An attempt to justify anthro moths for Wingthing, my visual novel (to which this is probably only slightly canon), including notes on evolution, anatomy, ontogeny, and pathology.
Anatomy
Pathology
Ontogeny
Juvenility
Adolescence
Adulthood
Known phylogeny
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- † Pandemonium sp.
Plesiadapidae - † Protoramus sp.
Plesiadapidae - † Protoramus silvicola
Plesiadapidae - † Protoramus sp.
Plesiadapidae - † Protoramus sp.
Plesiadapidae - † Arboromorphus gracilipes
Calaeopteridae - † Arboromorphus sp.
Calaeopteridae - † Glidomys vulgaris
Calaeopteridae - † Glidomys pavon
Calaeopteridae - † Tetrachir elegans
Calaeopteridae - † Tetrachir manicheli
Calaeopteridae - † Arboromorphus sp.
Calaeopteridae
Pandemonium sp.
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Pandemonium is an extinct genus of the family Plesiadapidae.
Protoramus sp.
Protoramus is another extinct genus within the family Plesiadapidae.
Protoramus silvicola
Protoramus silvicola is another extinct genus within the family Plesiadapidae.
Protoramus sp.
Protoramus is another extinct genus within the family Plesiadapidae.
Protoramus sp.
Protoramus is another extinct genus within the family Plesiadapidae.
Family Calaeopteridae
Genus Arboromorphus
Arboromorphus gracilipes
Protoramus is another extinct genus within the family Calaeopteridae.
Arboromorphus sp.
Protoramus is another extinct genus within the family Calaeopteridae.
Arboromorphus sp.
Protoramus is another extinct genus within the family Calaeopteridae.
Genus Glidomys
Glidomys
Anatomy
Locomotion
Biomechanic analyses unanimously clock Glidomys as an arboreal genus, quadrupedal on the ground. It was capable of gliding short distances via thoracic membranes and had well-developed hind leg muscles for launches, alongside robust claws on fore- and hindlimbs for landings and climbing.
Wings
Glidomys' most prominent trait was the bifurcation of the spinous process in vertebra T5, located imediately below the scapulae. This vertebra's process is elongated alongside their tails to support a large, thin membrane, used for gliding in a manner similar to that of Petatarsus.
Mating displays
Members of the genus had large vibrissae used in mating displays with no obvious sexual dimorphism. Later members show keratinization beginning near the attachment sites of wing membranes, a precursor to similar displays on the wings of later genera and potentially already used for such a purpose in Glidomys.
Ecology
Ecological niche
Members were arboreal, crepuscular ambush predators which mainly fed on insects and reptiles. TK.
Social structure
Glidomys were strongly eusocial. TK.
Glidomys vulgaris
Glidomys vulgaris
Biometrics
Height | TK |
---|---|
Length | TK |
Weight | TK |
Anatomy
G. vulgaris is currently the earliest known occurence of the gliding wings seen in early Calaeopterids, although it may not have been the first. Its fifth thoracic vertebra is bifurcated in a manner adjacent to certain cervical vertebrae, with a thin wing membrane attached to the process and the side of their longer tails. These wings were smaller than those of descendants like G. pavon and lacked the keratinous supports and mobility seen in the succeeding genera Tetrachir and Calaeopteryx and were likely only usable across short distances.
Ecology
TK
Glidomys pavon
Glidomys pavon
Biometrics
Height | TK |
---|---|
Length | TK |
Weight | 350-400g |
Anatomy
Seperately from other members of its genus, G. pavon is known to have had keratinous scales at the base of its wing membranes, thought to have served as mechanical support as they grew larger than their initial forms. These scales are also hypothesized to have been used in mating displays, as seen in the subsequent genus Tetrachir.
Ecology
TK
Genus Tetrachir
Tetrachir
Anatomy
Secondary thoracic structures
Tetrachir's most striking characteristic is the repetition of its upper torso including forelimbs and wings. This is almost certainly caused by a mutation either of or of the regulatory elements of homeobox genes HOXC6 and HOXC8, although genetic tests have not been performed.
All secondary structures are degraded in size and functionality compared to the primary sets. This enabled Tetrachir and subsequent taxa to develop precision grips and therefore complex tool use without leaving their arboreal habitats, as the less dextrous secondary pair was able to specialize into grasping branches while the primary pair developed fine motor control comparable to those of late hominin genus Australopithecus. This undoubtedly generated a similar feedback loop to that seen in hominins, ultimately compounding in the "human-level" intelligence of contemporaneous members of Calaeopteryx.
Wings
While similar to the later wings of their preceding genus Glidomys, Tetrachir wings were seperate from their tails and covered in keratinous scales along the frontal plane, which were thickened and hardened at the edges for structural support. Mid to late members show a complete degredation of the tail, thought to have compensated for the vast energy cost of the developing wings.
Mating displays
Alongside retaining the display function of vibrissae, Tetrachir also displays significant mating display function in the scale patterns of its wings - indeed, this was likely the primary selection pressure behind their evolution given that they somewhat hinder flight, even contemporaneously.
Chemical analyses, while limited, suggest that these scales covered a large spectrum of vibrant colors and patterns. Such scales persist in the extant lineage in both form and function.
Ecology
TK.
Tetrachir elegans
Tetrachir elegans
Tetrachir manicheli
Tetrachir manicheli