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Suplement of Enhancing hypermarket competitive advantage through ergonomic elderly trolley design: an Indonesian-based design
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FIGURE 1 in The genus Coricuma Watling & Breedy, 1988 (Crustacea, Cumacea, Bodotriidae) in Indonesian waters
FIGURE 1. SEM photos of Coricuma insolita n. comb. (Petrescu 1992), adult male from Lembeh Island: a: habitus, b: carapace, c: uropods, d: antenna 2, e: second antenna, detail.
FIGURE 2 in The genus Coricuma Watling & Breedy, 1988 (Crustacea, Cumacea, Bodotriidae) in Indonesian waters
FIGURE 2. SEM photos of Coricuma insolita n. comb. (Petrescu 1992), adult female from Lembeh Island: a: habitus, b: carapace, c: uropods, d: first antenna.
FIGURE 4 in The genus Coricuma Watling & Breedy, 1988 (Crustacea, Cumacea, Bodotriidae) in Indonesian waters
FIGURE 4. SEM photos of Coricuma insolita n. comb. (Petrescu 1992), adult female from Raja Ampat: a: habitus, b: carapace, c: uropods, d: first antenna.
FIGURE 3 in The genus Coricuma Watling & Breedy, 1988 (Crustacea, Cumacea, Bodotriidae) in Indonesian waters
FIGURE 3. SEM photos of Coricuma insolita n. comb. (Petrescu 1992), adult male from Raja Ampat: a: habitus, b: carapace, c: uropods, d: first antenna, e: second antenna, f and g: second antenna, detail.
Distribution. Mainland SE Asia, Peninsular Malaysia, and Sumatra. The Javan Mongoose or the Small Indian Mongoose is said to occur on Hong Kong (since the 1980s), and to have been introduced to some Indonesian islands. in Herpestidae
Distribution. Mainland SE Asia, Peninsular Malaysia, and Sumatra. The Javan Mongoose or the Small Indian Mongoose is said to occur on Hong Kong (since the 1980s), and to have been introduced to some Indonesian islands.
Distribution. SW Asia from Iraq and Iran to Afghanistan, Pakistan, India, Nepal, and Bhutan; also Bangladesh, Myanmar and S China (including Hainan I). Introduced to Antigua, Barbados, Beef Island, Buck Island, Carriacou, Croatia, Cuba, Fiji, French Guiana, Goat Island, Grenada, Guadeloupe, Guyana, Hawaii, Hispaniola, Jamaica, Japan, Jost Van Dyke, La Desirade, Lavango, Mafia (Tanzania), Marie Galante, Martinique, Maui, Mauritius, Molokai, Nevis, Oahu, Puerto Rico, St. Croix, St. John, St. Kitts, St. Lucia, St. Martin, St. Thomas, St. Vincent, Surinam, Tortola, Trinidad, Vieques, and Water Island. Introduction was unsuccessful in the Dominican Republic. The Small Indian Mongoose or the Javan Mongoose is said to occur on Hong Kong since the 1980s, and to have been also introduced to some Indonesian islands (particularly Ambon). in Herpestidae
Distribution. SW Asia from Iraq and Iran to Afghanistan, Pakistan, India, Nepal, and Bhutan; also Bangladesh, Myanmar and S China (including Hainan I). Introduced to Antigua, Barbados, Beef Island, Buck Island, Carriacou, Croatia, Cuba, Fiji, French Guiana, Goat Island, Grenada, Guadeloupe, Guyana, Hawaii, Hispaniola, Jamaica, Japan, Jost Van Dyke, La Desirade, Lavango, Mafia (Tanzania), Marie Galante, Martinique, Maui, Mauritius, Molokai, Nevis, Oahu, Puerto Rico, St. Croix, St. John, St. Kitts, St. Lucia, St. Martin, St. Thomas, St. Vincent, Surinam, Tortola, Trinidad, Vieques, and Water Island. Introduction was unsuccessful in the Dominican Republic. The Small Indian Mongoose or the Javan Mongoose is said to occur on Hong Kong since the 1980s, and to have been also introduced to some Indonesian islands (particularly Ambon).
Subspecies and Distribution. V. t. tangalunga Gray, 1832 — Peninsular Malaysia, Sumatra, Borneo, several Indonesian islands (Amboina I, Banggi I, Langkawi I, Rhio-Lingga Archipelago, Bangka I, Karimata I & Sulawesi), and the Philippines; also two records from Java, but no evidence of native population. V. t. lankavensis Robinson & Kloss, 1920 — Malaysia (Langkawi I). in Viverridae
Subspecies and Distribution. V. t. tangalunga Gray, 1832 — Peninsular Malaysia, Sumatra, Borneo, several Indonesian islands (Amboina I, Banggi I, Langkawi I, Rhio-Lingga Archipelago, Bangka I, Karimata I & Sulawesi), and the Philippines; also two records from Java, but no evidence of native population. V. t. lankavensis Robinson & Kloss, 1920 — Malaysia (Langkawi I).
