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1,994 results for “Tailings”

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Reduction Results for an Artificial Fish Tail

<p>Computation Results for an extensive comparison of model reductions methods for structure preserving reduction of second order mechanical systems applied to an artificial fishtail model.</p>

opencc-by-4.0Feb 2019View details →
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Reconstruction of the skeletons of Struthiomimus altus (left) and Ornitholestes hermanni (right). Struthiomimus 1/10, Ornitholestes 1/6 natural size, The Ornitholestes restoration replaces the original restoration by Osborn in 1903 which is very faulty. The Struthiomimus, Amer. Mus. 5339, mount has the distal end of the tail restored from Amer. Mus. 5355; dotted vertebra from Amer. Mus. 5262, In both restorations the pollex is too closely appressed to the other digits, see Fig. 3. in Skeletal Adaptations of Ornitholestes, Struthiomimus, Tyrannosaurus

Reconstruction of the skeletons of Struthiomimus altus (left) and Ornitholestes hermanni (right). Struthiomimus 1/10, Ornitholestes 1/6 natural size, The Ornitholestes restoration replaces the original restoration by Osborn in 1903 which is very faulty. The Struthiomimus, Amer. Mus. 5339, mount has the distal end of the tail restored from Amer. Mus. 5355; dotted vertebra from Amer. Mus. 5262, In both restorations the pollex is too closely appressed to the other digits, see Fig. 3.

opencc-by-4.0Dec 1917View details →
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Figures 21-26 in Two new cave-dwelling genera of short-tailed whip-scorpions from Brazil (Arachnida: Schizomida: Hubbardiidae)

Figures 21-26. Photographs of habitat and live schizomids: (21) view of plateau at Carajás region, limit between canga and ombrophilous vegetation types; (22-23) entrance region of a canga cave; (24) invertebrate manual collecting on ground of the interior of a canga cave; (25) live male of Naderiore carajas gen. nov., sp. nov. on ground; (26) live female of Cangazomus xikrin gen. nov., sp. nov. on ground. Photos: (21-24) Renata de Andrade, (25) Igor Cizauskas, (26) Marcus Oliveira.

opencc-by-4.0Apr 2016View details →
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Figures 1-6 in Two new cave-dwelling genera of short-tailed whip-scorpions from Brazil (Arachnida: Schizomida: Hubbardiidae)

Figures 1-6. Male flagellum. Naderiore carajas gen. nov., sp. nov.: (1) dorsal; (2) ventral; (3) lateral. Cangazomus xikrin gen. nov., sp. nov.: (4) dorsal; (5) ventral; (6) lateral. Scale bars: 1, 3-4 = 0.1; 2, 5-6 = 0.05 mm. Note: the setae named in parentheses correspond to the nomenclature of the flagellar setation proposed by VILLARREAL et al. (2014) and MORENO-GONZáLEZ et al. (2014).

opencc-by-4.0Apr 2016View details →
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Figures 7-10 in Two new cave-dwelling genera of short-tailed whip-scorpions from Brazil (Arachnida: Schizomida: Hubbardiidae)

Figures 7-10. Female flagellum. Naderiore carajas gen. nov., sp. nov.: (7) ventral; (8) dorsal. Cangazomus xikrin gen. nov., sp. nov.: (9) dorsal; (10) ventral. Scale bar: 0.05 mm. Note: The setae named in parentheses correspond to the nomenclature of the flagellar setation proposed by VILLARREAL et al. (2014) and MORENO-GONZáLEZ et al. (2014).

opencc-by-4.0Apr 2016View details →
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Figures 14-20 in Two new cave-dwelling genera of short-tailed whip-scorpions from Brazil (Arachnida: Schizomida: Hubbardiidae)

