40 results on '"Pailler, T."'
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2. Auto-pollination in a long-spurred endemic orchid (Jumellea stenophylla) on Reunion Island (Mascarene Archipelago, Indian Ocean)
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Micheneau, C., Fournel, J., Gauvin-Bialecki, A., and Pailler, T.
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- 2008
3. Flower size dimorphism in diclinous plants native to La Réunion Island
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Humeau, L., Pailler, T., and Thompson, J. D.
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- 2003
4. Variation in the breeding system of two sympatric Dombeya species on La Réunion island
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Humeau, L., Pailler, T., and Thompson, J. D.
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- 1999
5. Distyly and heteromorphic incompatibility in oceanic island species of Erythroxylum (Erythroxylaceae)
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Pailler, T., Humeau, L., and Thompson, J. D.
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- 1998
6. Variation in the breeding system of two sympatricDombeya species on La Réunion island
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Humeau, L., Pailler, T., and Thompson, J. D.
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- 1999
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7. Combining pollination ecology and fine-scale spatial genetic structure analysis to unravel the reproductive strategy of an insular threatened orchid
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Gigant, R.L., primary, De Bruyn, A., additional, M'sa, T., additional, Viscardi, G., additional, Gigord, L., additional, Gauvin-Bialecki, A., additional, Pailler, T., additional, Humeau, L., additional, Grisoni, M., additional, and Besse, P., additional
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- 2016
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8. Spatial patterns of AFLP diversity in Bulbophyllum occultum (Orchidaceae) indicate long-term refugial isolation in Madagascar and long-distance colonization effects in La Réunion
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Jaros, U, primary, Fischer, G A, additional, Pailler, T, additional, and Comes, H P, additional
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- 2016
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9. Orchid conservation: Making the links
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Fay, M., Pailler, T., Dixon, Kingsley, Fay, M., Pailler, T., and Dixon, Kingsley
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Orchidaceae, one of the largest families of flowering plants, present particular challenges for conservation, due in great part to their often complex interactions with mycorrhizal fungi, pollinators and host trees. In this Highlight, we present seven papers focusing on orchids and their interactions and other factors relating to their conservation.
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- 2015
10. Jumellea recurva (Orchidaceae): not a rediscovery in Mauritius
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Baider, C., Francois Benjamin Vincent Florens, and Pailler, T.
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Biodiversity ,Taxonomy - Abstract
Baider, Claudia, Florens, F.B. Vincent, Pailler, Thierry (2012): Jumellea recurva (Orchidaceae): not a rediscovery in Mauritius. Phytotaxa 40: 31-32, DOI: 10.11646/phytotaxa.40.1.5
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- 2012
11. Glomeremus paraorchidophilus Hugel & Micheneau & Fournel & Warren & Gauvin-Bialecki & Pailler & Chase & Strasberg 2010, n. sp
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Hugel, S., Micheneau, C., Fournel, J., Warren, B. H., Gauvin-Bialecki, A., Pailler, T., Chase, M. W., and Strasberg, D.
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Gryllacrididae ,Insecta ,Glomeremus paraorchidophilus ,Arthropoda ,Animalia ,Orthoptera ,Biodiversity ,Glomeremus ,Taxonomy - Abstract
Glomeremus paraorchidophilus n. sp. (Figs. 5, 8, 11, 14, 17, 20, tab. 2) Holotype. Male. Indian Ocean, Mascarene archipelago, Maurice, Savanne District, Parc National de Rivière Noire, Cocotte, 745 m Alt., 20°26’29’’S 57°28’20’’E, 22.IV.2005, S. Hugel, MNHN (MNHN-ENSIF2644). Allotype. Female. Same as holotype, 22.IV.2005, S. Hugel, MNHN (MNHN-ENSIF2645). Paratypes. Males. 2♂, same as holotype, 22.II.2008, BIOTAS2008212, S. Hugel, MHNR; 22.IV.2005, S. Hugel leg & coll. 1♂, Maurice, Savanne District, Parc National de Rivière Noire, Plaine Champagne, point de vue sur les Gorges, 681 m alt., 20°25’39’’S 57°25’43’’E, 22.IV.2005. S. Hugel, MSIRI. 1♂, Maurice, Plaines Wilhems District, Petrin, 604 m alt., 20°24’27’’S 57°28’21’’E, 23.II.2008, BIOTAS2008122, S. Hugel leg & coll. 1♂, Maurice, Port Louis District, le Pouce (dernier plateau), 733 m alt., 20°12’13’’S 57°31’43’’E, 08.V.2009, BIOTAS2009217, S. Hugel leg & coll. 2♂, Maurice, Plaines Wilhems District, Brise Fer vieille parcelle, 648 m alt., 20°23’02’’S 57°26’23’’E, 24.II.2008, BIOTAS2008176, S. Hugel, CIRAD Réunion; BIOTAS2008177, S. Hugel, CIRAD Réunion. 1♂, Maurice, Black River District, Parc National de Rivière Noire, Piton Brise Fer, 617 m alt., 20°23’02’’S 57°25’51’’E, 13.V.2009, BIOTAS2009349, S. Hugel leg & coll. Females. 1♀, same as holotype, 07.V.2009, BIOTAS2009164, S. Hugel leg & coll. 1♀, Maurice, Savanne District, Parc National de Rivière Noire, Cocotte, 745 m Alt., 20°26’29’’S 57°28’20’’E, 22.IV.2005, S. Hugel leg & coll. 3♀, Maurice, Plaines Wilhems District, Florin, 610 m alt., 20°23’28’’S 57°27’37’’E, 25.II.2008, BIOTAS2008191, S. Hugel leg & coll; BIOTAS2008190, S. Hugel leg & coll; BIOTAS2008192, S. Hugel, MSIRI. 4♀, Maurice, Plaines Wilhems District, Petrin, 604 m alt., 20°24’27’’S 57°28’21’’E, 23.II.2008, BIOTAS2008130, S. Hugel, BMNH; BIOTAS2008131, S. Hugel, BMNH; BIOTAS2008123, S. Hugel leg & coll. BIOTAS2008124, S. Hugel leg & coll. 1♀, Maurice, Port Louis District, le Pouce (dernier plateau), 733 m alt., 20°12’13’’S 57°31’43’’E, 08.V.2009, BIOTAS2009206, S. Hugel leg & coll. 2♀, Maurice, Plaines Wilhems District, Brise Fer vieille parcelle, 648 m alt., 20°23’02’’S 57°26’23’’E, 04.V.2009, BIOTAS2009188, S. Hugel leg & coll; 24.II.2008, BIOTAS2008178, S. Hugel, CIRAD Réunion. Diagnosis. See the diagnosis of G. orchidophilus n. sp.. Description. In addition to generic characters. Body length: size small for the genus. Head: slightly broader than the thorax; fastigium frontis wider than scapus; median and lateral ocelli weakly distinct. Thorax. Pronotum: maximal width (including lateral lobes) slightly wider than long; anterior margin weakly convex (in dorsal view), arched; posterior margin strait (in dorsal view), almost horizontal; sulci not distinct on the discus, converging on lateral lobes. Wings. FW well distinct, half as long as Pro. Legs. TI and TII with usual spurs formula (4 pairs of subapical + 1 pair of apical spurs ventrally, and one single apical spur on TII posterior dorsal angle); subapical spurs of usual length (roughly at least as long as T width). Hind legs: femora 2.5–3.0 times as long as wide (Fig. 5); FIII with 2–8 (usually 6) ventral anterior spines; FIII with 3–7 ventral posterior spines; TIII with 6–8 dorsal anterior spines; with 6–7 dorsal posterior spines. Abdomen. Stridulatory files present. Sexual dimorphism: apart from primary sexual characters, ♂♂ and ♀♀ are similar, males are smaller. Male: terminalia (Fig. 8, 11, 14). Tergite VIII slightly extended posteriorly (compared to preceding tergites); posterior margin forming a 45° angle (in side view). Tergite IX vertically oriented (side view); distal end of tergite pointing ventrally (side view) with a distinct emargination separating two lobes (ventral/ posterior view; Fig. 14). Tergite X sclerites (see Hugel, 2009) forming an upwards/sideward-directed lamellar process (Fig. 11, 14). Cerci shortened (Fig. 14). SGP distal end with a distinct process between the styli; lateral margins of the process weakly converging; process with a distinct posterior notch (Fig. 8); styli hardly exceeding the SGP distal process; styli not thickened (Fig. 8). Female: sternite before SGP (VII) not modified; SGP (Figs. 17, 20) with rounded lateral margins; with anterior bulge (side view, Fig. 17) posterior margin with a shallow emargination (Fig. 20); with two distal lateral sclerifications. Ovipositor regularly arched, regularly narrowing towards the apex; pointing distally, 0.7 – 0.8 times as long as FIII, dorsal valves with a distinct ventrally directed protrusion near the basis. Colour: general coloration brown yellowish; occiput with a black pattern forming a triangle pointing on the fastigium frontis (as in G. orchidophilus n. sp.; Fig. 2); pronotum with a black pattern on the anterior margin, forming a triangle pointing backwards, sometimes with a black sagittal line and black on the posterior margin; legs without black pattern; knees sometimes darkened; anterior part of abdominal tergites darkened.
