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304 results for “eucalyptus”

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zenodo32/100

FIGURE 14 in Notes on Endoclita C. & R. Felder (Lepidoptera: Hepialidae) feeding on Eucalyptus in Vietnam, with new records and a new species

FIGURE 14. Endoclita spp. male genitalia. Endoclita marginenotatus (14a–f), E. undulifer (14g). Photos 14a–c by Nikolai Ignatev; 14d–e by John Grehan; 14f–g reproduced from Tindale (1941: figs 15, 16 respectively).

opennotspecifiedMay 2024View details →
zenodo32/100

FIGURE 1 in Notes on Endoclita C. & R. Felder (Lepidoptera: Hepialidae) feeding on Eucalyptus in Vietnam, with new records and a new species

FIGURE 1. Endoclita phuthoensis sp. n.: holotype female (1a dorsal, 1b ventral), and two paratype females (1c–d). Photos by Nguyen Minh Chi.

opennotspecifiedMay 2024View details →
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FIGURE 16 in Notes on Endoclita C. & R. Felder (Lepidoptera: Hepialidae) feeding on Eucalyptus in Vietnam, with new records and a new species

FIGURE 16. Endoclita spp. larval feeding webs and feeding chamber around tunnel entrance Endoclita phuthoensis sp. n. (16a–b) and E. coomani (16c–f). Photos by Duy Long Pham.

opennotspecifiedMay 2024View details →
zenodo32/100

FIGURE 21 in Notes on Endoclita C. & R. Felder (Lepidoptera: Hepialidae) feeding on Eucalyptus in Vietnam, with new records and a new species

FIGURE 21. Endoclita spp. Presence of fused sternum VIII in three species of Endoclita. Photo (21a) by Duy Long Pham, (21c, e) by Benny de Groof, (21b) by Loren Jones, 21d, f) by Nikolai Ignatev.

opennotspecifiedMay 2024View details →
zenodo32/100

FIGURE 18 in Notes on Endoclita C. & R. Felder (Lepidoptera: Hepialidae) feeding on Eucalyptus in Vietnam, with new records and a new species

FIGURE 18. Endoclita spp. larval activity and impact of Endoclita phuthoensis sp. n. (18a–b, e–f), and E. coomani: (18c–d) vacated tunnels showing regrowth of callus tissue around tunnel entrance; (18e) head and thorax of larva visible within feeding chamber; (18f) cross sectional cut across stem showing typical circular shape of larval tunnel, typical for Hepialidae in general, and its central position within the sapling stem. Photos by Duy Long Pham.

opennotspecifiedMay 2024View details →
zenodo32/100

FIGURE 20 in Notes on Endoclita C. & R. Felder (Lepidoptera: Hepialidae) feeding on Eucalyptus in Vietnam, with new records and a new species

FIGURE 20. Live adults of Endoclita phuthoensis sp. n. (20b, e) and E. coomani (20a, c–d, f) at rest. Photos by Nguyen Minh Chi.

opennotspecifiedMay 2024View details →
zenodo32/100

Supplementary material 1 from: Ridenbaugh RD, Barbeau E, Sharanowski BJ (2018) Description of four new species of Eadya (Hymenoptera, Braconidae), parasitoids of the Eucalyptus Tortoise Beetle (Paropsis charybdis) and other Eucalyptus defoliating leaf beetles. Journal of Hymenoptera Research 64: 141-175. https://doi.org/10.3897/jhr.64.24282

Table S1 : Explanation note: List of all materials examined along with collecting localities, its type designation and location of deposition, and associated DNA voucher number or unique identifier. Eadya annleckieae Ridenbaugh, sp. n. is referred to as Eadya sp.1, Eadya spitzer Ridenbaugh, sp. n. is referred to as Eadya sp.2, and Eadya daenerys Ridenbaugh, sp. n. is referred to as Eadya sp.3.

opencc-zeroJul 2018View details →
zenodo32/100

FIGURES 8–13 in New species of gall fly (Diptera: Fergusoninidae) from Eucalyptus camaldulensis (Myrtaceae) in southern Australia and its associated parasitoids and inquilines

FIGURES 8–13. Fergusonina nodulosa sp. nov.: Fig. 8, Male epandrium; Fig. 10, Aedeagus; Figs 11–13, Female postabdomen: Fig. 11, dorsal aspect; Fig. 12, ventral aspect; Fig. 13 lateral aspect. Scale = 0.5 mm in Figs 8, 11–13; 0.2 mm in Figs 9–10.

opennotspecifiedDec 2019View details →
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FIGURE 14 in New species of gall fly (Diptera: Fergusoninidae) from Eucalyptus camaldulensis (Myrtaceae) in southern Australia and its associated parasitoids and inquilines

