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Figs. 1–4 in A New Species ofEnoclerusGahan (Coleoptera: Cleridae: Clerinae) from the Sierra Sur of Oaxaca, Mexico
Figs. 1–4. Enoclerus juquilensis, holotype female and habitat. 1) Habitus; 2) Living specimen; 3) Vines (probably Ipomoea sp. or Aristolochia sp.) from which the holotype was beaten; 4) Type locality: pine-oak forest with second growth vegetation along roadside, south of Juquila, Oaxaca, Mexico.
FIGURE 3 in Rhytidhysteron mexicanum sp. nov. (Dothideomycetes, Ascomycota) from the Sierra of Guadalupe, Trans Mexican Volcanic Belt
FIGURE 3. Macroscopical morphological features of Rhytidhysteron mexicanum. A. Appearance of hysterothecia on host. B. Ascomata hysterothecial close-up.
FIGURE 2 in Rhytidhysteron mexicanum sp. nov. (Dothideomycetes, Ascomycota) from the Sierra of Guadalupe, Trans Mexican Volcanic Belt
FIGURE 2. Maximum-likelihood analysis tree from analysis of combined dataset of ITS and LSU sequence alignment of Rhytidhysteron species. The tree was rooted using Gloniopsis calami as the out-group. Bootstrap support values from 1,000 replicates are shown at the nodes only for branches supported by more than 50%. The scale bar at the bottom of the tree indicates a genetic change of 0.02. Newly generated sequences are in green.
FIGURE 1 in Rhytidhysteron mexicanum sp. nov. (Dothideomycetes, Ascomycota) from the Sierra of Guadalupe, Trans Mexican Volcanic Belt
FIGURE 1. Maximum-likelihood analysis tree from analysis of combined dataset of ITS and LSU sequence alignment of Pleoporomycetidae. The tree was rooted using Roccella fuciformis as the out-group. Bootstrap support values from 1,000 replicates are shown at the nodes only for branches supported by more than 50%. The scale bar at the bottom of the tree indicates a genetic change of 0.02. Newly generated sequences are in green. The species in bold are the Ex-type strain.
FIGURE 4 in Rhytidhysteron mexicanum sp. nov. (Dothideomycetes, Ascomycota) from the Sierra of Guadalupe, Trans Mexican Volcanic Belt
FIGURE 4. Microscopical features of Rhytidhysteron mexicanum stained with alcohol (70%) and KOH (10%) reagent. A. Hysterothecium cross-section without KOH. B. Hysterothecium cross-section with KOH. C. Hysterothecium cross section, showing the epithecium, haemathecium (hymenium), exciple and subhymenium. D. Exciple of iso-diametric cells (globulosa-angularis) close-up. E. Asci and ascospores. F. Peridium of iso-radiating cells (textura prismatica) close-up. G. Pseudoparaphyses. H. Ascospores.
FIGURE. Typical habitats of Ramalina species on northern South America. A. High paramo, Laguna Anteojos, Sierra Nevada de Merida, where grows on rocks R. anteojina at 4100 m. B. Sub-paramo (timberline), La Aguada, Sierra Nevada de Merida, 3100 m, where are found R. dictyota and R. reducta on shrubs. C. Andean cloud forest, La Victoria, Sierra Nevada de Merida where R. cochlearis, R. cumanensis and R. victoriana are found growing as epiphytes. D. Populations of R. usnea, R. morrocoyensis and R. paradisensis growing as epiphytes on mangroves and Suriana maritima at sea level, National Park Morrocoy, state Falcón; the latter two species are known only from this locality. E. Ramalina usnea is the only species of this genus reported from the Alto Orinoco, Amazonas, near La Esmeralda, 150 m, growing as corticolous in submontane forests, at the top of the picture the Cerro Duida. F. Xerophytic forests from the National Park Cerro Santa Ana, state Falcón, where Ramalina santanensis and R. microphylla are known only growing on soil and rocks at 200–400 m. Photos V. Marcano. in The genus Ramalina Acharius (Ascomycota, Lecanoromycetes, Ramalinaceae) in northern South America
FIGURE. Typical habitats of Ramalina species on northern South America. A. High paramo, Laguna Anteojos, Sierra Nevada de Merida, where grows on rocks R. anteojina at 4100 m. B. Sub-paramo (timberline), La Aguada, Sierra Nevada de Merida, 3100 m, where are found R. dictyota and R. reducta on shrubs. C. Andean cloud forest, La Victoria, Sierra Nevada de Merida where R. cochlearis, R. cumanensis and R. victoriana are found growing as epiphytes. D. Populations of R. usnea, R. morrocoyensis and R. paradisensis growing as epiphytes on mangroves and Suriana maritima at sea level, National Park Morrocoy, state Falcón; the latter two species are known only from this locality. E. Ramalina usnea is the only species of this genus reported from the Alto Orinoco, Amazonas, near La Esmeralda, 150 m, growing as corticolous in submontane forests, at the top of the picture the Cerro Duida. F. Xerophytic forests from the National Park Cerro Santa Ana, state Falcón, where Ramalina santanensis and R. microphylla are known only growing on soil and rocks at 200–400 m. Photos V. Marcano.