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- 2010
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12. Glomeremus tikasignatus Hugel & Micheneau & Fournel & Warren & Gauvin-Bialecki & Pailler & Chase & Strasberg 2010, n. sp
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Hugel, S., Micheneau, C., Fournel, J., Warren, B. H., Gauvin-Bialecki, A., Pailler, T., Chase, M. W., and Strasberg, D.
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Gryllacrididae ,Insecta ,Arthropoda ,Animalia ,Orthoptera ,Biodiversity ,Glomeremus tikasignatus ,Glomeremus ,Taxonomy - Abstract
Glomeremus tikasignatus n. sp. (Figs. 3, 6, 9, 12, 15, 18, 21, tab. 3) Holotype. Male. Indian Ocean, Mascarene archipelago, Maurice, Savanne District, Parc National de Rivière Noire, Plaine Champagne, point de vue sur les Gorges, 681 m alt., 20°25’39’’S 57°25’43’’E, 22.IV.2005. S. Hugel, MNHN (MNHN-ENSIF2646). Allotype. Female. Same as holotype, 13.VIII.2001. S. Hugel, MNHN (MNHN-ENSIF2647). Paratypes. Males. 2♂, Maurice, Savanne District, Parc National de Rivière Noire, Cocotte, 745 m Alt., 20°26’29’’S 57°28’20’’E, 22.II.2008, BIOTAS2008210, S. Hugel leg & coll.; 07.V.2009, BIOTAS2009163, S. Hugel leg & coll. Females. 1♀, Maurice, Black River District, Parc National de Rivière Noire, Piton Brise Fer, 617 m alt., 20°23’02’’S 57°25’51’’E, 13.V.2009, BIOTAS2009286, S. Hugel, MSIRI. 5♀, Maurice, Savanne District, Parc National de Rivière Noire, Cocotte, 745 m Alt., 20°26’29’’S 57°28’20’’E, 22.II.2008, BIOTAS2008211, S. Hugel leg & coll.; 06.III.2008, BIOTAS2008412, S. Hugel leg & coll.; 22.IV.2005, S. Hugel leg & coll.; 22.IV.2005, S. Hugel, CIRAD Réunion; 19.IV.2005, S. Hugel leg & coll. Diagnosis. This species differs from the other Glomeremus in the following characters: TI and TII with 4 ventral subapical spurs on both sides, in addition to the apical spur (3 in G.shelfordi); FW reduced, but clearly distinct (all other Glomeremus species are wingless except G. orchidophilus n. sp., G. paraorchidophilus n. sp., G. mediopictus Uvarov, 1957, and G. feanus (Griffini, 1908)); the thorax and head without black pattern; male cerci not particularly extended (extended and thin in G. brevifalcatus); male tergite X sclerites forming an upwards directed lamellar process (Fig. 12, 15); male SGP with a shallow emargination (Fig. 9); female SGP with a “W”-shaped end margin (Fig. 21); ovipositor falciform, pointing apically, as long as FIII, dorsal valves without ventrally directed protrusion (Fig. 20; ovipositor roughly straight after the base in G. feanus, G. glomerinus, G.sphinx, G. mediopictus, G. pileatus, G. shelfordi, G. sphingoides). Description. In addition to generic characters. Body length: size medium to large for the genus. Head (Fig. 3): as broad or slightly broader than the thorax; fastigium frontis wider than scapus; median and lateral ocelli clearly distinct (less obvious on specimens dried from alcohol), median ocellus circular, less wide than scapus. Thorax. Pronotum: maximal width (including lateral lobes) as wide as or slightly wider than long; anterior margin convex (in dorsal view), arched; posterior margin strait (in dorsal view), almost horizontal; anterior sulcus deep on lateral lobes and well distinct on discus; posterior sulcus shallower and less distinct on discus; both sulci converging on lateral lobes; prozona elevated. Wings. FW well distinct, half as long as Pro. Legs. TI and TII with usual spurs formula (4 pairs of subapical + 1 pair of apical spurs ventrally, and one single apical spur on TII posterior dorsal angle); subapical spurs of usual length (at least as long as T width). Hind legs: femora 3.4–3.7 times as long as wide (Fig. 6); FIII with 5–7 ventral anterior spines; FIII with 6–11 ventral posterior spines; TIII with 5–7 dorsal anterior spines; with 6–8 dorsal posterior spines. Abdomen. Stridulatory files present. Sexual dimorphism: apart from primary sexual characters, ♂♂ and ♀♀ are similar. Male: terminalia (Fig. 9, 12, 15). Tergite VIII slightly extended posteriorly (compared to preceding tergites); posterior margin forming a 45° angle (in side view). Tergite IX vertically oriented (side view); distal end of tergite pointing ventrally (side view) with a shallow emargination separating two small bulges (ventral/ posterior view; Fig. 15). TX sclerites (see Hugel, 2009) forming an upwards directed lamellar process (Fig. 12, 15). Cerci not particularly elongated (Fig. 15). SGP distal end with an indistinct emargination (Fig. 9); styli exceeding distinctly the SGP distal end, not thickened (Fig. 9). Female: sternite before SGP (VII) not modified; SGP (Figs. 18, 21) with strait lateral margins, posterior margin pointing ventrally (side view, Fig. 18), the posterior end corresponds to the SGP dorsal surface, with a shallow “W” shape (ventral view, Fig. 21). Ovipositor regularly arched, pointing distally, as long as FIII, dorsal valves without ventrally directed protrusion. Colour: general coloration brown; head, legs pronotum without black pattern (knees sometimes darkened); anterior part of abdominal tergites darkened; median and lateral ocelli white., Published as part of Hugel, S., Micheneau, C., Fournel, J., Warren, B. H., Gauvin-Bialecki, A., Pailler, T., Chase, M. W. & Strasberg, D., 2010, Glomeremus species from the Mascarene islands (Orthoptera, Gryllacrididae) with the description of the pollinator of an endemic orchid from the island of Réunion, pp. 58-68 in Zootaxa 2545 (1) on pages 64-66, DOI: 10.11646/zootaxa.2545.1.6, http://zenodo.org/record/5303685, {"references":["Hugel, S. (2009) Gryllacrididae and Tettigoniidae (Insecta, orthoptera, ensifera) from espiritu Santo, Vanatu. Zoosystema, 31 (3), pp. 525 - 576."]}
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- 2010
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13. Glomeremus shelfordi
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Hugel, S., Micheneau, C., Fournel, J., Warren, B. H., Gauvin-Bialecki, A., Pailler, T., Chase, M. W., and Strasberg, D.