FIGURE 14. Frequency of number of locules for galls of Fergusonina nodulosa sp. nov. on Eucalyptus camaldulensis, Adelaide, South Australia. n = 245.

opennotspecifiedDec 2019View details →
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Bacterial fertilizer and filtered sludge enhance soil quality and eucalyptus growth in a eucalyptus plantation

Open the record for dataset details and reuse information.

opencc-by-nc-4.0Aug 2024View details →
dryad32/100

Data from: Enhanced decomposition and nitrogen mineralisation sustain rapid growth of Eucalyptus regnans after wildfire

Eucalyptus regnans grows rapidly from seed after wildfires, out-competing other species, thereby forming pure stands of mature forests that rank amongst the world's most carbon dense. By global standards, these forests grow on infertile soils. It is unclear how E. regnans is able to obtain large amounts nitrogen (N) from these infertile soils to support its rapid growth after fire. We measured carbon (C) and N stored in plant biomass and photosynthetic rates of E. regnans 2 years after a wildfire and examined whether E. regnans stimulated its own N supply through root-induced increases in microbial decomposition and N mineralization. We compared microbial biomass, gross N mineralization rates and soil C in trenched and rooted plots. Photosynthetic rates of E. regnans seedlings were high and comparable to photosynthetic rates observed in fertilized crops. Presence of roots of E. regnans and allied microflora enhanced gross N mineralization more than fivefold compared to soil without roots present. Soil microbial biomass was more than doubled by root presence. The soil N pulse caused by the fire and N mineralization rates in the absence of roots were too small to account for the large amount of N stored in E. regnans 2 years after the fire. Our results suggest that E. regnans facilitated its rapid growth by enhancing microbial activity and N mineralization. This enhanced microbial activity also contributed to a substantial loss of soil C (˜62% of carbon gained in plant biomass was concurrently lost from soil). Synthesis. At the ecosystem scale, the synergistic effects of plant growth and soil N mineralization need to be carefully assessed against costs to soil C for forests regenerating after disturbance.

opencc-zeroDec 2015View details →
zenodo32/100

FIGURE 10. Shield forms from L3 in Nematodes from galls on Myrtaceae. III. Fergusobia from flower bud and stigma galls on Eucalyptus, with descriptions of four new species

FIGURE 10. Shield forms from L3 fergusoninid larvae from flower bud galls (A–C redrawn from Currie (1937); D, E = automontage images, original): A, Fn. nicholsoni from flower bud galls on E. macrorrhyncha; B, Larva (Currie's Sp. 5) from flower bud galls on E. pauciflora; C, Fn. tillyardi (newly moulted) from flower bud gall on E. camaldulensis; D, larva from style gall on E. fasciculosa; E, larva from flower bud gall on E. fibrosa. Scale bars = 50 µm.

opennotspecifiedDec 2012View details →
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FIGURE 9 in Nematodes from galls on Myrtaceae. III. Fergusobia from flower bud and stigma galls on Eucalyptus, with descriptions of four new species

FIGURE 9. Dried flower bud galls (arrowed): A, from E. eugenioides associated with F. eugenioidae n. sp.; B, from E. camaldulensis associated with F.?curriei; and C, from E. obliqua associated with MSp 65. Scale bars = 5 mm.

opennotspecifiedDec 2012View details →
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FIGURE 8 in Nematodes from galls on Myrtaceae. III. Fergusobia from flower bud and stigma galls on Eucalyptus, with descriptions of four new species

FIGURE 8. Spicules from Fergusobia spp. collected from flower bud galls (K–L redrawn from Siddiqi 1994): A, F. eugeniodae n. sp. from E. eugenioides; B, F. juliae n. sp. from E. macrorrhyncha; C, MSp 65 from E. obliqua; D, MSp 27 from E. obliqua; E, F.?curriei from E. camaldulensis; F, F.?curriei from E. camaldulensis; G, F. fasciculosae n. sp. from E. fasciculosae; H, MSp 71 from E. largiflorens; MSp 75 from E. populnea; J, MSp 62 from E. pruinosa; K, F. brevicauda from E. deglupta; L, F. philippinensis from E. deglupta; M, from E. pauciflora; N, F. m o r r i s a e n. sp. from E. fibrosa; and O, MSp 54 from E. tereticornis. Scale bars = 5 µm. MSp numbers as in Davies et al. (2012).

opennotspecifiedDec 2012View details →
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FIGURE 7 in Nematodes from galls on Myrtaceae. III. Fergusobia from flower bud and stigma galls on Eucalyptus, with descriptions of four new species

