
Adult females average 15 mm in length (range 7 to 22 mm). Females may have the same color pattern as males, but usually females have the black dorsal areas of the body covered with colored scales. These scales may be gray, tan, brown, orange, or combinations of any or all of the above colors. Those females that are completely covered with orange scales are particularly attractive. Most of the more colorful females are found in the southern two-thirds of Florida and in the Greater Antilles. Cheliceral color is iridescent (either green or red- violet), but less noticeable than in males because the chelicerae are usually covered by the palpi, small leg-like appendages which are densely covered with long white setae. The cheliceral tubercles are absent. Leg-fringes are present, but not as distinct as in males. Females also have four tufts of setae in the region of the dorsal eyes; males lack these tufts.
Phidippus regius is one of the few spiders that can be sexed in the early instars. Juvenile females of more southern populations attain a scale cover as early as the 3rd instar; males are stark black and white throughout their life cycle.
1. Posterior abdominal spots orange and quadrangular . . . . . P. otiosus
1'. Posterior abdominal spots white and not quadrangular . . . . . 2
2. Posterior abdominal spots oval, black spots absent . . . . . P. regius
2'. Posterior abdominal spots linear, 4 pair of dull black, quadrangular spots on
dorsum of abdomen . . . . . P. audax
As with all jumping spiders, P. regius uses its excellent vision to locate prey and potential mates. Prey is caught by jumping on it, hence the common name of the family. Males court females with a species-specific dance in which the leg fringes are displayed (Edwards 1975). The chelicerae are also believed to be of use in recognition between the sexes, as no other jumping spiders within the geographic range of the genus Phidippus have iridescent chelicerae.
Although jumping spiders do not make webs to capture prey, they do use silk. Hunting spiders trail a dragline behind them to break their fall in case they miss a jump. Silken nests, ellipsoid structures with an opening at each end, are used for resting at night, molting, and egg-laying. Juveniles may make their nests in the tops of herbs or in rolled leaves, while subadults and adults frequently make their nests along the inner mid-veins of palm fronds. Adult males often cohabit with subadult and occasionally adult females in order to mate. A cohabiting male will mate with a subadult female soon after she matures. Jackson (1977) showed that males of P. johnsoni (Peckham & Peckham) were able to employ a tactile type of courtship to females inside nests, which was much different than the visually-oriented courtship males employed for females outside nests. A similar tactile courtship has been noted for P. regius, P. cardinalis (Hentz), and P. whitmani Peckham & Peckham (Edwards 1980). Other species of Phidippus, including P. audax (Hentz), P. clarus Keyserling (Snetsinger 1955), and P. otiosus (Hentz) (Hill 1978) are known to cohabit.
Females of P. regius make thick silken nests under the bark of various trees, particularly oak and pine, in which to lay their eggs. Cracks and spaces in old houses and barns also provide suitable shelter for nests of egg-laying females. Females lay up to four batches of eggs; the 1st batch averages 183 eggs, the number of eggs declining with each successive batch. Assuming a female laid four batches of eggs, the average total of all batches was 402 eggs, but the maximum egg production was calculated at 715 eggs (Edwards 1980). Even this total might underestimate the maximum reproductive potential of P. regius, since Anderson (1978) reported a large female to lay a single eggsac with 570 eggs.
Phidippus regius individuals are known to feed on a wide variety of other arthropods. Smaller immatures feed heavily on Diptera, while older juveniles and adults feed on large Orthoptera and Hemiptera, and larval and adult Lepidoptera (Edwards 1980). A male of P. regius was collected while feeding on an adult of Diaprepes abbreviatus (Linnaeus), a pest of citrus and sugarcane (D. Gowan, collector).
Author: G.B. Edwards,
Florida Department of Agriculture and Consumer Services, Division of Plant Industry.
Originally published as DPI Entomology Circular 223.
Photographs: G.B. Edwards, Division of Plant Industry
Project Coordinator: Thomas R. Fasulo, University of Florida
Publication Number: EENY-152
Publication Date: September 2000
Copyright 2000 University of Florida
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Department of Entomology and Nematology
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