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Gryllacrididae ,Insecta ,Arthropoda ,Glomeremus shelfordi ,Animalia ,Orthoptera ,Biodiversity ,Glomeremus ,Taxonomy - Abstract
Glomeremus shelfordi (Griffini, 1909) Eremus sphinx var. shelfordi Griffini, 1909: 333 (original description). Glomeremus shelfordi, Karny, 1937: 115. Material examined. Unpublished high quality pictures of female holotype (OUMNH). This type specimen is badly damaged: only a part of the head, the thorax, four abdominal tergites, the right foreleg and the left fore femora are remaining. Type locality. As specified in Griffini’s original description, the holotype is labelled “ Mauritius?”. In accordance with the original description, this specimen displays 3 ventral subapical spurs on both sides of the remaining fore tibia (according to Griffini, both fore tibia and mid tibia had the same spur formula) and it is wingless. These characters clearly distinguish G. shelfordi from the three other Glomeremus species recorded in the archipelago. In addition, the ovipositors of G.shelfordi and of the other species recorded in the archipelago are clearly distinct: 19 mm for G. shelfordi (vs. G.shelfordi (vs. clearly falciform in the three other species we recorded in the archipelago). In spite of the numerous nights spent in the field in Mauritius, no specimen corresponding to G. shelfordi was recorded during our study, suggesting either that this island is not the type locality, or that the species is very rare or extinct. Diagnosis. This species differs from all other Glomeremus species by the following character combination: face and thorax without black patterns; TI and TII with 3 ventral subapical spurs on both sides; wingless; ovipositor more than twice as long as hind femora (this latter character by itself distinguishes G. shelfordi from all other Glomeremus)., Published as part of Hugel, S., Micheneau, C., Fournel, J., Warren, B. H., Gauvin-Bialecki, A., Pailler, T., Chase, M. W. & Strasberg, D., 2010, Glomeremus species from the Mascarene islands (Orthoptera, Gryllacrididae) with the description of the pollinator of an endemic orchid from the island of Réunion, pp. 58-68 in Zootaxa 2545 (1) on page 59, DOI: 10.11646/zootaxa.2545.1.6, http://zenodo.org/record/5303685, {"references":["Griffini, A. (1909) Studi sui Grillacridi del Museo di Oxford. Parte Ia, specie etiopiche, indo-malesi ed australiane. Atti della Societa Italiana di Scienze Naturali, 47, pp. 300 - 338.","Karny, H. H. (1937) Orthoptera Fam. Gryllacrididae Subfamiliae omnes. In: Wytsman, P (Ed). Genera Insectorum, V. Verteneuil & L. Desmet, Bruxelles. 317 pp."]}
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- 2010
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14. Permanent genetic resources added to Molecular Ecology Resources Database 1 April 2010-31 May 2010
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Andree, K., Axtner, J., Bagley, M. J., Barlow, E. J., Beebee, T. J. C., Bennetzen, J. L., Bermingham, E., Boisselier-Dubayle, M. C., Bozarth, C. A., Brooks, C. P., Brown, R. P., Catanese, G., Cavers, S., Ceron-Souza, I., Chak, S. T. C., Chan, M. N., Charles-Dominique, P., Chen, C. Y., Chen, J. D., Chinchilla, L., Da Silva, D., Dafreville, S., Daunt, F., Delatte, H., Dorge, T., Duncan, N., Durand, Jean-Dominique, Duvernell, D., Estep, M., Fan, S., Fattahi, R., Villela, O. F., Fong, Y., Freville, H., Funes, V., Gallardo-Escarate, C., Ganeshaiah, K. N., Ghaffari, M. R., Girod, C., Gomez-Moliner, B. J., Gonzalez-Porter, G. P., Gosa, A., Govers, F., Guerin, F., Guindo, D., Hailer, F., Haye, P. A., Hoelmer, K. A., Hofmann, S., Hong, Y., Hu, C. Q., Huang, S. W., Humeau, L., Infante, C., Jackson, S. A., Jacobsen, E., Jowkar, A., Kafi, M., Kermani, M. J., Kim, H., Kim, K. S., Kim, M. Y., Knibb, W., Koita, O. A., Korpelainen, H., Lambourdiere, J., Lasso, E., Leblois, R., Lee, H., Lee, S. W., Leung, F. C. C., Leung, K. M. Y., Li, C. H., Li, Y., Lieckfeldt, D., Lizana, M., Loughry, W. J., Luo, P., Madeira, M. J., Mahmoodi, P., Maldonado, J. E., Mardi, M., Mendes, O., Miehe, G., Muth, P., Nacci, D., Kumar, L. N., Ng, W. C., Pailler, T., Parzies, H. K., Perez, L., Pfunder, M., Pietilaeinen, M., Pirseyedi, S. M., Porta, D., Porta, J., Porta, J. M., Quilici, S., Rakotoarivelo, F. P., Ramesha, B. T., Ravikanth, G., Riera, B., Risterucci, A. M., Roberts, D. A., Samadi, Sarah, Sarasola-Puente, V., Sarrazin, E., Sarthou, C., Schmidt, A., Segovia, N. I., Shen, K. N., Simiand, C., Bin Sman, M. H., Solhoy, T., Sommer, S., Sumangala, R. C., Taubert, R., Tejangkura, T., Telford, A., Testa, A., Tollon-Cordet, C., Tzeng, W. N., Shaanker, R. U., van der Lee, T. A. J., Van Mourik, T. A., Vasudeva, R., Wai, T. C., Wang, R. L., Welch, M. E., Weltzien, E., Whitehead, A., Woodard, A., Xia, J. J., Zeinolabedini, M., and Zhang, L.
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This article documents the addition of 396 microsatellite marker loci to the Molecular Ecology Resources Database. Loci were developed for the following species: Anthocidaris crassispina, Aphis glycines, Argyrosomus regius, Astrocaryum sciophilum, Dasypus novemcinctus, Delomys sublineatus, Dermatemys mawii, Fundulus heteroclitus, Homalaspis plana, Jumellea rossii, Khaya senegalensis, Mugil cephalus, Neoceratitis cyanescens, Phalacrocorax aristotelis, Phytophthora infestans, Piper cordulatum, Pterocarpus indicus, Rana dalmatina, Rosa pulverulenta, Saxifraga oppositifolia, Scomber colias, Semecarpus kathalekanensis, Stichopus monotuberculatus, Striga hermonthica, Tarentola boettgeri and Thermophis baileyi. These loci were cross-tested on the following species: Aphis gossypii, Sooretamys angouya, Euryoryzomys russatus, Fundulus notatus, Fundulus olivaceus, Fundulus catenatus, Fundulus majalis, Jumellea fragrans, Jumellea triquetra Jumellea recta, Jumellea stenophylla, Liza richardsonii, Piper marginatum, Piper aequale, Piper darienensis, Piper dilatatum, Rana temporaria, Rana iberica, Rana pyrenaica, Semecarpus anacardium, Semecarpus auriculata, Semecarpus travancorica, Spondias acuminata, Holigarna grahamii, Holigarna beddomii, Mangifera indica, Anacardium occidentale, Tarentola delalandii, Tarentola caboverdianus and Thermophis zhaoermii.
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- 2010
15. Phylogeny and generic limits in the sister tribes Psychotrieae and Palicoureeae (Rubiaceae): Evolution of schizocarps in Psychotria and origins of bacterial leaf nodules of the Malagasy species
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Razafimandimbison, S. G., primary, Taylor, C. M., additional, Wikstrom, N., additional, Pailler, T., additional, Khodabandeh, A., additional, and Bremer, B., additional
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- 2014
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16. Permanent Genetic Resources added to Molecular Ecology Resources Database 1 April 2010 – 31 May 2010: Isolation and characterization of microsatellite markers for the European shag, Phalacrocorax aristotelis.
