(= clavipes)
Aranea longimana Fabricius 1781: 536.
Epeira clavipes: Walckenaer 1805: 54.
Nephila clavipes: MacLeay 1834: 12.
Nephila fasciculata: Koch, C.L. 1839a: 30.
Nephila plumipes Koch, C.L. 1839b: 138.
Epeira vespucea Walckenaer 1842: 98.
Epeira janeira Walckenaer 1842: 100.
Nephila sylphurea Taczanowski 1873: 148.
Nephila wilderi McCook 1894: 87.
Nephila wistariana McCook 1894: 252.
Nephila concolor McCook 1894: 256.
Trichonephila clavipes Dahl 1911: 271.
Discussion: The genus Aranea Linnaeus and its synonym Epeira Walckenaer each consisted of a large
conglomerate of species, related and unrelated, some of which are still in the process of revision. One
of the distinct groups of species that was recognized and named relatively early in the history of araneoid
nomenclature was Nephila (Leach 1815). MacLeay (1834) apparently was the first to recognize that
Aranea clavipes Linnaeus belonged in the genus Nephila.
Nephila clavipes is the only species of the genus occurring in the Western Hemisphere. It occurs
throughout Florida, the West Indies, as far north as North Carolina, across the Gulf States, through
Central America, and into South America as far south as Argentina. Other even larger relatives occur
in the South Pacific, southeast Asia, and Madagascar.
N. clavipes females are among the largest non-tarantula-like spiders in North America and are perhaps
the largest orb-weavers in this country, rivaled in size only by Argiope aurantia (Fabricius) and the
largest Araneus species, including A. bicentenarius (McCook). Females range from 24 mm to 40 mm
in length. The female color pattern, consisting of silvery carapace, yellow spots on a dull orange to tan
cylindrical body, brown and orange banded legs, plus the hair brushes (gaiters) on the tibial segment of
legs, I, II, and IV, make this spider one of the most easily recognized. The males, on the other hand,
are rather inconspicuous dark brown, slender spiders averaging 6 mm in length which would often go
unnoticed if not for the fact that they are often found in the webs of females.
male and female
N. clavipes in temperate North America has one generation per year under field conditions. Adult
males are present from July to September, with most females maturing in August. Mature females are
found late into the fall, when they make at least two large eggsacs 2.5 to 3 cm in diameter consisting of
several hundred eggs surrounded by a basket of curly yellow silk. Populations in the tropical parts of
the range probably produce more eggsacs, as the related N. maculata (Fabricius) averaged nearly nine
eggsacs per female in New Guinea (Robinson and Robinson 1973a). The life history of N. clavipes
has not been studied through all the instars, but it is probably quite similar to N. maculata (Robinson
and Robinson 1976), with one or two fewer instars.
The finely meshed, large web of N. clavipes (often 1 to 2 meters in diameter) is placed to best exploit
insect flight paths (i.e., above the herbaceous stratum). In tropical America, webs are found most
frequently at edges of forest clearings, alongside forest trails, and across forest watercourses (Robinson
and Mirick 1971). The hub of the web where the spider waits is located near the top of the web,
making an asymmetrical orb. Kaston (1972) gives an illustration of a portion of a web in detail. The
web is a semipermanent structure, i.e., it is not destroyed and created periodically as is the case with
many members of the similar family Araneidae. Large portions of the web may be repaired leaving the remainder undisturbed (Peters
1955). Occasionally stabilimenta (bands of zigzag silk) are incorporated into complete webs of
immatures, and more frequently are found on skeleton webs (webs lacking viscid spiral) made by
immatures and used as molting platforms (Robinson and Robinson 1973b).
adult female
Prey-capture behavior by Nephila species is considered primitive compared to species of Argiope and Eriophora. The large species in these latter genera make webs nearly as large as those of Nephila, yet the mesh of these webs are coarse when compared to those of Nephila. N. clavipes capture smaller prey on the average than do, for example, Argiope argentata (Fabricius) or Eriophora fuliginea (C.L. Koch) webs of similar size. However, due to their use of immobilization wrapping as a primary attack weapon (Robinson 1969, Robinson and Olazarri 1971, Robinson et al. 1969),
Argiope and Eriophora species are able to capture larger prey on the average than do Nephila species which directly employ biting to subdue the prey. Differences in web mesh size and attack
behaviors between the two types of orb-weavers can be viewed as an evolutionary advancement by these other large orb-weavers to reduce competition for prey with Nephila.
Webs of Nephila species, as well as of other large orb-weavers, are liable to kleptoparasitism by small
(3 to 4 mm) silvery spiders of the genus Argyrodes Simon (family Theridiidae). Robinson and
Robinson (1976) recorded as many as 30 of these kleptoparasites in a single web of N. maculata, and
we have seen over 40 Argyrodes in an abandoned N. clavipes web. This latter observation was
noteworthy, since Robinson and Robinson (1976) demonstrated that Nephila species could reduce the
kleptoparasitic load by periodically moving their webs even if the web site was productive of prey.
