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78 results for “Pipistrellus pipistrellus”

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FIGURE 6 in Systematics and taxonomy of Pipistrellus kuhlii (Kuhl, 1817) in Central Europe and the Balkans

FIGURE 6. Bayesian phylogram tree for combined mitochondrial data. Two haplotypes obtained in this study (H1 and H2) were put together in consensus tree with haplotypes available from GenBank (accession numbers are given) for Pipistrellus kuhlii s. l. Posterior probabilities are given for each clade.

opennotspecifiedDec 2017View details →
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FIGURE 2 in Systematics and taxonomy of Pipistrellus kuhlii (Kuhl, 1817) in Central Europe and the Balkans

FIGURE 2. Orange penis coloration of P. k. lepidus, Przemyśl, Poland (A) and pinkish-brown penis coloration of P. k. kuhlii, Drenovë, Albania (B) (photos: K. Sachanowicz).

opennotspecifiedDec 2017View details →
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Distribution. Madeira Archipelago (Madeira and Porto Santo) and W Canary Is (La Palma, La Gomera, El Hierro, and Tenerife). Individuals classified as Pipistrellus sp. from the Azores have been suggested to be Madeira Pipistrelles. in Vespertilionidae

Distribution. Madeira Archipelago (Madeira and Porto Santo) and W Canary Is (La Palma, La Gomera, El Hierro, and Tenerife). Individuals classified as Pipistrellus sp. from the Azores have been suggested to be Madeira Pipistrelles.

opennotspecifiedOct 2019View details →
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Fig. 6 in Unusual Pipistrelle: Taxonomic Position of the Malayan Noctule (Pipistrellus stenopterus; Vespertilionidae; Chiroptera)

Fig. 6. Penial bones (baculum) of selected Vespertilionine species: 1, Pipistrellus abramus (ZMMU n/n, Vietnam). 2, Glischropus bucephalus (ZMMU S-184658). 3, Pipistrellus nathusii (ZMMU S-183034). 4, Hypsugo joffrei (ZMMU S-186691). 5, P. stenopterus (ZMMU S-103149). 6, P. coromandra (ZMMU S-184690). 7, Nyctalus noctula (ZMMU S-180228). 8, Philetor brachypterus. 9, Scotozous dormeri. 10, H. pulveratus. 1-7, original drawings; dorsal, lateral and ventral views. 8-10, after Hill & Harrison, 1987, dorsal and lateral views. Scale bar = 3 mm.

opennotspecifiedDec 2018View details →
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Fig. 4 in Unusual Pipistrelle: Taxonomic Position of the Malayan Noctule (Pipistrellus stenopterus; Vespertilionidae; Chiroptera)

Fig. 4. Scatter plot of the two first Principal Components, calculated for 43 species of Pipistrellus, Nyctalus, Glischropus, Scotozous, Philetor, Hypsugo, Tylonycteris, Falsistrellus and Arielulus (322 specimens, including 17 P. stenopterus) based on 22 skull measurements. PC I (28.54% of total variance) have high correlations with C and CC; PC II (19.46%) – with BCW, ZW and POC. Genotyped specimen of P. stenopterus is marked by asterisk.

opennotspecifiedDec 2018View details →
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Fig. 5 in Unusual Pipistrelle: Taxonomic Position of the Malayan Noctule (Pipistrellus stenopterus; Vespertilionidae; Chiroptera)

Fig. 5. Skull features of Pipistrellus stenopterus: (A) general skull shape; (B) mandible shape in lateral view of P. stenopterus (ZMMU S-103149; B1) and Nyctalus (N. plancyi ZMMU S-164496; B2); (C) upper incisors and canine in lateral view of (C1) Philetor brachypterus (ROM MAM 113087) and (C2) P. stenopterus (ROM MAM 41436).

opennotspecifiedDec 2018View details →
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Fig. 2 in Unusual Pipistrelle: Taxonomic Position of the Malayan Noctule (Pipistrellus stenopterus; Vespertilionidae; Chiroptera)

Fig. 2. Phylogenetic ML tree reconstructed from alignment of the mitochondrial gene cytb. Numbers on tree nodes indicate bootstrap values (BS) and posterior probabilities (PP) for ML/BI, respectively.

opennotspecifiedDec 2018View details →
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Fig. 1 in Unusual Pipistrelle: Taxonomic Position of the Malayan Noctule (Pipistrellus stenopterus; Vespertilionidae; Chiroptera)

