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Fig. 3. A in Platybinthus, a new genus of Lebinthina crickets (Orthoptera, Gryllidae, Eneopterinae) from Maluka, Indonesia

Fig. 3. A. Maximum likelihood phylogenetic tree based on concatenated sequences of eight molecular markers. Values under branches indicate bootstrap values; bootstrap value> 99 is indicated with an asterisk (*). B. Close-up view of the maximum likelihood phylogenetic tree showing the relationships among species of Platybinthus gen. nov. and with Macrobinthus Robillard & Dong, 2016. C. Morphological comparison of the males (habitus, genitalia and FW) between Platybinthus and Macrobinthus. The red arrows indicate diagnostic characters for Platybinthus. Scale bar (for habitus) = 10 mm.

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Fig. 7. FWs. A–B in Platybinthus, a new genus of Lebinthina crickets (Orthoptera, Gryllidae, Eneopterinae) from Maluka, Indonesia

Fig. 7. FWs. A–B. ♂♂. C–D. ♀♀. A, C. Platybinthus striolatus (Brunner von Wattenwyl, 1898) gen. et comb. nov. (♂ ZIN; ♀ MNHN-ENSIF1449). B, D. Platybinthus sandyi gen. et sp. nov. (♂ holotype MZB.ORTH.1786; ♀ paratype MZB.ORTH.1787) Scale bar = 2 mm.

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Fig. 5 in Platybinthus, a new genus of Lebinthina crickets (Orthoptera, Gryllidae, Eneopterinae) from Maluka, Indonesia

Fig. 5.Head in dorsal view (A–C) and face in anterior view (D–F). A, D. Platybinthus punctatus (Brunner von Wattenwyl, 1898) gen. et comb. nov., syntype, ♀ (MNHN-EO-ENSIF1448). B, E. Platybinthus striolatus (Brunner von Wattenwyl, 1898) gen. et comb. nov., ♂ (ZIN). C, F. Platybinthus sandyi gen. et sp. nov., holotype, ♂ (MZB.ORTH.1786). Scale bar = 2 mm.

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Fig. 4. Habitus. A–D in Platybinthus, a new genus of Lebinthina crickets (Orthoptera, Gryllidae, Eneopterinae) from Maluka, Indonesia

Fig. 4. Habitus. A–D. Platybinthus striolatus (Brunner von Wattenwyl, 1898) gen. et comb. nov. (♂ ZIN; ♀ MNHN-ENSIF1449). E–H. Platybinthus sandyi gen. et sp. nov. (♂ holotype MZB.ORTH.1786; ♀ paratype MZB.ORTH.1787). A–B, E–F. ♂♂. C–D, G–H. ♀♀. Scale bar = 1 cm.

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Fig. 8. Genitalia. A–F in Platybinthus, a new genus of Lebinthina crickets (Orthoptera, Gryllidae, Eneopterinae) from Maluka, Indonesia

Fig. 8. Genitalia. A–F. ♂♂. G–H. ♀♀. A–C, H. Platybinthus striolatus (Brunner von Wattenwyl, 1898) gen. et comb. nov. (ZIN). D–F. Platybinthus sandyi gen. et sp. nov., holotype (MZB.ORTH.1786) G. Platybinthus punctatus (Brunner von Wattenwyl, 1898) gen. et comb. nov., syntype (MNHN-EO- ENSIF1448). Scale bars: A–F = 1 mm; G–H = 0.5 mm.

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The State of Open Science in Indonesia: a preliminary analysis of digitalisation's impact on science regimes

<p>This presentation is a discussion on Open Science in Indonesia from the field of the Sociology of Knowledge Approach to Discourse.&nbsp; Boasting the largest number of Open Access Journals in the world, and steadily capitalising on a burgeoning technological economy, Indonesia would seem ripe for a science and knowledge-sharing renaissance.&nbsp; In the past five years, science and education institutions have been consolidated into one &ldquo;super entity&rdquo;, the Indonesian National Research and Innovation Agency (BRIN), stirring the imagination for a publicly funded and centralised open access system for indexing, storing and sharing scientific research, data and results. Further, on the back of the 2022 G20 Presidency, Indonesia holds the 2023 ASEAN Presidency, which provides it with agenda setting powers towards regional science and technology cooperation. The potential is high for Open Science, and thus the global sustainable development agenda, to find precedence in Indonesia&rsquo;s policymaking discourse. Interviews conducted with BRIN staff, professors and PhD Candidates of leading Indonesian universities, think-tank policy advisers, and grass roots organisers illuminate common challenges to implementation of Open Science policies and the Open Science mindset. This discussion addresses where Open Science sits in Indonesia&rsquo;s development agenda, where there are promises, where there are challenges and what the role of CSIS is in facilitating the transition to Open Science.</p>

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Fig. 1. A in Caridina clandestina, new species, an unusual new freshwater shrimp (Crustacea: Decapoda: Atyidae) from the remote high elevation Napu Valley of Sulawesi, Indonesia

Fig. 1. A, map of Sulawesi with the study area framed in red as shown on the detail map (B) of the Napu and Bada Valleys; B, the symbols show the sampling locations of Caridina clandestina, new species (black circles), C. sulawesi Cai &amp; Ng, 2009 (white circles), C. parvidentata J. Roux, 1904 (square), and C. villadolidi Blanco, 1939 (diamond).

