scholarly journals The first record of Fistulina hepatica (Schaeff.) With. on Castanea sativa Mill. in Poland

2018 ◽  
Vol 53 (1) ◽  
Author(s):  
Jacek Piętka ◽  
Wojciech Ciurzycki

This paper discusses details of the locality of <em>Fistulina hepatica</em> recorded on <em>Castanea sativa</em>, a new host species in Poland. Since 2014, <em>F. hepatica</em> has been featured on the list of species under partial protection, and has been marked as “R” (rare species) on the “Red list of the macrofungi in Poland”. A new locality of <em>F. hepatica</em> has been found in Warsaw, in the Mokotów neighborhood, on the premises of the Central Clinical Hospital of Ministry of the Interior and Administration. Two basidiomata of <em>F. hepatica</em> were discovered at the base of a declining sweet chestnut tree.


Mycotaxon ◽  
2014 ◽  
Vol 127 (1) ◽  
pp. 185-190 ◽  
Author(s):  
Lu-Chao Bai ◽  
Zhi-Min Cao ◽  
Zhong-Dong Yu


2012 ◽  
Vol 2012 ◽  
pp. 1-3 ◽  
Author(s):  
Albena Lapeva-Gjonova ◽  
Kadri Kiran ◽  
Volkan Aksoy

The extreme inquiline antAnergates atratulus(Schenck, 1852) (Hymenoptera, Formicidae) was collected in ant nests ofTetramorium moravicumKratochvil, 1941 in Bulgaria and ofT. chefketiForel, 1911 in Bulgaria and Turkey. The reported ant hosts belong to theTetramorium chefketispecies complex in contrast with the typical hosts fromTetramorium caespitum/impurumcomplex. This finding confirms the assumption that a broader range of host species for the socially parasitic speciesA. atratulusmay be expected. Present data on the new host species expand knowledge about biology of this rare ant species, included in the IUCN Red List of threatened species.



2021 ◽  
Vol 126 (4) ◽  
pp. 509-512
Author(s):  
Pieter Kan ◽  
Mark R. Shaw ◽  
Brigitte Kan-van Linburg Stirum ◽  
Sylvie Warot ◽  
Géraldine Groussier

Telenomus kolbei is newly reported in France, parasitizing two new host species: Aglais io and Nymphalis antiopa. Oviposition by the parasitoid into eggs of both species was observed. Films were made, to which links are given. DNA sequences were obtained and deposited in Genbank.



Plants ◽  
2021 ◽  
Vol 10 (8) ◽  
pp. 1538
Author(s):  
Ana Teresa Alhinho ◽  
Miguel Jesus Nunes Ramos ◽  
Sofia Alves ◽  
Margarida Rocheta ◽  
Leonor Morais-Cecílio ◽  
...  

The sweet chestnut tree (Castanea sativa Mill.) is one of the most significant Mediterranean tree species, being an important natural resource for the wood and fruit industries. It is a monoecious species, presenting unisexual male catkins and bisexual catkins, with the latter having distinct male and female flowers. Despite the importance of the sweet chestnut tree, little is known regarding the molecular mechanisms involved in the determination of sexual organ identity. Thus, the study of how the different flowers of C. sativa develop is fundamental to understand the reproductive success of this species and the impact of flower phenology on its productivity. In this study, a C. sativa de novo transcriptome was assembled and the homologous genes to those of the ABCDE model for floral organ identity were identified. Expression analysis showed that the C. sativa B- and C-class genes are differentially expressed in the male flowers and female flowers. Yeast two-hybrid analysis also suggested that changes in the canonical ABCDE protein–protein interactions may underlie the mechanisms necessary to the development of separate male and female flowers, as reported for the monoecious Fagaceae Quercus suber. The results here depicted constitute a step towards the understanding of the molecular mechanisms involved in unisexual flower development in C. sativa, also suggesting that the ABCDE model for flower organ identity may be molecularly conserved in the predominantly monoecious Fagaceae family.



2021 ◽  
Author(s):  
Erin K. Zess ◽  
Yasin F. Dagdas ◽  
Esme Peers ◽  
Abbas Maqbool ◽  
Mark J. Banfield ◽  
...  

AbstractIn order to infect a new host species, the pathogen must evolve to enhance infection and transmission in the novel environment. Although we often think of evolution as a process of accumulation, it is also a process of loss. Here, we document an example of regressive evolution in the Irish potato famine pathogen (Phytophthora infestans) lineage, providing evidence that a key sequence motif in the effector PexRD54 has degenerated following a host jump. We began by looking at PexRD54 and PexRD54-like sequences from across Phytophthora species. We found that PexRD54 emerged in the common ancestor of Phytophthora clade 1b and 1c species, and further sequence analysis showed that a key functional motif, the C-terminal ATG8-interacting motif (AIM), was also acquired at this point in the lineage. A closer analysis showed that the P. mirabilis PexRD54 (PmPexRD54) AIM appeared unusual, the otherwise-conserved central residue mutated from a glutamate to a lysine. We aimed to determine whether this PmPexRD54 AIM polymorphism represented an adaptation to the Mirabilis jalapa host environment. We began by characterizing the M. jalapa ATG8 family, finding that they have a unique evolutionary history compared to previously characterized ATG8s. Then, using co-immunoprecipitation and isothermal titration calorimetry assays, we showed that both full-length PmPexRD54 and the PmPexRD54 AIM peptide bind very weakly to the M. jalapa ATG8s. Through a combination of binding assays and structural modelling, we showed that the identity of the residue at the position of the PmPexRD54 AIM polymorphism can underpin high-affinity binding to plant ATG8s. Finally, we conclude that the functionality of the PexRD54 AIM was lost in the P. mirabilis lineage, perhaps owing to as-yet-unknown pressure on this effector in the new host environment.Author SummaryPathogens evolve in concert with their hosts. When a pathogen begins to infect a new host species, known as a “host jump,” the pathogen must evolve to enhance infection and transmission. These evolutionary processes can involve both the gain and loss of genes, as well as dynamic changes in protein function. Here, we describe an example of a pathogen protein that lost a key functional domain following a host jump, a salient example of “regressive evolution.” Specifically, we show that an effector protein from the plant pathogen Phytopthora mirabilis, a host-specific lineage closely related to the Irish potato famine pathogen Phytopthora infestans, has a derived amino acid polymorphism that results in a loss of interaction with certain host machinery.



