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78 results for “Pipistrellus pipistrellus”
Fig. 47. Distribution maps. A–B. Pipistrellus nanulus Thomas, 1904. C–D in The bats of the Congo and of Rwanda and Burundi revisited (Mammalia: Chiroptera)
Fig. 47. Distribution maps. A–B. Pipistrellus nanulus Thomas, 1904. C–D. Pipistrellus rueppellii (Fischer, 1826). E–F. Scotoecus albofuscus (Thomas, 1890). A, C, E. Distribution in the CRB area. B, D, F. Pan-African distribution.
Figure 3 in The first record of Scotozous dormeri Dobson, 1875 from Nepal with new locality records of Pipistrellus coromandra (Gray, 1838) and P. tenuis (Temminck, 1840) (Chiroptera: Vespertilionidae)
Figure 3. Dorsal (d) and lateral (l) views of the bacula of Pipistrellus coromandra (CDZ TU_BAT 022) and Pipistrellus tenuis (CDZ TU_BAT 021).
Figure 2. Koshi Tappu W.R in The first record of Scotozous dormeri Dobson, 1875 from Nepal with new locality records of Pipistrellus coromandra (Gray, 1838) and P. tenuis (Temminck, 1840) (Chiroptera: Vespertilionidae)
Figure 2. Koshi Tappu W.R. and buffer zone. Black dots indicate the following localities: 1 - Kusaha; 2 - Goithi Tole; 3 - Samsul Tole.
Figure 1 in The first record of Scotozous dormeri Dobson, 1875 from Nepal with new locality records of Pipistrellus coromandra (Gray, 1838) and P. tenuis (Temminck, 1840) (Chiroptera: Vespertilionidae)
Figure 1. Map of Nepal showing the location of Koshi Tappu WR (K.T.) and Royal Bardia NP (R.B.) and the delineation within the country's borders of the terrestrial ecoregions, Terai-Duar Savanna and Grasslands (area shaded dark grey) and Himalayan subtropical broadleaf forests (area shaded light grey). The area within the black box is depicted in greater detail in Fig. 2.
Figure 3. The phylogenetic relationship between G in The Complete Mitochondrial Genome of Glischropus bucephalus (Vespertilionidae; Chiroptera) Provides New Evidence for Pipistrellus Paraphyly
Figure 3. The phylogenetic relationship between G. bucephalus and the other Pipistrellini species is inferred by maximum likelihood analysis based on cytb sequences. The numbers in the branches show the bootstrap values. Vespertilio species are used as outgroups.
Figure 1 in The Complete Mitochondrial Genome of Glischropus bucephalus (Vespertilionidae; Chiroptera) Provides New Evidence for Pipistrellus Paraphyly
Figure 1. Map of the G. bucephalus mitogenome. Gray color indicates the PCG regions; red color— tRNAs; yellow color—rRNAs. The heavy strand in the outer circle encodes 28 genes, whereas 9 genes are encoded in the light strand in the inner circle.
Figure 2. The phylogenetic relationship between G in The Complete Mitochondrial Genome of Glischropus bucephalus (Vespertilionidae; Chiroptera) Provides New Evidence for Pipistrellus Paraphyly
Figure 2. The phylogenetic relationship between G. bucephalus and the other Vespertilioninae species is inferred by the maximum likelihood analysis based on the concatenated protein-coding gene sequences. The bootstrap values (indicated by the slashes on the branches) correspond to the trees constructed on full sequences (three codon positions), the first two codon positions (third positions omitted), and two positions with the exclusion of the Nd6 gene. The asterisks mark branches that in the second or third case have a different topology than shown. Myotis species are used as outgroups.
