Sphingidae

Life-forms

Superregnum: Eukaryota
Cladus: Unikonta
Cladus: Opisthokonta
Cladus: Holozoa
Regnum: Animalia
Subregnum: Eumetazoa
Cladus: Bilateria
Cladus: Nephrozoa
Cladus: Protostomia
Cladus: Ecdysozoa
Cladus: Panarthropoda
Phylum: Arthropoda
Subphylum: Hexapoda
Classis: Insecta
Cladus: Dicondylia
Subclassis: Pterygota
Cladus: Metapterygota
Infraclassis: Neoptera
Cladus: Eumetabola
Cladus: Endopterygota
Superordo: Panorpida
Cladus: Amphiesmenoptera
Ordo: Lepidoptera
Subordo: Glossata
Cladus: Coelolepida
Cladus: Myoglossata
Cladus: Neolepidoptera
Infraordo: Heteroneura
Cladus: Eulepidoptera
Cladus: Ditrysia
Cladus: Apoditrysia
Cladus: Obtectomera
Cladus: Macroheterocera
Superfamilia: Bombycoidea

Familia: Sphingidae
Subfamiliae (3): Macroglossinae - Smerinthinae - Sphinginae
Name

Sphingidae Latreille, 1802.
References

Becker, V.O. & S.E. Miller, 2002: The large moths of Guana Island, British Virgin Islands: a survey of efficient colonizers (Sphingidae, Notodontidae, Noctuidae, Arctiidae, Geometridae, Hyblaeidae, Cossidae). The Journal of the Lepidopterists' Society 56 (1): 9–44. Full article: [1].
Cadiou, J.-M., 1995: Seven new species of Sphingidae. Lambillionea XCV 4 déc.: 499–515.
Chu, H.F. & Y. Wang, 1980: New species and new subspecies of the family Shingidae (Lepidoptera). Acta Zootaxonomica Sinica 5 (4): 418–426.
Clark, B.P., 1917: New American Sphingidae. Proceedings of the New England zoological Club 6: 57–72.
Clark, B.P., 1917: New American Sphingidae. Proceedings of the New England zoological Club 6: 99–114.
Clark, B.P., 1922: Twenty-five new Sphingidae. Proceedings of the New England zoological Club 8: 1–23.
Clark, B.P., 1923: Thirty-three new Sphingidae. Proceedings of the New England zoological Club 8: 47–77.
Clark, B.P., 1924: Twelve new Sphingidae. Proceedings of the New England zoological Club 9: 11–21.
Correa-Carmona, Y., Vélez-Bravo, A.H. & Echeverri, M.I.W. 2015. Current status of knowledge of Sphingidae Latreille, 1802 (Lepidoptera: Bombycoidea) in Colombia. Zootaxa 3987(1): 1–73. DOI: 10.11646/zootaxa.3987.1.1. Preview (PDF) ISBN 978-1-77557-745-4 (paperback); ISBN 978-1-77557-746-1 (Online edition) Reference page.
J. Haxaire et D. Herbin, 2000: Les Lépidoptères Sphingidae de Bolivie. Ecologie et systématique: deuxième partie: les sous-familles des Smerinthinae et des Macroglossinae (Lepidoptera). Revue de l’Association Roussillonnaise d’Entomologie 9 (1): 4–19.
Haxaire, J. & T. Melichar, 2011: Description de deux nouveaux Sphingidae du sud de la péninsule arabique (Lepidoptera: Sphingidae). The European Entomologist 3 (3): 159–168.
Hogenes, W. & C.G. Treadaway, 1998: The Sphingidae (Lepidoptera) of the Philippines. Nachrichten des Entomologischen Vereins Apollo Supplement 17: 17–132.
Pitkin, B. & P. Jenkins. Butterflies and Moths of the World: Generic Names and their Type-species. Natural History Museum.[2]
Kitching, I.J. & Cadiou, J.-M. 2000. Hawkmoths of the world: an annotated and illustrated revisionary checklist. Cornell University Press, Ithaca.
Rafi, M.A. et al. 2014: The hawkmoth fauna of Pakistan (Lepidoptera: Sphingidae). Zootaxa 3794(3): 393–418. DOI: 10.11646/zootaxa.3794.3.4 Reference page.
Rothschild, Lionel Walter & Jordan, Heinrich Ernst Karl: A revision of the lepidopterous family Sphingidae, The Zoological Museum, Tring, 1903.
Yen, Shen-Horn , Ian J. Kitching & Chao-Shian Tzen, 2003: A new subspecies of hawkmoth from Lanyu, with a revised and annotated checklist of the Taiwanese Sphingidae (Lepidoptera). Zoological Studies 42 (2): 292–306. Full article: [3]

