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304 results for “eucalyptus”

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zenodo32/100

FIGURE 2 in Re-description and first host and biology records of Entedon magnificus (Girault & Dodd) (Hymenoptera, Eulophidae), a natural enemy of Gonipterus weevils (Coleoptera, Curculionidae), a pest of Eucalyptus trees

FIGURE 2. Entedon magnificus, female, SEM. A, habitus, dorsal view; B, head, frontal view; C, propodeum; D, lower face; E, head and anterior mesosoma; F, occiput.

opennotspecifiedDec 2015View details →
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FIGURE 5. Entedon magnificus, final instars. A in Re-description and first host and biology records of Entedon magnificus (Girault & Dodd) (Hymenoptera, Eulophidae), a natural enemy of Gonipterus weevils (Coleoptera, Curculionidae), a pest of Eucalyptus trees

FIGURE 5. Entedon magnificus, final instars. A, body of completely eaten Gonipterus larva filled with final instars of E. magnificus; B–E, parasitoid larvae emerging from remnants of its host, mature larva of Gonipterus sp.; F and G, pupae.

opennotspecifiedDec 2015View details →
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FIGURE 1. Entedon magnificus. A, B in Re-description and first host and biology records of Entedon magnificus (Girault & Dodd) (Hymenoptera, Eulophidae), a natural enemy of Gonipterus weevils (Coleoptera, Curculionidae), a pest of Eucalyptus trees

FIGURE 1. Entedon magnificus. A, B. Female, habitus: A, dorsal view; B, lateral view. C, D. Male, habitus: C, lateral view; D, dorsal view.

opennotspecifiedDec 2015View details →
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FIGURE 4. A and B in Re-description and first host and biology records of Entedon magnificus (Girault & Dodd) (Hymenoptera, Eulophidae), a natural enemy of Gonipterus weevils (Coleoptera, Curculionidae), a pest of Eucalyptus trees

FIGURE 4. A and B, Gonipterus platensis weevils, habitus. C and D, female of Entedon magnificus ovipositing into Gonipterus platensis larva feeding on Eucalyptus leaf.

opennotspecifiedDec 2015View details →
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FIGURES 8–12 in A new species of invasive gall wasp (Hymenoptera: Eulophidae: Tetrastichinae) on blue gum (Eucalyptus globulus) in California

FIGURES 8–12. Selitrichodes globulus Ƥ. 8, Head, frontal view. 9, Head, lateral view. 10, Mesosoma, dorsal. 11, Antenna. 12, Fore wing.

opennotspecifiedDec 2009View details →
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FIGURES 1–6. Selitrichodes globulus. 1–2 in A new species of invasive gall wasp (Hymenoptera: Eulophidae: Tetrastichinae) on blue gum (Eucalyptus globulus) in California

FIGURES 1–6. Selitrichodes globulus. 1–2, Gall damage on Eucalyptus globulus. 3, Galls showing adult emergence holes. 4, Dissected section of stem showing galls containing larvae and pupae. 5–6, Larvae within dissected galls.

opennotspecifiedDec 2009View details →
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FIGURES 8–9 in A new genus and species of Tetrastichinae (Hymenoptera: Eulophidae) inducing galls in seed capsules of Eucalyptus

FIGURES 8–9. Leprosa milga and galled seeds of Eucalyptus?camaldulensis. 8. L. milga Ψ; 9. seeds with emergence hole in a seed capsule.

opennotspecifiedDec 2008View details →
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FIGURES 1–7 in A new genus and species of Tetrastichinae (Hymenoptera: Eulophidae) inducing galls in seed capsules of Eucalyptus

FIGURES 1–7. Leprosa milga Ψ. 1. Antenna, inner side; 2. Pedicel, outer side; 3. Face, frontal view; 4. Mesosoma, dorsal view; 5. Mesosoma, lateral view; 6. Gaster, lateral view; 7. Forewing.

opennotspecifiedDec 2008View details →
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Long-term effects of intercropping on multi-trophic structure and bio-thermodynamic health of mixed Eucalyptus-native tree plantations

