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Figure 6 in Host status and susceptibility of Cannabis sativa cultivars to root-knot nematodes
Figure 6: Cannabis sativa (cv. Panacea) 60 days after planting in RKN-infested field soil. (Left) naturally infested soil, (middle) nematicide-treated (fluopyram) soil, (right) steamed soil (Photo J. Coburn).
Figure 4 in Host status and susceptibility of Cannabis sativa cultivars to root-knot nematodes
Figure 4: Hemp plant dry weights (g) for RKN inoculated (+) and uninoculated (-) plants with two CBD and two Chinese fiber hemp cultivars. Factor levels not connected by the same letter are significantly different according to Tukey's HSD with P ≤ 0.05 (Trial 3).
Figure 2 in First report of northern root-knot nematode, Meloidogyne hapla (Chitwood, 1949) on strawberry in Turkey
Figure 2: PCR product at 440 bp using species-specific SCAR primers (JMV1, JMV2 and JMVhapla). M: 100 bp molecular size marker, 1,2 and 3: larvae from field infected samples. +k: positive control and –k: negative control.
Figure 3 in Characterization of root-knot nematodes infecting mulberry in Southern China
Figure 3: Phylogenetic relationships within root-knot nematodes on mulberry as inferred from Bayesian analysis of the D2-D3 region of the 28S gene sequences. Posterior probability values more than 70% are given on appropriate clades.
Figure 1 in Characterization of root-knot nematodes infecting mulberry in Southern China
Figure 1: Representative morphological characteristics of M. enterolobii. (A, whole female; B, C, female head; D, E, female perineal pattern; F, male entire; G, male head and tail; H, male posture; I, head of G second instar larva; J, middle of second instar larva; K, tail of second instar larva).
Figure 2 in Characterization of root-knot nematodes infecting mulberry in Southern China
Figure 2: Phylogenetic relationships within root-knot nematodes on mulberry as inferred from Bayesian analysis of the rDNA-ITS gene sequences. Posterior probability values more than 70% are given on appropriate clades.
Figure 2 in New Hosts and Records in Portugal for the Root-Knot Nematode Meloidogyne luci
Figure 2: Phylogenetic relationship of MelOidOgyne spp. sequences based on the alignment of sequences of cytochrome oxidase subunit I (A) and cytochrome oxidase subunit II (B) of mitochondrial DNA with available sequences of other MelOidOgyne species. The phylogenetic tree was generated in MEGA7 using the Neighbour-Joining method. The percentage of replicate trees in which the associated MelOidOgyne spp. clustered together in the bootstrap test (500 replicates) is shown next to the branches. The evolutionary distances were computed using the Jukes-Cantor method. All positions with less than 95% site coverage were eliminated. That is, fewer than 5% alignment gaps, missing data, and ambiguous bases were allowed at any position. *Recently, reclassified as M. lUCi, according to Stare et al. (2017).
Figure 1 in New Hosts and Records in Portugal for the Root-Knot Nematode Meloidogyne luci
Figure 1: Esterase phenotypes of protein homogenates from five egglaying females of MelOidOgyne species isolates. C – M. lUCi (positive control); 1 – M. ethiOpiCa isolate from Brazil; J3 – M. jaVaniCa (reference isolate); 2 – M. lUCi (COrdyline aUStraliS); 3 – M. lUCi (SOlanUM lyCOperSiCUM) and 4 – M. lUCi (OXaliS COrniCUlata).
Figure. 2 in First Report of the Peach Root-Knot Nematode, Meloidogyne floridensis Infecting Almond on Root-Knot Nematode Resistant´Hansen 536µ and´Brightµs Hybrid 5µ Rootstocks in California, USA
Figure. 2: Meloidogyne floridensis. (A–C) Anterior region of J2s; (D and E) Head region of males; (F–H) Posterior region of J2s; (I and J) Posterior region of males; (K) Lateral field of male; (L–N) Perineal patterns of females. Scale = 10 μm for A–J and 20 μm for L–N.
