The growing adult female red scale was the most preferred stage for A. melinus, followed by the second growing instar and lastly the male prepupa. The numbers of scale parasitized, the total of eggs laid, the number of eggs per scale, sex ratio and size of the parasites produced were all ranked in the same order. The mean size of parasites produced within the third instar decreased as the number of parasites per host increased. In the absence of the preferred host stages, female A. melinus laid readily in the unpreferred stages. In both A. melinus and A, chrysomphali it was noted that in multi- parasitism pupation, pupal development and adult emergence of all parasites in one host were synchronized. In A. melinus the sex and number of eggs laid per host are influenced by the host's size and quality. When A. melinus laid more than one egg in one host, it laid female eggs first and male eggs later; apparently the spermatheca goes through a period of fatigue, and is incapable of delivering sperm to the eggs descending the oviduct. Sex ratio decreases with increase in number of parasites per host and density of parasite population relative to hosts. The deposition of parasite eggs in a host by one female was observed during a short cycle of oviposition. A. melinus laid its eggs both 'above' and 'below' the body of the scale, whereas A. chrysomphali did so exclusively 'below'. In young mated A. melinus, eggs laid above the body of the scale were females and those below were males, but in old mated females all eggs, wherever laid, were male. Host development stops as soon as a parasite egg is laid. A. melinus avoids laying eggs in already parasitized hosts. The stages of red scale were ranked according to the percentage of mutilated individuals as: first moult (most mutilated), second instar, first instar, third instar, male prepupa and male pupa; second-moult females, egg-maturation stage and crawler-producing stage were unmutilated. A. melinus sometimes partitions her clutch of eggs into two hosts, particularly when host density is high. Partitioning in A. melinus may substitute for the generally accepted practice of super- parasitism, which would not be appropriate because the parasite is able to distinguish between parasitized and unparasitized hosts, is able to sense host density and to distribute her progeny on available hosts. Partitioning is advantageous for biological control. Behaviour of oviposition, mutilation and mutilation feeding in A. melinus are described in detail.

A, melinus produced more female progeny and more than twice as many total progeny as A. chrysomphali; it also destroyed almost twice as many hosts through oviposition and mutiliation. A. chrysomphali had a longer post-oviposition period than A. melinus, especially at 30�C. The proportion of single progeny in a host was higher for A, chrysomphali than for A. melinus at all temperatures, and was related to temperature positively in A. chrysomphali and inversely in A. melinus. Large old female A. melinus produced only males at the end of their lives; they did not mate at that stage when offered males, not because they were aged but because they mate only once in their lives. As temperature decreased, female A. melznus ceased producing females earlier, probably because temperature affected either longevity of sperms or the mechanism controlling their release. Differential mortality, temperature, and age of mothers all influenced sex ratio. Pupal mortality was inversely related to temperature within the observed range 20-30�C; in female pupae of A. chrysomphali it was lower than that in either female or male pupae of A. melinus; it was higher in male than female pupae in A. melinus. A. melinus lived longer than A. chrysomphali at all temperatures. Duration of development was longer for A. chrysomphali than for A. melinus at 30�C, but shorter at 20 and 25�C. The threshold of development was 8.5C for A. chrysomphali and 11C for A. melinus. A. chrysomphali had a higher rm at 20 and 25�C than A. melinus, but much lower at 30�C. The highest rate of increase was at > 30�C for A. melinus, and at about 25�C for A. chrysomphali. The rm of the parasites was 3.1-5.0 times that of red scale, depending on parasite species and temperature. A. chrysomphali is smaller than A. melinus, and from the positive relationship between adaptation to cold and speed of development, and the negative relationship between speed of development and size, a negative relationship between size and adaptation to cold within Aphytis spp. may be postulated. A. chrysomphali is more adapted to cold and less to heat than A. melinus. This explains the seasonal and annual fluctuation in their relative abundance in southern Australia. The species would complement each other in controlling red scale; from the data presented here it is possible that Aphytis spp. in Australia may have evolved into more efficient control agents of red scale than elsewhere. Knowledge on the searching ability of Aphytis at different host densities is wanting.

The lethality of malathion to all stages of red scale of three different strains was tested. Scales from areas subjected to spraying were 1.87 times as tolerant as those from unsprayed areas, which in turn were 1.52 times as tolerant as the laboratory strain. Of the seven distinguishable stages of red scale only the first moult (males and females), second moult females, and young-producing females proved to be significantly more tolerant than the other stages, the second moult female being three times as tolerant as the young-producing female, or nine times as tolerant if the body weight and surface area are taken into account. The latter finding is important, because it has been customary to estimate the efficiency of spray treatments by mortality in the young-producing stage. This would leave many of the second moult females alive after spraying and the infestation would continue.

I

A laboratory spraying apparatus is described. It consists of an atomizer carried on a mechanical carriage that moves at constant speed back and forth at a fixed height above the target; after each passage the carriage is moved forward on another carriage. A large area (about 30 by 60 cm) can be sprayed in this way. Tests of the performance of the apparatus showed it to be capable of giving a reasonably even and reproducible deposit of spray over the target area. A method for converting the dose in percentage concentration to quantity per unit area is presented.