Elevated atmospheric CO2: effects on phytochemistry, insect performance and insect-parasitoid interactions

This study was conducted to examine the effects of CO₂-mediated changes in tree chemistry on the performance of the gypsy moth ((Lymantria dispar L.) and the parasitold Cotesia melanoscela (Ratz.). We used carbon-nutrient balance theory to develop hypotheses regarding changes in tree chemistry and the performance of both insects under elevated CO₂. As predicted, levels of foliar nitrogen declined and concentrations of carbon-based compounds (e.g. starch and phenolics) increased under elevated CO₂. Gypsy moth performance (e.g. growth, development) was altered by CO₂-mediated changes in foliar chemistry, but the magnitude was small and varied across tree species. Larvae feeding on high CO₂ aspen exhibited the largest reduction in performance, relative to larvae feeding on birch, oak, or maple. Parasitism by C. melanoscela significantly prolonged gypsy moth development and reduced growth rates. Overall, the effect of parasitism on gypsy moth performance did not differ between CO₂ treatments. Altered gypsy moth performance on high CO₂ foliage in turn affected parasitoid performance, but the response was variable: parasitoid mortality increased and adult female size declined slightly under high CO₂, while development time and adult male size were unaffected. Our results suggest that CO₂-induced changes in plant chemistry were buffered to the extent that effects on third trophic level interactions were weak to non-existent for the system examined in this study.     

New species, anatomy, and systematic position of the hydrothermal vent and hydrocarbon seep gastropod family Provannidae fam.n. (Caenogastropoda)

The anatomy of the hydrothermal vent gastropod Provanna is described. It is shown to be a primitive neotaenioglossan with mainly plesiomorphic features in all systems, including open pallial gonoducts, epiathroid nervous system with accessory pedal ganglia and a circulatory system where a considerable portion of the venous blood from the coelomic spaces enters the pallial skirt. Apomorphic features include the possession of an anterior notch, or short canal in the shell (and mantle edge), an annulated sensory pallial tentacle, paraspermatozoa modificd as nurse cells. multiple seminal receptacles, a posterior bursa copulatrix, and a renal oviduct with three distinct regions. the middle one expanded. Comparisons are madc with Abyssochrysos, a genus assumed to be a relict member of the Loxonematoidea, which appears to be the closest known relative. A new family. Provannidae fam.n., is created and tentatively included in the Loxonematoidea. The following new specics are described: Provanna segonzaci sp.n. (from hydrothermal vents at the Fiji Back Arc), P. laevis sp.n. (from hydrothermal seeps in the Gulf of California), P. sculpta sp.n. and P. admetoides sp.n. (from hydrocarbon seeps in the Gulf of Mexico). New records are added for previously described species of Provanna.     

Variation in cell composition and utilization of N and P for growth of Selenastrum capricornutum

Cell material from different phases of growth for the green alga Selenastrum capricornutum Printz was analysed for major elements and chlorophyll a content. The ranges in percentage of the dry weight were 50–80%, 4.4–8.8%, 0.24–3.0%, and 0.20–3.23% for C, N, P and chlorophyll a, respectively. The dry weight per cell varied 2.3 times between different growth phases. A N/P-quotient of about 10 (by weight) was found to be a critical level for Selenastrum when these elements were the most limiting nutrients for growth. 31 different organic N-compounds were tested as single N sources in growth experiments with Selenastrum. At least 19 of them could be utilized to varying extent for algal growth. Three organic P-compounds of six tested, were utilized for algal growth. Yield coefficients (mm³ cell volume/mg limiting nutrient element) for Selenastrum were determined with NO₃, -N (y_N= 134). NH₄-N (Y_N= 111) and PO₄-P (Y_P= 2580).     

The cost of secondary sexual characters and the evolution of cost-reducing traits

Secondary sexual traits are characterized by their exaggerated expression relative to homologous nonsexual characters in other species. All models of sexual selection assume that sex traits are costly to produce and maintain, and individuals with reduced costs of production and maintenance of secondary sexual characters would be at a selective advantage. A number of morphological, physiological and behavioural traits may have evolved as a result of their cost-reducing properties: (1) body size, which does not change throughout life, that allows certain individuals to develop exaggerated sex traits, (2) cost-reducing traits, such as muscle size, that improve with practice and (3) actual cost-reducing traits, such as wing size in birds with song flight, which are produced in advance of or simultaneously with the sex trait. Cost-reducing traits may coevolve with secondary sexual characters and allow more extreme sexual signalling than would otherwise have been possible in their absence or in reduced versions.     

