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883 results for “termites”
Figure 1 from: Scheffrahn RH (2016) Parvitermes (Isoptera, Termitidae, Nasutitermitinae) in Central America: Two new termite species and reassignment of Nasutitermes mexicanus. ZooKeys 617: 47-63. https://doi.org/10.3897/zookeys.617.10040
Figure 1 - Parvitermes brooksi. A Dorsal left view of gut: M = mesenteron, P1-P4 = proctodeal segments 1-4 (limits of P2 highlighted) B Whole mount of P2 with musculature removed. Posterior (end attached to P3) at top of image C P2 splayed open; bacterial pellet attached to spines of the central pad.
Figure 4 from: Scheffrahn RH (2016) Parvitermes (Isoptera, Termitidae, Nasutitermitinae) in Central America: Two new termite species and reassignment of Nasutitermes mexicanus. ZooKeys 617: 47-63. https://doi.org/10.3897/zookeys.617.10040
Figure 4 - Parvitermes worker head and thorax, lateral views. A Parvitermes mexicanus comb. n. B Parvitermes mesoamericanus sp. n. C Parvitermes yucatanus sp. n.
Figure 7 from: Scheffrahn RH (2016) Parvitermes (Isoptera, Termitidae, Nasutitermitinae) in Central America: Two new termite species and reassignment of Nasutitermes mexicanus. ZooKeys 617: 47-63. https://doi.org/10.3897/zookeys.617.10040
Figure 7 - Collection localities of three Parvitermes species in the UF Termite collection. The far western sample of Parvitermes mexicanus comb. n. was taken near the type locality.
Figure 8 from: Scheffrahn RH (2016) Parvitermes (Isoptera, Termitidae, Nasutitermitinae) in Central America: Two new termite species and reassignment of Nasutitermes mexicanus. ZooKeys 617: 47-63. https://doi.org/10.3897/zookeys.617.10040
Figure 8 - Field photograph of Parvitermes mesoamericanus sp. n. foragers feeding within a crevice of damp wood (Coyolito, Honduras; paratype locality, HN431).
Supplementary material 2 from: Duquesne E, Fournier D (2024) Connectivity and climate change drive the global distribution of highly invasive termites. NeoBiota 92: 281-314. https://doi.org/10.3897/neobiota.92.115411
Occurrences of the 22 invasive termites as well as their source
Supplementary material 1 from: Duquesne E, Fournier D (2024) Connectivity and climate change drive the global distribution of highly invasive termites. NeoBiota 92: 281-314. https://doi.org/10.3897/neobiota.92.115411
Supplementary tables and figures (S1 to S7)
FIGURE 10 in Termite nests in eolian backshore settings: An unusual record throughout the Quaternary in the Neotropical realm
FIGURE 10. Termites collected in site A, identified as Termitidae. Other investigated sites are also represented by termitids. A. General view of an egg (below), a minor worker and a bigger worker (above). B. Detail of an egg with visible termite inside. C. General view of a Termitidae soldier. D. Detail of a soldier with rounded cephalic capsule bearing a conical frontal tube (nasus), with fine extremity.
FIGURE 9 in Termite nests in eolian backshore settings: An unusual record throughout the Quaternary in the Neotropical realm
FIGURE 9. Features of the casted nests. A. Photomosaic evidencing the hypogean portion of nest D.4; observe that the structure present two main disposition of passages, with concentrated passages very similar to epigeal portion going up to ~70 deep, and elongated passages mostly vertically-oriented with lateral chambers occurring only in deeper part of the structure; horizontally-oriented passages are more common in the middle of the underground portion, with local globous chambers. Dotted lines colored in yellow represent inferred connections, lost during removal of the cast. B. Plan view of the bottom of epigeal portion, with concentrated pattern of passages (central chamber is absent). C. Casted concentrated passages evidencing a random distribution. D. Walls of passages in epigeal portion, showing high concentration of sand lined by organic matter in its interior (this sample was not casted).
FIGURE 6 in Termite nests in eolian backshore settings: An unusual record throughout the Quaternary in the Neotropical realm
FIGURE 6. Successive cuts in nest C.2 (a-c). Observe a second enlargement below the general funnel in the central portion of the nest (c), while the margins present only a general downward reduction in size (a, b).
FIGURE 3 in Termite nests in eolian backshore settings: An unusual record throughout the Quaternary in the Neotropical realm
FIGURE 3. Detail of the internal chamber found in nest A.3 (a, b) and the rhizome of ferns used by termites (c).
FIGURE 2. Termite nests from site A in Termite nests in eolian backshore settings: An unusual record throughout the Quaternary in the Neotropical realm
FIGURE 2. Termite nests from site A. General view of the nests close to the shoreline (a), with sparse vegetation of grasses and ferns around the mounds, and detail of external nest morphology with no open chimneys (b) (nest A.6). The hypogean portion of nest A.10 with bottom passages vertically oriented is shown in (c). The schematic disposition of termite nests in site A allow observing that the closest nest is less than 30 m from shoreline (d), and nest's concentration in the flat areas of foredunes (e), almost 60 m far from shoreline.
Figure 3 from: Castro D, Scheffrahn RH, Carrijo TF (2018) Echinotermes biriba, a new genus and species of soldierless termite from the Colombian and Peruvian Amazon (Termitidae, Apicotermitinae). ZooKeys 748: 21-30. https://doi.org/10.3897/zookeys.748.24253
Figure 3 Bayesian gene tree of all described soldierless New World genera using the mitochondrial COI barcode gene showing posterior probabilities. Tree rooted on terminal Heterotermes crinitus.
