Immobile and tough versus mobile and weak: effects of ultraviolet B radiation on eggs and larvae of Manduca sexta

Although indirect effects of solar ultraviolet (UV) radiation on insects are well known (e.g. UV radiation can modify plant chemistry), direct effects of solar radiation on insects have received little attention. Radiation in the UVB range (300–320 nm) is damaging because it is absorbed directly by proteins and DNA. UVB should be toughest on immobile or small life stages, such as eggs or early larval instars. In the present study, the effects of UVB radiation on eggs and larvae of the tobacco hornworm Manduca sexta L. (Lepidoptera: Sphingidae) are examined. The present study aimed to address: what natural levels of UV do they experience; how does UVB affect the performance of eggs; and how does it affect the performance of larvae? In addition, do M. sexta larvae use behaviour to avoid UVB exposure and, consequently, are they physiologically less robust to UVB? In these experiments, eggs and late larval instars of M. sexta are found to be robust to natural levels of UV radiation. By contrast, young larvae are not only more susceptible to damage from UVB, but also they use behavioural means to avoid it. The strategy of using behaviour may relax selection pressures on morphological and physiological mechanisms for preventing (or recovering from) damage by environmental UV radiation.     

Translation of Rabbit Haemoglobin Messenger RNA by Thalassaemic and Non-thalassaemic Ribosomes

Globin mRNA from rabbit reticulocytes can be translated equally well by human ribosomes from thalassaemic and normal reticulocytes. This implies that the defect in β-thalassaemia is not in the ability of ribosomes to translate mRNA but is probably in the mRNA itself.     

A developmental approach to the problem of variation in evolutionary rates

Certain general features are widely recognized in evolution, one of which is the variability in the rate at which morphological characters evolve and taxa are replaced by others. Although some rate-variability in evolution no doubt arises because of different rates of ecological change, it is proposed that some of the variability also arises from developmental, rather than ecological, sources. A theory is outlined whereby early-acting genes influencing the course of development evolve more slowly, but have individually larger effects, than genes affecting development at a later stage in the life-cycle. The erratic course of morphological evolution that results is illustrated by computer simulation. It is suggested that the applicability of the theory is restricted to long-term evolution and that variability in the rate of evolution over shorter periods may be of an entirely different nature.     

Relative influence of habitat structure,species interactions and rainfall on the post‐fire population dynamics of ground‐dwelling vertebrates

The long‐term impacts of wildfires on animal populations are largely unknown. We used time‐series data based on a tracking index, from coastal NSW spanning 28 years after a wildfire, to investigate the relative influence of habitat structure, species interactions and climate on post‐fire animal population dynamics. The fire had an immediate impact on habitat structure, reducing and simplifying vegetation cover, which then underwent post‐fire successional change including an increase and plateau in tree canopy cover; an increase, stabilization and then decline in shrub cover; and an increase in ground litter cover. Population changes of different animal species were influenced by different components of successional change, but there was also evidence that species interactions were important. For example, bandicoots (Isoodon obesulus and Perameles nasuta combined) increased concurrent with an increase in shrub cover then declined at a faster rate than a direct association with senescing shrub cover would suggest, while the feral cat (Felis catus) population changed with the bandicoot population, suggesting a link between these species. Potoroos (Potorous tridactylus) increased 10 years after the fire concurrent with the closing tree canopy, but there was also evidence of a negative association with feral foxes (Vulpes vulpes). Variation in rainfall did not have significant effects on the population dynamics of any species. Our results suggest that changes in habitat structure play a key role in the post‐fire dynamics of many ground‐dwelling animals and hence different fire regimes are likely to influence animal dynamics through their effects on habitat structure. However, the role of predator–prey interactions, particularly with feral predators, is less clear and further study will require manipulative experiments of predators in conjunction with fire treatments to determine whether feral predator control should be integrated with fire management to improve outcomes for some native species.     

Comparison of epilithic and epixylic biofilm development in a boreal river

SUMMARY. 1. We assessed substratum effects on lotic biofilm development by placing glass and white pine sampling units in a fourth-order boreal river, and analysing, at 6-week intervals, upper-surface biofilms for ATP, chlorophyll, ergosterol, and the activities of nine exoenzymes.
2. All parameters, except chlorophyll standing stock (range 80–320 μg dm⁻²) and β-xylosidase activity (range 0.4–4.8 μmol h⁻¹ dm⁻²), were significantly greater for epixylic biofilms than for epilithic ones, but the magnitude of the increases varied from 2 to 5 fold, showing that, even under similar hydrodynamic conditions, epilithic and epixylic biofilms are structurally and functionally distinct. For example, ergosterol concentrations ranged from undetectable to 0.93 μg dm⁻² for epilithon and from 11–49 μg dm⁻² for epixylon; corresponding ranges for ATP were 1.6–3.7 (epilithon) and 4.2–7.7 μg dm⁻² (epixylon), for acid phosphatase activity: 2.3–4.9 and 20–41 μmolh⁻¹dm⁻², and for alkaline phosphatase activity: 1.9–8.1 and 29–150 μmol h⁻¹dm⁻², respectively.
3. The more extensive epixylic development was attributed to utilization of the wood substratum as a supplemental carbon source and to a higher density of microbial attachment sites.     

Tracing carbon and oxygen isotope signals from newly assimilated sugars in the leaves to the tree-ring archive

The analysis of δ ¹³C and δ ¹⁸O in tree-ring archives offers retrospective insights into environmental conditions and ecophysiological processes. While photosynthetic carbon isotope discrimination and evaporative oxygen isotope enrichment are well understood, we lack information on how the isotope signal is altered by downstream metabolic processes.
In Pinus sylvestris , we traced the isotopic signals from their origin in the leaf water ( δ ¹⁸O) or the newly assimilated carbon ( δ ¹³C), via phloem sugars to the tree-ring, over a time-scale that ranges from hours to a growing season.
Seasonally, variable ¹³C enrichment of sugars related to phloem loading and transport did lead to uncoupling between δ ¹³C in the tree-ring, and the c _i/ c _a ratio at the leaf level. In contrast, the oxygen isotope signal was transferred from the leaf water to the tree-ring with an expected enrichment of 27‰, with time-lags of approximately 2 weeks and with a 40% exchange between organic oxygen and xylem water oxygen during cellulose synthesis.
This integrated overview of the fate of carbon and oxygen isotope signals within the model tree species P. sylvestris provides a novel physiological basis for the interpretation of δ ¹³C and δ ¹⁸O in tree-ring ecology.     

The Ovule and 'Seed' of Araucaria Bidwillii with Discussion of the Taxonomy of the Genus: III. Anatomy of Multi-ovulate Cone Scales

This paper deals with the anatomy of two- and three-ovulatecone scales which are found occasionally in the cones of A.Bidwillii. The manner in which each ovule receives its vascularsupply from bundles lateral to the ovule is discussed, togetherwith a hypothetically primitive type of araucarian cone scalewith three ovules possibly resembling the fossil Schizolepis.The interpretation of the vascular system of the scales as givenin this paper is a correction of that presented in the firstpaper of this series by the same authors.