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American Giant Millipede

Narceus americanus (Palisot de Beauvouis 1817)

Behavior

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North American millipedes sense their environment using their antennae, which can taste food, smell odors, feel, measure temperature, find water, and sense pheromones. Their Tömösváry organs, found at the base of the antennae, specifically measure humidity and possibly act as chemoreceptors. In addition, they have eyes on either side of the head which detect light and movement. Potential mates communicate using pheromones and silk trails.

Communication Channels: visual ; tactile ; chemical

Other Communication Modes: pheromones ; vibrations

Perception Channels: visual ; tactile ; vibrations ; chemical

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Millican, K. 2013. "Narceus americanus" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Narceus_americanus.html
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Kelli Millican, University of Michigan-Ann Arbor
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Jeremy Wright, University of Michigan-Ann Arbor
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Associations

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Millipedes have a variety of defenses against predators. North American millipedes secrete a substance containing large amounts of benzoquinones that may cause dermal burns and discoloration. In addition to defensive secretions, millipedes will roll up in a tight ball to expose their hard exoskeleton as armor. In spite of these defenses, North American millipedes are prey items to many other animals, including ants, beetles, birds, centipedes, cockroaches, dogs, foxes, frogs, lizards, moles, opossums, raccoons, salamanders, scorpions, shrews, skunks, toads, and turtles.

Known Predators:

  • American robin (Turdus migratorius)
  • American toad (Anaxyrus americanus)
  • Brown-headed cowbird (Molothrus ater)
  • Common black ground beetle (Pterostichus melanarius)
  • Cockroach (Order Blattodea)
  • Dog (Canis lupis familiaris)
  • Eastern mole (Scalopus aquaticus)
  • European starling (Sturnus vulgaris)
  • Fire ant (Solenopsis sp.)
  • Five-lined skink (Plestiodon fasciatus)
  • Frogs (Order Anura, Class Amphibia)
  • Fox (Family Canidae, Order Carnivora)
  • Garden centipedes (Class Chilopoda)
  • Least shrew (Cryptotis parva)
  • Lizards (Order Squamata, Class Reptilia)
  • Raccoon (Procyon lotor)
  • Scorpions (Order Scorpiones, Class Arachnida)
  • Spotted salamander (Ambystoma maculatum)
  • Striped skunk (Mephitis mephitis)
  • Three-lined salamander (Eurycea guttolineata)
  • Turtle (Order Testudines, Class Reptilia)
  • Virginia opossum (Didelphis virginiana)
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Millican, K. 2013. "Narceus americanus" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Narceus_americanus.html
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Kelli Millican, University of Michigan-Ann Arbor
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Jeremy Wright, University of Michigan-Ann Arbor
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Morphology

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Although their common name, "millipede," implies that these animals have one thousand legs, the highest number of legs on record for an individual is 375 pairs; most millipedes have fewer than 50 pairs. North American millipedes have two pairs of legs attached to each body segment (except for a few segments at the anterior and posterior ends that have one pair). Centipedes, a closely related group of animals, can be distinguished from millipedes as they have only one pair of legs per body segment and venomous claws below their mouths. In general, bodies of millipedes are long and cylindrical, with many segments that are covered by a cuticle consisting of three layers. North American millipedes can reach up to 2.5 grams in weight and 10.2 centimeters in length. Individuals are mainly black, though the edges of their body segments show a range of colors including yellow, purple and pink. All millipedes have spiracles on their body segments, which are connected to their tracheal respiratory system and pairs of ozadenes (stink glands) connected to ozopores. These ozopores release a noxious substance, produced by the ozadenes, which contains large amounts of benzoquinones and may cause chemical burns. Unlike many millipedes, North American millipedes do not release hydrogen cyanide when threatened. Sub-species of North American millipede differ in the number and appearance of legs and body segments as well as color. Typically, males of this species have longer legs and antennae than females.

Average mass: 2.5 g.

Range length: 10.2 (high) cm.

Other Physical Features: ectothermic ; bilateral symmetry

Sexual Dimorphism: sexes shaped differently

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Millican, K. 2013. "Narceus americanus" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Narceus_americanus.html
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Kelli Millican, University of Michigan-Ann Arbor
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Life Expectancy

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North American millipedes typically live for several years. The longest recorded lifespan in this species is 11 years.

Typical lifespan
Status: wild:
1 to 11 years.

Typical lifespan
Status: captivity:
1 to 11 years.

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Millican, K. 2013. "Narceus americanus" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Narceus_americanus.html
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Kelli Millican, University of Michigan-Ann Arbor
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Habitat

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These millipedes are terrestrial animals most often found in forests and agricultural areas in the soil-litter layer interface under rocks, boards, dead trees, and piles of moist dead leaves, and occasionally in moist animal corpses. They are also found in urban and suburban areas. Because their cuticles are permeable to water, they are restricted to habitats where humidity is high, otherwise they quickly become dehydrated. While different species of millipedes have been found from sea level up to snow lines of mountains, the elevation boundaries of this species are unknown.

