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218 results for “Aculeata”
Figure 4 in Contribution to the knowledge of the Chrysididae (Hymenoptera, Aculeata) in the south of Iran, with nine new records
Figure 4. Hedychridium femoratum (Dahlbom, 1854): A) head, frontal view; B) head, lateral view; C) head, dorsal view; D) mesosoma, dorsal view; E) metasoma, dorsal view.
Figure 2 in Contribution to the knowledge of the Chrysididae (Hymenoptera, Aculeata) in the south of Iran, with nine new records
Figure 2. Hedychridium virescens (du Buysson, 1908): A) head, frontal view; B) head, lateral view; C) head, dorsal view; D) mesosoma, dorsal view; E) metasoma, dorsal view; F) metasoma, lateral view.
Figure 1 in Contribution to the knowledge of the Chrysididae (Hymenoptera, Aculeata) in the south of Iran, with nine new records
Figure 1. Southern Iran, Hormozgan Province, where the specimens were collected: A) Zakin, B) Faryab, C) Tezerj, D) Chelo.
Figure 3. Hedychridium verhoeffi Linsenmaier, 1959 in Contribution to the knowledge of the Chrysididae (Hymenoptera, Aculeata) in the south of Iran, with nine new records
Figure 3. Hedychridium verhoeffi Linsenmaier, 1959: A) head, frontal view; B) head, lateral view; C) head, dorsal view; D) mesosoma, dorsal view; E) metasoma, dorsal view.
Fig. 1 in Mutillidae (Hymenoptera, Aculeata) do estado de Mato Grosso do Sul, Brasil
Fig. 1. Mapa com as localidades de coleta das espécies de Mutillidae registradas para o estado de Mato Grosso do Sul neste estudo (Na, AnastÁcio; Aq, Aquidauana; Ba, BataYporã; BEP, Base de Estudo do Pantanal (UFMS); C, CorumbÁ; CG, Campo Grande; Cox, Coxim; D, Dourados; I, Ivinhema; Ma, Maracaju; Mir, Miranda; NA, Nova Andradina; NH, Fazenda Nhumirim (Embrapa Pantanal); PM, Porto Murtinho; RB, Rio Brilhante; SB, Serra da Bodoquena; Sel, Selvíria; Sid, Sidrolândia; TL, Três Lagoas).
Figs 6-14 in Tiphiidae (Hymenoptera, Aculeata) of Turkey
Figs 6-14: Tiphia bahattini nov.sp. Paratypus 3: (6) head and pronotum, dorsal aspect; (7) head, frontal spect; (8) metasternum; (9) sensorial area of hindfemur; (10) 5 th sternum, particular; (11) gonostylus and volsella, ¾ inner lateral aspect; (12) Gonostylus and volsella, inner lateral aspect. Tiphia persica 3: (13) metasternum5 th; (14) sternum, particular. (6, 7, 8, 13: scale bar = 1 mm) (9, 10, 11, 12, 14: scale bar = 0.5 mm).
Figs 1-5 in Tiphiidae (Hymenoptera, Aculeata) of Turkey
Figs 1-5: Tiphia bahattini nov.sp. Holotypus ♀: (1) head, frontal aspect; (2) mesosoma, dorsal aspect; (3) metasternum; (4) hindfemur. Tiphia persica Lectotypus ♀: (5) metasternum. (1, 3, 4, 5: scale bar = 1mm; 2: Scale bar = 2mm).
Abb. 1 in Die Stechimmenfauna (Hymenoptera Aculeata) im Naturpark Tiroler Lech in Österreich
Abb. 1: Lage der Fundstellen im Tiroler Lechtal bei Reutte: 1 = Weisshaus, 2 = Pinswang, 3 = Forchach/Schotterwerk, 4 = Forchach, 5 = Namlos.
Abb. 3 in Die Stechimmenfauna (Hymenoptera Aculeata) im Naturpark Tiroler Lech in Österreich
Abb. 3: Celonites abbreviatus, hier ein Männchen, ist eine in Südeuropa weit verbreitete Honigwespenart, die nördlich der Alpen nur sehr punktuell auftritt. Foto H. Bellmann.
Abb. 2 in Die Stechimmenfauna (Hymenoptera Aculeata) im Naturpark Tiroler Lech in Österreich
Abb. 2: Die parasitische Grabwespe Nysson ganglbaueri, hier ein Weibchen, ist ausschliesslich alpin verbreitet und wird sehr selten gefunden.
Abb. 3 in Mitteleuropäische Wälder als Primärlebensraum von Stechimmen (Hymenoptera, Aculeata)
Abb. 3: Verteilung von Wildbienen und Wespen im Jahresverlauf aus dem NSG Wulsenberg (KUHLMANN 1998).
