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On following pages: 228. Christie's Long-eared Bat (Plecotus christii); 229. Mediterranean Long-eared Bat (Plecotus turkmenicus); 232. Strelkov's Long-eared Bat (Plecotus strelkovi); 233. Ognev's Long-eared Bat (Plecotus ognevi); Long-eared Bat (Plecotus homochrous); 237. Taiwan Long-eared Bat (Plecotus taivanus); 238. Japanese Long-eared macrobullaris); 241. Sardinian Long-eared Bat (Plecotus sardus); 242. Brown Long-eared Bat (Plecotus auritus); 243 245. Rafinesque's Big-eared Bat (Corynorhinus rafinesquii); 246. Townsend's Big-eared Bat (Corynorhinus townsendii kolombatovici); 230. Ethiopian Long-eared Bat (Plecotus balensis); 231. Turkmen Long-eared Bat (Plecotus 234. Kozlov's Long-eared Bat (Plecotus kozlovi); 235. Sichuan Long-eared Bat (Plecotus ariel); 236. Himalayan Bat (Plecotus sacrimontis); 239. Ward's Long-eared Bat (Plecotus ward): 240. Alpine Long-eared Bat (Plecotus. Desert Long-eared Bat (Otonycteris hemprichii); 244. Turkestani Long-eared Bat (Otonycteris leucophaea) '); 247. Mexican Big-eared Bat (Corynorhinus mexicanus); 248. Allen's Big-eared Bat (/dionycteris phyllotis). in Vespertilionidae
On following pages: 228. Christie's Long-eared Bat (Plecotus christii); 229. Mediterranean Long-eared Bat (Plecotus turkmenicus); 232. Strelkov's Long-eared Bat (Plecotus strelkovi); 233. Ognev's Long-eared Bat (Plecotus ognevi); Long-eared Bat (Plecotus homochrous); 237. Taiwan Long-eared Bat (Plecotus taivanus); 238. Japanese Long-eared macrobullaris); 241. Sardinian Long-eared Bat (Plecotus sardus); 242. Brown Long-eared Bat (Plecotus auritus); 243 245. Rafinesque's Big-eared Bat (Corynorhinus rafinesquii); 246. Townsend's Big-eared Bat (Corynorhinus townsendii kolombatovici); 230. Ethiopian Long-eared Bat (Plecotus balensis); 231. Turkmen Long-eared Bat (Plecotus 234. Kozlov's Long-eared Bat (Plecotus kozlovi); 235. Sichuan Long-eared Bat (Plecotus ariel); 236. Himalayan Bat (Plecotus sacrimontis); 239. Ward's Long-eared Bat (Plecotus ward): 240. Alpine Long-eared Bat (Plecotus. Desert Long-eared Bat (Otonycteris hemprichii); 244. Turkestani Long-eared Bat (Otonycteris leucophaea) '); 247. Mexican Big-eared Bat (Corynorhinus mexicanus); 248. Allen's Big-eared Bat (/dionycteris phyllotis).
