Biology of Ixodes Rubicundus Ticks under Laboratory Conditions: Observations on Oviposition and Egg Development

Observations on oviposition and egg development of Ixodes rubicundus were made under laboratory conditions. Engorged females were exposed to temperatures in the range 10–25°C and relative humidities (RHs) of 33 and 93%. The pre-oviposition period, oviposition period, incubation period, conversion efficiency index (CEI) values and fecundity were determined. The mean pre-oviposition period varied from 13.3 days (temperature 25°C and RH 33%) to 68.3 days (temperature 10°C and RH 93%). Oviposition extended from a mean of 39 days (temperature 25°C and RH 93%) to 201.7 days (temperature 10°C and RH 93%). The developmental zero temperature for the pre-oviposition period was 9.2°C. The mean total number of eggs produced by engorged I. rubicundus females varied from 2045.7 (temperature 10°C and RH 93%) to 3777.7 (temperature 20°C and RH 93%). Both female mass and RH significantly (p < 0.01) influenced the number of eggs produced. CEI values varied between 43.1–54.4% (RH 93%) and 34.1–42.5% (RH 33%). At 93% RH females produced between 14.2 and 17.7 eggs per mg body mass compared to the 13.2–14.6 eggs per mg body mass at 33% RH. The shortest mean incubation period recorded was 164.3 days (temperature 25°C and RH 93%). The developmental zero temperature for incubation was 6.5°C. Both the pre-oviposition and oviposition periods of I. rubicundus are more extended compared to other species of the genus. Ixodes rubicundus produces a large number of small eggs compared to other prostriate ticks.     

Factors affecting oviposition and fecundity in the grain miteAcarus siro L. (Acarina:Acaridae), especially temperature and relative humidity

Oviposition and fecundity in the grain miteAcarus siro were studied at 5–30°C and 62.5–90% RH. At and above 20°C, 80% RH, mating and oviposition occurred soon after emergence, but at lower temperatures and humidities egg laying was progressively delayed from one to several days. Females needed to mate repeatedly in order to achieve maximum egg production, optimum conditions for which were 15°C, 90% RH, where total output per female averaged 435 with a maximum of 858. Oviposition rates were highest at higher temperatures, the mean daily rate at 20 and 25°C, 90% RH, rising to maximum levels of 28/29 eggs per female per day on day six.Oviposition followed clearly defined patterns, favourable conditions producing rapid increases in the mean daily oviposition rate to high peak levels reached at an early stage in the oviposition period. Less favourable conditions resulted in reduced outputs and lower, more uniform rates of egg laying. The mean oviposition period, varying with humidity, fell from 72–122 days at 5°C to 9–13 days at 30°C and the mean incubation period from 42–70 days at 5°C to 3–4 days at 30°C. Egg viability increased with increasing humidity but was little affected by temperature and unaffected by age of the female at time of oviposition.Males tended to live longer than females at most conditions; longevity—depending on humidity—averaging 13–15 days at 30°C and 129–175 days at 5°C. Adult life for females averaged 12–19 days at 30°C and 88–169 days at 5°C. An index of suitability, calculated from egg number, viability and duration of the egg stage and oviposition period, indicated that the most favourable conditions for oviposition and hatching were 20–25°C and 80–90% RH.     

Temperature-controlled under-water egg dormancy and postflood hatching in Isotoma viridis (Collembola) as forms of adaptation to annual long-term flooding

Summary Incubation experiments with eggs of a population of Isotoma viridis, which is exposed to annual long-term flooding from about April to July, as well as field observations show that temperature controls both, underwater egg dormancy and immediate postflood hatching. The population is located at the Eder Freshwater Reservoir in Germany.If constant experimental temperatures are above 14°C, almost all eggs are nondormant. Dormancy is established at temperatures below 15°C, but embryonic development is completed. Experiments indicate that of the environmental factors that change drastically at the end of submergence (light, turgor pressure, oxygen, a.o.), only temperature acts as a hatching trigger. Hatching of the previously dormant eggs occurs at a constant threshold temperature of 16°C, mainly within 2 to 20 days after temperature elevation, but most of these eggs need even higher temperatures to hatch. Remaining eggs were partly stimulated to hatch by recooling them at 7°C for some days and then rewarming them again.The threshold temperatures observed are unusually high for Collembola and seem to be the result of selection by the special floodplain conditions. During normal years, the surface temperatures of submerged soil usually do not exceed threshold limits before summer drainage. This allows both, protection from under-water hatching and an optimal timing of hatching at the very beginning of the main terrestrial period. The experiments show that above the threshold temperature (in warm summers), individuals can hatch under water and survive submerged for 10–15 days. They can survive even longer in the water habitat, if emergent structures enable them to climb onto the water surface. Furthermore, a considerable polymorphism observed in some hatching properties improves the chance to survive under the unpredictable floodplain conditions.     

