@ARTICLE{TreeBASE2Ref21462,
author = {Gregory Michael Bonito},
title = {Historical biogeography and diversification of truffles in the Tuberaceae and their newly identified Southern hemisphere sister lineage},
year = {2012},
keywords = {fungal evolution, phylogenetics, divergence time estimation, Tuber, ectomycorrhizal lineages, hypogeous fungi, biogeography},
doi = {},
url = {http://},
pmid = {},
journal = {PLOSone},
volume = {},
number = {},
pages = {},
abstract = {Truffles have evolved from epigeous (aboveground) ancestors in nearly every major lineage of fleshy fungi. Because accelerated rates of morphological evolution accompany the transition to the truffle form, closely related epigeous ancestors remain unknown for most truffle lineages. This is the case for the quintessential truffle genus Tuber, which includes species with socio-economic importance and esteemed culinary attributes. Ecologically, Tuber spp. form obligate mycorrhizal symbioses with a diverse species of plant hosts including pines, oaks, poplars, orchids, and commercially important trees such as hazelnut and pecan. Unfortunately, limited geographic sampling and inconclusive phylogenetic relationships have obscured our understanding of their origin, biogeography, and diversification. To address this problem, we present a global sampling of Tuberaceae based on DNA sequence data from four loci for phylogenetic inference and molecular dating. Our well-resolved Tuberaceae phylogeny shows high levels of regional and continental endemism. We also identify a previously unknown epigeous member of the Tuberaceae ? the South American cup-fungus Nothojafnea thaxteri (Cash) Gamund?. Phylogenetic resolution was further improved through the inclusion of a previously unrecognized Southern hemisphere sister group of the Tuberaceae. This morphologically diverse assemblage of fungi includes truffle forms endemic to Australia and South America (e.g. Gymnohydnotrya spp.) and non-truffle species. The Southern hemisphere taxa appear to have diverged more recently than the Northern hemisphere lineages. Our analysis of the Tuberaceae suggests that Tuber evolved from an epigeous ancestor. Molecular dating estimates that the Tuberaceae diverged in the late Jurassic (~156 million years ago), with subsequent radiations in the Cretaceous and Paleogene. Intra-continental diversification, limited long-distance dispersal, and ecological adaptations have driven truffle evolution and Tuberaceae biodiversity.}
}
Taxa for matrix 14819 of Study 13537

Citation title:
"Historical biogeography and diversification of truffles in the Tuberaceae and their newly identified Southern hemisphere sister lineage".

Study name:
"Historical biogeography and diversification of truffles in the Tuberaceae and their newly identified Southern hemisphere sister lineage".