Subspecies and Distribution. E.f.fuscusPalisotdeBeauvois,1796—SECanadaandEUSA. E.f.bahamensisG.S.Miller,1897—Bahamas(NewProvidenceandSanSalvadorIs). E.f.bernardinusRhoads,1902—SWCanada(BritishColumbia)andWUSA. E.f.dutertreusP.Gervais,1837—Bahamas(Andros,Exumas,Long,Crooked,andAcklinsIs),Cuba,andCaymanIs(CaymanBrac). E.f.hispaniolaeG.S.Miller,1918—JamaicaandHispaniola. E.f.miradorensisH.Allen,1866—mostofMexico,CentralAmerica,andAndesofWVenezuela,NColombia,andNEcuador. E.f.osceolaRhoads,1902—-Florida,SEUSA. E.f.pallidusYoung,1908—WCCanada,C,WC&SWUSA,andNW&NCMexico. E.f.peninsulaeThomas,1898—BajaCaliforniaSur,NWMexico. E.f.petersoniSilva-Taboada,1974—IsladelaJuventud(Cuba). E. f. wetmorei H. T. T. Jackson, 1916 — Puerto Rico, Dominica, and Barbados. in Vespertilionidae
Subspecies and Distribution. E.f.fuscusPalisotdeBeauvois,1796—SECanadaandEUSA. E.f.bahamensisG.S.Miller,1897—Bahamas(NewProvidenceandSanSalvadorIs). E.f.bernardinusRhoads,1902—SWCanada(BritishColumbia)andWUSA. E.f.dutertreusP.Gervais,1837—Bahamas(Andros,Exumas,Long,Crooked,andAcklinsIs),Cuba,andCaymanIs(CaymanBrac). E.f.hispaniolaeG.S.Miller,1918—JamaicaandHispaniola. E.f.miradorensisH.Allen,1866—mostofMexico,CentralAmerica,andAndesofWVenezuela,NColombia,andNEcuador. E.f.osceolaRhoads,1902—-Florida,SEUSA. E.f.pallidusYoung,1908—WCCanada,C,WC&SWUSA,andNW&NCMexico. E.f.peninsulaeThomas,1898—BajaCaliforniaSur,NWMexico. E.f.petersoniSilva-Taboada,1974—IsladelaJuventud(Cuba). E. f. wetmorei H. T. T. Jackson, 1916 — Puerto Rico, Dominica, and Barbados.
Distribution. SW Western Australia, E & SE Queensland (including Fraser I), C & E New South Wales, Victoria, and SE South Australia, SW & E Australia. A specimen is known from Fiji, but this is suspected to represent the New Caledonian Long-eared Bat (NV. nebulosus) or a mislabeled specimen. in Vespertilionidae
Distribution. SW Western Australia, E & SE Queensland (including Fraser I), C & E New South Wales, Victoria, and SE South Australia, SW & E Australia. A specimen is known from Fiji, but this is suspected to represent the New Caledonian Long-eared Bat (NV. nebulosus) or a mislabeled specimen.
Heterogeneity in resource competition covaries with individual variation in long-term social relationships
<p>Resource competition among conspecifics is central to social evolution, as it serves as one of the primary selective pressures of group living. This is because the degree of competition for resources impacts the costs and benefits of social interactions. Despite this, how heterogeneity in resource competition drives variation in the type and quantity of long-term social relationships individuals foster has been overlooked. By measuring male mating competition and female foraging competition in a highly social, long-lived mammal, we demonstrate that individual variation in long-term intrasexual social relationships covaries with preferred habitat and experienced resource competition, and this effect differs based on the sex of the individual. Specifically, greater resource competition resulted in fewer social preferences, but the magnitude of the effect varied by both habitat and sex, whereas for social avoidances, both the directionality and magnitude of the effect of resource competition varied by habitat and sex. Together our work shows how fine-scale variation in individual socioecological niches (i.e., unique physical and social environments) can drive extensive variation in individual social behavior (here long-term relationships) within a population, thereby broadening current theories of social evolution.</p>