Figures 14-20. Pedipalp, chelicerae and spermathecae: (14-17) Naderiore carajas gen. nov., sp. nov.: (14) Male homeomorphic pedipalp (holotype); (15) Male heteromorphic pedipalp, paratype MZSP-68883; (16) Male chelicerae, holotype: top-movable finger, bottom-fixed finger; (17) female paratype spermathecae, MZSP-65724; (18-20) Cangazomus xikrin gen. nov., sp. nov.: (18) male pedipalp, holotype; (19) male chelicerae, holotype: top-movable finger, bottom-fixed finger; (20) female paratype spermathecae. Scale bars: 14-15, 18 = 0.20 mm; 17, 20 = 0.05 mm. (Fe1) Femur ectal 1, (Fe2) femur ectal 2, (Fv1) femur ventral 1, (Fv2) femur ventral 2.

opencc-by-4.0Apr 2016View details →
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Figures 11-13 in Two new cave-dwelling genera of short-tailed whip-scorpions from Brazil (Arachnida: Schizomida: Hubbardiidae)

Figures 11-13. Glandular pores: (11) Cangazomus xikrin gen. nov., sp. nov.; (12-13) Naderiore carajas gen. nov., sp. nov. Scale bars: 11 = 0.002, 12 = 0.005, 13 = 0.01 mm.

opencc-by-4.0Apr 2016View details →
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Figure 2 in Occurrence of regenerated tail in Indian freshwater spiny eel, Macrognathus pancalus Hamilton, 1822 (Teleostei: Mastacembelidae), in northern West Bengal, India

Figure 2. Lateral view, preopercular spines, scales, and X-ray impression of regenerated tail of Macrognathus pancalus.

opencc-by-4.0Jun 2013View details →
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Figures 1–5 in Rediscovery of the scorpion tailed orb-weaver, Arachnura melanura Simon 1867 (Araneae: Araneidae) from India

Figures 1–5. Arachnura melanura Simon, female: 1. Habitus, dorsal view, 2. Same, ventral view, 3. Tip of abdominal tail, 4. Epigynum, ventral view, 5. Internal genitalia, dorsal view. Scale bars= (1, 2, 4) 0.5 mm, (3, 5) 0.3 mm. Abbreviations: S = Scape, L = Lateral lobe, Sp = Spermatheca, Cd = Copulatory duct, Fd = Fertilization duct, Co = Copulatory opening.

opencc-by-4.0Dec 2020View details →
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Figure 4 in Ensemble distribution modeling of the Mesopotamian spiny-tailed lizard, Saara loricata (Blanford, 1874), in Iran: an insight into the impact of climate change

Figure 4. Overlay of Iranian Conservation Network with the habitat suitability map of the Mesopotamian spiny-tailed lizard.

opencc-by-4.0Dec 2016View details →
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Figure 3 in Ensemble distribution modeling of the Mesopotamian spiny-tailed lizard, Saara loricata (Blanford, 1874), in Iran: an insight into the impact of climate change

Figure 3. Model of habitat suitability for the species based on the present climatic data (A) and 2.6 (B) and 8.5 (C) scenarios of the CCSM for the future.

opencc-by-4.0Dec 2016View details →
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Figure 1 in Ensemble distribution modeling of the Mesopotamian spiny-tailed lizard, Saara loricata (Blanford, 1874), in Iran: an insight into the impact of climate change

Figure 1. The presence records (black dots) used for the development of a maximum entropy model for predicting the habitat suitability of the Mesopotamian spiny-tailed lizard.

opencc-by-4.0Dec 2016View details →
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Figure. The adult male of Podarcis lilfordi from Sa Dragonera, Mallorca (Balearic Islands), presenting a tail-like appendage in the left hind limb. in A case of limb regeneration in a wild adult Podarcis lilfordi lizard

Figure. The adult male of Podarcis lilfordi from Sa Dragonera, Mallorca (Balearic Islands), presenting a tail-like appendage in the left hind limb.

opencc-by-4.0Jul 2017View details →
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Figure 4 in Composition and structure of soil fauna community in the Dexing Copper Mine tailings pool after revegetation

