No abstract

Logging to "salvage" economic returns from forests affected by natural disturbances has become increasingly prevalent globally. Despite potential negative effects on biodiversity, salvage logging is often conducted, even in areas otherwise excluded from logging and reserved for nature conservation, inter alia because strategic priorities for post-disturbance management are widely lacking.A review of the existing literature revealed that most studies investigating the effects of salvage logging on biodiversity have been conducted less than 5 years following natural disturbances, and focused on non-saproxylic organisms.A meta-analysis across 24 species groups revealed that salvage logging significantly decreases numbers of species of eight taxonomic groups. Richness of dead wood dependent taxa (i.e. saproxylic organisms) decreased more strongly than richness of non-saproxylic taxa. In contrast, taxonomic groups typically associated with open habitats increased in the number of species after salvage logging.By analysing 134 original species abundance matrices, we demonstrate that salvage logging significantly alters community composition in 7 of 17 species groups, particularly affecting saproxylic assemblages. Our results suggest that salvage logging is not consistent with the management objectives of protected areas. Substantial changes, such as the retention of dead wood in naturally disturbed forests, are needed to support biodiversity. Future research should investigate the amount and spatio-temporal distribution of retained dead wood needed to maintain all components of biodiversity.

Following individual development by means of the 'sandwich method' the duration of egg, larval, and pupal stages, as well as of adult maturation feeding of the spruce bark beetle (Ips typographus) was measured at constant temperatures in the range between 12" and 33°C. At 20°C complete development from egg to adult emerging from pupa averaged 29 days. The proportion of the duration of larval development relative to total preimaginal development increased with temperature. Developmental rates, i.e. the speed of development increased linearly with temperature in a range between 15" and 25°C. Based on linear regressions, lower developmental thresholds were calculated to be 10.6"C (eggs), 8.2"C (larvae), 9.9"C (pupae), and 8.3"C (preimaginal development egg to pupa), respectively. Differing heat sums reported in the literature matched ours when recalculated with our developmental thresholds. A nonlinear model (Logan/Lactin) was fitted to the data which allowed to describe development in the entire temperature range. It further permits to identify lower and upper ( FZ 40°C) developmental thresholds as well as optimum temperatures (30-33°C) of the instars.

1. In several dry inner Alpine valleys higher mortality levels of pine have been observed in recent years. This paper evaluates the role of xylophagous insects in the current pine decline and the influence of climate change on the infestation dynamics.2. More than 200 trees of different levels of crown transparency (needle loss) were felled between 2001 and 2005 and sections of them incubated in insect emergence traps. Colonisation densities were related to the transparency level of each host tree at the time of attack.3. Trees with more than 80% needle loss were colonised most frequently, but the breeding density was highest in trees with 65–80% needle loss.4. The scolytine Ips acuminatus and the buprestid Phaenops cyanea colonised trees with 30–90% needle loss in high densities. The bark beetle Tomicus minor was less aggressive, preferring trees with 60–85% needle loss. The hymenopteran Sirex noctilio and the cerambycid Acanthocinus aedilis were restricted to greatly weakened trees with 50–85% needle loss. Most species colonised trees that had experienced a decline in vigour, that is an increase in crown transparency shortly before attack.5. The infestation dynamics of P. cyanea covaried with the drought index as well as with temperature.6. Increased temperatures not only trigger a drought stress rendering the host trees susceptible to insect attack, but also accelerate insect development. As more frequent drought periods are likely as a result of climate change, even trees only slightly or temporarily weakened will be more subject to attack by aggressive species such as I. acuminatus and P. cyanea.

Summary 1. The spruce bark beetle Ips typographus (L.) is one of the most important forest pests in Central Europe, but despite this the effects of temperature on life history and population growth are largely unknown. This study examines the effects of temperature on reproduction and intrinsic demographic statistics. 2. Laboratory experiments on oviposition were carried out at six temperatures in the range 12–33 °C, using the so‐called sandwich rearing technique for bark beetles. 3. A linear relationship between oviposition rates and temperatures in the range 15–25 °C was used to estimate the lower temperature threshold for oviposition as 11.4 °C. With a nonlinear model fitted to the data across the whole range of experimental temperatures, the lower and upper limiting temperatures and optimum temperature were found to be 7.9, 33.7, and 28.9 °C, respectively. A model for daily oviposition rate was fitted, which describes the pattern of oviposition over the entire oviposition period. 4. The analysis of life tables, combining developmental rates, reproduction, mortality, and sex ratio, suggests maximum population growth (rm) at near 30 °C. 5. After generating a first brood, spruce bark beetles often re‐emerge from the tree and produce other sister broods. The effects of temperature and number of sister broods on demography were evaluated using age‐specific life‐table analyses. It is hypothesized that sister broods play an important role in regions where I. typographus is monovoltine, but have only moderate significance where this species has more than one generation per season.