FIGURE 7. Habitus drawings of Fergusobia spp. (most undescribed) collected from flower bud galls (P and Q redrawn from Siddiqi 1994): A, F. ptychocarpae from C. ptychocarpa; B, F. eugeniodae n. sp. from E. eugenioides; C, F. j u l i a e n. sp. from E. macrorrhyncha; D, MSp 27 from E. obliqua; E, MSp 65 from E. obliqua; F, MSp 64 from E. pauciflora; G, F. tumifaciens from E. bridgesiana (formerly stuartiana); H, MSp 54 from E. tereticornis; I, F. fasciculosae n. sp. from E. fasciculosa; J, F. morrisae n. sp. from E. fibrosa; K, MSp 71 from E. largiflorens; L, MSp 72 from E. melliodora; M, Msp 22 from E. microcarpa; N, Msp 75 from E. populnea; O, Msp 62 from E. pruinosa; P, F. brevicauda from E deglupta; Q, F. philippinensis from E. deglupta. Scale bars = 50 μm. MSp numbers as in Davies et al. (2012).

opennotspecifiedDec 2012View details →
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FIGURE 3. Fergusobia eugenioidae n in Nematodes from galls on Myrtaceae. III. Fergusobia from flower bud and stigma galls on Eucalyptus, with descriptions of four new species

FIGURE 3. Fergusobia eugenioidae n. sp. (all in lateral view): A, Entire infective female; B, Head of infective female; C, Entire parthenogenetic female; D, Head of parthenogenetic female; E, Tails of parthenogenetic females; F, Entire male; G, Head of males; H, Tails of males. Scale bars: A, C, F = 50 μm. B, D, G = 5 μm. Tails not drawn to scale. Line drawings indicate ranges of habitus of the various stages.

opennotspecifiedDec 2012View details →
zenodo32/100

FIGURE 1. The Bayesian consensus tree inferred from D2 in Nematodes from galls on Myrtaceae. III. Fergusobia from flower bud and stigma galls on Eucalyptus, with descriptions of four new species

FIGURE 1. The Bayesian consensus tree inferred from D2/D3 under TVM+I+G model (lnL=4001.6121; freqA=0.2903; freqC=0.1443; freqG=0.2394; freqT=0.3259; R(a)=0.8475; R(b)=3.4236; R(c)=1.9889; R(d)=0.455; R(e)=3.4236; R(f)=1; Pinva=0.522; Shape=0.5933). Posterior probability values exceeding 50% are given on appropriate clades. (Tree labels comprise nematode species, location (Australia state code), gall type, host plant species and GenBank accession number.

opennotspecifiedDec 2012View details →
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FIGURE 2 in Nematodes from galls on Myrtaceae. III. Fergusobia from flower bud and stigma galls on Eucalyptus, with descriptions of four new species

FIGURE 2. The Bayesian consensus tree inferred from COI under GTR+I+G model (lnL=3999.9661; freqA=0.2104; freqC=0.1017; freqG=0.1948; freqT=0.4931; R(a)=1.2258; R(b)=7.2392; R(c)=1.5064; R(d)=0.0698; R(e)=4.1806; R(f)=1; Pinva=0.5476; Shape=1.5992). Posterior probability values exceeding 50% are given on appropriate clades.

opennotspecifiedDec 2012View details →
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FIGURE 4. Fergusobia fasciculosae n in Nematodes from galls on Myrtaceae. III. Fergusobia from flower bud and stigma galls on Eucalyptus, with descriptions of four new species

FIGURE 4. Fergusobia fasciculosae n. sp. (all in lateral view): A, Entire infective female; B, Head of infective female; C, Tails of infective females; D, Entire parthenogenetic female; E, Head of parthenogenetic female; F, Tails of parthenogenetic females; G, Entire male; H, Head of male; I, Tails of males. Scale bars: A, D, G = 50 μm. B, E, H = 5 μm. Tails not drawn to scale. Line drawings indicate ranges of habitus of the various stages.

opennotspecifiedDec 2012View details →
zenodo32/100

FIGURE 5. Fergusobia juliae n in Nematodes from galls on Myrtaceae. III. Fergusobia from flower bud and stigma galls on Eucalyptus, with descriptions of four new species

FIGURE 5. Fergusobia juliae n. sp. (all in lateral view): A, Entire infective female; B, Head of infective female; C, Tails of infective females; D, Entire parthenogenetic female; E, Head of parthenogenetic female; F, Tails of parthenogenetic females; G, Entire male; H, Head of male; I, Tails of males. Scale bars: A, D, G = 50 μm. B, E, H = 5 μm. Tails not drawn to scale. Line drawings indicate ranges of habitus of the various stages.

opennotspecifiedDec 2012View details →

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