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113 results for “Myotis bats”
Fig. 3 in Contribution To Ecology Of Brandt'S Bat, Myotis Brandtii (Chiroptera, Vespertilionidae) In The North-Eastern Ukraine: Comparison Of Local Summer And Winter Bat Assemblages
Fig. 3. Body mass (g) characteristic of females (F) and (M) of M. brandtii in periods of spring departure April (S_dep) and swarming August (Swarm) from the Tetlega mines (dot — mean value, line — median value, whiskers — min and max values, not filling circles — outliers).
Fig. 2 in Contribution To Ecology Of Brandt'S Bat, Myotis Brandtii (Chiroptera, Vespertilionidae) In The North-Eastern Ukraine: Comparison Of Local Summer And Winter Bat Assemblages
Fig. 2. Forearm length (mm) of females (F) and males (M) of M. brandtii from Tetlega mines (dot — mean value, line — median value, whiskers — min and max values).
Fig. 1 in Contribution To Ecology Of Brandt'S Bat, Myotis Brandtii (Chiroptera, Vespertilionidae) In The North-Eastern Ukraine: Comparison Of Local Summer And Winter Bat Assemblages
Fig. 1. Allocation of M. brandtii (Mbra) and M. daubentonii (Mdau) inside the Tetlega mines from November to April (n — number of counted bats); A — in crevices or open, B — on walls or ceiling.
Fig. 4 in Is parasite load dependent on host aggregation size? The case of the greater mouse-eared bat Myotis myotis (Mammalia: Chiroptera) and its parasitic mite Spinturnix myoti (Acari: Gamasida)
Fig. 4 Relationship between the size of bat maternity aggregation (a), percentage of forest cover (b), body condition index (c), and parasite infection of the examined bats in the Carpathians Mountains (2007).
Fig. 1 in Is parasite load dependent on host aggregation size? The case of the greater mouse-eared bat Myotis myotis (Mammalia: Chiroptera) and its parasitic mite Spinturnix myoti (Acari: Gamasida)
Fig. 1 Distribution of greater mouse-eared bat (Myotis myotis) maternity aggregations (grey circles) and single founding individuals (black dots) in the Beskids (Carpathian Mountains, Poland). Data pooled from Kozakiewicz (2003), Szkudlarek et al. (2008), and our data. For the investigated maternity colonies, forested areas within a 10-km radius is shown
Fig. 3 in Is parasite load dependent on host aggregation size? The case of the greater mouse-eared bat Myotis myotis (Mammalia: Chiroptera) and its parasitic mite Spinturnix myoti (Acari: Gamasida)
Fig. 3 Proportions of protonymph (PN), deutonymph (DN), and adult (AD) stages of S. myoti mites, collected from Myotis myotis (bars), and the sex ratios of deutonymph and adult mites (circles)
Fig. 2 in Is parasite load dependent on host aggregation size? The case of the greater mouse-eared bat Myotis myotis (Mammalia: Chiroptera) and its parasitic mite Spinturnix myoti (Acari: Gamasida)
Fig. 2 Micrograph of the adult female Spinturnix myoti, dorsal view. Scanning electron microscopy image, original magnification ×40
Text-fig. 7. a–e, h, i – Myotis cf. reductus: a – BSP 1974 XIV 1209, left M2, Erkertshofen 2, occlusal view; b – BSP 1974 XIV 1208, right M1, Erkertshofen 2, occlusal view; c – left maxillary fragment with M1–2, NMA P28/0345, Petersbuch 28, ventral view; d – BSP 1974 XIV 1199, left C inf., Erkertshofen 2, lingual (c1) and occlusal (c2) views; e – SNSB-BSPG 1962 XIX 4200, left mnd without teeth; Erkertshofen 1, occlusal (e1) and lateral (e2) views; h – BSP 1974 XIV 1202, left p4, Erkertshofen 2, occlusal view; i – PCMRCh87, right m3, Petersbuch 2, occlusal view; f, g – cf. Myotis sp., right C inf., Petersbuch 2, lingual view: f – PCMRCh25, g – PCMRCh88; j – M. aff. reductus, NMA P62/0331, right dentary fragment with p4–m1, Petersbuch 62, occlusal view. in The Early Miocene Bats (Chiroptera, Mammalia) From The Karstic Sites Of Erkertshofen And Petersbuch 2 (Southern Germany)
Text-fig. 7. a–e, h, i – Myotis cf. reductus: a – BSP 1974 XIV 1209, left M2, Erkertshofen 2, occlusal view; b – BSP 1974 XIV 1208, right M1, Erkertshofen 2, occlusal view; c – left maxillary fragment with M1–2, NMA P28/0345, Petersbuch 28, ventral view; d – BSP 1974 XIV 1199, left C inf., Erkertshofen 2, lingual (c1) and occlusal (c2) views; e – SNSB-BSPG 1962 XIX 4200, left mnd without teeth; Erkertshofen 1, occlusal (e1) and lateral (e2) views; h – BSP 1974 XIV 1202, left p4, Erkertshofen 2, occlusal view; i – PCMRCh87, right m3, Petersbuch 2, occlusal view; f, g – cf. Myotis sp., right C inf., Petersbuch 2, lingual view: f – PCMRCh25, g – PCMRCh88; j – M. aff. reductus, NMA P62/0331, right dentary fragment with p4–m1, Petersbuch 62, occlusal view.