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Andree, K., Axtner, Jan, Bagley, M.J., Barlow, E.J., Beebee, T.J.C., Bennetzen, Jeffrey L., Bermingham, Eldredge, Boisselier-Dubayle, M.C., Bozart, Christine A., Brooks, Christopher P., Brown, R.P., Catanese, Gaetano, Cavers, S., Ceron-Souza, Ivania, Chak, Solomon T.C., Chan, M.N., Charles-Dominique, P., Chen, C.Y., Chen, J.D., Chinchilla, Leah, Da Silva, D., Dafreville, S., Daunt, F., Delatte, H., Dorge, T., Duncan, N., Durand, J.D., Duvernell, D., Estep, Matt, Fan, Sigang, Fattahi, R., Villela, Oscar Flores, Fong, Yokking, Freville, H., Funes, Victoria, Gallardo-Escarte, C., Ganeshaiah, K.N., Ghaffari, M.R., Girod, C., Gomez-Moliner, B.J., Gonzalez-Porter, Gracia P., Gosa, A., Govers, F., Guerin, F., Guindo, Diarah, Hailer, Frank, Haye, P.A., Hoelmer, Kim A., Hofmann, S., Hong, Yan, Hu, Chaoqun, Huang, S.W., Humeau, L., Infante, Carlos, Jackson, S.A., Jacobsen, E., Jowkar, A., Kafi, M., Kermani, J., Kim, Hyojoong, Kim, Kyung Seok, Knibb, W., Koita, Ousmane A., Korpelainen, H., Lambourdiere, J., Lasso, Eloisa, Leblois, R., Lee, Hang, Lee, Seunghwan, Leung, F.C.C., Leung, Kenneth M.Y., Li, Chunjong, Li, Y., Lieckfeldt, Dietmar, Lizana, M., Loughry, W.J., Luo, Peng, Madeira, M.J., Mahmoodi, P., Maldonado, Jesus E., Mardi, M., Mendes, O., Miehe, G., Muth, Peter, Nacci, D., Kumar, Naveen, Ng, Wai-Chuen, Pailler, T., Parzies, Heiko K., Perez, Laura, Pfunder, M., Pietilainen, M., Pirseyedi, S.M., Porta, D., Porta, J., Porta, J.M., Quilici, S., Rakotoarivelo, F.P., Ramesha, B.T., Ravikanth, G., Riera, B., Risterucci, A.M., Roberts, D.A., Samadi, S., Sarasola-Puente, V., Sarrazin, E., Sarthou, C., Schmidt, Anke, Segovia, N.I., Shen, K.N., Simiand, C., Sman, Muhammad Hidayat Bin, Solhoy, T., Sommer, Simone, Sumangala, R.C., Taubert, Ramona, Tejangkura, T., Telford, A., Testa, A., Tollon-Cordet, C., Tzeng, W.N., Uma-Shaanker, R., Van Der Lee, T.A.J., Van Mourik, Thomas A., Vasudeva, R., Wai, T.C., Wang, R.L., Welch, Mark E., Weltzein, Eva, Whitehead, A., Woodard, Anastasia, Xia, Jianjun, Zeinolabedini, M., Zhang, Lvping, Andree, K., Axtner, Jan, Bagley, M.J., Barlow, E.J., Beebee, T.J.C., Bennetzen, Jeffrey L., Bermingham, Eldredge, Boisselier-Dubayle, M.C., Bozart, Christine A., Brooks, Christopher P., Brown, R.P., Catanese, Gaetano, Cavers, S., Ceron-Souza, Ivania, Chak, Solomon T.C., Chan, M.N., Charles-Dominique, P., Chen, C.Y., Chen, J.D., Chinchilla, Leah, Da Silva, D., Dafreville, S., Daunt, F., Delatte, H., Dorge, T., Duncan, N., Durand, J.D., Duvernell, D., Estep, Matt, Fan, Sigang, Fattahi, R., Villela, Oscar Flores, Fong, Yokking, Freville, H., Funes, Victoria, Gallardo-Escarte, C., Ganeshaiah, K.N., Ghaffari, M.R., Girod, C., Gomez-Moliner, B.J., Gonzalez-Porter, Gracia P., Gosa, A., Govers, F., Guerin, F., Guindo, Diarah, Hailer, Frank, Haye, P.A., Hoelmer, Kim A., Hofmann, S., Hong, Yan, Hu, Chaoqun, Huang, S.W., Humeau, L., Infante, Carlos, Jackson, S.A., Jacobsen, E., Jowkar, A., Kafi, M., Kermani, J., Kim, Hyojoong, Kim, Kyung Seok, Knibb, W., Koita, Ousmane A., Korpelainen, H., Lambourdiere, J., Lasso, Eloisa, Leblois, R., Lee, Hang, Lee, Seunghwan, Leung, F.C.C., Leung, Kenneth M.Y., Li, Chunjong, Li, Y., Lieckfeldt, Dietmar, Lizana, M., Loughry, W.J., Luo, Peng, Madeira, M.J., Mahmoodi, P., Maldonado, Jesus E., Mardi, M., Mendes, O., Miehe, G., Muth, Peter, Nacci, D., Kumar, Naveen, Ng, Wai-Chuen, Pailler, T., Parzies, Heiko K., Perez, Laura, Pfunder, M., Pietilainen, M., Pirseyedi, S.M., Porta, D., Porta, J., Porta, J.M., Quilici, S., Rakotoarivelo, F.P., Ramesha, B.T., Ravikanth, G., Riera, B., Risterucci, A.M., Roberts, D.A., Samadi, S., Sarasola-Puente, V., Sarrazin, E., Sarthou, C., Schmidt, Anke, Segovia, N.I., Shen, K.N., Simiand, C., Sman, Muhammad Hidayat Bin, Solhoy, T., Sommer, Simone, Sumangala, R.C., Taubert, Ramona, Tejangkura, T., Telford, A., Testa, A., Tollon-Cordet, C., Tzeng, W.N., Uma-Shaanker, R., Van Der Lee, T.A.J., Van Mourik, Thomas A., Vasudeva, R., Wai, T.C., Wang, R.L., Welch, Mark E., Weltzein, Eva, Whitehead, A., Woodard, Anastasia, Xia, Jianjun, Zeinolabedini, M., and Zhang, Lvping
- Abstract
This article documents the addition of 396 microsatellite marker loci to the Molecular Ecology Resources Database. Loci were developed for the following species: Anthocidaris crassispina, Aphis glycines, Argyrosomus regius, Astrocaryum sciophilum, Dasypus novemcinctus, Delomys sublineatus, Dermatemys mawii, Fundulus heteroclitus, Homalaspis plana, Jumellea rossii, Khaya senegalensis, Mugil cephalus, Neoceratitis cyanescens, Phalacrocorax aristotelis, Phytophthora infestans, Piper cordulatum, Pterocarpus indicus, Rana dalmatina, Rosa pulverulenta, Saxifraga oppositifolia, Scomber colias, Semecarpus kathalekanensis, Stichopus monotuberculatus, Striga hermonthica, Tarentola boettgeri and Thermophis baileyi. These loci were cross-tested on the following species: Aphis gossypii, Sooretamys angouya, Euryoryzomys russatus, Fundulus notatus, Fundulus olivaceus, Fundulus catenatus, Fundulus majalis, Jumellea fragrans, Jumellea triquetra Jumellea recta, Jumellea stenophylla, Liza richardsonii, Piper marginatum, Piper aequale, Piper darienensis, Piper dilatatum, Rana temporaria, Rana iberica, Rana pyrenaica, Semecarpus anacardium, Semecarpus auriculata, Semecarpus travancorica, Spondias acuminata, Holigarna grahamii, Holigarna beddomii, Mangifera indica, Anacardium occidentale, Tarentola delalandii, Tarentola caboverdianus and Thermophis zhaoermii.