Habitat Regions: temperate ; terrestrial

Terrestrial Biomes: forest

Other Habitat Features: urban ; suburban ; agricultural

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Millican, K. 2013. "Narceus americanus" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Narceus_americanus.html
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Kelli Millican, University of Michigan-Ann Arbor
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Distribution

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North American millipedes, including several sub-species, are found in the United States in all states east of the Mississippi River and nine states to the west (Minnesota, Iowa, Missouri, Arkansas, Louisiana, Nebraska, Kansas, Oklahoma, and Texas) and Canada (Quebec and Ontario provinces). This distribution is likely to change, however, as recent analysis of the taxonomy and distribution records of this species indicates that it probably represents a complex of multiple species.

Biogeographic Regions: nearctic (Native )

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Millican, K. 2013. "Narceus americanus" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Narceus_americanus.html
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Kelli Millican, University of Michigan-Ann Arbor
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Trophic Strategy

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Millipedes are detritivores and prefer decaying leaves, wood, and roots, especially if the decaying matter has bacteria and fungi, which may increase the availability of nutrients and palatability. They sometimes eat live vegetation but rarely animal tissue. Most are coprophages and eat their own feces, which allows them to digest nutrients that were not digested the first time. They use their mandibles to bite and crush food into small pieces. Salivary glands open in the foregut and secrete a lubricating solution. Microorganisms in the gut help to digest tougher material.

Plant Foods: leaves; roots and tubers; wood, bark, or stems; algae

Other Foods: fungus; detritus ; dung; microbes

Primary Diet: mycophage ; detritivore ; coprophage

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Millican, K. 2013. "Narceus americanus" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Narceus_americanus.html
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Kelli Millican, University of Michigan-Ann Arbor
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Jeremy Wright, University of Michigan-Ann Arbor
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Associations

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North American millipedes are important in their ecosystems as decomposers, stimulators of microbial activity, and are very important in the cycling of terrestrial calcium. While this species does not act as a predator or parasite itself, they do engage in mutualism with certain species of ants, providing sanitary services in return for protection from predators. This species is an intermediate host to parasitic worms such as Oligacanthorhynchus tortuosa (before its definitive host, Didelphis virginiana) and Macracanthorhynchus ingens (before its definitive hosts, which include dogs, foxes and raccoons), protists (Enterobryus elegans and Enterobryus euryuri), and nematodes (Rhigonema sp.). They are also commensals with some species of mites (Narceolaelaps americanus in particular)

Ecosystem Impact: biodegradation

Species Used as Host:

  • None known

Mutualist Species:

  • Narceolaelaps americanus (Family Laelapidae, Subclass Acari)

Commensal/Parasitic Species:

  • Enterobryus elegans (Family Eccrinaceae, Phylum Choanozoa)
  • Enterobryus euryuri (Family Eccrinaceae, Phylum Choanozoa)
  • Macracanthorhynchus ingens (Family Oligacanthorhynchida, Order Archiacanthocephala)
  • Oligacanthorhynchus tortuosa (Family Oligacanthorhynchida, Order Archiacanthocephala)
  • Nematodes (Rhigonema sp.)
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Millican, K. 2013. "Narceus americanus" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Narceus_americanus.html
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Kelli Millican, University of Michigan-Ann Arbor
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Benefits

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Millipedes are model organisms for studying arthropod physiology and segmentation. Their defensive secretions may also show promise as sources of new pharmaceuticals.

Positive Impacts: source of medicine or drug ; research and education

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Millican, K. 2013. "Narceus americanus" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Narceus_americanus.html
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Kelli Millican, University of Michigan-Ann Arbor
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Benefits

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These millipedes produce a substance that irritates and discolors human skin. In addition, they can do significant economic damage to root crops and are a nuisance when they swarm into homes and cover railroad tracks and roadways.

Negative Impacts: crop pest; household pest

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Millican, K. 2013. "Narceus americanus" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Narceus_americanus.html
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Kelli Millican, University of Michigan-Ann Arbor
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Life Cycle

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Fertilized eggs are laid in a nest made of chewed up leaves and excrement that is made by the female. Although most millipedes lay hundreds of eggs at a time, the scientific literature indicates that each North American millipede nest typically contains only one egg. When they hatch, young have three pairs of legs and seven body segments. With each molt, they gain more body segments, legs, and other structures. North American millipedes molt many times throughout their lifetimes and size is directly related to age.

Development - Life Cycle: indeterminate growth

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Millican, K. 2013. "Narceus americanus" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Narceus_americanus.html
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Kelli Millican, University of Michigan-Ann Arbor
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Conservation Status

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This species has no special conservation status.

US Federal List: no special status

CITES: no special status

State of Michigan List: no special status

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Millican, K. 2013. "Narceus americanus" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Narceus_americanus.html
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Kelli Millican, University of Michigan-Ann Arbor
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Untitled

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Millipedes first appeared in the fossil record 400 million years ago and are some of the first animals to have lived on land. It is hypothesized that these ancient species are the largest animals without backbones to have walked on earth. Modern forms appear in the late Paleozoic. While North American millipedes are currently classified as diplopods, Linnaeus classified them as apterate insects, Lamarck said they were arachnids, and others have called them worms or crustaceans. They belong to a diverse group with more than 10,000 described species.

