Ostriches Sleep like Platypuses

Mammals and birds engage in two distinct states of sleep, slow wave sleep (SWS) and rapid eye movement (REM) sleep. SWS is characterized by slow, high amplitude brain waves, while REM sleep is characterized by fast, low amplitude waves, known as activation, occurring with rapid eye movements and reduced muscle tone. However, monotremes (platypuses and echidnas), the most basal (or ‘ancient’) group of living mammals, show only a single sleep state that combines elements of SWS and REM sleep, suggesting that these states became temporally segregated in the common ancestor to marsupial and eutherian mammals. Whether sleep in basal birds resembles that of monotremes or other mammals and birds is unknown. Here, we provide the first description of brain activity during sleep in ostriches (Struthio camelus), a member of the most basal group of living birds. We found that the brain activity of sleeping ostriches is unique. Episodes of REM sleep were delineated by rapid eye movements, reduced muscle tone, and head movements, similar to those observed in other birds and mammals engaged in REM sleep; however, during REM sleep in ostriches, forebrain activity would flip between REM sleep-like activation and SWS-like slow waves, the latter reminiscent of sleep in the platypus. Moreover, the amount of REM sleep in ostriches is greater than in any other bird, just as in platypuses, which have more REM sleep than other mammals. These findings reveal a recurring sequence of steps in the evolution of sleep in which SWS and REM sleep arose from a single heterogeneous state that became temporally segregated into two distinct states. This common trajectory suggests that forebrain activation during REM sleep is an evolutionarily new feature, presumably involved in performing new sleep functions not found in more basal animals

Phylogeny and Taxonomy of the Round-Eared Sengis or Elephant-Shrews, Genus Macroscelides (Mammalia, Afrotheria, Macroscelidea)

The round-eared sengis or elephant-shrews (genus Macroscelides) exhibit striking pelage variation throughout their ranges. Over ten taxonomic names have been proposed to describe this variation, but currently only two taxa are recognized (M. proboscideus proboscideus and M. p. flavicaudatus). Here, we review the taxonomic history of Macroscelides, and we use data on the geographic distribution, morphology, and mitochondrial DNA sequence to evaluate the current taxonomy. Our data support only two taxa that correspond to the currently recognized subspecies M. p. proboscideus and M. p. flavicaudatus. Mitochondrial haplotypes of these two taxa are reciprocally monophyletic with over 13% uncorrected sequence divergence between them. PCA analysis of 14 morphological characters (mostly cranial) grouped the two taxa into non-overlapping clusters, and body mass alone is a relatively reliable distinguishing character throughout much of Macroscelides range. Although fieldworkers were unable to find sympatric populations, the two taxa were found within 50 km of each other, and genetic analysis showed no evidence of gene flow. Based upon corroborating genetic data, morphological data, near sympatry with no evidence of gene flow, and differences in habitat use, we elevate these two forms to full species

Male mate guarding in a socially monogamous mammal, the round-eared sengi: on costs and trade-offs

Abstract Mate guarding is predicted to be one of the driving forces for the evolution of monogamy, but supporting evidence in free-living mammals is rare. The goals of our study were three-pronged. First, we tested if mate guarding, measured as intrapair distance, occurs as a behavioral tactic in round-eared sengis (Macroscelides proboscideus), a socially monogamous species lacking paternal care and in which females breed asynchronously, producing 2–3 litters during an 8-month long breeding season. Second, we determined if mate guarding involves costs which we identified as changes in male body mass. Third, we investigated whether variation in individual investment in mate guarding depended on the males’ body mass and the number of neighboring males. Field data were collected in a semidesert in South Africa using radio-tracking, trapping, and direct observations during three successive breeding seasons. Mate guarding strongly depended on the females’ reproductive state, and all males started to guard their mates prior to and during estrus, as exemplified by reduced intrapair distance. Mate guarding incurred costs: overall, males lost about 5% of body mass. Male body mass loss and initial body mass were negatively related to the intensity of precopulatory mate guarding. Furthermore, during estrus intrapair distance was inversely correlated with the number of neighboring males. The results show that mate guarding is the predominant male tactic in round-eared sengis. However, since mate guarding imposed costs, males may balance benefits and costs associated with guarding by varying their effort in relation to their physical capabilities and the competitive environment