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139 results for “Species replacement”

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zenodo28/100

Figure 3 from: Liao M, Zeng S-J, Zeng L-Y, Yin H-J, Yan M-L, Zhang C-F, Tang G-D (2024) A new species and a replacement name in Cynanchum (Apocynaceae, Asclepiadeae) from China. PhytoKeys 241: 49-63. https://doi.org/10.3897/phytokeys.241.111499

Figure 3 Cynanchum pingtaoi S.Jin Zeng, G.D.Tang & Miao Liao a follicle and leaves b inflorescence c glands at the base of leaf d top view of flower e side view of flower with two corolla lobes removed f calyx g corolla lobes (each lobe attached to part of the corolla tube), outer surface on the right, inner surface on the left (four drawn) h corolla separation, showing gynostegium with corona lobes i pollinarium j seed. Illustration based on Si-Jin Zeng & Lin-Ya Zeng SJ4825 (IBSC), and drawn by Ding-Han Cui.

opencc-by-4.0Apr 2024View details →
zenodo28/100

Figure 2 from: Liao M, Zeng S-J, Zeng L-Y, Yin H-J, Yan M-L, Zhang C-F, Tang G-D (2024) A new species and a replacement name in Cynanchum (Apocynaceae, Asclepiadeae) from China. PhytoKeys 241: 49-63. https://doi.org/10.3897/phytokeys.241.111499

Figure 2 Cynanchum longhushanense G.D.Tang & Miao Liao a flowering branch b cross-section of hollow stem c node with small glands d petiole with glands at the top e inflorescence f bracteoles at the base of the pedicel g flower bud (above: top view; below: side view) h flower (1) top view, (2) lateral view, showing the connivent corona-scales apex, not exceeding the throat of the corolla, (3) side view, showing corolla lobes overlapping to the right and corolla tube i opened corolla, adaxial (above) and abaxial (below) view j ovary with calyx (above: top view, showing glands at the base of the calyx, below: side view of ovary, calyx and pedicel) k ovary l calyx lobes m gynostegium with corona lobes n gynostegium o corona lobes p pollinarium. All photos based on Miao Liao LM78.

opencc-by-4.0Apr 2024View details →
zenodo28/100

Figure 1 from: Liao M, Zeng S-J, Zeng L-Y, Yin H-J, Yan M-L, Zhang C-F, Tang G-D (2024) A new species and a replacement name in Cynanchum (Apocynaceae, Asclepiadeae) from China. PhytoKeys 241: 49-63. https://doi.org/10.3897/phytokeys.241.111499

Figure 1 Simplified maximum likelihood tree of Cynanchum based on two nuclear regions (nrETS and nrITS) and three plastid markers (rps16 and trnL introns, and trnL-F spacer). Bootstrap support values are given for each node. See Suppl. material 3 for maximum likelihood tree. Clade designations follow those of Khanum et al. (2016) and names in parentheses are the corresponding names that were used in Khanum et al. (2016).

opencc-by-4.0Apr 2024View details →
zenodo28/100

Figure 1 in A new species of Scaphisoma Leach, 1815 from New Guinea and a new replacement name (Coleoptera: Staphylinidae: Scaphidiinae)

Figure 1. Scaphisoma telnovi sp. nov.: Antennomeres 3 to 11 [scale bar 0.1 mm].

opennotspecifiedNov 2017View details →
zenodo28/100

Figure 6 in Are invasive hymenopteran species replacing native mud dauber wasp-associated taxa on the Seychelles Archipelago?

Figure 6. Change of hymenopteran assemblage associated with nests of the mud dauber wasp Sceliphron fuscum (Sphecidae) in Seychelles (Mahé and Praslin) from the 1930s to 2016 (Vesey-Fitzgerald 1950; this study). The differences in frequencies of native and invasive taxa between the two periods are significant (χ2 = 4.055; df = 1; p = 0.044).

opencc-by-4.0Jan 2022View details →
zenodo28/100

Figure 3 in Are invasive hymenopteran species replacing native mud dauber wasp-associated taxa on the Seychelles Archipelago?

Figure 3. Mud dauber wasp Sceliphron fuscum (Sphecidae) from Seychelles (2016). (A, B) Specimen reared from preimaginal stages. (C, D) Specimen dead at the pupal stage. (E–H) Post-emergence cocoons. Scale bar = 5 mm. (Photos: Elizaveta A. Spitsyna).

opencc-by-4.0Jan 2022View details →
zenodo28/100

Figure 2 in Are invasive hymenopteran species replacing native mud dauber wasp-associated taxa on the Seychelles Archipelago?

