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FIGURE 4 in Effects Of Host Plants On Distribution, Abundance, Developmental Time And Life Table Parameters Of Oligonychus Afrasiaticus (Mcgregor) (Acari: Tetranychidae)

FIGURE 4: Population dynamics of O. afrasiaticus at 27°C on different supports collected at Segdoud oasis, South of Tunisia.

FIGURE 3 in Effects Of Host Plants On Distribution, Abundance, Developmental Time And Life Table Parameters Of Oligonychus Afrasiaticus (Mcgregor) (Acari: Tetranychidae)

FIGURE 3: Survivorship curve (lX) and age-specific fecundity (mx) of O. afrasiaticus on six alimentary supports at 27°C.

FIGURE 1 in Effects Of Host Plants On Distribution, Abundance, Developmental Time And Life Table Parameters Of Oligonychus Afrasiaticus (Mcgregor) (Acari: Tetranychidae)

FIGURE 1: Seasonal fluctuations of O. afrasiaticus densities on Deglet Noor pinnae and fruits and on sorghum leave, at Segdoud, South of Tunisia in 2004-2006.

FIGURE 2 in Effects Of Host Plants On Distribution, Abundance, Developmental Time And Life Table Parameters Of Oligonychus Afrasiaticus (Mcgregor) (Acari: Tetranychidae)

FIGURE 2: Densities of O. afrasiaticus motile stages, at Segdoud, South of Tunisia, (A) 2006 (B) 2007, on date varieties 'Deglet Noor', 'Alig', 'Bessr', and 'Kentichi'.

opennotspecifiedJun 2020View details →

Fig. 9 in How whale and dolphin barnacles attach to their hosts and the paradox of remarkably versatile attachment structures in cypris larvae

Fig. 9 Comparative cyprid morphology between Xenobalanus globicipitis and four of the species used in this study. a, b Xenobalanus globicipitis. c, d Amphibalanus amphitrite. e, f Trevathana jensi. g, h Lepas pectinata. i, j Scalpellum scalpellum. Compared with C. paguri (Fig. 8). Terminology is explained in supplementary table 1. Roman

opencc-by-4.0Apr 2024View details →

Alignment of ITS sequences of Erysiphe specimens from Koelreuteria hosts, with Golovinomyces spp. as outgroup. The scientific names are followed by the respective GenBank accession number.

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opennotspecifiedMar 2015View details →

Figure 1 in Interaction between Tephritidae (Insecta, Diptera) and plants of the family Asteraceae: new host and distribution records for the state of Rio Grande do Sul, Brazil

Figure 1. Localities in Rio Grande do Sul, Brazil, where the fauna of Tephritidae (Dip* tera) from capitula of Asteraceae was sampled.

opencc-by-4.0Aug 2024View details →

Datasets - Unveiling Host-Parasite Relationships through Conserved MITEs in Prokaryote and Viral Genomes

Title: Unveiling Host-Parasite Relationships through Conserved MITEs in Prokaryote and Viral Genomes   Authors: Francisco Nadal-Molero(1), Riccardo Roselli(1), Silvia Garcia-Juan(1), Alicia Campos-Lopez(1), Ana-Belen Martin-Cuadrado(1*)   SUPPLEMENTARY FILES   Supplementary File S1. Sequences of cMITEs detected in Bacteria genomes (fasta format). The hosting microbial species and inferred NCBI-taxonomy are indicated in the name of each sequence. The structure of the MITE name is: “Accession|Genome|start|end|TSD|TIRlength|MITETracker_group|Lineage”. Supplementary File S2. Sequences of cMITEs detected in the Archaea genomes (fasta format). The hosting microbial species and inferred NCBI-taxonomy are indicated in the name of each sequence. The structure of the MITE name is: “Accession|Genome|start|end|TSD|TIRlength|MITETracker_group|Lineage”. Supplementary File S3. Sequences of vMITEs detected in the virus sequences from the NCBI and IMG/VR v.4.1 database (fasta format). Virus, microbial host (if known) and inferred NCBI-taxonomy is stated in the name of each sequence. The structure of the MITE name is: “Accession|Genome|start|end|TSD|TIRlength|MITETracker_group|Virus|Name|Host”. Supplementary File S4. Sequences of si-vMITEs detected in the virus sequences from the NCBI and IMG/VR v.4.1 database (fasta format). Virus, microbial host (if known) and inferred NCBI-taxonomy are stated in the name of each sequence. The structure of the MITE name is: “Accession|Genome|start|end|Ident.Method.by.DB|Host”. Supplementary Files S5. Cytoscape networks. (A) Figure 1A, (B) Figure 1B. Supplementary File S6. Sequences of cMITEs obtained from 5837 genomes of Neisseriales. The structure of the MITE name is: “Accession|NucleotideID|start|end|TSD|TIRlength|MITETracker_group|Genome|Lineage”. Supplementary File S7. Sequences of si-vMITEs obtained from 5837 genomes of Neisseriales. The structure of the MITE name is: “Accession|Genome|start|end|Host”. Supplementary File S8. Sequences of cMITEs obtained from 46051 genomes of Bacteroidota. The structure of the MITE name is: “Accession|NucleotideID|start|end|TSD|TIRlength|MITETracker_group|Genome|Lineage”. Supplementary File S9. Sequences of si-vMITEs obtained from 46051 genomes of Bacteroidota. The structure of the MITE name is: “Accession|Genome|start|end|Host”.

opennotspecifiedJan 2017View details →

FIGURE 3. Host and habitat. A in Phelipanche sevanensis (Orobanchaceae): a new species from the Caucasus, and nomenclatural notes on similar species

FIGURE 3. Host and habitat. A. Heracleum trachyloma – general habit of flowering host. B. Habitat with the dominant host species. C, D, E. Host with attached Phelipanche sevanensis. Photos by Renata Piwowarczyk.