Fig. 3 in Acoustic Discrimination Of Pipistrellus Kuhlii And Pipistrellus Nathusii (Chiroptera: Vespertilionidae) And Its Application To Assess Changes In Species Distribution
Fig. 3. Bar graph about the number of settlements where P. kuhlii and P. nathusii occurred or were absent in case of the two studied areas, from North and South Hungary
Fig. 2 in Acoustic Discrimination Of Pipistrellus Kuhlii And Pipistrellus Nathusii (Chiroptera: Vespertilionidae) And Its Application To Assess Changes In Species Distribution
Fig. 2. Occurrences of the two species in the two studied areas from North and South Hungary. (open circle = none of the species found, black square = P. nathusii, black triangle = P. kuhlii, black circle =
Fig. 1 in Acoustic Discrimination Of Pipistrellus Kuhlii And Pipistrellus Nathusii (Chiroptera: Vespertilionidae) And Its Application To Assess Changes In Species Distribution
Fig. 1. The distribution of the canonical scores between P. kuhlii and P. nathusii resulted from the discriminant function analysis based on 5 call parameters
Figure 2 in Unusual finding of chewing louse Quadraceps cf. junceus (Scopoli, 1763) (Phthiraptera: Ischnocera) on Nathusius pipistrelle Pipistrellus nathusii (Keyserling & Blasius, 1839) (Mammalia: Chiroptera) with review of findings of lice reported from bats
Figure 2. Lice of genus Quadraceps parasitizing birds of the genus Tringa: A. Q. furvus; B. Q. junceus; C. Q. obscurus; D. Q. obtusus; E. Q. ochropi; F. Q. similis (Sychra, own data).
Figure 4. Small mammals recorded from Farasan Archipelago. A. Rhinopoma cystops. B. Asellia patrizii. C. Pipistrellus kuhlii. D. Acomys dimidiatus E. Rattus rattus. F in Small mammals from Farasan Archipelago, Saudi Arabia
Figure 4. Small mammals recorded from Farasan Archipelago. A. Rhinopoma cystops. B. Asellia patrizii. C. Pipistrellus kuhlii. D. Acomys dimidiatus E. Rattus rattus. F. Gerbillus nanus.
Trace metals (Cd, Cu, Pb and Zn) concentrations in tissues of Pipistrellus kuhlii from NE Ukraine
<p>The dataset contains information on level of cadmium (Cd), copper (Cu), lead (Pd) and zinc (Zn) in internal and external tissues of <em>Pipistrellus kuhlii </em>from industrial (Mariupol city) and agricultural (Karlovka village). Bats were taken for analysis from Ukrainian Bat Rehabilitation Centre (Kharkiv, Ukraine) in 2021. </p>
Trace metals (Cd, Cu, Pb and Zn) concentrations in tissues of Pipistrellus kuhlii lepidus with identified age from unpolluted area - Karlovka village NE Ukraine
<div> <p>The dataset contains information on level of cadmium (Cd), copper (Cu), lead (Pd) and zinc (Zn) in internal and external tissues of <em>Pipistrellus kuhlii lepidus </em>from agricultural area (Karlovka village). Bats were taken for analysis from Ukrainian Bat Rehabilitation Centre (Kharkiv, Ukraine) in 2021-2022. In addition, age of each individual was identified using osteochronological technique. </p> <p> </p> </div>
Temporal mismatches in flight activity patterns between Pipistrellus kuhlii and Prays oleae in Mediterranean olive farms: Implications for biocontrol services potential
<ol> <li>Biocontrol services are widely recognized as providing key incentives for bat conservation. However, we have virtually no information on whether and how disruptions in bat-mediated biocontrol services are driven by mismatches between the temporal activity patterns of insectivorous bats and insect pests.</li> <li>2. We investigated the temporal relationship between the nightly activity patterns of the common pipistrelle bat (<em>Pipistrellus</em> <em>kuhlii</em>) and the olive fruit moth (<em>Prays</em> <em>oleae</em>). Temporal mismatches between species pairs were estimated as the time difference (expressed as a percentage of the night) at which <em>P. kuhlii </em>and<em> P. oleae</em> reached 50% of their abundance.