Vernacular names
беларуская: Бражнікі
čeština: Lišajovití
Deutsch: Schwärmer
suomi: Kiitäjät
français: Sphingidés
magyar: Szenderfélék
日本語: スズメガ科
Nederlands: Pijlstaarten
polski: zawisakowate
српски / srpski: Вјештице
svenska: Svärmare
українська: Бражники
中文: 天蛾科

The Sphingidae are a family of moths (Lepidoptera) called sphinx moths, also colloquially known as hawk moths, with many of their caterpillars known as “hornworms”; it includes about 1,450 species.[1] It is best represented in the tropics, but species are found in every region.[2] They are moderate to large in size and are distinguished among moths for their agile and sustained flying ability, similar enough to that of hummingbirds as to be reliably mistaken for them.[2] Their narrow wings and streamlined abdomens are adaptations for rapid flight. The family was named by French zoologist Pierre André Latreille in 1802.

Some hawk moths, such as the hummingbird hawk-moth or the white-lined sphinx, hover in midair while they feed on nectar from flowers, so are sometimes mistaken for hummingbirds. This hovering capability is only known to have evolved four times in nectar feeders: in hummingbirds, certain bats, hoverflies, and these sphingids[3] (an example of convergent evolution). Sphingids have been much studied for their flying ability, especially their ability to move rapidly from side to side while hovering, called "swing-hovering" or "side-slipping". This is thought to have evolved to deal with ambush predators that lie in wait in flowers.[3]

Sphingids are some of the faster flying insects; some are capable of flying at over 5.3 m/s (19 km/h).[4] They have wingspans from 4 cm (1+1⁄2 in) to over 10 cm (4 in).

Description
Frenulum of a male comma nephele hawk moth as seen when the forewing is pulled back. It pierces a retinaculum on vein Sc on the ventral side of the forewing,[5] and couples the wings in flight for efficiency.[6] In males it consists of a single but compound bristle while in females it consists of several compound bristles.[7] A reduced frenulum is found in some Smerinthini.[6]

Antennae are generally not very feathery, even in males.[2] They lack tympanal organs, but members of the group Choerocampini have hearing organs on their heads.[2] They have a frenulum and retinaculum to join hindwings and forewings.[2] The thorax, abdomen, and wings are densely covered in scales. Some sphingids have a rudimentary proboscis, but most have a very long one,[2] which is used to feed on nectar from flowers. Most are crepuscular or nocturnal, but some species fly during the day.[8] Both males and females are relatively long-lived (10 to 30 days).[8] Prior to flight, most species shiver their flight muscles to warm them up, and, during flight, body temperatures may surpass 40 °C (104 °F).[8]

In some species, differences in form between the sexes is quite marked. For example, in the African species Agrius convolvuli (the convolvulus or morning glory hawk moth), the antennae are thicker and wing markings more mottled in the male than in the female. Only males have both an undivided frenular hook and a retinaculum. Also, all male hawkmoths have a partial comb of hairs along with their antennae.[9] Females call males to them with pheromones. The male may douse the female with a pheromone[8] before mating.
Behavior

Some species fly only for short periods either around dusk or dawn, while other species only appear later in the evening and others around midnight, but such species may occasionally be seen feeding on flowers during the day. A few common species in Africa, such as the Oriental bee hawk (Cephonodes hylas virescens), Macroglossum hirundo, and Macroglossum trochilus, are diurnal.[9]

A number of species are known to be migratory, all in the Sphingini and Macroglossinae, and specially in the genera Agrius, Cephonodes, Macroglossum, Hippotion and Theretra.[10]
Flight

In studies with Manduca sexta, moths have dynamic flight sensory abilities due to their antennae. The antennae are vibrated in a plane so that when the body of the moth rotates during controlled aerial maneuvers, the antennae are subject to the inertial Coriolis forces that are linearly proportional to the angular velocity of the body.[11] The Coriolis forces cause deflections of the antennae, which are detected by the Johnston's organ at the base of each antenna, with strong frequency responses at the beat frequency of the antennae (around 25 Hz) and at twice the beat frequency. The relative magnitude of the two frequency responses enables the moth to distinguish rotation around the different principal axes, allowing for rapid course control during aerial maneuvers.[12]
Vine hawk moth larva (Hippotion celerio)
An example of the posterior "horn" seen on the tomato hornworm
Life cycle

Most species are multivoltine, capable of producing several generations a year if weather conditions permit.[8] Females lay translucent, greenish, flattened, smooth eggs, usually singly on the host plants. Egg development time varies highly, from three to 21 days.
A Hyles gallii caterpillar seeking a place to pupate: the color of the caterpillar darkens before pupation.
Hyles euphorbiae pupa

