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FIGURE 12 in Taxonomic implications of anatomical characteristics of the genus Tulipa (Liliaceae) in Turkey and their place in the historical subgeneric classifications
FIGURE 12. The scape transverse sections of the genus Tulipa (A˗R). A. T. agenensis. B. T. aleppensis. C. T. armena var. armena. D. T. armena var. galatica. E. T. julia. F. T. raddii. G. T. sintenisii. H. T. undulatifolia var. undulatifolia. I. T. clusiana. J. T. biflora. K. T. cinnabarina subsp. cinnabarina. L. T. humilis. M. T. koyuncui. N. T. orphanidea. O. T. pulchella. P. T. saxatilis. Q. T. sylvestris subsp. australis. R. T. sylvestris subsp. sylvestris, cu: cuticle, ep: epidermis, cl: collenchyma, co: cortex, ph: phloem, xy: xylem, sc: sclerenchyma.
FIGURE 13 in Taxonomic implications of anatomical characteristics of the genus Tulipa (Liliaceae) in Turkey and their place in the historical subgeneric classifications
FIGURE 13. The leaf transverse sections of the genus Tulipa (A˗R). A. T. agenensis. B. T. aleppensis. C. T. armena var. armena. D. T. armena var. galatica. E. T. julia. F. T. raddii. G. T. sintenisii. H. T. undulatifolia var. undulatifolia. I. T. clusiana. J. T. biflora. K. T. cinnabarina subsp. cinnabarina. L. T. humilis. M. T. koyuncui. N. T. orphanidea. O. T. pulchella. P. T. saxatilis. Q. T. sylvestris subsp. australis. R. T. sylvestris subsp. sylvestris, cu: cuticle, ue: upper epidermis, le: lower epidermis, p: parenchyma, ph: phloem, xy: xylem, st: stomata.
FIGURE 14 in Taxonomic implications of anatomical characteristics of the genus Tulipa (Liliaceae) in Turkey and their place in the historical subgeneric classifications
FIGURE 14. The leaf surface section of the genus Tulipa (each photo represents 1 mm2): 1˗T. agenensis, 2˗T. aleppensis, 3˗T. armena var. armena, 4˗T. armena var. galatica, 5˗T. julia, 6˗T. raddii, 7˗T. sintenisii, 8˗T. undulatifolia var. undulatifolia, 9˗T. clusiana, 10˗T. biflora, 11˗T. cinnabarina subsp. cinnabarina, 12˗T. humilis, 13˗T. koyuncui, 14˗T. orphanidea, 15˗T. pulchella, 16˗T. saxatilis, 17˗T. sylvestris subsp. australis, 18˗T. sylvestris subsp. sylvestris, a-lower epidermis, b-upper epidermis, epc: epidermis cell, st: stoma.
FIGURE 11 in Taxonomic implications of anatomical characteristics of the genus Tulipa (Liliaceae) in Turkey and their place in the historical subgeneric classifications
FIGURE 11. The root transverse sections of the genus Tulipa (A˗R). A. T. agenensis. B. T. aleppensis. C. T. armena var. armena. D. T. armena var. galatica. E. T. julia. F. T. raddii. G. T. sintenisii. H. T. undulatifolia var. undulatifolia. I. T. clusiana. J. T. biflora. K. T. cinnabarina subsp. cinnabarina. L. T. humilis. M. T. koyuncui. N. T. orphanidea. O. T. pulchella. P. T. saxatilis. Q. T. sylvestris subsp. australis. R. T. sylvestris subsp. sylvestris, ep: epidermis, ex: exodermis, co: cortex, en: endodermis, pe: pericycle, mx: metaxylem, ph: phloem, px: protoxylem.
FIGURE 10 in Taxonomic implications of anatomical characteristics of the genus Tulipa (Liliaceae) in Turkey and their place in the historical subgeneric classifications
FIGURE 10. Dendrogram of average linkage (between groups)-squared euclidean distance in the hierarchical cluster analysis of 42 populations (OTUs).
FIGURE 9 in Taxonomic implications of anatomical characteristics of the genus Tulipa (Liliaceae) in Turkey and their place in the historical subgeneric classifications
FIGURE 9. Dendrogram of average linkage (between groups)-Manhattan distance in the hierarchical cluster analysis of 42 populations (OTUs).
FIGURE 2 in Taxonomic implications of anatomical characteristics of the genus Tulipa (Liliaceae) in Turkey and their place in the historical subgeneric classifications
FIGURE 2. Measurements of quantitavive characters related to leaf (µm) ― 21˗RPL: row number of parenchymatous cells at leaf section, 22a˗UPW: width of upper epidermal cells at leaf section, 22b˗UPL: length of upper epidermal cells at leaf section, 23a˗LOW: width of lower epidermal cells at leaf section, 23b˗LOL: length of lower epidermal cells at leaf section, 24a˗PLW: width of parenchymatous cells at leaf section, 24b˗PLL: length of parenchymatous cells at leaf section, 25a˗XEW: width of xylem elements at leaf section, 25b˗XEL: length of xylem elements at leaf section, 26a˗PMW: width of phloem elements at leaf section, 26b˗PML: length of phloem elements at leaf section, 27˗RSI: ratio of stoma index (not indicated on figure).
