Effects of temperature on acaricidal and insecticidal activities of the benzoylureas flucycloxuron and diflubenzuron

Effects of temperature on the activity of flucycloxuron on larval stages of Panonychus ulmi (Koch), based on LC₅₀ values, were highly significant (P < 0.001) with temperature coefficients of-1.7 in both the ranges of 15° to 25°C and 20° to 30°C. The slopes of probit regression lines at 15° and 20°C were significantly steeper than those at 25° and 30°C. As a consequence the temperature coefficients based on LC₉₀ values were-4.4 and-2.2, for the 2 temperature ranges. The ovicidal activity of flucycloxuron on P. ulmi was low and was only statistically detectable at 20°C (LC₉₀ of 84 mg a.i./l). In studies with larvae of Aedes aegypti (Linnaeus), Leptinotarsa decemlineata (Say), Plutella xylostella (Linnaeus), Spodeptera exigua (Hübner) and Spodoptera littoralis (Boisduval) probit regression lines were parallel over temperature. The activity of flucycloxuron on these five insect species was not affected by temperature. Based on LC₅₀ values, diflubenzuron showed positive temperature coefficients on P. xylostella of + 2.1 at 15° to 25°C and + 2.5 at 20° to 30°C. For S. littoralis the temperature coefficient was positive (+ 2.4) at 15° to 25°C but negative (-1.9) at the 20° to 30°C range. Temperature coefficients of diflubenzuron were neutral for A. aegypti, L. decemlineata and S. exigua. In the design and analysis of these studies special allowance was made for date effects and variation in natural mortality over temperature.     

Temperature effects on solute accumulation by Candida utilis

Summary A study was made of the effect of temperature on accumulation of glucosamine and 2-aminoisobutyrate by Candida utilis NCYC 321 grown at 30° C or 10° C. Exponential-phase cells contained greater proportions of C_16:1 and C_18:3 acids, and smaller proportions of C_13:1 and C_18:2 acids, when grown in a defined medium at 10° C compared with 30° C. Cells grown at 30° C or 10° C were able to accumulate extracellular (10 mM) glucosamine and 2-aminoisobutyrate against concentration gradients. 2-Aminoisobutyrate was not metabolised by the cells; glucosamine was accumulated probably as a mixture of glucosamine 1- and 6-phosphates. Rates of accumulation of glucosamine and 2-aminoisobutyrate by cells grown at 30° C or 10° C decreased markedly when the test temperature was decreased from 30° C to 15° C. The rate of accumulation of glucosamine by cells grown at 10° C was considerably lower at each of the test temperatures compared with the corresponding rates for cells grown at 30° C; the rate of accumulation of 2-aminoisobutyrate was much less affected by the temperature at which the cells were grown and then only when measured at temperatures below about 20° C. Apparent K _m values for accumulation of glucosamine by cells grown at 30° C or 10° C decreased considerably when the test temperature was lowered from 20° C to 15° C. The extent of the decrease in K _m value was approximately the same for cells grown at 30° C or 10° C. Apparent K _m values for accumulation of 2-aminoisobutyrate were hardly affected by test temperature. Apparent V _max values for accumulation of glucosamine or 2-aminoisobutyrate were much lower when measured at 15° C than at 30° C. When measured at 30° C, apparent V _max values for accumulation of either solute were slightly lower with cells grown at 10° C compared with cells grown at 30° C; when measured at 15° C, the values were slightly greater with cells grown at 10° C. Net accumulation of glucosamine, at 30° C or 20° C, by cells grown at 30° C or 10° C ceased after 4–6 h. Cells grown at either temperature continued to accumulate 2-aminoisobutyrate at 30° C or 20° C for at least 12 h. The rate of efflux of glucosamine by cells grown at 30° C was slower when measured at 20° C compared with 30° C. With cells grown at 10° C, the rate of efflux at 30° C was slower than with cells grown at 30° C; when measured at 20° C, the rates were about equal. The temperature at which the cells were grown did not affect the ability of d-glucose, d-mannose or d-ribose to compete with d-glucosamine, or with the ability of l-alanine to compete with 2-aminoisobutyrate, when tested at 30° C or 20° C. Cells grown 30° C or 10° C had very similar ATP contents. The results are discussed in relation to the effect of temperature on the rate of solute accumulation by micro-organisms.Abbreviation AIB 2-Aminoisobutyrate     

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.     

