Table 1. Strains used in phylogenetic analysis, their origin and GenBank numbers.
| Strain1 |
Species |
Geography |
GenBank
|
|
|
|
|
|
|
ITS 1+2
|
act
|
cal
|
tef1
|
|
| G.J.S. 02-134 |
T. atroviride |
Sri Lanka |
DQ315466 |
|
|
DQ307547 |
| G.J.S. 02-135 |
T. atroviride |
Sri Lanka |
DQ315467 |
|
|
DQ307548 |
| G.J.S. 02-139 |
T. atroviride |
Sri Lanka |
DQ315463 |
|
|
DQ307546 |
| G.J.S. 02-96 |
T. atroviride |
Sri Lanka |
DQ315469 |
|
|
DQ307550 |
| G.J.S. 98-8 |
T. atroviride |
France |
DQ315462 |
|
|
DQ307545 |
| C.T.R. 85-57 |
T. austrokoningii |
U.S.A. (FL) |
DQ315469 |
DQ333551 |
DQ379003 |
DQ307564 |
| CBS 247.63 |
T. austrokoningii |
New Zealand |
DQ315470 |
DQ341183 |
DQ381953 |
DQ307568 |
| G.J.S. 00-73 |
T. austrokoningii |
Russia |
DQ315465 |
DQ341177 |
DQ379006 |
DQ307569 |
| G.J.S. 96-163 |
T. austrokoningii |
Taiwan |
DQ323408 |
DQ367709 |
DQ378997 |
DQ307565 |
| G.J.S. 99-146 |
T. austrokoningii (T) |
Australia (QL) |
DQ323423 |
DQ367716 |
DQ379001 |
DQ307561 |
| G.J.S. 99-147 |
T. austrokoningii |
Australia (QL) |
DQ323422 |
DQ333569 |
DQ379000 |
DQ307562 |
| G.J.S. 99-116 |
T. austrokoningii |
New Zealand |
DQ333546 |
DQ379011 |
DQ379004 |
|
| G.J.S. 97-3 |
T. caribbaeum (T) |
Guadeloupe |
DQ313131 |
DQ328607 |
DQ367688 |
DQ284977 |
| G.J.S. 98-43 |
T. caribbaeum |
Puerto Rico |
DQ313139 |
DQ328606 |
DQ367673 |
DQ284976 |
| DIS 320c |
T. caribbaeum var. aeqatoriale (T) |
Ecuador |
DQ323436 |
DQ328610 |
DQ367704 |
DQ289010 |
| G.J.S. 02-87 |
PS E |
Sri Lanka |
DQ315461 |
|
|
DQ307544 |
| G.J.S. 02-50 |
T. dingleyae (T) |
New Zealand |
DQ333548 |
DQ367718 |
DQ370461 |
DQ284978 |
| G.J.S. 99-105 |
T. dingleyae |
New Zealand |
DQ313151 |
|
DQ378998 |
AF348117 |
|
|
|
|
|
|
DQ289008 |
| G.J.S. 99-203 |
T. dingleyae |
New Zealand |
AY380899 |
AY376674 |
DQ367666 |
AF348111, AY376040 |
| G.J.S. 99-194 |
T. dorotheae |
Australia (VI) |
DQ313136 |
DQ328602 |
DQ367674 |
DQ284974 |
| G.J.S. 99-202 |
T. dorotheae (T) |
New Zealand |
DQ313144 |
DQ323454 |
DQ367706 |
DQ307536 |
| G.J.S. 99-97 |
T. dorotheae |
New Zealand |
DQ333547 |
DQ379009 |
|
DQ288990 |
| DIS 7 |
T. erinaceus |
Peru |
DQ109534 |
DQ111968 |
DQ122162 |
DQ109547 |
| DIS 8 |
T. erinaceus |
Peru |
DQ313147 |
DQ323450 |
DQ384930 |
DQ284970 |
| G.J.S. 96-13 |
T. intricatum |
Puerto Rico |
DQ381955 |
AY376683 |
DQ367679 |
AY376059 |
| G.J.S. 97-88 |
T. intricatum (T) |
Thailand |
AY380913 |
AY376684 |
DQ367680 |
AY376060 |
| ATCC 64262 |
T. koningii |
Hungary |
AY380903 |
AY376679 |
DQ367671 |
AY376046 |
| DAOM 167645 = CBS 979.70 |
T. koningii |
Netherlands |
DQ323410 |
DQ379007 |
DQ367682 |
DQ288994 |
| G.J.S. 00-156 |
T. koningii |
U.S.A. (PA) |
DQ323433 |
DQ379010 |
|
DQ288991 |
| G.J.S. 00-168 |
T. koningii |
U.S.A. (?MD) |
DQ323427 |
DQ333562 |
|
DQ307571 |
| G.J.S. 89-122 = CBS 989.97 = IMI 378801 |
T. koningii (T of H. koningii) |
U.S.A. (MD) |
AY380902 |
AY376678 |
DQ367693 |
AY376045 |
| G.J.S. 90-18 = CBS 988.97 |
T. koningii |
U.S.A. (WI) |
DQ323409 |
DQ341181 |
DQ370463 |
DQ289007 |
| G.J.S. 92-18 = CBS 987.97 |
T. koningii |
Canada |
DQ323435 |
DQ367712 |
DQ370458 |
DQ289005 |
| G.J.S. 96-118 |
T. koningii |
Netherlands |
DQ323444 |
DQ341178 |
DQ367683 |
DQ288996 |
| CBS 458.96 |
|
|
|
|
|
|
| G.J.S. 96-119 |
T. koningii |
Netherlands |
DQ323424 |
DQ341179 |
DQ367681 |
DQ289003 |
| CBS 460.96 |