Text-fig. 9. Bats from Late Miocene deposits, North Caucasus. a – Myotis sp. 1, right M2, GIN-1143-411; b – Myotis sp. 1, M2, dex, GIN-1143-412; c – Myotis sp. 2, m1 or m2, dex, GIN-1144- 311; e – Myotis sp. 2, M2, dex, GIN-1144-312; d – Eptesicus sp., M1 or M2, sin, GIN-1143-413. a, b, d – Volchaya Balka; c, e – Gaverdovsky. in Late Miocene (Early Turolian) Vertebrate Faunas And Associated Biotic Record Of The Northern Caucasus: Geology, Taxonomy, Palaeoenvironment, Biochronology
Text-fig. 9. Bats from Late Miocene deposits, North Caucasus. a – Myotis sp. 1, right M2, GIN-1143-411; b – Myotis sp. 1, M2, dex, GIN-1143-412; c – Myotis sp. 2, m1 or m2, dex, GIN-1144- 311; e – Myotis sp. 2, M2, dex, GIN-1144-312; d – Eptesicus sp., M1 or M2, sin, GIN-1143-413. a, b, d – Volchaya Balka; c, e – Gaverdovsky.
Data and code for: Roost selection by male northern long-eared bats (Myotis septentrionalis) in a managed fire-adapted forest
<p>Data and code for: Roost selection by male northern long-eared bats (<em>Myotis septentrionalis</em>) in a managed fire-adapted forest</p>
Data from: Diversification rates have no effect on the convergent evolution of foraging strategies in the most speciose genus of bats, Myotis
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Data and code from: A multifaceted approach reveals complex genomic mediation of white-nose syndrome resistance in the little brown bat (<em>Myotis lucifugus</em>)
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Drivers of longitudinal telomere dynamics in the long-lived bat species, Myotis myotis
<p>Age related telomere shortening is considered a hallmark of the ageing process. <a name="_Hlk10395680">However, a recent cross-sectional ageing study of relative telomere length (rTL) in bats failed to detect a relationship between rTL and age in the long-lived genus <i>Myotis</i> (<i>M. myotis</i> and <i>M. bechsteinii</i>), suggesting some other factors are responsible for driving telomere dynamics in these species</a>. Here, we test if longitudinal rTL data show signatures of age-associated telomere attrition in <i>M. myotis</i> and differentiate which intrinsic or extrinsic factors are likely to drive telomere length dynamics.<a name="_Hlk30419416"> </a><a name="_Hlk26682824"></a><a name="_Hlk14445670">Using qPCR, rTL was measured in 504 samples from a marked population, from Brittany, France</a>, captured between 2013 and 2016. These represent 174 individuals with an age range of 0 to 7+ years. We find no significant relationship between rTL and age (<i>p</i> = 0.762), but demonstrate that within-individual rTL is highly variable from year to year. To investigate the heritability of rTL, a population pedigree (n=1744) was constructed from genotype data generated from a 16 microsatellite multiplex, designed from an initial, low coverage, Illumina genome for <i>M. myotis</i>. Heritability was estimated in a Bayesian, mixed model framework, and showed that little of the observed variance in rTL <a name="_Hlk513597000">is heritable (<i>h<sup>2</sup>= </i>0.06 – 0.01)</a>. Rather, correlations of first differences, correlating yearly changes in telomere length and weather variables, demonstrate that, during the spring transition, average temperature, minimum temperature, rainfall and windspeed correlate with changes in longitudinal telomere dynamics. <a name="_Hlk10396857">As such, rTL may represent a useful biomarker to quantify the physiological impact of various environmental stressors in bats.</a></p>
Code and source data for the paper: Global warming leads to larger bats with a faster life history pace in the long-lived Bechstein's bat (Myotis bechsteinii)
