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272 results for “HARDI”
Figure 15 in A Review of the Australian Species of Thevenetimyia Bigot, 1875 (Bombyliidae, Bombyliinae, Eclimini), with Description of Four New Species and the Pupal Case of T. longipalpis (Hardy)
Figure 15. Thevenetimyia longipalpis (Hardy, 1921) genitalia (a–e ♂; f, g ♀): (a) genital capsule, dorsal; (b) genital capsule, ventral; (c) genital capsule, lateral; (d) epandrium, dorsal; (e) epandrium, lateral; (f) sternite 8, ventral; (g) genitalia and spermathecae. Scale bars = 0.1 mm.
Figure 1. Thevenetimyia australiensis Hall, 1969 in A Review of the Australian Species of Thevenetimyia Bigot, 1875 (Bombyliidae, Bombyliinae, Eclimini), with Description of Four New Species and the Pupal Case of T. longipalpis (Hardy)
Figure 1. Thevenetimyia australiensis Hall, 1969 ♂ (holotype): (a) dorsal; (b) lateral; (c) flagellum; (d) wing; (e) head, dorsal; (f) head, lateral; (g) head, frontal; (h) head, profile. Scale bars = 1 mm (a, b, d–h); = 0.1 mm (c).
Figure 20 in A Review of the Australian Species of Thevenetimyia Bigot, 1875 (Bombyliidae, Bombyliinae, Eclimini), with Description of Four New Species and the Pupal Case of T. longipalpis (Hardy)
Figure 20. Thevenetimyia nigrapicalis (Roberts, 1929) ♂: (a) dorsal; (b) lateral; (c) flagellum; (d) head, dorsal; (e) head, lateral; (f) head, frontal; (g) head, profile. Scale bars = 1 mm (a, b, d–h); = 0.1 mm (c).
Figure 3. Thevenetimyia australiensis Hall, 1969 in A Review of the Australian Species of Thevenetimyia Bigot, 1875 (Bombyliidae, Bombyliinae, Eclimini), with Description of Four New Species and the Pupal Case of T. longipalpis (Hardy)
Figure 3. Thevenetimyia australiensis Hall, 1969 Genitalia (a–e (♂); f, g (♀)): (a) genital capsule, dorsal; (b) genital capsule, ventral; (c) genital capsule, lateral; (d) epandrium, dorsal; (e) epandrium, lateral; (f) sternite 8, ventral; (g) genitalia and spermathecae. Scale bars = 0.1 mm.
Figure 8 in A Review of the Australian Species of Thevenetimyia Bigot, 1875 (Bombyliidae, Bombyliinae, Eclimini), with Description of Four New Species and the Pupal Case of T. longipalpis (Hardy)
Figure 8. Thevenetimyia furvicostata (Roberts, 1929) ♀: (a) dorsal; (b) lateral; (c) head, dorsal; (d) head, lateral; (e) wing; (f) head, frontal; (g) head, profile. Scale bars = 1 mm.
Figs. 42–46 in Biology And Description Of The Third Instar Larva And Puparium Of Ichneumonopsis Burmensis Hardy (Diptera: Tephritidae: Dacinae: Gastrozonini), A Bamboo-Breeding Fruit Fly From The Oriental Region
Figs. 42–46. Puparium of I. burmensis (SEM photographs). 42, Apical end of the puparium showing the anterior spiracles. 43, Detail of invaginated frontal part of prothorax showing the locations of the paired sensilla. 44, Detail of the anterior spiracle showing three papillae. 45, Caudal end of the puparium. 46, Posterior spiracles. an = anus; as = anterior spiracle; pts 2–9 = prothoracic sensillae.
Figs. 34–41 in Biology And Description Of The Third Instar Larva And Puparium Of Ichneumonopsis Burmensis Hardy (Diptera: Tephritidae: Dacinae: Gastrozonini), A Bamboo-Breeding Fruit Fly From The Oriental Region
Figs. 34–41. Thoracic and abdominal segments of the I. burmensis larva. 34, Pseudocephalon and prothorax, dorsal view. 35, Prothoracic paired sensilla and anterior spiracle (lateral view). 36, Prothoracic paired sensilla (dorsal view). 37, Enlarged paired prothoracic sensilla (pts5). 38, Detail of anterior spiracle showing the papillae. 39, Detail of a creeping welt showing the spinules. 40, Caudal segment showing the posterior spiracle, anus and the locations of some sensilla. 41, Posterior spiracles. T1 = prothorax; an = anus; as = anterior spiracle; es = ecdysial scar; I1, I2 = intermediate sensilla; p ceph = pseudocephalon; pts 1–10 = prothoracic sensilla; ps = posterior spiracle; sh = spiracular hairs.