The effect of temperature on development and fecundityof Scymnus levaillanti

Development and fecundity of Scymnus levaillanti(Mulsant) were recorded at fiveconstant temperatures ranging from 15 to 35 ± 1 °C in 5 °C increments, 60 ± 5% RHand 16 h of artificial light (5000 Lux). Developmentaltime (egg to adult) of S. levaillantisignificantly decreased with increasing temperatures,ranging from 63.9 days at 15 °C to 11.1 days at35 °C. Development from egg to adult required305.2 DD above a developmental threshold estimated as11.7 °C. Oviposition periods lasted 86.5, 76.1,47.2, and 31.5 days at 20, 25, 30 and 35 °C,respectively. No eggs were deposited at 15 °C.Higher temperatures resulted in shorter generationtimes (T_O) and in decreased net reproductiverates (R_O) of the coccinellid. S.levaillanti kept at 30 °C produced 0.151females/female/day, the highest per capita rate ofpopulation growth (r_m). The `functional response'of larvae and adults of S. levaillanti matcheswell that described by Holling (1959) as Type 2.Daily number of eggs deposited by females increased toa plateau with increasing prey density. Resultsobtained here provide information about the biology ofS. levaillanti, and its feeding capacityindicates that it may act as an important control agent.     

The respiratory chain of the facultative thermophile,Bacillus coagulans

Two oxidases were found to be present in membranes from the facultative thermophile Bacillus coagulans grown at 55°C, compared to one in cells grown at 37°C. Cytochrome spectra and inhibitors of the respiratory chain identified them as cytochrome oxidases aa ₃ and d. Both were present in membranes from 55°C grown cells, but only cytochrome oxidase aa ₃ was found in membranes from 37°C grown cells. The presence of cytochrome d in 55°C grown cultures was found to be due to decreased oxygen tension and not to the high growth temperature. This was confirmed by (a) induction of cytochrome d at 37°C under conditions of oxygen limitation and (b) its repression at 55°C under conditions of high aeration and its subsequent induction on lowering the dissolved oxygen concentration in chemostat cultures. Two cytochromes b (_max 558 and _max 562) were present in both 37°C and 55°C grown cells. Results from the inhibition of substrate oxidation by membranes suggested different pathways of electron transport by the respiratory chain.     

Effect of temperature on production of aflatoxin on rice by Aspergillus flavus

Summary The effect of temperature on formation of aflatoxin on solid substrate (rice) byAspergillus flavus NRRL 2999 has been studied in some detail. The optimum temperature for production of both aflatoxin B₁ and G₁ under the conditions employed is 28° C. Comparable yields of B₁ were obtained at 32° C, but considerably less G₁ was produced at this temperature. Both B₁ and G₁ were found in lesser amounts at temperatures above 32° C, and the aflatoxin content of rice incubated at 37° C was low (300–700 ppb) even though growth was good.Reducing the temperature from 28° to 15° C resulted in progressively less aflatoxin, but 100 ppb of B₁ was detected in cultures incubated 3 weeks at 11° C. No aflatoxin was produced at 8° C.The ratio of the four aflatoxins is affected by temperature. At the lower temperatures, essentially equal amounts of aflatoxin B₁ and G₁ were produced, whereas at 28° C, approximately four times as much B₁ was detected as G₁. At the higher temperatures, relatively less G was formed, until at 37° C, less than 10 ppb was detected.This is a laboratory of the Northern Utilization Research and Development Division, Agricultural Research Service, U.S. Department of Agriculture.     

Long-Term Temperature Acclimation of Photosynthesis in Steady-State Cultures of the Polar Diatom <Emphasis Type="Italic">Fragilariopsis cylindrus</Emphasis>