Induction of diapausing amictic eggs in Synchaeta pectinata

Amictic females of a clone of S. pectinata from Star Lake (Norwich, Vermont) may produce diapausing as well as non-diapausing (subitaneous) eggs. The proportion of diapausing eggs produced in cultures was unaffected by temperature (12 vs 19 °C) or rotifer population density (minima of 0.33 vs 3 ind. ml^–1) at 19 °C. However, at 19 °C this proportion was higher in cultures maintained at a low food level suppressing reproduction (5 × 10³ cells ml^–1 Cryptomonas erosa) than in those maintained at a high food level (2 × 10⁴ cells ml^–1); the treatment effect was marginally significant (p=0.067). Consistent with the effect of low food availability, a period of starvation was very effective in inducing the development of diapausing eggs. None of 19 females cultured individually from hatching at 19 °C on C. erosa (2 × 10⁴ cells ml^–1) in 1-ml volumes produced any diapausing eggs in 4 days (0 out of 349 eggs), while 13 out of 16 females subjected to a 15-hour starvation period 6 hours after birth produced one or more diapausing eggs during that time (34% of the 158 eggs produced by the 16 females were diapausing). Diapausing eggs produced and left at 19 °C hatched after 4 to 13 days. Those produced in cultures with a low food level took significantly longer to hatch (9.7 days) than those produced in cultures with a high food level (8.1 days) (p=0.022). In natural communities, S. pectinata should be able to respond directly and rapidly to poor food conditions by producing eggs that undergo an obligatory dormant period before resuming development.     

Field and laboratory studies on the timing of oviposition and hatching of the western black-legged tick, Ixodes pacificus (Acari: Ixodidae)

The timing of oviposition and hatching of Ixodes pacificus was investigated in the field and at constant temperatures in the laboratory. Replete females held at temperatures between 9 and 29°C began depositing eggs a mean of 9–70 days after drop off. Egg masses held between 12 and 25°C commenced hatching 25–178 days after the onset of oviposition. Eggs held at 9 or 29°C did not hatch. The lower temperature thresholds for development (LTD) for oviposition and hatching were 6.5 and 9°C, respectively. The number of degree days required for oviposition and hatching was 173 and 588, respectively. Replete females placed in the field on 2 December through to 8 March deposited eggs from 2 February through to 24 April; the eggs commenced hatching between 2 July and 21 August. Unfed larvae from two of 20 egg masses survived through the winter and fed readily when exposed to deer mice (Peromyscus maniculatus) on 22 April. Replete larvae were returned to the field and moulted between 9 and 21 August. Larvae exposed to deer mice in August, 4 weeks after hatching, also fed readily. Although further studies are needed to clarify the timing of nymphal development, the present study suggests that I. pacificus requires more than 1 year to complete its life cycle.     

Biological aspects of the geranium mites,Coptophylla caroliniani andAceria mississippiensis (Prostigmata: Eriophyidae)

Aceria mississippiensis andCoptophylla caroliniani (Prostigmata: Eriophyidiae) were found on wild geranium,Geranium carolinianum L., in northern Mississippi. About onehalf of the total developmental time was spent in the egg stage for each species. The developmental threshold forA. mississippiensis was 5.5±1.04°C and 7.3±0.93°C forC. caroliniani. The optimum temperature for each developmental stage was between 25 and 29°C.C. caroliniani failed to develop at 36°C, whereasA. mississippiensis failed at 40°C. Day-degree requirements to complete development were 100.7±3.6 D^o and 154.6±4.1 D^o forC. caroliniani andA. mississippiensis, respectively.Mean female longevity at 20°C was 17.4 (range 12–21) days forC. caroliniani and 16.5 (range 15–19) days forA. mississippiensis. The shortest pre-oviposition period was 2.2 days forC. caroliniani at 20°C and 1.7 days forA. mississippiensis at 25°C, and the length of pre-oviposition period increased with temperature above 25°C for both species.Maximum egg production ofC. caroliniani andA. mississippiensis occurred at 20°C. There were no differences (P0.05) in number of eggs per day at temperatures of 20, 25 and 32°C for each species, but there was a tendency to lay more eggs per day with increasing temperature. The percentages of egg hatch were not significantly different at these temperatures. The sex ratio of laboratory-rearedA. mississippiensis was 1:1.8, whereas field-collectedC. caroliniani showed a ratio of 1:1.     