Figure. 1 in First Report of the Peach Root-Knot Nematode, Meloidogyne floridensis Infecting Almond on Root-Knot Nematode Resistant´Hansen 536µ and´Brightµs Hybrid 5µ Rootstocks in California, USA
Figure. 1: (A) Root galls on 'Hansen 536' rootstock of almond trees (Prunus dulcis) as scion; (B) Almond tree infected tree with Meloidogyne floridensis; (C) Almond tree, healthy.
Figure 2 in Evaluation of root-knot nematode resistance assays for sugarcane accession lines in Australia
Figure 2: Regressions to show the relationship between root biomass and ln(eggs per g roots+1) in eight nematode trials.
Figure 1 in Evaluation of root-knot nematode resistance assays for sugarcane accession lines in Australia
Figure 1: Examples of root-knot nematode gall ratings for sugarcane based on percentage of root system with galls. 1 = ≤1 to 2%, 2 = 2 to 25%, 3 = 25 to 50%, 4 = 51 to 75%, 5 ≥ 75% (modified from Shepherd 1979).
Figure 3 in Dynamics of arbuscular mycorrhizal fungi in relation to root colonization, spore density, and soil properties among different spreading stages of the exotic plant threeflower beggarweed (Desmodium triflorum) in a ZoysiO tenuifoliO lawn
Figure 3. Dynamics of the soil arbuscular mycorrhizal fungal spore density within Desmodium triflorum coverage levels and seasons.
Figure 6 in Dynamics of arbuscular mycorrhizal fungi in relation to root colonization, spore density, and soil properties among different spreading stages of the exotic plant threeflower beggarweed (Desmodium triflorum) in a ZoysiO tenuifoliO lawn
Figure 6. Conceptual framework demonstrating possible mechanisms of soil arbuscular mycorrhizal fungi (AMF) during the spreading process of Desmodium triflorum in the Zoysia tenuifolia lawn. Numbers 1, 2, 3, and 4 indicate different spreading stages of the invasive plant D. triflorum. Corresponding mycorrhizal structures were shown as the four microscopic views. Light-green and medium-yellow circles indicate AM fungal spores predominantly produced by the root mycorrhizal structures of Z. tenuifolia and D. triflorum, respectively. Medium-green and dark-yellow lines indicate the life cycle of spores in Z. tenuifolia plants and in D. triflorum plants, respectively. The AM fungi might influence the spread of D. triflorum by the following steps: (1) the early stage of the lawn's development with only Z. tenuifolia growing but without D. triflorum present. This occurs at the very beginning of the lawn establishment, and the AM fungal spores that previously existed in the lawn soil first infected the fine roots of Z. tenuifolia and completed the life cycle on their own. (2) The early spreading stage of D. triflorum (level 1). The roots of the two plants come into contact with each other, inducing the external hyphae that originally grow closely on the Z. tenuifolia roots to infect the roots of D. triflorum. The difference between the mycorrhizal infections of the two host plants contributes to higher root mycorrhizal colonizations of D. triflorum compared with Z.tenuifolia. However, at this stage,D. triflorum is not as competitive as Z. tenuifolia in the lawn, although it has advantages in terms of mycorrhizal infections. Therefore, the soil AM fungal spores are still predominantly produced by the mycorrhizal structures of the AMF-infected Z. tenuifolia roots. (3) The intermediate spreading stage of D. triflorum (levels 2 and 3). Desmodium triflorum continues to spread in the lawn. The contact of the two plants becomes more frequent and further induces a much closer relationship between the AM infections of the two plants. The increased D. triflorum plants in the lawn and the advantage of D. triflorum in root mycorrhizal infections facilitate the contribution of the mycorrhizal structures of the D. triflorum roots to sporulation. Thus, in this stage, the soil AM fungal spores were produced by the mycorrhizal structures of both plants, thereby inducing insignificant correlations between the spore densities and the root colonizations of either Z. tenuifolia or D. triflorum. (4) The late spreading stage of D. triflorum (levels 4 and 5). Desmodium triflorum is dominant in the lawn.The large numbers of D. triflorum plants and the AM infection advantage of D. triflorum facilitate AMF sporulation in the soil, thereby inducing significant correlations between the spore densities and the root colonizations of D. triflorum. At the different spreading stages of D. triflorum, the soil AM fungal communities also change as a result of the changed contributions of the AMF-infected host plants to the sporulation.
