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Distribution. Top End of Northern Territory, Australia, from Table Top Range in the NW to Wollogorang Station, and E just over the Queensland border; also occurs on Marchinbar in the Wessel Is. in Dasyuridae
Distribution. Top End of Northern Territory, Australia, from Table Top Range in the NW to Wollogorang Station, and E just over the Queensland border; also occurs on Marchinbar in the Wessel Is.
Subspecies and Distribution. P.m.maculataGould,1851—EAustralia,NQueensland(CapeYork),SthroughoutEQueenslandtoENewSouthWales(Gosford),alsoinFraserandBribieIs. P.m. sinualis Thomas, 1926 — N Australia, N Western Australia, N Northern Territory (Top End and Groote Eylandt I). Individuals from Barrow I, N Western Australia, are included here but possibly represent a differentstill undescribed species. in Dasyuridae
Subspecies and Distribution. P.m.maculataGould,1851—EAustralia,NQueensland(CapeYork),SthroughoutEQueenslandtoENewSouthWales(Gosford),alsoinFraserandBribieIs. P.m. sinualis Thomas, 1926 — N Australia, N Western Australia, N Northern Territory (Top End and Groote Eylandt I). Individuals from Barrow I, N Western Australia, are included here but possibly represent a differentstill undescribed species.
On following pages 34 Red-bel ıed Tarnann (Saguınus labıatusi 35 Emperor Tamann (Saguınus mpemron 36 Mıdas Tamann (Saguınus nudes) 37 Black-handed Tamann (Saguınııs nıgen 38 Pıed Tamann (Soguınus bıoolofi 39 Mamns s Bare-faced Tamann (Saguınus mamnsl) 40 Mottled-face Tırnann (Saguınus ınustusl 41 Whıte-fooıed Tamann (Saguınus Ieuoopus) 42 Cotton-top Tımann (Saguınus oedvøus). 43 Geoffroys Tamann (Saguınus gsafhoyñ in Callitrichiade
On following pages 34 Red-bel ıed Tarnann (Saguınus labıatusi 35 Emperor Tamann (Saguınus mpemron 36 Mıdas Tamann (Saguınus nudes) 37 Black-handed Tamann (Saguınııs nıgen 38 Pıed Tamann (Soguınus bıoolofi 39 Mamns s Bare-faced Tamann (Saguınus mamnsl) 40 Mottled-face Tırnann (Saguınus ınustusl 41 Whıte-fooıed Tamann (Saguınus Ieuoopus) 42 Cotton-top Tımann (Saguınus oedvøus). 43 Geoffroys Tamann (Saguınus gsafhoyñ
FIGURES –. Rare taxa (SEM, New Caledonia, Melanesia). Cocconeis sp. 2 in Riaux-Gobin et al. 2015 (31, 32), short marginal SV striae between each short raised virgae (31, arrow; 32, arrowhead), SV narrow sternum, siliceous pearls (31), C. sp. 4 in Riaux-Gobin et al. 2015 (33–34), strong marginal crista marginalis, short marginal striae on top of each short raised virga (33, arrow; 34, arrowhead),?C. sp. 5 in Riaux-Gobin et al. 2015 (35–36), short SV striae and a raised axial structure (35, arrow). Scale bars = 3 µm (31), 2 µm (33, 35), 1 µm (32, 36), 500 nm (34). in Marine Achnanthales (Bacillariophyceae) from New Caledonia (Melanesia): assemblage specificities, ultramafic environment
FIGURES –. Rare taxa (SEM, New Caledonia, Melanesia). Cocconeis sp. 2 in Riaux-Gobin et al. 2015 (31, 32), short marginal SV striae between each short raised virgae (31, arrow; 32, arrowhead), SV narrow sternum, siliceous pearls (31), C. sp. 4 in Riaux-Gobin et al. 2015 (33–34), strong marginal crista marginalis, short marginal striae on top of each short raised virga (33, arrow; 34, arrowhead),?C. sp. 5 in Riaux-Gobin et al. 2015 (35–36), short SV striae and a raised axial structure (35, arrow). Scale bars = 3 µm (31), 2 µm (33, 35), 1 µm (32, 36), 500 nm (34).