This study is part of submission 13537
(Status: Published).
Taxa
Return to matrix row view
| ID |
Taxon Label |
NCBI taxid |
uBIO namebankID |
| 920773 |
Balsamia MES84 |
|
|
| 920751 |
Balsamia SRC395 |
|
|
| 920763 |
Balsamia SRC868 |
|
|
| 920746 |
Choiromyces meandriformis RH691 Iowa |
68612
|
3058906
|
| 920725 |
Dingleya JT20122 Australia |
|
|
| 920731 |
Dingleya JT27860 Australia |
|
|
| 920738 |
Dinglyea JT27686 Australia |
|
|
| 920680 |
Dinglyea JT31036 Australia |
|
|
| 920758 |
Gymnohydnotrya australiana JT19760 |
|
3047852
|
| 920656 |
Gymnohydnotrya australiana OSC130601 |
|
3047852
|
| 920745 |
Helvella acetabulum MES215 |
|
3034256
|
| 920722 |
Helvella lacunosa MES218 |
44625
|
3058787
|
| 920681 |
Helvella lacunosa MES286 |
44625
|
3058787
|
| 920664 |
Labyrinthomyces JT25359 Australia |
|
|
| 920707 |
Labyrinthomyces JT28801 Australia |
|
|
| 920728 |
Leppia JT28813 Australia |
|
|
| 920757 |
Leppia holotype Australia |
|
|
| 920713 |
Nothojafnia cf thaxterii N10 Argentina |
|
|
| 920740 |
Reddellomyces JT27799 Australia |
|
|
| 920753 |
Reddellomyces JT4985 Australia |
|
|
| 920748 |
Reddellomyces JT6873 Australia |
|
|
| 920760 |
Tuber aestivum GB202 Italy |
59557
|
1454762
|
| 920693 |
Tuber aestivum OSC61974 Serbia |
59557
|
1454762
|
| 920686 |
Tuber anniae JT13209 Washington holotype |
|
3279228
|
| 920716 |
Tuber anniae JT22695 Oregon |
|
3279228
|
| 920771 |
Tuber asa M1828 Italy |
381831
|
10309018
|
| 920747 |
Tuber beyeleri JT32597 Oregon |
|
|
| 920734 |
Tuber borchii GB1 Italy |
42251
|
1454765
|
| 920774 |
Tuber borchii GB14 Italy |
42251
|
1454765
|
| 920723 |
Tuber californicum JT28058 California |
92708
|
3126315
|
| 920691 |
Tuber canaliculatum JT28215 New Jersey |
349718
|
3126184
|
| 920704 |
Tuber canaliculatum OSC59072 West Virginia |
349718
|
3126184
|
| 920674 |
Tuber cf borchii China |
|
|
| 920678 |
Tuber dryophilum GB35 Italy |
64384
|
3918243
|
| 920676 |
Tuber dryophilum GB37 Italy |
64384
|
3918243
|
| 920739 |
Tuber ferrugineum MA2721 Italy |
42250
|
3125014
|
| 920675 |
Tuber fulgens M2435 Italy |
554502
|
3121353
|
| 920709 |
Tuber gennadii BM667 Spain |
|
|
| 920692 |
Tuber gennadii JT9627 Spain paratype |
|
|
| 920766 |
Tuber gennadii M1904 Italy |
|
|
| 920714 |
Tuber gibbosum JT26632 Washington |
353052
|
3095001
|
| 920663 |
Tuber gibbosum JT30580 Oregon |
353052
|
3095001
|
| 920679 |
Tuber indicum A GB236 China |
|
|
| 920777 |
Tuber indicum A GB240 China |
|
|
| 920743 |
Tuber indicum B JT29410 Oregon |
|
|
| 920764 |
Tuber liaotongense OSC87602 China |
381835
|
3263489
|
| 920719 |
Tuber macrosporum JT13362 Italy |
92903
|
3094904
|
| 920696 |
Tuber magnatum GB12 Italy |
42249
|
1454769
|
| 920703 |
Tuber magnatum GB13 Italy |
42249
|
1454769
|
| 920660 |
Tuber malacodermum JT32319 Spain |
|
|
| 920673 |
Tuber melanosporum GB200 Italy |
39416
|
3096480
|
| 920690 |
Tuber mesentericum CW105 Sweden |
92904
|
3086647
|
| 920699 |
Tuber multimaculatum OSC62169 Spain paratype |
|
|
| 920752 |
Tuber nitidum BM105 Spain |
382148
|
3106649
|
| 920724 |
Tuber oregonense JT27985 Oregon paratype |
|
|
| 920754 |
Tuber oregonense JT30493 Oregon paratype |
|
|
| 920720 |
Tuber regimontanum ITCV909 Mexico holotype |
512386
|
|
| 920772 |
Tuber rufum GB213 Italy |
119233
|
3918833
|
| 920700 |
Tuber sancarloensis ITCV181 Mexico holotype |
|
|
| 920659 |
Tuber sancarloensis ITCV885 Mexico |
|
|
| 920736 |
Tuber sp JT9953 Quebec |
|
|
| 920729 |
Tuber sp ITCV884 Mexico |
|
|
| 920655 |
Tuber sp ITCV910 Mexico |
|
|
| 920769 |
Tuber sp JT32567 Mexico |
|
|
| 920761 |
Tuber sp RH73 Iowa |
|
|
| 920667 |
Tuber sp RH8270753 Iowa |
|
|
| 920701 |
Tuber sp TB10248 New York |
|
|
| 920671 |
Tuber sp1 K201 Japan |
|
|
| 920768 |
Tuber sp14 K186 Japan |
|
|
| 920730 |
Tuber sp2 K215 Japan |
|
|
| 920721 |
Tuber sp7 K408 Japan |
|
|
| 920711 |
Tuber sp8 K228 Japan |
|
|
| 920712 |
Tuber sp9 K213 Japan |
|
|
| 920727 |
Tuber sp9 K214 Japan |
|
|
| 920755 |
Tuber sphaerosporum JT12487 Oregon |
|
3148481
|
| 920654 |
Tuber spinoreticulatum U188 Maryland isotype |
|
3203493
|
| 920759 |
Underwoodia beatonii JT28375 Australia |
|
3217837
|
| 920687 |
Underwoodia beatonii JT28380 Australia |
|
3217837
|
| 920744 |
Underwoodia singeri mes161 Chile |
|
3203662
|