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FIGURE 19 in Contribution to the knowledge of Chinese Gryllacrididae (Orthoptera) V: Further study on the Chinese Capnogryllacris and comment on the phylogenetic relationships of the Gryllacrididae
FIGURE 19. Capnogryllacris nigromarginata rectispina ssp. nov.. Male: A–B. habitus in lateral view; C–D. tegmina in dorsal view: C. left tegmen, D. right tegmen.
FIGURE 21 in Contribution to the knowledge of Chinese Gryllacrididae (Orthoptera) V: Further study on the Chinese Capnogryllacris and comment on the phylogenetic relationships of the Gryllacrididae
FIGURE 21. Capnogryllacris sequestris sp. nov.. Male: A–B. habitus in lateral view; C–D. tegmina in dorsal view: C. left tegmen, D. right tegmen.
FIGURE 17 in Contribution to the knowledge of Chinese Gryllacrididae (Orthoptera) V: Further study on the Chinese Capnogryllacris and comment on the phylogenetic relationships of the Gryllacrididae
FIGURE 17. Capnogryllacris nigromarginata hainanensis ssp. nov.. Male: A. head in frontal view; B–C. head and pronotum: B. lateral view, C. dorsal view; D–G. apex of abdomen: D. lateral view, E. apical view, F. apico-ventral view, G. ventral view; H–I. tegmina in dorsal view: H. left tegmen, I. right tegmen.
FIGURE 15 in Contribution to the knowledge of Chinese Gryllacrididae (Orthoptera) V: Further study on the Chinese Capnogryllacris and comment on the phylogenetic relationships of the Gryllacrididae
FIGURE 15. Capnogryllacris nigromarginata hainanensis ssp. nov.. Male: A. head in frontal view; B–C. head and pronotum: B. dorsal view, C. lateral view; D. second and third abdominal tergites in lateral view; E–H. apex of abdomen: E. lateral view, F. dorsal view, G–H. ventral view.
FIGURE 23 in Contribution to the knowledge of Chinese Gryllacrididae (Orthoptera) V: Further study on the Chinese Capnogryllacris and comment on the phylogenetic relationships of the Gryllacrididae
FIGURE 23. Capnogryllacris spinosa (Li, Liu & Li, 2014). Male (from Mao´ershan, Guangxi, XZ61): A–B. head and pronotum: A. dorsal view, B. lateral view; C–F. apex of abdomen: C. dorsal view, D–E. lateral view, F. ventral view.
FIGURE 11 in Contribution to the knowledge of Chinese Gryllacrididae (Orthoptera) V: Further study on the Chinese Capnogryllacris and comment on the phylogenetic relationships of the Gryllacrididae
FIGURE 11. Capnogryllacris nigromarginata nigromarginata (Karny, 1928). Male: A. head in frontal view; B–C. head and pronotum: B. dorsal view, C. lateral view; D. second and third abdominal tergites in lateral view; E–I. apex of abdomen: E. dorso-apical view, F. lateral view, G. dorsal view, H. ventral view, I. apical view.
FIGURE 10 in Contribution to the knowledge of Chinese Gryllacrididae (Orthoptera) V: Further study on the Chinese Capnogryllacris and comment on the phylogenetic relationships of the Gryllacrididae
FIGURE 10. Capnogryllacris melanocrania (Karny, 1929). Male: A–B. habitus in lateral view; C–D. tegmina in dorsal view: C. left tegmen, D. right tegmen.
FIGURE 2 in Contribution to the knowledge of Chinese Meconematinae (Orthoptera: Tettigoniidae) I: One new species of Neocyrtopsis Liu & Zhang, 2007 with key to species
FIGURE 2. Neocyrtopsis (Neocyrtopsis) tristrigata sp. nov.. Female: A. head in frontal view; B–C. head and pronotum: B. dorsal view, C. lateral view; D. apex of abdomen in lateral view; E. subgenital plate in ventral view; F–G. genicular lobes of postfemora: F. internal view, G. external view.
