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240 results for “gall-inducer”
FIGURES 159–167 in Holopothrips diversity-a Neotropical genus of gall-inducing insects (Thysanoptera, Phlaeothripidae)
FIGURES 159–167. Holopothrips longisetus sp. nov. holotype and paratypes. (159) body; (160) head and pronotum, with long pronotal setae, including am; (161) fore tarsus, showing robust hamus (black arrow); (162) detail of pronotum, showing shorter am setae (white arrows); (163) mesonotum; (164) pelta; (165) spermatheca; (166) male abdominal sternite VIII, showing absence of pore plate; (167) metanotum.
FIGURES 10–15 in Holopothrips diversity-a Neotropical genus of gall-inducing insects (Thysanoptera, Phlaeothripidae)
FIGURES 10–15. Leaf-galls induced by Holopothrips (white arrows). (10) galls on Myrtaceae (by H. flavisetis); (11) galls on Acca sellowiana (by H. infestans); 12–13. galls on Ƒochysia cf. obovata (by H. kaminskii) (Photos: Lucas A. Kaminski): (12) general view; (13) opened gall; (14) galls on Miconia sp. (by H. brevicapitatum); (15) galls on Tabebuia heterophylla (by H. tabebuia) (Photo: Irma Cabrera).
FIGURES 1–9 in Holopothrips diversity-a Neotropical genus of gall-inducing insects (Thysanoptera, Phlaeothripidae)
FIGURES 1–9. Leaf-galls induced by Holopothrips (white arrows). (1) galls on Siphoneugena reitzii (by H. curiosus); (2) galls on Myrciaria floribunda (by H. spermathecus) (Photo: André Santana); (3) gall on Myrcia guianensis (by H. molzi); (4) gall on Myrcia retorta (by H. striatus); (5) gall on Myrcia sp. (by H. cardosoi) (Photo: João C. Cardoso); (6) gall on Myrcia splendens (by H. conducans); (7) gall on Myrcia splendens (by H. longisetus); (8) gall on Myrcia selloi (by H. acrioris); (9) galls on Neomitranthes obscura (by H. varicolor) (Photo: Sheila Carvalho-Fernandes).
Supplementary material 3 from: Ebinghaus M, Maier W, Wingfield MJ, Begerow D (2018) New host associations and a novel species for the gall-inducing acacia rust genus Ravenelia in South Africa. MycoKeys 43: 1-21. https://doi.org/10.3897/mycokeys.43.25090
Table S1 : Explanation note: List of measurements of teliospore characters of R.evansii. Obtained values were sorted by voucher and by individual teliospores. All measurements are given in μm.
Supplementary material 4 from: Ebinghaus M, Maier W, Wingfield MJ, Begerow D (2018) New host associations and a novel species for the gall-inducing acacia rust genus Ravenelia in South Africa. MycoKeys 43: 1-21. https://doi.org/10.3897/mycokeys.43.25090
Table S2 : Explanation note: List of measurements of teliospore characters of R.macowaniana and R.xanthophloeae. Obtained values were sorted by voucher and by individual teliospores. All measurements are given in μm.
Supplementary material 2 from: Ebinghaus M, Maier W, Wingfield MJ, Begerow D (2018) New host associations and a novel species for the gall-inducing acacia rust genus Ravenelia in South Africa. MycoKeys 43: 1-21. https://doi.org/10.3897/mycokeys.43.25090
Figure S2 : Explanation note: Boxplot of measurements of the six defined teliospore characteristics of R.macowaniana and R.xanthophloeae. Values were obtained from teliospores derived from three different host species of in total 10 individual trees. The boxplots are based on mean values calculated for all investigated teliospores for each specimen, respectively.
Supplementary material 1 from: Ebinghaus M, Maier W, Wingfield MJ, Begerow D (2018) New host associations and a novel species for the gall-inducing acacia rust genus Ravenelia in South Africa. MycoKeys 43: 1-21. https://doi.org/10.3897/mycokeys.43.25090
Figure S1 : Explanation note: Boxplot of measurements of the six defined teliospore characters of R.evansii. Values were obtained from teliospores derived from seven different host species of in total 18 individual trees. The boxplots are based on mean values calculated for all investigated teliospores for each specimen, respectively.
FIGURES 8–16 in Eurynothrips Bagnall (Thysanoptera, Phlaeothripinae): a rare and long-lost Australian genus, with one new gall-inducing species
FIGURES 8–16. Eurynothrips laheyi sp.n. (8) Female; (9–10) Head and pronotum of large and small females. (11) Antenna. (12) Prosternum. (13) Holotype head ventral surface. (14) Pronotum. (15) Metanotum and pelta. (16) Specimens from Imbil (QDPC Brisbane).
FIGURES 1–7 in Eurynothrips Bagnall (Thysanoptera, Phlaeothripinae): a rare and long-lost Australian genus, with one new gall-inducing species
FIGURES 1–7. Eurynothrips species. Leaf galls on Planchonella pohlmaniana 1–5: (1) Young gall; (2) Galls on terminal leaves; (3) Adults wandering on gall surface; (4–5) Mature galls. (6) Head of E. magnicollis paralectotype, lateral view. (7) Head of E. laheyi paratype, lateral view.
Figure 3 in A unique seasonal cycle in a leaf gall-inducing insect: the formation of stem galls for dormancy
Figure 3. Light micrographs of the Pseudotectococcus rolliniae metathoracic leg distal portion. (A) Exuviae from the first moult. (B) Crawler (5first instar). (C) Leaf nymph (5secondinstar). Scale bars: 10 mm.