Experimental tail elongation in male Barn Swallows Hirundo rustica reduces provisioning of young, but only in second broods

At the beginning of the breeding season, the outermost tail feathers of 31 male Barn Swallows Hirundo rustica were either shortened by 20 mm, elongated by 20 mm or left unmanipulated. In first broods, the number of feeding bouts (per nestling per hour) by males and females did not differ significantly among experimental groups. However, in second broods, males with elongated tails fed their nestlings less often than males with shortened or unmanipulated tails. Male tail elongation may have been detrimental to flight, making capture of insects more difficult. Females paired to long-tailed males did not compensate for this reduction in feeding by males and their nestlings received less food. Neither feeding rates nor brood size differed significantly between first and second broods. Variation in abundance of large insects at different times of the day (high around noon and low in the morning and afternoon) matched variation in feeding rates, supporting the importance of large insects in the Barn Swallow diet. Different feeding rate patterns in first and second broods by males with elongated tails could have at least three explanations: (1) such males were able to adjust their parental effort to some extent, temporarily compensating for an imposed handicap; (2) they were more sensitive than males in the other experimental groups to late season food shortage (a decrease in numbers of large insects, the main Barn Swallow prey, was observed as the season progressed); and (3) they were more sensitive than males in the other experimental groups to the deterioration in their physical condition after first broods.     

Pelagic and benthic net production of dissolved inorganic carbon in an unproductive subarctic lake

1. Both the pelagic and benthic net dissolved inorganic carbon (DIC) productions were measured in situ on four occasions from June to September 2004, in the unproductive Lake Diktar-Erik in subarctic Sweden. The stable isotopic signal ( δ ¹³C) of respired organic material was estimated from hypolimnion water data and data from a laboratory incubation using epilimnion water.
2. Both pelagic and benthic habitats were net heterotrophic during the study period, with a total net DIC production of 416 mg C m⁻² day⁻¹, of which the pelagic habitat contributed approximately 85%. The net DIC production decreased with depth both in the pelagic water and in the sediments, and most of the net DIC production occurred in the upper water column.
3. Temporal variations in both pelagic and benthic DIC production were small, although we observed a significant decrease in pelagic net DIC production after the autumn turnover. Water temperature was the single most important factor explaining temporal and vertical variations in pelagic DIC production. No single factor explained more than 10% of the benthic net DIC production, which probably was regulated by several interacting factors.
4. Pelagic DIC production, and thus most of the whole-lake net production of DIC, was mainly due to the respiration of allochthonous organic carbon. Stable isotope data inferred that nearly 100% of accumulated DIC in the hypolimnion water had an allochthonous carbon source. Similarly, in the laboratory incubation using epilimnion water, c. 85% of accumulated DIC was indicated to have an allochthonous organic carbon source.     

On the distribution of developmental errors: comparing the normal, gamma, and log-normal distribution

The amount of between‐individual variation in the unobservable developmental instability (DI) has been the subject of intense recent debates. The unexpectedly high estimates of between‐individual variation in DI based on distributional characteristics of observable asymmetry values (of on average bilaterally symmetric traits) rely on statistical models that assume an underlying normal distribution of developmental errors. This prompted doubts on the assumption of the Gaussian nature of developmental errors. However, when applying other candidate distributions [log‐normal and gamma (γ)], recent analyses of empirical datasets have indicated that estimates remain generally high. Yet, all estimates were based on bilaterally symmetric traits, which did not allow for a formal comparison of the alternative distributions. In the present study, we extend a recent statistical model to allow statistical comparison of the different distributions based on traits that developed repeatedly under the same conditions, such as flower traits and regrown feathers. We analyse simulated and empirical data and show that: (1) it is statistically difficult to differentiate among the three alternatives when variances are small relative to the mean, as is often the case with DI; (2) the normal distribution fits the log‐normal or γ relatively well under those circumstances; (3) the deviance information criterion (DIC) is able to pick up differences in model fit among the three alternative distributions, yet more strongly so when levels of DI were high; (4) empirical datasets show a better fit of the normal over the log‐normal and γ‐distributions as judged by the DIC; and (5) estimates of between‐individual variation in DI in the three empirical datasets were relatively high (> 50%) under each distributional assumption. In conclusion, and based on our three datasets, the normal approximation appears to be a reasonable choice for statistical models of DI and the remarkably high estimates of variation in DI cannot be attributed to non‐normal developmental noise. Nevertheless, our method should be applied to a broad range of traits and organisms to evaluate the generality of this result. We argue that there is an urgent need for studies that reveal the underlying mechanisms of developmental noise and stability, as well as the role of developmental selection, in order to be able to determine the biological importance of the highly skewed distributions of developmental instability often observed. © 2007 The Linnean Society of London, Biological Journal of the Linnean Society, 2007, 92 , 197–210.