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- 2010
17. Genetic and floral variation in two colosely related Jumella spp. (Orchidaceae) in Mascarene Islands
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Mallet, B., primary, Dafreville, S., additional, Blambert, L., additional, Pailler, T., additional, and Humeau, L., additional
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- 2013
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18. Promotion of aromatic orchids endemic to the Mascarene Islands within a framework of sustainable development
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Blambert, L., primary, Mallet, B., additional, Palama, T.L., additional, Couprie, J., additional, Sing, A. Shum Cheong, additional, Grisoni, M., additional, Suzanne, W., additional, Chatel, A., additional, Humeau, L., additional, and Pailler, T., additional
- Published
- 2013
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19. Glomeremus species from the Mascarene islands (Orthoptera, Gryllacrididae) with the description of the pollinator of an endemic orchid from the island of Réunion
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HUGEL, S., primary, MICHENEAU, C., additional, FOURNEL, J., additional, WARREN, B. H., additional, GAUVIN-BIALECKI, A., additional, PAILLER, T., additional, CHASE, M. W., additional, and STRASBERG, D., additional
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- 2010
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20. Reproductive trait variation in the functionally dioecious and morphologically heterostylous island endemicChassalia corallioides(Rubiaceae)
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PAILLER, T, primary
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- 1998
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21. Two new records of Jumellea (Orchidaceae) for Mauritius (Mascarene Islands) and their conservation status
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Claudia Baider, Vincent Florens, F. B., Rakotoarivelo, F., Bosser, J., Pailler, T., Université de Maurice, Peuplements végétaux et bioagresseurs en milieu tropical (UMR PVBMT), Centre de Coopération Internationale en Recherche Agronomique pour le Développement (Cirad)-Institut de Recherche pour le Développement (IRD)-Institut National de la Recherche Agronomique (INRA)-Université de La Réunion (UR), Université d'Antananarivo, Institut de Recherche pour le Développement (IRD), and Muséum national d'Histoire naturelle (MNHN)
- Subjects
Tracheophyta ,Liliopsida ,Asparagales ,[SDV.BV]Life Sciences [q-bio]/Vegetal Biology ,Biodiversity ,Plantae ,Orchidaceae ,Taxonomy - Abstract
International audience; Two new records of Jumellea for the island of Mauritius (Indian Ocean), J. exilis and J. rossii are reported from incorrectly attributed past collections. Sampling over the last four decades on Mauritius recorded only a few localities for J. exilis, while J. rossii is known from only a single collection. Recent surveys confirm that J. exilis is very rare, qualifying as Critically Endangered on Mauritius according to the IUCN Red List Criteria, and J. rossii should be considered as probably Extinct. An updated key to the Jumellea of Mauritius is provided. Threats besetting the species and other orchids in general in Mauritius are discussed and conservation measures suggested.
22. Morphological differences and identification of Jumellea rossii and Jumellea fragrans (Orchidaceae) in Reunion Island: Implications for conservation,Différences morphologiques et identification de Jumellea rossii et Jumellea fragrans (Orchidaceae) à l'île de La Réunion: Implications pour la conservation
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Mallet, B., Humeau, L., Blambert, L., Rakotoarivelo, F., Claudia Baider, and Pailler, T.
23. Saprotrophic fungal mycorrhizal symbionts in achlorophyllous orchids: Finding treasures among the 'molecular scraps'?
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Selosse, M. -A, Martos, F., Perry, B. A., Mahajabeen Padamsee, Roy, M., and Pailler, T.
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Mini-Reviews ,Species Specificity ,Mycorrhizae ,fungi ,food and beverages ,Orchidaceae ,Symbiosis ,Biological Evolution ,Phylogeny - Abstract
Mycoheterotrophic plants are achlorophyllous plants that obtain carbon from their mycorrhizal fungi. They are usually considered to associate with fungi that are (1) specific of each mycoheterotrophic species and (2) mycorrhizal on surrounding green plants, which are the ultimate carbon source of the entire system. Here we review recent works revealing that some mycoheterotrophic plants are not fungal-specific, and that some mycoheterotrophic orchids associate with saprophytic fungi. A re-examination of earlier data suggests that lower specificity may be less rare than supposed in mycoheterotrophic plants. Association between mycoheterotrophic orchids and saprophytic fungi arose several times in the evolution of the two partners. We speculate that this indirectly illustrates why transition from saprotrophy to mycorrhizal status is common in fungal evolution. Moreover, some unexpected fungi occasionally encountered in plant roots should not be discounted as 'molecular scraps', since these facultatively biotrophic encounters may evolve into mycorrhizal symbionts in some other plants.
24. Genetic and floral variation in two colosely related Jumella spp. (Orchidaceae) in Mascarene Islands.
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Anonymous, Dafreville, S., Blambert, L., Pailler, T., and Humeau, L.
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- 2013
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25. Promotion of aromatic orchids endemic to the Mascarene Islands within a framework of sustainable development.
- Author
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Anonymous, Mallet, B., Palama, T.L., Couprie, J., Sing, A. Shum Cheong, Grisoni, M., Suzanne, W., Chatel, A., Humeau, L., and Pailler, T.
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- 2013
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- View/download PDF
26. Phylogenetic relationships amongst the African genera of subtribe Orchidinae s.l. (Orchidaceae; Orchideae): Implications for subtribal and generic delimitations.
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Ngugi G, Le Péchon T, Martos F, Pailler T, Bellstedt DU, and Bytebier B
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- Africa, Bayes Theorem, DNA, Plant genetics, Orchidaceae genetics, Plastids genetics, Orchidaceae classification, Phylogeny
- Abstract
Phylogenetic relationships within the Orchideae sensu Pridgeon et al, remain one of the biggest unresolved issues in our understanding of the taxonomy of the orchids. Members of the Orchideae are numerous and widespread in Africa but remain poorly represented in phylogenetic research. In this study we included a broad sampling of African taxa for which we sequenced three plastid (rbcl, matK and trnL + trnL-F) and two nuclear regions (ITS and 18S). We used 368 sequences representing 278 species and 49 genera to infer relationships using the Bayesian Inference and Maximum Likelihood method. Our results show strong support for three clades, two of which almost entirely match the historical circumscription of Orchidinae and Habenariinae, and the third, Bartholininae, sister to the former two, includes the genera Holothrix and Bartholina. Stenoglottis should be assigned to Orchidinae and not to Habenariinae. Several genera such as Habenaria, Cynorkis and Benthamia are shown to be para- or polyphyletic: Bonatea, Centrostigma, Platycoryne and Roeperocharis are all embedded in Habenaria; Physoceras, Arnottia and part of Benthamia are embedded in Cynorkis. We propose a subdivision of Orchideae sensu lato into nine subtribes, but refrain from making generic re-arrangements until more extensive or more in-depth studies have been done., (Copyright © 2020 Elsevier Inc. All rights reserved.)
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- 2020
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27. Reproductive patterns, genetic diversity and inbreeding depression in two closely related Jumellea species with contrasting patterns of commonness and distribution.
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Blambert L, Mallet B, Humeau L, and Pailler T
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- Genetics, Population, Pollen genetics, Pollination, Reproduction, Reunion, Self-Fertilization, Genetic Variation, Inbreeding Depression, Orchidaceae genetics
- Abstract
Backgrounds and Aims: Theory predicts that the long-term persistence of plant populations exposed to size reduction can be threatened by a loss of genetic diversity and increased inbreeding. However, several life-history and ecological traits can influence the response to population size reduction. The reproductive patterns, levels of genetic diversity and magnitude of inbreeding depression of the rare and fragmented Jumellea fragrans and of its widespread congener J. rossii were studied. The aim was to evaluate the effects of over-collection and fragmentation on J. fragrans and to enhance our knowledge of the biology and ecology of the two species, used for their aromatic and medicinal properties on Réunion., Methods: Hand pollination experiments were conducted to determine the breeding system and to evaluate the potential for inbreeding depression in both species. Nuclear microsatellite markers were used to investigate selfing rates and levels of genetic diversity., Key Results: Jumellea rossii revealed a mixed-mating system, and inbreeding depression at the germination stage (δ = 0·66). Levels of genetic diversity were relatively high [allelic richness (AR) = 8·575 and expected heterozygosity (He) = 0·673]. In J. fragrans, selfing rates suggest a mainly outcrossing mating system. Genetic diversity was lower than in J. rossii, but not yet critically low (AR = 4·983 and He = 0·492), probably because of the mainly outcrossing mating system and the relatively high density of individuals in the studied population. Jumellea fragrans did not show inbreeding depression, and it is hypothesized that the population had progressively purged its genetic load during successive fragmentation events., Conclusions: Even if the persistence of the J. fragrans population is not threatened in the short term, its genetic diversity has probably been reduced by fragmentation and over-collection. In situ conservation actions for J. fragrans and ex situ cultivation of both species are recommended in order to meet the demand of local people., (© The Author 2016. Published by Oxford University Press on behalf of the Annals of Botany Company. All rights reserved. For Permissions, please email: journals.permissions@oup.com.)
- Published
- 2016
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28. Orchid conservation: making the links.
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Fay MF, Pailler T, and Dixon KW
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- Conservation of Natural Resources, Orchidaceae physiology
- Abstract
Orchidaceae, one of the largest families of flowering plants, present particular challenges for conservation, due in great part to their often complex interactions with mycorrhizal fungi, pollinators and host trees. In this Highlight, we present seven papers focusing on orchids and their interactions and other factors relating to their conservation., (© The Author 2015. Published by Oxford University Press on behalf of the Annals of Botany Company. All rights reserved. For Permissions, please email: journals.permissions@oup.com.)
