@ARTICLE{TreeBASE2Ref18182,
author = {Doris Wolff and Sigrid Liede-Schumann},
title = {Evolution of flower morphology, pollen dimorphism, and nectar composition in Arcytophyllum, a distylous genus of Rubiaceae},
year = {2006},
keywords = {},
doi = {},
url = {},
pmid = {},
journal = {Organisms Diversity & Evolution},
volume = {},
number = {},
pages = {},
abstract = {A phylogenetic study of Arcytophyllum based on ITS was conducted and compared with an earlier study based on cpDNA. The position of the widespread A. thymifolium as sister to all other species was confirmed and several well-supported clades could be retrieved. The Central American A. lavarum is well embedded between exclusively or predominantly South American species. To understand the expression of heterostyly in the genus, we analyzed inter- and intraspecific variation in floral morphology, nectar, pollen-ovule-ratio and seed set of ten species in eleven populations. Stigma and anther levels differed significantly between the morphs in the species/populations investigated except for A. filiforme, in which anther levels differed not significantly between the two morphs. Different expressions of heterostyly in Arcytophyllum seem independent of phylogenetic relationships. Nectar sugar composition was similar between the morphs. Nectar of most species presented a larger proportion of hexoses than of sucrose, only the most derived species, A. macbridei and A. vernicosum, have higher sucrose proportions. There is a significant positive correlation between corolla tube length and the proportion of sucrose. Pollen dimorphism, both with regard to the number (long-styled > short-styled) and to the size (short-styled > long-styled) was observed in all taxa investigated except for A. filiforme. According to the pollen-ovule-ratios the breeding systems range from facultative autogamy to facultative xenogamy. The lowest P/O-ratios were found in A. filiforme the highest in A. rivetii. Hymenoptera, Diptera and Coleoptera were observed as flower visitors. Seed production did not differ significantly between the morphs in eight of the eleven species/populations investigated. There is, however a tendency in all species/populations (except for A. macbridei Peru) that the short-styled morph has a higher percentage of seeds per ovule indicating that the short-styled morphs display higher female reproductive success.}
}
Taxa for matrix 20535 of Study 1503

Citation title:
"Evolution of flower morphology, pollen dimorphism, and nectar composition in Arcytophyllum, a distylous genus of Rubiaceae".

This study was previously identified under the legacy study ID S1447
(Status: Published).
Taxa
Return to matrix row view
| ID |
Taxon Label |
NCBI taxid |
uBIO namebankID |
| 1377259 |
Antrodia alpina RLG6107 |
|
3022226
|
| 1377283 |
Antrodia carbonica FP105585-R |
40416
|
3023620
|
| 1377274 |
Antrodia xantha TFRI879 |
|
3188915
|
| 1377247 |
Bjerkandera adusta DAOM215869 |
5331
|
3018775
|
| 1377299 |
Diplomitoporus lindbladii Dai6414 |
83258
|
3022493
|
| 1377255 |
Diplomitoporus lindbladii HHB5629 |
83258
|
3022493
|
| 1377266 |
Perenniporia corticola Cui 2655 |
|
3362961
|
| 1377279 |
Perenniporia corticola Cui1248 |
|
3362961
|
| 1377229 |
Perenniporia corticola Cui1465 |
|
3362961
|
| 1377243 |
Perenniporia corticola Dai7330 |
|
3362961
|
| 1377282 |
Perenniporia detrita MUCL42649 |
644906
|
|
| 1377257 |
Perenniporia fraxinea Cui7154 |
157708
|
3167290
|
| 1377263 |
Perenniporia fraxinea Cui8871 |
157708
|
3167290
|
| 1377246 |
Perenniporia fraxinea Cui8885 |
157708
|
3167290
|
| 1377277 |
Perenniporia fraxinea DP83 |
157708
|
3167290
|
| 1377236 |
Perenniporia latissima Cui6625 |
595651
|
3048371
|
| 1377242 |
Perenniporia maackiae Cui5605 |
|
3262126
|
| 1377271 |
Perenniporia maackiae Cui8929 |
|
3262126
|
| 1377249 |
Perenniporia martia Cui7992 |
|
|
| 1377273 |
Perenniporia martia MUCL41677 |
|
|
| 1377261 |
Perenniporia martia MUCL41678 |
|
|
| 1377239 |
Perenniporia medulla-panis Cui3274 |
137755
|
3919570
|
| 1377234 |
Perenniporia medulla-panis Dai10780 |
137755
|
3919570
|
| 1377233 |
Perenniporia medulla-panis MUCL43250 |
137755
|
3919570
|
| 1377258 |
Perenniporia medulla-panis MUCL49581 |
137755
|
3919570
|
| 1377275 |
Perenniporia ochroleuca Dai11486 |
270278
|
3198283
|
| 1377264 |
Perenniporia ochroleuca MUCL39563 |
270278
|
3198283
|
| 1377269 |
Perenniporia ochroleuca MUCL39726 |
270278
|
3198283
|
| 1377256 |
Perenniporia ohiensis Cui5714 |
644908
|
3198284
|
| 1377276 |
Perenniporia ohiensis MUCL41036 |
644908
|
3198284
|
| 1377241 |
Perenniporia pyricola Cui9149 |
|
|
| 1377270 |
Perenniporia pyricola Dai10265 |
|
|
| 1377252 |
Perenniporia robiniophila Cui5644 |
|
3025998
|
| 1377230 |
Perenniporia robiniophila Cui7144 |
|
3025998
|
| 1377265 |
Perenniporia robiniophila Cui9174 |
|
3025998
|
| 1377248 |
Perenniporia tenuis Cui5523 |
|
3198286
|
| 1377260 |
Perenniporia tephropora Cui6331 |
483159
|
3198287
|
| 1377245 |
Perenniporia tephropora Cui8040 |
483159
|
3198287
|
| 1377231 |
Perenniporia tephropora Cui9029 |
483159
|
3198287
|
| 1377320 |
Perenniporia truncatospora Cui6987 |
|
3043615
|
| 1377313 |
Perenniporia truncatospora Dai 5125 |
|
3043615
|
| 1377232 |
Pyrofomes albomarginatus Cui8838 |
|
3200850
|
| 1377228 |
Pyrofomes albomarginatus Cui8844 |
|
3200850
|
| 1377268 |
Trametes elegans BCC23751 |
252818
|
3084708
|
| 1377237 |
Trametes elegans Cui10748 |
252818
|
3084708
|
| 1377244 |
Trametes hirsuta Cui7784 |
5327
|
3156561
|
| 1377262 |
Trametes ochracea PRM900601 |
230624
|
3046354
|
| 1377254 |
Trametes suaveolens Dai10729 |
40454
|
1224622
|
| 1377280 |
Yuchengia narymica 0308/21-J |
|
|
| 1377251 |
Yuchengia narymica 0709/157 |
|
|
| 1377312 |
Yuchengia narymica 0709/42 |
|
|
| 1377267 |
Yuchengia narymica 0808/10 |
|
|
| 1377284 |
Yuchengia narymica 0809/3 |
|
|
| 1377281 |
Yuchengia narymica 1009/22 |
|
|
| 1377253 |
Yuchengia narymica Dai10510 |
|
|
| 1377240 |
Yuchengia narymica Dai6989 |
|
|
| 1377227 |
Yuchengia narymica Dai6998 |
|
|
| 1377272 |
Yuchengia narymica Dai7016 |
|
|
| 1377250 |
Yuchengia narymica Dai7050 |
|
|