Laboratory studies of factors affecting egg hatch of triops longicaudatus (LeConte) (Notostraca : Triopsidae)

Egg hatch was greatest (78.33%) for eggs not previously desiccated. A reduction in numbers hatched occurred as the relative humidity at which they were dried decreased. Some eggs hatched (0.67–79.33%) at pH levels of 3.10–10.01 with the highest hatch at pH 5.60. Water temperature greatly affected egg hatch. No hatch occurred until temperatures were above 14°C. A constant 29°C significantly inhibited hatching. Egg hatch increased 13.00 to 43.42% as salinity decreased from 2200 to 9.24 micromhos/cm. As little as 13 mm of flooded soil covering the eggs prevented them from hatching for 14 days. Eighteen percent hatch resulted when soil and eggs were redistributed to a 1 mm soil layer. Egg samples from the same parent, even though treated similarly, often hatched at greatly varying rates and only rarely was hatching 100% within a replication.     

Biology of the shore fly Scatella stagnalis in rockwool under greenhouse conditions

The development times and survival of immature stages in rockwool and the fecundity and longevity of adult Scatella stagnalis were determined and stage-specific life-tables constructed for the species at constant 20 and 25 °C and at a fluctuating temperature (23–34 °C, mean 28.5 °C). Development time from egg to adult decreased with temperature, being 15.9±0.1 days at 20 °C, 11.4±0.1 days at 25 °C and 10.1±0.2 days at fluctuating temperature with mean of 28.5 °C. The lower threshold for egg-to-adult development was 6.4±2.7 °C and the total quantity of thermal energy required to complete development was 212.8±.0 °C. The proportion of females in two populations studied was 0.521. High temperature increased the mortality of pupae from 7% (20 °C) and 10% (25 °C) to 29% at 28.5 °C. At 25 °C, female longevity was 15.5±0.7 days and fecundity 315±19 eggs/female (20.4 eggs/female/day). Males lived for 22.0±1.1 days. At constant 25 °C, the net reproductive rate was 126.1 female eggs/female, generation time was 18.4 days, the doubling time of the population 5.3 days, and the intrinsic rate of increase (r _m) 0.263 day^–1.     

Mixed oviposition in individual females of Gryllus firmus: Graded proportions of fast-developing and diapause eggs

Summary Eggs of field crickets (Gryllus spp.) held at 25±1°C hatch in 2–4 weeks (fast-developing eggs) or 5–28 weeks (diapause eggs). Most species lay but one type: at least 10 species lay only fast-developing eggs, and pennsylvanicus and ovisopis lay only diapause eggs. Gryllus firmus from Gainesville, Florida, lays both types, and individual females do so for as long as 8 weeks. The proportion of diapause eggs laid weekly by captive females exposed to outdoor photoperiods and temperatures varies seasonally from <5% (March–June) to ca. 50% (November–December). At outdoor temperatures in late fall some eggs that are presumptively fast-developing (at 25° C) enter diapause.Some firmus from Carolina Beach, North Carolina, lay both diapause and fast-developing eggs. Outdoor rearing experiments established that spring adults could result from fast-developing eggs of fall adults, refuting the hypothesis that spring and fall adults at that locality represent temporally isolated demes.High variance in hatching times for eggs laid by one female is appropriate to the unpredictable extremes of moisture and temperature that occur in the open, sandy habitats of G. firmus. Physiological mechanisms of the mixed oviposition and specific environmental determinants of the varying proportions are unknown.     

Responses and song pattern copying of Omega-type I-neurons in the cricket,Gryllus bimaculatus,at different prothoracic temperatures