Abb. 2 in Mitteleuropäische Wälder als Primärlebensraum von Stechimmen (Hymenoptera, Aculeata)
Abb. 2: Verteilung von Wildbienen und Wespen im Jahresverlauf in Bernwood (England) von 1980 bis 1982 (verändert nach Archer 1988: 26).
Fig. 4 in Overview of the Distribution and Biogeography of Tiphiidae (Hymenoptera: Aculeata) in Turkey
Fig. 4: Ordination of the seven biogeographical regions of Turkey in the reduced space of the first two principal coordinates for 20 species of Tiphiidae. (Dice, r = 0.86). For names of regions see Figure 3.
Figure 6. Holothuria aculeata Semper, 1868, holotype. A in Taxonomy of the heavily exploited Indo-Pacific sandfish complex (Echinodermata: Holothuriidae)
Figure 6. Holothuria aculeata Semper, 1868, holotype. A, tables of dorsal body wall; B, large table of dorsal body wall; C, buttons of dorsal body wall; D, table of dorsal papillae; E, perforated plates of dorsal papillae; F, rods of the dorsal papillae; G, buttons of dorsal papillae; H, table of ventral body wall; J, buttons of ventral body wall; K, table of ventral tube foot; L, buttons of ventral tube feet; M, perforated plates and rods of ventral tube feet. Scale bars: A–M = 50 Mm.
Figure 3 in The Chrysidoidea Wasps (Hymenoptera, Aculeata) in Conventional Coffee Crops and Agroforestry Systems in Southeastern Brazil
Figure 3. Venn diagram showing exclusive and shared genera of Chrysidoidea among conventional, agroforestry and transitional systems in the "Pontal do Paranapanema" region, São Paulo, Brazil. Bethylidae in blue, Chrysididae in red and Dryinidae in green color.
Figure 2 in The Chrysidoidea Wasps (Hymenoptera, Aculeata) in Conventional Coffee Crops and Agroforestry Systems in Southeastern Brazil
Figure 2. Malaise trap (Townes model) installed in the conventional system (S.J.F. – Conv.), in the "Pontal do Paranapanema" region, São Paulo, Brazil.
Figure 1 in The Chrysidoidea Wasps (Hymenoptera, Aculeata) in Conventional Coffee Crops and Agroforestry Systems in Southeastern Brazil
Figure 1. Map showing the collection sites of Chrysidoidea wasps in the conventional, agroforestry and transitional systems in the "Pontal do Paranapanema" area, state of São Paulo, Brazil. The different colored squares represent: S.A. - Conv. (red); S.J.F. - Conv. (green); S.F.- SAF (yellow), S.J.M. - SAF (blue); S.S. - SAF (white); S.M.-Trans. (light blue).
Using a coalescent approach to assess gene flow and effective population size of Acrocomia aculeata (Jacq.) Lodd. Ex Mart. in the Brazilian Atlantic Forest
<p><i>Acrocomia aculeata</i> is a tropical palm tree native to Central and South America that has significant economic, social, and environmental potential. However, land encroachment due to the expansion of agribusiness, and other factors such as urban sprawl, have resulted in the fragmentation and destruction of its habitat, leading to the loss of genes and genotypes in <i>A. aculeata</i> populations. In this context, the objective of this study was to characterize the genetic variability of <i>A. aculeata</i> populations by estimating gene flow and effective population size using an approach based on coalescent theory. Four populations located in the municipalities of Teodoro Sampaio (TSI and TSII), Rosana (RA), and Amparo (AP) in São Paulo State, Brazil, were genotyped with nine microsatellite markers. Gene flow and effective population size were estimated using a coalescent-based Bayesian inference implemented in the MIGRATE-N software. The effective population size (<i>N<sub>e</sub></i>) was obtained considering an assumed mutation rate of <a name="_Hlk6565387">5x10<sup>-5</sup>. </a>Gene flow (<i>Nm</i>) for pairwise populations ranged from 0.28 to 1.17, with higher levels of migration between the three geographically proximal locations (TSI, TSII, and RA). The estimates of effective population size (<i>N<sub>e</sub></i>) were 444, 835, 838, and 874 for AP, TSII, RA, and TSI, respectively, showing that the effects caused by genetic drift may be more pronounced when <i>N<sub>e</sub></i> is smaller. The coalescent-based results add to our understanding of <i>A. aculeata</i> population genetics and suggest that some traditional assessment methods may be ineffective in characterizing historical evolutionary processes.</p>
FIGURE 1 in Trap-nesting bees and wasps (Hymenoptera, Aculeata) in a Semidecidual Seasonal Forest fragment, southern Brazil
FIGURE 1: Trap nests installed on Parque Estadual São Camilo.
Fig. 5 in Protocol for collecting Mutillidae (Hymenoptera, Aculeata) in ecological studies: species-area effects on Mutillidae communities
Fig. 5. Direct ordering analysis of Mutillidae community in relation to the sample area gradient.
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