Subspecies and Distribution. V. i. indica Geoffroy Saint-Hilaire, 1803 — S peninsular India. V. i. atchinensis Sody, 1931 — Sumatra. V. i. baliensis Sody, 1931 — Bali. V. i. baptistae Pocock, 1933 — Bangladesh to NE India (Assam), and Bhutan. V. i. deserti Bonhote, 1898 — Pakistan through C India to Nepal. V. i. klossi Pocock, 1933 — Malaysia. V. i. mayori Pocock, 1933 — Sri Lanka. V. i. muriavensis Sody, 1931 — Java. V.i. taivana Schwarz, 1911 — Taiwan. V.i. thai Kloss, 1919 — Myanmar and Thailand through Indochina to China. V. i. wellsi Pocock, 1933 — NW India. It has been introduced to Madagascar, Zanzibar Island, the Comoro Islands, and Socotra Island for the production of civet or to be used as rat catchers; its presence on some of the Indonesian islands (Bali, Bawean, Kangean, Lombok, and Sumbawa) could also have resulted from introductions. in Viverridae
Subspecies and Distribution. V. i. indica Geoffroy Saint-Hilaire, 1803 — S peninsular India. V. i. atchinensis Sody, 1931 — Sumatra. V. i. baliensis Sody, 1931 — Bali. V. i. baptistae Pocock, 1933 — Bangladesh to NE India (Assam), and Bhutan. V. i. deserti Bonhote, 1898 — Pakistan through C India to Nepal. V. i. klossi Pocock, 1933 — Malaysia. V. i. mayori Pocock, 1933 — Sri Lanka. V. i. muriavensis Sody, 1931 — Java. V.i. taivana Schwarz, 1911 — Taiwan. V.i. thai Kloss, 1919 — Myanmar and Thailand through Indochina to China. V. i. wellsi Pocock, 1933 — NW India. It has been introduced to Madagascar, Zanzibar Island, the Comoro Islands, and Socotra Island for the production of civet or to be used as rat catchers; its presence on some of the Indonesian islands (Bali, Bawean, Kangean, Lombok, and Sumbawa) could also have resulted from introductions.
Subspecies and Distribution. A. t. trivirgata Gray, 1832 — Peninsular Thailand and Malaysia, Sumatra, and Borneo; also found on several small Indonesian Is. A. t. leucotis Horsfield, 1851 — NE India (Assam), Bangladesh, China (Yunnan), and Mainland SE Asia to the Isthmus of Kra. A. t. tnilineata Wagner, 1841 — Java. in Viverridae
Subspecies and Distribution. A. t. trivirgata Gray, 1832 — Peninsular Thailand and Malaysia, Sumatra, and Borneo; also found on several small Indonesian Is. A. t. leucotis Horsfield, 1851 — NE India (Assam), Bangladesh, China (Yunnan), and Mainland SE Asia to the Isthmus of Kra. A. t. tnilineata Wagner, 1841 — Java.