FIGURE. Drosera tomentosa (a–d): a, rosette; b, rosette and base of inflorescences of D. tomentosa var. glabrata (Serra do Cipó, MG); c, inflorescence of the "type morphotype" of D. tomentosa (Chapada Diamantina, BA); d, inflorescence with open flower of the "glabrate morphotype" of D. tomentosa, side view (Diamantina, MG). Drosera villosa (e, f): e, habit; f, flower (Parque Estadual da Serra Negra da Mantiqueira, MG). Drosera viridis (g–i): g, rosettes of D. viridis (bottom) and D. communis (single plant, top; Imbituva, PR); h, leaf, detail (Piraquara, PR); i, flower (Balsa Nova, PR). Photo credits: a, b, d–f by PMG; c by FR; g–i by Carlos Rohrbacher. in A synopsis of the genus Drosera (Droseraceae) in Brazil
FIGURE. Drosera tomentosa (a–d): a, rosette; b, rosette and base of inflorescences of D. tomentosa var. glabrata (Serra do Cipó, MG); c, inflorescence of the "type morphotype" of D. tomentosa (Chapada Diamantina, BA); d, inflorescence with open flower of the "glabrate morphotype" of D. tomentosa, side view (Diamantina, MG). Drosera villosa (e, f): e, habit; f, flower (Parque Estadual da Serra Negra da Mantiqueira, MG). Drosera viridis (g–i): g, rosettes of D. viridis (bottom) and D. communis (single plant, top; Imbituva, PR); h, leaf, detail (Piraquara, PR); i, flower (Balsa Nova, PR). Photo credits: a, b, d–f by PMG; c by FR; g–i by Carlos Rohrbacher.
FIGURE. Drosera hirtella (a–i): a, b, c, habit of the "type morphotype"; d, habit of the "western morphotype"; e, rosette of the "type morphotype"; f, emerging inflorescence, highlighting the red scape with red eglandular trichomes characteristic of the species; g, fertile individuals of D. hirtella (left plant, with inflorescence emerging to the bottom) and D. lutescens (right plant, with inflorescence emerging to the top left) growing under shaded conditions side by side, highlighting the morphological differences between the two species regarding leaf shape and scape and indumentum color; h, i, flower. a–c, f and h at Serra do Cipó, MG; d and h at Chapada dos Veadeiros, GO; e at Diamantina, MG; g at Cristalina, GO. Photo credits: all by PMG. in A synopsis of the genus Drosera (Droseraceae) in Brazil
FIGURE. Drosera hirtella (a–i): a, b, c, habit of the "type morphotype"; d, habit of the "western morphotype"; e, rosette of the "type morphotype"; f, emerging inflorescence, highlighting the red scape with red eglandular trichomes characteristic of the species; g, fertile individuals of D. hirtella (left plant, with inflorescence emerging to the bottom) and D. lutescens (right plant, with inflorescence emerging to the top left) growing under shaded conditions side by side, highlighting the morphological differences between the two species regarding leaf shape and scape and indumentum color; h, i, flower. a–c, f and h at Serra do Cipó, MG; d and h at Chapada dos Veadeiros, GO; e at Diamantina, MG; g at Cristalina, GO. Photo credits: all by PMG.
Subspecies and Distribution. M.f.fuscusThomas,1882—nowrestrictedtoN&WTasmania,butsubfossilevidence(owlpellets)indicatesaformerlymoreextensiverangeacrossTasmania. M. f. mordicus Thomas, 1922 — highly fragmented in mainland SE Australia, including the Otway and Dandenong ranges, coastal areas of Gippsland and SE New South Wales, and the Great Dividing Range around Barrington Tops and from near the Brindabella Range S to Warburton. in Muridae
Subspecies and Distribution. M.f.fuscusThomas,1882—nowrestrictedtoN&WTasmania,butsubfossilevidence(owlpellets)indicatesaformerlymoreextensiverangeacrossTasmania. M. f. mordicus Thomas, 1922 — highly fragmented in mainland SE Australia, including the Otway and Dandenong ranges, coastal areas of Gippsland and SE New South Wales, and the Great Dividing Range around Barrington Tops and from near the Brindabella Range S to Warburton.