Figure 2 from: Castro D, Scheffrahn RH, Carrijo TF (2018) Echinotermes biriba, a new genus and species of soldierless termite from the Colombian and Peruvian Amazon (Termitidae, Apicotermitinae). ZooKeys 748: 21-30. https://doi.org/10.3897/zookeys.748.24253
Figure 2 Worker enteric valve of Echinotermes biriba sp. n. A Spliced mount B whole mount, showing in situ position of armature. Note the filamentous bacteria attached to the spines. The trilobed seating anterior to the spines (removed in this preparation) is full of bacteria and devoid of food particles, referred by Noirot (2001) as the "bacterial pouch".
Figure 1 from: Castro D, Scheffrahn RH, Carrijo TF (2018) Echinotermes biriba, a new genus and species of soldierless termite from the Colombian and Peruvian Amazon (Termitidae, Apicotermitinae). ZooKeys 748: 21-30. https://doi.org/10.3897/zookeys.748.24253
Figure 1 Worker of Echinotermes biriba sp. n.: A dorsal and lateral views of head and pronotum B mandibles C right fore-tibia D digestive tube from left to right: dorsal, right, ventral and left views. Abbreviations: C = crop, EVS = enteric valve seating, MS = mesenteron, MT = mesenteric tongue, P1–P5 = proctodeal segments.
Figure 3 from: Scheffrahn RH, Bourguignon T, Akama PD, Sillam-Dussès D, Šobotník J (2018) Roisinitermes ebogoensis gen. & sp. n., an outstanding drywood termite with snapping soldiers from Cameroon (Isoptera, Kalotermitidae). ZooKeys 787: 91-105. https://doi.org/10.3897/zookeys.787.28195
Figure 3 Brachypterous nymph of Roisinitermesebogoensis gen. & sp. n. Top: Dorsal view of mandibles. Bottom: lateral view of head and thorax.
Figure 2 from: Scheffrahn RH, Bourguignon T, Akama PD, Sillam-Dussès D, Šobotník J (2018) Roisinitermes ebogoensis gen. & sp. n., an outstanding drywood termite with snapping soldiers from Cameroon (Isoptera, Kalotermitidae). ZooKeys 787: 91-105. https://doi.org/10.3897/zookeys.787.28195
Figure 2 Imago of Roisinitermesebogoensis gen. & sp. n. A Dorsal view of head and thorax B Oblique view of head C Lateral view of head and thorax D Right forewing (arrow on subcosta) and right hind wing.
Figure 1 from: Scheffrahn RH, Bourguignon T, Akama PD, Sillam-Dussès D, Šobotník J (2018) Roisinitermes ebogoensis gen. & sp. n., an outstanding drywood termite with snapping soldiers from Cameroon (Isoptera, Kalotermitidae). ZooKeys 787: 91-105. https://doi.org/10.3897/zookeys.787.28195
Figure 1 Phylogenetic tree of Kalotermitidae based on full mitochondrial genomes. The tree depicted was reconstructed with RAxML using the data matrix without third codon position. Node labels are the Maximum Likelihood bootstrap supports and the Bayesian posterior probabilities in the following order, from left to right: posterior probability of the analysis with third codon position included, posterior probability of the analysis without third codon position, bootstrap support of the analysis with third codon position included, bootstrap support of the analysis without third codon position, *indicates 100% bootstrap support and 1.0 posterior probability for all four analyses.
Figure 5 from: Scheffrahn RH, Bourguignon T, Akama PD, Sillam-Dussès D, Šobotník J (2018) Roisinitermes ebogoensis gen. & sp. n., an outstanding drywood termite with snapping soldiers from Cameroon (Isoptera, Kalotermitidae). ZooKeys 787: 91-105. https://doi.org/10.3897/zookeys.787.28195
Figure 5 Dorsal view of frons and mandibles of Roisinitermesebogoensis gen. n. sp. n. Inset: oblique ventral view of columnar hump (arrow).
Figure 4 from: Scheffrahn RH, Bourguignon T, Akama PD, Sillam-Dussès D, Šobotník J (2018) Roisinitermes ebogoensis gen. & sp. n., an outstanding drywood termite with snapping soldiers from Cameroon (Isoptera, Kalotermitidae). ZooKeys 787: 91-105. https://doi.org/10.3897/zookeys.787.28195
Figure 4 Soldier (holotype) of Roisinitermesebogoensis gen. & sp. n. Dorsal (A), lateral (B), and ventral (C) views of head and pronotum.
Figure 3 from: Scheffrahn RH, Roisin Y (2018) Anenteotermes cherubimi sp. n., a tiny dehiscent termite from Central Africa (Termitidae: Apicotermitinae). ZooKeys 793: 53-62. https://doi.org/10.3897/zookeys.793.28342
Figure 3 Gut of Anenteotermescherubimi sp. n. worker. A dorsal B right with area near mixed segment and mesenteric tongue (MT) torn (see Figure 1D) C ventral with position of enteric valve armature (EVA) and enteric valve seating (EVS) drawing superimposed to scale D left views. Abbreviations: C = crop, LD = dehiscence line; M = mesenteron; P1, P3, P4, and P5 = proctodeal segments.
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