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Fig. 4. A in Caridina clandestina, new species, an unusual new freshwater shrimp (Crustacea: Decapoda: Atyidae) from the remote high elevation Napu Valley of Sulawesi, Indonesia

Fig. 4. A, Lariang River, natural habitat of Caridina clandestina, new species; B, colouration of living specimen; C, specimen with chelae adapted for filter feeding.

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Fig. 5. A in Caridina clandestina, new species, an unusual new freshwater shrimp (Crustacea: Decapoda: Atyidae) from the remote high elevation Napu Valley of Sulawesi, Indonesia

Fig. 5. A, scatterplot analysis of chelae morphology in both forms of Caridina clandestina, new species; B, chelae morphology in both forms of Caridina clandestina is not related to size of specimens.

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Fig. 3. A–C, F, G, J–O in Caridina clandestina, new species, an unusual new freshwater shrimp (Crustacea: Decapoda: Atyidae) from the remote high elevation Napu Valley of Sulawesi, Indonesia

Fig. 3. A–C, F, G, J–O, Caridina clandestina, new species, paratype male filter feeding morph (CL 5.6 mm) (ZMB 30207a), Lariang River, Central Sulawesi; D, E, H, I, Caridina clandestina, new species, paratype male short chelae morph (CL 4.7 mm) (ZMB 30203b), Napu Valley, stream, tributary of Lariang River, Central Sulawesi. A, third maxilliped; B, first pereiopod; C, fingers of first pereiopod; F, second pereiopod; G, fingers of second pereiopod; J, third pereiopod; K, dactylus of third pereiopod; L, fifth pereiopod; M, dactylus of fifth pereiopod; N, endopod of male's first pleopod; O, endopod and appendix masculina on second pleopod. Scale bars: A–F, H–J, L, N, O = 1.0 mm; G, K, M = 0.5 mm.

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Fig. 2. A, C–N in Caridina clandestina, new species, an unusual new freshwater shrimp (Crustacea: Decapoda: Atyidae) from the remote high elevation Napu Valley of Sulawesi, Indonesia

Fig. 2. A, C–N, Caridina clandestina, new species, paratype male filter feeding morph (CL 5.6 mm) (ZMB 30207a), Lariang River, Central Sulawesi; B, Caridina clandestina, new species, paratype male short chelae morph (CL 4.7 mm) (ZMB 30203b), Napu Valley, stream, tributary of Lariang River, Central Sulawesi. A, cephalothorax and cephalic appendages; B, rostrum; C, telson; D, distal part of telson; E, preanal carina; F, uropodal diaeresis; G, antennular peduncle; H, scaphocerite; I, distal part of mandible; J, maxillula; K, maxilla; L, first maxilliped; M, palp of first maxilliped; N, second maxilliped. Scale bars: A–C, G–I, K–N = 1.0 mm; D, E, F, J = 0.5 mm.

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Fig. 6 in Caridina clandestina, new species, an unusual new freshwater shrimp (Crustacea: Decapoda: Atyidae) from the remote high elevation Napu Valley of Sulawesi, Indonesia

Fig. 6. Molecular phylogeny of all described endemic species of Caridina from Sulawesi. Topology based on BI analysis of concatenated dataset of two mitochondrial gene fragments (16S and COI). Numbers on branches are, from the top, Bayesian posterior probabilities (&gt;0.9) and ML/MP bootstrap values (&gt;70). An asterisk indicates nodes with full support (1/100/100). The scale bar indicates the substitution rate.

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Fig. 1 in Cymonomus dwi, a new species of deep-water cymonomid crab from Indonesia (Crustacea: Brachyura)

Fig. 1. Cymonomus dwi, new species, male holotype, cl 2.78 mm, pcl 2.41 mm, cw 2.69 mm, MZB: A, dorsal habitus; B, fronto-orbital region, dorsal view; C, right epistomial spine mesial to base of antenna, ventral view; D, right maxilliped 3, external view; E, thoracic sternite 3, ventral view; F, right G1, pleonal view; G, right G2, pleonal view; H, left P4 dactylus, dorsal view; I, left P5 dactylus, dorsal view. Scale: A = 1.0 mm; B–G = 0.5 mm; H, I = 0.25 mm.