Distribution. Sulawesi and adjacent Is (Buton, Kabaena, Muna, Peleng, Lembeh, and on some of the Togian Is); thought to be extinct on Selayar I. Pigs have been widely domesticated through the Indonesian archipelago and beyond. This primarily involved the Eurasian Wild Pig (S. scrofa), but also S. celebensis, the only other species of pig successfully domesticated. Mitochondrial DNA studies of the dispersion of these domesticated forms agree on three major dispersal events, two involving S. scrofa and one S. celebensis. Evidence supports an early human-mediated translocation of S. celebensis to Flores and Timor and two later, separate human-mediated dispersals of domestic pig through islands of SE Asia into Oceania. In addition to Flores and Timor, S. celebensis is also thought to occur in its domesticated form on Halmahera, Lendu, Roti, and Savur Is, and even on Simeulue and Nias Is to the W of Sumatra and far from its island of origin, Sulawesi. In the Moluccas, and possibly elsewhere in this region, introduced S. celebensis are thought to have hybridized with other introduced pigs of S. scrofa derivation, and apparent hybrids between these species are now reported to survive on a number of islands, including Salawatti, Great Kei, Dobu, Seram, Ambon, Bacan, Ternate, Morotai, and New Guinea. It is also reported that in the 19" century the sows of domestic pigs in Sulawesi frequently mated with wild animals, after which they returned to their villages. in Suidae
Distribution. Sulawesi and adjacent Is (Buton, Kabaena, Muna, Peleng, Lembeh, and on some of the Togian Is); thought to be extinct on Selayar I. Pigs have been widely domesticated through the Indonesian archipelago and beyond. This primarily involved the Eurasian Wild Pig (S. scrofa), but also S. celebensis, the only other species of pig successfully domesticated. Mitochondrial DNA studies of the dispersion of these domesticated forms agree on three major dispersal events, two involving S. scrofa and one S. celebensis. Evidence supports an early human-mediated translocation of S. celebensis to Flores and Timor and two later, separate human-mediated dispersals of domestic pig through islands of SE Asia into Oceania. In addition to Flores and Timor, S. celebensis is also thought to occur in its domesticated form on Halmahera, Lendu, Roti, and Savur Is, and even on Simeulue and Nias Is to the W of Sumatra and far from its island of origin, Sulawesi. In the Moluccas, and possibly elsewhere in this region, introduced S. celebensis are thought to have hybridized with other introduced pigs of S. scrofa derivation, and apparent hybrids between these species are now reported to survive on a number of islands, including Salawatti, Great Kei, Dobu, Seram, Ambon, Bacan, Ternate, Morotai, and New Guinea. It is also reported that in the 19" century the sows of domestic pigs in Sulawesi frequently mated with wild animals, after which they returned to their villages.
FIGURE 1. Chartocinus rarus n. gen., n in A new genus and new species of Hymenosomatidae (Crustacea: Brachyura) from Indonesian Papua
FIGURE 1. Chartocinus rarus n. gen., n. sp., holotype male (2.9 x 3.1 mm) (MZB Cru 5342), Papua, Indonesia. A, overall dorsal habitus; B, ventral view.
FIGURE 2. Chartocinus rarus n. gen., n in A new genus and new species of Hymenosomatidae (Crustacea: Brachyura) from Indonesian Papua
FIGURE 2. Chartocinus rarus n. gen., n. sp., holotype male (2.9 x 3.1 mm) (MZB Cru 5342), Papua, Indonesia. A, dorsal view of carapace (setae not drawn); B, frontal view showing left antennule, antenna, orbit, proepistome and epistome (setae not drawn); C, right third maxilliped (setae not drawn); D, thoracic sternum and sternopleonal cavity; E, pleon (setae not drawn); F, left chela; G–J, P2–P5, respectively; K, left G1 (dorsal view); L, left G1 (ventral view); M, left G2. Scales: A, D, F–J = 0.5 mm; B, C, E = 0.2 mm; K–M = 0.1 mm.
Indonesian soil and litter Collembola species and trait matrix with environmental data
