Nineteen lichens new to sub-Antarctic Heard Island are recorded. Three species are described as new: Gyalideopsis heardense Øvstedal, Mycobilimbia subbyssoidea Øvstedal and Psoroma absconditum Øvstedal. Altogether the total number of lichen species recorded on the island is now 90.

The importance of organic chemistry in the classification of lichens is well established, but inorganic chemistry has been largely overlooked. Six lichen species were studied over a period of 23 years that were growing in 11 protected areas of the northern Great Lakes ecoregion, which were not greatly influenced by anthropogenic particulates or gaseous air pollutants. The elemental data from these studies were aggregated in order to test the hypothesis that differences among species in tissue element concentrations were large enough to discriminate between taxa faithfully. Concentrations of 16 chemical elements that were found in tissue samples from Cladonia rangiferina, Evernia mesomorpha, Flavopunctelia flaventior, Hypogymnia physodes, Parmelia sulcata, and Punctelia rudecta were analyzed statistically using multivariate discriminant functions and CART analyses, as well as t-tests. Genera and species were clearly separated in element space, and elemental discriminant functions were able to classify 91–100 of the samples correctly into species. At the broadest level, a Zn concentration of 51 ppm in tissues of four of the lichen species effectively discriminated foliose from fruticose species. Similarly, a S concentration of 680 ppm discriminated C. rangiferina and E. mesomorpha, and a Ca concentration of 10 436 ppm discriminated H. physodes from P. sulcata. For the three parmelioid species, a Ca concentration >32 837 ppm discriminated Punctelia rudecta from the other two species, while a Zn concentration of 56 ppm discriminated Parmelia sulcata from F. flaventior. Foliose species also had higher concentrations than did fruticose species of all elements except Na. Elemental signatures for each of the six species were developed using standardized means. Twenty-four mechanisms explaining the differences among species are summarized. Finally, the relationships of four species based on element concentrations, using additive-trees clustering of a Euclidean-distance matrix, produced identical relationships as did analyses based on secondary product chemistry that used additive-trees clustering of a Jaccard similarity matrix. At least for these six species, element composition has taxonomic significance, and may be useful for discriminating other taxa.

Six new species of foliicolous lichenized fungi are described as new to science from Bolivian lowland Amazon forest: Asterothyrium vezdae Flakus & Lücking (Asterothyriaceae), Keratosphaera multiseptata Flakus & Lücking (Pseudoperisporiaceae), Phylloblastia bielczykiae Flakus & Lücking (Verrucariaceae), Porina boliviana Flakus & Lücking (Porinaceae), Tapellaria intermedia Flakus & Lücking (Pilocarpaceae) and Trichothelium subargenteum Flakus & Lücking (Porinaceae). In addition, new records of 70 lichen species in Bolivia are listed. Of these, 52 are new to Bolivia.

The distribution of different ecological groups of lichens (acidophytes, ‘nitrophytes’, indifferent species) was compared on 1–24 year-old twigs of Abies sibirica sampled in the ‘pristine’ West Sayan and the polluted East Sayan Mountains (Krasnoyarsk District, South Siberia, Russia) to test their value as indicators of current pollution effects. Bark pH of twigs and bark chemistry (N, S, Ca, Mg, Al, Fe) were measured, and a preliminary estimate of emissions in the Krasnoyarsk District from livestock animal populations was calculated. In both regions, an unusually high twig bark pH and an abnormal species composition for A. sibirica canopy were found (e.g. Physcia aipolia, P. dubia, P. tenella, Phaeophyscia sp., Melanelia exasperatula and Candelariella vitellina), with P. tenella (East Sayan) and M. exasperatula (West Sayan) as dominants. The results confirm that the distribution of lichen species on Abies sibirica twigs is a valuable indicator of current changes in atmospheric conditions.

In the European Alps, subalpine forests are important for lichen diversity conservation at multiple levels. However, the potential role of coarse woody debris (CWD) has been only marginally considered in the previous literature. The aims of this case study are (i) to provide a first evaluation of the effects of different types of CWD (stumps, logs, and snags) and wood decay on lichen diversity in Pinus-Larix forests in the Italian Alps, and (ii) to increase the knowledge of the lichen biota on CWD in Italy. Seventy-eight species were found, including 12 nationally rare and 10 calicioid species; Placynthiella hyporhoda is new to Italy. Different types of CWD in different decay stages had significantly different lichen communities. Snags seem to be particularly effective for conservation, since they host the highest number of nationally rare species. Our survey suggests that CWD could be an important substratum for several nationally rare species, indicating that further surveys at a regional scale are urgently required in order to evaluate the role of CWD for lichen diversity conservation in the Alps.

The study aimed to determine how the response of the epiphytic lichen vegetation to sulphur air pollution is affected by interaction with other factors (distance from pollution sources, habitat, altitude, initial eutrophication of the tree bark). It was based on a series of four successive recordings taken over a period of 18 years with increasing pollution levels and on the same set of 139 solitary trees. Relationships between habitat variables and lichen community composition are assessed using canonical correspondence analysis. The data set comprised 69 lichen species. Ordination of initial species composition on trees revealed two major gradients: eutrophication and acidity.