One aspect of prey capture by Nephila species, that of always bringing the prey back to the hub rather
than leaving wrapped prey in situ, has been hypothesized to be a preventative action to reduce the
amount of food stolen by Argyrodes, since detection of the theft action of the kleptoparasites would be
difficult on such a large web (Robinson and Robinson 1973a).
Another problem faced by golden silk spiders in tropical and subtropical climates is overheating. Special behaviors and body features have evolved in Nephila to protect against the problem. The silvery carapace reflects sunlight, while the long, cylindrical body may be pointed directly at the sun, thus reducing the area of exposed body surface. Force evaporative cooling may be employed by manipulating a drop of fluid with the chelicerae. Cooling responses generally occur above 35°C (Krakauer 1972). The web does not have to be perpendicular to the sun in order for the spider to employ orientation; in fact, webs are generally placed so as to capture the most insects regardless of the sun's position, and the spider's orientation movements can be quite complex (Robinson and Robinson 1974).
In the South Pacific, females of N. maculata are induced to build webs on bamboo frames, which are
then used as fish nets. The natives also relish the gravid females as a protein supplement, eating them
either raw or roasted. Different reports say that the flavor is somewhat like mixed raw potato and lettuce
mixed, or nutty flavored like peanut butter with a sticky consistency (Robinson and Robinson 1976).
- Dahl F. 1911. Die Verbreitung der Spinnen spricht gegen eine fruhere Landverbindung der Sudspitzen unserer Kontinente. Zool. Anz. 37: 270-282.
- DeGeer C. 1778. Memoires pour servir à l'histoire des insectes. Stockholm 7:176-324.
- Fabricius JC. 1781. Species insectorum exhibentes eorum differentias specificas, synonyma auctorum, loca notalia, metamorphos in adiectis observationibus, descriptionibus. Hamburgi & Kilonii 1: 536-547.
- Kaston BJ. 1972. How to Know the Spiders. Wm. C. Brown Co. Publishers, Dubuque, Iowa. 289 p.
- Koch CL. 1839a. Die Arachniden. Nurnberg 5: 1-158.
- Koch CL. 1839b. Die Arachniden. Nurnberg 6: 1-156.
- Krakauer T. 1972. Thermal responses of the orb-weaving spider, Nephila clavipes (Araneae: Argiopidae). American Midland Naturalist 88: 245-250.
- Leach WE. 1815. Zoological miscellany; being descriptions of new and interesting animals. London 2: 1-154.
- Linnaeus C. 1767. Systema Naturae (12th edition) per regna trianaturae, secundum classes, ordines, genera, species, cum characteribus differentiis, synonymis, locis. Editio duodecima, reformata, Holmiae 1: 553-1327.
- MacLeay WS. 1834. A few remarks tending to illustrate the natural history of two annulose genera,
namely Uranis of Fabricius and Mygale of Walckenaer. Proceedings of the Zoology Society London 2: 10-12.
- McCook HC. 1894. American spiders and their spinningwork. Philadelphia 3: 1-285.
- Muma MH. 1975. Spiders in Florida citrus groves. Florida Entomologist 58: 83-90.
- Pallas PS. 1772. Spicilegia Zoologica. Continens Quadrupedium, Avium, Amphibiorum, Piscium, Insectorum, Molluscorum Aliorumque Marinorum Fasciculos decem. Berolini 1: 44-50.
- Peters HM. 1955. Contribuciones sobre la etología y ecología comparada de las arañas tejedoros tropicales. Comunicaciones del Instituto Tropical de la Universidad de El Salvador 1-2: 37-56.
- Robinson MH. 1969. Predatory behavior of Argiope argentata (Fabricius). Amererican Zoologist 9: 161-173.
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- Robinson MH, Robinson B. 1973b. The stabilimenta of Nephila clavipes and the origins of stabilimentum-building in araneids. Psyche 80: 277-288.
- Robinson MH, Robinson B. 1974. The thermoregulatory postures of the golden-web spider, Nephila clavipes, at low latitudes. American Midland Naturalist 92: 386-396.
- Robinson MH, Robinson B. 1976. The ecology and behavior of Nephila maculata: A supplement. Smithsonian Contributions to Zoology 218: 1-22.
- Taczanowski L. 1872. Les Araneides de la Guyane française. Horae Soc. Ent. Ross. 9: 64-150, 261-286, Sep. 1-87.
- Walckenaer CA. 1805. Tableau des Araneides ou caractères essentiels des tribus, genres, familles
et races que renferme le genre Aranea de Linné, avec la designation de espèces comprises dan chacune de ces divisions. Paris, 1-88.
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Authors: H.V. Weems, Jr., and G.B. Edwards, Jr., Florida
Department of Agriculture and Consumer Services, Division of Plant Industry.
Originally published as DPI Entomology Circular 193.
Photographs: University of Florida, and De Anne M. Shellenbarger
Project Coordinator: Thomas R. Fasulo, University of Florida
Publication Number: EENY-229
Publication Date: August 2001. Latest revision: October 2004.
Copyright 2001-2004 University of Florida
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