|
|
|
|
|
|
| G.J.S. 96-120 |
T. koningii |
Netherlands |
DQ109536 |
DQ111972 |
DQ122168 |
DQ109548 |
| CBS 459.96 |
|
|
|
|
|
|
| G.J.S. 96-117 |
T. koningii (neotype) |
Netherlands |
Z79628 |
DQ341180 |
DQ367686 |
AF456909 |
| CBS 457.96 |
|
|
|
|
|
|
| DAOM 222105 |
T. koningiopsis |
Canada (ON) |
DQ313146 |
DQ379012 |
DQ367668 |
AY376042 |
| DIS 172ai = CBS 119067 = IMI 385811 |
T. koningiopsis |
Brazil |
DQ313138 |
DQ323453 |
DQ367675 |
DQ284972 |
| DIS 205f = CBS 119068 = IMI 385805 |
T. koningiopsis |
Ecuador |
DQ323419 |
DQ328609 |
DQ367698 |
DQ288993 |
| DIS 229d = CBS 119069 = IMI 391590 |
T. koningiopsis |
Ecuador |
DQ313143 |
DQ323452 |
DQ367676 |
DQ284971 |
| DIS 326h = CBS 119070 = IMI 393639 |
T. koningiopsis |
Ecuador |
DQ379015 |
DQ379008 |
DQ367695 |
DQ288997 |
| DIS 339c = CBS 119065 = IMI 391591 |
T. koningiopsis |
Ecuador |
DQ313142 |
DQ323447 |
DQ367677 |
DQ284968 |
| DIS 94c = CBS 119066 = IMI 391592 |
T. koningiopsis |
Peru |
DQ313130 |
DQ379014 |
DQ367678 |
DQ284967 |
| G.J.S. 01-07 |
T. koningiopsis |
Ecuador |
DQ313132 |
AY376676 |
DQ367669 |
AY376043 |
| G.J.S. 01-08 |
T. koningiopsis |
Ecuador |
— |
— |
— |
— |
| G.J.S. 01-09 |
T. koningiopsis |
Ecuador |
— |
— |
— |
— |
| G.J.S. 01-10 |
T. koningiopsis |
Ecuador |
— |
— |
— |
— |
| G.J.S. 01-11 |
T. koningiopsis |
Ecuador |
— |
— |
— |
— |
| G.J.S. 01-12 |
T. koningiopsis |
Ecuador |
— |
— |
— |
— |
| G.J.S. 04-10 |
T. koningiopsis |
Texas |
DQ323413 |
DQ341184 |
DQ367692 |
DQ284981 |
| G.J.S. 04-11 |
T. koningiopsis |
Texas |
DQ323421 |
DQ341182 |
DQ367687 |
DQ289009 |
| G.J.S. 04-373 |
T. koningiopsis |
Brazil |
DQ323437 |
DQ367713 |
DQ367703 |
DQ289006 |
| G.J.S. 04-379 |
T. koningiopsis |
Brazil |
DQ323439 |
DQ367719 |
DQ367702 |
DQ289001 |
| G.J.S. 04-378 |
T. koningiopsis |
Brazil |
DQ323432 |
DQ367714 |
DQ367699 |
DQ289011 |
| G.J.S. 04-375 |
T. koningiopsis |
Brazil |
DQ323411 |
DQ367711 |
DQ367697 |
DQ288989 |
| G.J.S. 04-376 |
T. koningiopsis |
Brazil |
DQ323425 |
DQ341176 |
DQ367696 |
DQ288992 |
| G.J.S. 04-377 |
T. koningiopsis |
Brazil |
DQ323416 |
DQ333552 |
DQ367701 |
DQ289002 |
| G.J.S. 04-374 |
T. koningiopsis |
Brazil |
DQ323412 |
DQ367709 |
DQ367700 |
DQ288995 |
| G.J.S. 91-6 |
T. koningiopsis |
Brazil |
DQ313135 |
DQ323446 |
DQ367705 |
DQ307539 |
| G.J.S. 91-7 |
T. koningiopsis |
Brazil |
DQ313137 |
DQ323449 |
DQ367689 |
DQ284969 |
| G.J.S. 95-175 |
T. koningiopsis |
U.S.A. (KY) |
AF456923 |
DQ323448 |
DQ367707 |
AF456910 |
| G.J.S. 96-47 |
T. koningiopsis |
Puerto Rico |
DQ313133 |
AY376677 |
DQ367670 |
AY376044 |
| G.J.S. 93-20 |
T. koningiopsis (T) |
Cuba |
DQ313140 |
DQ381954 |
DQ367694 |
DQ284966 |
| G.J.S. 97-273 = BBA 65450 |
T. koningiopsis |
Germany |
DQ109537 |
DQ111973 |
DQ122169 |
DQ109549 |
| DIS 172h |
T. ovalisporum |
Brazil |
AY380896 |
AY376670 |
DQ122167 |
AY387660 |
| DIS 172i |
T. ovalisporum |
Brazil |
DQ323438 |
DQ328611 |
— |
DQ288999 |
| DIS 203c |
T. ovalisporum |
Brazil |
DQ315458 |
DQ328608 |
DQ378996 |
DQ307540 |
| DIS 70a |
T. ovalisporum (T) |
Ecuador |
AY380897 |
AY376671 |
DQ379005 |
AY376037 |
| DAOM 165782 |
T. petersenii |
U.S.A. (NC) |
DQ313149 |
DQ328604 |
DQ367690 |
DQ289000 |
| G.J.S. 04-164 |
T. petersenii |
U.S.A. (TN) |
DQ323442 |
DQ333566 |
DQ367684 |
DQ289004 |
| G.J.S. 04-351 |
T. petersenii |
U.S.A. (TN) |
DQ323440 |
DQ333568 |