</li> <li>The study was carried out during spring, summer, and fall between 2017 and 2019 in 60 olive farms representing increasing levels of structural simplification (as a surrogate of agricultural intensification). Olive farms were classified as exhibiting high (i.e., HIGH olive farms; n = 27), intermediate (MID; n = 18), and low (LOW; n = 15) structural complexity. </li> <li>Temporal mismatches between the activity levels of<em> P. kuhlii </em>and<em> P. oleae</em> varied between seasons and types of olive farms, being comparatively lower in summer than in spring and fall. Furthermore, summer was the only season in which temporal mismatches between species pairs differed between types of olive farms, with higher temporal mismatches found in LOW than in HIGH and MID olive farms.</li> <li>Overall, our work demonstrates the existence of temporal mismatches between the nightly activity patterns of <em>P. kuhlii </em>and<em> P. oleae</em>. Furthermore, it demonstrates that the structural simplification of olive farms increases temporal mismatches between species pairs, particularly in summer when bat-mediated biocontrol services are most needed.</li> <li> <em>Synthesis and applications</em>. Future research should consider mismatches between the temporal activity patterns of insectivorous bats and insect pests. Otherwise, the actual impact of agricultural intensification on bat-mediated biocontrol services as well as the economic impact of their loss on the agriculture industry might be underestimated. To enhance biocontrol services, we propose increasing the availability of suitable roosting and foraging sites as well as conserving areas of remnant native woodland and scattered hollow-bearing trees.</li> </ol>
Table 2 in The Complete Mitochondrial Genome of Glischropus bucephalus (Vespertilionidae; Chiroptera) Provides New Evidence for Pipistrellus Paraphyly
<p><b>Table 2.</b> GenBank accession numbers for mitochondrion and <i>cytb</i> sequences used in analysis.</p><table><tbody><tr><th>Species</th><th>Mitochondrion</th><th>cytb</th></tr></tbody><tbody><tr><th><i>Glischropus aquilus</i></th><td></td><td>KR612333.1</td></tr><tr><th><i>G. bucephalus</i></th><td>OR667258</td><td>KR612331.1, KR612332.1, OR667259, OR667260, OR667261</td></tr><tr><th><i>G. tylopus</i></th><td></td><td>JX570898.1, EU521632.1, OR667262, OR667263</td></tr><tr><th><i>“</i> <i>Pipistrellus coromandra”</i></th><td>NC_029191.1</td><td>NC_029191.1</td></tr><tr><th><i>Nyctalus aviator</i></th><td>NC_060309.1</td><td>NC_060309.1, MK167360.1</td></tr><tr><th><i>N. labiata</i></th><td>NC_027237.1, NC_041160.1</td><td>NC_027237.1, NC_041160.1, KX467596.1</td></tr><tr><th><i>N. lasiopterus</i></th><td></td><td>DQ120867.1, EU360680.1, JX570900.1</td></tr><tr><th><i>N. leisleri</i></th><td></td><td>DQ120877.1, JX570901.1, EU360690.1</td></tr><tr><th><i>N. noctula</i></th><td>MN122876.1, MN122907.1</td><td>MN122907.1, MN122876.1, DQ120872.1</td></tr><tr><th><i>Pipistrellus abramus</i></th><td>KX355640.1, NC_005436.1</td><td>GQ332529.1, KX355640.1, NC_005436.1</td></tr><tr><th><i>P. deserti</i></th><td></td><td>KM252759.1</td></tr><tr><th><i>P. coromandra</i></th><td></td><td>OR667264, OR667265, OR667266, OR667267</td></tr><tr><th><i>P. dhofarensis</i></th><td></td><td>KX375145.1, KX375148.1</td></tr><tr><th><i>P. hesperidus</i></th><td></td><td>MN790830.1, MT778037.1, MN790820.1</td></tr><tr><th><i>P. javanicus</i></th><td></td><td>KX496357.1</td></tr><tr><th><i>P. kuhlii</i></th><td>KU058655.1</td><td>KU058655.1, DQ120845.1, EU360657.1</td></tr><tr><th><i>P. maderensis</i></th><td></td><td>KC520771.1, KC520774.1, MT374272.1</td></tr><tr><th><i>P. nanulus</i></th><td></td><td>MK188530.1</td></tr><tr><th><i>P. nathusii</i></th><td>MN122