The nocturnal bottleneck hypothesis is a hypothesis to explain several mammalian traits. In 1942,
Gordon Lynn Walls described this concept which states that
placental mammals were mainly or even exclusively
nocturnal through most of their evolutionary history, from their origin 225 million years ago to after the
Cretaceous–Paleogene extinction event, 66 million years ago.[1] While some mammal groups later adapted to
diurnal (daytime) lifestyles to fill newly unoccupied
niches, the approximately 160 million years spent as nocturnal animals has left a lasting legacy on
basal mammalian
anatomy and physiology, and most mammals are still nocturnal.[2]
Mammals evolved from
cynodonts, a group of superficially dog-like
synapsids in the wake of the
Permian–Triassic mass extinction. The emerging
archosaurian groups that flourished after the extinction, including
crocodilians and
dinosaurs and their ancestors, drove the remaining larger cynodonts into extinction, leaving only the smaller forms.[3] The surviving cynodonts could only succeed in
niches with minimal competition from the
diurnal dinosaurs, evolving into the typical small-bodied
insectivorous dwellers of the nocturnal undergrowth.[4] While the early mammals continued to develop into several probably quite common groups of animals during the
Mesozoic, they all remained relatively small and nocturnal.
Only with the massive extinction at the end of the
Cretaceous did the dinosaurs leave the stage open for the establishment of a new fauna of mammals. Despite this, mammals continued to be small-bodied for millions of years.[5] While all the
largest animals alive today are mammals, the majority of mammals are still small nocturnal animals.[6]
Mammalian nocturnal adaptions
Numerous features of mammalian physiology, especially features relating to the sensory organs, appear to be adaptations to a nocturnal lifestyle. These include:
Senses
An acute sense of hearing, with coiling
cochleae, external
pinnae and auditory
ossicles in the ear.
Mitochondria with respiration rates five to seven times higher than those of reptiles of similar size.[11]
Fur to assist in thermo-regulation in a cold (night) environment.
Lack of an ocular shielding mechanism against (diurnal)
ultraviolet light.[12]
Loss of the ability to produce
gadusol, a chemical which protects against the sun.[13][14]
The
photolyase DNA repair mechanism, which relies on visible light, does not work in the placental mammals, despite being present and functional in bacteria, fungi, and most other animals.[15][16]
Burrowing lifestyle allowing sheltering from climate and diurnal predators appears to be a basal mammalian trait.[19]
References
^
abGerkema MP, Davies WI, Foster RG, Menaker M, Hut RA. The nocturnal bottleneck and the evolution of activity patterns in mammals. Proc Biol Sci. 2013 Jul 3;280(1765):20130508. doi: 10.1098/rspb.2013.0508
^Gamberale-Stille, G.; Hall, K. S. S.; Tullberg, B. S. (10 August 2006). "Signals of profitability? Food colour preferences in migrating juvenile blackcaps differ for fruits and insects". Evolutionary Ecology. 20 (5): 479–490.
doi:
10.1007/s10682-006-0015-y.
S2CID45267536.
^Cannon, B. (1 January 2004). "Brown Adipose Tissue: Function and Physiological Significance". Physiological Reviews. 84 (1): 277–359.
doi:
10.1152/physrev.00015.2003.
PMID14715917.