<p>Contains two R scripts necessary to perfom the analysis for the paper "Global warming leads to a faster life history pace in the long-lived Bechstein’s bat (Myotis bechsteinii)"</p> <ul> <li>1st Script (" Script_analysis paper_bodysize_AFR_fecundity_LRS_GAMs_revised": Descriptive statistics, calculation of all GAMs and code for figure 1, 2 and 3</li> <li>2nd Script (" Script_size specific generation times"): Calculation of reproductive and mortality rates, calculation of generation time and population growth rates (lambda) as well as code for figure 4 and 5</li> </ul> <p>And also .csv files with the data points of all figures.</p>
Active season body mass patterns of Little Brown Bats and Northern Myotis: Raw and fitted mass values, environmental conditions and inflection point estimates
<p><span>Animals are expected to adjust their behavioural patterns to improve fitness outcomes, such as fecundity or offspring survival. For long-lived hibernators, decisions made in each annual cycle may reflect considerations not just for concurrent survival and reproduction, but also the pressure to maximize overwinter survival and future reproductive success. We examined how these elements manifest themselves in the body mass variation patterns of North American northern latitude temperate bats, whose size and roosting habits present considerable monitoring challenges. We characterized and compared the summer and fall mass variation patterns of little brown myotis (<em>Myotis lucifugus</em>) and northern myotis (<em>M. septentrionalis</em></span><span>) from a historic dataset. In summer, the estimated date of parturition was strongly associated with spring foraging conditions (low wind, low precipitation, warm temperatures), and mass gain associated with female reproduction conferred considerable differentiation between the mass variation patterns of females and males. In fall, differences were most apparent among species, although adults exhibited a greater capacity for rapid mass gain than juveniles. These results demonstrate how reproductive constraints and interannual survival have important influences on the behaviour of temperate bats. Future work should seek to quantify the fitness benefits of patterns identified in this study, such as the rate of prehibernation mass gain.</span></p>
Appendix 1 in On the distribution and taxonomy of bats of the Myotis mystacinus morphogroup from the Caucasus region (Chiroptera: Vespertilionidae)
<p><b>Appendix 1.</b> (Continued).</p><table><tbody><tr><th></th><th></th><th></th><th>Slovakia</th><th>Boťany, Trebišov Dist.</th><th>48°28′N, 22°07′E</th><th>NMP 94586</th></tr></tbody><tbody><tr><th>hap24</th><td>KU060277</td><td><i>M. alcathoe</i></td><td>Bulgaria</td><td>Gorna Breznica, Blagoevgrad Prov.</td><td>41°45′N, 23°07′E</td><td>NMP 48344</td></tr><tr><th>hap25</th><td>KU060274</td><td><i>M. alcathoe</i></td><td>Bulgaria</td><td>Malko Târnovo, Burgas Prov.</td><td>42°00′N, 27°31′E</td><td>Biopsy</td></tr><tr><th>hap26</th><td>KU060275</td><td><i>M. alcathoe</i></td><td>Bulgaria</td><td>Kaleto Cave, Mladežko, Burgas Prov.</td><td>42°09′N, 27°21′E</td><td>Biopsy</td></tr><tr><th>hap27</th><td>KU060280</td><td><i>M.</i> cf. <i>alcathoe</i></td><td>Russia</td><td>Utriš Peninsula, Krasnodar Prov.</td><td>44°47′N, 37°24′E</td><td>NMP 95306</td></tr><tr><th>hap28</th><td>KU060278</td><td><i>M.</i> cf. <i>alcathoe</i></td><td>Russia</td><td>Psekabs River, Thamaha, Krasnodar Prov.</td><td>44°39′N, 38°54′E</td><td>NMP 95307</td></tr><tr><th></th><td></td><td></td><td>Russia</td><td>Bol’šaâ Fanagorijskaâ Cave, Fanagorijskoe, Krasnodar Prov.</td><td>44°28′N, 38°59′E</td><td>NMP 95309</td></tr><tr><th></th><td></td><td></td><td>Russia</td><td>Gebeus Mt., Gešebs, Krasnodar Prov.</td><td>44°23′N, 38°36′E</td><td>NMP 95313</td></tr><tr><th></th><td></td><td></td><td>Russia</td><td>Gebeus Mt., Gešebs, Krasnodar Prov.</td><td>44°23′N, 38°36′E</td><td>NMP 95314</td></tr><tr><th></th><td></td><td></td><td>Russia</td><td>Gebeus Mt., Gešebs, Krasnodar Prov.</td><td>44°23′N, 38°36′E</td><td>NMP 95315</td></tr><tr><th></th><td></td><td></td><td>Russia</td><td>Gebeus Mt., Gešebs, Krasnodar Prov.