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Figure 2 from: McPartland JM, Small E (2020) A classification of endangered high-THC cannabis (Cannabis sativa subsp. indica) domesticates and their wild relatives. PhytoKeys 144: 81-112. https://doi.org/10.3897/phytokeys.144.46700
Figure 2 Shifts in THC/CBD ratios over time; data from 47 numbered studies in Suppl. material 1: SF.9. Central Asian landraces in unitalicized red (n =13 studies); "Indica" in underlined unitalicized red (n= 9); South Asian landraces in italicized green (n =18 studies); "Sativa" in underlined italicized green (n =7 studies). Size of numeral reflects the number of accessions analyzed in that study.
Figure 7 from: McPartland JM, Small E (2020) A classification of endangered high-THC cannabis (Cannabis sativa subsp. indica) domesticates and their wild relatives. PhytoKeys 144: 81-112. https://doi.org/10.3897/phytokeys.144.46700
Figure 7 Distribution of herbarium specimens. Red circles: var. asperrima; green triangles: var. himalayensis. Floristic zones based on Djamali et al. (2012): Red area: Irano-Turanian region; green area: Indian region; lilac area: Saharo-Sindian region. Other floristic regions not demarcated and unlabeled. Background base map by Natural Earth, free open-source map data (https:// www.naturalearthdata.com).
Figure 4 from: McPartland JM, Small E (2020) A classification of endangered high-THC cannabis (Cannabis sativa subsp. indica) domesticates and their wild relatives. PhytoKeys 144: 81-112. https://doi.org/10.3897/phytokeys.144.46700
Figure 4 Two varieties of C. sativa subsp. indica from South Asia. On left a var. indica. On right b var. himalayensis.
Figure 6 from: McPartland JM, Small E (2020) A classification of endangered high-THC cannabis (Cannabis sativa subsp. indica) domesticates and their wild relatives. PhytoKeys 144: 81-112. https://doi.org/10.3897/phytokeys.144.46700
Figure 6 Type specimens of C. sativa subsp. indica var. asperrima. Lectotype on left (a), epitype on right (b).
Figure 3 from: McPartland JM, Small E (2020) A classification of endangered high-THC cannabis (Cannabis sativa subsp. indica) domesticates and their wild relatives. PhytoKeys 144: 81-112. https://doi.org/10.3897/phytokeys.144.46700
Figure 3 Representative achenes of four varieties Aindica, Rajshahi (Bangladesh), Clarke 1877 (BM) Bindica, Coimbatore (India), Bircher 1893 (K) Cindica, South Africa, Hillig 1996; (IND) Dhimalayensis neotype Ehimalayensis, Bareilly (India), Roxburgh 1796 (K). Fhimalayensis, East Bengal (Bangladesh) Griffith 1835 (GH) Gafghanica neotype Hafghanica epitype Iafghanica Yarkant (Xīnjiāng), Henderson 1871 (LE) Jasperrima lectotype Kasperrima Nuristān (Afghanistan), Street 1965 (F) L Kailiyskiy Alatau (Kazakhstan), Semenov-Tyan-Shansky 1857 (LE).
Figure 4 from: Cuevas CC, Sanhueza R (2020) Geographic boundaries and natural history notes of the microendemic endangered frog Eupsophus migueli Formas, 1977 (Alsodidae) in the Mahuidanche Range, southern Chile. ZooKeys 929: 79-92. https://doi.org/10.3897/zookeys.929.35984
Figure 4 Scheme of the life history data of E. migueli (this paper) and E. altor. Data for E. altor were obtained from Núñez et al. (2012).
Figure 1 from: Cuevas CC, Sanhueza R (2020) Geographic boundaries and natural history notes of the microendemic endangered frog Eupsophus migueli Formas, 1977 (Alsodidae) in the Mahuidanche Range, southern Chile. ZooKeys 929: 79-92. https://doi.org/10.3897/zookeys.929.35984
Figure 1 A Distribution map of Eupsophus migueli. The red polygon corresponds to an updated distribution area of E. migueli, and it is formed by georeferenced landmarks including new records (this paper), old records (including the type locality, Mehuín, and nearby localities Queule and Pichicuyín) and other documented points (Méndez et al. 2005, Contreras 2014, Miranda 2015) B specimen of E. migueli from Colehual Alto.
Figure 3 from: Cuevas CC, Sanhueza R (2020) Geographic boundaries and natural history notes of the microendemic endangered frog Eupsophus migueli Formas, 1977 (Alsodidae) in the Mahuidanche Range, southern Chile. ZooKeys 929: 79-92. https://doi.org/10.3897/zookeys.929.35984
Figure 3 Habitat of Eupsophus migueliA, D native forest with anthropogenic disturbance in Boroa Norte 1 B pine monoculture with undergrowth habitat of Aristotelia chilensis in Boroa Norte 4 C, E native forest in El Socorro.