On following pages: 3. Small Long-fingered Bat (Miniopterus pusillus); 4. Intermediate Long-fingered Bat (Miniopterus medius); 5. Ryukyu Long-fingered Bat (Miniopterus fuscus); 6. Eschscholtz's Long-fingered Bat (Miniopterus eschscholtzil); 7. Philippine Long-fingered Bat (Miniopterus paululus); 8. Great Long-fingered Bat (Miniopterus tristis); 9. Shortridge's Long-fingered Bat (Miniopterus shortridgel); 10. Javanese Long-fingered Bat (Miniopterus blepotis); 11. Little Long-fingered Bat (Miniopterus australis); 12. Small Melanesian Long-fingered Bat (Miniopterus macrocneme); 13. Loyalty Long-fingered Bat (Miniopterus robustior); 14. Australian Long-fingered Bat (Miniopterus orianae); 15. Pallid Long-fingered Bat (Miniopterus pallidus); 16. Schreibers's Long-fingered Bat (Miniopterus schreibersii); 17. Maghrebian Long-fingered Bat (Miniopterus maghrebensis). in Miniopteridae
On following pages: 3. Small Long-fingered Bat (Miniopterus pusillus); 4. Intermediate Long-fingered Bat (Miniopterus medius); 5. Ryukyu Long-fingered Bat (Miniopterus fuscus); 6. Eschscholtz's Long-fingered Bat (Miniopterus eschscholtzil); 7. Philippine Long-fingered Bat (Miniopterus paululus); 8. Great Long-fingered Bat (Miniopterus tristis); 9. Shortridge's Long-fingered Bat (Miniopterus shortridgel); 10. Javanese Long-fingered Bat (Miniopterus blepotis); 11. Little Long-fingered Bat (Miniopterus australis); 12. Small Melanesian Long-fingered Bat (Miniopterus macrocneme); 13. Loyalty Long-fingered Bat (Miniopterus robustior); 14. Australian Long-fingered Bat (Miniopterus orianae); 15. Pallid Long-fingered Bat (Miniopterus pallidus); 16. Schreibers's Long-fingered Bat (Miniopterus schreibersii); 17. Maghrebian Long-fingered Bat (Miniopterus maghrebensis).
On following pages: 21. Least Long-fingered Bat (Miniopterus minon; 22. Sandy Long-fingered Bat (Miniopterus arenarius); 23. African Long-fingered Bat (Miniopterus africanus); 24. Natal Long-fingered Bat (Miniopterus natalensis); 25. Mozambican Long-fingered Bat (Miniopterus mossambicus); 26. Lesser Long-fingered Bat (Miniopterus fraterculus); 27. Aellen's Long-fingered Bat (Miniopterus aelleni); 28. Griveaud's Long-fingered Bat (Miniopterus griveaud)); 29. Glen's Long-fingered Bat (Miniopterus gleni); 30. Madagascar Long-fingered Bat (Miniopterus brachytragos); 31. Montagne dAmbre Long-fingered Bat (Miniopterus ambohitrensis); 32. Major's Long-fingered Bat (Miniopterus majori); 33. Eger's Long-fingered Bat (Miniopterus egeri); 34. Manavil Long-fingered Bat (Miniopterus manavi); 35. Sororcula Long-fingered Bat (Miniopterus sororculus); 36. Peterson's Long-fingered Bat (Miniopterus petersoni); 37. Mahafaly Long-fingered Bat (Miniopterus mahafaliensis); 38. Griffiths's Long-fingered Bat (Miniopterus griffithsi) in Miniopteridae
On following pages: 21. Least Long-fingered Bat (Miniopterus minon; 22. Sandy Long-fingered Bat (Miniopterus arenarius); 23. African Long-fingered Bat (Miniopterus africanus); 24. Natal Long-fingered Bat (Miniopterus natalensis); 25. Mozambican Long-fingered Bat (Miniopterus mossambicus); 26. Lesser Long-fingered Bat (Miniopterus fraterculus); 27. Aellen's Long-fingered Bat (Miniopterus aelleni); 28. Griveaud's Long-fingered Bat (Miniopterus griveaud)); 29. Glen's Long-fingered Bat (Miniopterus gleni); 30. Madagascar Long-fingered Bat (Miniopterus brachytragos); 31. Montagne dAmbre Long-fingered Bat (Miniopterus ambohitrensis); 32. Major's Long-fingered Bat (Miniopterus majori); 33. Eger's Long-fingered Bat (Miniopterus egeri); 34. Manavil Long-fingered Bat (Miniopterus manavi); 35. Sororcula Long-fingered Bat (Miniopterus sororculus); 36. Peterson's Long-fingered Bat (Miniopterus petersoni); 37. Mahafaly Long-fingered Bat (Miniopterus mahafaliensis); 38. Griffiths's Long-fingered Bat (Miniopterus griffithsi)
Measurement report: On the contribution of long-distance transport to the secondary aerosol formation and aging
