This article is the 14th in the Fungal Diversity Notes series, wherein we report 98 taxa distributed in two phyla, seven classes, 26 orders and 50 families which are described and illustrated. Taxa in this study were collected from Australia, Brazil, Burkina Faso, Chile, China, Cyprus, Egypt, France, French Guiana, India, Indonesia, Italy, Laos, Mexico, Russia, Sri Lanka, Thailand, and Vietnam. There are 59 new taxa, 39 new hosts and new geographical distributions with one new combination. The 59 new species comprise Angustimassarina kunmingense , Asterina lopi , Asterina brigadeirensis , Bartalinia bidenticola , Bartalinia caryotae , Buellia pruinocalcarea , Coltricia insularis , Colletotrichum flexuosum , Colletotrichum thasutense , Coniochaeta caraganae , Coniothyrium yuccicola , Dematipyriforma aquatic , Dematipyriforma globispora , Dematipyriforma nilotica , Distoseptispora bambusicola , Fulvifomes jawadhuvensis , Fulvifomes malaiyanurensis , Fulvifomes thiruvannamalaiensis , Fusarium purpurea , Gerronema atrovirens , Gerronema flavum , Gerronema keralense , Gerronema kuruvense , Grammothele taiwanensis , Hongkongmyces changchunensis , Hypoxylon inaequale , Kirschsteiniothelia acutisporum , Kirschsteiniothelia crustaceum , Kirschsteiniothelia extensum , Kirschsteiniothelia septemseptatum , Kirschsteiniothelia spatiosum , Lecanora immersocalcarea , Lepiota subthailandica , Lindgomyces guizhouensis , Marthe asmius pallidoaurantiacus , Marasmius tangerinus , Neovaginatispora mangiferae , Pararamichloridium aquisubtropicum , Pestalotiopsis piraubensis , Phacidium chinaum , Phaeoisaria goiasensis , Phaeoseptum thailandicum , Pleurothecium aquisubtropicum , Pseudocercospora vernoniae , Pyrenophora verruculosa , Rhachomyces cruralis , Rhachomyces hyperommae , Rhachomyces magrinii , Rhachomyces platyprosophi , Rhizomarasmius cunninghamietorum , Skeletocutis cangshanensis , Skeletocutis subchrysella , Sporisorium anadelphiae-leptocomae , Tetraploa dashaoensis , Tomentella exiguelata , Tomentella fuscoaraneosa , Tricholomopsis lechatii , Vaginatispora flavispora and Wetmoreana blastidiocalcarea . The new combination is Torula sundara . The 39 new records on hosts and geographical distribution comprise Apiospora guiyangensis , Aplosporella artocarpi , Ascochyta medicaginicola , Astrocystis bambusicola , Athelia rolfsii , Bambusicola bambusae , Bipolaris luttrellii , Botryosphaeria dothidea , Chlorophyllum squamulosum , Colletotrichum aeschynomenes , Colletotrichum pandanicola , Coprinopsis cinerea , Corylicola italica , Curvularia alcornii , Curvularia senegalensis , Diaporthe foeniculina , Diaporthe longicolla , Diaporthe phaseolorum , Diatrypella quercina , Fusarium brachygibbosum , Helicoma aquaticum , Lepiota metulispora , Lepiota pongduadensis , Lepiota subvenenata , Melanconiella meridionalis , Monotosporella erecta , Nodulosphaeria digitalis , Palmiascoma gregariascomum , Periconia byssoides , Periconia cortaderiae , Pleopunctum ellipsoideum , Psilocybe keralensis , Scedosporium apiospermum , Scedosporium dehoogii , Scedosporium marina , Spegazzinia deightonii , Torula fici , Wiesneriomyces laurinus and Xylaria venosula . All these taxa are supported by morphological and multigene phylogenetic analyses. This article allows the researchers to publish fungal collections which are important for future studies. An updated, accurate and timely report of fungus-host and fungus-geography is important. We also provide an updated list of fungal taxa published in the previous fungal diversity notes. In this list, erroneous taxa and synonyms are marked and corrected accordingly.

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Background and aims The amount of DNA in an unreplicated gametic chromosome complement is known as the C-value and is a key biodiversity character of fundamental significance with many practical and predictive uses. Since 1976, Bennett and colleagues have assembled eight compilations of angiosperm C-values for reference purposes and subsequently these have been pooled into the Angiosperm DNA C-values Database (http://data.kew.org/cvalues/). Since the last compilation was published in 2005, a large amount of data on angiosperm genome size has been published. It is therefore timely to bring these data together into a ninth compilation of DNA amounts. Scope The present work lists DNA C-values for 2221 species from 151 original sources (including first values for 1860 species not listed in previous compilations). Combining these data with those published previously shows that C-values are now available for 6287 angiosperm species. Key findings Analysis of the dataset, which is by far the largest of the nine compilations published since 1976, shows that angiosperm C-values are now being generated at the highest rate since the first genome sizes were estimated in the 1950s. The compilation includes new record holders for the smallest (1C = 0·0648 pg in Genlisea margaretae) and largest (1C = 152·23 pg in Paris japonica) genome sizes so far reported, extending the range encountered in angiosperms to nearly 2400-fold. A review of progress in meeting targets set at the Plant Genome Size meetings shows that although representation for genera, geographical regions and some plant life forms (e.g. island floras and parasitic plants) has improved, progress to increase familial representation is still slow. In terms of technique it is now clear that flow cytometry is soon likely to become the only method available for plant genome size estimations. Fortunately, this has been accompanied by numerous careful studies to improve the quality of data generated using this technique (e.g. design of new buffers, increased awareness and understanding of problems caused by cytosolic inhibitors). It is also clear that although the speed of DNA sequencing continues to rise dramatically with the advent of next-generation and third-generation sequencing technologies, 'complete genome sequencing' projects are still unable to generate accurate plant genome size estimates.