Figure 2 from: Cuevas CC, Sanhueza R (2020) Geographic boundaries and natural history notes of the microendemic endangered frog Eupsophus migueli Formas, 1977 (Alsodidae) in the Mahuidanche Range, southern Chile. ZooKeys 929: 79-92. https://doi.org/10.3897/zookeys.929.35984
Figure 2 Dorsal (capitals) and ventral (lowercase) patterns of pigmentation in Eupsophus migueli from different localities along its distribution range. A Dorsal pattern of dark brown (Socorro) a ventral white with longitudinal spots (El Socorro, Boroa Norte) B dorsal yellow pattern and b belly with yellow crosslinks (El Socorro) C dorsal pattern yellow with brown spots and c belly with yellow longitudinal spots (El Socorro, Boroa Norte) D dorsal pattern dark brown and d belly with whitish faded spots. All specimens were adults ranging in size from 4 to 5 cm.
Figures 6-11 from: Fukushima CS, Cardoso P, Bertani R (2020) Description of the male of the Critically Endangered tarantula Typhochlaena curumim Bertani, 2012 (Araneae, Theraphosidae), with comments on tarantula trade and conservation. ZooKeys 938: 125-136. https://doi.org/10.3897/zookeys.938.51442
Figures 6-11 Typhochlaena curumim male (MNRJ 6915) 6−10 palpal bulb, left side 6 retrolateral 7 prolateral 8 dorsal 9 frontal 10 left palp, prolateral 11 urticating setae type II. Scale bars: 1 mm (6–10); 0.1 mm (11)
Figures 2-5 from: Fukushima CS, Cardoso P, Bertani R (2020) Description of the male of the Critically Endangered tarantula Typhochlaena curumim Bertani, 2012 (Araneae, Theraphosidae), with comments on tarantula trade and conservation. ZooKeys 938: 125-136. https://doi.org/10.3897/zookeys.938.51442
Figures 2-5 Typhochlaena curumim male (MNRJ 6915) 2 carapace, dorsal 3 abdomen, dorsal 4 maxillae, labium, sternum, and coxae 5 spinnerets, ventral. Scale bars: 1 mm.
Figure 1 from: Fukushima CS, Cardoso P, Bertani R (2020) Description of the male of the Critically Endangered tarantula Typhochlaena curumim Bertani, 2012 (Araneae, Theraphosidae), with comments on tarantula trade and conservation. ZooKeys 938: 125-136. https://doi.org/10.3897/zookeys.938.51442
Figure 1 Typhochlaena curumim Bertani, 2012 habitus, male from southern Rio Grande do Norte, Brazil. Photo: Rogério Bertani.
Figure 12 from: Fukushima CS, Cardoso P, Bertani R (2020) Description of the male of the Critically Endangered tarantula Typhochlaena curumim Bertani, 2012 (Araneae, Theraphosidae), with comments on tarantula trade and conservation. ZooKeys 938: 125-136. https://doi.org/10.3897/zookeys.938.51442
Figure 12 Approximate distribution of Typhochlaena curumim Bertani, 2012. A large spatial error has been introduced to avoid revealing exact localities.
Figure 1 in Improved local inventory and regional contextualization for anuran (Amphibia) diversity assessment at an endangered habitat in southeastern Brazil
Figure 1. Result of the WPGMA (Jaccard's index) showing (A) dissimilarities among localities with published anuran inventories at the Quadrilátero Ferrífero, southeastern Brazil, and (B) their spatial distribution. Locality names are as in Table 2.
Figure 4 from: Baasanmunkh S, Nyamgerel N, Bayarmaa G-A, Oyuntsetseg B, Oyundelger K, Choi HJ (2020) A new record of critically endangered Saussurea bogedaensis (Asteraceae) from Dzungarian Gobi, Mongolia. PhytoKeys 160: 109-121. https://doi.org/10.3897/phytokeys.160.55603
Figure 4 Phylogenetic tree based on concatenated sequence alignments of nrDNA (ITS) and cpDNA (trnK, trnH-psbA, and rbcL) regions. Bayesian Inference (BI) posterior probability support values above 90% (bold), Maximum Likelihood (ML) and Maximum Parsimony (MP) bootstrap support values above 70% are shown in the branches in the following order BI/ML/MP. The new samples of S. bogedaensis and S. orgaadayi originated from Mongolia are in red and black bolds, respectively.