</td><td>44°23′N, 38°36′E</td><td>NMP 95316</td></tr><tr><th></th><td></td><td></td><td>Russia</td><td>Gebeus Mt., Gešebs, Krasnodar Prov.</td><td>44°23′N, 38°36′E</td><td>NMP 95317</td></tr><tr><th></th><td></td><td></td><td>Russia</td><td>Bol’šaâ Fanagorijskaâ Cave, Fanagorijskoe, Krasnodar Prov.</td><td>44°28′N, 38°59′E</td><td>NMP 95325</td></tr><tr><th></th><td></td><td></td><td>Russia</td><td>Bol’šaâ Fanagorijskaâ Cave, Fanagorijskoe, Krasnodar Prov.</td><td>44°28′N, 38°59′E</td><td>NMP 95326</td></tr><tr><th></th><td></td><td></td><td>Russia</td><td>Bol’šaâ Fanagorijskaâ Cave, Fanagorijskoe, Krasnodar Prov.</td><td>44°28′N, 38°59′E</td><td>NMP 95327</td></tr><tr><th></th><td></td><td></td><td>Russia</td><td>Bol’šaâ Fanagorijskaâ Cave, Fanagorijskoe, Krasnodar Prov.</td><td>44°28′N, 38°59′E</td><td>NMP 95328</td></tr><tr><th></th><td></td><td></td><td>Russia</td><td>Aše, Krasnodar Prov.</td><td>43°58′N, 39°16′E</td><td>NMP 95329</td></tr><tr><th></th><td></td><td></td><td>Russia</td><td>Tahira Cave, Kalež, Krasnodar Prov.</td><td>44°01′N, 39°21′E</td><td>NMP 95331</td></tr><tr><th></th><td></td><td></td><td>Russia</td><td>Utriš Peninsula, Krasnodar Prov.</td><td>44°47′N, 37°24′E</td><td>Biopsy</td></tr><tr><th></th><td></td><td></td><td>Russia</td><td>Utriš Peninsula, Krasnodar Prov.</td><td>44°47′N, 37°24′E</td><td>Biopsy</td></tr><tr><th>hap29</th><td>KU060279</td><td><i>M.</i> cf. <i>alcathoe</i></td><td>Russia</td><td>Psekabs River, Thamaha, Krasnodar Prov.</td><td>44°39′N, 38°54′E</td><td>NMP 95312</td></tr><tr><th></th><td></td><td></td><td>Russia</td><td>Bol’šaâ Fanagorijskaâ Cave, Fanagorijskoe, Krasnodar Prov.</td><td>44°28′N, 38°59′E</td><td>NMP 95324</td></tr></tbody></table>
Appendix 1 in On the distribution and taxonomy of bats of the Myotis mystacinus morphogroup from the Caucasus region (Chiroptera: Vespertilionidae)
<p><b>Appendix 1.</b> (Continued).</p><table><tbody><tr><th></th><th></th><th></th><th>Russia</th><th>Aše, Krasnodar Prov.</th><th>43°58′N, 39°16′E</th><th>NMP 95330</th></tr></tbody><tbody><tr><th>hap30</th><td>KU060281</td><td><i>M. hyrcanicus</i></td><td>Iran</td><td>Ali Abad, Golestan Prov.</td><td>36°53′N, 54°53′E</td><td>NMP 90857</td></tr><tr><th>hap31</th><td>KU060282</td><td><i>M. brandtii</i></td><td>Russia</td><td>Dzyhra Lake, Ahštyr’, Krasnodar Prov.</td><td>43°32′N, 40°01′E</td><td>NMP 95310</td></tr><tr><th></th><td></td><td></td><td>Russia</td><td>Staraâ Ladoga, Leningrad Prov.</td><td>60°01′N, 32°19′E</td><td>NMP 49272</td></tr><tr><th></th><td></td><td></td><td>Crimea</td><td>Partizanskoe, Âlta Dist.</td><td>44°33′N, 34°15′E</td><td>NMP pb4345</td></tr><tr><th></th><td></td><td></td><td>Montenegro</td><td>Stabna, Plužine Dist.</td><td>43°10′N, 18°46′E</td><td>NMP 90227</td></tr><tr><th></th><td>JX570902</td><td><i>Nyctalus noctula</i></td><td></td><td></td><td></td><td>Heaney et al. (2012)</td></tr><tr><th></th><td>JX570901</td><td><i>Nyctalus leisleri</i></td><td></td><td></td><td>Heaney et al. (2012)</td></tr><tr><th></th><td>AF376834</td><td><i>Vespertilio murinus</i></td><td></td><td></td><td></td><td>Ruedi and Mayer (2001)</td></tr></tbody></table>
Appendix 1 in On the distribution and taxonomy of bats of the Myotis mystacinus morphogroup from the Caucasus region (Chiroptera: Vespertilionidae)