— |
DQ284979 |
| G.J.S. 04-355 |
T. petersenii (T) |
U.S.A. (TN) |
DQ323441 |
DQ333570 |
DQ367691 |
DQ284980 |
| G.J.S. 90-86 |
T. petersenii |
U.S.A. (NC) |
DQ313153 |
DQ328605 |
DQ367708 |
DQ284975 |
| G.J.S. 91-99 |
T. petersenii |
U.S.A. (VA) |
DQ313134 |
AY376673 |
— |
AY376039 |
| G.J.S. 98-139 |
T. petersenii |
France |
DQ323426 |
DQ379013 |
DQ378999 |
DQ288998 |
| G.J.S. 98-140 |
T. petersenii |
France |
DQ313148 |
AY376675 |
DQ367667 |
AY376041 |
| G.J.S. 99-48 |
T. petersenii |
Costa Rica |
AY380898 |
AY376672 |
DQ367665 |
AY376038 |
| G.J.S. 04-157 |
T. rogersonii |
U.S.A. (TN) |
DQ323415 |
DQ333565 |
DQ370454 |
DQ307558 |
| G.J.S. 04-158 |
T. rogersonii (T) |
U.S.A. (TN) |
DQ323434 |
DQ333567 |
DQ370460 |
DQ307563 |
| G.J.S. 90-108 |
T. rogersonii |
U.S.A. (MD) |
DQ333550 |
DQ333561 |
DQ370448 |
DQ307570 |
| G.J.S. 90-125 |
T. rogersonii |
U.S.A. (NC) |
DQ323417 |
DQ341175 |
DQ370453 |
DQ307567 |
| G.J.S. 90-78 |
T. rogersonii |
U.S.A. (NC) |
DQ333549 |
DQ333558 |
DQ370457 |
DQ307556 |
| G.J.S. 90-79 |
T. rogersonii |
U.S.A. (NC) |
DQ381956 |
DQ333563 |
DQ370451 |
DQ381959 |
| G.J.S. 90-93 |
T. rogersonii |
U.S.A. (NC) |
DQ313154 |
DQ333560 |
DQ370450 |
DQ307559 |
| G.J.S. 92-116 |
T. rogersonii |
U.S.A. (MD) |
DQ313150 |
DQ333554 |
DQ370455 |
DQ307557 |
| G.J.S. 94-115 |
T. rogersonii |
U.S.A. (MO) |
Z95927 |
DQ333555 |
DQ370452 |
AF456906 |
| G.J.S. 95-217 |
T. rogersonii |
Austria |
DQ323445 |
DQ333553 |
DQ370462 |
DQ307566 |
| G.J.S. 98-75 |
T. rogersonii |
U.S.A. (NJ) |
DQ323443 |
DQ333556 |
DQ370449 |
DQ307560 |
| G.J.S. 98-77 |
T. rogersonii |
U.S.A. (NJ) |
DQ323414 |
DQ333559 |
|
DQ307572 |
| G.J.S. 98-82 |
T. rogersonii |
U.S.A. (NJ) |
AY380910 |
AY376682 |
DQ367672 |
AY376055 |
| G.J.S. 96-32 |
T. stilbohypoxyli |
Puerto Rico |
AY380915 |
AY376686 |
DQ122160 |
AY376062 |
| G.J.S. 96-30 = CBS 992.97 |
T. stilbohypoxyli (T) |
Puerto Rico |
DQ109533 |
DQ111967 |
DQ122161 |
DQ109546 |
| G.J.S. 96-30A |
T. stilbohypoxyli |
Puerto Rico |
AY380916 |
AY376687 |
- |
AY376063 |
| G.J.S. 96-42A |
T. stilbohypoxyli |
Puerto Rico |
AY380914 |
AY376685 |
- |
AY376061 |
| G.J.S. 96-43 |
T. stilbohypoxyli |
Puerto Rico |
- |
- |
- |
- |
| G.J.S. 95-93 |
T. taiwanense (T) |
Taiwan |
DQ313141 |
DQ323455 |
DQ367685 |
DQ284973 |
| C.P.K. 9842 |
T. viride VB |
Sweden |
- |
- |
- |
- |
| C.P.K. 9652 |
T. viride VB |
Czech Republic |
- |
- |
- |
- |
| ATCC 28020 |
T. viride VB |
U.S.A. (WA) |
DQ109535 |
DQ111970 |
DQ122164 |
AY937449 |
| CBS 101526 |
T. viride VB |
Netherlands |
X93979 |
- |
- |
AY376053 |
| C.P.K. 1001 |
T. viride VB |
Russia |
- |
- |
- |
- |
| C.P.K. 1002 |
T. viride VB |
Russia |
- |
- |
- |
- |
| C.P.K. 1006 |
T. viride VB |
Russia |
- |
- |
- |
- |
| C.P.K. 1007 |
T. viride VB |
Russia |
- |
- |
- |
- |
| C.P.K. 1008 |
T. viride VB |
Russia |
- |
- |
- |
- |
| C.P.K. 1009 |
T. viride VB |
Russia |
- |
- |
- |
- |
| G.J.S. 04-369 |
T. viride VB |
Austria |
DQ323430 |
- |
- |
DQ307553 |
| G.J.S. 04-370 |
T. viride VB |
Austria |
DQ323429 |
- |
- |
DQ307554 |
| G.J.S. 04-371 |
T. viride VB |
France |
DQ323431 |
- |
- |
DQ307552 |
| G.J.S. 04-372 |
T. viride VB |
Czech Rep. |
DQ323428 |
- |
- |
DQ307555 |
| G.J.S. 90-95 = CBS 120066 |
T. viride VB |
U.S.A. (NC) |
DQ315455 |
- |
- |
DQ307535 |
| G.J.S. 92-14 |
T. viride VB |
New Zealand |
DQ313155 |
- |
- |