<p>(1) Chemical composition of PM2.5 in four transport sectors.<br> (2) Time series of organic aerosol factors resolved by PMF&ME-2 in four transport sectors.<br> (3) Meteorological data corresponded to the ACSM and PMF&ME-2 data.<br> (4) f44 and f43 ratio in four transport sectors.</p>
A one-year-long evaluation of a wind-farm parameterisation in HARMONIE-AROME -- Model data
<p>This file contains supporting data for the manuscript "A one-year-long evaluation of a wind-farm parameterisation in HARMONIE-AROME" by van Stratum et al. 2022 in JAMES. </p> <p>- model_output: contains NetCDF files with HARMONIE-AROME for specific columns for the lidar locations, only for the WIPAFF flight comparison the full 3D hourly fields are given for one day. Files containing "DOWA_40h12tg2_fERA5_ptE" are the reference simulations and files containing "DOWA_40h12tg2_fERA5_WF2019_fix" are output from the wind farm parameterisation simulations. <br> - input_HARMONIE_WFP: contains the input files used for the wind farm parameterisation, where wind_turbine_coordinates.tab contains the locations of all wind turbines and the turbine type, and wind_turbine_0XX.tab the cp/ct curves, radius and hub height for each turbine type. </p> <p>The measurements used in the manuscript are from various external sources and should be downloaded separately.</p>
On following pages: 74. Greater Long-tongued Blossom Bat (Macroglossus sobrinus); 75. Southern Blossom Bat (Syconycteris australis); 76. Halmaheran Blossom Bat (Syconycteris carolinae); 77. Moss-forest Blossom Bat (Syconycteris hobbit); 78. Manado Fruit Bat (Boneia bidens); 79. Sulawesi Harpy Fruit Bat (Harpyionycteris celebensis); 80. Philippine Harpy Fruit Bat (Harpyionycteris whitehead); 81. Bulmer's Fruit Bat (Aproteles bulmerae); 82. Lesser Naked-backed Fruit Bat (Dobsonia minor); 83. Moluccan Naked-backed Fruit Bat (Dobsonia moluccensis); 84. Western Naked-backed Fruit Bat (Dobsonia peronii); 85. Andersen's Naked-backed Fruit Bat (Dobsonia anderseni): 86. Panniet Naked-backed Fruit Bat (Dobsonia pannietensis); 87. Philippine Naked-backed Fruit Bat (Dobsonia chapman); 88. Biak Naked-backed Fruit Bat (Dobsonia emersa); 89. Sulawesi Naked-backed Fruit Bat (Dobsonia exoleta): 90. Greenish Naked-backed Fruit Bat (Dobsonia viridis); 91. Beaufort's Naked-backed Fruit Bat (Dobsonia beaufort); 92. Halmahera Naked-backed Fruit Bat (Dobsonia crenulata); 93. Solomons Naked-backed Fruit Bat (Dobsonia inermis); 94. New Britain Naked-backed Fruit Bat (Dobsonia praedatrix). in Pteropodidae
On following pages: 74. Greater Long-tongued Blossom Bat (Macroglossus sobrinus); 75. Southern Blossom Bat (Syconycteris australis); 76. Halmaheran Blossom Bat (Syconycteris carolinae); 77. Moss-forest Blossom Bat (Syconycteris hobbit); 78. Manado Fruit Bat (Boneia bidens); 79. Sulawesi Harpy Fruit Bat (Harpyionycteris celebensis); 80. Philippine Harpy Fruit Bat (Harpyionycteris whitehead); 81. Bulmer's Fruit Bat (Aproteles bulmerae); 82. Lesser Naked-backed Fruit Bat (Dobsonia minor); 83. Moluccan Naked-backed Fruit Bat (Dobsonia moluccensis); 84. Western Naked-backed Fruit Bat (Dobsonia peronii); 85. Andersen's Naked-backed Fruit Bat (Dobsonia anderseni): 86. Panniet Naked-backed Fruit Bat (Dobsonia pannietensis); 87. Philippine Naked-backed Fruit Bat (Dobsonia chapman); 88. Biak Naked-backed Fruit Bat (Dobsonia emersa); 89. Sulawesi Naked-backed Fruit Bat (Dobsonia exoleta): 90. Greenish Naked-backed Fruit Bat (Dobsonia viridis); 91. Beaufort's Naked-backed Fruit Bat (Dobsonia beaufort); 92. Halmahera Naked-backed Fruit Bat (Dobsonia crenulata); 93. Solomons Naked-backed Fruit Bat (Dobsonia inermis); 94. New Britain Naked-backed Fruit Bat (Dobsonia praedatrix).
