Partially dehydrated third-stage larvae of Xenopsylla cheopis take up water vapour from the air after transference to higher humidities. A net uptake of vapour occurs at relative humidities from close to saturation down to 65 per cent r.h., the critical equilibrium humidity. The amount of vapour taken up from the air, until the larvae achieve equilibrium, is greater the higher the relative humidity (Fig. 1); the larvae maintain this equilibrium at a high environmental humidity with a high water content and at a lower humidity with a lower water content. At 93 per cent r.h. and 25°C water vapour is transported from the air into partially dehydrated larvae at an approximately constant rate of 11 μg/hr per larva or 2·0 μg/hr per mm2 surface area and continuously for an average period of 6 hr until the equilibrium water content is achieved. The uptake curve, then, rather abruptly takes a horizontal course (Fig. 2); water loss and water uptake become balanced and the starving larvae remain unchanged in weight for 24 to 48 hr. Water is transferred faster into partially dehydrated larvae the higher the humidity to which the larvae are exposed. The rate of transpiration at 0 per cent r.h. and 25°C is 4·7 μg/hr per larva or 0·9 μg/hr per mm2 surface area. Net sorption of vapour from almost saturated air is approximately twice as fast as transpiration into dry air.Vapour uptake is related to the r.h. (relative vapour pressure) of the air and not to its absolute vapour pressure or to its saturation deficit; we have to infer that the equilibrium vapour pressure at the absorbing site on the surface of the larvae increases with temperature by the same amount as the vapour pressure in the air. This relationship shifts at temperatures not far from the upper lethal limit of the larvae.Equilibrium water contents are established not only by partially dehydrated larvae which are transferred to humidities above the critical equilibrium humidity but also by hydrated larvae which are transferred to lower humidities, as long as these are above the critical equilibrium humidity. These hydrated larvae lose water until their water content is depleted to a level which corresponds to the humidity to which the larvae are exposed. As soon as this level is reached, equilibrium is established (Figs. 3, 4).Uptake of water vapour by dehydrated larvae and retention of water by hydrated ones are temperature-dependent. Equilibrium water contents cannot be established below 13°C, whereas 35°C is close to the upper limit (Figs. 5, 6, 7). Within the favourable range the rate of uptake increases markedly with temperature.The equilibrium water content is delicately balanced. Regaining water occurs whenever the water content of the larvae is lowered below the equilibrium level characteristic for the humidity to which the larvae are exposed (Fig. 8).Larvae, after their final defaecation (prepupae), absorb four to five times more water vapour from the air than larvae in the feeding stage (Fig. 9). While the feeding larvae reach an equilibrium water content within approximately 6 hr, water uptake continues in the prepupae for an additional 42 hr. The increased vapour uptake by the prepupae is initiated invariably shortly after the final defaecation, while there is neither an increase in the ambient humidity nor a preceding adequate decrease of the water content of the organism; in fact it takes place even when the prepupae are transferred to a lower humidity. Vapour uptake ceases 2 days before the larval-pupal ecdysis takes place.Larvae do not develop into pupae at humidities substantially below the critical equilibrium humidity. The lower limit for development at different temperatures is related to the r.h. of the air just as the equilibria follow the r.h. and not the saturation deficit. Equilibria can be achieved only at temperatures at which the larvae develop into pupae.The vapour pressure of the haemolymph of insects can be taken as in equilibrium with an r.h. of not less than approximately 99 per cent r.h. Net uptake of atmospheric water into the haemolymph of flea larvae, however, takes place at 65 per cent r.h. This requires that osmotic forces of some 584 atm must be overcome by the animal. Uptake and retention of water depend upon metabolically driven processes. The mechanism is not known.
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