Fig. 1. Phylogenetic ML tree reconstructed from alignment of the mitochondrial gene COI. Numbers on tree nodes indicate bootstrap values (BS) and posterior probabilities (PP) for ML/BI, respectively.

opennotspecifiedDec 2018View details →
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Fig. 3 in Unusual Pipistrelle: Taxonomic Position of the Malayan Noctule (Pipistrellus stenopterus; Vespertilionidae; Chiroptera)

Fig. 3. Phylogenetic ML tree reconstructed from alignment of the nuclear gene RAG-2. Numbers on tree nodes indicate bootstrap values (BS) and posterior probabilities (PP) for ML/BI, respectively. © 2018 Academia Sinica, Taiwan

opennotspecifiedDec 2018View details →
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FIG. 4 in Small scale habitat preferences of Myotis daubentonii, Pipistrellus pipistrellus, and potential aerial prey in an upland river valley

FIG. 4. Relationship between aerial insect number (pooled for altitude and all habitat types) with air temperature (r² = 0.092)

opennotspecifiedNov 2017View details →
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F. 7 in Small scale habitat preferences of Myotis daubentonii, Pipistrellus pipistrellus, and potential aerial prey in an upland river valley

F. 7. Bat activity expressed as 0 ± SD bat passes hr-1 in relation to habitat type (water state) of both M. daubentonii and IG P. pipistrellus, pooled for all four altitudes

opennotspecifiedNov 2017View details →
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FIG. 6 in Small scale habitat preferences of Myotis daubentonii, Pipistrellus pipistrellus, and potential aerial prey in an upland river valley

FIG. 6. Percentage of most prevalent aerial insects found during the 40 nights of sweep net sampling along river Wharfe. Samples been pooled for altitude and habitat type. Insect families represented by <0.1 % not shown

opennotspecifiedNov 2017View details →
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FIG. 3 in Small scale habitat preferences of Myotis daubentonii, Pipistrellus pipistrellus, and potential aerial prey in an upland river valley

FIG. 3. Mean ± SD of number of aerial insects caught with sweep net above water surface (and over grass = control), pooled for all four altitudes (n = 40 nights)

opennotspecifiedNov 2017View details →
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FIG. 5 in Small scale habitat preferences of Myotis daubentonii, Pipistrellus pipistrellus, and potential aerial prey in an upland river valley

FIG. 5. Relationship between numbers of aerial insects caught with a sweep net (pooled for all altitudes and habitat types) above the water surface with minimum wind speed

opennotspecifiedNov 2017View details →
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FIG. 2 in Small scale habitat preferences of Myotis daubentonii, Pipistrellus pipistrellus, and potential aerial prey in an upland river valley

FIG. 2. Wind direction (degrees) expressed as windroses at for 10 nights from highest (a) to lowest (d) altitudes along river Wharfe

opennotspecifiedNov 2017View details →
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Figure 1 in Bats can migrate farther than it was previously known: a new longest migration record by Nathusius' pipistrelle Pipistrellus nathusii (Chiroptera: Vespertilionidae)

Figure 1: Long-distance movement of a Nathusius' pipistrelle Pipistrellus nathusii from Borok (Russia) to Lully (France).

opennotspecifiedApr 2022View details →
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Figure 2 in First record of a Nathusius' pipistrelle (Pipistrellus nathusii) overwintering at a latitude above 60 N

Figure 2: Known breeding colonies (round symbols) and overwintering site (square symbol) of Pipistrellus nathusii in Finland.

opennotspecifiedAug 2020View details →
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Figure 1 in First record of a Nathusius' pipistrelle (Pipistrellus nathusii) overwintering at a latitude above 60 N

Figure 1: Sonogram of Pipistrellus nathusii calls recorded at Härmälä cleft (Finland) on February 15, 2019.

opennotspecifiedAug 2020View details →
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Data from: Habitat usage of Daubenton's bat (Myotis daubentonii), common pipistrelle (Pipistrellus pipistrellus), and soprano pipistrelle (Pipistrellus pygmaeus) in a North Wales upland river catchment

Open the record for dataset details and reuse information.

publicMay 2019View details →
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Data from: Managing conflict between bats and humans: the response of soprano pipistrelles (Pipistrellus pygmaeus) to exclusion from roosts in houses

Open the record for dataset details and reuse information.

publicJul 2016View details →

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International Brain Laboratory public data

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