COMPARING THE CO2 EMISSION INTENSITY OF THE STEEL INDUSTRIES IN THE EU AND CHINA RESULTING FROM TOP-DOWN AND BOTTOM-UP APPROACHES SUPPLEMENTARY
<p>The provided .xlsx file contains the following addtional data for the conference paper "Comparing CO<sub>2</sub> emission intensity of the steel industries in EU and China resulting from top-down and bottom-up approaches":</p> <ul> <li>The data used to plot Figure 1, 4, 5 and 6</li> <li>Scope adaption calculation</li> <li>EAF case study</li> </ul>
Data from: What drives diversification? Range expansion tops climate, life history, habitat, and size in lizards and snakes
<p><strong>Aim: </strong>A major challenge in ecology and evolutionary biology is to explain the dramatic differences in species richness among clades. Much variation in richness is explained by differences in diversification rates among clades, and variation in diversification rates is often linked to various traits. But what types of traits are most important for explaining diversification? Here, we compared the impacts of different types of traits on diversification rates among lizard and snake families, and tested predictions about the relative importance of ecology vs. morphology, static vs. dynamic traits, and alpha vs. beta niche traits.</p> <p><strong>Location: </strong>Global.</p> <p><strong>Time period:</strong> Recent to ~200 million years ago.</p> <p><strong>Major taxa studied:</strong> Squamata.</p> <p><strong>Methods: </strong>We compared the relative impacts of traits related to biogeography (range size, range expansion), climate, life history (viviparity), microhabitat, and morphology (body-size) on diversification rates among all 72 family-level clades of squamates. We compiled data on traits, and tested for relationships between traits and diversification rates using phylogenetic multiple regression models.</p> <p><strong>Results: </strong>The best-fitting model explained ~60% of the variation in diversification rates across squamate families. This model included only microhabitat (proportion of arboreal species) and a novel, dynamic, ecological/biogeographic beta-niche trait (rate of range expansion), which explained most variance. Other variables had more variable or non-significant contributions, including rates of climatic-niche change. Rates of range expansion were related to species richness, larger body size, and faster rates of climatic-niche change.</p> <p><strong>Main conclusions:</strong> Overall, we provide possibly the most comprehensive comparison of the types of traits that can drive diversification. We also help explain diversity patterns in one of the largest vertebrate clades. We show that the rate of range expansion is the most important variable for explaining diversification rates and richness patterns in squamates. We also identify traits that help explain variation in rates of range expansion among clades.</p>
NASA TOPS Logos
<p>NASA Transform to Open Science badges and wordmark</p>
Mesa Top Dig, Mesa Verde
This dig has exposed two sites from different times. Created in RealityCapture by Capturing Reality from 219 images in 01h:32m:18s. Source: Objaverse 1.0 / Sketchfab
Harrison Marble Top Table - Preview
For more information about this item visit: https://bhpsite.org/ Source: Objaverse 1.0 / Sketchfab
Jeanbille_et_al_2024_Exclusion_experiment_ANALYSIS: code and data for "Size exclusion experiment in a grassland field unravels top-down control of the soil fauna on microbial community assembly"
<p>Release of code and data associated with the publication "Size exclusion experiment in a grassland field unravels top-down control of the soil fauna on microbial community assembly".</p>
Top-down control of ammonia oxidizers in the North Pacific
<p>necessary data and programs for the submitted manuscript</p>
Jeanbille_et_al_2024_Exclusion_experiment_ANALYSIS: code and data for "Size exclusion experiment in a grassland field unravels top-down control of the soil fauna on microbial community assembly"
<p>Release of code and data associated with the publication "Size exclusion experiment in a grassland field unravels top-down control of the soil fauna on microbial community assembly".</p>
Jeanbille_et_al_2024_Exclusion_experiment_ANALYSIS: code and data for "Size exclusion experiment in a grassland field unravels top-down control of the soil fauna on microbial community assembly"