Summary Omega-type I-neurons (ON/1) (Fig. 1A) were recorded intracellularly with the prothoracic ganglion kept at temperatures of either 8–9°, or 20–22° or 30–33 °C and the forelegs with the tympanal organs kept at ambient temperature (20–22 °C). The neurons were stimulated with synthetic calling songs (5 kHz carrier frequency) with syllable periods (SP in ms) varying between 20 and 100, presented at sound intensities between 40 and 80 dB SPL. The amplitude and duration of spikes as well as response latency decreased at higher temperatures (Figs. 1 B, 2, 6). At lower prothoracic temperatures (8–9 °C) the neuron's responses to songs with short SP (20 ms) failed to copy single syllables, or with moderate SP (40 ms) copied the syllable with low signal to noise ratio (Fig. 3). The auditory threshold of the ON/1 type neuron, when tested with the song model, was temperature-dependent. At 9° and 20 °C it was between 40 and 50 dB SPL and at 33 °C it was less than 40 dB SPL (Fig. 4). For each SP, the slope of the intensity-response function was positively correlated with temperature, however, at low prothoracic temperatures the slope was lower for songs with shorter SPs (Fig. 5). The poor copying of the syllabic structure of the songs with short SPs at low prothoracic temperatures finds a behavioral correlate because females when tested for phonotaxis on a walking compensator responded best to songs with longer SPs at a similar temperature.Abbreviations epsps excitatory postsynaptic potentials - ON/1 omega-type I-neuron - SP syllable period - SPL sound pressure level     

Interactions between photoperiodism and temperature with respect to the control of dormancy in the adult stage of Pterostichus oblongopunctatus F. (Col., Carabidae)

Summary Pterostichus oblongopunctatus belongs to the type of spring breeding carabids with adult hibernation. Ovarian maturation is under the control of photoperiod: the females need a change of day length to mature. The first step of egg maturation (previtellogenesis) is bound to short day, the second step (vitellogenesis) to long day.The short day effect is achieved almost only at temperatures of 10 to 15°C; it is completely suppressed by 20°.The males mature under very different photoperiods and temperatures, but long day diminishes the percentage of mature males slightly, as well as does the higher temperature of 20°C in short day as compared with 15°C.Simulation of climatic conditions as experienced by the beetles from autumn throughout winter until spring in the laboratory showed that a short span of favourable temperatures at short day as experienced in nature in autumn allows the females to accomplish the short day development. But this maturation effect is still more diminished the longer temperatures below 5°C act on the beetles. Following that, a second period of temperatures between 10–15°C must restore the short day maturation effect if full maturity shall be gained in the following long day.The beetles are able to store reserve materials under long day at 20°C. After such a period they are able to have a normal previtellogenesis in spite of a severe shortage of food during short day. These experiments indicate that the failure in short day development outside the temperature range of 10–15°C is not a matter of an especially well balanced over-all metabolism in this favourable temperature range. It seems rather that hormonal systems involved in the short day phase of oogenesis act only within this span of temperature.Supportet by the Deutsche Forschungsgemeinschaft.     

Cold-hardiness of Dermacentor marginatus (Acari: Ixodidae)

The cold-hardiness of Dermacentor marginatus using laboratory-reared offspring of ticks collected in Germany was characterized. Investigations of unfed stages revealed that adult ticks suffered 50% mortality at –10°C after 4–5 months, but larvae and nymphs suffered mortality within few days, whereas –15°C was lethal for all stages within a very short period. Larval hatch and moulting of engorged larvae and nymphs did not occur at 10°C. Embryonic development of eggs with larval hatch was considerably reduced by exposure of eggs to 10°C. Engorged females did not lay eggs at 10°C, the oviposition capability, however, persisted over 6 months at 10°C, 5 months at 5°C, 3 months at 0°C and 2 months at –10°C without substantial decrease of the oviposition capacity or reduction of viable eggs. These results present evidence that unfed adult ticks are the ecoepidemiologically most effective stages, which are capable to tolerate long and extremely cold winters without substantial impairment of the population density. It is also considered that engorged females interrupt their oviposition at low and subzero temperatures delaying it for months and so contribute in bypassing winter conditions. None of the stages survived supercooling indicating that D. marginatus is freeze intolerant. Mean supercooling point (SCP) ranged between –26°C in eggs and –12, 6°C in engorged females. Compared with eggs, the SCP of the other stages was significantly higher. In conclusion, the SCP is considered to have no predictive value in the context with cold-hardiness.     

Induction of sexual reproduction and resting egg production in Brachionus Plicatilis reared in sea water

Brachionus plicatilis raised in our laboratory in sea water reproduces asexually even under high crowding conditions (at least 40 individuals per ml). Amictic females were induced to produce mictic females, males and resting eggs by reducing the concentration of the sea water culture medium. Mictic females and males appeared predominantly among the progeny produced by the amictic females during 4 days following their transfer into 25% sea water. Resting eggs appeared first 5–12 days after the onset of the experiment. Following the disappearance of males, the culture consisted of amictic females.Resting eggs produced by the method described above may be preserved for at least three months at –14°C or by desiccation at room temperature. Under the appropriate experimental conditions, resting eggs hatch into amictic females. Since B. plicatilis is one of the most commonly used food sources of fish larvae in aquaculture, the methods reported here may offer an easy and versatile way of preserving rotifer culture stock to be used on demand.     