On following pages: 35. Short-palated Fruit Bat (Casinycteris argynnis); 36. Pohle's Fruit Bat (Casinycteris ophiodon); 37. Campo-Ma'an Fruit Bat (Casinycteris campomaanensis); 38. Lesser Dawn Bat (Eonycteris spelaea); 39. Greater Dawn Bat (Eonycteris major); 40. Philippine Dawn Bat (Eonycteris robusta); 41. Geoffroy's Rousette (Rousettus amplexicaudatus): 42. Bare-backed Rousette (Rousettus spinalatus); 43. Leschenault's Rousette (Rousettus leschenaultil); 44. Linduan Rousette (Rousettus linduensis); 45. Sulawesi Rousette (Rousettus celebensis); 46. Egyptian Rousette (Rousettus aegyptiacus); 47 Malagasy Rousette (Rousettus madagascariensis); 48. Comoro Rousette (Rousettus obliviosus); 49. Long-haired Fruit Bat (Stenonycteris lanosus). in Pteropodidae
On following pages: 35. Short-palated Fruit Bat (Casinycteris argynnis); 36. Pohle's Fruit Bat (Casinycteris ophiodon); 37. Campo-Ma'an Fruit Bat (Casinycteris campomaanensis); 38. Lesser Dawn Bat (Eonycteris spelaea); 39. Greater Dawn Bat (Eonycteris major); 40. Philippine Dawn Bat (Eonycteris robusta); 41. Geoffroy's Rousette (Rousettus amplexicaudatus): 42. Bare-backed Rousette (Rousettus spinalatus); 43. Leschenault's Rousette (Rousettus leschenaultil); 44. Linduan Rousette (Rousettus linduensis); 45. Sulawesi Rousette (Rousettus celebensis); 46. Egyptian Rousette (Rousettus aegyptiacus); 47 Malagasy Rousette (Rousettus madagascariensis); 48. Comoro Rousette (Rousettus obliviosus); 49. Long-haired Fruit Bat (Stenonycteris lanosus).
