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636 results for “LM”

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Figure 6 from: Cao LM, van Achterberg C, Tang YL, Yang ZQ, Wang XY, Cao TW (2020) Redescriptions of two parasitoids, Metapelma beijingense Yang (Hymenoptera, Eupelmidae) and Spathius ochus Nixon (Hymenoptera, Braconidae), parasitizing Coraebus cavifrons Descarpentries & Villiers (Coleoptera, Buprestidae) in China with keys to genera or species groups. ZooKeys 926: 53-72. https://doi.org/10.3897/zookeys.926.48688

Figure 6 Spathius ochus Nixon, ♀, China, Guizhou. A Habitus, lateral aspect B head, dorsal aspect C head, anterior aspect D antennae, lateral aspect E mesosoma, dorsal aspect.

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Figure 4 from: Cao LM, van Achterberg C, Tang YL, Yang ZQ, Wang XY, Cao TW (2020) Redescriptions of two parasitoids, Metapelma beijingense Yang (Hymenoptera, Eupelmidae) and Spathius ochus Nixon (Hymenoptera, Braconidae), parasitizing Coraebus cavifrons Descarpentries & Villiers (Coleoptera, Buprestidae) in China with keys to genera or species groups. ZooKeys 926: 53-72. https://doi.org/10.3897/zookeys.926.48688

Figure 4 Metapelma beijingenseYang, ♀, China, Guizhou. A Head and mesosoma, lateral aspect B metasoma, lateral aspect, C metasoma, dorsal aspect D mid and hind legs, lateral aspect E wings.

opencc-by-4.0Apr 2020View details →
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Figure 5 from: Cao LM, van Achterberg C, Tang YL, Yang ZQ, Wang XY, Cao TW (2020) Redescriptions of two parasitoids, Metapelma beijingense Yang (Hymenoptera, Eupelmidae) and Spathius ochus Nixon (Hymenoptera, Braconidae), parasitizing Coraebus cavifrons Descarpentries & Villiers (Coleoptera, Buprestidae) in China with keys to genera or species groups. ZooKeys 926: 53-72. https://doi.org/10.3897/zookeys.926.48688

Figure 5 Metapelma beijingense Yang, ♂, China, Guizhou. A Habitus, dorsal aspect B habitus, ventral aspect.

opencc-by-4.0Apr 2020View details →
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Figure 5 from: Bernard J, Lumley LM, Buck M, Cobb TP (2020) A new species of rake-legged mite, Caeculus cassiopeiae (Prostigmata, Caeculidae), from Canada and a systematic analysis of its genus. ZooKeys 926: 1-23. https://doi.org/10.3897/zookeys.926.48741

Figure 5 Caeculus cremnicolus, female. Micrograph of dorsal idiosoma, collected and slide mounted in 1978 by E.E. Lindquist. Scale bar: 0.5 mm.

opencc-by-4.0Apr 2020View details →
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Figure 2 from: Bernard J, Lumley LM, Buck M, Cobb TP (2020) A new species of rake-legged mite, Caeculus cassiopeiae (Prostigmata, Caeculidae), from Canada and a systematic analysis of its genus. ZooKeys 926: 1-23. https://doi.org/10.3897/zookeys.926.48741

Figure 2 Caeculus cassiopeiae sp. nov., female idiosoma A dorsum B venter; PG, progenital valve; AG, aggenital sclerite; AD, adanal sclerite; PS, pseudanal sclerite C detail of bs seta, exemplifying typical clavate idiosomal seta. Scale bar: 0.5 mm (A, B).

opencc-by-4.0Apr 2020View details →
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Figure 3 from: Cao LM, van Achterberg C, Tang YL, Yang ZQ, Wang XY, Cao TW (2020) Redescriptions of two parasitoids, Metapelma beijingense Yang (Hymenoptera, Eupelmidae) and Spathius ochus Nixon (Hymenoptera, Braconidae), parasitizing Coraebus cavifrons Descarpentries & Villiers (Coleoptera, Buprestidae) in China with keys to genera or species groups. ZooKeys 926: 53-72. https://doi.org/10.3897/zookeys.926.48688

Figure 3 Metapelma beijingense Yang, ♀, China, Guizhou. A Habitus, dorsal aspect B head, dorsal aspect C head, anterior aspect D antennae, lateral aspect E mesosoma, dorsal aspect.

