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FIGURES 14 – 15. Omniops hanseni holotype. — 14. Ventral habitus. — 15 in Omniops gen. n. and two new species of Hydrophilini from Papua New Guinea (Coleoptera: Hydrophilidae)
FIGURES 14 – 15. Omniops hanseni holotype. — 14. Ventral habitus. — 15. Pro, meso, and metasternum.
FIGURE 2 in Rhinobatos manai sp. nov., a new species of guitarfish (Rhinopristiformes: Rhinobatidae) from New Ireland, Papua New Guinea
FIGURE 2. Head of preserved adult male holotype, 731 mm TL (NTUM 11500): A. dorsal view; B. ventral view.
FIGURE 1 in Rhinobatos manai sp. nov., a new species of guitarfish (Rhinopristiformes: Rhinobatidae) from New Ireland, Papua New Guinea
FIGURE 1. Dorsal view of Rhinobatos manai sp. nov., adult male holotype, 731 mm TL (NTUM 11500): A. freshly caught; B) preserved.
Data from: What goes in must come out? The metabolic profile of plants and caterpillars, frass, and adults of Asota (Erebidae: Aganainae) feeding on Ficus (Moraceae) in New Guinea
<p>Insect herbivores have evolved a broad spectrum of adaptations in response to the diversity of chemical defences employed by plants. Here we focus on two species of New Guinean Asota and determine how these specialist moths deal with the leaf alkaloids of their fig (Ficus) hosts. As each focal Asota species is restricted to one of three chemically distinct species of Ficus, we also test whether these specialized interactions lead to similar alkaloid profiles in both Asota species. We reared Asota caterpillars on their respective Ficus hosts in natural conditions and analyzed the alkaloid profiles of leaf, frass, caterpillar, and adult moth samples using UHPLC–MS/MS analyses. We identified 43 alkaloids in our samples. Leaf alkaloids showed various fates. Some were excreted in frass or found in caterpillars and adult moths. We also found two apparently novel indole alkaloids likely synthesized de novo by the moths or their microbiota—in both caterpillar and adult tissue but not in leaves or frass. Overall, alkaloids unique or largely restricted to insect tissue were shared across moth species despite feeding on different hosts. This indicates that a limited number of plant compounds have a direct ecological function that is conserved among the studied species. Our results provide evidence for the importance of phytochemistry and metabolic strategies in the formation of plant–insect interactions and food webs in general. Furthermore, we provide a new potential example of insects acquiring chemicals for their benefit in an ecologically relevant insect genus.</p>
Fig. 6 in The Taxonomy And Phylogenetic Relationships Of Species In The Bactrocera Musae Complex Of Fruit Flies (Diptera: Tephritidae: Dacinae) In Papua New Guinea
Fig. 6. Neighbour joining tree showing relationships between CO1 haplotypes from species in the Bactrocera musae complex. Values at nodes are for 1000 bootstrap replicates of the maximum likelihood calculations using the Kimura two-parameter model of sequence evolution (left) and Bayesian posterior probability (right). Clade A = B. musae, Clade B = B. rufivitta, Clade C = B. contermina. Note: the numbers at the branch tips represent the field collection codes given to individual specimens.
Fig. 7 in The Taxonomy And Phylogenetic Relationships Of Species In The Bactrocera Musae Complex Of Fruit Flies (Diptera: Tephritidae: Dacinae) In Papua New Guinea
Fig. 7. Diagram showing clustering of individuals at (A) the highest hierarchical level of structuring in the Bactrocera musae complex using STRUCTURE, and (B) the sub-group structuring into two further clusters of the individuals from the red cluster in A. Vertical bars represent individuals and colours denote the proportion of ancestry from each cluster based on eight microsatellite loci. Note at the highest level (A), individuals are clearly assigned to either the B. musae or the 'others' cluster. At the next level (B), individuals from the 'others' cluster are assigned to either the B. rufivitta cluster (red) or the B. contermina cluster (green). Note: The numbers below the vertical bars represent the field collection codes given to individual specimens.
Fig. 12. Oreophryne geislerorum, AMNH A 75042, SVL 26.3 in Systematics of Microhylid Frogs, Genus Oreophryne, from the North Coast Region of New Guinea
Fig. 12. Oreophryne geislerorum, AMNH A 75042, SVL 26.3, from Lae, Morobe Prov., Papua New Guinea (R. Zweifel photo).
Fig. 8 in Systematics of Microhylid Frogs, Genus Oreophryne, from the North Coast Region of New Guinea
Fig. 8. Audiospectrograms of calls of Oreophryne. A. O. biroi, UPNG 8134, Kowat, Adelbert Mtns., Madang Prov., Papua New Guinea, air 25.0°C; first 35 notes of a 67note call graphed with 59Hz and 300Hz filters. B. O. hypsiops, AMNH A83044, vicinity of Sempi, Madang Prov., Papua New Guinea, air 25.8°C; first 19 notes of a longer call graphed with 59Hz filter.