FIGURE 3. Sideroxylon cochranei. A in Sideroxylon cochranei (Sapotoideae, Sapotaceae): a new cloud forest tree species from the Sierra de Manantlán and Cuale in western México
FIGURE 3. Sideroxylon cochranei. A. Immature fruits, from El Fresnal. Sierra de Manantlán, Cuevas-G. et al. 7694. B. Mature fruits from Sierra de Cuale, Santana-M. et al. 11384. Photographs by R. Cuevas-G.
FIGURE 2. Sideroxylon cochranei. A. Fruiting branch. B. Floriferous branch. C in Sideroxylon cochranei (Sapotoideae, Sapotaceae): a new cloud forest tree species from the Sierra de Manantlán and Cuale in western México
FIGURE 2. Sideroxylon cochranei. A. Fruiting branch. B. Floriferous branch. C. The entire flower (left) and gynoecium showing the open corolla and staminodes (right). D. Fruit. E. Seed. Illustration by Enrique V. Sánchez R.
FIGURE 1 in Sideroxylon cochranei (Sapotoideae, Sapotaceae): a new cloud forest tree species from the Sierra de Manantlán and Cuale in western México
FIGURE 1. Distribution of Sideroxylon cochranei and other geographically close species of Sideroxylon in the state of Jalisco, Mexico.
FIGURE 4. Hechtia marthae. A in In disentangling two species limits of Hechtia (Bromeliaceae: Hechtioideae) from Sierra Madre Occidental, a new species is discovered from Durango, Mexico
FIGURE 4. Hechtia marthae. A. Pistillate plant in bloom. B. Staminate plant in bloom. C. Detail of inflorescence with young fruits. D. Female flowers at anthesis. E. Male flowers at anthesis. Illustration by Alberto Guerra based on photographs by A, D. Ricardo Quirino-Olvera. B. Gustavo Romero-González. C. Adolfo Espejo-Serna from the specimen A. R. López-Ferrari et al. 2989 (UAMIZ). E and staminate rosette based of photographs by Ivón Ramírez-Morillo. D and pistillate rosette in based of photographs by Ricardo Quirino-Olvera.
FIGURE 1 in In disentangling two species limits of Hechtia (Bromeliaceae: Hechtioideae) from Sierra Madre Occidental, a new species is discovered from Durango, Mexico
FIGURE 1. Geographical distribution of Hechtia jaliscana, H. marthae and H. subalata. Biogeographical provinces are depicted in different colors; their limits are based on Morrone et al. (2017).
FIGURE 7. Hechtia subalata portraying a in In disentangling two species limits of Hechtia (Bromeliaceae: Hechtioideae) from Sierra Madre Occidental, a new species is discovered from Durango, Mexico
FIGURE 7. Hechtia subalata portraying a rosette in bloom, note the red coloration on the leaves. A. Pistillate inflorescence. B. Female flowers at anthesis. C. Branch with open fruits. D. Staminate inflorescence. E. Details of the male flowers with open exposing the pollen. F. Open flowers before anthesis. (Illustration by Alberto Guerra based of photographs by A, B. Omar Góngora. C-F, Ivón Ramírez-Morillo).
FIGURE 3. Hechtia jaliscana. A in In disentangling two species limits of Hechtia (Bromeliaceae: Hechtioideae) from Sierra Madre Occidental, a new species is discovered from Durango, Mexico
FIGURE 3. Hechtia jaliscana. A. General structure of a male individual in bloom. B. Bee visiting fragrant male flowers. C. Origin of the inflorescence in a female plant. D. Details of male flowers. E. Details of female flowers. F. Branch with male flowers. G. Branch with female flowers. H. Preserved ripe fruits. (Credits: A, D, F. Claudia Ramírez-Díaz. B, C. Ivón Ramírez-Morillo. E, G. Pablo Carrillo-Reyes. H. Fruit features taken from P. Carrillo-Reyes & D. Cabrera-Toledo 8880-A♀ (IBUG)).