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Fig. 4 in Pectinaria nusalautensis (Pectinariidae, Annelida): a new polychaete species from Maluku, Indonesia

Fig. 4. Close-up of body parts of Pectinaria nusalautensis, new species (MZB. Pol. 00236). A, ventral view of the anterior part; B, transitional region from thorax to abdomen; C, scaphal hooks; D, scaphe (ventral view). Abbreviations: abd = abdomen; af = anal flap; avl = antero-ventral lobe; br = branchia; ch = chaetiger; cv = cephalic veil; cvc = cephalic veil cirri; lh = lateral hump; np = notopodial paleae; or = opercular rim; pp = peristomial palp; savl = small antero-ventral lobe; sh = scaphal hooks; tc = tentacular cirrus; tra = trapezoidal glandular area; tri = triangular glandular area; un = uncini; vf = ventral flap; vl = ventral lappet. Numbers 1–5 are the last five posterior segments forming scaphe. Scale bars: A, B = 2 mm; C = 0.25 mm; D = 1 mm.

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Fig. 2 in Pectinaria nusalautensis (Pectinariidae, Annelida): a new polychaete species from Maluku, Indonesia

Fig. 2. Pectinaria nusalautensis, new species (MZB. Pol. 00236). A, dorsal view; B, ventral view. Abbreviations: ag = abdominal glandular area; avl = antero-ventral lobe; br1 = first branchia; br2 = second branchia; cvc = cephalic veil cirrus; dlf = dorso-lateral flap; dlp = dorsolateral pad; lh = lateral hump; no = notopodium; np = notopodial palea; op = opercular plate; or = opercular rim; pp = peristomial palp; savl = small antero-ventral lobe; tra = trapezoidal glandular area; tri = triangular glandular area; vf = ventral flap; vl = ventral lappet. Scale bar = 2 mm.

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Fig. 7 in Pectinaria nusalautensis (Pectinariidae, Annelida): a new polychaete species from Maluku, Indonesia

Fig. 7. SEM of chaetae of Pectinaria nusalautensis, new species (MZB. Pol. 00236). A, notochaetae of chaetiger 5; B, uncini of chaetiger 5. Scale bars: A = 200 μm; B = 10 μm.

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Fig. 1 in Pectinaria nusalautensis (Pectinariidae, Annelida): a new polychaete species from Maluku, Indonesia

Fig. 1. Distributional map of Indonesian pectinariids. Dark grey and white areas indicate Indonesian islands and nearby regions. Pectinaria nusalautensis, new species, and (?)P. brevispinis were collected from the same island. The record of A. capensis is doubtful due to such a long distance between South Africa and Sunda Strait that may restrict the distribution of the species. Pectinaria brevispinis was originally described from the Philippines and was later recorded to occur in Indonesia by Caullery (1944), but this record cannot be verified.

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Fig. 3 in Pectinaria nusalautensis (Pectinariidae, Annelida): a new polychaete species from Maluku, Indonesia

Fig. 3. Pectinaria nusalautensis, new species (MZB. Pol. 00236), stained using methylene blue. A, dorsal view; B, ventral view. Abbreviations: ag = abdominal glandular area; avl = antero-ventral lobe; br = branchia; cvc = cephalic veil cirrus; dlf = dorso-lateral flap; dlp = dorso-lateral pad; lh = lateral hump; no = notopodium; np = notopodial palea; op = opercular plate; or = opercular rim; pp = peristomial palp; savl = small antero-ventral lobe; tra = trapezoidal glandular area; tri = triangular glandular area; vf = ventral flap; vl = ventral lappet. Scale bar = 2 mm.

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Fig. 6 in Pectinaria nusalautensis (Pectinariidae, Annelida): a new polychaete species from Maluku, Indonesia

Fig. 6. Chaetae of Pectinaria nusalautensis, new species (MZB. Pol. 00236). A, chaetae of chaetiger 3; B, chaetae of chaetiger 5. Scale bars: A = 100 μm; B = 200 μm.

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Fig. 5 in Pectinaria nusalautensis (Pectinariidae, Annelida): a new polychaete species from Maluku, Indonesia

Fig. 5. Close-up of some body parts of Pectinaria nusalautensis, new species (MZB. Pol. 00236). A, notopodial paleae showing faint transverse lines; B, scaphal hooks showing blunt tips; C, anal flap (ventral view) showing a triangular shape with longitudinal striations. Scale bars: A = 1 mm; B = 0.05 mm; C = 0.5 mm.

opencc-by-4.0Jan 2023View details →

ScienceDex guides

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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.

allen-brain-atlas
neuroscienceopenDocumentation, web resources, and API references are available online.
Last verified 2026-04-30Open record

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.

abode-home-cage
behavioral-neuroscienceopenThe DataShare record exposes download links for annotations, documentation, license text, and the zipped per-snippet data directory.
Last verified 2026-04-30Open record

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.

dandi-nwb
electrophysiologyopenPublished Dandiset metadata and archive endpoints are available through the production DANDI API.
Last verified 2026-04-30Open record

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.

ibl
behavioral-neuroscienceopenPublic sessions can be searched and loaded from the IBL public data server through ONE.
Last verified 2026-04-29Open record

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.

openneuro
neuroscienceopenPublished datasets are available on demand over the internet.
Last verified 2026-04-29Open record

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