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503 results for “Indonesian”
FIG. 12 in Indonesian chitons of the genera Belknapchiton Sirenko, Saito et Schwabe, 2022 and Leptochiton Gray, 1847 (Mollusca: Polyplacophora: Leptochitonidae)
FIG. 12. Leptochiton commandorensis, Banda Sea, Indonesia, 3200 m, BL–5.0 mm. A. Head valve, dorsal view. B. Valve II, dorsal view. C. Valve IV, dorsal view. D. Valve VIII, dorsal view. E. Valve V, ventral view. F. Valve IV, tegmentum sculpture in central area. G. Valve IV, frontal view. H. Valve VIII, lateral view. РИС. 12. Leptochiton commandorensis, море Банда, ИндонеЗиЯ, 3200 м, BL–5,0 мм. A. Головной Щиток, вид сверху. B. Щиток II, вид сверху. C. Щиток IV, вид сверху. D. Щиток VIII, вид сверху. E. Щиток V, вид сниЗу. F. Щиток IV, скульптура тегментума на центральном поле. G. Щиток IV, вид спереди. H. Щиток VIII, вид сбоку.
Figs 4–12 in On the Phytophagous Scarabs of the Subfamilies Dynastinae, Rutelinae, and Melolonthinae from the Schouten Islands ( Kepulauan Biak), Indonesian Papua (Coleoptera: Scarabaeidae)
Figs 4–12. Neoheteronyx calliseta (4–6), N. schoutensis (7–10), and N. tanythrix (11–12) spp. n., holotypes: 4, 7, 11–dorsal view; 5, 9– aedeagus, lateral view; 6, 10–aedeagus, dorsal view; 8, antenna (weakly lamellate fifth joint arrowed); 12–setosity of middle third of elytral epipleura, dorsal view. Scale bars: 4, 7–9, 11=1 mm; 5, 10=0.5 mm; 6=0.25 mm; 12=0.2 mm.
Figs 1–3 in On the Phytophagous Scarabs of the Subfamilies Dynastinae, Rutelinae, and Melolonthinae from the Schouten Islands ( Kepulauan Biak), Indonesian Papua (Coleoptera: Scarabaeidae)
Figs 1–3. Scalation of the elytral interspaces in Engertia amboinae, Yapen I. (1); E. papuana, Papua New Guinea: Sentani (2), and E. setifera, Ceram I. (3). Scale bar (common)=1 mm.
Traits data of naturalized and non-naturalized alien species of four Indonesian Botanic Gardens
<p>The establishment of new botanic gardens in tropical regions highlights a need for weed risk assessment tools suitable for tropical ecosystems. The relevance of plant traits for invasion into tropical rainforests has not been well studied. </p> <p>Working in and around four botanic gardens in Indonesia where 590 alien species have been planted, we estimated the effect of four plant traits, plus time since species introduction, on: a) the naturalization probability and b) abundance (density) of naturalized species in adjacent native tropical rainforests; and c) the distance that naturalized alien plants have spread from the botanic gardens. </p> <p>We found that specific leaf area (SLA) strongly differentiated 23 naturalized from 78 non-naturalized alien species (randomly selected from 577 non-naturalized species) in our study. These trends may indicate that exotics with high SLA benefit from at least two factors when establishing in tropical forests: high growth rates and occupation of forest gaps. We also found that height was unrelated to naturalization probability, but naturalized aliens were having high SLA and were short. </p> <p>Exotic species that were present in the gardens for over 30 years and those with small seeds also had higher probabilities of becoming naturalized, indicating that garden plants can invade the understorey of closed canopy tropical rainforests, especially when invading species are shade-tolerant and have sufficient time to establish.</p> <p>On average, exotic species that were not animal dispersed spread 78 m further into the forests than animal-dispersed species. We did not detect relationships between the measured traits and estimated density of naturalized exotics in the adjacent forests.</p> <p>Synthesis: Traits were able to differentiate exotic species from botanic gardens that naturalized in native forest from those that did not; this is promising for developing trait-based risk assessment in the tropics. To limit the risk of invasion and spread into adjacent native forests, we suggest tropical botanic gardens avoid planting exotic species with fast carbon capture strategies and those that are shade tolerant.</p>
Traveling Waves: The Indonesian Tsunami Warning System - STS Webinar Series #1