FIGURE 1 in Contribution to the knowledge of Chinese Meconematinae (Orthoptera: Tettigoniidae) I: One new species of Neocyrtopsis Liu & Zhang, 2007 with key to species
FIGURE 1. Neocyrtopsis (Neocyrtopsis) tristrigata sp. nov.. Male: A. head in frontal view; B–C. head and pronotum: B. dorsal view, C. lateral view; D–I. apex of abdomen: D. lateral view, E, G–H. apico-dorsal view, F. apical view, I. ventral view; J–K. apices of posttibiae: J. internal view, K. external view; L–M. genicular lobes of postfemora: L. external view, M. internal view.
Data from: Coastal darkening substantially limits the contribution of kelp to coastal carbon cycles
<p>Macroalgal-dominated habitats are rapidly gaining recognition as important contributors to marine carbon cycles and sequestration. Despite this recognition, relatively little is known about the production and fate of carbon originating from these highly productive ecosystems, or how anthropogenic and climate related stressors affect the role of macroalgae in marine carbon cycles. Here, we examine the impact of increasing turbidity on carbon storage, fixation and loss in southern hemisphere kelp forests. We quantified net primary production (NPP) and biomass accumulation (BA), and estimated carbon release via detritus and dissolved organic carbon (DOC) across a large-scale turbidity gradient. We show that increased turbidity, resulting in a 63 % reduction in light, can result in a 95 % reduction in kelp productivity. When averaged annually, estimates of NPP and BA per plant at high light sites were nearly 6 and 2 times greater than those at low light sites, respectively. Furthermore, the quantity of carbon fixed annually by kelp forests was up to 4.7 times greater than that stored as average annual standing stock. At low light sites, the majority of C goes directly into tissue growth and is subsequently eroded. In contrast, excess production at high light sites accounts for up to 39 % of the total carbon fixed and is likely released as DOC. Turbidity is expected to increase in response to climate change and our results suggest this will have significant impacts on the capacity of kelp forests to contribute to carbon sequestration pathways. In addition to demonstrating that turbidity significantly reduces the quantity of carbon fixed by kelp forests, and subsequently released as detritus, our results highlight the negative impacts of turbidity on a large source of previously unaccounted for carbon.</p>
FIGURE 4 in A contribution to the knowledge of leaf-mining Phyllocnistis Zeller, 1848 associated with Baccharis (Asteraceae), with description of two new species from Peru (Lepidoptera: Gracillariidae)
FIGURE 4. Distribution of Phyllocnistis (Gracillariidae) species associated with Baccharis (Asteraceae) in Peru. (A) Records are for P. canta n. sp. (green circles), P. furcata Vargas & Cerdeña (red circles) and P. elongata n. sp. (yellow circles). (B) and (C) Type localities of P. canta n. sp. (Canta, Lima) and P. elongata n. sp. (Tarata, Tacna), respectively. Baccharis host plants of P. canta n. sp. and P. elongata n. sp. are indicated in both cases by red arrows.
FIGURE 3 in A contribution to the knowledge of leaf-mining Phyllocnistis Zeller, 1848 associated with Baccharis (Asteraceae), with description of two new species from Peru (Lepidoptera: Gracillariidae)
FIGURE 3. Female genitalia of Phyllocnistis canta n. sp. (A–C), Phyllocnistis elongata n. sp. (D–F) and Phyllocnistis furcata Vargas & Cerdeña (G-I) under light microscopy. (A, D, G) lateral view, (B, E, H) last abdominal tergum in dorsal view, (C, F, I) corpus bursae in detail. Arrows indicate expansion of VIII abdominal segment (A: also marked with asterisk in B), signum bearing two small spines (C) and additional sclerotized areas bearing micro-spines (I). Scale bars: 0.5 mm (A, D, G), 0.2 mm (B, E, H), 0.1 mm (C, F, I).
