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Fetal exposure to the Ukraine famine of 1932-1933 and adult Type 2 Diabetes Mellitus (Public data and analytical code)
<p><strong>Abstract</strong></p> <p>The short-term impact of famines on death and disease is well documented but it is difficult to estimate their potential long-term impact. We used the setting of the man-made Ukrainian Holodomor famine of 1932-1933 to examine the relationship between prenatal famine and adult Type 2 diabetes mellitus (T2DM). This ecological study included 128,225 T2DM cases diagnosed between 2000-2008 among 10,186,016 male and female Ukrainians born between 1930 and 1938. Individuals who were born in the first half-year of 1934, and hence exposed in early gestation to the mid-1933 peak famine period, had a larger than two-fold likelihood of T2DM (OR 2.21; 95% CI 2.00-2.45) compared to unexposed controls. There was a dose-response relationship between severity of famine exposure and adult T2DM risk comparing individuals born in regions with severe, very severe, and extreme famine to births in the no-famine region.</p> <p> </p> <p><strong>Description of the data and analytical code</strong></p> <p>In exploratory analyses we first examined whether the odds for T2DM were elevated for any month of birth in the period January 1930 to December 1938 in any of the four regions of varying famine intensity. This was achieved by comparing, within each region, the T2DM odds for births in any month and year of birth relative to the T2DM odds for births in the same month combining all other years of birth. The analysis served to identify potential relations of famine with specific months and years of birth, controlling for month of birth effects. We observed increased T2DM odds ratios for births between January and June 1934 in famine-exposed oblasts, with smaller increases for births in 1935 and 1936 in these months. Our findings suggested that in multivariate modelling statistical control for month of birth effects could be accomplished by adjusting for the January-June period. Our findings are presented in the data file '01 Odds Ratio for T2DM Over Time' and show the odds ratios (ORs) for Type 2 Diabetes Mellitus (T2DM) comparing the region-specific T2DM odds for each birth year and month relative to births in the same months but combining all other years of birth. The R syntax file '01 Odds of T2DM Over Time Figure' provides the code necessary to reproduce the figure.</p> <p> </p> <p>For confirmatory analyses we employed a Difference-in-Differences approach to quantify associations between prenatal exposure to famine and T2DM, taking into account year of birth, half-year of birth (Jan-Jun vs Jul-Dec), region, and their interactions. This analysis was conducted initially for each gender separately and then for both genders combined, adjusting for We carried out sensitivity analyses to assess potential changes in T2DM odds arising from the use of pre-famine births vs post-famine births as controls. Our findings are presented in the data file '02 Ukraine Famine 1932-33 Main Data'. Information on the number of T2DM cases by gender, region of residence, and year and month of birth 1930-1938 in Ukraine was collected by the national Ukraine Diabetes Register (Komisarenko Institute of Endocrinology and Metabolism, Kyiv) between 2000-2008. The number of births in the same subgroups, representing the populations at risk for T2DM, was estimated by demographic population reconstruction methods as reported in the publication. We classified the birth counts by year of birth, the semi-annual birth period (January-June vs. July-December), region of birth, and gender. The SPSS syntax file titled '02 Ukraine Famine 1932-33 Main Analysis' provides the code to replicate our main findings as presented in the publication.</p> <p> </p> <p>In a separate analysis we visualized by a meta-regression approach the relation between famine intensity at the oblast level in 1933 and the odds for adult T2DM. The data required for the replication of our findings are included in the file '03 Odds Ratio for T2DM and Famine Intensity at Oblast Level'. The R syntax file titled '03 Ukraine Famine 1932-33 Meta-regression' provides details on conducting the meta-regression using the R package ‘metafor’.