Figure 2. Examples of mud dauber wasps Sceliphron fuscum (Sphecidae) nest aggregations in Seychelles. (A) Mahé: under a rocky shelter. The blue arrow shows a female of Nephilingis livida (Vinson, 1863) (Araneae: Araneidae), a large spider species, whose webs are often accompanying massive conglomerations of mud dauber and potter wasp nests on the island. (B) Praslin: on the ceiling of a crumbling house. The red arrows show Megachile (Callomegachile) disjuncta (Megachilidae) females constructing their cells inside the nests of Sceliphron fuscum (note black, wax-like substance around entrances – a diagnostic feature of mud dauber wasp cells colonized by this bee species). (C) Silhouette: under a leaf of Coco De Mer Palm Lodoicea maldivica. (Photos: Ivan N. Bolotov [A, C] and Yulia Kolosova [B]).

opencc-by-4.0Jan 2022View details →
dryad28/100

Data from: A signature of dynamic biogeography: enclaves indicate past species replacement

Understanding how species have replaced each other in the past is important to predicting future species turnover. While past species replacement is difficult to detect after the fact, the process may be inferred from present-day distribution patterns. Species with abutting ranges sometimes show a characteristic distribution pattern, where a section of one species range is enveloped by that of the other. Such an enclave could indicate past species replacement: when a species is partly supplanted by a competitor, but a population endures locally while the invading species moves around and past it, an enclave forms. If the two species hybridize and backcross, the receding species is predicted to leave genetic traces within the expanding one under a scenario of species replacement. By screening dozens of genes in hybridizing crested newts, we uncover genetic remnants of the ancestral species, now inhabiting an enclave, in the range of the surrounding invading species. This independent genetic evidence supports the past distribution dynamics we predicted from the enclave. We suggest that enclaves provide a valuable tool in understanding historical species replacement, which is important because a major conservation concern arising from anthropogenic climate change is increased species replacement in the future.

opencc-zeroDec 2016View details →
zenodo28/100

Figures 10-15 from: Perez-Miles F, Bragio Bonaldo A, Miglio L (2014) Bumba, a replacement name for Maraca Pérez-Miles, 2005 and Bumba lennoni, a new tarantula species from western Amazonia (Araneae, Theraphosidae, Theraphosinae). ZooKeys 448: 1-8. https://doi.org/10.3897/zookeys.448.7920

Figures 10-15 - Bumba lennoni sp. n.: 10–13 male paratype (MPEG 975) 14–15 female paratype (MPEG 19039). 10–12 Copulatory bulb: 10 Prolateral 11 Prolateral, tegular apophysis (TA), detail 12 Prolateral, ring-shaped keel, detail 13 Type III urticating hair, silhouette 14–15 Type IV urticating hair: 14 Silhouette; 15 Tip, detail.

opencc-by-4.0Oct 2014View details →
zenodo28/100

Figures 1-9 from: Perez-Miles F, Bragio Bonaldo A, Miglio L (2014) Bumba, a replacement name for Maraca Pérez-Miles, 2005 and Bumba lennoni, a new tarantula species from western Amazonia (Araneae, Theraphosidae, Theraphosinae). ZooKeys 448: 1-8. https://doi.org/10.3897/zookeys.448.7920

Figures 1-9 - Bumba lennoni sp. n.: 1–4 and 6–8 male holotype (MPEG 983) 5, 9 female paratype (MPEG 19039). 1–2 Tibiae and metatarsi of left leg I: 1 Prolateral 2 Ventral 3–4 Copulatory bulb: 3 Prolateral 4 Retrolateral 5 Spermathecae, dorsal 6 carapace, dorsal 7 abdomen, dorsal 8 retrolateral process in male palpal tibiae 9 sternum, ventral Scales: 1–2: 3 mm; and 3–5: 1 mm.

opencc-by-4.0Oct 2014View details →
zenodo28/100

Figs 71–76 in Four new species of Tipula (Sinotipula) Alexander (Diptera, Tipulidae) from China and a new replacement name in Tipula (Vestiplex) Bezzi, 1924