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Millican, K. 2013. "Narceus americanus" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Narceus_americanus.html
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Kelli Millican, University of Michigan-Ann Arbor
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Reproduction

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North American millipedes breed seasonally, beginning in the spring and early summer. Males spin a silken thread and emit pheromones in order to attract females. During millipede mating, males walk along females' backs in order to stimulate them. Females will raise their front segments, allowing males to pass a packet of stored sperm (spermatophore) to females. Some females mate only once, using stored sperm to fertilize all the eggs laid while others mate multiple times with other males. Males typically mate with several different females.

Mating System: polygynandrous (promiscuous)

North American millipedes' breeding season begins in the late spring/early summer and continues into autumn. Eggs hatch within a few weeks of being laid, although development times can shift with temperature changes. A female lays one egg in her prepared nest then wraps herself around the egg for brooding. Once the egg hatches there is no further parental involvement. Young millipedes take 1-2 years to reach maturity, with males usually reaching maturity first.

Breeding interval: North American millipedes may mate multiple times during their breeding season

Breeding season: Late spring through autumn

Range number of offspring: 1 (low) .

Range gestation period: 2 to 10 weeks.

Range age at sexual or reproductive maturity (female): 1 to 4 years.

Range age at sexual or reproductive maturity (male): 1 to 4 years.

Key Reproductive Features: iteroparous ; seasonal breeding ; gonochoric/gonochoristic/dioecious (sexes separate); sexual ; fertilization (Internal ); oviparous ; sperm-storing ; delayed fertilization

After mating, females may delay fertilization and protect the unfertilized eggs within their bodies. Females protect fertilized eggs by curling their body around them.

Parental Investment: pre-fertilization (Provisioning, Protecting: Female); pre-hatching/birth (Protecting: Female)

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Millican, K. 2013. "Narceus americanus" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Narceus_americanus.html
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Comprehensive Description