<p>Rainforest conversion and expansion of plantations in tropical regions is associated with changes in animal communities and biodiversity decline. In soil, Collembola are one of the most numerous invertebrate groups that control microbial processes and support arthropod predators. Despite that, information on the impact of changes in land use in the tropics on species and trait composition of Collembola communities is very limited. We investigated the response of Collembola to the conversion of rainforest into rubber agroforest ('junge rubber'), rubber and oil palm plantations in Jambi province (Sumatra, Indonesia), a region that experienced one of the strongest deforestation globally during the last decades. Collembola from litter and soil layers were collected in 2013 and 2016 using heat extraction. In the litter layer, density and species richness in plantation systems declined by 25-38% and 30-40%, respectively, compared to rainforest. By contrast, in the soil layer, density, species richness and trait diversity of Collembola were only slightly affected by land-use change contrasting the response of many other animal groups. Species and trait composition of Collembola communities in litter and soil layers differed between all land-use systems. Water content and pH were identified as main factors related to the differences in species and trait composition both in litter and soil layers, followed by the density of micro- and macropredators. Dominant Collembola species in rainforest and jungle rubber were characterized by small body size, absence of furca and absent or intense pigmentation, while in plantations larger species with long furca and diffuse or patterned coloration were more abundant. The trait-based responses were similar to those observed in Collembola from temperate regions and to those in a similar study on spiders at our study sites. Overall, land-use change negatively affected Collembola communities in the litter layer, but only little affected Collembola communities in soil. Several pantropical Collembola genera (i.e., <i>Isotomiella</i>, <i>Pseudosinella</i> and <i>Folsomides</i>) dominated across land-use systems, reflecting their high environmental adaptability or efficient dispersal calling for studies on their ecology and genetic diversity. The decline in species richness and density of litter-dwelling Collembola with the conversion of rainforest into plantation systems calls for management practices mitigating negative effects of the deterioration of the litter layer in rubber but in particular in oil palm plantations.</p>
On following pages: 42. Steppe Polecat (Mustela eversmanii); 43. Colombian Weasel (Mustela felipei); 44. Long-tailed Weasel (Mustela frenata); 45. Japanese Weasel (Mustela itatsi); 46. Yellow-bellied Weasel (Mustela kathiah); 47. European Mink (Mustela lutreola); 48. Indonesian Mountain Weasel (Mustela lutreolina); 49. Black-footed Ferret (Mustela nigripes); 50. Least Weasel (Mustela nivalis); 51. Malay Weasel (Mustela nudipes); 52. European Polecat (Mustela putorius); 53. Siberian Weasel (Mustela sibirica); 54. Back-striped Weasel (Mustela strigidorsa); 55. Egyptian Weasel (Mustela subpalmata); 56. American Mink (Neovison vison); 57. Patagonian in Mustelidae
On following pages: 42. Steppe Polecat (Mustela eversmanii); 43. Colombian Weasel (Mustela felipei); 44. Long-tailed Weasel (Mustela frenata); 45. Japanese Weasel (Mustela itatsi); 46. Yellow-bellied Weasel (Mustela kathiah); 47. European Mink (Mustela lutreola); 48. Indonesian Mountain Weasel (Mustela lutreolina); 49. Black-footed Ferret (Mustela nigripes); 50. Least Weasel (Mustela nivalis); 51. Malay Weasel (Mustela nudipes); 52. European Polecat (Mustela putorius); 53. Siberian Weasel (Mustela sibirica); 54. Back-striped Weasel (Mustela strigidorsa); 55. Egyptian Weasel (Mustela subpalmata); 56. American Mink (Neovison vison); 57. Patagonian
On following pages: 42. Steppe Polecat (Mustela eversmanii); 43. Colombian Weasel (Mustela felipei); 44. Long-tailed Weasel (Mustela frenata); 45. Japanese Weasel (Mustela itatsi); 46. Yellow-bellied Weasel (Mustela kathiah); 47. European Mink (Mustela lutreola); 48. Indonesian Mountain Weasel (Mustela lutreolina); 49. Black-footed Ferret (Mustela nigripes); 50. Least Weasel (Mustela nivalis); 51. Malay Weasel (Mustela nudipes); 52. European Polecat (Mustela putorius); 53. Siberian Weasel (Mustela sibirica); 54. Back-striped Weasel (Mustela strigidorsa); 55. Egyptian Weasel (Mustela subpalmata); 56. American Mink (Neovison vison); 57. Patagonian Weasel (Lyncodon patagonicus). in Mustelidae
On following pages: 42. Steppe Polecat (Mustela eversmanii); 43. Colombian Weasel (Mustela felipei); 44. Long-tailed Weasel (Mustela frenata); 45. Japanese Weasel (Mustela itatsi); 46. Yellow-bellied Weasel (Mustela kathiah); 47. European Mink (Mustela lutreola); 48. Indonesian Mountain Weasel (Mustela lutreolina); 49. Black-footed Ferret (Mustela nigripes); 50. Least Weasel (Mustela nivalis); 51. Malay Weasel (Mustela nudipes); 52. European Polecat (Mustela putorius); 53. Siberian Weasel (Mustela sibirica); 54. Back-striped Weasel (Mustela strigidorsa); 55. Egyptian Weasel (Mustela subpalmata); 56. American Mink (Neovison vison); 57. Patagonian Weasel (Lyncodon patagonicus).