<p><b>Appendix 1.</b> (Continued).</p><table><tbody><tr><th>hap17</th><th>KU060269</th><th><i>M. alcathoe</i></th><th>Czech Republic</th><th>Klíčava, Rakovník Dist.</th><th>50°04′N, 13°56′E</th><th>NMP 94580</th></tr></tbody><tbody><tr><th>hap18</th><td>KU060268</td><td><i>M. alcathoe</i></td><td>Czech Republic</td><td>Vůznice Reserve, Nižbor, Rakovník Dist.</td><td>50°02′N, 13°59′E</td><td>NMP 94582</td></tr><tr><th></th><td></td><td></td><td>Czech Republic</td><td>Ledové sluje Cave, Čížov, Znojmo Dist.</td><td>48°53′N, 15°51′E</td><td>NMP 94577</td></tr><tr><th></th><td></td><td></td><td>Czech Republic</td><td>Ledové sluje Cave, Čížov, Znojmo Dist.</td><td>48°53′N, 15°51′E</td><td>NMP 94575</td></tr><tr><th></th><td></td><td></td><td>Czech Republic</td><td>Ledové sluje Cave, Čížov, Znojmo Dist.</td><td>48°53′N, 15°51′E</td><td>NMP 94571</td></tr><tr><th></th><td></td><td></td><td>Czech Republic</td><td>Baštův Mill, Havraníky, Znojmo Dist.</td><td>48°49′N, 15°59′E</td><td>SMZ 6713</td></tr><tr><th></th><td></td><td></td><td>Montenegro</td><td>Stabna, Plužine Dist.</td><td>43°10′N, 18°46′E</td><td>NMP 90228</td></tr><tr><th></th><td></td><td></td><td>Czech Republic</td><td>Vůznice Reserve, Nižbor, Rakovník Dist.</td><td>50°02′N, 13°59′E</td><td>NMP 94569</td></tr><tr><th></th><td></td><td></td><td>Czech Republic</td><td>Vůznice Reserve, Nižbor, Rakovník Dist.</td><td>50°02′N, 13°59′E</td><td>NMP 94570</td></tr><tr><th></th><td></td><td></td><td>Czech Republic</td><td>Vlkov Pond, Šumná, Znojmo Dist.</td><td>48°56′N, 15°55′E</td><td>NMP 94584</td></tr><tr><th>hap19</th><td>KU060276</td><td><i>M. alcathoe</i></td><td>Bulgaria</td><td>Gorna Breznica, Blagoevgrad Prov.</td><td>41°45′N, 23°07′E</td><td>NMP 48343</td></tr><tr><th>hap20</th><td>KU060271</td><td><i>M. alcathoe</i></td><td>Slovakia</td><td>Stĺpová Cave, Šurice, Romavská Sobota Dist.</td><td>48°12′N, 19°55′E</td><td>NMP 50446</td></tr><tr><th>hap21</th><td>KU060272</td><td><i>M. alcathoe</i></td><td>Czech Republic</td><td>Ledové sluje Cave, Čížov, Znojmo Dist.</td><td>48°53′N, 15°51′E</td><td>NMP 94573</td></tr><tr><th></th><td></td><td></td><td>Slovakia</td><td>Boťany, Trebišov Dist.</td><td>48°28′N, 22°07′E</td><td>NMP 94587</td></tr><tr><th></th><td></td><td></td><td>Czech Republic</td><td>Ledové sluje Cave, Čížov, Znojmo Dist.</td><td>48°53′N, 15°51′E</td><td>NMP 94576</td></tr><tr><th></th><td></td><td></td><td>Ukraine</td><td>Čizaj, Beregove, Zakarpats’ka Prov.</td><td>48°13′N, 22°38′E</td><td>Biopsy</td></tr><tr><th>hap22</th><td>KU060270</td><td><i>M. alcathoe</i></td><td>Czech Republic</td><td>Líšná, Přerov Dist.</td><td>49°24′N, 17°33′E</td><td>NMP 94578</td></tr><tr><th></th><td></td><td></td><td>Czech Republic</td><td>Líšná, Přerov Dist.</td><td>49°24′N, 17°33′E</td><td>NMP 94579</td></tr><tr><th></th><td></td><td></td><td>Czech Republic</td><td>Vůznice Reserve, Nižbor, Rakovník Dist.</td><td>50°02′N, 13°59′E</td><td>NMP 94581</td></tr><tr><th></th><td></td><td></td><td>Czech Republic</td><td>Smrdutá Reserve, Chvalčov, Kroměříž Dist.</td><td>49°22′N, 17°45′E</td><td>NMP 94583</td></tr><tr><th>hap23</th><td>KU060273</td><td><i>M. alcathoe</i></td><td>Czech Republic</td><td>Tvořihráz, Znojmo Dist.</td><td>48°54′N, 16°07′E</td><td>NMP 94585</td></tr><tr><th></th><td></td><td></td><td>Slovakia</td><td>Stĺpová Cave, Šurice, Romavská Sobota Dist.</td><td>48°12′N, 19°55′E</td><td>NMP 50447</td></tr></tbody></table>
Appendix 1 in On the distribution and taxonomy of bats of the Myotis mystacinus morphogroup from the Caucasus region (Chiroptera: Vespertilionidae)
<p><b>Appendix 1.</b> (Continued).</p><table><tbody><tr><th>hap10</th><th>KU060263</th><th><i>M. davidii</i></th><th>Russia</th><th>Egerskaâ Karaulka, Adygea Prov.</th><th>44°10′N, 39°50′E</th><th>NMP 95320</th></tr></tbody><tbody><tr><th>hap11</th><td>KU060260</td><td><i>M. davidii</i></td><td>Russia</td><td>Karamyk River, Sablinskoe, Stavropol’ Prov.</td><td>44°30′N, 43°10′E</td><td>Biopsy</td></tr><tr><th></th><td></td><td></td><td>Russia</td><td>Karamyk River, Sablinskoe, Stavropol’ Prov.</td><td>44°30′N, 43°10′E</td><td>Biopsy</td></tr><tr><th></th><td></td><td></td><td>Russia</td><td>Karamyk River, Sablinskoe, Stavropol’ Prov.</td><td>44°30′N, 43°10′E</td><td>Biopsy</td></tr><tr><th></th><td></td><td></td><td>Russia</td><td>Karamyk River, Sablinskoe, Stavropol’ Prov.</td><td>44°30′N, 43°10′E</td><td>Biopsy</td></tr><tr><th></th><td></td><td></td><td>Russia</td><td>Karamyk River, Sablinskoe, Stavropol’ Prov.