<p>Previously published on YouTube: https://www.youtube.com/watch?v=CWK1_Nxi__Y</p> <p>(Indonesian)</p> <p>Seri webinar ini diadakan oleh Pusat Riset Kewilayahan (PRW) BRIN untuk mendiskusikan tema-tema terkait Science, Technology, and Society Studies, salah satu program kajian yang dikembangkan di PRW-BRIN. Webinar ini membahas kelindan antara diskursus, aktor, mesin deteksi, serta praktik sains dan teknologi untuk menghadapi risiko dan ketidakpastian sistem pengetahuan peringatan dini tsunami di Indonesia. Dengan menggunakan pendekatan etnografis, diskusi ini akan berusaha menjawab pertanyaan terkait teknologi sistem peringatan dini tsunami Indonesia sebagai infrastruktur sosial dan jaringan konektivitas pakar Jerman - Indonesia dalam pengembangan sistem teknologi tersebut di Indonesia.</p> <p>(English)</p> <p>This webinar series was held by the BRIN Regional Research Center (PRW) to discuss themes related to Science, Technology, and Society Studies, one of the study programs developed at PRW-BRIN. This webinar discusses the interplay between discourse, actors, detection machines, as well as science and technology practices to deal with the risks and uncertainties of the tsunami early warning knowledge system in Indonesia. Using an ethnographic approach, this discussion will attempt to answer questions related to the technology of the Indonesian tsunami early warning system as a social infrastructure and connectivity network of German-Indonesian experts in developing the technology system in Indonesia.</p>
The impact of Indonesian Throughflow constrictions on eastern Pacific upwelling and water-mass transformation
<p>Netcdf data and Matlab processing scripts for the article: </p> <p>Eabry, Holmes and Sen Gupta (2022): The impact of Indonesian Throughflow constrictions on eastern Pacific upwelling and water-mass transformation. Journal of Geophysical Research: Oceans. <a href="https://doi.org/10.1029/2022JC018509">https://doi.org/10.1029/2022JC018509</a></p> <p>Included are netcdf files with output from the ACCESS-OM2 1-degree ocean model averaged over years 500-600 of the spin-up simulation. CONTROL indicates the control simulation (realistic ITF topography), OPENITF indicates the Open ITF experiment and DIFF indicates difference files between the two. Please refer to the meta-data within the netcdf files for more information. Scripts to help with plotting standard variables are part of the COSIMA cookbook repository at <a href="https://github.com/COSIMA/cosima-recipes">https://github.com/COSIMA/cosima-recipes</a>.</p> <p>An example script Control_WMT_budget.m is provided to plot the control WMT budget and can be easily modified to plot the Open ITF or anomalous WMT budget. This script uses the Pacific masks found in mask.mat. The small tendency term is provided separately as dV_dt_nrho.mat.</p>
Data from : Genomic Sequence of Klebsiella pneumoniae IIEMP-3, a Vitamin B12-Producing Strain from Indonesian Tempeh
<p>Klebsiella pneumoniae strain IIEMP-3, isolated from Indonesian tempeh, is a vitamin B<sub>12</sub>-producing strain that exhibited a different genetic profile from pathogenic isolates. Here we report the draft genome sequence of strain IIEMP-3, which may provide insights on the nature of fermentation, nutrition, and immunological function of Indonesian tempeh.</p>
Fig. 5. A in Morphometric Analysis And Interrelationship Of Seven Indonesian Hornbill Species (Aves, Bucerotidae) Utilizing Principal Component And Cluster Analysis
Fig. 5. A dendrogram illustrating the relationships among the seven Indonesian hornbill species based on 14 morphometric characters, constructed using the Average Linkage model. Legend: Aa = Anthracoceros albirostris, Am = Anthracoceros malayanus, Ru = Rhyticeros undulatus, Rp = Rhyticeros plicatus, Ac = Aceros cassidix, Br = Buceros rhinoceros, dan Bb = Buceros bicornis.
Fig. 1 in Morphometric Analysis And Interrelationship Of Seven Indonesian Hornbill Species (Aves, Bucerotidae) Utilizing Principal Component And Cluster Analysis
Fig. 1. Hornbill genus grouping based on a combination of body length characters (PC1) and beak characters (PC3): A — genus Rhyticeros; B — genus Buceros; C — genus Anthracoceros.
Fig. 3 in Morphometric Analysis And Interrelationship Of Seven Indonesian Hornbill Species (Aves, Bucerotidae) Utilizing Principal Component And Cluster Analysis
Fig. 3. The combination of tail length and head length of two hornbill species within the genus Anthracoceros.