Figure 4. One-way ANOVA of Shannon–Wiener diversity index (H'), Pielou index (Js), and Margalef index (D) across the different samples (mean ± SE). Means with different letters are significantly different as assessed by LSD test, α = 0.05.

opencc-by-4.0Jan 2018View details →
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Figure 3 in Composition and structure of soil fauna community in the Dexing Copper Mine tailings pool after revegetation

Figure 3. One-way ANOVA of the functional groups across the different samples (mean ± SE). Means with different letters are significantly different as assessed by LSD test, α = 0.05.

opencc-by-4.0Jan 2018View details →
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Figure 5 in Composition and structure of soil fauna community in the Dexing Copper Mine tailings pool after revegetation

Figure 5. Results of the principal components analysis (PCA) of the soil fauna data. The values are means (n = 3) with bidirectional error bars of axis 1 and 2. For all the PCA plots, the values on the x- and y-axes represent the percent variation explained by axis 1 and axis 2, respectively. I, II, III, and IV refer to the sample I, sample II, sample III, and sample IV, respectively.

opencc-by-4.0Jan 2018View details →
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Figure 2 in Composition and structure of soil fauna community in the Dexing Copper Mine tailings pool after revegetation

Figure 2. One-way ANOVA of the abundance (A) and taxonomic richness (B) across different samples (mean ± SE). Means with different letters are significantly different as assessed by LSD test, α = 0.05.

opencc-by-4.0Jan 2018View details →
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Figure. Comparison of longest primary feather, tail length, and chest circumference in male and female common snipe (* = p <0.05; **= p <0.01). Table 3. Weight of gut variables in male and female common snipe. in Revision of common snipe, Gallinago gallinago in morphometric analysis and building the standard reference haematological values for further studies

Figure. Comparison of longest primary feather, tail length, and chest circumference in male and female common snipe (* = p &lt;0.05; **= p &lt;0.01). Table 3. Weight of gut variables in male and female common snipe.

opencc-by-4.0Jun 2021View details →
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Fig. 4 in Molecular screening for rickettsial bacteria and piroplasms in ixodid ticks surveyed from white-tailed deer (Odocoileus virginianus) and nilgai antelope (Boselaphus tragocamelus) in southern Texas

Fig. 4. Phylogentic analysis of sca0 (rompA) sequences from putative Rickettsia sp. endosymbionts of Amblyomma maculatum and Ixodes scapularis ticks collected from white-tailed deer in southern Texas. This is a maximum-likelihood tree that is rooted at midpoint. Branch support was assessed with 10,000 replicates of UFBoot bootstrap replication, and bootstrap percentages are indicated at each branch point in the tree. Sequences from GenBank used in the comparative analysis were annotated as rickettsial endosymbionts. Accession numbers and tick species from which sequence was identified are included on the branch label.

opencc-by-4.0Dec 2020View details →
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Fig. 3 in Molecular screening for rickettsial bacteria and piroplasms in ixodid ticks surveyed from white-tailed deer (Odocoileus virginianus) and nilgai antelope (Boselaphus tragocamelus) in southern Texas

Fig. 3. Phylogentic analysis of Theileria sp. fragments from Anocenter nitens ticks. Representative Type F, Type G, and 'divergent' Theileria sp. sequences were identified from individual A. nitens ticks collected from white-tailed deer and a single nilgai host (bold labels). A maximum-likelihood tree was constructed using Toxoplasma gondii as the outgroup, as it is from a different axpicomplexan class than Theileria. Branch support was assessed with 10,000 replicates of UFBoot bootstrap replication, and bootstrap percentages are indicated at each branch point in the tree. GenBank accession numbers and annotated identification for sequences used in the comparative analysis are indicated on the branch labels. Accession numbers in italics are those T. cervi sequences from white-tailed deer on the East Foundation's San Antonio Viejo Ranch in Starr and Jim Hogg Counties, Texas (Yu et al., 2020).

opencc-by-4.0Dec 2020View details →

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