provided by Memoirs of the American Entomological Society
Narceus americanus (Palisot de Beauvois)
Figures 17, 30-31, 44-51, 69-74, 84-85, 89-91
Jtilus americae borealis Palisot de Beauvois, Insectes recueillis en Afrique et en
Amerique, livr. 9, p. 155. 1817. Julus americanus Palisot de Beauvois, ibid., Apteres, pi. IV, fig. 3. Narceus tinctorius Rafinesque, Annals of Nature, p. 8. 1920. New synonymy. lulus americanus, Gervais, Hist. Nat. Insectes, vol. 4, Apteres, p. 181. 1947. Julus atratus Girard, in Marcy, Exploration of Red River of Louisiana, p. 244.
1853. New synonymy. Julus crassus Motschulsky [not Linnaeus, 1758], Etudes Entomologiques, Cin-
quieme annee 1856, p. 4, 1857. New synonymy. Spirostreptus zvoodi Humbert and Saussure, Rev. Mag. Zool., ser. 2, vol. 22, p.
177. 1870. New synonymy. Spirobolus marginatus, Bollman, Ann. New York Acad. Sci., vol. 4, p. 28. 1887. Spirobolus pensacolae Bollman, ibid., p. 29. New synonymy. Spirobolus atratus, Bollman, ibid., p. 43. Spirobolus woodi, Bollman, ibid., p. 44.
Spirobolus pensacolae Bollman, Entomologica Americana, vol. 2, p. 227. 1887. Spirobolus marginatus, Bollman (in part), Proc. U. S. Nat. Mus., vol. 11, p. 343.
1888. Jxdus americae-borealis, Bollman, U. S. Nat. Mus. Bull., no. 46, p. 146. 1893. Arctobolus marginatus. Cook, Harriman Alaska Exped., vol. 8, p. 65. 1904. Spirobolus marginatus, Williams and Hefner (in part), Ohio State Univ. Bull.,
vol. 33, p. 123. 1928. Spirobolus oklahomae Chamberlin, Ent. News, vol. 42, p. 98. fig. 1. 1931. New
synonymy. Arctobolus dolleyi Loomis, Bull. Mus. Comp. Zool., vol. 92, p. 398, fig. 13. 1943.
New synonymy. Spirobolus ramstadti Chamberlin, Bull. Univ. Utah, biol. ser., vol. 8, no. 2, p. 7,
figs. 12-16. 1943. New synonymy. Spiroholus meJanior Chamberlin, ibid., p. 9. New synonymy.
Spirobolus dolleyi, Hoffman, Journ. Elisha Mitchell Sci. Soc, vol. 66, p. 31. 1950.
Julus americae borealis, Hoffman, Florida Ent., vol. 34, p. 15. 1951.
Julus americanus, Hoffman, ibid., pp. 15-16.
Spirobolus marginatus, Hoffman, ibid., p. 16.
Spirobolus americanus, Hoffman (in part), ibid., p. 16.
Narceus tinctorius, Hoffman and Crabill, Florida Ent., vol. 36, pp. 80, 82. 1953.
Narceus americanus, Chamberlin (in part), Amer. Midi. Nat., vol. 50, p. 150.
1953. Narceus melanior Chamberlin, ibid., p. 150.
Narceus tinctorius. Causey, Journ. Kansas Ent. Soc, vol. 28, p. 71, fig. 2. 1955. Julus atratus. Causey, ibid., p. 71. Spirobolus agilis. Causey, ibid., p. 71. Spirobolus woodi. Causey, ibid., p. 71. Arctobolus dolleyi, Causey, ibid., p. 71. Narceus americanus. Causey, ibid., p. 72. Julus americae borealis, Causey, ibid., p. 72. Julus americanus. Causey, ibid., p. 72. Julus americanus borealis [sic], Causey, ibid., p. 72. Narceus oklahomae. Causey, ibid., pp. 71, 74. Narceus orophilus. Causey, ibid., pp. 71, 75. Narceus pensacolae, Causey, ibid., p. 75. Narceus melanior, Causey, ibid., p. 75. Narceus ramstadti. Causey, ibid., p. 75. Narceus tinctorius, Hoffman, Proc. Biol. Soc. Washington, vol. 70, p. 65, figs. 1,
4. 1957. Narceus ramstadi. Causey, Proc. Biol. Soc. Washington, vol. 70, p. 205. 1957. Narceus americanus, Chamberlin and Hoffman, U. S. Nat. Mus. Bull., no. 212,
p. 165. 1958. Narceus atratus, Chamberlin and Hoffman, ibid., p. 166. Narceus dolleyi, Chamberlin and Hoffman, ibid., p. 166. Narceus melanior, Chamberlin and Hoffman, ibid., p. 166. Narceus oklahomae, Chamberlin and Hoffman, ibid., p. 167. Narceus pensacolae, Chamberlin and Hoffman, ibid., p. 167. Narceus ramstadi, Chamberlin and Hoffman, ibid., p. 167. Narceus tinctorius, Chamberlin and Hoffman, ibid., p. 167. Narceus woodi, Chamberlin and Hoffman, ibid., p. 168.
Nomenclatorial Considerations. — The oldest specific names in the Spirobolidae are americae borealis and americanus, both pubHshed in 1817 (according to Griffin, 1937) by Palisot de Beauvois, and both applied to the same species. Exercising the " right of the first reviser ", Hoffman (1951) selected americanus as the name to be used. There
has been no agreement, however, as to which species Palisot described.
The original description of americanus gave Httle information on which to base an identification. It is my opinion, however, that it gave enough. Three characters must be considered : PaUsot's statement that his specimen had 49 segments, and the color and size as indicated by the figure (which is supposed to be natural size). Four species occur in the area in which Palisot traveled. Chicobolus spinigerus can be eliminated by its color. Narceus gordanus can be eliminated by its body proportions. The common northern species, Narceus annularis, never has as few as 49 segments (see Table 14). This leaves only the common southern species of Narceus, and it is herein designated americanus.