</td><td>44°30′N, 43°10′E</td><td>Biopsy</td></tr><tr><th></th><td></td><td></td><td>Russia</td><td>Karamyk River, Sablinskoe, Stavropol’ Prov.</td><td>44°30′N, 43°10′E</td><td>Biopsy</td></tr><tr><th></th><td></td><td></td><td>Russia</td><td>Razvalka Mine, Voronov, Stavropol’ Prov.</td><td>44°10′N, 43°02′E</td><td>Biopsy</td></tr><tr><th></th><td></td><td></td><td>Russia</td><td>Apšeronsk, Krasnodar Prov.</td><td>44°26′N, 39°44′E</td><td>NMP 95308</td></tr><tr><th></th><td></td><td></td><td>Russia</td><td>Egerskaâ Karaulka, Adygea Prov.</td><td>44°10′N, 39°50′E</td><td>NMP 95318</td></tr><tr><th></th><td></td><td></td><td>Russia</td><td>Egerskaâ Karaulka, Adygea Prov.</td><td>44°10′N, 39°50′E</td><td>NMP 95319</td></tr><tr><th>hap12</th><td>KU060261</td><td><i>M. davidii</i></td><td>Russia</td><td>Karamyk River, Sablinskoe, Stavropol’ Prov.</td><td>44°30′N, 43°10′E</td><td>Biopsy</td></tr><tr><th></th><td></td><td></td><td>Russia</td><td>Karamyk River, Sablinskoe, Stavropol’ Prov.</td><td>44°30′N, 43°10′E</td><td>Biopsy</td></tr><tr><th>hap13</th><td>KU060265</td><td><i>M. davidii</i></td><td>Russia</td><td>Kumtor-Kala Station, Dagestan Prov.</td><td>43°00′N, 47°14′E</td><td>NMP 95303</td></tr><tr><th></th><td></td><td></td><td>Russia</td><td>Kumtor-Kala Station, Dagestan Prov.</td><td>43°00′N, 47°14′E</td><td>NMP 95302</td></tr><tr><th>hap14</th><td>KU060264</td><td><i>M. davidii</i></td><td>Crimea</td><td>Suuk-Koba Cave, Čatyr-Dag Âjla, Simferopol’ Dist.</td><td>44°47′N, 34°17′E</td><td>NMP pb4354</td></tr><tr><th></th><td></td><td></td><td>Crimea</td><td>Suuk-Koba Cave, Čatyr-Dag Âjla, Simferopol’ Dist.</td><td>44°47′N, 34°17′E</td><td>NMP pb4357</td></tr><tr><th></th><td></td><td></td><td>Crimea</td><td>Kamenskoe, Lenino Dist.</td><td>45°17′N, 35°32′E</td><td>NMP pb4406</td></tr><tr><th></th><td></td><td></td><td>Crimea</td><td>Kamenskoe, Lenino Dist.</td><td>45°17′N, 35°32′E</td><td>NMP pb4408</td></tr><tr><th>hap15</th><td>KU060266</td><td><i>M. davidii</i></td><td>Azerbaijan</td><td>Kiş, Şəki Dist.</td><td>41°15′N, 47°12′E</td><td>Biopsy</td></tr><tr><th>hap16</th><td>KU060267</td><td><i>M. davidii</i></td><td>Iran</td><td>Bastam, Azarbaijan-e Gharbi Prov.</td><td>38°53′N, 44°57′E</td><td>NMP 48119</td></tr><tr><th></th><td></td><td></td><td>Iran</td><td>Bastam, Azarbaijan-e Gharbi Prov.</td><td>38°53′N, 44°57′E</td><td>NMP 48120</td></tr></tbody></table>
Table 4 in On the distribution and taxonomy of bats of the Myotis mystacinus morphogroup from the Caucasus region (Chiroptera: Vespertilionidae)
<p><b>Table 4</b>. Results of the analysis of variance between the Caucasian and European sample sets of <i>Myotis alcathoe</i> and dimensions of the European samples of <i>M. alcathoe</i>. See Section 2.3 for explanation of the dimension acronyms. a – external, skull, and tooth dimensions (in millimetres); b – relative dimensions and phenetic characters.</p><table><tbody><tr><th><b>a</b></th><th>ANOVA</th><th></th><th>Lineage III</th><th></th><th></th><th></th><th><b>b</b></th><th>ANOVA</th><th></th><th>Lineage III</th><th></th><th></th><th></th></tr></tbody><tbody><tr><th></th><td>results</td><td></td><td><i>M. alcathoe</i> Europe</td><td></td><td></td><td></td><td>results</td><td></td><td><i>M. alcathoe</i> Europe</td><td></td><td></td><td></td></tr><tr><th></th><td>df</td><td>F</td><td>p</td><td>n</td><td><b>M</b></td><td>min</td><td>max</td><td>SD</td><td></td><td>df</td><td>F</td><td>p</td><td>n</td><td><b>M</b></td><td>min</td><td>max</td><td>SD</td></tr><tr><th>LAt</th><td>40</td><td>0.025</td><td>0.876</td><td>25</td><td><b>32.28</b></td><td>27.2</td><td>35.3</td><td>1.401</td><td>CM3/LCr</td><td>42</td><td>0.060</td><td>0.808</td><td>27</td><td><b>0.379</b></td><td>0.364</td><td>0.387</td><td>0.006</td></tr><tr><th>LPol</th><td>36</td><td>4.845</td><td>0.034</td><td>21</td><td><b>4.39</b></td><