Cultures of the obligate psychrophilic diatom Fragilariopsis cylindrus (Grunow) were grown for 4 months under steady-state conditions at −1 °C and +7 °C (50 μmol photons m⁻² s⁻¹) prior to measurements in order to investigate long-term acclimation of photosynthesis to both temperatures. No differences in maximum intrinsic quantum yield of PS II (F_V/F_M) and relative electron transport rates could be detected at either temperature after 4 months of acclimation. Measurements of photosynthesis (relative electron transport rates) vs. irradiance (P vs. E curves) revealed similar values for relative light utilization efficiency (α = 0.57 at −1 °C, α = 0.60 at +7 °C) but higher values for irradiance levels at which photosynthesis saturates (E_K) at −1 °C and, therefore, higher maximum photosynthesis (P_MAX = 54 (relative units) at −1 °C, P_MAX = 49 at +7 °C). Nonphotochemical quenching (NPQ) measurements at 385 μmol photons m⁻² s⁻¹ indicated higher (37%) NPQ for diatoms grown at −1 °C compared to +7 °C, which was possibly related to a 2-fold increase in the concentration of the pigment diatoxanthin and a 9-fold up-regulation of a gene encoding a fucoxanthin chlorophyll a,c-binding protein. Expression of the D1 protein encoding gene psbA was ca. 1.5-fold up-regulated at −1 °C, whereas expression levels of other genes from Photosystem II (psbC, psbU, psbO), as well as rbcL, the gene encoding the Rubisco large subunit were similar at both temperatures. However, a 2-fold up-regulation of a plastid glyceraldehyde-P dehydrogenase at −1 °C indicated enhanced Calvin cycle activity. This study revealed for the first time that a polar diatom could efficiently acclimate photosynthesis over a wide range of polar temperatures given enough time. Acclimation of photosynthesis at −1 °C was probably regulated similarly to high light acclimation.     

The temperature dependence of the acute toxicity of copper to a freshwater pond snail,Viviparus bengalensis L.

Static bioassays with copper (as CuSO₄ · 5H₂O) were conducted in laboratory with a freshwater pond snailViviparus bengalensis, at different environmental temperatures. The 96 hr LC50 values in ppm of Cu were 0.060 at 32.5 °C; 0.066 at 24 °C; 0.09 at 27.3 °C and 0.39 at 20.3 °C. In higher copper concentrations some behavioural changes such as secretion of mucus, discharge of eggs and embryos were noted. The results indicate that toxicity to copper increases with temperature increase.     

Effects of temperature and CO2 enrichment on kinetic properties of phospho-enol-pyruvate carboxylase in two ecotypes of Echinochloa crus-galli (L.) Beauv., a C4 weed grass species

Summary Two populations of Echinochloa crus-galli (Québec, Mississippi) were grown at the Duke University Phytotron under 2 thermoperiods (28°/22°C, 21°/15°C day/night) and 2 CO₂ regimes (350 and 675 l l^-1). Thermostability, energy of activation (E _a ),K _m (PEP), K _m (Mg⁺⁺), and specific activity of phospho-enol-pyruvate carboxylase (PEP_c) were analyzed in partially purified enzyme preparations of plants grown for 5 weeks. Thermostability of PEP_c from extracts (in vitro) and leaves (in situ) was significantly higher in Mississippi plants. In vitro denaturation was not appreciably modified by thermal acclimation but CO₂ enrichment elicited higher thermostability of PEP_c. In situ thermostability was significantly higher than that of in vitro assays and was higher in Mississippi plants acclimated at 28°/22°C and in plants of the two ecotypes grown at 675 l l^-1 CO₂. E _a (Q ₁₀ 30°/20°C) for PEP_c was significantly lower in Québec plants as compared to Mississippi and no acclimatory shifts were observed. Significantly higher K _m's (PEP) in 20°C assays were obtained for Mississippi as compared to Québec plants but values were similar at 30°C and 40°C assays. K _m (Mg⁺⁺) decreased at higher assay temperatures and were significantly lower for PEP_c of the Québec ecotype. No significant changes in K _m (Mg⁺⁺) values were associated with modifications in temperature on CO₂ regimes. PEP_c activity measured at 30°C was significantly higher for Québec plants when measured on a leaf fresh weight, leaf area or protein basis but not on a chlorophyll basis. Significantly higher PEP_c activity for both genotypes was observed for plants acclimated at 21°/15°C or grown at 675 l l^-1 CO₂. Net photosynthesis (Ps) and net assimilation rates (NAR) were higher in Québec plants and were enhanced by CO₂ enrichment. NAR was higher in plants acclimated at low temperature, while an opposite trend was observed for Ps. PEP_c activities were always in excess of the amounts required to support observed rates of CO₂ assimilation.     