Fig. 11 in Systematics of Microhylid Frogs, Genus Oreophryne, from the North Coast Region of New Guinea
Fig. 11. Head width and tibia length ratios of Oreophryne geislerorum (crosses) and O. biroi (diamonds) compared. Solid diamonds represent specimens from Madang Prov., open diamonds specimens from East Sepik Prov.
Fig. 4 in Systematics of Microhylid Frogs, Genus Oreophryne, from the North Coast Region of New Guinea
Fig. 4. Regression of internarial span on snoutvent length in two samples of Oreophryne biroi from Papua New Guinea. Squares, specimens from Madang Prov.; crosses, specimens from East Sepik Prov.
Fig. 3 in Systematics of Microhylid Frogs, Genus Oreophryne, from the North Coast Region of New Guinea
Fig. 3. Regression of head width and eye diameter on snoutvent length in two samples of Oreophryne biroi from Papua New Guinea. Squares, specimens from Madang Prov.; crosses, specimens from East Sepik Prov.
Fig. 2 in Systematics of Microhylid Frogs, Genus Oreophryne, from the North Coast Region of New Guinea
Fig. 2. Plantar and palmar aspects of feet and hands of five species of Oreophryne. A.O. biroi, AMNH A83041. B. O. hypsiops, AMNH A83044. C. O. parkeri, BMNH 1955.1.1.17. D. O. geislerorum, AMNH A75041. E. O. brachypus, AMNH A84513. Scale in mm.
Fig. 7 in Systematics of Microhylid Frogs, Genus Oreophryne, from the North Coast Region of New Guinea
Fig. 7. Regressions of internarial span and width of third finger disk on snoutvent length in two samples of Oreophryne from Madang Prov., Papua New Guinea. Squares, O. biroi; crosses, O. hypsiops.
Fig. 6 in Systematics of Microhylid Frogs, Genus Oreophryne, from the North Coast Region of New Guinea
Fig. 6. Regressions of head width and eye diameter on snoutvent length in two samples of Oreophryne from Madang Prov., Papua New Guinea. Squares, O. biroi; crosses, O. hypsiops. The solid spot plots estimated head width of larger syntype of O. biroi (not used in calculating regression).
Fig. 10 in Systematics of Microhylid Frogs, Genus Oreophryne, from the North Coast Region of New Guinea
Fig. 10. Regressions of head width and tibia length on snoutvent length in Oreophryne geislerorum. The solid spots plot the estimated head width and tibia length of the larger syntype of O. biroi.
Fig. 14 in Systematics of Microhylid Frogs, Genus Oreophryne, from the North Coast Region of New Guinea
Fig. 14. Distribution of two species of Oreophryne in Papua New Guinea. Solid circles, O. geislerorum; open circles, O. hypsiops.
Fig. 9 in Systematics of Microhylid Frogs, Genus Oreophryne, from the North Coast Region of New Guinea
Fig. 9. Distribution of four species of Oreophryne in New Guinea and New Britain. Solid circles, O. biroi; open circles, O. brachypus; crosses, O. parkeri. The heavy line marks the course of two expeditions on one of which Ernst Tappenbeck collected the unique specimen of O. wolterstorffi.
Fig. 13 in Systematics of Microhylid Frogs, Genus Oreophryne, from the North Coast Region of New Guinea
Fig. 13. Audiospectrograms of calls of Oreophryne graphed with 59Hz filter. A. O. geislerorum, AMNH A81195, Lae, Morobe Prov., Papua New Guinea, air 23.8°C; one complete call, wave form at right at 2× expansion. B. O. parkeri, MZB 8155, vicinity of Lake Sentani, Papua, air 24.4°C; first 11 notes of a longer call.
Fig. 1. Oreophryne biroi. Left, UPNG 7355, SVL 20.5 in Systematics of Microhylid Frogs, Genus Oreophryne, from the North Coast Region of New Guinea
Fig. 1. Oreophryne biroi. Left, UPNG 7355, SVL 20.5, from Nobanob (Mt. Hanseman), Madang Prov., Papua New Guinea (J. Menzies photo). Right, specimen from series AMS R31031–31035, not measured, from Passam, E. Sepik Prov., Papua New Guinea (H. Cogger photo).
Figure 5 in A new species of Sicyopterus (Teleostei: Gobioidei: Sicydiinae) from Papua New Guinea
Figure 5. – Sicyopterus elomionearum, Holotype, MNHN 2019-0107 (tag 10634), male, 69.4 mm SL. Elnge Creek, New Britain (Papua New Guinea), 12 Nov. 2015, Amick et al. coll.
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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.