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88 results for “Erythraeus”
Figure 5 in New host detection of the parasitic mite, Erythraeus pistacicus (Trombidiformes: Erythraeidae) from Iran and indication of possible infection with bacterial symbionts
Figure 5. Phylogenetic tree based on 16S rRNA sequences of Cardinium, constructed by a neighbor-joining procedure. Cardinium strains are depicted by the host name. The accession numbers are shown after the host name. Numbers on the nodes indicate bootstrap percent confidence values.
Figure 2 in New host detection of the parasitic mite, Erythraeus pistacicus (Trombidiformes: Erythraeidae) from Iran and indication of possible infection with bacterial symbionts
Figure 2. Neighbor-joining tree of COI sequences of the Erythraeidae mites of the present study and the Genbank sequence data. Numbers above/below nodes represent bootstrap values.
Figure 1 in New host detection of the parasitic mite, Erythraeus pistacicus (Trombidiformes: Erythraeidae) from Iran and indication of possible infection with bacterial symbionts
Figure 1. Erythraeus (Erythraeus) pistacicus Haitlinger, Mehrnejad & Šundić, 2016 larva (Black arrow)inside the gall, feeding on the aphid, Forda hirsuta Mordvilko, 1928, on pistachio trees. June 2022, Mashhad, Northeast of Iran.
Figure 7 in New host detection of the parasitic mite, Erythraeus pistacicus (Trombidiformes: Erythraeidae) from Iran and indication of possible infection with bacterial symbionts
Figure 7. Phylogenetic relationship of Planomicrobium symbiont identified from Erythraeus (Erythraeus) pistacicus with related sequences retrieved from GenBank. The tree was constructed using neighbor-joining procedure. The sequence obtained from E. (E.) pistacicus in this study is in red box. Sequence from Bacillus subtilis was used as an
Fig. 14 Erythraeus regalis, larva. a in Towards resolving the double classification in Erythraeus (Actinotrichida: Erythraeidae): matching larvae with adults using 28S sequence data and experimental rearing
Fig. 14 Erythraeus regalis, larva. a Gnathosoma and idiosoma, dorsal view. b Dorsal opisthosomal seta. c Gnathosoma and idiosoma, ventral view
Fig. 11 Erythraeus cinereus, larva. a Leg I. b Leg II. c Leg III. d Tarsus I. e Tarsus II in Towards resolving the double classification in Erythraeus (Actinotrichida: Erythraeidae): matching larvae with adults using 28S sequence data and experimental rearing
Fig. 11 Erythraeus cinereus, larva. a Leg I. b Leg II. c Leg III. d Tarsus I. e Tarsus II (d, e, only specialized setae shown)
Fig. 9 Erythraeus cinereus, larva. a Chelicera. b in Towards resolving the double classification in Erythraeus (Actinotrichida: Erythraeidae): matching larvae with adults using 28S sequence data and experimental rearing
Fig. 9 Erythraeus cinereus, larva. a Chelicera. b Gnathosoma (and scutum), dorsal view. c Gnathosoma, ventral view. d Palp tibia. e Palp tarsus
Fig. 8 Erythraeus cinereus, adult. a Palp, medial view. b Crista metopica and eyes. c Dorsal opisthosomal setae. d in Towards resolving the double classification in Erythraeus (Actinotrichida: Erythraeidae): matching larvae with adults using 28S sequence data and experimental rearing
Fig. 8 Erythraeus cinereus, adult. a Palp, medial view. b Crista metopica and eyes. c Dorsal opisthosomal setae. d Serratala on genu I. e Serratala on genu IV. f Diversity of serratalae and setae of non-serratalae type on telofemora, genua, and tibiae of legs I–IV
Fig. 6 Erythraeus phalangoides, larva. a in Towards resolving the double classification in Erythraeus (Actinotrichida: Erythraeidae): matching larvae with adults using 28S sequence data and experimental rearing
Fig. 6 Erythraeus phalangoides, larva. a Gnathosoma and idiosoma, dorsal view. b Dorsal opisthosomal setae. c Gnathosoma and idiosoma, ventral view. d Seta ps
Fig. 10 Erythraeus cinereus, larva. a in Towards resolving the double classification in Erythraeus (Actinotrichida: Erythraeidae): matching larvae with adults using 28S sequence data and experimental rearing
Fig. 10 Erythraeus cinereus, larva. a Gnathosoma and idiosoma, dorsal view. b Dorsal opisthosomal setae. c Gnathosoma and idiosoma, ventral view. d Seta ps
Fig. 12 Erythraeus regalis, adult. a Palp, medial view. b Crista metopica and eyes. c Dorsal opisthosomal setae. d in Towards resolving the double classification in Erythraeus (Actinotrichida: Erythraeidae): matching larvae with adults using 28S sequence data and experimental rearing
Fig. 12 Erythraeus regalis, adult. a Palp, medial view. b Crista metopica and eyes. c Dorsal opisthosomal setae. d Serratala on genu I. e Serratala on genu IV. f Diversity of serratalae and setae of non-serratalae type on telofemora, genua, and tibiae of legs I–IV
Fig. 16 Erythraeus regalis, larva. a Leg I. b Leg II. c Leg III. d Genu-tarsus I. e Genu-tarsus II in Towards resolving the double classification in Erythraeus (Actinotrichida: Erythraeidae): matching larvae with adults using 28S sequence data and experimental rearing