</p> <p> </p> <p><strong>Funding</strong></p> <p>Ukraine State complex program Diabetes Mellitus, project number 0106U000844 (M.K.). Holodomor Research and Education Consortium in Canada (L.H.L., O.W.). NIDI-NIAS Fellowship of the Royal Netherlands Academy of Sciences (L.H.L.). National Institute of Aging R01 AG028593 (L.H.L.). National Institute of Aging R01 AG06687 (L.H.L.).</p> <p> </p> <p><strong>Sharing/Access information</strong></p> <p>Data sharing and use are unrestricted with acknowledgement of the original publication and listing of the funding sources as per the above. Researchers are encouraged to contact the Principal Investigators (PIs) for consultations on data structure and use as needed (L.H. Lumey, <a href="mailto:lumey@columbia.edu">lumey@columbia.edu</a>; Oleh Wolowyna, <a href="mailto:olehw@aol.com">olehw@aol.com</a>).</p>
Trento 1936 - Building 1932
<u>Coordinates</u>: N/A <br><u>Length</u>: 18.85 m<br><u>Width</u>: 9.66 m<br><u>Height</u>: 11.13 m<br><u>Points</u>: 16 <br><u>Vertices</u>: 84 <br><u>Primitives</u>: 28 <br><br><u>Main Files:</u><br><table><tbody><tr><th>Filename</th><th>.glb</th><th>.xml</th><th>.obj</th></tr><tr><td><a href="https://zenodo.org/api/records/12694163/files/building_1932.obj/content">building_1932.obj</a></td><td></td><td></td><td><a href="https://zenodo.org/api/records/12694163/files/building_1932.obj/content">Link</a></td></tr><tr><td><a href="https://zenodo.org/api/records/12694163/files/building_1932.glb/content">building_1932.glb</a></td><td><a href="https://zenodo.org/api/records/12694163/files/building_1932.glb/content">Link</a></td><td></td><td></td></tr><tr><td><a href="https://zenodo.org/api/records/12694163/files/11574436_edm.xml/content">11574436_edm.xml</a></td><td></td><td><a href="https://zenodo.org/api/records/12694163/files/11574436_edm.xml/content">Link</a></td><td></td></tr><tr><td><a href="https://zenodo.org/api/records/12694163/files/11574436_metsmods.xml/content">11574436_metsmods.xml</a></td><td></td><td><a href="https://zenodo.org/api/records/12694163/files/11574436_metsmods.xml/content">Link</a></td><td></td></tr></tbody></table><br><br><u>Thumbnails:</u><br><table><tbody><tr><th>Perspective</th><th>1000x1000</th><th>512x512</th><th>256x256</th><th>128x128</th></tr><tr><td>Perspective 1</td><td><a href="https://zenodo.org/api/records/12694163/files/building_1932_perspective_1.png/content">Link</a></td><td><a href="https://zenodo.org/api/records/12694163/files/building_1932_perspective_1_512x512.png/content">Link</a></td><td><a href="https://zenodo.org/api/records/12694163/files/building_1932_perspective_1_256x256.png/content">Link</a></td><td><a href="https://zenodo.org/api/records/12694163/files/building_1932_perspective_1_128x128.png/content">Link</a></td></tr><tr><td>Perspective 2</td><td><a href="https://zenodo.org/api/records/12694163/files/building_1932_perspective_2.png/content">Link</a></td><td><a href="https://zenodo.org/api/records/12694163/files/building_1932_perspective_2_512x512.png/content">Link</a></td><td><a href="https://zenodo.org/api/records/12694163/files/building_1932_perspective_2_256x256.png/content">Link</a></td><td><a href="https://zenodo.org/api/records/12694163/files/building_1932_perspective_2_128x128.png/content">Link</a></td></tr><tr><td>Perspective 3</td><td><a href="https://zenodo.org/api/records/12694163/files/building_1932_perspective_3.png/content">Link</a></td><td><a href="https://zenodo.org/api/records/12694163/files/building_1932_perspective_3_512x512.png/content">Link</a></td><td><a href="https://zenodo.org/api/records/12694163/files/building_1932_perspective_3_256x256.png/content">Link</a></td><td><a href="https://zenodo.org/api/records/12694163/files/building_1932_perspective_3_128x128.png/content">Link</a></td></tr><tr><td>Perspective 4</td><td><a