VENTRAL SURFACE Setae: Ventral submarginal setae (Fig. 8, P) are arranged in an even or irregular row around the submargin of body. Although there is some variation in shape and number (Fig. 9, C), most of them are slender and acute; therefore, they are not important as taxonomic characters. Body setae (Fig. 8, D) numerous in some species, sparse in others, usually resemble ventral sub- marginal setae, and are scattered randomly over the body. However, sometimes several setae are found clustered near the coxa. A varying number of interantennal setae is not normally used as a primary character except for a few taxa such as Pulvinaria citricola (Fig. 70, K) which has inter- antennal setae that often have bulbous expan- sions near the apex. Interantennal setae, how- ever, are occasionally used as secondary characters. Usually 3 pairs of large setae, termed prevulvar setae, are found anterior to the vulva on abdominal segments 6, 7, and 8; but, in Cero- plastes, Kilifia, and Protopulvinaria there is only one pair. In Toumeyella, the prevulvar setae are variable. Eyes: Eyes were detected in many of the species studied. They occur on or near the margin anterior to the antennae. They are ap- parently of no taxonomic importance. Antennae (Fig. 8, A): In most Coccidae, the antennae are long, fairly slender, 6 to 8-segmented, with the third segment usually longest. The second antenna segment in all species seen has a sensory pore. The terminal or apical segment has several fleshy and several more slender, hair-like setae. The 2 subapical segments usually possess 1 fleshy sensory seta each, which extends toward the antenna apex. Occasionally, the 3rd and 4th segments are par- tially or completely fused, in 1 or both antennae. Antennae of the Coccidae may be well developed (Fig. 8, A), slightly reduced (Fig. 23, F), or greatly reduced (Fig. 92, K). In Inglisia vitrea, the antennae are reduced to 1 segment. The size and number of antennal segments is useful in separating some genera and species. Clypeolabral shield: Located on the head, between the bases of the anterior legs; often possessing a pair of slender setae. Labium: Cone-shaped, appears I-segmented, usually with 3 to 5 setae on each side. Legs: The legs are 5-segmented and generally well developed in most genera of Coccidae. The trochanter of all species studied had 2 sensory pores on each face, and each tarsus 'was fitted with a claw. Legs may be well developed, as in Ceroplastes floridensis (Fig. 19); slightly re- duced, as in Eulecanium caryae (Fig. 43); greatly reduced, as in Toumeyella cerifera (Fig. 92), or entirely absent, as in Inglisia vitrea (Fig. 45). The tibia and tarsus may articulate and have an articulatory sclerosis (Fig. 10, A); the tibia and tarsus may be fused, without a sclerosis (Fig. 10, B); or the tibiotarsal sclerosis may be present, without free articulation (Fig. 10, C). The tarsus and claw of each leg possess a pair of digitules. The tarsal digitules are equal, slender, apically knobbed; the claw digitules may be unequal in shape (Fig. 10, D) or equal in shape (Fig. 10, E). The claw may have a denticle (Fig. 10, D), or may be simple without a denticle (Fig. 10, E). The reduction of legs, the presence or absence of tibiotarsal sclerosis and free articulation, shape of the claw digitules, and presence or absence of a claw denticle are useful taxonomic characters. Spiracles: The two pairs of spiracles are located on the thorax; the anterior pair believed to be on the borderline between the prothorax and mesothorax, the posterior pair between the mesothorax and metathorax. The posterior pair is normally larger. In most species studied, the spiracles are similar in structure and do not ap- pear to be of use in classification. However, in Pulvinaria psidii, each spiracle is surrounded by a sclerotic plate (Fig. 10, F), a character which immediately separates it from other members of the genus. In the genus Toumeyella, the spiracles are larger in proportion to the body size than in most other genera. In the genus Eulecanium, the peritreme of the thoracic spiracles is longer than the length of the coxae (Fig. 43) and is used as a generic character. Pores: Quinquelocular pores (Fig. 8, C) are found in the spiracular pore bands and around the spiracles in most species. In the genera In- glisia, Toumeyella, Pseudophilippia, and Neolecanium, they are also found in the ab- dominal region (Fig. 94, K) where they replace the mqltilocular pores found in most species. In Eulecanium caryae, quinquelocular pores are also located on the inner margin of the anal cleft (Fig. 43, F). Multilocular pores, most of which are 10-loculed (Fig. 8, F), occur in the anal area, in transverse bands on the abdomen, and occa- sionally on the thorax near the coxae; sometimes a few occur in the spiracular furrows of some species, but are numerous in Toumeyella cerifera (Fig. 92, M). In Pulvinariafloccifera (Fig. 75, P) the multilocular pores in the anal area are mostly 7-loculed, and in P. citricola (Fig. 70, N), most are 8-loculed. Various types of ventral pores are illustrated in Fig. 10, G. The type, position, and number of pores are useful taxonomic characters. Ducts: Microducts (Fig. 8, B) were detected