DQ288988 |
| G.J.S. 92-15 |
T. viride VB |
Canada |
DQ315452 |
- |
- |
DQ307537 |
| G.J.S. 97-271 = BBA 70239 = ITB 8212 |
T. viride VB |
Denmark |
DQ315456 |
- |
- |
AF348116 |
| G.J.S. 99-16 = FP 5563 |
T. viride VB |
Japan? |
DQ315460 |
- |
- |
DQ307543 |
| TR 2 = ATCC 18652 = CBS 240.63 |
T. viride VB |
U.S.A. (WA) |
DQ315457 |
- |
- |
DQ307538 |
| TR 21 = ATCC 28038 |
T. viride VB |
U.S.A. (VA) |
AY380909 |
AY376681 |
DQ122165 |
AY376054 |
| G.J.S. 04-40 |
T. viride VB? |
Brazil |
DQ315454 |
- |
- |
DQ307534 |
| 301rufa2 = C.P.K. 1999 |
T. viride VB |
Austria |
- |
- |
- |
- |
| 19d2 = G.J.S. 89-127 |
T. viride VB |
U.S.A. (NC) |
- |
- |
- |
- |
| 292rufa2 = C.P.K. 1997 |
T. viride VB |
Czech Republic |
- |
- |
- |
- |
| 6138i2 = C.P.K. 947 |
T. viride VD |
Austria |
- |
- |
- |
- |
| 7123412 = C.P.K. 2341 |
T. viride VD |
Italy (Sardinia) |
- |
- |
- |
- |
| ATCC 20898 |
T. viride VD |
U.S.A. (NY) |
DQ315434 |
- |
- |
DQ307518 |
| ATCC 32630 |
T. viride VD |
Sweden |
DQ315445 |
- |
- |
DQ307526 |
| CBS 274.79 |
T. viride VD |
Austria |
DQ315428 |
- |
- |
DQ307513 |
| CBS 333.72 |
T. viride VD |
Netherlands |
DQ315441 |
- |
- |
DQ307523 |
| CBS 438.95 |
T. viride VD |
U.K. |
DQ315438 |
- |
- |
DQ307522 |
| CBS 439.95 |
T. viride VD |
Northern Ireland |
DQ315439 |
- |
- |
AY937413 |
| 2732 |
T. viride VD |
U.K. |
|
- |
- |
- |
| C.P.K. 998 |
T. viride VD |
Russia |
|
- |
- |
- |
| C.P.K. 999 |
T. viride VD |
Russia |
|
- |
- |
- |
| 2462 |
T. viride VD |
U.K. |
|
- |
- |
- |
| 2342 |
T. viride VD |
Germany |
- |
- |
- |
- |
| G.J.S. 00-67 |
PS F T. viride VD |
U.S.A. (WV) |
DQ315418 |
- |
- |
DQ307502 |
| G.J.S. 89-142 = CBS 120065 |
T. viride VD |
U.S.A. (NC) |
DQ109532 |
DQ111965 |
DQ122157 |
AY376049 |
| G.J.S. 92-11 |
T. viride VD |
New Zealand |
DQ315422 |
- |
- |
DQ307524 |
| G.J.S. 94-10 |
PS F T. viride VD |
Taiwan |
DQ315420 |
- |
- |
DQ307506 |
| G.J.S. 94-11 |
PS F T. viride VD |
Taiwan |
DQ313156 |
- |
- |
DQ307508 |
| G.J.S. 94-118 |
T. viride VD |
France |
DQ315424 |
- |
- |
DQ307510 |
| G.J.S. 94-9 |
PS F T. viride VD |
Taiwan |
DQ315421 |
- |
- |
DQ307507 |
| G.J.S. 97-243 |
PS F T. viride VD |
U.S.A. (GA) |
DQ315419 |
- |
- |
DQ307503 |
| G.J.S. 97-272 = BBA 66069 |
T. viride VD |
Germany |
DQ315429 |
- |
- |
DQ307504 |
| G.J.S. 97-274 = BBA 68432 |
T. viride VD |
Russia |
DQ315440 |
- |
- |
DQ307505 |
| G.J.S. 98-129 |
T. viride VD |
France |
AY737773 |
- |
- |
DQ307542 |
| G.J.S. 98-182 = W.J. 1223 = CBS 120067 |
T. viride VD |
Austria |
DQ315425 |
- |
- |
DQ307511 |
| G.J.S. 98-86 |
T. viride VD |
Mexico |
DQ315423 |
- |
- |
DQ307509 |
| G.J.S. 99-10 = NR 5510 |
T. viride VD |
Czech Rep. |
DQ315430 |
- |
- |
DQ307514 |
| G.J.S. 99-128 |
T. viride VD |
Australia (VI) |
DQ315431 |
- |
- |
DQ307515 |
| G.J.S. 99-142 |
T. viride VD |
Australia (VI) |
DQ315427 |
- |
- |
DQ307512 |
| G.J.S. 99-175 |
T. viride VD |
Australia (VI) |
DQ315437 |
- |
- |
DQ307521 |
| G.J.S. 99-8 = NR 5541 |
T. viride VD |
Japan |
DQ315433 |
- |
- |
DQ307517 |
| G.J.S. 99-18 = FP 5564 |
T. viride VD |
Japan? |
DQ315435 |
- |
- |
DQ307519 |
| TR 4 |
T. viride VD |
U.S.A. (OR) |
DQ315436 |
- |
- |
DQ307520 |
| TR 5 |
T. viride VD |
U.S.A. (OR) |
DQ315443 |
- |
- |
DQ307525 |
| TR 6 |
T. viride VD |
U.S.A. (OR) |
DQ315444 |
- |
- |
AY376050 |
| CBS 433.34 |
T. viride VD, T of Eidamia viridescens |