href="https://zenodo.org/api/records/12694163/files/building_1932_perspective_4.png/content">Link</a></td><td><a href="https://zenodo.org/api/records/12694163/files/building_1932_perspective_4_512x512.png/content">Link</a></td><td><a href="https://zenodo.org/api/records/12694163/files/building_1932_perspective_4_256x256.png/content">Link</a></td><td><a href="https://zenodo.org/api/records/12694163/files/building_1932_perspective_4_128x128.png/content">Link</a></td></tr><tr><td>Perspective Top</td><td><a href="https://zenodo.org/api/records/12694163/files/building_1932_perspective_top.png/content">Link</a></td><td><a href="https://zenodo.org/api/records/12694163/files/building_1932_perspective_top_512x512.png/content">Link</a></td><td><a href="https://zenodo.org/api/records/12694163/files/building_1932_perspective_top_256x256.png/content">Link</a></td><td><a href="https://zenodo.org/api/records/12694163/files/building_1932_perspective_top_128x128.png/content">Link</a></td></tr></tbody></table><br><br><br><u>Changelog</u>: <br> - v<a href="https://doi.org/10.5281/zenodo.12542827">0.0.2</a>: Thumbnails added, Description updated with Link Tables.<br> - v<a href="https://doi.org/10.5281/zenodo.12694163">0.0.3</a>: Added XMLs for Europeana Data Model (EDM) and MetsMods.<br>
Annual summaries of daily observations from the USGS Streamflow Gauging Station on the Altamaha River near Doctortown, Georgia, for 1932 to 2004
Daily averaged river discharge data were obtained from the United States Geological Survey for streamflow gauging station USGS 02226000 on the Altamaha River near Doctortown, Georgia. Processed tabular data were downloaded from the USGS real-time web server (http://waterdata.usgs.gov/nwis/) by the Georgia Coastal Ecosystems LTER project, documented, and standardized to metric units. Missing values of mean discharge were estimated by cubic spline interpolation to fill in data gaps of five or fewer consecutive days. Annual summary statistics were then calculated from daily values aggregated by year.
Fig. 12. Rochinia debilis Rathbun, 1932, overall dorsal view. A in Deep-sea spider crabs of the families Epialtidae MacLeay, 1838 and Inachidae MacLeay, 1838, from the South China Sea, with descriptions of two new species (Decapoda, Brachyura, Majoidea)
Fig. 12. Rochinia debilis Rathbun, 1932, overall dorsal view. A. Holotype, ♀ (10.8 × 7.0 mm) (USNM49572), Japan. B. ♂ (23.1 × 15.8 mm) (SMF49904), Japan. C. ♂ (28.9 × 21.0 mm) (SMF49905), Japan, carapace half cleaned. Scale bars: A = 5 mm; B–C = 10 mm.
FIGURES 6 – 7 in Redescription of the type of Siphlonurus davidi (Navás, 1932) (Ephemeroptera: Siphlonuridae)
FIGURES 6 – 7, Siphlonurus davidi, photographs: 6, pinned specimen (photographie J. Legrand, Entomologie, MNHN, Paris); 7, genitalia (cleared), ventral view (photograph by Sartori).
FIGURES 32 – 39 in Parasitic copepods infesting the olfactory sacs of skates from the southwestern Atlantic with the description of a new species of Kroeyerina Wilson, 1932
FIGURES 32 – 39. Kroeyerina sudamericana sp. nov. SEM micrographs (adult female). 32, general habitus, ventral; 33, caudal rami; 34, detail of distal armature of caudal ramus; 35, fifth leg; 36, rostral processes; 37, mouth tube and maxillules; 38, maxilla; 39, maxilliped. Scale bars: 32 = 500 µm; 33, 37, 39 = 50 µm; 34 – 36 = 10 µm; 38 = 20 µm.
FIGURES 48 – 56. Brianella corniger Wilson, 1915 in Parasitic copepods infesting the olfactory sacs of skates from the southwestern Atlantic with the description of a new species of Kroeyerina Wilson, 1932
FIGURES 48 – 56. Brianella corniger Wilson, 1915. SEM micrographs (female). 48, tip of cephalothorax (oral region), ventral; 49, tip of antennule; 50, antenna (arrows indicate the three naked setae); 51, maxillule; 52, mouth tube, with tips of mandibles inside, 53; fused tip of maxillae and origin of the two processes of the attachment organ (distal portion of maxillae); 54, detail of vestigial bulla; 55, attachment organ; 56, attachment organ (dissected from base) showing asymmetric branching. Scale bars: 48, 54 = 50 µm; 49, 52 = 10 µm; 50 – 51 = 20 µm; 53 = 200 µm; 55 – 56 = 1 mm.