<p><span>1. </span><span>The intercropping approach of <em>Eucalyptus</em> and native trees has been widely recommended, as an ideal replacement for monoculture <em>Eucalyptus</em> plantations (EUs), to ameliorate global biodiversity loss and mitigate environmental change. However, both suitable native tree species and the best intercropping ratio between <em>Eucalyptus</em> and native trees have not been determined. </span></p> <p><span>2. </span><span>To fill this gap, a four-level intercropping gradient of <em>Eucalyptus urophylla</em> planted with eight native tree species was set up (i.e., 20%NS, 30%NS, 40%NS, 50%NS), monitored and compared to a monoculture <em>E. urophylla</em> plantation (EU) and a randomly mixed plantation of nine native tree species (NS) in southern China. </span></p> <p><span>3. </span><span>The results showed that the intercropping ratio of <em>Eucalyptus</em> and native trees had a long-term effect on tree layer structure and health status and a cascading effect on the thermodynamic health state of soil microbes. Shade-tolerant woody species are more suitable for intercropping with <em>Eucalyptus</em>. Intercropping plantations with not less than 30% native trees were more favorable for long-term survival and growth of both planted <em>Eucalyptus</em> and native trees and provided much more favorable conditions for the natural immigration of other native trees, which leads to a healthy plant community with significantly higher eco-exergy compared to EU. The initial mixing ratio between <em>Eucalyptus</em> and high diversity native trees affected soil fertility through its long-term effects on the biodiversity and bio-thermodynamic state of trees and soil microbes.</span></p> <p><span>4. </span><span><em>Synthesis and applications</em>.</span><span> Our results highlight the long-term positive effect of the intercropping ratio of <em>Eucalyptus</em> and high diversity native trees on multi-trophic biodiversity conservation, bio-thermodynamic health development, and soil fertility conservation. In the conversion of monoculture <em>Eucalyptus</em> plantations (EU) to multi-species plantations, it is recommended to mix more than 30% native tree species that have different ecological niches with <em>Eucalyptus</em>.</span></p>

opencc-zeroNov 2023View details →
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FIGURE 3. Pathogenicity test results for C in Eucalyptus leaf spot disease caused by Coniella eucalyptorum in Sri Lanka

FIGURE 3. Pathogenicity test results for C. eucalyptorum on E. camaldulensis leaves. a1–a4 wounded leaves inoculated with C. eucalyptorum spore suspensions. b1–b2 non-wounded leaves inoculated with C. eucalyptorum spore suspensions. c1–c2 non-wounded leaves inoculated with sterile water (control). d1–d2 wounded leaves inoculated with sterile water (control). e1–e4 wounded leaves inoculated with C. eucalyptorum mycelial plugs. f1–f2 non-wounded leaves inoculated with C. eucalyptorum mycelial plugs. g1–g2 wounded leaves inoculated with sterile PDA plugs (control). h1–h2 non-wounded leaves inoculated with sterile PDA plugs (control).

opennotspecifiedDec 2023View details →
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FIGURE 1 in Eucalyptus leaf spot disease caused by Coniella eucalyptorum in Sri Lanka

FIGURE 1. Phylogram generated for Coniella species from ML and BI analyses based on a combined dataset of ITS, LSU, and tef1-α sequences. The tree is rooted with Melanconiella sp. (CBS110385). Bootstrap support values for ML ≥ 65 % and Bayesian posterior probabilities (PP) ≥ 0.95 are shown at the nodes. The strain from the current study is in red. All ex-type strains are in bold black. Some branches were shortened to fit them to the pages, and these are indicated by two diagonal lines with the number of times a branch was shortened indicated next to the lines.

opennotspecifiedDec 2023View details →
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Fig. 6 in A phylogenetic investigation of the taxonomically problematic Eucalyptus odorata complex (E. section Adnataria series Subbuxeales): evidence for extensive interspecific gene flow and reticulate evolution

Fig. 6. Isolation by distance plot of core E. odorata complex samples (E. odorata, E. cajuputea, E. wimmerensis, E. walshii, E. yarriambiack, E. filiformis, E. polybractea and E. viridis from south-eastern Queensland). Geographic distances are kilometres between collection coordinates and genetic distances are uncorrelated-P distances.

opennotspecifiedOct 2022View details →
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Fig. 3 in A phylogenetic investigation of the taxonomically problematic Eucalyptus odorata complex (E. section Adnataria series Subbuxeales): evidence for extensive interspecific gene flow and reticulate evolution

Fig. 3. Plot of PCA analyses of SNPs generated using (a) ddRADseq and (b) DArTseq. Points are coloured by species consistent with Fig. 1, with shapes used to distinguish different major groups: the grey-box taxa (diamonds), mallee members of E. series Subbuxeales not in the E. odorata complex (squares), and the E. odorata complex (circles).

opennotspecifiedOct 2022View details →
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Fig. 5 in A phylogenetic investigation of the taxonomically problematic Eucalyptus odorata complex (E. section Adnataria series Subbuxeales): evidence for extensive interspecific gene flow and reticulate evolution

Fig. 5. Maximum-likelihood phylogeny generated using RAXML, excluding samples with strong evidence for hybridisation and introgression in the combined ddRADseq and DArTseq dataset. Support values on branches are those from the ML and MP analysis, with branches with greater than 80% bootstrapping support in both analyses thickened. Series are labelled as per Nicolle (2019).

opennotspecifiedOct 2022View details →
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Fig. 1 in A phylogenetic investigation of the taxonomically problematic Eucalyptus odorata complex (E. section Adnataria series Subbuxeales): evidence for extensive interspecific gene flow and reticulate evolution