U.K. |
AF456922 |
- |
- |
AF456905, AY376048 |
| G.J.S. 04-09 |
PS C |
U.S.A. (TX) |
DQ315459 |
- |
- |
DQ307541 |
| G.J.S. 92-60 |
PS C |
Australia |
DQ315448 |
- |
- |
DQ307529 |
| C.P.K. 1011 |
PS C |
Central Russia |
- |
- |
- |
DQ641674 |
| C.P.K. 1010 |
PS C |
Central Russia |
- |
- |
- |
DQ641673 |
| G.J.S. 02-54 |
H. vinosa |
New Zealand |
DQ315447 |
- |
- |
DQ307528 |
| G.J.S. 99-156 |
H. vinosa |
U.S.A. (TX) |
DQ315446 |
- |
- |
DQ307527 |
| G.J.S. 99-158 |
H. vinosa |
New Zealand |
AY380904 |
AY376680 |
DQ122158 |
AY376047 |
| DIS 217i |
PS B |
Ecuador |
DQ323420 |
- |
- |
DQ307549 |
| G.J.S. 04-353 |
PS B |
U.S.A. (TN) |
DQ323418 |
- |
- |
DQ307551 |
| G.J.S. 90-97 |
PS B |
U.S.A. (NC) |
DQ315449 |
- |
- |
DQ307530 |
| G.J.S. 99-127 |
PS A |
Australia (VI) |
DQ315453 |
- |
- |
DQ307533 |
| G.J.S. 99-83 |
PS A |
Australia (VI) |
AF456921 |
DQ111966, DQ333557 |
DQ122159 |
AF348118 |
| G.J.S. 99-191 |
PS A |
Australia (VI) |
DQ315451 |
- |
- |
DQ307532 |
| G.J.S. 99-86 |
PS A |
Australia (VI) |
DQ315432 |
- |
- |
DQ307516 |
| G.J.S. 99-204 |
PS A |
New Zealand |
DQ315450 |
- |
- |
DQ307531 |
| 371Tsp27Bnov = J. B. ID424 |
PS A |
- |
- |
- |
- |
- |
| 230T.spnov.278 = J. B. ID422 |
PS A |
- |
- |
- |
- |
- |
| G.J.S. 98-170 |
T. hamatum |
New Zealand |
DQ109530 |
DQ111963 |
DQ122155 |
DQ109544 |
| DAOM 167057 |
T. hamatum (ex-neotype) |
Canada |
Z48816 |
DQ111962 |
DQ122154 |
AF456911, AY750893 |
| DAOM 166162 |
T. hamatum |
U.S.A. (NC) |
DQ083016 |
DQ111961 |
DQ122153 |
AY750887 |
| G.J.S. 04-217 |
T. asperellum |
Peru |
DQ381957 |
DQ333564 |
DQ379002 |
DQ381958 |
Tr 3 = CBS 433.97
|
T. asperellum
|
U.S.A. (MD)
|
X93981
|
DQ111974
|
DQ122170
|
AY376058
|
|
1 Abbreviations of culture collections and collectors: ATCC = American Type Culture Collection, Manassas, VA, U.S.A., BBA = Biologisches Bundesanstalt, Berlin, Germany; CBS = Centraalbureau voor Schimmelcultures, Utrecht, The Netherlands; C.P.K. = Collection of C.P. Kubicek, Technische Universität, Abteilung für Mikrobielle Biochemie, Vienna; C.T.R., G.J.S., TR = Culture collection of the United States Department of Agriculture, Systematic Botany and Mycology Lab, Beltsville, MD U.S.A. (BPI); DAOM = Canadian Collection of Fungal Cultures, Ottawa, Canada; DIS refers to CABI-Bioscience, Ascot, cultures held by G.J.S; FP = unknown provenance, received from Toru Okuda, Nippon Roche Corp., Tokyo, Japan; IBT = Culture Collection of Fungi, Technical University of Denmark, Lyngby, Denmark; IMI = CABI-Bioscience, Egham, U.K.; J.B. = John Bissett, Agriculture and Agri-Food, Eastern Cereal and Oilseed Research Centre, Ottawa, Canada; W.J. = Culture collection of Walter Jaklitsch, Technische Universität, Abteilung für Mikrobielle Biochemie, Vienna; NR = Nippon Roche Corp. Tokyo, Japan.
2 Collection of C.P. Kubicek, Technische Universität, Abteilung für Mikrobielle Biochemie, Vienna.
Table 2. Principal Components Analysis Eigenvalues
|
Axis 1
|
Axis 2
|
Axis 3
|
Axis 4
|
Axis 5
|
Axis 6
|
|
| Eigenvalues |
8.041 |
4.125 |
3.038 |
1.854 |
1.814 |
1.536 |
| Percentage |
26.803 |
13.750 |
10.128 |
6.179 |
6.048 |
5.120 |
Cumulative Percentage
|
26.803
|
40.554
|
50.682
|
56.861
|
62.909
|
68.028
|
|
Table 3. Continuous characters, geographic distribution and colony phenotype of the Trichoderma species discussed.