Sphingid caterpillars are medium to large in size, with stout bodies. They have five pairs of prolegs.[8] Usually, their bodies lack any hairs or tubercules, but most species have a "horn" at the posterior end,[2] which may be reduced to a button, or absent, in the final instar.[8] Many are cryptic greens and browns, and have countershading patterns to conceal them. Others are more conspicuously colored, typically with white spots on a black or yellow background along the length of the body. A pattern of diagonal slashes along the side is a common feature. When resting, the larva usually holds its legs off the surface and tucks its head underneath (praying position), which, resembling the Great Sphinx of Giza, gives rise to the name "sphinx moth".[8] Some tropical larvae are thought to mimic snakes.[2][13] Larvae are quick to regurgitate their sticky, often toxic, foregut contents on attackers such as ants and parasitoids.[8] Development rate depends on temperature, and to speed development, some northern and high-altitude species sunbathe.[8] Larvae burrow into the soil to pupate, where they remain for two to three weeks before they emerge as adults.

In some Sphingidae, the pupa has a free proboscis, rather than being fused to the pupal case as is most common in the macrolepidoptera.[2] They have a cremaster at the tip of the abdomen.[8] Usually, they pupate off the host plant, in an underground chamber, among rocks, or in a loose cocoon.[8] In most species, the pupa is the overwintering stage.
Food plants
Larvae
Bee hawk moth (Cephonodes kingii), Crows Nest, New South Wales, Australia

Sphingid larvae tend to be specific feeders, rather than generalists.[8] Compared to similarly sized saturniids, sphingids eat soft young leaves of host plants with small toxic molecules, and chew and mash the food into very small bits.[14] Some species can tolerate quite high concentrations of specific toxins. Tobacco hornworms (Manduca sexta) detoxify and rapidly excrete nicotine, as do several other related sphinx moths in the subfamilies Sphinginae and Macroglossinae, but members of the Smerinthinae that were tested are susceptible.[15] The species that are able to tolerate the toxin do not sequester it in their tissues; 98% was excreted. However, other species, such as Hyles euphorbiae and Daphnis nerii, do sequester toxins from their hosts, but do not pass them on to the adult stage.[8]
Adults
Hummingbird clearwing moth (Hemaris thysbe) feeding on lantana flowers
A feeding hawk moth at Olympiaki Akti, Greece
Hummingbird hawk moth (Macroglossum stellatarum), wing action frozen using electronic flash.

Most adults feed on nectar, although a few tropical species feed on eye secretions, and the death's-head hawkmoths steal honey from bees.[8] Night-flying sphingids tend to prefer pale flowers with long corolla tubes and a sweet odor, a pollination syndrome known as "sphingophily".[3] Some species are quite general in visitations, while others are very specific, with the plant only being successfully pollinated by a particular species of moth.[3] Orchids frequently have such specific relations with hawk moths and very long corolla tubes. The comet orchid (Angraecum sesquipedale), a rare Malagasy flower with its nectar stored at the bottom of a 30-centimetre-long (12 in) tube, was described in 1822 by Louis-Marie Aubert du Petit-Thouars, and later, Charles Darwin famously predicted there must be some specialized moth to feed from it:

[A. sesquipetale has] nectaries 11 and a half inches long [29 cm], with only the lower inch and a half [4 cm] filled with very sweet nectar [...] it is, however, surprising, that any insect should be able to reach the nectar: our English sphinxes have probosces as long as their bodies, but in Madagascar, there must be moths with probosces capable of extension to a length of between 10 and 12 inches! [25 and 30 cm][16]

Alfred Russel Wallace published a sort of "wanted poster" (properly, a drawing in a book)[17] of what this lepidopteran might look like, and, concurring with his colleague, added:

[The proboscis of a hawk moth] from tropical Africa ([Xanthopan] morganii) is seven inches and a half [19 cm]. A species having a proboscis two or three inches longer [8 cm] could reach the nectar in the largest flowers of Angraecum sesquipedale, whose nectaries vary in length from ten to fourteen inches [36 cm]. That such a moth exists in Madagascar may be safely predicted, and naturalists who visit that island should search for it with as much confidence as astronomers searched for the planet Neptune, – and they will be equally successful.[18]

