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Butterfly classification and species discovery using genomics.

Taxon Rep Int Lepid Surv

October 2023

Department of Biophysics, University of Texas Southwestern Medical Center, 5323 Harry Hines Blvd., Dallas, TX 75390-9050, USA.

Genomic sequencing of worldwide butterfly fauna followed by phylogenetic analysis of protein-coding genes informs butterfly classification throughout the taxonomic hierarchy, from families to species. As a rule, we attribute the same taxonomic rank to more prominent clades of comparable divergence (i.e.

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During macrofungal surveys in 2019-2024, several specimens belonging to the family Psathyrellaceae were collected from the bed of the Indus River, Punjab, Pakistan. Phylogenetic analyses, based on ITS, LSU, and tef-1α sequences and morpho-anatomical study, confirmed the novelty and placement of three taxa in the genus . They are described as , , and .

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Genomic analysis reveals new species and subspecies of butterflies.

Taxon Rep Int Lepid Surv

December 2023

Department of Biophysics, University of Texas Southwestern Medical Center, 5323 Harry Hines Blvd., Dallas, TX 75390-9050, USA.

Large-scale genomic sequencing of butterfly taxa reveals new findings that are presented here. While we focus on detecting species by comparative genomics and define subspecies as groups of populations genetically differentiated from each other but not as strongly as species (i.e.

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Descriptions of one hundred new species of Hesperiidae.

Insecta mundi

December 2023

Departments of Biophysics and Biochemistry, University of Texas Southwestern Medical Center, 5323 Harry Hines Blvd., Dallas, TX, 75390-9050 USA.

A century and a half since the time of Hewitson, we are experiencing a renaissance in species discovery fueled by whole genome sequencing. A large-scale genomic analysis of Hesperiidae Latreille, 1809 (Lepidoptera), including primary type specimens, reveals a deluge of species new to science. One hundred of them (one in a new genus) are described here from the New World (type localities are given in parenthesis): () Grishin, (Ecuador: Napo), Grishin, (Ecuador: Esmeraldas), Grishin, (Panama: Panama), () Grishin, (Ecuador: Zamora-Chinchipe), () Grishin, (Panama: Darien), () Grishin, (Ecuador: Napo), () Grishin, (Panama: Panama), () Grishin, (Ecuador: Pastaza), Grishin, (Panama: Colón), Grishin, (Ecuador: Napo), Grishin, (Ecuador: Esmeraldas), Grishin, (Guyana), Grishin, (Peru: Cuzco), Grishin, (Peru: Cuzco), Grishin, (Panama: Panama), Grishin, (Brazil: Mato Grosso), () Grishin, (Brazil: Rondônia), () Grishin, (Panama: Panama), () Grishin, (Ecuador: Napo), Grishin, (Brazil: Rondônia), Grishin, (Peru: Loreto), Grishin, (Suriname: Para), Grishin, (Brazil: Santa Catarina), Grishin, (Panama: Panama), Grishin, (Brazil: Santa Catarina), Grishin, (Ecuador: Orellana), Grishin, (Venezuela: Aragua), Grishin, (Guatemala), Grishin, (Guyana), () Grishin, (Panama: Darien), () Grishin, (Mexico: Guerrero.

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The effects of rhizosphere microorganisms on plant growth and the associated mechanisms are a focus of current research, but the effects of exogenous combined inoculation with arbuscular mycorrhizal fungi (AMF) and plant growth-promoting rhizobacteria (PGPR) on seedling growth and the associated rhizosphere microecological mechanisms have been little reported. In this study, a greenhouse pot experiment was used to study the effects of single or double inoculation with AM fungi () and two PGPR ( sp., sp.

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