Species
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
T. austrokoningii |
T. caribbaeum var. caribbaeum |
T. caribbaeum var. aequatoriale |
T. dingleyeae |
T. dorotheae |
T. intricatum |
T. koningii |
T. koningiopsis |
T. ovalisporum |
T. petersenii |
T. rogersonii |
T. stilbohypoxyli |
T. taiwanense |
|
22
|
22
|
12,4
|
32
|
32
|
22
|
112
|
232
|
42
|
82
|
132
|
112
|
12
|
Geography1
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Australia (Queensland), also New Zealand, Taiwan, U.S.A. (Florida), Russia
|
Puerto Rico, Guadeloupe
|
Ecuador
|
New Zealand
|
Australia (Victoria), New Zealand
|
Puerto Rico, Thailand
|
Eastern N. America, Europe
|
Probably pantropical, also Eastern North America and Europe
|
Brazil (Amazonia), Ecuador
|
Europe, Eastern North America and Central America
|
Eastern North America, Europe
|
Central & South America, West Africa, U.K.
|
Taiwan
|
Conidium characters
|
|
|
|
|
|
|
|
|
|
|
|
|
|
| Conidium L1 (µm) |
(2.5-)3.0-3.7(-4.2) |
(3.5-)3.7-4.5(-4.7) |
(3.0-)3.5-3.7(-4.0)7 |
(3.2-)3.7-4.5(-6.2) |
(3.0-)3.5-4.2(-5.0) |
(3.0-)3.5-4.0(-4.5) |
(3.0-)3.7-4.5(-4.7) |
(3.0-)3.5-4.5(-6.2) |
(2.7-)3.2-4.0(-4.2) |
(2.5-)3.5-4.5(-5.5) |
(2.7-)3.5-4.5(-5.5) |
(2.5-)3.0-4.0(-5.0) |
(3.5-)3.7-4.2(-4.7) |
95% CI
|
3.3-3.4
|
4.0-4.1
|
3.5-3.7
|
4.2-4.3
|
3.8-3.9
|
3.6-3.7
|
4.1-4.2
|
3.9-4.0 x
|
3.5-3.6
|
3.9-4.0
|
4.0-4.1
|
3.5-3.6
|
3.9-4.1
|
| Conidium W1 (µm) |
(2.0-)2.2-2.7(-3.2) |
(2.2-)2.5-3.2(-3.5) |
(2.0-)2.2-2.7(-3.0)7 |
(2.5-)3.0-3.5(-3.7) |
(2.5-)2.7-3.2(-3.7) |
(2.5-)2.7-3.2(-3.5) |
(2.0-)2.5-3.0(-3.5) |
(2.0-)2.5-3.0(-3.5) |
(2.5-)3.0-3.2(-3.7) |
(2.2-)2.7-3.0(-3.5) |
(2.2-)2.5-3.2(-4.2) |
(1.7-)2.5-3.0(-3.5) |
(2.5-)2.7-3.2(-3.5) |
95% CI
|
2.5-2.6
|
2.8-3.0
|
2.4-2.6
|
3.1-3.2
|
3.0-3.1
|
3.0-3.1
|
2.6-2.7
|
2.6-2.7
|
3.0-3.1
|
2.8-2.9
|
2.8-2.9
|
2.6-2.7
|
2.8-3.1
|
| Conidium L/W1 |
(0.9-)1.2-1.6(-1.7) |
(1.0-)1.2-1.6(-1.9) |
(1.2-)1.3-1.5(-1.9)7 |
(1.1-)1.2-1.6(-2.1) |
(1.1-)1.2-1.4(-1.6) |
(0.9-)1.1-1.3(-1.5) |
(1.3-)1.5-1.7(-2.0) |
(1.0-)1.3-1.8(-2.5) |
1.1-1.3(-1.6) |
(1.0-)1.3-1.5(-1.8) |
(0.8-)1.3-1.7(-2.2) |
(0.9-)1.1-1.5(-1.9) |
(1.0-)1.2-1.6(-1.8) |
95% CI
|
1.3-1.4
|
1.4-1.5
|
1.4-1.5
|
1.3-1.4
|
1.2-1.3
|
1.2-1.3
|
1.5-1.6
|
1.49-1.52
|
1.15-1.19
|
1.35-1.39
|
1.4-1.5
|
1.3-1.4
|
1.3-1.5
|
Phialide characters
|
|
|
|
|
|
|
|
|
|
|
|
|
|
| Phialide length1 |
(5.2-)7.0-10.5(-13) |
3.5-9.0(-15.0) |
(5.5-)6.0-10.2(-14.0)7 |
(4.2-)6.7-11.2(-15.0) |
(4.7-)6.5-10.0(-13.7) |
(5.0-)5.7-8.2(-11.5) |
(4.2-)6.2-10.0(-15.5) |
(3.5-)5.5-9.2(-16.0) |
(4.0-)5.7-9.2(-13.5) |
(4.0-)6.2-10.2(-16.5) |
(3.5-)6.0-10.0(-17.5) |
(4.2-)5.5-9.0(-12.5) |
(5.2-)7.0-10.2(-13.2) |
95% CI
|
8.3-9.2
|
5.2-6.2
|
7.4-9.0
|
8.5-9.5
|
7.9-8.7
|
6.6-7.2
|
7.9-8.3
|
7.2-7.5
|
7.2-7/8
|
8.1-8.6
|
7.8-8.3
|
7.1-7.5
|
8.0-9.2
|
| Phialide at widest point1 |
(2.0-)2.5-3.0(-3.5) |
(2.0-)2.5-3.2(-4.0) |
(2.2-)2.5-3.2(-3.7)7 |
(1.7-)2.2-3.2(-4.0) |
(1.7-)2.2-3.0(-3.5) |
