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Figs 110–115. 110–112. Trilychnia flavipes Motschulsky, 1854a in New world lampyrid types at the Zoological Institute of the Russian Academy of Sciences
Figs 110–115. 110–112. Trilychnia flavipes Motschulsky, 1854a, holotype, sex undetermined. 110. Habitus, dorsal view. 111. Habitus, ventral view. 112. Labels. 113–115. Trilychnia ruficollis Motschulsky, 1854a, syntype, sex undetermined. 113. Habitus, dorsal view. 114. Habitus, ventral view. 115. Labels.
Figs 92–97. 92–94. Pygolampis quadrinotata Motschulsky, 1854b in New world lampyrid types at the Zoological Institute of the Russian Academy of Sciences
Figs 92–97. 92–94. Pygolampis quadrinotata Motschulsky, 1854b, paralectotype, ♂. 92. Habitus, dorsal view. 93. Habitus, ventral view. 94. Labels.. 95–97. Pyractomena vitticollis Motschulsky, 1853, syntype, ♂. 95. Habitus, dorsal view. 96. Habitus, ventral view. 97. Labels.
Figs 98–103. 98–100. Telephoroides fruticola Motschulsky, 1854b in New world lampyrid types at the Zoological Institute of the Russian Academy of Sciences
Figs 98–103. 98–100. Telephoroides fruticola Motschulsky, 1854b, paralectotype, ♂. 98. Habitus, dorsal view. 99. Habitus, ventral view. 100. Labels. 101–103. Telephoroides lineatocollis Motschulsky, 1854b, lectotype, ♂. 101. Habitus, dorsal view. 102. Habitus, ventral view. 103. Labels.
Figs 80–85. 80–82. Pseudolychnuris suturalis Motschulsky, 1854a in New world lampyrid types at the Zoological Institute of the Russian Academy of Sciences
Figs 80–85. 80–82. Pseudolychnuris suturalis Motschulsky, 1854a, lectotype, ♂. 80. Habitus, dorsal view. 81. Habitus, ventral view. 82. Labels. 83–85. Pseudolychnuris vittata Motschulsky, 1853, paralectotype, ♂. 83. Habitus, dorsal view. 84. Habitus, ventral view. 85. Labels.
Figs 86–91. 86–88. Pygolampis blanda Motschulsky, 1854b in New world lampyrid types at the Zoological Institute of the Russian Academy of Sciences
Figs 86–91. 86–88. Pygolampis blanda Motschulsky, 1854b, Syntype, ♂. 86. Habitus, dorsal view. 87. Habitus, ventral view. 88. Labels. 89–91. Pygolampis interrupta Motschulsky, 1854b, syntype, ♀. 89. Habitus, dorsal view. 90. Habitus, ventral view. 91. Labels.
Figs 74–79. 74–76. Nyctophanes palliata Motschulsky, 1854a in New world lampyrid types at the Zoological Institute of the Russian Academy of Sciences
Figs 74–79. 74–76. Nyctophanes palliata Motschulsky, 1854a, holotype, ♀. 74. Habitus, dorsal view. 75. Habitus, ventral view. 76. Labels. 77–79. Nyctophanes pellucida Motschulsky, 1854a, holotype, ♀. 77. Habitus, dorsal view. 78. Habitus, ventral view. 79. Labels.
Figs 68–73. 68–70. Nyctophanes cassidea, 1854a in New world lampyrid types at the Zoological Institute of the Russian Academy of Sciences
Figs 68–73. 68–70. Nyctophanes cassidea, 1854a, holotype, sex undetermined. 68. Habitus, dorsal view. 69. Habitus, ventral view. 70. Labels. 71–73. Nyctophanes lineolata Motschulsky, 1854a, holotype, ♂. 71. Habitus, dorsal view. 72. Habitus, ventral view. 73. Labels.