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Spatial patterns of genetic variation provide information central to many ecological, evolutionary, and conservation questions. This spatial variability has traditionally been analyzed through summary statistics between pairs of populations, therefore missing the simultaneous influence of all populations. More recently, a network approach has been advocated to overcome these limitations. This network approach has been applied to a few cases limited to a single species at a time. The question remains whether similar patterns of spatial genetic variation and similar functional roles for specific patches are obtained for different species. Here we study the networks of genetic variation of four Mediterranean woody plant species inhabiting the same habitat patches in a highly fragmented forest mosaic in Southern Spain. Three of the four species show a similar pattern of genetic variation with well-defined modules or groups of patches holding genetically similar populations. These modules can be thought of as the long-sought-after, evolutionarily significant units or management units. The importance of each patch for the cohesion of the entire network, though, is quite different across species. This variation creates a tremendous challenge for the prioritization of patches to conserve the genetic variation of multispecies assemblages.

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Background Adaptive radiation in Mediterranean plants is poorly understood. The white-flowered Cistus lineage consists of 12 species primarily distributed in Mediterranean habitats and is herein subject to analysis. Methodology/principal findings We conducted a "total evidence" analysis combining nuclear (ncpGS, ITS) and plastid (trnL-trnF, trnK-matK, trnS-trnG, rbcL) DNA sequences and using MP and BI to test the hypothesis of radiation as suggested by previous phylogenetic results. One of the five well-supported lineages of the Cistus-Halimium complex, the white-flowered Cistus lineage, comprises the higher number of species (12) and is monophyletic. Molecular dating estimates a Mid Pleistocene (1.04+/-0.25 Ma) diversification of the white-flowered lineage into two groups (C. clusii and C. salviifolius lineages), which display asymmetric characteristics: number of species (2 vs. 10), leaf morphologies (linear vs. linear to ovate), floral characteristics (small, three-sepalled vs. small to large, three- or five-sepalled flowers) and ecological attributes (low-land vs. low-land to mountain environments). A positive phenotype-environment correlation has been detected by historical reconstructions of morphological traits (leaf shape, leaf labdanum content and leaf pubescence). Ecological evidence indicates that modifications of leaf shape and size, coupled with differences in labdanum secretion and pubescence density, appear to be related to success of new species in different Mediterranean habitats. Conclusions/significance The observation that radiation in the Cistus salviifolius lineage has been accompanied by the emergence of divergent leaf traits (such as shape, pubescence and labdanum secretion) in different environments suggets that radiation in the group has been adaptive. Here we argued that the diverse ecological conditions of Mediterranean habitats played a key role in directing the evolution of alternative leaf strategies in this plant group. Key innovation of morphological characteristics is supported by our dated phylogeny, in which a Mediterranean climate establishment (2.8 Ma) predated the adaptive radiation of the white-flowered Cistus.

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Doñana National Park (DNP) in southern Spain is a UNESCO Biosphere Reserve where commercial hunting and wildlife artificial feeding do not take place and traditional cattle husbandry still exists. Herein, we hypothesized that Mycobacterium bovis infection prevalence in wild ungulates will depend on host ecology and that variation in prevalence will reflect variation in the interaction between hosts and environmental risk factors. Cattle bTB reactor rates increased in DNP despite compulsory testing and culling of infected animals. In this study, 124 European wild boar, 95 red deer, and 97 fallow deer were sampled from April 2006 to April 2007 and analyzed for M. bovis infection. Modelling and GIS were used to identify risk factors and intra and inter-species relationships. Infection with M. bovis was confirmed in 65 (52.4%) wild boar, 26 (27.4%) red deer and 18 (18.5%) fallow deer. In the absence of cattle, wild boar M. bovis prevalence reached 92.3% in the northern third of DNP. Wild boar showed more than twice prevalence than that in deer (p<0.001). Modelling revealed that M. bovis prevalence decreased from North to South in wild boar (p<0.001) and red deer (p<0.01), whereas no spatial pattern was evidenced for fallow deer. Infection risk in wild boar was dependent on wild boar M. bovis prevalence in the buffer area containing interacting individuals (p<0.01). The prevalence recorded in this study is among the highest reported in wildlife. Remarkably, this high prevalence occurs in the absence of wildlife artificial feeding, suggesting that a feeding ban alone would have a limited effect on wildlife M. bovis prevalence. In DNP, M. bovis transmission may occur predominantly at the intra-species level due to ecological, behavioural and epidemiological factors. The results of this study allow inferring conclusions on epidemiological bTB risk factors in Mediterranean habitats that are not managed for hunting purposes. Our results support the need to consider wildlife species for the control of bTB in cattle and strongly suggest that bTB may affect animal welfare and conservation.

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