(2.2-)3.0-3.7(-4.5) |
(2.0-)2.7-3.5(-4.2) |
(2.0-)2.7-3.5(-4.5) |
(2.0-)2.5-3.5(-4.2) |
(2.0-)2.5-3.5(-4.0) |
(2.0-)2.5-3.5(-4.0) |
(2.0-)2.7-3.5(-4.5) |
(2.2-)2.5-3.2(-3.5) |
95% CI
|
2.6-2.8
|
2.8-3.0
|
2.8-3.1
|
2.7-2.9
|
2.6-2.8
|
3.2-3.4
|
3.0-3.1
|
3.1-3.2
|
3.0-3.2
|
2.9-3.0
|
3.0-3.1
|
3.1-3.2
|
2.6-2.9
|
| Phialide base1 |
(1.5-)1.5-2.2(-3.2) |
(1.2-)1.5-2.2(-2.5) |
1.5-2.2(-2.5) |
(1.2-)1.7-2.5(-4.0)7 |
(1.2-)1.5-1.5(-2.7) |
(1.2-)1.5-2.5(-3.0) |
(1.0-)1.5-2.2(-3.0) |
(1.0-)1.5-2.2(-3.7) |
(1.0-)1.5-2.5(-3.2) |
(1.0-)1.5-2.5(-3.5) |
(1.2-)1.7-2.5(-3.2) |
(1.2-)1.7-2.5(-3.5) |
(1.5-)1.8-2.5(-2.5) |
95% CI
|
1.8-2.0
|
2.8-3.0
|
1.8-2.0
|
2.0-2.2
|
1.9-2.0
|
1.9-2.2
|
1.9-2.0
|
1.9-2.0
|
1.9-2.1
|
2.9-3.0
|
2.05-2.13
|
2.0-2.1
|
2.0-2.7
|
| L/W of Phialide1 |
(1.8-)2.4-3.7(-5.4) |
1.2-3.1(-6.6) |
(1.6-)1.9-3.9(-5.7)7 |
(1.8-)2.5-4.5(-6.3) |
(1.5-)2.3-4.1(-6.8) |
(1.4-)1.6-2.8(-4.0) |
(1.2-)1.8-3.6(-6.6) |
(1.0-)1.7-3.3(-6.0) |
(1.2-)1.7-3.3(-6.8) |
(1.3-)2.1-3.9(-6.9) |
(1.0-)2.7-3.7(-8.3) |
(1.2-)1.4-3.1(-5.6) µm |
(2.1-)2.7-4.0(-5.1) |
95% CI
|
3.1-3.6
|
1.8-2.4
|
2.5-3.3
|
3.3-3.7
|
3.0-3.3
|
2.0-2.3
|
2.6-2.8
|
2.4-2.5
|
1.6-3.4
|
2.8-3.0
|
2.6-2.8
|
2.3-2.4 µm
|
2.9-3.5
|
| Phialide supporting cell1 |
(1.5-)2.0-3.0(-3.5) |
(1.5-)2.0-3.0(-3.7) |
(1.7-)2.0-2.7(-3.0)7 |
(1.7-)2.2-4.2(-6.5) |
(1.5-)1.7-5.0(-9.5) |
(2.0-)2.5-3.5(-4.0) |
(1.5-)2.2-3.0(-4.0) |
(1.7-)2.2-3.5(-7.7) |
(1.7-)2.2-4.0(-6.2) |
(1.5-)1.7-2.2(-8.0) |
(1.5-)2.5-3.2(-4.0) |
(1.6-)2.2-3.2(-5.0) µm |
(2.0-)2.0-3.0(-3.5) |
95% CI
|
2.4-2.6
|
2.4-2.6
|
2.2-2.5
|
3.1-3.5
|
3.0-3.7
|
2.9-3.1
|
2.6-2.7
|
2.8-2.9
|
3.0-3.3
|
2.9-3.1
|
2.7-2.8
|
2.7-2.8 µm
|
2.4-2.7
|
Ascus characters
|
|
|
|
|
|
|
|
|
|
|
|
|
|
| Ascus length |
(65-)75-90(-100) |
65-75(-85) |
|
(45-)66-95(-105) |
ca. 703 |
(56-)65-77(-84) |
(56-)62-72(-80) |
(60-)65-75(-80) |
|
(55-)67-85(-105) |
(51-)69-89(-128) |
(65-)72-88(-98) µm |
(60-)63-73(-78) |
95% CI
|
81-85
|
70-75
|
|
76-85
|
|
70-73
|
66-70
|
69-72
|
|
75-78
|
78-80
|
79-82 µm
|
63-72
|
| Ascus width |
(3.2-)4.2-5.7(-6.5) |
(3.5-)4.5-6.0(-7.0) |
|
(3.0-)4.0-6.0(-7.7) |
4.5-5.53 |
(2.7-)4.0-5.2(-6.2) |
(4.2-)4.5-6.2(-7.0) |
(3.5-)4.0-6.0(-7.5) |
|
(3.0-)4.5-6.2(-8.0) |
(3.5-)4.2-6.2(-8.2) |
(4.0-)5.0-6.5(-7.7) µm |
(3.2-)3.7-5.0(-5.2) |
95% CI
|
4.8-5.2
|
4.9-5.4
|
|
4.8-5.4
|
|
4.4-4.8
|
5.2-5.8
|
4.7-5.3
|
|
5.2-5.4
|
5.3-5.5
|
5.5-5.8 µm
|
3.7-4.8
|
Ascospore characters
|
|
|
|
|
|
|
|
|
|
|
|
|
|
| Distal part-ascospore length |
(3.2-)3.5-4.2(-5.0) |
(2.7-)3.2-4.2(-4.7) |
|
(2.0-)3.0-4.2(-5.0) |
3.0-4.5(-6.5) |
(2.5-)3.0-3.7(-4.0) |
(2.7-)3.5-4.5(-4.6) |
(2.7-)3.2-4.0(-4.5) |
|
(2.2-)3.5-4.5(-5.5) |
(3.0-)3.5-4.5(-5.2) |
(3.2-)3.5-4.5(-5.0) µm |
(2.7-)3.0-4.0(-4.7) |
95% CI
|
3.8-3.9
|
3.7-3.8
|
|
3.6-3.9
|
3.6-4.0
|
3.2-3.4
|
3.9-4.2
|
3.7-3.8
|
|
3.8-4.0
|
3.9-4.0
|
3.9-4.1 µm
|
3.2-3.7
|
| Distal part-ascospore width |
(2.7-)3.2-3.7(-4.2) |
(2.5-)3.0-3.5(-4.0) |
|