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- 2015
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29. Chemical and morphological filters in a specialized floral mimicry system.
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Martos F, Cariou ML, Pailler T, Fournel J, Bytebier B, and Johnson SD
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- Animals, Behavior, Animal, Drosophila physiology, Pollination, Volatile Organic Compounds analysis, Flowers anatomy & histology, Flowers chemistry, Orchidaceae physiology
- Abstract
Many plant species attract insect pollinators through chemical mimicry of their oviposition sites, often detaining them in a trap chamber that ensures pollen transfer. These plant mimics are considered to be unspecialized at the pollinator species level, yet field observations of a mycoheterotrophic rainforest orchid (Gastrodia similis), which emits an odour reminiscent of rotting fruit, indicate that it is pollinated by a single drosophilid fly species (Scaptodrosophila bangi). We investigated the roles of floral volatiles and the dimensions of the trap chamber in enforcing this specialization, using gas chromatography-mass spectrometry analyses, bioassays and scanning electron microscopy. We showed that G. similis flowers predominantly emit three fatty-acid esters (ethyl acetate, ethyl isobutyrate and methyl isobutyrate) that were shown in experiments to attract only Scaptodrosophila flies. We additionally showed that the trap chamber, which flies enter into via a touch-sensitive 'trapdoor', closely matches the body size of the pollinator species S. bangi and plays a key role in pollen transfer. Our study demonstrates that specialization in oviposition site mimicry is due primarily to volatile chemistry and is reflected in the dimensions of the trapping apparatus. It also indicates that mycoheterotrophic plants can be specialized both on mycorrhizal fungi and insect pollinators., (© 2015 The Authors. New Phytologist © 2015 New Phytologist Trust.)
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- 2015
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30. Evidence for isolation-by-habitat among populations of an epiphytic orchid species on a small oceanic island.
- Author
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Mallet B, Martos F, Blambert L, Pailler T, and Humeau L
- Subjects
- Adaptation, Physiological genetics, Altitude, Flowers genetics, Gene Flow, Genetics, Population, Genotype, Geography, Indian Ocean, Islands, Phenotype, Population Dynamics, Seasons, Selection, Genetic, Ecosystem, Genetic Variation, Microsatellite Repeats genetics, Orchidaceae genetics
- Abstract
Identifying factors that promote population differentiation is of interest for understanding the early stages of speciation. Gene flow among populations inhabiting different environments can be reduced by geographical distance (isolation-by-distance) or by divergent selection resulting from local adaptation (isolation-by-ecology). Few studies have investigated the influence of these factors in small oceanic islands where the influence of geographic distance is expected to be null but where habitat diversity could have a strong effect on population differentiation. In this study, we tested for the spatial divergence of phenotypes (floral morphology and floral scent) and genotypes (microsatellites) among ten populations of Jumellea rossii, an epiphytic orchid endemic to Réunion growing in three different habitats. We found a significant genetic differentiation between populations that is structured by habitat heterogeneity rather than by geographic distance between populations. These results suggest that ecological factors might reduce gene flow among populations located in different habitats. This pattern of isolation-by-habitat may be the result of both isolation-by-ecology by habitat filtering and asynchrony in flowering phenology. Furthermore, data on floral morphology match these findings, with multivariate analysis grouping populations by habitat type but could be only due to phenotypic plasticity. Indeed floral scent compounds were not significantly different between populations indicating that specific plant-pollinator mutualism does not seem to play a major role in the population differentiation of J. rossii. In conclusion, the results from our study emphasize the importance of habitat diversity of small oceanic islands as a factor of population differentiation.
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- 2014
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31. The role of epiphytism in architecture and evolutionary constraint within mycorrhizal networks of tropical orchids.
- Author
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Martos F, Munoz F, Pailler T, Kottke I, Gonneau C, and Selosse MA
- Subjects
- DNA, Fungal genetics, DNA, Ribosomal Spacer genetics, Models, Genetic, Molecular Sequence Data, Mycorrhizae classification, Phylogeny, Plant Roots microbiology, Reunion, Sequence Analysis, DNA, Biological Evolution, Mycorrhizae genetics, Orchidaceae genetics, Orchidaceae microbiology, Symbiosis genetics
- Abstract
Characterizing the architecture of bipartite networks is increasingly used as a framework to study biotic interactions within their ecological context and to assess the extent to which evolutionary constraint shape them. Orchid mycorrhizal symbioses are particularly interesting as they are viewed as more beneficial for plants than for fungi, a situation expected to result in an asymmetry of biological constraint. This study addressed the architecture and phylogenetic constraint in these associations in tropical context. We identified a bipartite network including 73 orchid species and 95 taxonomic units of mycorrhizal fungi across the natural habitats of Reunion Island. Unlike some recent evidence for nestedness in mycorrhizal symbioses, we found a highly modular architecture that largely reflected an ecological barrier between epiphytic and terrestrial subnetworks. By testing for phylogenetic signal, the overall signal was stronger for both partners in the epiphytic subnetwork. Moreover, in the subnetwork of epiphytic angraecoid orchids, the signal in orchid phylogeny was stronger than the signal in fungal phylogeny. Epiphytic associations are therefore more conservative and may co-evolve more than terrestrial ones. We suggest that such tighter phylogenetic specialization may have been driven by stressful life conditions in the epiphytic niches. In addition to paralleling recent insights into mycorrhizal networks, this study furthermore provides support for epiphytism as a major factor affecting ecological assemblage and evolutionary constraint in tropical mycorrhizal symbioses., (© 2012 Blackwell Publishing Ltd.)
- Published
- 2012
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32. Colour-scent associations in a tropical orchid: three colours but two odours.
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Delle-Vedove R, Juillet N, Bessière JM, Grison C, Barthes N, Pailler T, Dormont L, and Schatz B
- Subjects
- Alkenes metabolism, Animals, Flowers physiology, Pigmentation genetics, Pollination physiology, Odorants, Orchidaceae chemistry, Pigmentation physiology
- Abstract
Colour and scent are the major pollinator attractants to flowers, and their production may be linked by shared biosynthetic pathways. Species with polymorphic floral traits are particularly relevant to study the joint evolution of floral traits. We used in this study the tropical orchid Calanthe sylvatica from Réunion Island. Three distinct colour varieties are observed, presenting lilac, white or purple flowers, and named respectively C. sylvaticavar.lilacina (hereafter referred as var. lilacina), C. sylvaticavar. alba (var. alba) and C. sylvatica var. purpurea (var. purpurea). We investigated the composition of the floral scent produced by these colour varieties using the non-invasive SPME technique in the wild. Scent emissions are dominated by aromatic compounds. Nevertheless, the presence of the terpenoid (E)-4,8-dimethylnona-1,3,7-triène (DMNT) is diagnostic of var. purpurea, with the volatile organic compounds (VOC) produced by some individuals containing up to 60% of DMNT. We evidence specific colour-scent associations in C. sylvatica, with two distinct scent profiles in the three colour varieties: the lilacina-like profile containing no or very little DMNT (<2%) and the purpurea-like profile containing DMNT (>2%). Calanthe sylvatica var. alba individuals group with one or the other scent profile independently of their population of origin. We suggest that white-flowered individuals have evolved at least twice, once from var. lilacina and at least once from var. purpurea after the colonisation of la Réunion. White-flowered individuals may have been favoured by the particular pollinator fauna characterising the island. These flowering varieties of C. sylvatica, which display three colours but two scents profiles prove that colour is not always a good indicator of odour and that colour-scent associations may be complex, depending on pollination ecology of the populations concerned., (Copyright © 2011 Elsevier Ltd. All rights reserved.)
- Published
- 2011
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33. Permanent Genetic Resources added to Molecular Ecology Resources Database 1 April 2010 - 31 May 2010.
