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15 results for “Pipistrellus kuhlii”
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 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>
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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FIGURE 5 in Systematics and taxonomy of Pipistrellus kuhlii (Kuhl, 1817) in Central Europe and the Balkans
FIGURE 5. Scatter plot of forearm length against pale wing margin width in P. k. kuhlii (squares) and P. k. lepidus (triangles).
FIGURE 4 in Systematics and taxonomy of Pipistrellus kuhlii (Kuhl, 1817) in Central Europe and the Balkans
FIGURE 4. Scatter plot of forearm length against body mass in P. k. kuhlii males (empty squares) and females (filled squares) and P. k. lepidus males (circles) and females (triangles).
FIGURE 1 in Systematics and taxonomy of Pipistrellus kuhlii (Kuhl, 1817) in Central Europe and the Balkans
FIGURE 1. General appearance and coloration of Pipistrellus k. lepidus, Przemyśl, Poland (A, D); light (typical) individual of P. k. kuhlii, Divjakë, Albania (B); and dark individual of P. k. kuhlii, Michalovce, Slovakia (C, E) (photos: K. Sachanowicz).
FIGURE 7 in Systematics and taxonomy of Pipistrellus kuhlii (Kuhl, 1817) in Central Europe and the Balkans
FIGURE 7. Distribution of sampling localities of P. kuhlii s. l. in Central Europe and the Balkans. P. k. kuhlii—black circles, P. k. lepidus—white squares, both taxa—black-white square.
FIGURE 3 in Systematics and taxonomy of Pipistrellus kuhlii (Kuhl, 1817) in Central Europe and the Balkans
FIGURE 3. Broadened and diffused pale wing margin of P. k. lepidus, Przemyśl, Poland (A) and uniformly narrow pale wing margin of P. k. kuhlii, Michalovce, Slovakia (B) (photos: K. Sachanowicz).
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.
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).
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