The species composition significantly changed with time, with a general decrease of the total number of lichen species per tree. In general, species sensitive to air pollution decreased, while tolerant species increased in number. Change over time differed depending on the position of the tree within the landscape (relative to one major source of pollution, the town of Tábor, whereas the distance to the other source, Sezimovo Ústí, was not significant) and on the initial species composition found on the tree. Trees under the effect of eutrophication changed their species composition less, indicating that the effect of eutrophication (mainly increased bark pH) may ameliorate the effects of air pollution; a local effect of eutrophication also seems to play an important role. Distance to pollution sources had only a small impact on the rate of change and perhaps other local conditions (sheltered or humid position, altitude) play a role in this interaction. There was a decrease of the overall heterogeneity of the data set over time. This means that the gradients in species composition attributable to these variables became less important over time. Therefore, one of the effects of air pollution is also a general homogenization of the lichen vegetation of the solitary trees.

Alectorioid and foliose lichens were weighed from full-size branches of Picea abies cut at two canopy heights in 100 trees in an old subalpine forested area in eastern Norway. The mean lichen biomass per branch decreased from 46 to 37 g moving upwards from 2–3 to 5–6 m canopy height. The lichen biomass correlated strongly with branch size variables, branch diameter alone explaining 48 of the variation in lichen biomass per branch (n=200). The alectorioid/foliose biomass ratio increased from 0·149 at 2–3 m to 0·316 at 5–6 m. Site factors reflecting openness of the canopy were computed for the branch at 2–3 m in all trees. The alectorioid/foliose biomass ratio increased significantly with the indirect site factors, suggesting that light, or factors associated with light, determine the balance between these two growth forms in tree canopies. Within the alectorioid biomass component, genera with usnic acid (Alectoria, Usnea) decreased with height, whereas the genus Bryoria with melanic pigments increased. According to the literature, dark melanic pigments have higher visible light screening efficiency than the yellowish usnic acid. Such patterns suggest a functional role for cortical pigments in the niche differentiation of alectorioid lichens.

Ambient CO2 concentration (together with CO2 exchange and microclimate) was recorded every 30 min for 15 months for Lecanora muralis growing in the Botanical Garden Würzburg (Germany, northern Bavaria), a habitat on the outskirts of the city. Annual mean CO2 was around 17 ppm higher than the global average reported for the time of measurement (361 ppm; 1995/96), and daily values ranged from 317 to 490 ppm. Diel courses of CO2 could be classified into three different types. Type A, when CO2 levels rose overnight and then fell strongly to below global levels during the day, which predominated in the summer (about 75 of days); Type B, irregular diel courses occurred during all seasons with often very rapid changes apparently due to advective CO2 transport; Type C, CO2 concentration was typically almost stable at generally between c. 330 and 430 ppm which predominated in the winter (63 of days).

Under controlled conditions, CO2 saturation of net photosynthesis (NP) of L. muralis at optimal hydration and light occurred at around 1000 ppm. NP was also affected by low CO2 at limiting light and thallus water contents. Based upon these data, we estimated the improvement of NP of L. muralis due to transient increase of ambient CO2 (as compared with the global average) for one selected combination of environmental factors (nocturnal dew or frost). This combination is an important source of water for the lichen, resulting in 40 of its annual production and, especially in these situations, photosynthesis was increased by high ambient CO2 in the early morning under prevailing Type A conditions. After dew activation, light compensation point of NP occurred at an average concentration of 413 ppm and diel maxima of NP at 402 ppm. This allows a rough estimate that the transiently elevated CO2 increased the photosynthetic gain of the lichen after dew of 7, or an improvement to its annual carbon balance of about 3. Conditions, especially interrelationships between lichen hydration, light and CO2 are so complex that we are not yet able to extend our estimates to other environmental situations of photosynthetic activity of L. muralis.

Mongolia is one of the least densely populated countries of the world with 2·6 million people occupying an area of 1·5 million km2. A high proportion of the population and economy is concentrated in the capital Ulan Bator, which has 1 million inhabitants. Ulan Bator is characterized by its high elevation (1350 m), low precipitation (300 mm), high annual sunshine duration, and its location in a basin. The city is surrounded by mountain ranges to the north and to the south. Furthermore, it is the coldest capital of the world with an annual mean temperature of −3·7°C (Hilbig et al. 2004). Outside Ulan Bator and a few industrial areas, including a large copper plant near the second-largest city Erdenet, Mongolia’s air is extremely pure (ADB 2006). Therefore, Mongolia’s forests, which cover 10% of the country (Erdenechuluun 2006) harbour a rich epiphytic lichen vegetation (Cogt 1995). Most of these woodlands are conifer stands that form the southernmost range of the continuous Siberian taiga forests (Gunin et al. 1999). Eighty percent of the forest area of Mongolia is covered by Larix sibirica (Savin et al. 1978), while other important tree species in the taiga include Pinus sibirica, P. sylvestris, Picea obovata, Abies sibirica, and Betula platyphylla (Hilbig 1995; Dulamsuren et al. 2005). Dominant epiphytic lichen species in the larch-dominated taiga include Bryoria fuscescens, B. nadvornikiana, Evernia mesomorpha, Flavopunctelia soredica, Hypogymnia bitteri, H. physodes, Lecanora symmicta, Melanohalea septentrionalis, Parmelia sulcata, Usnea sp., and Vulpicida pinastri (Biazrov 1974; Hauck et al. 2007).