Fig. 1. Distributions of the 12 species of the E. odorata complex, using taxonomic concepts employed a priori in this study. (a) E. viridis and species most commonly considered its closest relatives. (b) E. odorata, E. polybractea and species commonly considered close relatives of these. Distributions are coloured by species and open circles are used to highlight geographically restricted populations. Closed points indicate the collecting localities and seed provenances for samples used in this study. Black circles indicate major regions where members of the E. odorata complex occur as applied in text, which may differ from the actual geographic extent.

opennotspecifiedOct 2022View details →
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Fig. 4 in A phylogenetic investigation of the taxonomically problematic Eucalyptus odorata complex (E. section Adnataria series Subbuxeales): evidence for extensive interspecific gene flow and reticulate evolution

Fig. 4. Maximum-likelihood phylogeny generated using RAXML including all samples in the combined ddRADseq and DArTseq dataset. Support values on branches are those from the ML and MP analysis, with branches with greater than 80% bootstrapping support in both analyses thickened. Series are labelled as per Nicolle (2019).

opennotspecifiedOct 2022View details →
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Data linked to publication entitled "Biochar derived from Acai agroindustry waste enhances nutritional status and biomass in young Eucalyptus urophylla plants: Evidence connected to root development and leaf performance"

<p>Data linked to publication entitled &quot;Biochar derived from Acai agroindustry waste enhances nutritional status and biomass in young Eucalyptus urophylla plants: Evidence connected to root development and leaf performance&quot;</p>

opencc-by-4.0Jan 2022View details →
dryad32/100

Response of 25-day old Eucalyptus globulus to elevated CO2

<p><span>Increasing [CO<sub>2</sub>] may influence commercial crop and timber yield. While selection of genotypes sensitive to elevated [CO<sub>2</sub>] (e[CO<sub>2</sub>]) appears possible in agricultural crops, there is limited evidence for genotype-by-CO<sub>2</sub> (G×CO<sub>2</sub>) interactions in commercial tree species. We examined [CO<sub>2</sub>] responsiveness in 124 open-pollinated <em>Eucalyptus globulus</em> subspecies globulus (<em>E. globulus</em>) families with the aim of assessing whether G×CO<sub>2</sub> interactions are detectable in seedlings for early-age screening. Plants were grown in ambient (a[CO<sub>2</sub>]; ~405 μmol mol<sup>-1</sup>) and e[CO<sub>2</sub>] (640 μmol mol<sup>-1</sup>) and harvested 25 days after germination. Total, shoot and root dry weights were determined for each plant. Carbon isotopic discrimination against 13C (Δ13C) was determined at the family level. We observed highly significant (p&lt;0.0001) increases in mean total, shoot, and root dry weights. Mixed-model equations were used to estimate the main and interaction effects of the G×CO<sub>2</sub> for each mass trait. The main effects from the mixed model output ([CO<sub>2</sub>] and individual-tree effects) were significant for all traits. However, [CO<sub>2</sub>]-by-individual tree interactions were non-significant for all traits, indicating little G×CO<sub>2</sub> interaction. A secondary aim was to examine the correlation between greenhouse and mature-age growth from breeding trials that use common families conducted under ambient [C<sub>O2</sub>]. These correlations were non-significant, suggesting early growth is not necessarily indicative of later-age responses.  </span>Our results suggest that while early growth of <em>E. globulus</em> is enhanced under e[CO<sub>2</sub>], genotypes respond relatively uniformly to e[CO<sub>2</sub>] and little opportunity exists for seedling-based selection at the population level based upon the response of plants during the first weeks of growth.</p>

opencc-zeroMar 2022View details →
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Raw Data Survival, Development and Reproduction of Gonipterus platensis on Eucalyptus genotypes

<p>Data used in the paper&nbsp;&quot;The survival, development, and reproduction of <em>Gonipterus platensis </em>(Coleoptera: Curculionidae) on the main <em>Eucalyptus </em>(Myrtaceae) genotypes planted in Brazil&quot;</p>

opencc-by-4.0Jun 2022View details →
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Supplementary material 1 from: Demetriou J, Koutsoukos E, Davranoglou L, Roy HE, Spodek M, Martinou AF (2022) First records of the alien Eucalyptus psyllids Blastopsylla occidentalis (Hemiptera, Aphalaridae) from Cyprus and Platyobria biemani (Hemiptera, Aphalaridae) from Cyprus and continental Greece. Travaux du Muséum National d'Histoire Naturelle "Grigore Antipa" 65(1): 25-36. https://doi.org/10.3897/travaux.65.e82873

Supplementary material 1 from: Demetriou J, Koutsoukos E, Davranoglou L, Roy HE, Spodek M, Martinou AF (2022) First records of the alien Eucalyptus psyllids Blastopsylla occidentalis (Hemiptera, Aphalaridae) from Cyprus and Platyobria biemani (Hemiptera, Aphalaridae) from Cyprus and continental Greece. Travaux du Muséum National d'Histoire Naturelle "Grigore Antipa" 65(1): 25-36. https://doi.org/10.3897/travaux.65.e82873

opencc-by-4.0Jun 2022View details →

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