Figure 1 from: Baasanmunkh S, Nyamgerel N, Bayarmaa G-A, Oyuntsetseg B, Oyundelger K, Choi HJ (2020) A new record of critically endangered Saussurea bogedaensis (Asteraceae) from Dzungarian Gobi, Mongolia. PhytoKeys 160: 109-121. https://doi.org/10.3897/phytokeys.160.55603
Figure 1 Saussurea bogedaensis in Buduun Khargait river, Baitag Bogd Mt, Uyench sum, Khovd Province, Mongolia. A general habit in Baitag Bogd Mt, DzG region B fruiting C leaves D pappus E phyllaries. Photos: 28 July 2019, Sh. Baasanmunkh.
Figure 5 from: Baasanmunkh S, Nyamgerel N, Bayarmaa G-A, Oyuntsetseg B, Oyundelger K, Choi HJ (2020) A new record of critically endangered Saussurea bogedaensis (Asteraceae) from Dzungarian Gobi, Mongolia. PhytoKeys 160: 109-121. https://doi.org/10.3897/phytokeys.160.55603
Figure 5 Multiple sequence alignment of combined nr DNA (ITS) and cpDNA (trnK, trnH-psbA and rbcL) sequences. ITS region shows more differences than cpDNA regions amongst those closely related species. (*) – no differences found between species.
Figure 3 from: Baasanmunkh S, Nyamgerel N, Bayarmaa G-A, Oyuntsetseg B, Oyundelger K, Choi HJ (2020) A new record of critically endangered Saussurea bogedaensis (Asteraceae) from Dzungarian Gobi, Mongolia. PhytoKeys 160: 109-121. https://doi.org/10.3897/phytokeys.160.55603
Figure 3 Distribution of S. bogedaensis (red dots), S. involucrata (blue dots) and S. orgaadayi (green dots) in Mongolia, Russia and Chinese Tien-Shan Mts based on field surveys and herbarium materials as well as specimens from China based on the publications of Chen and Wang (2018) and Chen et al. (2019). Region numbers on the Mongolian map are phytogeographical regions according to Grubov (1982): 6 – Khovd, 7 – Mongolian Altai, 10 – Depression of Great Lakes and 14 – Dzungarian Gobi.
Figure 2 from: Baasanmunkh S, Nyamgerel N, Bayarmaa G-A, Oyuntsetseg B, Oyundelger K, Choi HJ (2020) A new record of critically endangered Saussurea bogedaensis (Asteraceae) from Dzungarian Gobi, Mongolia. PhytoKeys 160: 109-121. https://doi.org/10.3897/phytokeys.160.55603
Figure 2 Saussurea orgaadayi in Khukh Nuur, Munkhkhairkhan sum, Khovd Province, Mongolia A general habit in Munkhkhairkhan Mt, MA region B fruiting C flowering D pappus E phyllaries. Photos: 29 July 2016, B. Oyuntsetseg (A, C) Sh. Baasanmunkh (B, D, E).
An endangered bird calls less when invasive birds are calling
<p>Novel noises can affect various animal behaviours, and changes to vocal behaviour are some of the most documented. The calls of invasive species are an important source of novel noise, yet their effects on native species are poorly understood. We examined the effects of invasive bird calls on the vocal activity of an endangered Australian finch to investigate whether: (i) native finch calling behaviour was affected by novel invasive bird calls, and (ii) the calls of the finches overlapped in frequency with those of invasive birds. We exposed a wild population of Black-throated Finch southern subspecies (<i>Poephila cincta cincta</i>) to the vocalisations of two invasive birds, Nutmeg Mannikins (<i>Lonchura punctulata</i>) and Common Mynas (<i>Acridotheres tristis</i>), a synthetic 'pink' noise, and a silent control. To determine whether the amount of Black-throated Finch calling differed in response to treatments, we recorded and quantified Black-throated Finch vocalisations, and assessed the amount of calling using a generalised linear mixed model followed by pairwise comparisons. We also measured, for both Black-throated Finches and the stimulus noises: dominant, minimum and maximum frequency, and assessed the degree of frequency overlap between Black-throated Finch calls and stimulus noises. Compared to silent controls, Black-throated Finches called less when exposed to Common Myna calls and pink noise, but not to Nutmeg Mannikin calls. We also found that pink noise overlapped most in frequency with Black-throated Finch calls. Common Myna calls also somewhat overlapped the frequency range of Black-throated Finch calls, whereas Nutmeg Mannikin calls overlapped the least. It is possible that masking interference is the mechanism behind the reduction in calling in response to Common Myna calls and pink noise, but more work is needed to resolve this. Regardless, these results indicate that the calls of invasive species can affect the behaviour of native species, and future research should aim to understand the scope and severity of this issue.</p>
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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
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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.