Figs 62–67. 62–64. Nyctophanes bisignata Motschulsky, 1854a in New world lampyrid types at the Zoological Institute of the Russian Academy of Sciences
Figs 62–67. 62–64. Nyctophanes bisignata Motschulsky, 1854a, holotype, ♀. 62. Habitus, dorsal view. 63. Habitus, ventral view. 64. Labels. 65-67. Nyctophanes bremei Motschulsky, 1854a, syntype, ♀. 65. Habitus, dorsal view. 66. Habitus, ventral view. 67. Labels.
Figs 56–61. 56–58. Nyctocrepis flabellicornis Motschulsky, 1854a in New world lampyrid types at the Zoological Institute of the Russian Academy of Sciences
Figs 56–61. 56–58. Nyctocrepis flabellicornis Motschulsky, 1854a, holotype, ♂. 56. Habitus, dorsal view. 57. Habitus, ventral view. 58. Labels. 59–61. Nyctocrepis lamellicornis Motschulsky, 1854a, paralectotype, ♂. 59. Habitus, dorsal view. 60. Habitus, ventral view. 61. Labels.
Figs 44–49. 44–46. Macrolampis cincta Motschulsky, 1854a in New world lampyrid types at the Zoological Institute of the Russian Academy of Sciences
Figs 44–49. 44–46. Macrolampis cincta Motschulsky, 1854a, paralectotype, ♂. 44. Habitus, dorsal view. 45. Habitus, ventral view. 46. Labels. 47–49. Macrolampis longipennis Motschulsky, 1854a, lectotype, ♂. 47. Habitus, dorsal view. 48. Habitus, ventral view. 49. Labels.
Figs 50–55. 50–52. Macrolampis longula Motschulsky, 1854a in New world lampyrid types at the Zoological Institute of the Russian Academy of Sciences
Figs 50–55. 50–52. Macrolampis longula Motschulsky, 1854a, holotype, ♂. 50. Habitus, dorsal view. 51. Habitus, ventral view. 52. Labels. 53–55. Nyctocrepis demoulini Motschulsky, 1853, holotype, ♂. 53. Habitus, dorsal view. 54. Habitus, ventral view. 55. Labels.
Figs 32–37. 32–34. Ellipolampis suturella Motschulsky, 1854a in New world lampyrid types at the Zoological Institute of the Russian Academy of Sciences
Figs 32–37. 32–34. Ellipolampis suturella Motschulsky, 1854a, paralectotype, ♂. 32. Habitus, dorsal view. 33. Habitus, ventral view. 34. Labels. 35–37. Lychnacris triguttula Motschulsky, 1854a, holotype, ♀. 35. Habitus, dorsal view. 36. Habitus, ventral view. 37. Labels.
Figs 14–19. 14–16. Ellychnia californica Motschulsky, 1854a in New world lampyrid types at the Zoological Institute of the Russian Academy of Sciences
Figs 14–19. 14–16. Ellychnia californica Motschulsky, 1854a, lectotype, ♀. 14. Habitus, dorsal view. 15. Habitus, ventral view. 16. Labels. 17–19. Ellychnia latipennis Motschulsky, 1854a, holotype, ♀. 17. Habitus, dorsal view. 18. Habitus, ventral view. 19. Labels.
Figs 38–43. 38–40. Lychnogaster cinctus Motschulsky, 1854a in New world lampyrid types at the Zoological Institute of the Russian Academy of Sciences
Figs 38–43. 38–40. Lychnogaster cinctus Motschulsky, 1854a, paralectotype, sex undetermined. 38. Habitus, dorsal view. 39. Habitus, ventral view. 40. Labels. 41–43. Lychnuris klugii Motschulsky, 1854a, lectotype, ♂. 41. Habitus, dorsal view. 42. Habitus, ventral view. 43. Labels.
Figs 8–13. 8–10. Dilychnia basalis Motschulsky, 1853 in New world lampyrid types at the Zoological Institute of the Russian Academy of Sciences
Figs 8–13. 8–10. Dilychnia basalis Motschulsky, 1853, syntype, sex undetermined. 8. Habitus, dorsal view. 9. Habitus, ventral view. 10. Labels. 11–13. Ellychnia albilatera Motschulsky, 1854a, holotype, ♀. 11. Habitus, dorsal view. 12. Habitus, ventral view. 13. Labels.