FIGURES 40 – 47 in Parasitic copepods infesting the olfactory sacs of skates from the southwestern Atlantic with the description of a new species of Kroeyerina Wilson, 1932
FIGURES 40 – 47. Kroeyerina sudamericana sp. nov. SEM micrographs (adult male). 40, general habitus, ventral; 41, caudal rami; 42, detail of distal armature of caudal rami; 43, spinulation in lateral fields of genital complex; 44, rostral processes; 45, antenna; 46, mouth tube and maxilla; 47, maxilliped. Scale bars: 40 = 200 µm; 41 = 50 µm; 42 – 44 = 10 µm; 45 – 47 = 20 µm.
Fig. 4. A in A new species of Anaglyphula Rensch, 1932 from an island off the coast of West Indonesia, with redescription of the type species (Gastropoda: Caenogastropoda: Assimineidae)
Fig. 4. A, Putative constriction position of Anaglyphula yanseni, new species, holotype MZB.Gst. 23.829; B, Constriction of Anaglyphula cancellata Rensch, 1932, syntype NHMUK 1897.8.3.150; C, Constriction of Anaglyphula whitteni Vermeulen, 1996, paratype NHMUK 20000247. Not to scale.
Fig. 1. Anaglyphula cancellata Rensch, 1932, syntype NHMUK 1897.8.3.150. A in A new species of Anaglyphula Rensch, 1932 from an island off the coast of West Indonesia, with redescription of the type species (Gastropoda: Caenogastropoda: Assimineidae)
Fig. 1. Anaglyphula cancellata Rensch, 1932, syntype NHMUK 1897.8.3.150. A, Shell; B, Upper whorls; C, Structure on body whorl; D, Detailed structure on penultimate whorl.
Fig. 3 in A new species of Anaglyphula Rensch, 1932 from an island off the coast of West Indonesia, with redescription of the type species (Gastropoda: Caenogastropoda: Assimineidae)
Fig. 3. Anaglyphula yanseni, new species, holotype MZB.Gst. 23.829. A–B, Shell; A, Visible light camera images; B, SEM images; C, Protoconch; D, Detailed structure on upper body whorl; E, Detailed structure on lower body whorl.
Fig. 2. A in A new species of Anaglyphula Rensch, 1932 from an island off the coast of West Indonesia, with redescription of the type species (Gastropoda: Caenogastropoda: Assimineidae)
Fig. 2. A, Anaglyphula cancellata Rensch, 1932, syntype NHMUK 1897.8.3.149; B–C, Anaglyphula whitteni Vermeulen, 1996, Paratype. NHMUK 20000247; B, Shell; C, Ribbing structure details.
Fig. 5. Acmella species. A in A new species of Anaglyphula Rensch, 1932 from an island off the coast of West Indonesia, with redescription of the type species (Gastropoda: Caenogastropoda: Assimineidae)
Fig. 5. Acmella species. A, Acmella cf. tersa, NHMUK; B, Acmella moreletiana G. Nevill, 1878, NHMUK 1891.3.17.944–7; C, Acmella mellilla Godwin-Austen, 1895, NHMUK 1903.7.1.1698.
Fig. 50. Scrapter semirufus Cockerell, 1932 in Revision of the nitidus species group of the bee genus Scrapter Lepeletier & Serville, 1828 (Hymenoptera: Apoidea)
Fig. 50. Scrapter semirufus Cockerell, 1932, ♂. A. Terga 1–2 (dorsal view). B. Genitalia (dorsal view). C. Sternum 7. D. Sternum 8.
Fig. 49. Scrapter semirufus Cockerell, 1932 in Revision of the nitidus species group of the bee genus Scrapter Lepeletier & Serville, 1828 (Hymenoptera: Apoidea)
Fig. 49. Scrapter semirufus Cockerell, 1932, ♂. A. Lateral view. B. Scutum and scutellum (dorsal view). C. Metanotum and propodeum (dorsal view). D. Metasoma (dorsal view).
Fig. 48. Scrapter semirufus Cockerell, 1932 in Revision of the nitidus species group of the bee genus Scrapter Lepeletier & Serville, 1828 (Hymenoptera: Apoidea)
Fig. 48. Scrapter semirufus Cockerell, 1932, ♀. A. Lateral view. B. Head (dorsal view). C. Scutum and scutellum (dorsal view). D. Metanotum and propodeum (dorsal view). E. Metasoma (dorsal view). F. Terga 1–2 (dorsal view).