I have examined the types of woodi, pensacolae, oklahomae, dolleyi, and melanior, and consider them conspecific. The male pregenital coxae of oklahomae are somewhat unusual but appear to be the result of incomplete development; the female allotype is not unusual in any way. Both atratus and crassus were described from a locality where only one species of spirobolid occurs. I have examined topotypes of ramsfadti that agree in every way with Chamberlin's description ; the mesal processes of the sterna of the anterior gonopods are narrower than usual but study of other Florida specimens indicates this is a variable character and not worthy of nomenclatorial recognition. Two species of Narceus occur in Kentucky, but I have accepted the definitions of tinctorius given by Causey (1955a) and by Hoffman (1957) ; these descriptions apply to the more common species in that area.
Diagnosis. — Distinguished from gordanus by shape of the collum, shallower antennal groove, lack of a carina on the parietal sclerite, longer legs, larger lobes on the male pregenital coxae, and characters of the genitalia of both sexes. Differs from anmdaris in the characters given in the key and in Table 13. These characters are discussed in the remarks section under anmdaris.
Description.— L of males 51-125 mm. (78.5), of females 42-103 mm. (78.5) ; W of males 5.0-11.9 mm. (7.92), of females 4.9-10.4 mm. (8.15) ; L/W of males 8.4-11.8 (10.1), of females 8.1-11.7 (9.8). Segments 47-55 (51.1). Generally medium to dark brown (averaging somewhat lighter than annularis) with reddish hindbelts and legs ; specimens of this species seem to fade worse in alcohol than do those of annularis. Antennal groove moderately deep, well-delimited both anteriorly and posteriorly. Surface of parietal sclerite undulate but without a carina; sclerite tapering caudad. Mandibular cheek moderately grooved. Eyes per patch 35-60 (43.7). Clypeal setae 7-16 (9.7) ; labral setae 12-25 (16.3).
Colliim usually covering only vertex of head, leaving eye patches, antennal grooves, and mandibular cheeks exposed; anterior margin of collum usually angling slightly caudad at level of eye patches, emarginate below angles, : Second segment produced below ends of collum, the production moderately long, usually broad and rounded or truncate (sometimes subacute) ; ridge along anterior margin of production, this usually curving around ventral end of production, the ridge usually not as large as that of annularis, not much stronger than striae on median surface of production.
Coxae of male 3rd legs with large ventral lobes, these usually long and expanded laterally (figure 44) ; a deep transverse groove usually present on cephalic surface. Coxal lobes of 4th and 5th legs usually long, relatively narrow, and usually turgid. Lobes of 6th legs similar but usually shorter and broader. Coxae of 7th legs sometimes slightly produced, often not. Third segments of male legs 3-7 longer than 2nd segments, compressed, usually concave on caudal surface. Coxae of female 3rd legs usually produced ventrad, the lobe sometimes bent caudad. Legs relatively long, exceeding sides of body when held horizontally.
Gonopods like those of annularis except coxal endites usually slightly broader and prefemoral endites often acute distally.
Cyphopod thinner distally than in annularis, distal lobe usually not curved caudad. Distal corner of lateral flange often produced to form a tooth, a second tooth sometimes present on more proximal portion of flange.
Type. — Presumed lost ; a personal communication from J. M. Demange of the Paris Museum indicates that Palisot's specimen is not in the collection of that institution. According to Merrill (1936), most of Palisot's American specimens were destroyed. Locality : " fitatsUnis d'Amerique ". Apparently Palisot's chief southern collecting spots were Savannah, Georgia and Charleston, South Carolina. Extant letters indicate that he found no new species of animals at Savannah. The type locality is, therefore, here restricted to Charleston County, South Carolina.
Type of tinctorius: presumed lost. Locahty: Kentucky; restricted by Causey (1955a) to Natural Bridge, Powell County, Kentucky (this antedates Hoffman's, 1957, restriction of the locality to " knobby hills of Estill county, in Kentucky ") . Type of atratus: unknown. Locality: prairie Mer Rouge, Louisiana. Type of crassiis: unknown. Lo