FIGURE 2 in A contribution to the knowledge of leaf-mining Phyllocnistis Zeller, 1848 associated with Baccharis (Asteraceae), with description of two new species from Peru (Lepidoptera: Gracillariidae)
FIGURE 2. Male genitalia of Phyllocnistis canta n. sp. (A–B), Phyllocnistis elongata n. sp. (C–D) and Phyllocnistis furcata Vargas & Cerdeña (E–F), under light microscopy. (A, C, E) ventral view, (B, D, F) aedeagus, lateral view. Arrow indicates invagination in the middle of tegumen arch (A). Scale bars: 0.2 mm (A, C, E), 0.1 mm (B, D, F).
FIGURE 5 in A contribution to the knowledge of leaf-mining Phyllocnistis Zeller, 1848 associated with Baccharis (Asteraceae), with description of two new species from Peru (Lepidoptera: Gracillariidae)
FIGURE 5. Distance tree (Neighbor-joining) based on sequences of a 658-bp fragment of the cytochrome c oxidase I (COI) gene, showing the monophyletic status of the new species of Phyllocnistis and their nearest neighbors among Neotropical Phyllocnistis lineages, and the position of P. baccharidis Hering. The use of species of Baccharis as host plant by members of Neotropical Phyllocnistis is indicated.
FIGURE 1 in A contribution to the knowledge of leaf-mining Phyllocnistis Zeller, 1848 associated with Baccharis (Asteraceae), with description of two new species from Peru (Lepidoptera: Gracillariidae)
FIGURE 1. Adults of Phyllocnistis canta n. sp. (A–B), Phyllocnistis elongata n. sp. (C–D) and Phyllocnistis furcata Vargas & Cerdeña (E–F). (A, C, E) dorsal view, (B, D, F) detail of right forewing. Scale bars: 2 mm (A, C, D, E), 1 mm (B, F).
FIGURES 25–30 in Contribution to the knowledge of the genus Barsine Walker, 1854 from Xizang, China with description of a new species (Lepidoptera: Erebidae: Arctiinae: Lithosiini)
FIGURES 25–30. Male genitalia of Barsine spp. Depositories of the slides: 25, 27–30 in SCAU; 26 in CHSY.
FIGURES 37–46 in Contribution to the knowledge of the genus Barsine Walker, 1854 from Xizang, China with description of a new species (Lepidoptera: Erebidae: Arctiinae: Lithosiini)
FIGURES 37–46. Female genitalia of Barsine spp. Depositories of the slides: 37–41, 46 in SCAU; 42, 44, 45 in MWM/ZSM.
FIGURES 13–24 in Contribution to the knowledge of the genus Barsine Walker, 1854 from Xizang, China with description of a new species (Lepidoptera: Erebidae: Arctiinae: Lithosiini)
FIGURES 13–24. Adults of Barsine spp. Depositories of the specimens: 13, 14, 21–24 in SCAU; 15, 16, 18–20 in MWM/ZSM; 17 in NHMUK (©The Trustees of NHMUK).
FIGURES 31–36 in Contribution to the knowledge of the genus Barsine Walker, 1854 from Xizang, China with description of a new species (Lepidoptera: Erebidae: Arctiinae: Lithosiini)
FIGURES 31–36. Male genitalia of Barsine spp. Depositories of the slides: 31, 34–36 in SCAU; 32, 33 in MWM/ZSM.
FIGURE 11 in Contribution to the knowledge of Chinese Gryllacrididae (Orthoptera) VII: Review the genus Apterolarnaca Gorochov, 2004
FIGURE 11. Apterolarnaca (Bianigryllacris) xinganensis sp. nov.. Female: A. head in frontal view; B–C. head and pronotum: B. dorsal view, C. lateral view; D. apex of abdomen in lateral view; E. subgenital plate in ventral view.
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Allen Brain Atlas
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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.