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Nigersaurus taqueti shows extreme adaptations for a dinosaurian herbivore including a skull of extremely light construction, tooth batteries located at the distal end of the jaws, tooth replacement as fast as one per month, an expanded muzzle that faces directly toward the ground, and hollow presacral vertebral centra with more air sac space than bone by volume.
Some species show extreme adaptations for nectar collections, such as the tube-lipped bat in Ecuador, which is the owner of an extraordinary tongue that's over one and a half times its body length, used for reaching into deep petals.
Its extreme adaptations for herbivory at ground-level challenge current hypotheses regarding feeding function and feeding strategy among diplodocoids, the larger clade of sauropods that includes Nigersaurus.
Extreme adaptations for aquatic ectoparasitism in a Jurassic fly larva.
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This long narrow wing with a high-lift airfoil is an extreme adaptation for fixed-wing gliding.
This habitual head posture is one of several extreme adaptations in Nigersaurus for ground-level browsing, a feeding strategy that may have played an important role in the diplodocoid radiation of the Jurassic.
Their extreme adaptations reflect the severe predation on pronghorns during the Ice Age.
The extreme adaptations and characteristics of the BMR, together with the reported genome and transcriptome, will empower future use of the BMR model for biomedical research in the fight against cancer, stroke and cardiovascular diseases.
In particular, parasites displaying host alternation may show extreme specificity and adaptations for two very distantly related hosts with few features in common [ 1].
The differences may be extreme, as in the adaptations for sexual selection seen in the exotic plumes and colours of the male bird-of-paradise (family Paradisaeidae) or in the adaptations for protection exemplified by the great size and huge canine teeth of the male baboon (Papio).
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