Figure 5 in A unique seasonal cycle in a leaf gall-inducing insect: the formation of stem galls for dormancy
Figure 5. (A,E) Rollinia laurifolia stems: scanning electron micrographs showing Pseudotectococcus rollinae nymphs. (B–D, F) Photomicrographs of transverse sections of dormancy galls. (A,B) Crawler (5first-instar nymph) inside a dormancy gall. (C) Sudan Red B test showing plant cuticle (arrow) delimiting the dormancy gall concavity. (D) Exuviae from the first moult left inside a dormancy gall. (E) Crawler (5first-instar nymph) before dormancy starting. (F) Stem nymph (5stationary crawler) with its stylets (arrow) inserted into stem tissues inducing a dormancy gall. Crawler (cr), exuviae (ex), phelloderm (pd). Scale bars: 100 mm (A,B, D–F), 50 mm (C).
Figure 4 in A unique seasonal cycle in a leaf gall-inducing insect: the formation of stem galls for dormancy
Figure 4. Rollinia laurifolia lenticel ontogenesis. (A) Young stem with epidermis covered by cuticle and adjacent cortical parenchyma. (B) Phellogen differentiation from the external cortical parenchyma layer. (C) Young lenticel with first divisions of phellogen and suber deposition. (D) Mature lenticel with complementary cells (white arrow) and closing layer (black arrow). Cortical parenchyma (cp), epidermis (ep), phellogen (pg). Scale bar: 25 mm (A– C), 100 mm (D).
Figure 2 in A unique seasonal cycle in a leaf gall-inducing insect: the formation of stem galls for dormancy
Figure 2. Pseudotectococcus rolliniae scanning electron micrographs (A–C, E) and photomicrographs (D,F). (A) Stem nymphs (5first instar5''stationary crawlers'') located into dormancy galls. (B) Detail of a stem nymph under dormancy, showing body wax exudation covering. (C,D) Leaf nymphs (5second-instar) collected from surfaces of young leaves. (E) Crawler, still inside leaf gall. (F) Exuviae, found in dormancy stem gall. Scale bars: 500 mm (A), 50 mm (B), 100 mm (C,D), 50 mm (E,F).
Figure 1 in A unique seasonal cycle in a leaf gall-inducing insect: the formation of stem galls for dormancy
Figure 1. Schematic representation of Pseudotectococcus rollinae annual life cycle on Rollinia laurifolia plants. Numbers from two to four represent nymphal instars.
FIGURE 8 in A new gall-inducing genus and species of Eriococcidae (Hemiptera: Sternorrhyncha: Coccoidea) on Sapindaceae from Brazil
FIGURE 8. Young adult female of B. maytabae prior to full maturity. For letters, see Fig. 7. Note that D is the dorsal plate as seen from underneath.
FIGURE 7 in A new gall-inducing genus and species of Eriococcidae (Hemiptera: Sternorrhyncha: Coccoidea) on Sapindaceae from Brazil
FIGURE 7. Old, fully-expanded adult female B. mataybae. Unless otherwise started, on this and subsequent figures A = dorsal spinose setae; B = dorsal setose setae; C = dorsal microtubular duct; D = "ventral" view of dorsal plate; E = ventral spinose seta; F = posterior leg; G = posterior spiracle; H = ventral microtubular duct; J = 5-locular disc pore; K = ventral setose seta, and L = antenna.
FIGURE 11 in A new gall-inducing genus and species of Eriococcidae (Hemiptera: Sternorrhyncha: Coccoidea) on Sapindaceae from Brazil
FIGURE 11. First-instar nymph of B. mataybae. For letters, see Fig. 7, but where D = anal ring; M = onion-dome-shaped marginal setae; N = labium and P = pore of unknown homology.
FIGURES 1–5 in A new gall-inducing genus and species of Eriococcidae (Hemiptera: Sternorrhyncha: Coccoidea) on Sapindaceae from Brazil
FIGURES 1–5. (1) Upper surface of leaf of Matayba guianensis with young galls of Bystracoccus mataybae Hodgson, Isaias & Oliveira, showing outer gall orifice. (2) Lower surface of leaf of M. guianensis with fairly well-developed galls of B. mataybae. (3) Upper leaf surface of M. guianensis with old galls of B. mataybae. (4) Pit gall on twig of M. guianensis with first-instar nymph of B. mataybae in centre. (5) Twig of M. guianensis with many pit galls induced by B. mataybae, some fused together, many with nymphs in their centres. [Photographs D. Oliveira].
FIGURE 15 in Cissococcus Cockerell (Hemiptera: Coccoidea: Coccidae), a unique gall-inducing soft scale genus on Vitaceae from South Africa, with description of a new species
FIGURE 15. Cissococcus braini Hodgson & Millar, first-instar nymph (sex unknown). Lettering as for Figure 4, except T1 = claw and part of tarsus of prothoracic leg, and T2 = claw and part of tarsus of metathoracic leg.
FIGURE 14 in Cissococcus Cockerell (Hemiptera: Coccoidea: Coccidae), a unique gall-inducing soft scale genus on Vitaceae from South Africa, with description of a new species
FIGURE 14. Cissococcus braini Hodgson & Millar, sp. n. third-instar female. Lettering as in Figure 4 apart from T = entire metathoracic leg.
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