opennotspecifiedApr 2018View details →

FIGURE 1 in Studies of botryosphaerialean fungi associated with canker and dieback of tree hosts in Dongling Mountain of China

FIGURE 1. Phylogram of Botryosphaeriales based on combined ITS, LSU, and TEF-1α genes. MP and ML bootstrap support values above 50 % are shown at the first and second position respectively. Thickened branches represent posterior probabilities above 0.95 from BI. Type species are in bold. Strains in the current study are in blue.

opennotspecifiedApr 2018View details →

FIGURE 2 in Studies of botryosphaerialean fungi associated with canker and dieback of tree hosts in Dongling Mountain of China

FIGURE 2. Morphology of Phaeobotryon rhoinum from Rhus typhina (CF 201782). A: Symptoms on the host. B, C: Habit of pycnidia on a twig. D: Transverse section of pycnidia. E: Longitudinal section through pycnidia. F–H: Conidiogenous cells and conidia. I: immature conidia. J–K: mature conidia. Scale bars: B = 1 mm; C–E = 500 μm; F–K = 10 μm.

opennotspecifiedJul 2018View details →

FIGURE 2. Orobanche arpica. A. General habit. B. Flower. C. Inflorescence. D. Habitat with host species Psephellus pulcherrimus. E in Orobanche arpica (Orobanchaceae): a new species from the Caucasus, and contributional notes on O. ser. Krylowianae

FIGURE 2. Orobanche arpica. A. General habit. B. Flower. C. Inflorescence. D. Habitat with host species Psephellus pulcherrimus. E. Flower of host species. Photos by Renata Piwowarczyk.

opennotspecifiedJul 2018View details →

FIGURE 3. Habitat and host. A in Orobanche javakhetica (Orobanchaceae): a new species from the Caucasus (Armenia)

FIGURE 3. Habitat and host. A. Habitat with the dominant host species of Lomelosia caucasica. B. Flower of host species. Photos by Renata Piwowarczyk.

FIGURE 1 in Redetermination of host plants reveals that the rust fungi Aecidium annonae, Aecidium chrysophaeum and Cerotelium xylopiae occur on Diospyros species (Ebenaceae) instead of Annonaceae

FIGURE 1. Micromorphological characteristics distinguishing Ebenaceae and Annonaceae: a. Diospyros sericea, surface of trichome tip covered with elongated spindle shaped warts; b. Annona holosericea Saff., section through leaf showing two globular secretory cells.

FIGURE 2 in Redetermination of host plants reveals that the rust fungi Aecidium annonae, Aecidium chrysophaeum and Cerotelium xylopiae occur on Diospyros species (Ebenaceae) instead of Annonaceae

FIGURE 2. Aecidium annonae: a. Infected leaves of Diospyros hispida (holotype). b–d. Aecia: b. peridial cells in longitudinal section (inner side on the left); c. inner side of peridial cells in face view; d. aeciospores in face view and optical sections.

FIGURE 3 in Redetermination of host plants reveals that the rust fungi Aecidium annonae, Aecidium chrysophaeum and Cerotelium xylopiae occur on Diospyros species (Ebenaceae) instead of Annonaceae

FIGURE 3. Aecidium chrysophaeum: a. Infected leaves of Diospyros artanthifolia (lectotype). c. Subepidermal spermogonium in section. c–f. Aecia: c. aecium in section; d. aeciospores with enlarged distal wall, insert shows single spore with lumen stained by cottonblue; e. inner side of peridial cells in face view; f. outer side of peridial cells in face view and optical section.

FIGURE 4 in Redetermination of host plants reveals that the rust fungi Aecidium annonae, Aecidium chrysophaeum and Cerotelium xylopiae occur on Diospyros species (Ebenaceae) instead of Annonaceae

FIGURE 4. Cerothelium diospyri: a–b. Comparison of size and shape between leaves of a. Xylopia sericea A. St.-Hill. (Annonaceae) infected by Dasyspora winteri (Pazschke) Beenken and b. Diospyros sericea (Ebenaceae) infected by Cerothelium diospyri. Upper leaf side is shown on the left and lower side is shown on the right. c–f. Telia of Cerotelium diospyri on Diospyros sericea (holotype); c. Telium breaking through the papillate leaf epidermis, in section; d. teliospores in gelatinous matrix; e. germinating teliospore; f. drawings of two teliospores germinating with basidia, with two of the six basidiospores germinating.

opennotspecifiedMar 2018View details →

FIGURE 1 in Enterographa confusa sp. nov. (Roccellaceae, Arthoniales) discovered by chance in type material of its host lichen Arthonia ochraceella, described more than a century ago

FIGURE 1. Enterographa confusa (A–E, holotype, G). A. E. confusa (black arrows point to ascomata of the lichenicolous fungi) forming a paler, whitish area in the thallus of its host, Arthonia ochraceella (white arrows point to ascomata of the host lichen). B. Ascomata of E. confusa. C. Asci in water. D. asci in KI showing the KI+ blue apical ring. E. Ascospores in water. Scale in A = 500 μm, in B = 100 μm, in C–D = 10 μm, in E = 5 μm. (Photos D. Ertz).

opennotspecifiedJan 2019View details →

FIGURE 61 in Holoparasitic Orobanchaceae (Cistanche, Diphelypaea, Orobanche, Phelipanche) in Armenia: distribution, habitats, host range and taxonomic problems

FIGURE 61. Orobanche rosea lectotype. Nakhichevan, peaks of low mountains 1.5‒2 km east of city of Ordubad, on Prangos ferulacea, 9 June 1956, T. Egorova, N. Tzvelev & S. Cherepanov (LE s.n.).