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Figure 2 from: Cao LM, van Achterberg C, Tang YL, Yang ZQ, Wang XY, Cao TW (2020) Redescriptions of two parasitoids, Metapelma beijingense Yang (Hymenoptera, Eupelmidae) and Spathius ochus Nixon (Hymenoptera, Braconidae), parasitizing Coraebus cavifrons Descarpentries & Villiers (Coleoptera, Buprestidae) in China with keys to genera or species groups. ZooKeys 926: 53-72. https://doi.org/10.3897/zookeys.926.48688

Figure 2 A A mature pupa of Metapelma beijingense Yang, near the buprestid larva B a new pupa of M. beijingense Yang, with the buprestid larva C empty cocoons of Spathius ochus Nixon D pupa of M. beijingense Yang and cocoons of S. ochus Nixon showing synparasitism.

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Figure 1 from: Cao LM, van Achterberg C, Tang YL, Yang ZQ, Wang XY, Cao TW (2020) Redescriptions of two parasitoids, Metapelma beijingense Yang (Hymenoptera, Eupelmidae) and Spathius ochus Nixon (Hymenoptera, Braconidae), parasitizing Coraebus cavifrons Descarpentries & Villiers (Coleoptera, Buprestidae) in China with keys to genera or species groups. ZooKeys 926: 53-72. https://doi.org/10.3897/zookeys.926.48688

Figure 1 A Tree (Symplocos stellaris Brand) damaged by Coraebus cavifrons Descarpentries & Villiers B trunk damaged by C. cavifrons Descarpentries & Villiers C gallery of larvae D adult of C. cavifrons Descarpentries & Villiers E pupal chamber F larva of C. cavifrons Descarpentries & Villiers.

opencc-by-4.0Apr 2020View details →
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Figure 5 from: Magro A, Churata-Salcedo J, Lecompte E, Hemptinne J-L, Almeida LM (2020) A new species of Nephus (Nephus) (Coleoptera, Coccinellidae) described from Reunion Island. ZooKeys 962: 123-137. https://doi.org/10.3897/zookeys.962.51520

Figure 5 Nephus (Nephus) apolonia Magro & Almeida, sp. nov. A dorsal view B ventral view C lateral view D frontal view E, F abdomen G–J male genitalia: G, H penis I, J tegmen (dorsal and lateral view) K, L female genitalia: K spermatheca L coxites.

opencc-by-4.0Aug 2020View details →
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Figure 4 from: Magro A, Churata-Salcedo J, Lecompte E, Hemptinne J-L, Almeida LM (2020) A new species of Nephus (Nephus) (Coleoptera, Coccinellidae) described from Reunion Island. ZooKeys 962: 123-137. https://doi.org/10.3897/zookeys.962.51520

Figure 4 Nephus (Nephus) voeltzkowi Weise, 1910 A dorsal view B ventral view C lateral view D frontal view E abdomen F, G female genitalia: F coxites G spermatheca.

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Figure 3 from: Magro A, Churata-Salcedo J, Lecompte E, Hemptinne J-L, Almeida LM (2020) A new species of Nephus (Nephus) (Coleoptera, Coccinellidae) described from Reunion Island. ZooKeys 962: 123-137. https://doi.org/10.3897/zookeys.962.51520

Figure 3 Nephus (Geminosipho) reunioni (Fürsch, 1974) A dorsal view B ventral view C lateral view D frontal view E, F abdomen G–J male genitalia: tegmen (dorsal and lateral view): I, J penis K, L female genitalia: K spermatheca L coxites.

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Figure 2 from: Magro A, Churata-Salcedo J, Lecompte E, Hemptinne J-L, Almeida LM (2020) A new species of Nephus (Nephus) (Coleoptera, Coccinellidae) described from Reunion Island. ZooKeys 962: 123-137. https://doi.org/10.3897/zookeys.962.51520

Figure 2 Nephus (Nephus) oblongosignatus Mulsant, 1850 A dorsal view B ventral view C lateral view D frontal view E, F abdomen G–K male genitalia: G spicula H, I tegmen (dorsal and lateral view) J, K penis L, M female genitalia: L spermatheca M coxites.

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Figure 6 from: Magro A, Churata-Salcedo J, Lecompte E, Hemptinne J-L, Almeida LM (2020) A new species of Nephus (Nephus) (Coleoptera, Coccinellidae) described from Reunion Island. ZooKeys 962: 123-137. https://doi.org/10.3897/zookeys.962.51520

Figure 6 Maximum likelihood phylogeny of Nephus (Nephus) apolonia Magro & Almeida, sp. nov. and four related species based on the mitochondrial genome (without the control region) reconstructed through 1000 non-parametric bootstrap replicates. The scale bar indicates 0.04 substitutions per site. Numbers on major nodes represent Maximum Likelihood bootstrap support.