Effect of acute pH depression on the survival of the freshwater amphipod Hyalella azteca at variable temperatures: field and laboratory studies

Field observations on temperature and pH of a small pond showed that a amphipod population of Hyalella azteca was exposed to variable seasonal pH between 5.10–5.85, and water temperatures between 2–21 °C. Laboratory experiments were designed to simulate seasonal temperatures and field pHs of a small pond habitat. Laboratory bioassay experiments were conducted to determine the survival of Hyalella azteca at pHs 4, 5, 6 and 7, and varying temperatures of 5°, 10°, 15°, 20° and 25 °C.The LT₁₀₀ at pH 4 and 25 °C was 5.7 ± 0.47 days, compared to 47.3 ± 2.49 days at 5 °C. An Analysis of Variance (ANOVA) showed temperature was a significant (p > 0.0001) source of variation in the acute lethality of pH to H. azteca. A Duncans Multiple Range Test (DMRT) further showed that in laboratory experiments at pH 4, there was a significant difference ( = 0.01) between the LT_100s at 5°, 10°, 15° and 20 °C, but not between temperatures 20° and 25 °C.     

Life-history traits of the acarophagous lady beetle,<Emphasis Type="Italic">Stethorus japonicus</Emphasis> at three constant temperatures

Stethorus japonicusKamiya (Coleoptera: Coccinellidae) is an indigenous ladybird beetle in Japan, which feeds on many spider mite species. We evaluated the development, survivorship and life-history parameters of this lady beetle on a diet of eggs of the two-spotted spider mite, Tetranychus urticae Koch (red form) (Acari: Tetranychidae). In addition, the effect of short photoperiod on its reproduction was assessed. Survival rates from egg to adult were more than 71% at temperatures between 17.5 and 30 °C. The highest immature mortality was 100% at 35 °C followed by 76% at 15 °C and 52% at 32.5 °C. The lower threshold temperature for development from egg to egg-laying adult was 13.0 °C and the thermal constant was calculated as 238.7° days. Based on these data, the maximum number of generations that could complete development in a year under field conditions in Ibaraki, central Japan, would be between five and seven. The intrinsic rates of natural increase (r_m) were 0.093 at 20 °C, 0.156 at 25 °C and 0.241 at 30 °C. Reproductive diapause was induced at photoperiods with light phases shorter than 13 h at 18 °C.     

Effects of temperature and thermal history on neuromuscular properties of two crustacean species

Summary The effect of temperature on the ability of neuromuscular junctions and muscle fibers to contract, release neurotransmitter, and maintein postsynaptic membrane properties, was measured in vivo and in vitro in claw closer muscles in stone crabsMenippe mercenaria (Say) and blues crabsCallinectes sapidus (Rathbun).In vivo muscle stress (defined as force generated per unit of muscle cross-sectional area) was measured in crabs of both species collected from northern populations (annual temperature range 2–30°C) and southern populations (annual temperature range 15–30°C). Muscle stress was compared between (1) crabs of both species maintained in the laboratory at 30°C (laboratory warmed); (2) crabs given a brief acclimation period (4 weeks for blue crabs; 7 weeks for stone crabs) at 8°C in the laboratory (laboratory colled), and (3) stone crabs that had been naturally acclimated from summer (30°C) to winter (8°C) temperatures over a 6 month period in the field (naturally cooled). No differences were found in the abilities of the northern and southern populations of either species to generate muscle stress when tested at summer temperatures (30°C) common to both populations. Northern and southern blue crabs produced similar levels of muscle stress whether laboratory warmed (30°C) or laboratory cooled (8°C). Conversely, northern and southern stone crabs showed significantly reduced muscle stress in laboratory cooled crabs compared with laboratory warmed crabs. Stone crabs from both populations generated the same amount of muscle stress after having been naturally cooled to 8°C as they had generated the previous summer (30°C).In vitro neuromuscular properties (i.e. (1) muscle stress as a measure of contractile ability; (2) excitatory junction potential (EJP) amplitude as a measure of neurotransmitter release; (3) specific membrane resistance (R_m) as a measure of postsynaptic membrane properties) were compared at 8, 20, and 30°C between northern cold acclimated (naturally cooled stone crabs and laboratory cooled blue crabs) and non-cold acclimated (laboratory cooled stone crabs. Muscle fibers in claws of stone crabs and blue crabs showing cold acclimation had higher R_m at 8°C than non-cold acclimated crabs. This higher R_m resulted in a broadening of EJP's which enhanced EJP summation, muscle fiber depolarization, and muscle stress.Abbreviations EJP excitatory junction potential - E _r resting membrane potential - F _e lacilitation - R _m specific membrane resistance     

Respiratory energy losses related to cell weight and temperature in ciliated protozoa

