Metabolic rate in diapause and nondiapause brown locust eggs correlated with embryonic development

Insects use dormancy to survive adverse conditions. Brown locust Locustana pardalina (Walk.) eggs offer a convenient model to study dormancy (diapause and quiescence), which contributes to their survival under arid conditions. The metabolic rates of developing nondiapause, diapause and quiescent eggs are compared in the present study using closed‐system respirometry. The embryo becomes committed to continue development and hatch or to enter diapause 6 days after the eggs are placed on moist soil. The metabolic rate of nondiapause eggs increases exponentially until hatching, whereas that of diapause eggs is low and stable. The metabolic rate of diapause laboratory eggs (1.9 ± 0.6 µL CO₂ mg^?1 h^?1) is significantly higher than that of field eggs (0.5 ± 0.3 µL CO₂ mg^?1 h^?1), although the ranges of metabolic rate overlap and the embryos are all in late anatrepsis. The metabolic rate of quiescent eggs is similar to that of diapause eggs but decreases with time. Low metabolic rates during arrested development allow eggs to persist over long periods before hatching.     

Low dissolved oxygen levels reduce anti-predation behaviours of the freshwater clam Corbicula fluminea

1. When dissolved oxygen levels decline in aquatic systems, prey may be unable to maintain behaviours protecting them from predators. We examined how oxygen availability affected anti‐predator responses in the freshwater clam, Corbicula fluminea. 2. When attacked, bivalves protect their soft tissues by closing their protective valves. This reduces vulnerability to small predators, but ventilation and oxygen uptake are suspended. We found that after a simulated attack, clams under low oxygen conditions reopened their valves sooner than clams under high oxygen conditions, suggesting that hypoxia increases vulnerability to predation. 3. Bivalves may also evade predators through burial into the substratum. Deeper burial confers greater refuge from predators, but increases the costs of ventilation. In a second experiment, we studied how burial depth of C. fluminea is affected by oxygen availability. Additionally, we examined whether clams changed burial depth following a simulated attack by a small predator, and whether this response was affected by oxygen availability. Our results offered partial support for the hypothesis that burial depth is reduced under hypoxic conditions, but the simulated attack did not affect burial depth in any oxygen treatments.     

Changing attitudes in nature conservation: the Nature Conservancy and Nature Conservancy Council

An official organization responsible for ecological research and nature conservation was formed in 1949. This paper traces its development and vicissitudes, first as an independent Nature Conservancy, then as a part of the Natural Environment Research Council, and finally as the Nature Conservancy Council. Much has been achieved: ecology is now a household word; there is a strong voluntary tide for nature conservation in the country; and there have been notable achievements in practical conservation. But the dangers to nature in Britain have proved to be much greater than anticipated.     

The inhibition of potato sprout growth by light.

The effect of light intensity on sprout growth in seed potato tubers (Solanum tuberosum) was examined using diffuse daylight in Peru and diffuse artificial light at Glasgow. Mean temperatures below 20 °C produced strong sprout growth that was inhibited by both daylight and artificial light, at visible irradiances above 0.01 Wm^-2. The percentage inhibition of sprout growth increased linearly with the logarithm of the irradiance, 50% inhibition being at 0.04 - 0.1 Wm^-2 provided that the temperature was suitable for substantial sprout growth in the absence of light. Cultivar and temperature had very little effect on the 50% inhibition point. At high irradiances growth inhibition was up to 95%, but the sprout length was never reduced to zero; short, robust green sprouts remained. Sprout numbers were increased by daylight, but not by artificial light. Diffuse daylight also reduced the total weight loss from seed tubers during a storage season of 180 days. At mean temperatures above 20 °C., sprout growth in the absence of light was much reduced and the effect of light on sprout elongation was less obvious.     

The effect of ammonia treatment on the solubilization of straw and the growth of cellulolytic rumen bacteria

Pre-treatment of straw with anhydrous ammonia increased its susceptibility to solubilization by the predominant cellulolytic bacteria from the rumen, Bacteroides succinogenes, Ruminococcus albus and R. flavefaciens. Ammonia treatment also increased the production of microbial protein and fermentation products by all three species. Scanning electron microscope observations of straw during digestion suggested that the attack of straw by these bacteria was accompanied by the formation of substantial numbers of adherent microcolonies.     

Tasmanian high altitude grassy vegetation: its distribution,community composition and conservation status

Grassy woodland, grassy shrubland, grassy sedgeland, tussock grassland and grassland are extensive on basalt, limestone and fine-textured Quaternary deposits, are occasional on dolerite, granite and fine-grained sedimentary rocks, but are absent from the siliceous mountains of Tasmania. With the exception of limestone lithosols, the grassy communities are confined to relatively deep soils with a low surface rock cover. Much of the area of the grassy communities below the climatic treeline has clearly been forest in the recent past, although some of the higher subalpine plains seem likely to have been grassy at least since the peak of the Last Glacial. The first axis of an ordination of floristic data from 190 quadrats had at one extreme the grassy communities which most resembled in their species composition the sedgelands and sclerophyll shrub woodlands of the west of Tasmania, and at the other extreme the grassy woodlands on relatively fertile, well drained sites in the centre and east of Tasmania. The second axis was correlated with altitude, probably inversely reflecting the growing season. The third axis was related most closely to a soil drainage index. Many of the 15 communities recognized from a polythetic divisive classification of the quadrats have highly local distributions. Six of the communities are totally unreserved and four are poorly reserved. An iterative method is used to develop a minimum reservation strategy involving seven areas.     

Comparison of nucleic acid hybridisation and other tests for detecting tobacco rattle virus in narcissus plants and potato tubers

All isolates of tobacco rattle virus (TRV) found in naturally infected narcissus leaves produced nucleoprotein particles, mostly in large concentrations but, because of antigenic diversity, less than half of the isolates were identified by immunosorbent electron microscopy (ISEM) and still fewer by enzyme-linked immunosorbent assay. All were identified by a nucleic acid hybridisation test in which DNA complementary to RNA-1 of strain PRN of TRV was allowed to react with nucleic acid extracted from leaf tissue. Spraing-affected tubers in some potato stocks yielded only NM isolates of TRV. These isolates do not produce virus particles and they were therefore not detected by ISEM. The infectivity of nucleic acid extracts from recently harvested tubers with spraing symptoms was much greater than that of extracts prepared from tubers after 8 months' storage. In other potato stocks, some spraing-affected tubers contained NM isolates and the rest contained particle-producing isolates (M isolates) of TRV. The infectivity of sap and of nucleic acid, extracted 7 months after harvest from tubers infected with M isolates, was much greater than that of nucleic acid extracted from comparable tubers infected with NM isolates. TRV was detected by nucleic acid hybridisation in extracts of almost all tubers containing either M or NM isolates, even when the tubers were not tested until 7–8 months after harvest. The probable sequence of events occurring after tubers are infected with TRV is outlined, and it is suggested that the virus will rarely become established in fields as a result of planting infected tubers.