FIGURE 1 in Taxonomic implications of anatomical characteristics of the genus Tulipa (Liliaceae) in Turkey and their place in the historical subgeneric classifications
FIGURE 1. Measurements of quantitavive characters (µm). A, B. Root; 1˗CXW: width of cortex region at root section, 2a˗ERW: width of epidermal cells at root section, 2b˗ERL: length of epidermal cells at root section, 3a˗EXW: width of exodermal cells at root section, 3b˗EXL: length of exodermal cells at root section, 4a˗COW: width of cortex parenchymatous cells at root section, 4b˗COL: length of cortex parenchymatous cells at root section, 5˗RER: row number of endodermal cells at root section, 6˗RPR: row number of pericycle cells at root section, 7a˗ENW: width of endodermal cells at root section, 7b˗ENL: length of endodermal cells at root section, 8a˗PEW: width of pericycle cells at root section, 8b˗PRL: length of pericycle cells at root section, 9˗NPR: number of protoxylem at root section, 10˗NMR: number of metaxylem elements at root section, 11a˗MXW: width of metaxylem elements at root section, 11b˗MXL: length of metaxylem elements at root section. C, D. Scape; 12˗DSS: diameter of scape section, 13˗ANP: the average number of cell in pith at scape section, 14a˗EPW: width of epidermal cells at scape section, 14b˗EPL: length of epidermal cells at scape section, 15a˗CLW: width of collenchyma cells at scape section, 15b˗CLL: length of collenchyma cells at scape section, 16a˗PAW: width of parenchymatous cells at scape section, 16b˗PAL: length of parenchymatous cells at scape section, 17˗RSS: row number of sclerenchyma cells at scape section, 18a˗PHW: width of phloem elements at scape section, 18b˗PEL: length of phloem elements at scape section, 19a˗SSW: width of sclerenchyma cells at scape section, 19b˗SSL: length of sclerenchyma cells at scape section, 20a˗XYW: width of xylem elements at scape section, 20b˗XYL: length of xylem elements at scape section.
FIGURE 3 in Taxonomic implications of anatomical characteristics of the genus Tulipa (Liliaceae) in Turkey and their place in the historical subgeneric classifications
FIGURE 3. Grouping and coding the character states of a quantitative character on a modified Whisker's graph.
Replication package for: Culture and the Historical Fertility Transition
<p>Replication package for: Beach, Brian and Hanlon, W. Walker (Forthcoming). "Culture and the Historical Fertility Transition," Review of Economic Studies. Package contains data, processing and analysis code, and results tables.</p>
Distribution. Highlands of S India; in Tamil Nadu it has been recorded from several localities in the Nilgiri Hills and there is an historical record from the Palni (= Palani) Hills; in Kerala it is recorded from the historical type locality of Thrissur and also the Erivakulam National Park. in Soricidae
Distribution. Highlands of S India; in Tamil Nadu it has been recorded from several localities in the Nilgiri Hills and there is an historical record from the Palni (= Palani) Hills; in Kerala it is recorded from the historical type locality of Thrissur and also the Erivakulam National Park.
Distribution. Originally distributed throughout the Indo-Malayan Region and S China, including Taiwan, Hainan, and Sri Lanka (only original range shaded in the map). Possible human-mediate introduced range in Maldives, islands of Malaysia, Indonesia, Brunei, Philippines, Japan (Kyushu and Ryukyu Is), Guam, Palau, and New Guinea. Introduced in historical times into East Africa (Egypt, Sudan, Eritrea, Djibouti, Kenya, Rwanda, and Tanzania), Pemba and Zanzibar (Unguja) Is, Madagascar, Comoro Is, Mauritius, Réunion I, and into coastal Arabia (in the vicinity of seaports in Iraq, Kuwait, Bahrain, Saudi Arabia, Yemen, and Oman). in Soricidae
Distribution. Originally distributed throughout the Indo-Malayan Region and S China, including Taiwan, Hainan, and Sri Lanka (only original range shaded in the map). Possible human-mediate introduced range in Maldives, islands of Malaysia, Indonesia, Brunei, Philippines, Japan (Kyushu and Ryukyu Is), Guam, Palau, and New Guinea. Introduced in historical times into East Africa (Egypt, Sudan, Eritrea, Djibouti, Kenya, Rwanda, and Tanzania), Pemba and Zanzibar (Unguja) Is, Madagascar, Comoro Is, Mauritius, Réunion I, and into coastal Arabia (in the vicinity of seaports in Iraq, Kuwait, Bahrain, Saudi Arabia, Yemen, and Oman).