FIGURE 2 in In disentangling two species limits of Hechtia (Bromeliaceae: Hechtioideae) from Sierra Madre Occidental, a new species is discovered from Durango, Mexico
FIGURE 2. Hechtia jaliscana in habitat. A. Structure of the rachis in the infructescence. B. Details of the structure of the staminate inflorescence at anthesis. C. Rosettes with male flowers in habitat. D. Individuals in habitat of tropical dry forests. (Credits: A, C. Ivón Ramírez-Morillo. B, D. Claudia Ramírez-Díaz).
FIGURE 6 in In disentangling two species limits of Hechtia (Bromeliaceae: Hechtioideae) from Sierra Madre Occidental, a new species is discovered from Durango, Mexico
FIGURE 6. Hechtia subalata: A. Detail of the branching with young fruits. B. Detail of a dry staminate inflorescence. C. Rosette with infructescence. D. Plants in habitat, showing the red coloration on leaves. (Credits: A, C. Sabina Ascencio. B. Ivón Ramírez-Morillo. D. Pablo Carrillo-Reyes).
FIGURE 5. Hechtia marthae. A in In disentangling two species limits of Hechtia (Bromeliaceae: Hechtioideae) from Sierra Madre Occidental, a new species is discovered from Durango, Mexico
FIGURE 5. Hechtia marthae. A. Plants in habitat. B. Infructescence with open fruits in habitat. C. Seeds. (Credits A-C. Ivón Ramírez-Morillo).
Supporting data for: Investigating conifer water use patterns across temporal and topographic gradients in the southern Sierra Nevada
<p>Access to a reliable water source plays an integral role in tree function and survival. Water is a critical component of tree physiological processes, with trees that experience water stress exhibiting lower stomatal conductance (Irvine et al. 1998, Panek and Goldstein 1999), reduced photosynthetic and growth rates (Grieu et al. 1988, DeLucia and Heckathorn 1989, Adams and Kolb 2005, Truettner et al. 2018), and increased risk of hydraulic failure (Brodribb and Cochrad 2009, Anderegg and Anderegg 2013). As droughts increase in frequency, severity, and duration globally (Allen et al. 2015), access to a reliable water source such as deep soil water or water stored in fractured bedrock (i.e, hydraulic refugia) may dictate how trees respond to periods of water stress (McDowell et al. 2019). For example, studies in the southwestern United States have indicated that trees with access to deeper, more reliable water sources experience lower rates of mortality during drought periods (Grossiord et al. 2017, McDowell et al. 2019). While the effect of water availability on tree function and survival is well studied, whether the primary water source used by trees varies through time and across topographic gradients remains poorly understood. Understanding variability in tree water use patterns may provide insight to how forests will respond to increasing water stress under climate change.</p>
Replication package for "Long Run Effects of Aid: Forecasts and Evidence from Sierra Leone"
<p>Replication package for "Long Run Effects of Aid: Forecasts and Evidence from Sierra Leone" by K.Casey, R. Glennerster, E. Miguel and M. Voors, in the Economic Journal 2022</p>
FIGURE 3. A–C, Pinguicula warijia. A. Summer rosette. B. Flower. C. Seed. D–F, Pinguicula zamudioana. D. Summer rosette. E. Flower. F. Seed. G–I. Pinguicula oblongiloba. G. Summer rosette. H. Flower. I. Seed. Photos A and B in Pinguicula warijia sp. nov. (Lentibulariaceae), a newly rediscovered species from the Sierra Obscura, northern Mexico
FIGURE 3. A–C, Pinguicula warijia. A. Summer rosette. B. Flower. C. Seed. D–F, Pinguicula zamudioana. D. Summer rosette. E. Flower. F. Seed. G–I. Pinguicula oblongiloba. G. Summer rosette. H. Flower. I. Seed. Photos A and B by Martín Mata-Rosas; D by David Juárez-Gutiérrez; E, G and H by Julián Hernández-Rendón; C, F and I by Greta Hanako Rosas-Saito.
FIGURE 1. Pinguicula warijia. A in Pinguicula warijia sp. nov. (Lentibulariaceae), a newly rediscovered species from the Sierra Obscura, northern Mexico
FIGURE 1. Pinguicula warijia. A. Habit with rosette, flower, fruit and flower bud. B. Leaf series with variation in size and form. C. Detail of the stipitate glands of the leaf. D. Calyx, back view. E. Flower, lateral view. F. Corolla shape variation, frontal view. G. Detail of the throat of the tube showing the multicellular trichomes and stigma. H. Trichomes of the tube. Drawing by María Teresa Jiménez-Segura.
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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.