Summary Respiratory energy losses in five species of ciliated protozoa, Tetrahymena pyriformis Ehrenberg, Vorticella microstoma Ehrenberg, Paramecium aurelia Ehrenberg, Spirostomum teres Claparède and Lachmann and Frontonia leucas Ehrenberg, were investigated at 8.5° C, 15° C and 20° C using Cartesian diver microrespirometry. Q ₁₀ values of 1.15–2.24 were found for four of the species between 8.5–15° C, while in S. teres a Q ₁₀ of 12.98 occurred between these temperatures. Between 15–20° C T. pyriformis and P. aurelia had Q ₁₀ values of 3.73 and 1.56, respectively. Linear double log regressions of oxygen consumption vs. dry weight were derived at each temperature and regression coefficients (b) of 0.2723 (8.5° C), 0.4364 (15° C) and 0.4171 (20° C) were obtained. The results are explained and discussed in relation to previous work on the energetics of ciliated protozoa.     

Recovery of photosynthetic reactions after high-temperature treatments of a heat-tolerant cactus

Inhibition and recovery of net CO₂ uptake and three photosynthetic electron transport reactions as well as plant survival following high-temperature treatments were investigated for Opuntia ficus-indica. For plants maintained at 30°C/20°C day/night air temperatures, treatment at 60°C for 1 h irreversibly inhibited net CO₂ uptake and photosynthetic electron transport, resulting in plant death in about 60 days. When a plant maintained at 30°C/20°C was treated at 55°C for 1 h, net CO₂ uptake was completely inhibited 1 d after the treatment but fully recovered in 60 d. Differential inactivation of photosystem (PS) I, PSII, and whole chain electron transport activities occurred; PSI was the most tolerant of 55°C and took the least time (45 d) for total recovery. All 30°C/20°C plants survived a 1-h treatment at 55°C, although some pale green areas were observed on the cladode surfaces. In contrast to growing at 30°C/20°C, plants acclimated to 45°C/35°C survived 60°C for 1 h without showing any necrotic or pale green areas on the cladode surfaces. When such a plant was transferred to 30°C/20°C following the high-temperature treatment, recovery in net CO₂ uptake began in 1 d and progressed to complete recovery by 30 d. Growth temperatures thus influence the possibility for recovery of photosynthetic reactions and ultimately the survival of O. ficus-indica following a high-temperature exposure.Abbreviations DCPIP 2,6-dichlorophenol indophenol - MV methyl viologen - PAR photosynthetically active radiation - PSI or PSII photosystem I or II - WC whole chain     

Effect of temperature and oxygen on cell growth and recombinant protein production in insect cell cultures

The effect of temperature and O₂ saturation on the production of recombinant proteins -galactosidase and human glucocerebrosidase by Spodoptera frugiperda cells (Sf9) infected with recombinant Autographa californica nuclear polyhedrosis virus was investigated. The rates of cell growth, glucose consumption, O₂ consumption and product expression were measured at temperatures between 22° C and 35° C. The results indicated that possible O₂ limitation may be alleviated without compromising the maximum cell yield by lowering the incubation temperature from 27° C to 25° C. The expression level of the recombinant proteins at 27° C was similar to that obtained at 22° C and 25° C; lower protein yields were obtained at 30° C. An increase in temperature from 22° C to 27° C led to earlier production of the proteins and to an increase in the proportion of the product released outside the cells. Correspondence to: J. Shiloach     

Untersuchung der Beziehung zwischen extracellulärer Glykolsäure-Ausscheidung und der photosynthetischen CO2-Aufnahme bei der Blaualge Anacystis nidulans

Summary The formations of transients in CO₂ exchange in the blue-green alga Anacystic nidulans is dependent on the temperature used during the measurements. The algae were grown in a low light intensity (4000 lux) under normal air conditions and measured in the same low CO₂ concentration (0.03 vol. %) but under a higher light intensity (10 000 lux). At a temperature of +20°C the stationary rate of CO₂ uptake was reached directly. At a temperature of +35°C, on the other hand, a maximum of CO₂ uptake could be observed at the beginning of the light period followed by a steady rate of photosynthesis, which was higher than at +20°C. In the beginning of the dark period a CO₂ outburst appeared at 35°C.Only at a low temperature (+20°C) did we find a light induced glycollate excretion; after a maximum at 7 1/2 minutes illumination the release of glycollate ceases and the level decreases to a lower value. A similar time course exists during illumination in red light (621 nm, 1.5·10^-8 einsteins) and a temperature of +20°C. In blue light (432 nm, 1,5·10^-8 einsteins, +20°C) and in white light at a high temperature (+35°C) we could not find any light induced glycollate excretion. Our results are discussed in reference to the photorespiration. We explain the formation of transients in CO₂ uptake of Anacystis at a high temperature (+35°C) and in blue light (+20°C) on the basis of the influence of photorespiration.     