Figs 16–21 in Redescription of Strombidium coronatum (Leegaard, 1915) Kahl, 1932 (Ciliophora, Spirotricha) based on live observation, protargol impregnation, and scanning electron microscopy
Figs 16–21. Strombidium coronatum, Irish Sea specimens (16–18, scanning electron micrographs; 19–21, protargol impregnation, micrographs of several focal planes were stacked, using the computer program CombineZP from Alan Hadley). 16 – ventrolateral view; 17 – left lateral view showing uniquely shaped peristome, which is roughly triangular in outline and almost flat, extending in the sagittal plane. The extrusomes insert in short oblique rows anteriorly to the girdle kinety; note that some of them are just ejected (arrowhead); 18 – posterior cell portion showing the sharp, longitudinal ridges that have already been illustrated in the original description by Leegaard (1915); 19 – left lateral view of an early divider; 20 – dorsolateral view of an early divider; 21 – ventrolateral view. AP – apical protrusion, BM – buccal membranelles, CM – collar membranelles, DC – distended cell surface, EX – extrusome attachment sites, GK – girdle kinety, MA – macronucleus, OP – oral primordium, VK – ventral kinety. Scale bars: 40 µm (16), 20 µm (17, 19–21), and 10 µm (18).
Fig. 30 in Review of the fritillary species systematically close to Melitaea lutko Evans, 1932 (Lepidoptera: Nymphalidae) with analysis of their geographic distribution and interrelations with host plants
Fig. 30 (continued on next page). Distribution of the lutko species group fritillaries in combination with the distribution of known and suspected species of host plants from the genus Phlomoides Blume. = Melitaea lutko Evans, 1932; = M. timandra timandra Coutsis & Oorschot, 2014; = M. timandra binaludica subsp. nov.; = M. shahvarica sp. nov.; = M. mimetica mimetica Higgins, 1940; = M. mimetica delerei Heidemann, 1954;? = unconfirmed findings of M. timandra; = M. timandra with an unclear subspecies status; = Phlomoides regeliana (Aitch. & Hemsl.) Adylov, Kamelin & Makhm.; = Phlomoides boissieriana (Regel) Adylov, Kamelin & Makhm.; = Phlomoides laciniata (L.) Kamelin & Makhm.; = Phlomoides labiosiformis (Popov) Adylov, Kamelin & Makhm.; = Phlomoides loasifolia (Benth.) Kamelin & Makhm.; = Phlomoides molucelloides (Bunge) Salmaki; = Phlomoides acaulis (Beck ex Rech.f.) Salmaki; = Phlomoides labiosa (Bunge) Adylov, Kamelin & Makhm. A. Pakistan, Chitral, Chaghbini CGNP, alt. 2700–3000 m. B. Pakistan, Khyber Pakhtunkhwa, Drosh. C. Pakistan, Khyber Pakhtunkhwa, Keon Nullah. D. Pakistan, Khyber Pakhtunkhwa, Malakand. E. Pakistan, Khyber Pakhtunkhwa, Birmoglasht. F. Turkmenistan, Badkhyz, Kepeli, alt. 700 m. G. Turkmenistan, Badkhyz, Kyzyl-Jar, alt. 700 m. H. Turkmenistan, Kushka, alt. 700 m. I. Turkmenistan, Murgab river, Sary-Yazy, alt. 300 m. J. Turkmenistan, 30 km E of BairamAli, Zahmet, alt. 240 m. K. Turkmenistan, Bairam-Ali, alt. 230 m. L. Turkmenistan, Kara-Kum desert, 30 km W of Mary, alt. 200 m.M. Turkmenistan, Dushak, alt. 250 m.N. Turkmenistan, Chaacha, alt. 400 m. O. Turkmenistan, Bakharden, alt. 200 m. P. Iran, Khorossan Razavi, Kuh-e-Binalud Mts, Qadamgah area, Gerina, alt. 2000 m. Q. Iran, Khorasan Razavi, Kuh-e-Binalud Mts, 15 km