Figs. 28–33 in Biology And Description Of The Third Instar Larva And Puparium Of Ichneumonopsis Burmensis Hardy (Diptera: Tephritidae: Dacinae: Gastrozonini), A Bamboo-Breeding Fruit Fly From The Oriental Region
Figs. 28–33. Cephalopharyngeal skeleton, anterior/ posterior spiracles and larval habitus of I. burmensis (light microscopy). 28, Anterior spiracle. 29, Detail of anterior spiracle showing the papillae. 30, Posterior spiracle. 31. Spiracular hairs. 32, Cephalopharyngeal skeleton. 33, Larval habitus. A1–A7 = abdominal segments; as = anterior spiracle; cs = caudal segment; cw = creeping welt; da = dorsal apodeme; db = dorsal bridge; dc = dorsal cornu; ec = ecdysial scar; hb = hypopharyngeal bridge; hs = hypopharyngeal sclerite; ls = labial sclerite; mh = mouth hook; p ceph = pseudocephalon; pb = parastomal bar; pt = praeapical tooth; sh = spiracular hairs; T1–T3 = thoracic segments; win = window; va = ventral apodeme; vb = ventral bridge; vc = ventral cornu; vs = ventral sclerite.
Figs. 15–21 in Biology And Description Of The Third Instar Larva And Puparium Of Ichneumonopsis Burmensis Hardy (Diptera: Tephritidae: Dacinae: Gastrozonini), A Bamboo-Breeding Fruit Fly From The Oriental Region
Figs. 15–21. Damage symptoms of bamboo shoots attacked by I. burmensis. 15, Tip of an unaffected Melocalamus compactiflorus bamboo shoot. 16, Tip of a Melocalamus compactiflorus bamboo shoot infested by I. burmensis. The leaves of the upper internodes have started to wither. 17, The apical internodes have dropped down to the ground, but the I. burmensis internode is still attached to the bamboo shoot. A part of the internode sheath was removed in order to show the location of the bud, the zone of intercalary growth and the predetermined breaking point. 18, The newly emerged branches at the base of the I. burmensis-internode have displaced the internode sheath. Most branches are not depicted in order to show the exit hole above the predetermined breaking point. 19, The I. burmensis internode has cracked at the level of the exit hole and dangles at the tip of the bamboo shoot. The puparium is still protected by the torn off vascular fibres. 20, The apical part of the I. burmensis-internode has dropped to the ground. The basal stump of the internode remains attached at the tip of the bamboo shoot and harbours the puparium. 21, Longitudinal section of the enlarged basal part of an I. burmensis-internode showing the location of the puparium. b = branch; bb = branch bud; cs = culm sheath; eh = exit hole; ii = I. burmensis-internode; n = node; p = puparium; pbp = predetermined breaking point; sb = sheath blade; vf = vascular fibres; zig = zone of intercalary growth.
Figs. 8–14 in Biology And Description Of The Third Instar Larva And Puparium Of Ichneumonopsis Burmensis Hardy (Diptera: Tephritidae: Dacinae: Gastrozonini), A Bamboo-Breeding Fruit Fly From The Oriental Region
Figs. 8–14. Damage of bamboo shoots caused by I. burmensis, and pupariation. 8, Basal part of an I. burmensis internode, early stage of infestation. The culm sheath was removed to show the branch bud, the zone of intercalary growth and the predetermined breaking point of the internode. 9, The apical part of the bamboo shoot has fallen down, but the I. burmensis-internode is still attached to the bamboo shoot. The emerging side branches have pushed away the culm sheath from the internode wall. 10, I. burmensis internode with side branches largely removed in order to show the slit-like exit hole. 11, The I. burmensis-internode has cracked at the level of the exit hole (above the predetermined breaking point). The exposed internode cavity is filled with torn off, compressed vascular fibres, which protect the puparium. 12, The cracked upper part of the I. burmensis-internode has dropped to the ground. The puparium rests inside the stump of the I. burmensis internode at the tip of the bamboo shoot. 13, I. burmensis puparium stuck in the basal part of the internode. The internode was broken at the predetermined breaking point in order to show the protruding puparium. 14, I. burmensis puparium stuck in the upper part of the internode cavity, anterior end on right hand side. as = anterior spiracle; bb = branch bud; cs = culm sheath; eh = exit hole; ii = I. burmensis-internode; p = puparium; pbp = predetermined breaking point; vf = vascular fibres; zig = zone of intercalary growth.
Figs 25–26. Ichneumonopsis spp., glans. 25. I. burmensis Hardy, 1973. 26. I in A revision of Ichneumonopsis Hardy, 1973 (Diptera: Tephritidae: Dacinae: Gastrozonini), Oriental bamboo-shoot fruit flies
Figs 25–26. Ichneumonopsis spp., glans. 25. I. burmensis Hardy, 1973. 26. I. taiwanensis sp. nov.