914.1</td><td>MN122914.1, AJ504446.1, DQ120849.1</td></tr><tr><th><i>P. paterculus</i></th><td></td><td>OR667268, OR667269, OR667270</td></tr><tr><th><i>P. pipistrellus</i></th><td>LR862378.1</td><td>KF874520.1, DQ120853.1, LR862378.1</td></tr><tr><th><i>P. pygmaeus</i></th><td>MN122927.1, OX465325.1</td><td>MN122927.1, OX465325.1, EU084882.1</td></tr><tr><th><i>P. raceyi</i></th><td></td><td>KM886094.1, KM886088.1</td></tr><tr><th><i>P. rusticus</i></th><td></td><td>KX375166.1, KX375167.1</td></tr><tr><th><i>P. stenopterus</i></th><td></td><td>MH540194.1</td></tr><tr><th><i>Plecotus auritus</i></th><td>MN122881.1, MT410875.1</td><td></td></tr><tr><th><i>P. macrobullaris</i></th><td>KR134372.1, KR134385.1</td><td></td></tr><tr><th><i>Hypsugo alaschanicus</i></th><td>MF459671.1, MK135784.1, NC_029939.1</td><td></td></tr><tr><th><i>Lasionycteris noctivagans</i></th><td>MT774150.1, MT774151.1, NC_050995.1</td><td></td></tr><tr><th><i>Chalinolobus tuberculatus</i></th><td>NC 002626.1</td><td></td></tr><tr><th><i>Eptesicus bottae</i></th><td>NC_070014.1, OP328299.1, OP328300.1</td><td></td></tr><tr><th><i>E. nilssonii</i></th><td>OX621305.1</td><td></td></tr><tr><th><i>Vespertilio murinus</i></th><td>NC_033347.1</td><td>NC_033347.1</td></tr><tr><th><i>V. sinensis</i></th><td>KJ081440.1, KM092493.1.</td><td>KJ081440.1, KM092493.1.</td></tr><tr><th><i>Myotis brandtii</i></th><td>NC_025308.1</td><td></td></tr><tr><th><i>M. horsfieldii</i></th><td>MF143494.1</td><td></td></tr><tr><th><i>M. muricola</i></th><td>KT213444.1</td><td></td></tr></tbody></table>
Table 3 in The Complete Mitochondrial Genome of Glischropus bucephalus (Vespertilionidae; Chiroptera) Provides New Evidence for Pipistrellus Paraphyly
<p><b>Table 3.</b> Gene organization and characterization of the <i>G. bucephalus</i> mitogenome.</p><table><tbody><tr><th></th><th><b>Start Position</b></th><th><b>Stop Position</b></th><th><b>Length (bp)</b></th><th><b>Anticodon</b></th><th><b>Start Codon</b></th><th><b>Stop Codon</b></th><th><b>Strand</b></th></tr></tbody><tbody><tr><th>tRNAPhe</th><td>1</td><td>73</td><td>73</td><td>GAA</td><td></td><td></td><td>+</td></tr><tr><th>12S rRNA</th><td>74</td><td>1010</td><td>937</td><td></td><td></td><td></td><td>+</td></tr><tr><th>tRNAVal</th><td>1011</td><td>1078</td><td>68</td><td>TAC</td><td></td><td></td><td>+</td></tr><tr><th>16S rRNA</th><td>1079</td><td>2644</td><td>1566</td><td></td><td></td><td></td><td>+</td></tr><tr><th>tRNALeu</th><td>2650</td><td>2725</td><td>76</td><td>TAA</td><td></td><td></td><td>+</td></tr><tr><th>Nd1</th><td>2731</td><td>3684</td><td>954</td><td></td><td>ATG</td><td>TA-</td><td>+</td></tr><tr><th>tRNAIle</th><td>3687</td><td>3755</td><td>69</td><td>GAT</td><td></td><td></td><td>+</td></tr><tr><th>tRNAGln</th><td>3753</td><td>3827</td><td>75</td><td>TTG</td><td></td><td></td><td>-</td></tr><tr><th>tRNAMet</th><td>3828</td><td>3896</td><td>69</td><td>CAT</td><td></td><td></td><td>+</td></tr><tr><th>Nd2</th><td>3897</td><td>4937</td><td>1041</td><td></td><td>ATT</td><td>T-</td><td>+</td></tr><tr><th>tRNATrp</th><td>4939</td><td>5005</td><td>67</td><td>TCA</td><td></td><td></td><td>+</td></tr><tr><th>tRNAAla</th><td>5013</td><td>5081</td><td>69</td><td>TGC</td><td></td><td></td><td>-</td></tr><tr><th>tRNAAsn</th><td>5082</td><td>5154</td><td>73</td><td>GTT</td><td></td><td></td><td>-</td></tr><tr><th>OR</th><td>5155</td><td>5189</td><td>35</td><td></td><td></td><td></td><td></td></tr><tr><th>tRNACys</th><td>5187</td><td>5252</td><td>66</td><td>GCA</td><td></td><td></td><td>-</td></tr><tr><th>tRNATyr</th><td>5253</td><td>5319</td><td>67</td><td>GTA</td><td></td><td></td><td>-</td></tr><tr><th>Cox1</th><td>5321</td><td>6862</td><td>1542</td><td></td><td>ATG</td><td>TAA</td><td>+</td></tr><tr><th>tRNASer</th><td>6869