Distribution. Mountainous areas in Morocco (Rif, High and Middle Atlas) and Algeria (Grande and Petite Kabylie); historically it also occurred in W Tunisia but is now extinct there. A free-ranging population occurs in Gibraltar introduced there by the British in 1740. in Cercopithecidae
Distribution. Mountainous areas in Morocco (Rif, High and Middle Atlas) and Algeria (Grande and Petite Kabylie); historically it also occurred in W Tunisia but is now extinct there. A free-ranging population occurs in Gibraltar introduced there by the British in 1740.
Corpus of historic Basque texts
<p>A corpus of historic Basque texts analyzed for this study, classified according to textual genre and dialect, with source references.</p>
Distribution. Known only from scattered localities on Peninsular Malaysia; it may be extirpated in most ofits historical distribution in SE Myanmar (Bago Division and Mon State) and W & Peninsular Thailand. in Muridae
Distribution. Known only from scattered localities on Peninsular Malaysia; it may be extirpated in most ofits historical distribution in SE Myanmar (Bago Division and Mon State) and W & Peninsular Thailand.
Phylogenomics resolves timing and patterns in the evolution of Australasian Cerambycinae (Coleoptera: Cerambycidae), and reveals new insights into the subfamily-level classification and historical biogeography of longhorn beetles
<p><span><span><span><span>Cerambycinae is the second-largest subfamily of longhorn beetles in the Southern Hemisphere. The phylogeny of Cerambycinae is poorly known, resulting in a highly artificial tribal-level classification and a largely speculative evolutionary history. We reconstructed the phylogenetic relationships of Cerambycinae at the generic level using anchored hybrid enrichment data from hundreds of nuclear genes, with a primary focus on the extraordinarily diverse faunas of Australia and New Zealand. We also estimated divergence times by incorporating fossil calibrations in our analyses. We identified two main clades within Cerambycinae, which can also be separated morphologically by a distinct type of antennal foramen. We recovered a Late Jurassic origin of crown Cerambycinae. Dorcasominae, which was newly found to have representatives in Australia, was notably derived from within Cerambycinae. We recovered two independent origins of Australian Cerambycinae: one clade originated in the Early Cretaceous and is likely endemic to the Southern Hemisphere, while the other clade appears to have immigrated to Australia, perhaps from the Northern Hemisphere. Within the Australian lineages were multiple independent origins of New Zealand taxa, all of which are relative host-plant generalists. Tribal relationships and assignments are discussed and, based on our results, the following major nomenclatural acts were made: Dorcasominae Lacordaire, 1868, is downgraded to a tribe Dorcasomini of Cerambycinae Latreille, 1804; Neostenini Lacordaire, 1868 syn. nov. is treated as a junior synonym of Uracanthini Blanchard, 1851.</span></span></span></span></p>
FIGURE 9 in A review of records of the Trimeresurus albolabris Gray, 1842 group from the Indian subcontinent: expanded description and range extension of Trimeresurus salazar, redescription of Trimeresurus septentrionalis and rediscovery of historical specimens of Trimeresurus davidi (Reptilia: Viperidae)
FIGURE 9. Trimeresurus septentrionalis live adult female from Kathmandu, Nepal, showing its diagnostic character of plain grass green colouration without any mix of yellow in it. Photo: Gernot Vogel
FIGURE 8. Trimeresurus septentrionalis Holotype MHNG 1404.31 in A review of records of the Trimeresurus albolabris Gray, 1842 group from the Indian subcontinent: expanded description and range extension of Trimeresurus salazar, redescription of Trimeresurus septentrionalis and rediscovery of historical specimens of Trimeresurus davidi (Reptilia: Viperidae)
FIGURE 8. Trimeresurus septentrionalis Holotype MHNG 1404.31 from Nähe Pokhara, Nepal. Photos: Gernot Vogel.
FIGURE 7. Trimeresurus davidi NMW 23925 in A review of records of the Trimeresurus albolabris Gray, 1842 group from the Indian subcontinent: expanded description and range extension of Trimeresurus salazar, redescription of Trimeresurus septentrionalis and rediscovery of historical specimens of Trimeresurus davidi (Reptilia: Viperidae)
FIGURE 7. Trimeresurus davidi NMW 23925:1, 2 entire views: (top right and left), tail profile (mid-left) photos: Gernot Vogel; NHMUK 1986.7.7.40–41 paratypes (mid-right and bottom left and right; photos: P.D. Campbell).
FIGURE 6. Trimeresurus salazar NHMUK 1937.3.1.14 in A review of records of the Trimeresurus albolabris Gray, 1842 group from the Indian subcontinent: expanded description and range extension of Trimeresurus salazar, redescription of Trimeresurus septentrionalis and rediscovery of historical specimens of Trimeresurus davidi (Reptilia: Viperidae)
FIGURE 6. Trimeresurus salazar NHMUK 1937.3.1.14 from 'Nagpur, Central Province', India. Photos: Gernot Vogel
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Allen Brain Atlas
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DANDI Archive for NWB datasets
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International Brain Laboratory public data
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OpenNeuro
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