Life history of Euseius scutalis feeding on citrus red mite Panonychus citri at various temperatures

The aim of this study was todetermine the biology and reproductivepotential of Euseius scutalis(Athias-Henriot) (Acari: Phytoseiidae) atvarious temperatures. These data are of valuein relation to mass rearing and the developmentof population dynamics models. The developmenttime, survival and fecundity of E.scutalis were determined at 20, 25 and30 ± 1 °C, 65 ± 10% RH and 16:8photoperiod. Total development times of E.scutalis were 6.7, 4.9 and 4.2 days at 20, 25and 30 ± 1 °C, respectively, using adiet of all life stages of the spider mite Panonychus citri (McGregor) (Acari:Tetranychidae). In general, preoviposition andpostoviposition periods of E. scutaliswere shortened as temperature increased, butthe oviposition period was longer at 25 °C than at 20 and 30 °C. Theshortest survival time of E. scutalis, at30 °C, was 10.1 days, followed by 23.7days and 28.6 days at 20 and 25 °C,respectively. Mated females laid on average1.1, 1.4 and 1.7 eggs per female per day and21.5, 39.7 and 17.1 eggs over their entire lifetime at 20, 25 and 30 °C, respectively.The sex ratios of E. scutalis were2.11/1, 2.24/1 and 2.11/1 female/male at 20, 25and 30 °C, respectively. The intrinsicrate of natural increase (r _m) increasedwith rising temperatures from 0.166 at 20 °C to 0.295 females/female/day at 30 °C. The net reproductive rate (R ₀)was highest at 25 °C (26.03females/female) and lowest at 30 °C(12.95 females/female). Mean generation time(T ₀) was longest at 25 °C (17.50days) and shortest (9.53 days) at 30 °C.     

Reptilian viviparity in cold climates: testing the assumptions of an evolutionary hypothesis

Viviparity (live-bearing) in reptiles often is interpreted as an adaptation to cold climates. This hypothesis relies on (i) body temperatures of gravid females being higher than soil (nest) temperatures; (ii) embryonic development being accelerated by this temperature difference; and (iii) survivorship of hatchlings being increased if eggs hatch before the advent of cold weather in autumn. I gathered data to test these assumptions, using eight species of scincid lizards in a high-elevation area of southeastern Australia. Due to behavioural thermoregulation, body temperatures of gravid lizards average ca. 7°C higher than soil (nest) temperatures. Oviparous female lizards retain eggs in utero for ca. 50% of development. Laboratory studies show that a temperature increase from 17°C (mean nest temperature) to 24°C (mean lizard temperature) reduces incubation periods of eggs by >40 days in heliothermic species, and <20 days in a thigmothermic species. In the field, soil temperatures drop to lethally low levels shortly after the usual time of hatching. Simple calculations show that without the acceleration of development caused by uterine retention, eggs could not hatch prior to the onset of these low temperatures in the field. These results support the major assumptions of the “cold climate hypothesis” for the evolution of reptilian viviparity.     

The effect of adult feeding on the fecundity,weight loss and survival of the pine beauty moth,Panolis flammea (D&S)

Summary Adult females of the pine beauty moth, Panolis flammea, fed on a saturated honey solution, laid significantly more eggs than those individuals given water only or not fed at all.At 20°, the longevity of both male and female moths was significantly increased when they were supplied with a food source. At 10° fed male months were not significantly longer lived than unfed moths. Fed female moths at 10° were however, significantly longer lived than unfed individuals. At 20°, fed male moths lived longer than fed females (8.17 days as compared with 5.95 days). At 10°, fed female moths lived longer than fed males (16.00 days compared with 11.41 days).At 20°, weight loss in unfed females over the reproductive period was proportional to the number of eggs laid and the survival time of the individual. In fed females, no significant weight loss occurred over the reproductive period, irrespective of the number of eggs laid or the longevity of the individual.Egg production, even in fed females, over the life span of an individual was only a fifth of the total eggs present in the reproductive tract at eclosion.It is concluded that adult females of P. flammea are likely to require an extra external food source to achieve their full reproductive potential.     