The predicted sphingid was discovered 21 years later and described as a subspecies of the one African species studied by Wallace: Xanthopan morganii praedicta,[19] for which, the subspecific name praedicta ("the predicted one") was given. The Madagascan individuals had a pink, rather than white, breast and abdomen and a black apical line on the forewing, broader than in mainland specimens. Molecular clock models using either rate- or fossil-based calibrations imply that the Madagascan subspecies X. morgani praedicta and the African subspecies morgani diverged 7.4 ± 2.8 Mya (million years ago), which overlaps the divergence of A. sesquipedale from its sister, A. sororium, namely 7.5 ± 5.2 Mya.[20] Since both these orchids have extremely long spurs, longspurs likely existed before that and were exploited by long-tongued moths similar to Xanthopan morganii praedicta. The long geological separation of subspecies morgani and praedicta matches their morphological differences in the color of the breast and abdomen.
Relationships and species
Oleander hawk moth (Daphnis nerii), in Mangaon, Maharashtra, India
A sphinx moth, subfamily Macroglossinae, in Cibodas Botanical Garden, Java

The Sphingidae is sometimes assigned its own exclusive superfamily, Sphingoidea, but is alternatively included with the more encompassing Bombycoidea. Following Hodges (1971) two subfamilies are accepted, namely the Sphinginae and Macroglossinae.[5] Around 1,450 species of hawk moths are classified into around 200 genera. Some of the best-known hawk moth species are:

Privet hawk moth (Sphinx ligustri)
White-lined Sphinx (Hyles lineata)
Death's-head hawk moth (Acherontia atropos)
Lime hawk moth (Mimas tiliae)
Poplar hawk moth (Laothoe populi)
Convolvulus hawk moth (Agrius convolvuli)
Catalpa sphinx (Ceratomia catalpae)
Hummingbird hawk-moth (Macroglossum stellatarum)
Elephant hawk moth (Deilephila elpenor)
Vine hawk moth (Hippotion celerio)
Spurge hawk moth (Hyles euphorbiae)
Oleander hawk moth (Daphnis nerii)
Pandora sphinx moth (Eumorpha pandorus)
Tomato worm (Manduca quinquemaculata)
Tobacco hornworm (Manduca sexta)

See also

List of moths of Great Britain (Sphingidae)
List of moths of India
Sphingidae species list
Twin-spotted sphinx moth

References

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Scoble, Malcolm J. (1995): The Lepidoptera: Form, Function and Diversity (2nd edition). Oxford University Press & Natural History Museum London. ISBN 0-19-854952-0
Kitching, Ian J (2002). "The phylogenetic relationships of Morgan's Sphinx, Xanthopan morganii (Walker), the tribe Acherontiini, and allied long-tongued hawkmoths (Lepidoptera: Sphingidae, Sphinginae)". Zoological Journal of the Linnean Society. 135 (4): 471–527. doi:10.1046/j.1096-3642.2002.00021.x.
Stevenson, R.; Corbo, K.; Baca, L.; Le, Q. (1995). "Cage size and flight speed of the tobacco hawkmoth Manduca sexta" (PDF). The Journal of Experimental Biology. 198 (Pt 8): 1665–1672. doi:10.1242/jeb.198.8.1665. PMID 9319572. Retrieved 10 August 2012.
Common, I.F.B. (1990). Moths of Australia. Leiden: Brill. p. 24. ISBN 9789004092273.
Schreiber, Harald (1978). Dispersal Centres of Sphingidae (Lepidoptera) in the Neotropical Region. Dordrecht: Springer Netherlands. p. 18. ISBN 9789400999602.
Messenger, Charlie (1997). "The Sphinx Moths (Lepidoptera: Sphingidae) of Nebraska". Transactions of the Nebraska Academy of Sciences (24): 91–93. Retrieved 18 April 2016.
Pittaway, A. R. (1993): The Hawkmoths of the Western Palaearctic. Harley Books & Natural History Museum, London. ISBN 0-946589-21-6
Pinhey, E. (1962): Hawk Moths of Central and Southern Africa. Longmans Southern Africa, Cape Town.
Holloway, J.D. (1987). "Family Sphingidae". The Moths of Borneo. Southene Sdn Bhd.
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Bernays, E. A.; Janzen, D. H. (1988). "Saturniid and sphingid caterpillars: two ways to eat leaves". Ecology. 69 (4): 1153–1160. doi:10.2307/1941269. JSTOR 1941269. S2CID 56310810.
Wink, M.; Theile, Vera (2002). "Alkaloid tolerance in Manduca sexta and phylogenetically related sphingids (Lepidoptera: Sphingidae)". Chemoecology. 12: 29–46. doi:10.1007/s00049-002-8324-2. S2CID 41120103.
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Netz, Christoph; Renner, Susanne S. (2017). "Long-spurred Angraecum orchids and long-tongued sphingid moths on Madagascar: A time-frame for Darwin's predicted Xanthopan/Angraecum coevolution". Biological Journal of the Linnean Society. 122 (Supplement): 469–478. doi:10.1093/biolinnean/blx086.