The relation between size and performance is central for understanding the evolution of sensory systems, and much interest has been focused on mammalian eyes and ears. However, we know very little about olfactory organ size (OOS), as data for a representative set of mammals are lacking. Here, we present a cranial endocast method for estimating OOS by measuring an easily accessible part of the system, the perforated part of the ethmoid bone, through which the primary olfactory axons reach the olfactory bulb. In 16 species, for which relevant data are available, the area of the perforated ethmoid bone is directly proportional to the area of the olfactory epithelium. Thus, the ethmoid bone is a useful indicator enabling us to analyse 150 species, and describe the distribution of OOS within the class Mammalia. In the future, a method using skull material may be applied to fossil skulls. In relation to skull size, humans, apes and monkeys have small olfactory organs, while prosimians have OOSs typical for mammals of their size. Large ungulates have impressive olfactory organs. Relating anatomy to published thresholds, we find that sensitivity increases with increasing absolute organ size.

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The evolution of a particular sensory organ is often discussed with no consideration of the roles played by other senses. Here, we treat mammalian vision, olfaction and hearing as an interconnected whole, a three-dimensional sensory space, evolving in response to ecological challenges. Until now, there has been no quantitative method for estimating how much a particular animal invests in its different senses. We propose an anatomical measure based on sensory organ sizes. Dimensions of functional importance are defined and measured, and normalized in relation to animal mass. For 119 taxonomically and ecologically diverse species, we can define the position of the species in a three-dimensional sensory space. Thus, we can ask questions related to possible trade-off vs. co-operation among senses. More generally, our method allows morphologists to identify sensory organ combinations that are characteristic of particular ecological niches. After normalization for animal size, we note that arboreal mammals tend to have larger eyes and smaller noses than terrestrial mammals. On the other hand, we observe a strong correlation between eyes and ears, indicating that co-operation between vision and hearing is a general mammalian feature. For some groups of mammals we note a correlation, and possible co-operation between olfaction and whiskers.

Three poorly known nocturnal mammal species from the montane forests of the Taita Hills in Kenya, were studied via vocalization analysis. Here, their acoustic behaviour is described. The studied animals were the tree hyrax (Dendrohyrax sp.), the small-eared greater galago (Otolemur garnettii), and the dwarf galago (Paragalago sp.). High-quality loud calls were analysed using RAVEN PRO, and compared to calls of presumed closest relatives. Our findings include the first detailed descriptions of tree hyrax songs. Moreover, our results suggest that the tree hyrax of Taita Hills may be a taxon new to science, as it produces a characteristic call, the ‘strangled thwack’, not previously known from other Dendrohyrax populations. Our data confirms that the small-eared greater galago subspecies living in the Taita Hills is Otolemur garnettii lasiotis. The loud calls of the elusive Taita Hills dwarf galago closely resemble those of the Kenya coast dwarf galago (Paragalago cocos). Thus, the population in the Taita Hills probably belongs to this species. The Taita Hills dwarf galagos are geographically isolated from other dwarf galago populations, and live in montane cloud forest, which is an unusual habitat for P. cocos. Intriguingly, two dwarf galago subpopulations living in separate forest patches in the Taita Hills, Ngangao and Mbololo, have clearly different contact calls. The Paragalagos in Mbololo Forest may represent a population of P. cocos with a derived call repertoire, or, alternatively, they may actually be mountain dwarf galagos (P. orinus). Hence, differences in habitat, behaviour, and contact call structure suggest that there may be two different Paragalago species in the montane forests of the Taita Hills.

We studied a previously almost unknown nocturnal mammal, an apparently undescribed species of tree hyrax (Dendrohyrax sp.) in the moist montane forests of Taita Hills, Kenya. We used thermal imaging to locate tree hyraxes, observe their behavior, and to identify woody plants most frequently visited by the selective browsers. We also documented acoustic behavior in forest fragments of different sizes. Data on calling type and frequency were analyzed together with lidar data to estimate population densities and to identify forest stand characteristics associated with large populations. Viable populations were found only in the largest forest fragments (> 90 ha), where tree hyraxes preferred most pristine forest stands with high, multilayered canopies. The estimated population sizes in smaller forest fragments were very limited, and hyraxes were heard to call only during late night and early morning hours, presumably in order to avoid detection. While we frequently recorded tree hyrax songs in the largest forest fragments, we almost never heard songs in the small ones. All remaining subpopulations of the Taita tree hyrax are under threat of human disturbance and further habitat deterioration. Conservation efforts should include protection of all remaining habitat patches, but also reforestation of former habitat is urgently needed.

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