</td><td>6937</td><td>69</td><td>TGA</td><td></td><td></td><td>-</td></tr><tr><th>tRNAAsp</th><td>6945</td><td>7011</td><td>67</td><td>GTC</td><td></td><td></td><td>+</td></tr><tr><th>Cox2</th><td>7012</td><td>7692</td><td>681</td><td></td><td>ATG</td><td>TAA</td><td>+</td></tr><tr><th>tRNALys</th><td>7699</td><td>7765</td><td>67</td><td>TTT</td><td></td><td></td><td>+</td></tr><tr><th>ATP8</th><td>7767</td><td>7967</td><td>201</td><td></td><td>ATG</td><td>TAA</td><td>+</td></tr><tr><th>ATP6</th><td>7928</td><td>8605</td><td>678</td><td></td><td>ATG</td><td>TAA</td><td>+</td></tr><tr><th>Cox3</th><td>8608</td><td>9390</td><td>783</td><td></td><td>ATG</td><td>TA-</td><td>+</td></tr><tr><th>tRNAGly</th><td>9392</td><td>9460</td><td>69</td><td>TCC</td><td></td><td></td><td>+</td></tr><tr><th>Nd3</th><td>9461</td><td>9805</td><td>345</td><td></td><td>ATT</td><td>TA-</td><td>+</td></tr><tr><th>tRNAArg</th><td>9809</td><td>9878</td><td>70</td><td>TCG</td><td></td><td></td><td>+</td></tr><tr><th>Nd4L</th><td>9880</td><td>10,173</td><td>294</td><td></td><td>ATG</td><td>TAA</td><td>+</td></tr><tr><th>Nd4</th><td>10,170</td><td>11,546</td><td>1377</td><td></td><td>ATG</td><td>T-</td><td>+</td></tr><tr><th>tRNAHis</th><td>11,548</td><td>11,616</td><td>69</td><td>GTG</td><td></td><td></td><td>+</td></tr><tr><th>tRNASer</th><td>11,617</td><td>11,675</td><td>59</td><td>GCT</td><td></td><td></td><td>+</td></tr><tr><th>tRNALeu</th><td>11,676</td><td>11,745</td><td>70</td><td>TAG</td><td></td><td></td><td>+</td></tr><tr><th>Nd5</th><td>11,764</td><td>13,552</td><td>1789</td><td></td><td>ATA</td><td>TAA</td><td>+</td></tr><tr><th>Nd6</th><td>13,544</td><td>14,062</td><td>519</td><td></td><td>ATG</td><td>TAA</td><td>-</td></tr><tr><th>tRNAGlu</th><td>14,066</td><td>14,133</td><td>68</td><td>TTC</td><td></td><td></td><td>-</td></tr><tr><th>CytB</th><td>14,139</td><td>15,275</td><td>1137</td><td></td><td>ATG</td><td>AGA</td><td>+</td></tr><tr><th>tRNAThr</th><td>15,279</td><td>15,348</td><td>70</td><td>TGT</td><td></td><td></td><td>+</td></tr><tr><th>tRNAPro</th><td>15,348</td><td>15,416</td><td>69</td><td>TGG</td><td></td><td></td><td>-</td></tr><tr><th>D-loop</th><td>15,416</td><td>17,023</td><td>1608</td><td></td><td></td><td></td><td></td></tr></tbody></table>
Table 1 in The Complete Mitochondrial Genome of Glischropus bucephalus (Vespertilionidae; Chiroptera) Provides New Evidence for Pipistrellus Paraphyly
<p><b>Table 1.</b> Model types for protein-coding gene analysis configured by IQtree ModelFinder through ultrafast bootstrap (10,000 replicates) for the phylogenetic tree with 3 codons.</p><table><tbody><tr><th>Model Type</th><th></th><th></th><th></th><th></th><th></th><th></th><th>Gene</th><th></th><th></th><th></th><th></th><th></th><th></th></tr></tbody><tbody><tr><th></th><td>ND1</td><td>ND2</td><td>COX1</td><td>COX2</td><td>ATP8</td><td>ATP6</td><td>COX3</td><td>ND3</td><td>ND4L</td><td>ND4</td><td>ND5</td><td>ND6</td><td>CYTB</td></tr><tr><th>GTR+F+G4</th><td>1st pos</td><td></td><td></td><td>1st pos</td><td></td><td>1st pos</td><td></td><td>1st pos</td><td></td><td></td><td></td><td></td><td>1st pos</td></tr><tr><th>TPM3u+F+I+G4</th><td>2nd pos</td><td></td><td>2nd pos</td><td>2nd pos</td><td></td><td>2nd pos</td><td>2nd pos</td><td></td><td></td><td></td><td></td><td></td><td>2rd pos</td></tr><tr><th>TIM+F+I+G4</th><td>3rd pos</td><td>3rd pos</td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td>3rd pos</td></tr><tr><th>TIM2+F+I+G4</th><td></td><td>1st pos</td><td></td><td></td><td>1st pos, 2nd pos</td><td></td><td></td><td></td><td>1st pos</td><td>1st pos</td><td>1st pos</td><td></td><td></td></tr><tr><th>TPM3u+F+I+G4</th><td></td><td>2nd pos</td><td></td><td></td><td></td><td></td><td></td><td>2nd pos</td><td>2nd pos</td><td>2nd