On following pages: 86. Thomas's Nectar Bat (Hsunycteris thomas); 87. Chestnut Long-tongued Bat (Lionycteris spurrell); 88. Brazilian Nectar Bat (Lonchophylla mordax); 89. Chocoan Nectar Bat (Lonchophylla chocoanal; 90. Goldman's Nectar Bat (Lonchophylla concava); 91. Pacific Forest Long-tongued Bat (Lonchophylla fornicata); 92. Orces's Long-tongued Bat (Lonchophylla orcesi); 93. Western Nectar Bat (Lonchophylla hesperia); 94. Eastern Cordilleran Nectar Bat (Lonchophylla orienticollina); 95. Handley's Nectar Bat (Lonchophylla handleyi); 96. Orange Nectar Bat (Lonchophylla robusta); 97. Dekeyser's Nectar Bat (Lonchophylla dekeyseri), 98. Pale-bellied Nectar Bat (Lonchophylla inexpectata); 99. Bokermann's Nectar Bat (Lonchophylla bokermanni); 100. Peracchi's Nectar Bat (Lonchophylla peracchii); 101. Long-snouted Bat (Platalina genovensium); 102. Vieira's Long-tongued Bat (Xeronycteris vieirai). in Phyllostomidae
On following pages: 86. Thomas's Nectar Bat (Hsunycteris thomas); 87. Chestnut Long-tongued Bat (Lionycteris spurrell); 88. Brazilian Nectar Bat (Lonchophylla mordax); 89. Chocoan Nectar Bat (Lonchophylla chocoanal; 90. Goldman's Nectar Bat (Lonchophylla concava); 91. Pacific Forest Long-tongued Bat (Lonchophylla fornicata); 92. Orces's Long-tongued Bat (Lonchophylla orcesi); 93. Western Nectar Bat (Lonchophylla hesperia); 94. Eastern Cordilleran Nectar Bat (Lonchophylla orienticollina); 95. Handley's Nectar Bat (Lonchophylla handleyi); 96. Orange Nectar Bat (Lonchophylla robusta); 97. Dekeyser's Nectar Bat (Lonchophylla dekeyseri), 98. Pale-bellied Nectar Bat (Lonchophylla inexpectata); 99. Bokermann's Nectar Bat (Lonchophylla bokermanni); 100. Peracchi's Nectar Bat (Lonchophylla peracchii); 101. Long-snouted Bat (Platalina genovensium); 102. Vieira's Long-tongued Bat (Xeronycteris vieirai).
Subspecies and Distribution. H. uw. underwoodi Thomas, 1903 — disjunct from 8S Mexico (Veracruz) to E Guatemala, S Belize, and N & W Honduras, and from SE Nicaragua to W Panama. H. u. minor C. J. Phillips & J. K. Jones, 1971 — Pacific slope in Mexico, from Nayarit and Jalisco to S Oaxaca. A.p. discontinuous distribution with gap in Nicaragua might just reflect lack of data because Underwood's Long-tongued bat always occursat rather low densities and is therefore not very often captured. in Phyllostomidae
Subspecies and Distribution. H. uw. underwoodi Thomas, 1903 — disjunct from 8S Mexico (Veracruz) to E Guatemala, S Belize, and N & W Honduras, and from SE Nicaragua to W Panama. H. u. minor C. J. Phillips & J. K. Jones, 1971 — Pacific slope in Mexico, from Nayarit and Jalisco to S Oaxaca. A.p. discontinuous distribution with gap in Nicaragua might just reflect lack of data because Underwood's Long-tongued bat always occursat rather low densities and is therefore not very often captured.
On following pages: 49. Commissaris's Long-tongued Bat (Glossophaga commissarisi); 50. Western Long-tongued Bat (Glossophaga moreno); 51. Gray's Long-tongued Bat (Glossophaga leachii); 52. Miller's Long-tongued Bat (Glossophaga longirostris); 53. Pallas''s Long-tongued Bat (Glossophaga soricina); 54. Southern Long-nosed Bat (Leptonycteris curasoae); 55. Greater Long-nosed Bat (Leptonycteris nivalis); 56. Lesser Long-nosed Bat (Leptonycteris yerbabuenae); 57. Antillean Fruit-eating Bat (Brachyphylla cavernarum); 58. Cuban Fruit-eating Bat (Brachyphylla nana); 59. Jamaican Flower Bat (Phyllonycteris aphylla); 60. Cuban Flower Bat (Phyllonycteris poeyi), 61. Brown Flower Bat (Erophylla bombifrons); 62. Buffy Flower Bat (Erophylla sezekorni). in Phyllostomidae
On following pages: 49. Commissaris's Long-tongued Bat (Glossophaga commissarisi); 50. Western Long-tongued Bat (Glossophaga moreno); 51. Gray's Long-tongued Bat (Glossophaga leachii); 52. Miller's Long-tongued Bat (Glossophaga longirostris); 53. Pallas''s Long-tongued Bat (Glossophaga soricina); 54. Southern Long-nosed Bat (Leptonycteris curasoae); 55. Greater Long-nosed Bat (Leptonycteris nivalis); 56. Lesser Long-nosed Bat (Leptonycteris yerbabuenae); 57. Antillean Fruit-eating Bat (Brachyphylla cavernarum); 58. Cuban Fruit-eating Bat (Brachyphylla nana); 59. Jamaican Flower Bat (Phyllonycteris aphylla); 60. Cuban Flower Bat (Phyllonycteris poeyi), 61. Brown Flower Bat (Erophylla bombifrons); 62. Buffy Flower Bat (Erophylla sezekorni).
