enables a cephalopod to change its appearance almost instantaneously, a key feature in some escape behaviours and during agonistic signalling. Equally important, it also enables them to generate the discrete patterns so essential for camouflage or for signalling. The primary function of the chromatophores is camouflage. They are used to match the brightness of the background and to produce components that help the animal achieve general resemblance to the substrate or break up the body's outline. Because the chromatophores are neurally controlled an individual can, at any moment, select and exhibit one particular body pattern out of many. Such rapid neural polymorphism (‘polyphenism’) may hinder search-image formation by predators. Another function of the chromatophores is communication. Intraspecific signalling is well documented in several inshore species, and interspecific signalling, using ancient, highly conserved patterns, is also widespread. Neurally controlled chromatophores lend themselves supremely well to communication, allowing rapid, finely graded and bilateral signalling.