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Figure 1 from: Magro A, Churata-Salcedo J, Lecompte E, Hemptinne J-L, Almeida LM (2020) A new species of Nephus (Nephus) (Coleoptera, Coccinellidae) described from Reunion Island. ZooKeys 962: 123-137. https://doi.org/10.3897/zookeys.962.51520

Figure 1 Scanning electron microscopy A–D antennae E–H prosternal process I–L tarsi M–P abdominal postcoxal line A, E, I, MNephus (Nephus) oblongosignatus Mulsant, 1850 B, F, J, NNephus (Geminosipho) reunioni (Fürsch, 1974) C, G, K, ONephus (Nephus) voeltzkowi Weise, 1910 D, H, L, PNephus apolonia Magro & Almeida, sp. nov.

opencc-by-4.0Aug 2020View details →
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Figure 9 from: Santos APM, Dumas LL, Henriques-Oliveira AL, Souza WRM, Camargos LM, Calor AR, Pes AMO (2020) Taxonomic Catalog of the Brazilian Fauna: order Trichoptera (Insecta), diversity and distribution. Zoologia 37: 1-13. https://doi.org/10.3897/zoologia.37.e46392

Figure 9 Number of caddisfly species described or reported to Brazil by year (from 1833 to July 2019).

opencc-by-4.0Sep 2020View details →
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Figures 1-3 from: Santos APM, Dumas LL, Henriques-Oliveira AL, Souza WRM, Camargos LM, Calor AR, Pes AMO (2020) Taxonomic Catalog of the Brazilian Fauna: order Trichoptera (Insecta), diversity and distribution. Zoologia 37: 1-13. https://doi.org/10.3897/zoologia.37.e46392

Figures 1-3 Map of Brazil in South America showing: (1) the six continental biomes following IBGE (2004); (2) the twelve hydrographic regions in the country following ANA (2015); (3) the 26 states plus the Federal District. For each geographic unity, the respective number of caddisfly species, total and endemic, is provided.

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Figure 8 from: Santos APM, Dumas LL, Henriques-Oliveira AL, Souza WRM, Camargos LM, Calor AR, Pes AMO (2020) Taxonomic Catalog of the Brazilian Fauna: order Trichoptera (Insecta), diversity and distribution. Zoologia 37: 1-13. https://doi.org/10.3897/zoologia.37.e46392

Figure 8 Contribution of the ten most diverse caddisfly families to the total richness of Trichoptera in Brazil, in Atlantic Forest, and in Amazon Forest, respectively, indicating the proportion of endemic species for each family in each area.

opencc-by-4.0Sep 2020View details →
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Figures 4-7 from: Santos APM, Dumas LL, Henriques-Oliveira AL, Souza WRM, Camargos LM, Calor AR, Pes AMO (2020) Taxonomic Catalog of the Brazilian Fauna: order Trichoptera (Insecta), diversity and distribution. Zoologia 37: 1-13. https://doi.org/10.3897/zoologia.37.e46392

Figures 4-7 Adults of Brazilian caddisflies: (4) Macrostemum brasiliense (Fisher, 1970), the first caddisfly species described from Brazil, originally as Phryganea maculata Perty, 1833 (photo by FF Salles), Espirito Santo state; (5) Centromacronema auripenne (Rambur, 1842), a problematic taxon with several synonyms and in need of a taxonomic revision, Rio de Janeiro state; (6) Nectopsyche sp., an unidentified species of this diverse and poorly studied genus, Rio de Janeiro; (7) Marilia sp., an unidentified species of another genus in need of taxonomic revision, Amazonas.

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Figure 12 from: Santos APM, Dumas LL, Henriques-Oliveira AL, Souza WRM, Camargos LM, Calor AR, Pes AMO (2020) Taxonomic Catalog of the Brazilian Fauna: order Trichoptera (Insecta), diversity and distribution. Zoologia 37: 1-13. https://doi.org/10.3897/zoologia.37.e46392

Figure 12 Unweighted pair-group average (UPGMA) dendrogram based on Jaccard dissimilarity index of the incidence data of Trichoptera in Brazilian hydrographic regions. Species recorded only in one region were removed from the analysis. Values near branches are bootstrap analyses with 10,000 pseudoreplicates. Dendrogram and bootstrap values were calculated in software PAST.

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Figures 10-11 from: Santos APM, Dumas LL, Henriques-Oliveira AL, Souza WRM, Camargos LM, Calor AR, Pes AMO (2020) Taxonomic Catalog of the Brazilian Fauna: order Trichoptera (Insecta), diversity and distribution. Zoologia 37: 1-13. https://doi.org/10.3897/zoologia.37.e46392

Figures 10-11 Accumulation curves of caddisfly species described or reported to occur in Brazil by year (from 1833 to July 2019): (10) total; (11) considering the citizenship of the first author of the species name.

opencc-by-4.0Sep 2020View details →

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dandi-nwb
electrophysiologyopenPublished Dandiset metadata and archive endpoints are available through the production DANDI API.
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International Brain Laboratory public data

The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.

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