Data for: Heritability and parental effects in telomere length in a color polymorphic long-lived bird
<p>Telomere length, an indicator of senescence, has been shown to be heritable but can also be affected by environmental factors, like parental effects. Investigating heritability as well as parental effects and rearing environment can help us to understand the factors affecting offspring telomeres. Moreover, how phenotypic parental traits linked with fitness can impact offspring telomere length is still unclear. A phenotypic marker closely associated with physiological traits and fitness is melanin-based color polymorphism, which in tawny owl (<em>Strix aluco</em>) is highly heritable and strongly associated with adult telomere shortening and survival. We studied narrow-sense heritability (h<sup>2</sup>) of telomere length (RTL), as well as the impact of parental age and color morph and their interaction on offspring telomere length. Offspring RTL at fledging was strongly positively correlated with both mother and father RTL at breeding. Offspring RTL was also negatively associated with father age, suggesting that older fathers sired offspring with shorter telomeres. Parental color morph did not explain offspring telomere length and there were no interactive effects of parental morph and age, despite previously documented morph-specific senescence patterns. Our results suggest that telomere length is highly heritable and affected by paternal age, but not related to color polymorphism. This suggests that either morph-specific telomere shortening as adult does not result in significantly shorter telomeres in their gametes, or that parents compensate morph-specific senescence via parental care. Morph-specific patterns of telomere dynamics in polymorphic species may thus emerge from different life-history strategies adopted in adulthood.</p>
Distribution. NE & C Vietnam, known only from Cat Ba I, Ha Long Bay (Haiphong Province) and Chu Mom Ray National Park (Kon Turn Province) in Hipposideridae
Distribution. NE & C Vietnam, known only from Cat Ba I, Ha Long Bay (Haiphong Province) and Chu Mom Ray National Park (Kon Turn Province)
Supplement table of mesozooplankton taxa obtained using long-read and short-read metabarcoding
<p>Supplement tables containing information about publications on mesozooplankton taxa in the Ross Sea using two metabarcoding analyses</p>
Patch-clamp dataset (SyncroPatch384PE) for control variants used in a calibrated functional patch clamp assay to enhance clinical variant interpretation in KCNH2-related long QT syndrome
<p><span>Modern sequencing technologies have revolutionised our detection of gene variants. However, in most genes, including <em>KCNH2</em>, the majority of missense variants are currently classified as variants of uncertain significance (VUS). The aim of this study </span><span class="normaltextrun"><span>was to investigate the utility of an automated patch-clamp assay for aiding clinical variant classification in the <em>KCNH2 </em>gene. </span></span><span>The assay was designed according to recommendations proposed by the ClinGen Sequence Variant Interpretation Working Group. Thirty-one variants (17 pathogenic/likely pathogenic, 14 benign/likely benign) were classified internally as variant controls. They were heterozygously expressed in Flp-In HEK293 cells for assessing the effects of variant on current density and channel gating in order to determine the sensitive and specificity of the assay. All 17 pathogenic variant controls had reduced current density and 13/14 benign variant controls had normal current density, which enabled determination of normal and abnormal ranges for applying moderate or supporting evidence strength for VUS reclassification. Inclusion of <em>KCNH2</em> functional assay evidence enabled us to reclassify 6 out of 44 VUS as likely pathogenic. The high-throughput patch clamp assay can provide moderate strength evidence for clinical interpretation of clinical <em>KCNH2</em> variants and </span><span>demonstrates the value of developing automated patch clamp assays for functional characterisation of ion channel gene variants.</span></p>