Figure 5 in Dynamics of arbuscular mycorrhizal fungi in relation to root colonization, spore density, and soil properties among different spreading stages of the exotic plant threeflower beggarweed (Desmodium triflorum) in a ZoysiO tenuifoliO lawn
Figure 5. The relative abundance and community composition at the family (A) and species levels (B) of arbuscular mycorrhizal fungi (AMF) in soils of different Desmodium triflorum coverage levels.
Figure 2 in Dynamics of arbuscular mycorrhizal fungi in relation to root colonization, spore density, and soil properties among different spreading stages of the exotic plant threeflower beggarweed (Desmodium triflorum) in a ZoysiO tenuifoliO lawn
Figure 2. Dynamics of the total, hyphal, and vesicular colonizations of Zoysia tenuifolia and Desmodium triflorum among different D. triflorum coverage levels and seasons. "Season," "Coverage," and "Species" indicate ANOVA results of each indicator among seasons and D. triflorum coverage levels and between the two plants, respectively.
Figure 4 in Dynamics of arbuscular mycorrhizal fungi in relation to root colonization, spore density, and soil properties among different spreading stages of the exotic plant threeflower beggarweed (Desmodium triflorum) in a ZoysiO tenuifoliO lawn
Figure 4. Correlations among the root mycorrhizal colonizations, arbuscular mycorrhizal fungal spore densities ("AMF spore density"), and soil properties in different coverage levels of Desmodium triflorum. ZTC, ZHC, and ZVC in light-green circles indicate the total colonization (TC), hyphal colonization (HC), and vesicular colonization (VC) of Zoysia tenuifolia, respectively. DTC, DHC, and DVC in light-red circles indicate the TC, HC, and VC of D. triflorum, respectively. Green lines and green-colored numbers indicate significant correlations between the colonization indicators of Z. tenuifolia and corresponding correlation coefficients, respectively. Red lines and red-colored numbers indicate significant correlations between the colonization indicators of Z. tenuifolia and corresponding correlation coefficients, respectively. Dark-green double arrows and dark-green numbers indicate the correlations between the colonizations of Z. tenuifolia and those of D. triflorum and corresponding correlation coefficients, respectively. Light-blue double arrows and light-blue numbers indicate the correlations between the spore densities and soil properties/root colonizations and corresponding correlation coefficients,respectively. Darkyellow double arrows and dark-yellow numbers indicate the correlations between the soil properties and root colonizations and corresponding correlation coefficients, respectively. Correlation is significant at: *P <0.05; **P <0.01; ***P <0.001. The minus sign indicates a negative correlation. Insignificant correlations are not shown.
Figure 1 in Dynamics of arbuscular mycorrhizal fungi in relation to root colonization, spore density, and soil properties among different spreading stages of the exotic plant threeflower beggarweed (Desmodium triflorum) in a ZoysiO tenuifoliO lawn
Figure 1. Dynamics of the soil physiochemical properties (average ± SE, n = 5) within different Desmodium triflorum coverage levels and seasons. "Season" and "Coverage" indicate ANOVA results of each indicator among seasons and D. triflorum coverage levels, respectively. Level 1, level 2, level 3, level 4, and level 5 indicate the coverage levels of D. triflorum in the Zoysia tenuifolia lawn, respectively, in this and all following figures.
Dataset: Root, Inc. (ROOT) Stock Performance
This dataset provides historical stock market performance data for specific companies. It enables users to analyze and understand the past trends and fluctuations in stock prices over time. This information can be utilized for various purposes such as investment analysis, financial research, and market trend forecasting.
Fig. 5 in Morphometric Differences Among Root Vole (Muridae: Microtus Oeconomus) Populations In Hungary
Fig. 5. Distribution of centroid sizes among the studied populations calculated from landmarks: a (top) = on the dorsal view of the cranium, b (bottom) = on the mandibule. Non-parametric median test
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