- Author
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Andree K, Axtner J, Bagley MJ, Barlow EJ, Beebee TJ, Bennetzen JL, Bermingham E, Boisselier-Dubayle MC, Bozarth CA, Brooks CP, Brown RP, Catanese G, Cavers S, Ceron-Souza I, Chak ST, Chan MN, Charles-Dominique P, Chen CY, Chen JD, Chinchilla L, DA Silva D, Dafreville S, Daunt F, Delatte H, Dorge T, Duncan N, Durand JD, Duvernell D, Estep M, Fan S, Fattahi R, Villela OF, Fong Y, Fréville H, Funes V, Gallardo-Escarate C, Ganeshaiah KN, Ghaffari MR, Girod C, Gomez-Moliner BJ, Gonzalez-Porter GP, Gosa A, Govers F, Guérin F, Guindo D, Hailer F, Haye PA, Hoelmer KA, Hofmann S, Hong Y, Hu C, Huang SW, Humeau L, Infante C, Jackson SA, Jacobsen E, Jowkar A, Kafi M, Kermani MJ, Kim H, Kim KS, Kim MY, Knibb W, Koita OA, Korpelainen H, Lambourdiere J, Lasso E, Leblois R, Lee H, Lee S, Leung FC, Leung KM, Li C, Li Y, Lieckfeldt D, Lizana M, Loughry WJ, Luo P, Madeira MJ, Mahmoodi P, Maldonado JE, Mardi M, Mendes O, Miehe G, Muth P, Nacci D, Naveen Kumar L, Ng WC, Pailler T, Parzies HK, Perez L, Pfunder M, Pietiläinen M, Pirseyedi SM, Porta D, Porta J, Porta JM, Quilici S, Rakotoarivelo FP, Ramesha BT, Ravikanth G, Riéra B, Risterucci AM, Roberts DA, Samadi S, Sarasola-Puente V, Sarrazin E, Sarthou C, Schmidt A, Segovia NI, Shen KN, Simiand C, Sman MH, Solhoy T, Sommer S, Sumangala RC, Taubert R, Tejangkura T, Telford A, Testa A, Tollon-Cordet C, Tzeng WN, Uma Shaanker R, Van Der Lee TA, VAN Mourik TA, Vasudeva R, Wai TC, Wang RL, Welch ME, Weltzien E, Whitehead A, Woodard A, Xia J, Zeinolabedini M, and Zhang L
- Abstract
This article documents the addition of 396 microsatellite marker loci to the Molecular Ecology Resources Database. Loci were developed for the following species: Anthocidaris crassispina, Aphis glycines, Argyrosomus regius, Astrocaryum sciophilum, Dasypus novemcinctus, Delomys sublineatus, Dermatemys mawii, Fundulus heteroclitus, Homalaspis plana, Jumellea rossii, Khaya senegalensis, Mugil cephalus, Neoceratitis cyanescens, Phalacrocorax aristotelis, Phytophthora infestans, Piper cordulatum, Pterocarpus indicus, Rana dalmatina, Rosa pulverulenta, Saxifraga oppositifolia, Scomber colias, Semecarpus kathalekanensis, Stichopus monotuberculatus, Striga hermonthica, Tarentola boettgeri and Thermophis baileyi. These loci were cross-tested on the following species: Aphis gossypii, Sooretamys angouya, Euryoryzomys russatus, Fundulus notatus, Fundulus olivaceus, Fundulus catenatus, Fundulus majalis, Jumellea fragrans, Jumellea triquetra Jumellea recta, Jumellea stenophylla, Liza richardsonii, Piper marginatum, Piper aequale, Piper darienensis, Piper dilatatum, Rana temporaria, Rana iberica, Rana pyrenaica, Semecarpus anacardium, Semecarpus auriculata, Semecarpus travancorica, Spondias acuminata, Holigarna grahamii, Holigarna beddomii, Mangifera indica, Anacardium occidentale, Tarentola delalandii, Tarentola caboverdianus and Thermophis zhaoermii., (© 2010 Blackwell Publishing Ltd.)
- Published
- 2010
- Full Text
- View/download PDF
34. Saprotrophic fungal mycorrhizal symbionts in achlorophyllous orchids: finding treasures among the 'molecular scraps'?
- Author
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Selosse MA, Martos F, Perry BA, Padamsee M, Roy M, and Pailler T
- Subjects
- Biological Evolution, Mycorrhizae genetics, Phylogeny, Species Specificity, Mycorrhizae physiology, Orchidaceae microbiology, Symbiosis
- Abstract
Mycoheterotrophic plants are achlorophyllous plants that obtain carbon from their mycorrhizal fungi. They are usually considered to associate with fungi that are (1) specific of each mycoheterotrophic species and (2) mycorrhizal on surrounding green plants, which are the ultimate carbon source of the entire system. Here we review recent works revealing that some mycoheterotrophic plants are not fungal-specific, and that some mycoheterotrophic orchids associate with saprophytic fungi. A re-examination of earlier data suggests that lower specificity may be less rare than supposed in mycoheterotrophic plants. Association between mycoheterotrophic orchids and saprophytic fungi arose several times in the evolution of the two partners. We speculate that this indirectly illustrates why transition from saprotrophy to mycorrhizal status is common in fungal evolution. Moreover, some unexpected fungi occasionally encountered in plant roots should not be discounted as 'molecular scraps', since these facultatively biotrophic encounters may evolve into mycorrhizal symbionts in some other plants.
- Published
- 2010
- Full Text
- View/download PDF
35. Orthoptera, a new order of pollinator.
- Author
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Micheneau C, Fournel J, Warren BH, Hugel S, Gauvin-Bialecki A, Pailler T, Strasberg D, and Chase MW
- Subjects
- Animals, Gryllidae classification, Gryllidae physiology, Magnoliopsida physiology, Pollen
- Abstract
Background and Aims: Pollinator-mediated selection and evolution of floral traits have long fascinated evolutionary ecologists. No other plant family shows as wide a range of pollinator-linked floral forms as Orchidaceae. In spite of the large size of this model family and a long history of orchid pollination biology, the identity and specificity of most orchid pollinators remains inadequately studied, especially in the tropics where the family has undergone extensive diversification. Angraecum (Vandeae, Epidendroideae), a large genus of tropical Old World orchids renowned for their floral morphology specialized for hawkmoth pollination, has been a model system since the time of Darwin., Methods: The pollination biology of A. cadetii, an endemic species of the islands of Mauritius and Reunion (Mascarene Islands, Indian Ocean) displaying atypical flowers for the genus (white and medium-size, but short-spurred) was investigated. Natural pollinators were observed by means of hard-disk camcorders. Pollinator-linked floral traits, namely spur length, nectar volume and concentration and scent production were also investigated. Pollinator efficiency (pollen removal and deposition) and reproductive success (fruit set) were quantified in natural field conditions weekly during the 2003, 2004 and 2005 flowering seasons (January to March)., Key Results: Angraecum cadetii is self-compatible but requires a pollinator to achieve fruit set. Only one pollinator species was observed, an undescribed species of raspy cricket (Gryllacrididae, Orthoptera). These crickets, which are nocturnal foragers, reached flowers by climbing up leaves of the orchid or jumping across from neighbouring plants and probed the most 'fresh-looking' flowers on each plant. Visits to flowers were relatively long (if compared with the behaviour of birds or hawkmoths), averaging 16.5 s with a maximum of 41.0 s. At the study site of La Plaine des Palmistes (Pandanus forest), 46.5 % of flowers had pollen removed and 27.5 % had pollinia deposited on stigmas. The proportion of flowers that set fruit ranged from 11.9 % to 43.4 %, depending of the sites sampled across the island., Conclusions: Although orthopterans are well known for herbivory, this represents the first clearly supported case of orthopteran-mediated pollination in flowering plants.