Figs 1–7. 1–4. Amydetes fucatus Motschulsky, 1854b in New world lampyrid types at the Zoological Institute of the Russian Academy of Sciences
Figs 1–7. 1–4. Amydetes fucatus Motschulsky, 1854b, holotype, ♂. 1. Habitus, dorsal view. 2. Habitus, ventral view. 3. Antenna, lateral view. 4. Labels. 5–7. Bicellonycha lividipennis Motschulsky, 1854b, lectotype, ♂. 5. Habitus, dorsal view. 6. Habitus, ventral view. 7. Labels.
Figs 20–25. 20–22. Ellychnia mexicana Motschulsky, 1854a in New world lampyrid types at the Zoological Institute of the Russian Academy of Sciences
Figs 20–25. 20–22. Ellychnia mexicana Motschulsky, 1854a, holotype, ♀. 20. Habitus, dorsal view. 21. Habitus, ventral view.22. Labels. 23–25. Ellipolampis elongata Motschulsky, 1854a, paralectotype, ♂. 23. Habitus, dorsal view. 24. Habitus, ventral view. 25. Labels.
Paradoxes in the co-evolution of contagions and institutions
<p>Epidemic models study the spread of undesired agents through populations, be it infectious diseases through a country, misinformation in social media, or pests infesting a region. In combating these epidemics, we rely neither on global top-down interventions, nor solely on individual adaptations. Instead, interventions commonly come from local institutions such as public health departments, moderation teams on social media platforms, or other forms of group governance. Classic models, which are often individual or agent-based, are ill-suited to capture local adaptations. We leverage developments of institutional dynamics based on cultural group selection to study how groups attempt local control of an epidemic by taking inspiration from the successes and failures of other groups. Incorporating institutional changes into epidemic dynamics reveals paradoxes: a higher transmission rate can result in smaller outbreaks as does decreasing the speed of institutional adaptation. When groups perceive a contagion as more worrisome, they can invest in improved policies and, if they maintain these policies long enough to have impact, lead to a reduction in endemicity. By looking at the interplay between the speed of institutions and the transmission rate of the contagions, we find rich co-evolutionary dynamics that reflect the complexity of known biological and social contagions.</p>
Рис. 1. Карта-схема заказника «УΑыΛь» с указанием станций отбора проб зообентоса (с сайта ФГБУ «ЗаповеΑное Приамурье». URL: http://www.zapovedamur.ru/zakaznik_udyl) Fig. 1. Map-scheme of the Udyl Nature Reserve with indication of zoobenthos sampling stations (from website of the Federal State Budgetary Institution "Zapovednoe Priamurye. Available at: http://www.zapovedamur.ru/zakaznik_udyl) in Quantitative zoobenthos characteristics of the Udyl Lake basin (Udyl Nature Reserve, Khabarovsky Region)
Рис. 1. Карта-схема заказника «УΑыΛь» с указанием станций отбора проб зообентоса (с сайта ФГБУ «ЗаповеΑное Приамурье». URL: http://www.zapovedamur.ru/zakaznik_udyl) Fig. 1. Map-scheme of the Udyl Nature Reserve with indication of zoobenthos sampling stations (from website of the Federal State Budgetary Institution "Zapovednoe Priamurye. Available at: http://www.zapovedamur.ru/zakaznik_udyl)
BRAIN Journal-Prediction of Thyroid Disease Using Data Mining Techniques-Figure 1. Factors that Affect Thyroid Function (The Institute for Functional Medicine, 2014)
<p> In Figure 1 are presented the main factors that affect the thyroid function. It is obvious that factors such as stress, infection, toxins, trauma and certain medication are directly responsible for the improper production of thyroid hormones. Symptoms identification and the early detection of abnormal values of thyroid hormones after clinical investigation will help in establishing the proper diagnostic and to prescribe the right medication. The patient must periodically evaluate his clinical state in order to receive the treatment as long as he needs it. </p>
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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.