Figs 20–21. Ichneumonopsis burmensis Hardy, 1973 in A revision of Ichneumonopsis Hardy, 1973 (Diptera: Tephritidae: Dacinae: Gastrozonini), Oriental bamboo-shoot fruit flies
Figs 20–21. Ichneumonopsis burmensis Hardy, 1973, abdomen, dorsal view. 20. ♂. 21. ♀.
Figs 18–19. Ichneumonopsis spp., wing. 18. I. burmensis Hardy, 1973. 19. I in A revision of Ichneumonopsis Hardy, 1973 (Diptera: Tephritidae: Dacinae: Gastrozonini), Oriental bamboo-shoot fruit flies
Figs 18–19. Ichneumonopsis spp., wing. 18. I. burmensis Hardy, 1973. 19. I. taiwanensis sp. nov.
Figs 5–6. I in A revision of Ichneumonopsis Hardy, 1973 (Diptera: Tephritidae: Dacinae: Gastrozonini), Oriental bamboo-shoot fruit flies
Figs 5–6. I. hancocki sp. nov., head, anterior view. 5. ♂. 6. ♀.
Fig. 1 in A revision of Ichneumonopsis Hardy, 1973 (Diptera: Tephritidae: Dacinae: Gastrozonini), Oriental bamboo-shoot fruit flies
Fig. 1. Collecting localities of Ichneumonopsis spp.
Hardy Tree (Camden, UK) and gravestones
This is the Hardy Tree in [St Pancras Old Church](https://goo.gl/9AiihJ), Camden, London, UK ([OSM](https://goo.gl/ydVXeA)). The tree was reportedly planted by the author Thomas Hardy and the roots are embedded in pile of gravestones.  The point cloud is a combination of a RIEGL VZ-400 scan and a ZEB-REVO (to get detail around the gravestones). Scanning done by University College London ([@kungphil](https://twitter.com/kungphil), [@mathiasdisney](https://twitter.com/mathiasdisney), [@UCLgeography](https://twitter.com/UCLgeography)). This work was funded by the NERC National Centre for Earth Observation (NCEO). Source: Objaverse 1.0 / Sketchfab
St Pancras Old Church Hardy Tree
Before becoming a novelist and poet, Thomas Hardy studied architecture. During the 1860s he was tasked with supervising the moving of headstones in the churchyard of Old St. Pancras church (London) to make way for the Midland Railway line. The headstones were moved to this location around an ash tree which has now grown amongst the stones. Source: Objaverse 1.0 / Sketchfab
Fig. 1 in Evaluation Of Winter Hardiness In Different Cultivated Tilia Taxa - Experience Of Some Most Valuable Dendrological Plantations In Central Latvia (Vidzeme) After Extremely Hard Winter In Year 2009/2010
Fig. 1. Location of inventoried dendrological objects in central part of Latvia.
Heteromudas bicolor Hardy, male genitalia: 82, ventral view; 83, dorsal view; 84, lateral view. in The American Genera of Mydidae (Diptera), with the Description of three new Genera and two new Species
Heteromudas bicolor Hardy, male genitalia: 82, ventral view; 83, dorsal view; 84, lateral view.
Data from Preliminary estimates of genetic parameters and familial selection for non-native poplars show good potential for genetic gains on growth, cold hardiness, trunk quality and Sphaerulina musiva susceptibility
<p>Data from Preliminary estimates of genetic parameters and familial selection for non-native poplars show good potential for genetic gains on growth, cold hardiness, trunk quality and <em>Sphaerulina musiva</em> susceptibility</p> <p><br> Abstract<br> Genetic parameters for growth, trunk quality and susceptibility to frost and <em>Sphaerulina musiva</em> attack was estimated from 34 half-sib families of hybrid poplar from the crossing of non-native parents, <em>Populus maximowiczii</em> A. Henry and <em>Populus trichocarpa</em> Torr. & Gray, 3 and 6 years after planting. The use of spatial analysis proved to be the best method for quantitative growth data. The proportion of the among-family variance to the total (phenotypic) variance as well as the high heritabilities of growth and susceptibility to frost and <em>Spaherulina musiva</em> showed a high potential for selection for these traits while the quality traits were under low genetic control. Some families showed gains for several traits, suggesting the possibility of developing a selection index to obtain superior families that show gain for not only growth but quality and adaptive traits as well. Type B correlations were high, suggesting that families responded in the same way regardless of the site. High type A correlation between growth traits at 3 and 6 years showed early selection potential, although these relationships should be confirmed with future measurements to evaluate this effect at maturity. These results can be integrated into the strategy for improving hybrid poplar parental populations and, in the longer term, will make it possible to optimize the selection of individuals with traits of interest for the operational deployment of hybrid poplar clones.</p>
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