Effect of fluctuating temperature on the duration of embryonic development in two Ecdyonurus spp. and Rhithrogena cf. hybrida (Ephemeroptera) from Austrian streams

Summary Eggs of Ecdyonurus picteti from the Herrnalmbach and Seebach, and E. venosus and Rhithrogena cf. hybrida from the Seebach were fertilized artificially and kept at fluctuating temperatures (range 2.8°–18.1° C) in the laboratory. The percentage of eggs that hatched at each sinusoidal temperature cycle ranged from 0 to 49% and values were similar to those obtained for eggs reared under constant temperature conditions. The hatching time (days after fertilization for 10, 50% and 90% of the eggs to hatch) decreased with increasing temperature and the relationship between the two variables was well described by a powerlaw within the range 2.8°–18.1° C for E. venosus. A similar relationship has been found for the effect of constant temperature on the hatching time of eggs of E. venosus. It appears that the effect of temperature on the rate of change in the hatching time and the rate of development is approximately similar for both constant and fluctuating temperatures.     

The biology and metabolism ofOrchomene plebs (Hurley 1965) (Amphipoda: Gammaridea) from McMurdo sound,Ross Sea,Antarctic

Summary O. plebs (Hurley 1965) is a dominant bottom species of amphipoda, occuring in the investigated area at 10 to 760 m. Population structure and sex proportions depend upon the depth and the season of the year of sampling. Development of eggs occurs in winter; the young hatch in spring; the number of eggs produced is proportional to the volume of females. A relationship has been established between length and wet/dry body weight ofO. plebs. The species is necrophagus, long enduring without food. At -1.8°C retention of food in the gut may last from several hours to several days. Heart beat frequency oscillates between 40–80 beats/min at -1.8°C and depends on temperature. A temperature near 8°C is lethal. Oxygen consumption ofO. plebs depends on their developmental stage and sex and on trophic conditions. The level of metabolism of starved animals can be half that of fed animals. The greatest differences in oxygen consumption occur at-1.8°C, the ambient temperature. Oxygen consumption as a reaction to higher temperatures is different for starved and fed animals.O. plebs are hypostenothermic organisms; that is, they can adapt to the lowest temperature occuring in the marine environment.In memory of Mary Alice McWhinnie (1922–1980)     

Reproductive bionomics of the soft tick, Ornithodoros turicata (Acari: Argasidae)

The effects of different temperatures and relative humidities (RHs) were tested on various reproductive parameters of Ornithodoros turicata, an argasid tick that inhabits gopher tortoise burrows in Florida, USA. The pre-oviposition, oviposition and incubation periods of the ticks decreased as temperature increased. These periods were also affected by the RH. The number of eggs oviposited was affected significantly by the combined effect of temperature and RH. Fewer eggs were laid by ticks in the 24°C regimes and the 27°C/95%RH regime compared to those in the other temperature/RH groups. There was an inverse relationship between the number of eggs oviposited and the percentage of hatched larvae that was correlated with the temperature and RH. Ticks reared at 27°C/90%RH and 30°C/90%RH laid more eggs than those reared in the other combinations of temperature and humidity but fewer larvae hatched from these eggs. The reproductive fitness index (RFI) values were highest in females held in the 24°C groups and the 30°C/95%RH group, although significantly more larvae hatched at the lower temperatures. The optimum reproductive conditions for O. turicata under laboratory conditions appear to be 24°C and 90–95%RH. While mating occurred at all temperatures, none of the females laid eggs at 22°C. The ticks may move preferentially to low temperatures when not feeding to remain above the critical equilibrium humidity and/or below the critical metabolic level necessary for prolonged survival. However, most female ticks oviposited after 45 days when moved to 27°C/95%RH. Ornithodoros turicata females may have a limited capability to delay oviposition until an optimal microenvironment for egg deposition can be located in the burrow.     

Survival of adults and developmental stages ofSarcoptes scabiei var.canis when off the host

All life-stages ofSarcoptes scabiei var.canis survive in the hosts' environment for several days to several weeks depending on r.h. and temperature. Survival of larvae was comparable to males; survival of nymphs was comparable to females. Females and nymphs generally survived longer than larvae and males.Low temperature (10–15°) and high r.h. prolonged survival of all life stages. At 10–15°C, females and nymphs survived 1–3 weeks at 97% r.h., 1–2 weeks at 75% r.h. and 5–8 days at 45% r.h. At 20–25°C, survival was significantly reduced but all life-stages survived at least 2 days at 25% r.h. and 5–6 days at 75–100% r.h. Long survival off the host coupled with host-seeking behavior of these mites make it likely that environmental contamination is a source of scabies in domestic and wild mammals, and in humans.