Data from: Knowledge, attitudes, and practices among Indonesian urban communities regarding HPV infection, cervical cancer, and HPV vaccination
<p><strong>Background</strong>: Few studies explored Indonesian understanding of cervical cancer (CC) and the human papillomavirus (HPV) vaccination. We aimed to investigate the association between knowledge, attitudes, and practices (KAP) and socio-demographical influences <span>related to</span> HPV, CC, and vaccination among Indonesian urban citizens.</p> <p><strong>Methods</strong>: We conducted an online survey during March 2020-August 2021 using the Snowball sampling technique. The socio-demographic characteristic and KAP responses were collected via Google Forms from 400 respondents in Jakarta. The knowledge and attitudes were divided into HPV and CC (aspect 1) and HPV vaccination (aspect 2). Correlation between KAP scores was performed using Spearman's test, and multiple logistic regression analyses were conducted to determine KAP predictors.</p> <p><strong>Results</strong>: Indonesian urban citizens in Jakarta were found to have poor knowledge in individual aspects of the inquiry but moderate knowledge overall, good attitude in inquiry both in each aspect and overall, and unsatisfying practices. Overall, in the general population, men, and women respectively: 50.8%, 32.4%, and 53.6% had good knowledge; 82.0%, 75.2%, and 84.4% expressed positive attitude; and 30.3%, 15.2%, and 35.6% applied favorable practice regarding questions inquired. Knowledge was weakly correlated towards attitude (ρ=0.385) but moderately correlated with practice (ρ=0.485); attitude was moderately correlated with practice (ρ=0.577), all results: p<0.001. Significant odds ratio (OR) for predictors to good knowledge were female sex (OR=2.99), higher education (OR=2.91), and higher mother's education (OR=2.15). Factors related to positive attitudes were higher mother's education (OR=4.13), younger age (OR=1.86), and better results in the knowledge inquiries (OR=2.96). Factors that suggested better practices were female sex (OR=2.33), being employed (OR=1.68), excellent knowledge scores (OR=4.56), and positive attitudes expressions (OR=8.05). Having done one vaccination dose and intention to receive vaccines were significantly influenced by good KAP.</p> <p><strong>Conclusions</strong>: KAP had inter-association to successful CC and HPV prevention programs, and socio-demographical characteristics are critical to influencing better KAP.</p>
On following pages: 4. White-collared Fruit Bat (Megaerops albicollis); 5. Greater Short-nosed Fruit Bat (Cynopterus (Cynopterus horsfieldil); 8. Peters's Short-nosed Fruit Bat (Cynopterus luzoniensis); 9. Minute Short-nosed Fruit Bat Short-nosed Fruit Bat (Cynopterus titthaecheilus); 12. Lesser Musky Fruit Bat (Ptenochirus minon; 13. Greater Musky sphinx); 6. Lesser Short-nosed Fruit Bat (Cynopterus brachyotis); 7. Horsfield's Short-nosed Fruit Bat (Cynopterus minutus); 10. Nusatenggara Short-nosed Fruit Bat (Cynopterus nusatenggara); 11. Indonesian Fruit Bat (Ptenochirus jagorii); 14. Mindanao Fruit Bat (Ptenochirus wetmorel). in Pteropodidae
On following pages: 4. White-collared Fruit Bat (Megaerops albicollis); 5. Greater Short-nosed Fruit Bat (Cynopterus (Cynopterus horsfieldil); 8. Peters's Short-nosed Fruit Bat (Cynopterus luzoniensis); 9. Minute Short-nosed Fruit Bat Short-nosed Fruit Bat (Cynopterus titthaecheilus); 12. Lesser Musky Fruit Bat (Ptenochirus minon; 13. Greater Musky sphinx); 6. Lesser Short-nosed Fruit Bat (Cynopterus brachyotis); 7. Horsfield's Short-nosed Fruit Bat (Cynopterus minutus); 10. Nusatenggara Short-nosed Fruit Bat (Cynopterus nusatenggara); 11. Indonesian Fruit Bat (Ptenochirus jagorii); 14. Mindanao Fruit Bat (Ptenochirus wetmorel).
Distribution. Mainland SE Asia, Philippines, Indonesian Archipelago, New Guinea (including Bismarck Archipelago), Solomon Is, and NE Australia; also on N Nicobar Is in Hipposideridae
Distribution. Mainland SE Asia, Philippines, Indonesian Archipelago, New Guinea (including Bismarck Archipelago), Solomon Is, and NE Australia; also on N Nicobar Is
Subspecies and Distribution. P.p.pygmaeusLinnaeus,1760—WBorneoinMalaysia(SSarawakState)andIndonesia(NWestKalimantanProvince). P.p.morioOwen,1837—N&EBorneoinMalaysia(SabahState)andIndonesia(EastKalimantanProvince);possiblyinNSarawak. P. p. wurmbii Tiedemann, 1808 — S Indonesian Borneo (S West & Central Kalimantan provinces). in Hominidae
Subspecies and Distribution. P.p.pygmaeusLinnaeus,1760—WBorneoinMalaysia(SSarawakState)andIndonesia(NWestKalimantanProvince). P.p.morioOwen,1837—N&EBorneoinMalaysia(SabahState)andIndonesia(EastKalimantanProvince);possiblyinNSarawak. P. p. wurmbii Tiedemann, 1808 — S Indonesian Borneo (S West & Central Kalimantan provinces).
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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)
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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.