We studied the effects of temperature (5, 10, 20, and 30 C) on the phytotoxic activity of decaying quackgrass [Agropyron repens (L.) Beauv.] leaves and rhizomes that were incubated in soils for 0, 1, 2, 4, and 6 weeks. Alfalfa (Medicago sativa L.) seeds were grown for 96 h in water, water extracts of control soils, and water extracts of soil with quackgrass rhizomes or leaves. Dried quackgrass rhizomes and leaves contained water-soluble toxins that inhibited alfalfa seedling development and growth. There was a strong interaction between incubation time and temperature on the development of additional toxins by decomposing quackgrass. High incubation temperature (30 C) accelerated toxin formation and ultimate decay. Intermediate temperature (20 C) delayed toxin formation and decay. Low incubation temperatures (5 C and 10 C) prevented formation of additional toxin. In all extracts of quackgrass and soil that had been incubated for 6 weeks, normal alfalfa seedling number equaled that in water. However, seedling growth varied with incubation temperatures.

Treatment of quackgrass with glyphosate [N-(phosphonomethyl) glycine] in the greenhouse did not influence the toxicity of decaying quackgrass leaves. The highest toxic effect was noted after 1 week of decay on the soil surface.

Amicarbazone has potential for selective annual bluegrass control in cool-season turfgrasses, but seasonal application timings may influence efficacy. To test this hypothesis, field experiments in New Jersey and Indiana investigated amicarbazone efficacy from fall or spring applications and growth chamber experiments investigated the influence of temperature on efficacy. Fall treatments were more injurious to creeping bentgrass and Kentucky bluegrass than spring applications, but fall applications were also more efficacious for annual bluegrass control. In growth chamber experiments, injury and clipping weight reductions were exacerbated by increased temperatures from 10 to 30 C on annual bluegrass, creeping bentgrass, Kentucky bluegrass, and perennial ryegrass. Results suggest that amicarbazone use for annual bluegrass control in cool-season turf may be limited to spring applications, but increased temperature enhances activity on all grasses.

Temperature effects on spectral properties of the two types of rod photoreceptors in toad retina, “red” and “green” rods, were studied in the range 0–38°C. Absorbance spectra of the visual pigments were recorded by single-cell microspectrophotometry (MSP) and spectral sensitivities of red rods were measured by electroretinogram (ERG) recording across the isolated retina. The red-rod visual pigment is a usual rhodopsin (λmax = 503.6 nm and 502.3 nm at room temperature (21°C) in, respectively, Bufo marinus and Bufo bufo), that of green rods (λmax = 432.6 nm in Bufo marinus) belongs to the “blue” cone pigment family. In red rods, λmax depended inversely and monotonically on temperature, shifting by −2.3 nm when temperature was raised from 0°C to 38°C. Green-rod λmax showed no measurable dependence on temperature. In red rods, warming caused a relative increase of sensitivity in the long-wavelength range. This effect can be used for estimating the energy needed for photoexcitation, giving Ea = 44.3 ± 0.6 kcal/mol for Bufo marinus rhodopsin and 48.8 ± 0.5 kcal/mol for Bufo bufo rhodopsin. The values are significantly different (P < 0.001), although the two rhodopsins have very similar absorption spectra and thermal isomerization rates. Our recording techniques did not allow measurement of the corresponding effect at long wavelengths in green rods. Although spectral effects of temperature changes in the physiological range are small and of little significance for visual function, they reveal information about the energy states and different spectral tuning mechanisms of the visual pigments.

The influence of post-treatment temperature on the insecticidal activity of Azadirachta indica (A. Juss) seed extract against the desert locust, Schistocerca gregaria (Forskål) is reported. In tests on adults, the toxicity of crude A. indica seed extract increased by about 10-fold when the post-treatment temperature was raised from 22°C to 40°C. This temperature-dependent toxicity was observed in insects treated either topically or via injection. This phenomenon could partly explain the wide variability in efficacy of neem extracts reported by different investigators.

Temperature is the major abiotic factor controlling the rate of morphogenesis in fish. The present work investigated hatching time and the transition from endogenous to exogenous feeding at five constant temperatures over the range 15-35 °C. Clarias gariepinus eggs can be successfully hatched in ambient water temperatures between 20 and 35 °C, although at 30 °C the hatching rate is significantly improved. At 15 °C embryos do not survive. The period of hatching is inversely related to temperature such that synchronous hatching is encouraged by high temperature within the specific temperature range. The extent to which development rate and metabolic rate in C. gariepinus are accelerated by temperature is not the same. The duration between first feeding, yolksac absorption and the point-of-no-retum is inversely related to temperature. The same threshold temperature, below which development is theoretically arrested, can be estimated for C. gariepinus from the linear relationship between development rate and temperature up to hatching, first feeding and yolksac absorption. This closely approximates the lower lethal temperature of 15 °C estimated directly from embryo survival. The effect of temperature can be usefully modelled in C. gariepinus using the linear relationship V = a + bt to estimate t0 (threshold temperature) and Deff0 (effective day-degrees) and the hyperbolic relationship τ = Deff0/(t – t0) to determine development time. From the present work, t0 is 14.5 °C and Deff0 is 13, 26.3 and 35.7 for hatching, first feeding and yolksac absorption respectively for C. gariepinus. Unlike day-degrees, effective day-degrees remain independent of temperature over the range 20-35 °C. An approximate guide to development time at different constant temperatures within this range is given.