td>4.2</td><td>4.6</td><td>0.128</td><td>LaN/LCr</td><td>41</td><td>1.868</td><td>0.179</td><td>26</td><td><b>0.490</b></td><td>0.466</td><td>0.511</td><td>0.011</td></tr><tr><th>LTib</th><td>35</td><td>0.127</td><td>0.724</td><td>20</td><td><b>14.25</b></td><td>12.8</td><td>15.3</td><td>0.573</td><td>ANc/LCr</td><td>40</td><td>0.146</td><td>0.704</td><td>25</td><td><b>0.356</b></td><td>0.338</td><td>0.374</td><td>0.009</td></tr><tr><th>LCr</th><td>42</td><td>2.066</td><td>0.158</td><td>27</td><td><b>12.99</b></td><td>12.38</td><td>13.38</td><td>0.259</td><td>ANc/LaN</td><td>41</td><td>1.801</td><td>0.187</td><td>26</td><td><b>0.727</b></td><td>0.681</td><td>0.779</td><td>0.020</td></tr><tr><th>LCb</th><td>42</td><td>2.623</td><td>0.113</td><td>27</td><td><b>12.43</b></td><td>11.88</td><td>12.84</td><td>0.241</td><td>ACo/LMd</td><td>40</td><td>12.539</td><td>0.001</td><td>28</td><td><b>0.289</b></td><td>0.273</td><td>0.302</td><td>0.006</td></tr><tr><th>LaZ</th><td>31</td><td>5.661</td><td>0.024</td><td>19</td><td><b>8.09</b></td><td>7.57</td><td>8.43</td><td>0.202</td><td>CC/LCr</td><td>41</td><td>9.547</td><td>0.004</td><td>26</td><td><b>0.254</b></td><td>0.237</td><td>0.266</td><td>0.008</td></tr><tr><th>LaI</th><td>43</td><td>6.301</td><td>0.016</td><td>28</td><td><b>3.25</b></td><td>3.07</td><td>3.48</td><td>0.098</td><td>CC/CM3</td><td>42</td><td>8.464</td><td>0.006</td><td>27</td><td><b>0.668</b></td><td>0.621</td><td>0.704</td><td>0.022</td></tr><tr><th>LaInf</th><td>43</td><td>0.377</td><td>0.543</td><td>28</td><td><b>3.23</b></td><td>3.03</td><td>3.41</td><td>0.092</td><td>CP4/M1M3</td><td>43</td><td>4.704</td><td>0.036</td><td>28</td><td><b>0.806</b></td><td>0.688</td><td>0.877</td><td>0.037</td></tr><tr><th>LaN</th><td>42</td><td>5.498</td><td>0.024</td><td>27</td><td><b>6.35</b></td><td>6.01</td><td>6.64</td><td>0.145</td><td>P2P3/LCr</td><td>42</td><td>0.356</td><td>0.554</td><td>27</td><td><b>0.056</b></td><td>0.050</td><td>0.064</td><td>0.004</td></tr><tr><th>AN</th><td>42</td><td>0.816</td><td>0.371</td><td>27</td><td><b>4.62</b></td><td>4.39</td><td>4.75</td><td>0.111</td><td>CnR</td><td>43</td><td>0.687</td><td>0.412</td><td>28</td><td><b>1.306</b></td><td>1.200</td><td>1.397</td><td>0.053</td></tr><tr><th>CC</th><td>42</td><td>13.766</td><td>0.001</td><td>27</td><td><b>3.29</b></td><td>3.02</td><td>3.43</td><td>0.103</td><td>LCn/CM3</td><td>43</td><td>0.122</td><td>0.728</td><td>28</td><td><b>0.168</b></td><td>0.154</td><td>0.182</td><td>0.008</td></tr><tr><th>M3M3</th><td>42</td><td>0.651</td><td>0.424</td><td>28</td><td><b>5.16</b></td><td>4.75</td><td>5.36</td><td>0.111</td><td>P3/LCn</td><td>43</td><td>1.856</td><td>0.180</td><td>28</td><td><b>0.422</b></td><td>0.342</td><td>0.494</td><td>0.031</td></tr><tr><th>IM3</th><td>42</td><td>3.157</td><td>0.083</td><td>27</td><td><b>5.97</b></td><td>5.70</td><td>6.16</td><td>0.115</td><td>M3/M1</td><td>43</td><td>0.003</td><td>0.957</td><td>28</td><td><b>1.038</b></td><td>0.984</td><td>1.116</td><td>0.032</td></tr><tr><th>CM3</th><td>43</td><td>0.806</td><td>0.374</td><td>28</td><td><b>4.91</b></td><td>4.68</td><td>5.09</td><td>0.101</td><td>MR</td><td>41</td><td>0.004</td><td>0.951</td><td>28</td><td><b>1.786</b></td><td>0.5</td><td>3.0</td><td>0.726</td></tr><tr><th>P4M3</th><td>43</td><td>6.953</td><td>0.012</td><td>28</td><td><b>3.59</b></td><td>3.34</td><td>3.76</td><td>0.101</td><td>ACin/P4</td><td>43</td><td>1.630</td><td>0.209</td><td>28</td><td><b>0.137</b></td><td>0.093</td><td>0.168</td><td>0.021</td></tr><tr><th>M1M3</th><td>43</td><td>3.434</td><td>0.071</td><td>28</td><td><b>2.95</b></td><td>2.76</td><td>3.42</td><td>0.125</td><td>P3pos</td><td>42</td><td>0.922</td><td>0.342</td><td>27</td><td><b>1.43</b></td><td>1</td><td>3</td><td>0.661</td></tr><tr><th>M1M2</th><td>43</td><td>16.282</td><td>0.000</td><td>28</td><td><b>2.24</b></td><td>2.09</td><td>2.34</td><