- Published
- 2010
- Full Text
- View/download PDF
36. Independent recruitment of saprotrophic fungi as mycorrhizal partners by tropical achlorophyllous orchids.
- Author
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Martos F, Dulormne M, Pailler T, Bonfante P, Faccio A, Fournel J, Dubois MP, and Selosse MA
- Subjects
- Basidiomycota classification, Basidiomycota genetics, Basidiomycota physiology, Carbon Isotopes, Climate, Food Chain, Mycorrhizae classification, Mycorrhizae genetics, Nitrogen Isotopes, Phylogeny, Symbiosis genetics, Symbiosis physiology, Tropical Climate, Mycorrhizae physiology, Orchidaceae microbiology
- Abstract
Mycoheterotrophic orchids have adapted to shaded forest understory by shifting to achlorophylly and receiving carbon from their mycorrhizal fungi. In temperate forests, they associate in a highly specific way with fungi forming ectomycorrhizas on nearby trees, and exploiting tree photosynthates. However, many rainforests lack ectomycorrhizal fungi, and there is evidence that some tropical Asiatic species associate with saprotrophic fungi. To investigate this in different geographic and phylogenetic contexts, we identified the mycorrhizal fungi supporting two tropical mycoheterotrophic orchids from Mascarene (Indian Ocean) and Caribbean islands. We tested their possible carbon sources by measuring natural nitrogen ((15)N) and carbon ((13)C) abundances. Saprotrophic basidiomycetes were found: Gastrodia similis associates with a wood-decaying Resinicium (Hymenochaetales); Wullschlaegelia aphylla associates with both litter-decaying Gymnopus and Mycena species, whose rhizomorphs link orchid roots to leaf litter. The (15)N and (13)C abundances make plausible food chains from dead wood to G. similis and from dead leaves to W. aphylla. We propose that temperature and moisture in rainforests, but not in most temperate forests, may favour sufficient saprotrophic activity to support development of mycoheterotrophs. By enlarging the spectrum of mycorrhizal fungi and the level of specificity in mycoheterotrophic orchids, this study provides new insights on orchid and mycorrhizal biology in the tropics.
- Published
- 2009
- Full Text
- View/download PDF
37. Phylogenetics and biogeography of Mascarene angraecoid orchids (Vandeae, Orchidaceae).
- Author
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Micheneau C, Carlsward BS, Fay MF, Bytebier B, Pailler T, and Chase MW
- Subjects
- Bayes Theorem, DNA, Plant genetics, Geography, Indian Ocean Islands, Madagascar, Orchidaceae classification, Plant Proteins genetics, Plastids genetics, Orchidaceae genetics, Phylogeny
- Abstract
The large angraecoid orchid clade (subtribe Angraecinae sensu lato) has undergone extensive radiation in the western Indian Ocean, which includes Africa, Madagascar, and a number of Indian Ocean islands, such as the Mascarene Archipelago. To investigate systematics and biogeography of these Mascarene orchids, phylogenetic relationships were inferred from four plastid DNA regions, trnL intron, trnL-F intergenic spacer, matK gene, and rps16 intron. Parsimony and Bayesian analyses provided identical sets of relationships within the subtribe; the large genus Angraecum as currently circumscribed does not form an exclusive clade. Bonniera, an endemic genus to Reunion, is shown to be embedded in part of Angraecum. Evidence from our research supports the main origin of Mascarene Angraecinae from Madagascar, and although there were many independent colonizations, only a few of the lineages radiated within the Mascarene Archipelago.
- Published
- 2008
- Full Text
- View/download PDF
38. Bird pollination in an angraecoid orchid on Reunion Island (Mascarene Archipelago, Indian Ocean).
- Author
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Micheneau C, Fournel J, and Pailler T
- Subjects
- Animals, Orchidaceae anatomy & histology, Reproduction physiology, Reunion, Birds physiology, Flowers anatomy & histology, Orchidaceae physiology, Pollen physiology
- Abstract
Background and Aims: Although numerous angraecoid orchids in Madagascar display typical sphingophilous syndrome (i.e. white, nectariferous, long-spurred flowers, producing a strong scent at the crepuscule that is attractive to moths), three species of Angraecum in Reunion, belonging to the endemic section Hadrangis, have atypical unscented and short-spurred flowers. The aim of the study was to investigate the implication of plant-pollinator interaction on the evolution of floral morphology of these peculiar island floral forms., Methods: The flower morphology of A. striatum (one of the three section Hadrangis species) was investigated by performing a set of floral measures, and the reproductive biology was investigated by a set of hand pollination experiments. Natural pollinators were observed by means of a digital video camera. Pollinator efficiency (pollen removal and deposition) and reproductive success (fruit set) were quantified once a week in natural field conditions during the 2005 flowering season (i.e. from January to March)., Key Results: The orchid is self-compatible but requires a pollinator to achieve fruit set. Only one pollinator was observed, the endemic white-eye Zosterops borbonicus (Zosteropidae). These birds perched on inflorescences, and probed most fresh-looking flowers on each plant for nectar. Nectar was both abundant (averaging 7.7 microL) and dilute (averaging 9.7 % sugar in sucrose equivalents). Birds were mostly active between 0830 and 0930 h. Visits to plants were extremely short, lasting from 9 to 27 s. At the study site, 60.9 % of flowers had pollen removed, and 46.4 % had pollinia deposited on stigmas. The proportion of flowers that initiated a fruit averaged 20.6 % in natural conditions., Conclusions: For the first time, a bird-pollinated orchid is described from a sub-tribe that is mainly specialized for moth pollination. This study documents a morphological shift in flowers in response to pollinator adaptations in the insular context of the Mascarene Archipelago.
- Published
- 2006
- Full Text
- View/download PDF
39. Cryptic dioecy and leaky dioecy in endemic species of Dombeya (Sterculiaceae) on La Reunion.
- Author
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Humeau L, Pailler T, and Thompson JD
- Abstract
The high frequency of dioecy on oceanic islands such as Hawaii and New Zealand has attracted a great deal of attention from plant evolutionary biologists. One reason suggested for the high prevalence of dioecy on oceanic islands is that taxa considered truly dioecious may have occasional hermaphrodite flowers, i.e., show leaky dioecy. In this study, we quantified the presence and distribution of leaky dioecy in a group of congeneric endemic species of the genus Dombeya (Sterculiaceae) on La Réunion island (Indian Ocean). All eight species show cryptic dioecy. Five species show strict dioecy and three species show leaky dioecy due to the presence of male trees that set fruit. Species with strict dioecy and large populations tend to occur in mid- to high-altitude moist tropical cloud forest, whereas species in smaller populations at lower altitude and in semidry tropical forest tend to show leaky dioecy. Two reasons for this differential distribution of strict dioecy and leaky dioecy are discussed. First, environmental variation along the altitudinal gradient, biotic and/or abiotic, may influence the breeding system. Second, leaky dioecy may be favored in lowland populations due to the small size and disturbed nature of such populations.
- Published
- 1999
40. Distyly and variation in heteromorphic incompatibility in Gaertnera vaginata (Rubiaceae) endemic to La Reunion Island.
- Author
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Pailler T and Thompson J
- Abstract
Documenting the floral biology of species throughout the Rubiaceae family is of particular interest since heterostyly and dioecy may have evolved more than once in this large family. Unfortunately many species in several tropical regions remain unstudied. The purpose of this paper is to describe the floral biology, the nature of self-incompatibility, morph ratios, and fecundity in natural populations of Gaertnera vaginata, a small tree endemic to the island of La Reunion in the Indian Ocean. Measurements of floral characters in populations across the entire distribution of this species showed that G. vaginata exhibits a reciprocal stigma height and anther height dimorphism characteristic of a distylous species. Pollen grain size and corolla tube length are consistently greater in short-styled plants and long-styled plants produce more pollen per flower. Controlled pollinations in a natural population showed that 25% of the short-styled plants gave at least one fruit on intramorph (illegitimate) pollination, whereas no long-styled plants set fruit on illegitimate pollination. In total, 19.4% of illegitimate pollinations produced fruit on short-styled plants. No self-pollination gave fruit on either morph and between-morph pollinations produced 92.2 and 92.8% for short and long-styled plants, respectively. Overall, short-styled plants were significantly more abundant than long-styled plants. Short-styled plants outnumbered long-styled plants in 16 of the 19 populations. In three of these populations the morph ratio was significantly different from 1:1. In two natural populations, fruit set was significantly higher on long-styled plants, although the number of seeds per fruit was not significantly different between the two morphs. The possible effect of variation in the strength of heteromorphic incompatibility on observed variation in morph abundance and the possible causes for the variation in fruit set are discussed.
- Published
- 1997
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