Figs 71–76. Tipula (Sinotipula) wardi EdwaRds, 1928, ♂ (CAU). 71. Tergite 9, dorsal view. 72. Hypopygium, ventral view. 73. Outer gonostylus, lateral external view. 74. Outer gonostylus, dorsal view. 75. Inner gonostylus, lateral external view. 76. Adminiculum, ventral view. Scale bars: 71–73, 76 = 0.2 mm; 74–75 = 0.1 mm.

opencc-by-4.0Jul 2023View details →
zenodo28/100

Figs 44–47 in Four new species of Tipula (Sinotipula) Alexander (Diptera, Tipulidae) from China and a new replacement name in Tipula (Vestiplex) Bezzi, 1924

Figs 44–47. Tipula (Sinotipula) hobsoni EdwaRds, 1928, ♂ (CAU). 44. Hypopygium, lateral view. 45. Habitus, lateral view. 46. Head and thorax, dorsal view. 47. Wing. Abbreviations: see Material and methods. Scale bars = 1.0 mm.

opencc-by-4.0Jul 2023View details →
zenodo28/100

Figs 25–28 in Four new species of Tipula (Sinotipula) Alexander (Diptera, Tipulidae) from China and a new replacement name in Tipula (Vestiplex) Bezzi, 1924

Figs 25–28. Tipula (Sinotipula) forcipicauda sp. nov., holotype, ♂ (CAU). 25. Habitus, lateral view. 26. Hypopygium, lateral view. 27. Head and thorax, dorsal view. 28. Wing. Abbreviations: see Material and methods. Scale bars = 1.0 mm.

opencc-by-4.0Jul 2023View details →
zenodo28/100

Figs 69–70 in Four new species of Tipula (Sinotipula) Alexander (Diptera, Tipulidae) from China and a new replacement name in Tipula (Vestiplex) Bezzi, 1924

Figs 69–70. Tipula (Sinotipula) wardi EdwaRds, 1928, ♀ (CAU). 69. Habitus, lateral view. 70. Ovipositor, lateral view. Scale bars = 1.0 mm.

opencc-by-4.0Jul 2023View details →
zenodo28/100

Figs 65–68 in Four new species of Tipula (Sinotipula) Alexander (Diptera, Tipulidae) from China and a new replacement name in Tipula (Vestiplex) Bezzi, 1924

Figs 65–68. Tipula (Sinotipula) wardi EdwaRds, 1928, ♂ (CAU). 65. Habitus, lateral view. 66. Head and thorax, dorsal view. 67. Hypopygium, lateral view. 68. Wing. Abbreviations: see Material and methods. Scale bars = 1.0 mm.

opencc-by-4.0Jul 2023View details →
dryad28/100

Data from: A signature of dynamic biogeography: enclaves indicate past species replacement

Open the record for dataset details and reuse information.

publicNov 2017View details →
zenodo20/100

Distribution. Poorly known, NC Colombia in the E of Boyaca Department, E to the highlands of Meta to at least 1500 m above sea level. It is unclear if this species occupies an enclave within the range of the Lemurine Night Monkey (A. lemurinus) or if it replaces it in the NE part ofits distribution. in Aotidae

Distribution. Poorly known, NC Colombia in the E of Boyaca Department, E to the highlands of Meta to at least 1500 m above sea level. It is unclear if this species occupies an enclave within the range of the Lemurine Night Monkey (A. lemurinus) or if it replaces it in the NE part ofits distribution.

opennotspecifiedMar 2013View details →
zenodo20/100

FIGURE 1 in A new fossil species of Pycnomerus Erichson (Coleoptera: Zopheridae) from Baltic amber, and a replacement name for a Recent North American congener

FIGURE 1. Pycnomerus agtsteinicus sp. nov., holotype 273-2 [CCHH]: A, B—dorsal habitus photomicrograph, and corresponding SR X-ray micro-CT rendering; C, D—ventral habitus photomicrograph, and corresponding SR X-ray micro-CT rendering. Scale bars represent 0.5 mm.

opennotspecifiedJan 2019View details →
zenodo20/100

Figure 9 in Replacement name for the homonym of subgenus Trimorus (Neotrimorus) (Hymenoptera: Platygastroidea: Scelionidae) with description of two new species from India

Figure 9. Trimorus (Lochana) ferrari (Veenakumari and Rajmohana 2013), male. (a) Head and mesoscutum (dorsal view); (b) frons; (c) head and lateral pronotal area; (d) head and mesosoma (lateral view); (e) pleuron; (f) metasoma.

opennotspecifiedNov 2022View details →

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Last verified 2026-04-29Open record