<p>Release of code and data associated with the publication "Size exclusion experiment in a grassland field unravels top-down control of the soil fauna on microbial community assembly".</p>
Jeanbille_et_al_2024_Exclusion_experiment_ANALYSIS: code and data for "Size exclusion experiment in a grassland field unravels top-down control of the soil fauna on microbial community assembly"
<p>Release of code and data associated with the publication "Size exclusion experiment in a grassland field unravels top-down control of the soil fauna on microbial community assembly".</p>
Dataset,MATLAB Programs, and supported model of "Top-down control of ammonia oxidizers by grazing in the North Pacific"
<p>Dataset,MATLAB Programs, and supported model of "Top-down control of ammonia oxidizers by grazing in the North Pacific". For the detailed information, see in the paper "Top-down control of ammonia oxidizers by grazing in the North Pacific".</p>
Top-down control of ammonia oxidizers in the North Pacific
<p>Dataset and Matlab programs in the submitted "Top-down control of ammonia oxidizers by grazing in the North Pacific ".</p>
Alphabetical comprehensive false friends lists and top 100 frequency lists in German-English & Chinese-Japanese
<p>The FF pairs in German and English were sourced from "False Friends: A Short Dictionary: Reclam premium Sprachtraining" by Burkhard Dretzke and Margaret Nester. I systematically compiled a list of all 794 pairs of FFs from the German-English dictionary, initially arranging them alphabetically in spreadsheets. Subsequently, I queried the frequency of each entry in both German and English corpora, sorting the word lists in each language in descending order based on frequency per million. I aimed to compile a list of the most relevant FFs by selecting those pairs present in the top 100 entries of both lists, resulting in 34 pairs that appeared prominently in both languages. Additionally, I collected data on FFs where one language exhibited high frequency although the other showed low or minimal occurrence. Excluding the aforementioned 34 pairs, I further filtered the German and English frequency lists to identify 33 words each, along with their corresponding FFs in the other language, yielding a total of 66 additional FF pairs. Thus, I compiled a comprehensive list of the top 100 FFs in German and English based on combined frequency of occurrence. Meanwhile, the Chinese and Japanese FFs were gathered from "2136 Japanese Kanji Character Dictionary" and published by Liaoning People's Publishing House. The methodology for collecting data on Chinese-Japanese FF pairs follows a similar procedure but with greater difficulty and complexity. Given that the concept and phenomenon of FFs originate from European linguistics, there is a relative scarcity of corresponding academic materials in Asian languages such as Chinese and Japanese, for instance, a readily available FFs' dictionary. Consequently, I used a Japanese kanji dictionary as my primary data source. This dictionary allows for the retrieval of Japanese kanji words using 2136 commonly used Chinese characters, selected by the Japanese Ministry of Culture for their high frequency of usage in social life and officially announced in November 2010. With nearly 15,000 entries, each word in the dictionary is accompanied by detailed Chinese interpretations and examples, facilitating the differentiation between true cognates and FFs with the same form. Following a meticulous examination of almost 15,000 entries, I identified 700 pairs of Chinese-Japanese FFs. Then I queried the frequency of each entry in both Chinese and Japanese corpora, sorting the word lists in each language in descending order based on frequencies. Subsequently, I selected 48 pairs that appeared in the top 100 frequency list in both Chinese and Japanese, and 26 words for Chinese and 26 words for Japanese on their own, akin to the methodology employed for German-English data collection, ultimately compiling a comprehensive list of the top 100 FFs in Chinese and Japanese based on combined frequency of occurrence.</p>
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Allen Brain Atlas
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International Brain Laboratory public data
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OpenNeuro
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