cality : " Les rives du lac Pontchartrain ", Louisiana. Type of woodi: male (NHMV; Chamberlin and Hoffman, 1958, incorrectly say, " Geneva Museum"). Locality: St. Louis, Missouri. Type of pensacolae: female (USNM). Locality: Pensacola, Florida. Type of oklahomae: male (RVC). Locality: Murray County, Oklahoma. Type of dolleyi: male (MCZ). Locality : Feemster's Lake area near Tupelo, Lee County, Mississippi. Type of ramstadti: male (RVC, Chamberlin says in publications, " Field Museum "). Locality: Punta Gorda, Florida. Type of melanior: female (RVC, " Field Museum "). Locality: Stephen E. [sic] [F.] Austin State Park, 5 miles east of Scaley [sic] [Sealey], Austin County, Texas.
Distribntion. — Southeastern United States; from peninsular (the single record from Key West may be a result of mixing specimens) Florida and the Gulf States north to Illinois, Indiana, and Ohio west of the Appalachian Mountains, and to southern Virginia in the mountains and east of them (see map 2).
Specimens Examined. — 178 {77 males, 101 females).
Alabama. — Baldwin County: Mobile Bay, Oak Bayou, April 4, 1958 (2 males, 1 female), S. Lazell (NBC). Cullman County: Ardell, May 4, 1915 (1 male), A. O. Howell (USNM). Mobile County: 10 mi. s. of Mobile, west shore Mobile Bay, Aug. 17-20, 1949 (1 male) (CNHM).
Arkansas. — Faulkner County : mountainside,4 miles nw. Conway, Aug. 7, 1955 (1 female), L. Hubricht (RLH). Hempstead County: Hope, June 11, 1954 (1 female), J. W. Green (CAS). Lawrence County: Imboden, 1923 (1 female), B. C. Marshall (MCZ). Logan County: Magazine Mtn., 1903 (1 female) H. A. Pilsbry (ANSP), 2800 ft, Aug. 12, 1939 (1 female), Rehn, Rehn (ANSP). Montgomery County: Caddo Mtn., 1.3 mi. se. Caddo Gap, Aug. 13, 1955 (1 male, 2 females), L. Hubricht (RLH). Pulaski County: Camp Robinson, April 21, 1943 (1 female), D. D. Davis (CNHM) ; Little Rock (1 male), Bollman (USNM), July-Aug., 1942 (1 female), W. Beecher (CNHM), 1943 (2 males), E, M. Nelson (CNHM). Saline County: 5 mi. e. Crows, Aug. 13, 1955 (1 female), L. Hubricht (RLH). Yell County: south side Magazine Mtn., 3 mi. n. Havana, Aug. 6. 1955 (1 female), L. Hubricht Florida. — "Magnolia" (2 females) (MCZ). Alachua County : (2 females) J. A. Oliver (RLH). Charlotte County: Punta Gorda, 1928 (2 males, 1 female), H. Ramstadt (CNHM). Duval County: Jacksonville, June 9, 1928 (2 females), O. F. Cook (USNM) ; in swamp, 5 mi. w. of Jacksonville, June 23, 1928 (5 males, 2 females), Cook (USNM). Escambia County: Pensacola (female, type of pensacolae) (USNM), Oct. 7, 1928 (1 male). Cook (USNM). Hernando County: Brooksville, March 22, 1928 (2 females). Cook (USNM). 91
Highlands County: Highlands Hammock State Park, July 15-18, 1956 (1 female), D. J. Pirone, E. F. Menhinick (WTK), March 29, 1957 (1 female), Cornell Exped. (WTK). Hillsborough County: Tampa Springs (1 male), W. M. Beakley (ANSP). Indian River County: Sebastian (2 females). Nelson (MCZ). Lake County: between Astor and Altoona, Sept. 20, 1928 (1 male, 2 females) (USNM). Monroe County: Key West (1 female) (MCZ). Volusia County: St. John's River, Volusia (2 females) (MCZ).
Georgia. — "Georgia" (1 female) (USNM). Bibb County: Macon (1 female), L. M. Underwood (USNM). Camden County: St. Marys, 1896 (1 female), Outram Bangs (MCZ). Floyd County: Spring Creek, Aug. 27, 1913 (1 female) (MCZ). Rabun County: Tallulah (1 male, 2 females), L. M. Underwood (USNM).
Illinois. — "Illinois" (1 female), Richards (MCZ). Champaign County: Urbana (2 females), Blake (MCZ). McLean County: Normal (1 male, 1 female) (MCZ). Richland County: 2 mi. n. of Olney, Bird Haven, May 14, 1943 (1 male), D. Lowrie (CNHM).
Indiana. — Carroll County: Delphi (1 male) (MCZ). Howard County: Kokomo (1 male), Moon (USNM). Monroe County: Bloomington (1 male, 1 female), Bollman (USNM). Porter County: Tremont, Aug. 21, 1943 (1 male, 1 female), H. Dybas (CNHM).
Kentucky. — Edmonson County : Bee Spring, Jan. 8, 1874 ( 1 male, 3 females), F. S. S. (MCZ); near Mammoth Cave (1 female) (MCZ). Estill County: 5 mi. e. of Irvine, Rt. 80, May 9, 1954 (2 males), Hoffman (RLH). Harlan County: Pine Mountain, July, 1946 (2 males, 2 females), W. L. and C. K. Necker (CNHM).