td>0.061</td><td>pcl</td><td>41</td><td>3.817</td><td>0.058</td><td>28</td><td><b>0.54</b></td><td>0.0</td><td>1.0</td><td>0.302</td></tr><tr><th>CP4</th><td>43</td><td>0.415</td><td>0.523</td><td>28</td><td><b>2.37</b></td><td>2.17</td><td>2.59</td><td>0.108</td><td>plph</td><td>42</td><td>0.143</td><td>0.707</td><td>28</td><td><b>0.63</b></td><td>0.0</td><td>1.0</td><td>0.259</td></tr><tr><th>P2P3</th><td>43</td><td>0.921</td><td>0.343</td><td>28</td><td><b>0.73</b></td><td>0.66</td><td>0.82</td><td>0.047</td><td>mcl</td><td>40</td><td>0.096</td><td>0.758</td><td>28</td><td><b>0.46</b></td><td>0.0</td><td>1.0</td><td>0.358</td></tr><tr><th>LMd</th><td>40</td><td>0.523</td><td>0.474</td><td>28</td><td><b>9.37</b></td><td>8.92</td><td>9.70</td><td>0.198</td><td>mlph</td><td>42</td><td>5.199</td><td>0.028</td><td>28</td><td><b>0.16</b></td><td>0.0</td><td>1.0</td><td>0.274</td></tr><tr><th>ACo</th><td>42</td><td>2.035</td><td>0.161</td><td>28</td><td><b>2.71</b></td><td>2.53</td><td>2.86</td><td>0.085</td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th>IM3</th><td>43</td><td>4.228</td><td>0.046</td><td>28</td><td><b>6.32</b></td><td>6.04</td><td>6.52</td><td>0.108</td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th>CM3</th><td>43</td><td>1.767</td><td>0.191</td><td>28</td><td><b>5.31</b></td><td>5.01</td><td>5.49</td><td>0.108</td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th>P4M3</th><td>43</td><td>7.067</td><td>0.011</td><td>28</td><td><b>3.91</b></td><td>3.58</td><td>4.03</td><td>0.107</td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th>M1M3</th><td>43</td><td>2.995</td><td>0.091</td><td>28</td><td><b>3.27</b></td><td>3.00</td><td>3.37</td><td>0.089</td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th>CP4</th><td>43</td><td>0.006</td><td>0.941</td><td>28</td><td><b>2.12</b></td><td>1.94</td><td>2.24</td><td>0.093</td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th>P2P3</th><td>43</td><td>1.083</td><td>0.304</td><td>28</td><td><b>0.84</b></td><td>0.75</td><td>0.90</td><td>0.041</td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th>LCn</th><td>43</td><td>0.527</td><td>0.472</td><td>28</td><td><b>0.83</b></td><td>0.75</td><td>0.89</td><td>0.036</td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th>LaCn</th><td>43</td><td>0.036</td><td>0.851</td><td>28</td><td><b>0.63</b></td><td>0.54</td><td>0.69</td><td>0.033</td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th>P3</th><td>43</td><td>0.698</td><td>0.408</td><td>28</td><td><b>0.35</b></td><td>0.27</td><td>0.41</td><td>0.027</td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th>P3</th><td>43</td><td>3.833</td><td>0.057</td><td>28</td><td><b>0.36</b></td><td>0.28</td><td>0.41</td><td>0.030</td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th>ACin</th><td>43</td><td>3.708</td><td>0.061</td><td>28</td><td><b>0.15</b></td><td>0.10</td><td>0.19</td><td>0.023</td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th>P4</th><td>43</td><td>5.555</td><td>0.023</td><td>28</td><td><b>1.11</b></td><td>1.02</td><td>1.21</td><td>0.047</td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th>M1</th><td>43</td><td>0.164</td><td>0.687</td><td>28</td><td><b>1.35</b></td><td>1.27</td><td>1.42</td><td>0.044</td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th>M2</th><td>43</td><td>2.114</td><td>0.153</td><td>28</td><td><b>1.54</b></td><td>1.40</td><td>1.63</td><td>0.056</td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th>M3</th><td>43</td><td>0.153</td><td>0.697</td><td>28</td><td><b>1.41</b></td><td>1.29</td><td>1.51</td><td>0.048</td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td></tr></tbody></table>
ScienceDex guides
Understand access before you commit
These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
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.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.