Einfluß der Temperatur auf die Lichtatmung der Blaualge Anacystis nidulans

Summary CO₂ exchange, ¹⁴CO₂ fixation and ¹⁴C-products of Anacystis nidulans (strain L 1402-1) were studied during the induction period at temperatures of +15°C and+35°C. At+15°C the stationary rates of CO₂ uptake and respiration were reached directly. At+35°C a maximum of CO₂ uptake could be observed at the beginning of the illumination period followed by a lower steady rate of photosynthesis. In the following dark period a CO₂ gush appeared at+35°C. The magnitude of the CO₂ outburst is relatively independent of the photosyntbetic period. The autoradiographic studies showed that the Calvin cycle is the main carboxylation pathway in Anucystis. At a temperature of +35°C serine was labelled after 20 sec of photosynthesis. At+15°C, on the other hand, a low radio-activity appeared in serine after 5 min of photosynthesis. The results show that photorespiration of Anacystis is stimulated by high temperatures.     

Structural and circulatory responses to hypoxia in the secondary lamellae ofSalmo gairdneri gills at two temperatures

Summary The first gill arch ofSalmo gairdneri was fixed from normoxic (O₂ saturation of the water >90%) and hypoxic (O₂ saturation 25–30% for 5 days) fish at 10 °C and 18 °C, and from fish after one-day recovery from hypoxia at 18 °C. The secondary lamellae of the gills were analysed with morphometric methods for structural, haemotological and circulatory changes. During hypoxia a marked vascular distension took place at both temperatures. At both temperatures the vascular distension coincided with a shortening of the diffusion distance (36% at 10 °C and 21% at 18 °C) and a swelling of the erythrocytes (60% at 10 °C and 42% at 18 °C). The effects of these changes on the oxygen uptake of the gills are discussed.     

Growth characteristics of an obligately psychrophilic Vibrio sp.

The growth characteristics of an obligately psychrophilic Vibrio sp. have been studied in a chemostat with glucose or lactose as the limiting substrate over a temperature range 0–23°C. Vibrio AF-1 has an optimum growth temperature of 15°C and maximum growth temperature which is dependent upon the carbon source. On glucose growth ceases at 20°C whereas on lactose growth continues to 23°C. Growth rate is also a function of the carbon source provided. When grown on glucose, fructose, sucrose, maltose and galactose _max values of 0.046 h^-1 at 15°C were recorded whereas on lactose, mannose, ribose and xylose _max values of 0.020 h^-1 were obtained. Substrate affinities (K _s ) for the 9 sugars also fall into 2 divisions as for _max and are temperature dependent. Those sugars which support a high growth rate have highest K _s values at 0°C whereas these which give a low growth rate show maximum affinities at 15°C. Vibrio AF-1 produces the maximum cell yield (0.6 g/g sugar consumed) at temperature <8°C irrespective of the carbon source utilised and correlated with maximum rates of sugar uptake and minimum O₂ consumption. Maintenance energy determination on glucose grown cells show that at 2° C 2% of the carbon input is used for maintenance whereas at 20°C the requirement increases to 10% of the carbon input.     

Effect of constant temperatures on germination, radial growth and virulence of Metarhizium anisopliae to three species of African tephritid fruit flies

The effect of temperatureon conidial germination, mycelial growth, andsusceptibility of adults of three tephritidfruit flies, Ceratitis capitata(Wiedemann), C. fasciventris (Bezzi) andC. cosyra (Walker) to six isolatesof Metarhizium anisopliae were studied inthe laboratory. There were significantdifferences among the isolates in the effect oftemperature on both germination and growth.Over 80% of conidia germinated at 20, 25 and30°C, while between 26 and 67% conidiagerminated at 35°C and less than 10% at15°C within 24 hours. Radial growth was slowat 15°C and 35°C with all of theisolates. The optimum temperature forgermination and mycelial growth was 25°C. Mortality caused by the six fungal isolatesagainst the three fruit fly species varied withtemperature, isolate, and fruit fly species.Fungal isolates were more effective at 25, 30and 35°C than at 20°C. The LT₉₀values decreased with increasing temperature upto the optimum temperature of 30°C. Therewere significant differences in susceptibilitybetween fly species to fungal infection at allthe temperatures tested.