Louisiana. — Jefferson Parish: Harahan, Sept. 20, 1944 (1 female), H. S. Dybas (CNHM). Natchitoches Parish: Creston, 1915 (1 male, 3 females), K. P. Schmidt (MCZ) ; Chastine, 2 mi. n. of Creston, April 29, 1947 (1 male), J. M. Schmidt (CNHM). Orleans Parish: New Orleans, June 22, 1883 (3 females), R. W. Shufeldt (USNM), Jan., 1917 (1 male, 1 female) (MCZ), Oct. 20, 1943 (1 male, 1 female), E. S. Ross (CAS). Rapides Parish: Forest Hill, Sept.-Oct., 1945 (3 males), R. L. Wenzel (CNHM). Red River Parish: East Carroll, Sept. 12, 1926 (1 female) (USNM). St. Charles Parish: Norco, Aug. 27, 1944 (4 males), H. S. Dybas (CNHM).
Mississippi. — Lee County : Feemster's Lake area near Tupelo, May, 1937 (1 male, type of dolleyi), J. S. Dolley (MCZ). Oktibbeha County: Agricultural College, April 1, 1917 (1 male, 2 females). Few, Franklin, Bailey (MCZ). Tishomingo County: luka, Sept. 7, 1932 (1 female), T. H. Hubbell (MCZ).
Missouri. — St. Louis County: St. Louis (4 females), M. Kaltenthaler (RLH) ; wagon road to Bridger's Pass, R. Mts., May 6, 1857 (1 female), Lt. F. T. Bryan (ANSP) ; St. Louis (1 male) (NHMV). Wayne County: S. A. Baker State Park, Aug. 28, 1946 (1 male), J. A. Peters (RLH).
North Carolina. — Buncombe County: Ashville, July 1896 (1 female) (USNM). Carteret County: Beaufort (1 female), J. G. Shute (MCZ). Clay County: White Oak Bottom, June 4, 1952 (1 male), C. E. Wood, C. L. Rodgers (RLH) ; Tuni Gap, July 20, 1952 (1 male), Thelma Howell (RLH). Macon County: Highlands, Aug. 1, 1949 (1 male), R. L. Hoffman (RLH). Richmond County: n. of Rockingham, Sept. 14, 1928 (1 male) (USNM). Wake County: Raleigh, April 15, 1927 (1 female), D. L. Wray (RLH).
Ohio. — Vinton County: Tar Hollow State Forest, April 27, 1946 (2 males, 4 females), J. R. Bailey and E. S. Thomas (RLH).
Oklahoma.— " Camp Boulder", June 12, 1926 (1 male), T. H. Hubbell (RLH). Murray County: (male holotype, female allotype of oklahomae)
South Carolina. — "South Carolina" (2 females) (MCZ). "Yellow Head" (1 female) (MCZ). Berkeley County: Bonneau, Aug. 23, 1929 (1 male), Cook (USNM). Oconee County: Cherry Hill Recreation Area, Route 107, Sept. 6, 1958 (1 male), J. G. Franclemont, R. W. Hodges (WTK) ; Whitewater River, Lower Falls, Aug. 22, 1949 (1 female), T. Howell (RLH).
Tennessee. — Cocke County: Newport, March 29, 1948 (1 male), M. Wright (RLH) ; Wolf Creek (1 female), C. B. Branner (USNM). Davidson County: Nashville, Glendale Hills, April 21, 1917 (1 male), H. Cummins (MCZ). Morgan County: Burrville, June 27, 1951 (1 female), B. Benesh (CNHM). Sevier County: Elkmont, el. 3,500 ft. (2 males), G. G. Ainslee (MCZ) ; Great Smoky Mountains National Park, Sept. 23, 1951 (1 male), Hoffman (RLH), Chimneys, May 19, 1956 (1 male, 2 females), Hoffman, Keeton, Lund (WTK).
Texas.— " Birkville ", March 29, 1943 (1 male), B. A. Maina (CNHM). "Between Lufkin and Houston", Jan., 1931 (1 female), O. F. Cook (USNM). Austin County: Stephen F. Austin State Park (female, type of melanior), K. P. Schmidt (RVC). Brazos County: College Station, Dec, 1905 (1 male) (MCZ). Galveston County : Galveston, 1871 (3 females) (MCZ). Leon County: 5 mi. w. of Marquez, April 18, 1945 (2 females), K. P. Schmidt (CNHM). Williamson County: Georgetown (1 male) (MCZ).
Virginia. — Montgomery County : Dry Run, 5 miles e. of Blacksburg, Sept., 1957 (1 male), R. L. Hoffman (WTK), April, 1957 (1 male, 1 female), R. L. Hoffman (RLH). Norfolk County: Dismal Swamp, June, 1897 (1 female), D. W. Prentiss (USNM). Pittsylvania County: Smith Mtn. Gorge, June 19. 19^5 (1 female), R. L. Hoffman (RLH). Russell County: summit of Clinch Mt., July 29, 1941 (1 female), Dr. and Mrs. S. T. Brooks (CMP). Surry County: Swann's Point, April 20, 1947 (1 male), Hoffman (RLH).
West Virginia. — Mingo County : along Pigeon Creek, 5 miles e. of Taylorsville (1 male), G. K. MacMillan, N. D. Richmond (CMP). Monongalia County: Cooper Rock, May 18, 1932 (1 female), M. G. Netting (CMP).
The following specimens are considered hybrids with annularis.
Illinois. — Champaign County: Champaign, Sept. 18, 1921 (1 male), A. O. Weese (MCZ) ; Urbana (1 male) (MCZ). Cook County: Willow Springs, Sept. 27, 1942 (1 female), H. S. Dybas (CNHM). McLean County: Normal (3 males) (MCZ).
Kentucky. — Edmonson County: Bee Spring, Jan. 8, 1874 (1 male), F. S. S. Missouri. — St. Louis (1 male), M. Kaltenthaler (RLH).
Nebraska. — Richardson County: 4 mi. e. of Barada, May 29, 1948 (2 males, 1 female), M. H. Muma and O. S. Bare (RLH).
Ohio. — Greene County: Yellow Springs, 1868 (1 female) (MCZ).
Tennessee. — Carter County: Burbank (1 male), R. Thaxter (MCZ).
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bibliographic citation
Keeton, W.T. 1960. A Taxonomic Study of the Milliped Family Spirobolidae (Diplopoda: Spirobolida). Memoirs of the American Entomological Society vol. 17. Philadelphia, USA