pos</td><td>2nd pos</td><td></td><td></td></tr><tr><th>TIM2e+I+G4</th><td></td><td></td><td>1st pos</td><td></td><td></td><td></td><td>1st pos</td><td></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th>TIM2+F+I+G4</th><td></td><td></td><td>3rd pos</td><td>3rd pos</td><td>3rd pos</td><td>3rd pos</td><td></td><td></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th>TN+F+I+G4</th><td></td><td></td><td></td><td></td><td></td><td></td><td>3rd pos</td><td>3rd pos</td><td>3rd pos</td><td>3rd pos</td><td>3rd pos</td><td></td><td></td></tr><tr><th>HKY+F+I+G4</th><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td>1st pos, 2nd pos</td><td></td></tr><tr><th>HKY+F+G4</th><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td>3rd pos</td><td></td></tr></tbody></table>
High vulnerability of juvenile Nathusius' pipistrelle bats (Pipistrellus nathusii) at wind turbines
<p>Large numbers of bats are killed by wind turbines globally, yet the specific demographic consequences of wind turbine mortality are still unclear. In this study, we compared characteristics of Nathusius’ pipistrelles (<em>Pipistrellus nathusii</em>) killed at wind turbines (N = 119) to those observed within the live population (N = 524) during the summer migration period in Germany. We used generalised linear mixed effects modelling to identify demographic groups most vulnerable to wind turbine mortality, including sex, age (adult or juvenile), and geographic origin (regional or long-distance migrant; depicted by fur stable hydrogen isotope ratios). Juveniles contributed with a higher proportion of carcasses at wind turbines than expected given their frequency in the live population suggesting that juvenile bats may be particularly vulnerable to wind turbine mortality. This effect varied with wind turbine density. Specifically, at low wind turbine densities, representing mostly inland areas with water bodies and forests where Nathusius’ pipistrelles breed, juveniles were found more often dead beneath turbines than expected based on their abundance in the live population. At high wind turbine densities, representing mostly coastal areas where Nathusius’ pipistrelles migrate, adults and juveniles were equally vulnerable. We found no evidence of increased vulnerability to wind turbines in either sex, yet we observed a higher proportion of females than males among carcasses as well as the live population, which may reflect a female bias in the live population most likely caused by females migrating from their north-eastern breeding areas migrating into Germany. A high mortality of females is conservation concern for this migratory bat species because it affects the annual reproduction rate of populations. A distant origin did not influence the likelihood of getting killed at wind turbines. A disproportionately high vulnerability of juveniles to wind turbine mortality may reduce juvenile recruitment, which may limit the resilience of Nathusius’ pipistrelles to environmental stressors such as climate change or habitat loss. Schemes to mitigate wind turbine mortality, such as elevated cut-in speeds, should be implemented throughout Europe to prevent population declines of Nathusius’ pipistrelles and other migratory bats.</p> <p> </p> <p>Supplementary material 1: DataS1: primary_data_Kruzynski_et_al (includes bats raw data of stable isotopes).</p> <p>Supplementary material 2 includes Fig S1: Hydrogen isotopic ratios of long-distance and regional Nathusius’ pipistrelle bats from carcasses (WT) and live population (BB) in Germany during the migratory period </p>
Temporal mismatches in flight activity patterns between Pipistrellus kuhlii and Prays oleae in Mediterranean olive farms: Implications for biocontrol services potential
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