SW of Zoshk, alt. 2300– 2500 m. R. Iran, S Khorosan, 75 km N of Birjant, Sedeh, alt. 1500 m. S. Iran, S Khorosan, 35 km N of Birjant, alt. 1500 m. T. Afghanistan, Bamian, Band-e-Amir, Dzhudoi-Kvak Gorge, alt. 3200 m. U. Afghanistan, Bamian, Band-e-Amir, Hazarajat, alt. 3000–3200 m. V. Afghanistan, Bamian, Koh-iBaba Mts, Joshanak, alt. 2800 m. W. Afghanistan, Heart, Qala-i-Naw, Kashka pass. X. Iran, Semnan, Shahvar Mt., alt. 2200–2500 m. Y. Turkmenistan, Kara-Kala, Monjukly Ridge, 300–700 m. Z. Iran, Golestan, E Maraveh Tappeh, N Ghazan Ghayeh, Palizan Mts. A". Pakistan, Balochistan, Quetta, Urak, alt. 2500 m. B". Pakistan, Balochistan, Ziarat, alt. 2500 m. C". Pakistan, Balochistan, Khojak, alt. 1700 m. D". Pakistan, Balochistan, Zaghum, alt. 1600 m; E". Pakistan, Punjab, Gawar, alt. 500 m. F". Pakistan, Balochistan, Sheik Wazil, alt. 1600 m. G". Afghanistan, Bamian, Hushkak, alt. 2700–2800 m. H". Afghanistan, Bamian, Punjub Distr., 10 km NE of Varas, alt. 2400 m. I". Afghanistan, Ghor, 17 km E of Changcharan, 15 km S of Bandi-Ali, Gazak Mts, alt. 2400 m. J". Afghanistan, Ghor, Bayan Range, 15 km S of Changcharan, Kindival valley, alt. 2700 m. K". Afghanistan, Bamiyan, Kohi-Baba Mts, Panjao, alt. 3000 m. Afghanistan, Bamiyan, Koh-i-Baba Mts, Shah-tu-Kotal, alt. 4000 m. L". Afghanistan, Kapisa, Pandshir valley, alt. 2200–2800 m. M". Afghanistan, Kabul. N". Iran, Tehran, Elburz Ridge, Demavend Mt., Ask, alt. 1800 m. O". Iran, Semnan, Foulad Mohaleh, alt. 2200 m. P". Pakistan, Punjab, Murree.
Fig. 29 in Review of the fritillary species systematically close to Melitaea lutko Evans, 1932 (Lepidoptera: Nymphalidae) with analysis of their geographic distribution and interrelations with host plants
Fig. 29.Differences in the structure of valva and aedeagus of the lutko species group.A. Melitaea shahvarica sp. nov. B, D, H. M. timandra binaludica subsp. nov. C–E. M. mimetica Higgins, 1940. F. M. lutko Evans, 1932. G. M. timandra timandra Coutsis &van Oorschot, 2014. A. Iran, Semnan Prov., Shahrud area, S macroslope of Shahvar Mts, alt. 2200–2400 m. B. Iran, Rezavi Khorassan Prov., Kuh-e-Binalud Mts, Dorrud v. vicinity, alt. 2430 m. C. Afghanistan, Bamian Prov., Punjub Distr., 10 km NE of Varas v., alt. 2400 m. D. Afghanistan, Band-i-Amir, Hazarajat. E. Pakistan, Balochistan, Quetta, Urak, alt. 2400– 2700 m. F. Pakistan, Chitral, Gol National Park, alt. 2700 m. G. Turkmenistan, Sary-Yazy, alt. 700 m. H. Iran, Rezavi Khorassan Prov., Kuh-e-Binalud Mts, Dorrud v. vicinity, alt. 2430 m.
Fig. 28 in Review of the fritillary species systematically close to Melitaea lutko Evans, 1932 (Lepidoptera: Nymphalidae) with analysis of their geographic distribution and interrelations with host plants
Fig. 28.Eggs and caterpillars of Melitaea shahvarica sp. nov. in nature and in the laboratory.A–B. Freshly laid eggs under a leaf of a host plant, May 2018, Iran, Shahvar Mt., alt. 2200 m. C–D. IV–V instar caterpillars on the leaves of the host plant Phlomoides molucelloides (Bunge) Salmaki, July 2019, Iran, Shahvar Mt., alt. 2500 m. E. I instar caterpillars in the laboratory, Moscow, May 2018. F. VI instar caterpillars during diapause, Moscow, October 2018.
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