Narceus americanus

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Narceus americanus is a large millipede of eastern North America. Common names include American giant millipede,[1] worm millipede, and iron worm.[2] It inhabits the eastern seaboard of North America west to Georgetown, Texas, north of the Ottine wetlands.[3] It has a nearly cylindrical gray body, reaching a length of 4 inches (100 mm).[4] They can be commonly found in or under decaying logs from March to October.[5] When threatened, they sometimes curl up or release a noxious liquid that contains large amounts of benzoquinones which can cause dermatological burns. This fluid may irritate eyes or skin. Many other millipedes secrete hydrogen cyanide, and while there have also been claims that N. americanus releases hydrogen cyanide, they are unsubstantiated. They do, however, excrete a substance that causes a temporary, non-harmful discoloration of the skin known as millipede burn.[6]

Ecology and behavior

Diet

N. americanus are detritivores, primarily consuming decaying wood and leaf litter. They have also been found to feed on deer scat and fresh fruit, preferring these to their typical diet when given the choice. [7] Most feeding activity occurs at night.

Behavior

Though capable of releasing irritating and foul-smelling liquid from ozopores when aggressively disturbed, they can typically be safely handled by humans and are not uncommon on the arthropod pet market.[8]

Their cuticle is somewhat water permeable, so they seek out damp or humid environments and have exhibited specific behaviors in response to desiccation stress. If exposed to a dry or actively desiccating environment, they will first expend energy trying to find a more favorable environment, and if this fails they reflexively curl into the typical defensive position. This position closes spiracles located at the base of legs, preventing further water loss.[9] From a partially dehydrated state they can reabsorb moisture from high-humidity air, but moisture-rich food is necessary for complete recovery to a fully hydrated state. Molting while burrowed into the ground or into rotting wood can also be a response to chronic dehydrating conditions.

Burrowing[10]

Burrowing is initiated by the millipede picking up sediment grains with its mandibles and using legs to pass them along its body segments, where the sediment is then deposited at the posterior end of the body. This process from start to finish can take anywhere between five and sixty minutes, depending on the size of the burrow and qualities of the soil.

Burrows can be used as temporary or more permanent dwellings, and are used to escape dry or cold surface conditions. Millipedes will typically spend non-feeding time in their burrows, which is why they are difficult to find during the day. Molting is almost exclusively done in burrows.

Reproduction[11]

The average lifespan of these millipedes is unknown, but they can live up to eleven years in captivity or in the wild. Sexual maturity is not reached until 1-2 years of age.

Mating occurs at the beginning of spring through to early summer. Males mate via transfer of a spermatophore, and females are able to store this sperm to fertilize eggs at a later time. Other millipede species may lay 20–300 eggs, but N. americanus lay just one egg in a nest made of chewed leaf litter and excrement. The female millipede will wrap herself around the egg and nest until it hatches several weeks later, producing a millipede with seven body segments and only three leg pairs. The number of body segments and leg pairs are increased with each molting, and there is no parental investment after egg hatching.

Photos

See also

References

  1. ^ Millipedes (Diplopoda), Jeff's Nature Page
  2. ^ Walker, Matt J; Stockman, Amy K; Marek, Paul E; Bond, Jason E (2009). "Pleistocene glacial refugia across the Appalachian Mountains and coastal plain in the millipede genus Narceus: Evidence from population genetic, phylogeographic, and paleoclimatic data". BMC Evolutionary Biology. 9 (1): 25. doi:10.1186/1471-2148-9-25. PMC 2652443. PMID 19183468.
  3. ^ Stephen Welton Taber & Scott B. Fleenor (2005). "Crustaceans, millipedes, and centipedes". Invertebrates of Central Texas Wetlands. Texas Tech University Press. pp. 263–272. ISBN 978-0-89672-550-8.
  4. ^ Jennifer Frick-Ruppert (2010). "Railroad worms and millipedes: predators and prey". Mountain Nature: a Seasonal Natural History of the Southern Appalachians. University of North Carolina Press. pp. 106–108. ISBN 978-0-8078-7116-4.
  5. ^ "American Giant Millipede Complex". iNaturalist.{{cite web}}: CS1 maint: url-status (link)
  6. ^ J. E. Percy, J. Weatherston (1971). "Studies of physiologically active arthropod secretions. V. Histological studies of the defence mechanism of Narceus annularis (Raf.) (Diplopoda: Spirobolida)". Canadian Journal of Zoology. 49 (2): 278–279. doi:10.1139/z71-040. PMID 4925896.
  7. ^ Silva, C. M., and R. L. Stewart. "Behavioral Dietary Preferences of Narceus americanus in a Controlled Environment."[1]
  8. ^ "Giant Pink Foot Millipede (Narceus americanus)".{{cite web}}: CS1 maint: url-status (link)
  9. ^ O'Neill, Robert V. (1969). "Adaptive Responses to Desiccation in the Millipede, Narceus americanus (Beauvois)". The American Midland Naturalist. 81 (2): 578–583. doi:10.2307/2423992. ISSN 0003-0031.
  10. ^ Bowen, Jared J.; Hembree, Daniel I. (2014-04-22). "Neoichnology of two spirobolid millipedes: improving the understanding of the burrows of soil detritivores". Palaeontologia Electronica. 17 (1): 1–48. doi:10.26879/395. ISSN 1094-8074.
  11. ^ Millican, Kelli. "Narceus americanus". Animal Diversity Web. Retrieved 2021-12-08.

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Narceus americanus: Brief Summary

provided by wikipedia EN

Narceus americanus is a large millipede of eastern North America. Common names include American giant millipede, worm millipede, and iron worm. It inhabits the eastern seaboard of North America west to Georgetown, Texas, north of the Ottine wetlands. It has a nearly cylindrical gray body, reaching a length of 4 inches (100 mm). They can be commonly found in or under decaying logs from March to October. When threatened, they sometimes curl up or release a noxious liquid that contains large amounts of benzoquinones which can cause dermatological burns. This fluid may irritate eyes or skin. Many other millipedes secrete hydrogen cyanide, and while there have also been claims that N. americanus releases hydrogen cyanide, they are unsubstantiated. They do, however, excrete a substance that causes a temporary, non-harmful discoloration of the skin known as millipede burn.

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