2015 ◽  
Vol 2015 ◽  
pp. 1-4
Author(s):  
Julia Giehr ◽  
Jürgen Heinze ◽  
Alexandra Schrempf

Data on host species and the distribution of the endoparasitic fungusMyrmicinosporidium durumincreased continuously in recent decades. Here, we add the antCardiocondyla elegansas new host species. Colonies of the monogynous species were found infested in the region of Languedoc-Roussillon (South France). Samples from the nest indicate high infection rates. All castes and sexes were infected by the spores. Variations of infection rates between sampling methods and species are discussed.



2020 ◽  
Vol 10 (20) ◽  
pp. 11192-11216
Author(s):  
Paola Pollegioni ◽  
Stefano Del Lungo ◽  
Ruth Müller ◽  
Keith E. Woeste ◽  
Francesca Chiocchini ◽  
...  


2016 ◽  
Vol 11 (3) ◽  
pp. 1934578X1601100 ◽  
Author(s):  
Margherita Campo ◽  
Patrizia Pinelli ◽  
Annalisa Romani

Sweet Chestnut ( Castanea sativa Mill.) wood extracts, rich in Hydrolyzable Tannins (HTs), are traditionally used in the tanning and textile industries, but recent studies suggest additional uses. The aim of this work is the HPLC-DAD-ESI-MS characterization of Sweet Chestnut aqueous extracts and fractions obtained through a membrane separation technology system without using other solvents, and the evaluation of their antioxidant and antiradical activities. Total tannins range between 2.7 and 138.4 mM; gallic acid ranges between 6% and 100%; castalagin and vescalagin range between 0% and 40%. Gallic Acid Equivalents, measured with the Folin-Ciocalteu test, range between 0.067 and 56.99g/100g extract weight; ORAC test results for the marketed fractions are 450.4 and 3050 μmol/g Trolox Equivalents/extract weight. EC50 values, measured with the DPPH test, range between 0.444 and 2.399 μM. These results suggest a new ecofriendly and economically sustainable method for obtaining chestnut fractions with differentiated, stable and reproducible chemical compositions. Such fractions can be marketed for innovative uses in several sectors.



Zootaxa ◽  
2018 ◽  
Vol 4479 (1) ◽  
pp. 1 ◽  
Author(s):  
CHARLES S. EISEMAN ◽  
OWEN LONSDALE

We present rearing records of Agromyzidae (Diptera) from five years of collecting throughout the United States. We review host and distribution data, and describe leaf mines, for 93 species, plus 28 others that could not be confidently identified in the absence of male specimens. We report 147 new host species records, including the first rearing records for Agromyza bispinata Spencer, A. diversa Johnson, A. parca Spencer, A. pudica Spencer, A. vockerothi Spencer, Calycomyza michiganensis Steyskal, Ophiomyia congregata (Malloch), and Phytomyza aldrichi Spencer. Phytomyza anemones Hering and (tentatively identified) Cerodontha (Dizygomyza) iraeos (Robineau-Desvoidy) are new to North America; Agromyza albitarsis Meigen, Amauromyza shepherdiae Sehgal, Aulagromyza populicola (Walker), Liriomyza orilliensis Spencer, Phytomyza linnaeae (Griffiths), P. solidaginivora Spencer, and P. solidaginophaga Sehgal are new to the USA. We also present confirmed USA records for Calycomyza menthae Spencer (previous records were based only on leaf mines), Ophiomyia maura (Meigen) (reported from the USA in older literature but deleted from the fauna in the most recent revision (Spencer & Steyskal 1986)), and Phytomyza astotinensis Griffiths and P. thalictrivora Spencer (previously only tentatively recorded from the USA). We provide 111 additional new state records. We describe the following 30 new species: Agromyza fission, A. soka, Melanagromyza palmeri, Ophiomyia euthamiae, O. mimuli, O. parda, Calycomyza artemisivora, C. avira, C. eupatoriphaga, C. vogelmanni, Cerodontha (Dizygomyza) edithae, Cer. (D.) feldmani, Liriomyza ivorcutleri, L. valerianivora, Phytomyza actaeivora, P. aesculi, P. confusa, P. doellingeriae, P. erigeronis, P. hatfieldae, P. hydrophyllivora, P. palmeri, P. palustris, P. sempervirentis, P. tarnwoodensis, P. tigris, P. triangularidis, P. vancouveriella, P. verbenae, and P. ziziae. 



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