Data for: Long duration advertisement calls of nesting male plainfin midshipman fish are honest indicators of size and condition
<p>The plainfin midshipman fish (Porichthys notatus) has long served as a model organism for neuroethology research on acoustic communication and related social behaviors. Type I or 'singing' males produce highly stereotyped, periodic advertisement calls that are the longest known uninterrupted vertebrate vocalizations. Despite the extensive literature on the acoustic behaviour of this species, it remains unclear whether reproductive males signal their quality via their highly energetic, multiharmonic advertisement calls. Here, we recorded the advertisement calls of 22 reproductive type I males at night in a controlled laboratory setting in which males were housed in aquaria maintained at a constant temperature (13.9±0.3°C). The duration of the advertisement calls from type I males was observed to increase from the first call of the night to the middle call after which call duration remained steady until the early morning hours and first light. A strong positive correlation was observed between loudness (sound pressure level and maximum sound pressure level) of the advertisement call and body size (mass and standard length; rs>0.8). In addition, an asymptotic relationship was observed between the harmonic frequencies (f0–f10) of the advertisement calls and male body condition, with harmonic frequencies initially increasing with body condition indices, but then plateauing when body condition measures were high. Taken together, our results suggest that type I male advertisement calls provide reliable honest information about male quality regarding size and body condition. Such condition-dependent information of calling males could potentially be used by receptive females to help facilitate mate choice decisions.</p>
On following pages: 211. Alpine Chamois (Rupicapra rupicapra); 212. Carpathian Chamois (Rupicapra carpatica); 213 Gray Goral (Nemorhaedus bedford); 216. Chinese Goral (Nemorhaedus griseus); 217. Burmese Goral (Nemorhaedus. Asia Minor Chamois (Rupicapra asiatica); 214. Himalayan Brown Goral (Nemorhaedus goral); 215. Himalayan evansi); 218. Long-tailed Goral (Nemorhaedus caudatus); 219. Red Goral (Nemorhaedus baileyi). in Bovidae
On following pages: 211. Alpine Chamois (Rupicapra rupicapra); 212. Carpathian Chamois (Rupicapra carpatica); 213 Gray Goral (Nemorhaedus bedford); 216. Chinese Goral (Nemorhaedus griseus); 217. Burmese Goral (Nemorhaedus. Asia Minor Chamois (Rupicapra asiatica); 214. Himalayan Brown Goral (Nemorhaedus goral); 215. Himalayan evansi); 218. Long-tailed Goral (Nemorhaedus caudatus); 219. Red Goral (Nemorhaedus baileyi).
On following pages 3 Sunda Pangolm (Mums pvamml 4 Palawan Pangolm IMams cuhonenslsl. 5 Grant Pangolm (Manıs gıganteel. 6 Ground Pangolln IMams temmınckıı) 7 Long-tolled Pangolm (Mams tetradactylal. 8 Common Alncan Pangolrn (Manrs tncuSPISI in Manidae
On following pages 3 Sunda Pangolm (Mums pvamml 4 Palawan Pangolm IMams cuhonenslsl. 5 Grant Pangolm (Manıs gıganteel. 6 Ground Pangolln IMams temmınckıı) 7 Long-tolled Pangolm (Mams tetradactylal. 8 Common Alncan Pangolrn (Manrs tncuSPISI
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.