Fig. 4 in Morphometric Analysis And Interrelationship Of Seven Indonesian Hornbill Species (Aves, Bucerotidae) Utilizing Principal Component And Cluster Analysis
Fig. 4. The combination of head length and tail length of three hornbill species within the genus Rhyticeros.
Figure 3 in Photographic evidence of freshwater whipray Urogymnus dalyensis (Myliobatiformes: Dasyatidae) in Indonesian waters
Figure 3. Map showing location of Urogymnus dalyensis (yellow circle) in Lampu Satu beach, Merauke district, Papua province, Indonesia.
Figure 1 in Photographic evidence of freshwater whipray Urogymnus dalyensis (Myliobatiformes: Dasyatidae) in Indonesian waters
Figure 1. The specimen of Urogymnus dalyensis caught on 24 December 2017 at Lampu Satu beach, Merauke district, Papua province, Indonesia (Photo: Lham Jr).
Fig. 3 in Molecular phylogeny of Indonesian Lymantria Tussock Moths (Lepidoptera: Erebidae) based on CO I gene sequences
Fig. 3. Neighbor-Joining tree based on K2P distance model of all substitutions of CO I gene (Bootstrap support are shown at the nodes; ID=specimens from Indonesia).
Fig. 4. Maximum likelihood tree for 43 in Molecular phylogeny of Indonesian Lymantria Tussock Moths (Lepidoptera: Erebidae) based on CO I gene sequences
Fig. 4. Maximum likelihood tree for 43 species of Lymantria based all substitutions of CO I gene (Bootstrap support are shown at the nodes; ID=specimens from Indonesia).
Fig. 5. Maximum likelihood tree for 10 in Molecular phylogeny of Indonesian Zeuzera (Lepidoptera: Cossidae) wood borer moths based on CO I gene sequence
Fig. 5. Maximum likelihood tree for 10 species of Zeuzera based on all substitution of CO I gene (Bootstrap support are shown ath the nodes).
Fig. 3 in Molecular phylogeny of Indonesian Zeuzera (Lepidoptera: Cossidae) wood borer moths based on CO I gene sequence
Fig. 3. Scatter plots of pairwise seqeunce divergence based on K2P model versus Transition/Transversion (Ts/Tv).
Fig. 4. A 50 in Molecular phylogeny of Indonesian Zeuzera (Lepidoptera: Cossidae) wood borer moths based on CO I gene sequence
Fig. 4. A 50% majority-rule consensus tree based on all substitutions of CO I gene (Bootstrap support are shown only for the nodes which have value>50%.
Fig. 1 in Molecular phylogeny of Indonesian Zeuzera (Lepidoptera: Cossidae) wood borer moths based on CO I gene sequence
Fig. 1. Cladogram of Zeuzera (Schoorl, 1990) (all the numbers showed in each branch are apomorphies charactes that are listed in Table 1).
Fig. 3 in The first female specimen of the poorly known Arfak Stout-tailed Snake, Calamophis sharonbrooksae Murphy, 2012 (Serpentes: Colubroidea: Homalopsidae), from the Vogelkop Peninsula of Indonesian West New Guinea, with comments on the taxonomic history of primitive homalopsids
Fig. 3. Detailed views of the head and tail of the first known female Calamophis sharonbrooksae (NRM 17803), presented as both photographic and line-drawn illustrations for improved clarity. (A, A′) Dorsal view of the head, illustrating rostral (R), single internasal (IN), fused prefrontal-preocular (PF-PR), frontal (F), paired supraocular (SO), and parietals (P). (B, B′) Ventral view of the head, showing a single pair of chin shields (CS), seven infralabials (IL1-IL7), mental (M), and the first ventral scute (V1). (C, C′) Left lateral view of the head, additionally illustrating the undivided nasal (N), single postocular (PO), single anterior temporal (AT), two posterior temporals (PT), and six supralabials (SL1-SL6). (D, D′) Right lateral view of the head, illustrating differences in scalation compared to left side, three posterior temporals (PT), and small scale separating the postocular and anterior temporal (*). (E, E′) Ventral view of the tail, showing the final ventral (V158), divided cloacal plate (CP), first paired subcaudal (SC1), and rounded terminal scute (TS). Scale = 10 mm for Fig. 3A-D and 10 mm for Fig. 3E.
ScienceDex guides
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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.