Fig. 16 Erythraeus regalis, larva. a Leg I. b Leg II. c Leg III. d Genu-tarsus I. e Genu-tarsus II. Tibia-tarsus III (d–f, only specialized setae shown)
Fig. 7 Erythraeus phalangoides, larva. a Leg I. b Leg II. c Leg III. d Tarsus I. e Tarsus II. f in Towards resolving the double classification in Erythraeus (Actinotrichida: Erythraeidae): matching larvae with adults using 28S sequence data and experimental rearing
Fig. 7 Erythraeus phalangoides, larva. a Leg I. b Leg II. c Leg III. d Tarsus I. e Tarsus II. f Tarsus III (d–f, only specialized setae shown)
Fig. 5 Erythraeus phalangoides, larva. a in Towards resolving the double classification in Erythraeus (Actinotrichida: Erythraeidae): matching larvae with adults using 28S sequence data and experimental rearing
Fig. 5 Erythraeus phalangoides, larva. a Gnathosoma (and scutum), dorsal view. b Odontus. c Gnathosoma, ventral view. d Palp tarsus
Mandible morphology as a tool to investigate origin, adaptation and stress in invasive alien species. First insights into Callosciurus erythraeus in Europe
<p>When an alien species is introduced in a new area, the number of founding individuals affects the severity of the population bottleneck, hence the new population may be distinctively different, both genetically and phenotypically, from the parent population from which it is derived. In this study we investigated the variation in shape and size of the mandible among and within three populations of the invasive Pallas’s squirrel, a tree squirrel native to SE Asia and introduced in Italy, Belgium and France. Significant differences in both size and shape of the mandible were found among all population pairs, with France being the most distinct. French squirrels showed a larger and slender mandible with a broad angular process, a restricted condyle, and a backward-oriented coronoid process. The Italian and the Belgian population differ at a lesser extent, the Italian squirrels having a lower coronoid process, a broader angular apophysis, and a restricted condyle. s. Size explained 15% of the total shape variation, but the orientation of allometric trajectories did not reveal any significant difference among populations. French squirrels showed the highest fluctuating asymmetry (both size and shape) of the right versus the left mandible, the Italians the highest directional asymmetry. Results are discussed in terms of different selective pressures in the invaded areas related to functionally mastication, and possible factors affecting fluctuating and directional asymmetry. The hypothesis of the classic mandibular two-module organization of rodent mandible (alveolar region vs ascending ramus) was confirmed both before and after correcting for size.</p>
Figure 1 in Two new records of dragonet fish, Callionymus sagitta Pallas, 1770 and Callionymus erythraeus Ninni, 1934 from Bangladesh
Figure 1. (★) Sampling location of Callionymus sagitta (F1612sb-184) and (▼) sampling location of Callionymus erythraeus (F1710SM-03).
Fig. 1 in Spillover and spillback risks of ectoparasites by an invasive squirrel Callosciurus erythraeus in Kanto region of Japan
Fig. 1. Location map of the study areas. The Pallas's squirrels examined in this study were collected by extermination programs operated by the local governments of Yokohama and Yokosuka. Detailed information on the sampling localities is refrained due to the intension of the cooperative organizations.
Fig. 3. NMDS plot for the parasite infracommunity composition recovered from 52 in Spillover and spillback risks of ectoparasites by an invasive squirrel Callosciurus erythraeus in Kanto region of Japan
Fig. 3. NMDS plot for the parasite infracommunity composition recovered from 52 host individuals. The influence of each parasite's abundance by discriminating the developmental stage on the score components of the two axes is represented by broken lines. The relationships with environmental variables are indicated by gray arrows. Abbreviations are as follows: M: male, F: female, YH: Yokohama, YS: Yokosuka, HfN: nymph of Haemaphysalis flava, HfL: larva of H. flava, Lep: larva of Leptotrombidium spp., EkA: adult of Enderleinellus kumadai, EkL: larva of E. kumadai, NoA: adult of Neohaematopinus callosciuri, NoL: larva of N. callosciuri, Ca: Ceratophyllus anisus, Ci: Ceratophyllus indages indages.
Figure 6 in New host detection of the parasitic mite, Erythraeus pistacicus (Trombidiformes: Erythraeidae) from Iran and indication of possible infection with bacterial symbionts
Figure 6. Haplotype network of Cardinium endosymbionts based on 16S rDNA sequences.
Figure 4 in New host detection of the parasitic mite, Erythraeus pistacicus (Trombidiformes: Erythraeidae) from Iran and indication of possible infection with bacterial symbionts
Figure 4. Haplotype network of Wolbachia endosymbionts based on wsp gene.
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