(1.7-)2.5-4.0(-4.5) |
(2.2-)2.7-3.7(-5.2) |
(2.2-)2.7-3.5(-3.7) |
(2.5-)3.0-3.5(-4.0) |
(2.0-)2.7-3.5(-4.0) |
|
(2.0-)3.2-4.2(-5.0) |
(2.5-)3.2-4.0(-5.0) |
(2.7-)3.2-3.7(-4.2) µm |
(2.5-)3.0-3.5(-4.0) |
95% CI
|
3.5-3.6
|
3.2-3.4
|
|
3.1-3.4
|
2.8-3.8
|
3.0-3.2
|
3.2-3.4
|
3.1-3.3
|
|
3.7-3.8
|
3.6-3.7
|
3.4-3.5 µm
|
3.1-3.3
|
| Proximal part-ascospore length |
(3.2-)2.5-4.5(-5.0) |
(2.7-)3.5-4.7(-5.2) |
|
(2.5-)3.0-4.7(-6.5) |
(3.5-)3.7-5.0(-6.5) |
(2.5-)2.5-4.2(-4.5) |
(3.2-)3.7-4.5(-5.2) |
(3.0-)3.7-4.7(-6.0) |
|
(2.7-)3.7-5.0(-6.5) |
(3-)4-5(-6) |
(3.2-)4.0-5.0(-6.0) µm |
(3.0-)3.5-4.5(-5.2) |
95% CI
|
3.9-4.1
|
4.1-4.4
|
|
3.8-4.1
|
4.2-4.6
|
3.6-3.9
|
4.0-4.3
|
4.1-4.4
|
|
4.4-4.6
|
4.4-4.5
|
4.5-4.7 µm
|
3.7-4.1
|
| Proximal-part width |
(2.7-)3.0-3.5(-4.2) |
(2.5-)2.7-3.2(-3.7) |
|
(1.7-)2.5-3.5(-4.2) |
2.5-3.5(-4.2) |
(2.2-)2.5-3.0(-3.2) |
(2.2-)2.5-3.0(-3.7) |
(1.7-)2.2-3.0(-3.5) |
|
(2.2-)2.7-3.7(-5.2) |
(2.0-)2.7-3.5(-4.0) |
(2.2-)2.7-3.2(-4.0) µm |
(2.2-)2.5-3.2 |
95% CI
|
3.1-3.2
|
3.0-3.1
|
|
2.9-3.2
|
2.9-3.1
|
2.7-2.8
|
2.6-2.9
|
2.6-2.8
|
|
3.2-3.3
|
3.1-3.2
|
3.0-3.1 µm
|
2.7-2.9
|
Colony radius and slope of growth curve on PDA after 72h (mm)
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Radius 15 °C1
|
65
|
13-155
|
7-104
|
11-175
|
16-175
|
8-105
|
(12-)15-19
|
(8-)9-17(-30)
|
(5-)6-13
|
(10-)11-13(-14)
|
(8-)8.5-11(-13)
|
(2-)3-13(-17)
|
10-125
|
Radius 20 °C1
|
18-205
|
365
|
25-424
|
22-375
|
31-425
|
25-425
|
(26-)31-38
|
(23-)30-40(-42)
|
(31-)31-37
|
(19-)23-29
|
(23-)24-28(-31)
|
(11-)15-39(-43)
|
21-295
|
Radius 25 °C1
|
33-355
|
53-565
|
41-504
|
24-295
|
39-415
|
40-506
|
(41-)49-58
|
(45-)51-63(-67)
|
(38-)43-66
|
(26-)33-45
|
(38-)40-48(-50)
|
(36-)38-54(-64)
|
43-465
|
Radius 30 °C1
|
(36-375
|
54-585
|
9-164
|
1-35
|
20-285
|
9-165
|
(35-)45-61
|
(20-)52-72
|
48-70
|
(25-)32-48
|
(40-)40-52(-60)
|
36-54(-69)
|
42-435
|
Radius 35 °C1
|
0.0-1.05
|
1-25
|
0-14
|
15
|
1-25
|
0-15
|
(0-)1-2(-3)
|
(0-)2-10(-12)
|
5-14
|
0-4
|
(0-)0.7-4(-5)
|
0-3
|
0
|
slope PDA 15 °C1
|
0.113-0.1355
|
0.204-0.2225
|
0.24
|
0.209-0.2635
|
0.272-0.3185
|
0.125-0.1695
|
(0.225-)0.255-0.311(-0.314)
|
(0.053-)0.163-0.281(-0.310)
|
0.125-0.1855
|
(0.178-) 0.187-0.223(-0.232)
|
(0.138-)0.151-0.191(-0.210)
|
(0.049-)0.092-0.222(-0.242)
|
0.163-0.2165
|
Species
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
T. austrokoningii |
T. caribbaeum var. caribbaeum |
T. caribbaeum var. aequatoriale |
T. dingleyeae |
T. dorotheae |
T. intricatum |
T. koningii |
T. koningiopsis |
T. ovalisporum |
T. petersenii |
T. rogersonii |
T. stilbohypoxyli |
T. taiwanense |
|
22
|
22
|
12,4
|
32
|
32
|
22
|
112
|
232
|
42
|
82
|
132
|
112
|
12
|
slope PDA 20 °C1
|
0.329-0.3365
|
0.580-0.5995
|
0.475-0.6254
|
0.353-0.4285
|
0.493-0.5545
|
0.329-0.4925
|
(0.492-)0.540-0.610
|
(0.272-)0.503-0.676
|
0.522-0.6545
|
(0.340-)0.396-0.475(-0.468)
|
(0.371-)0.414-0.504(-0.540)
|
(0.271)0.340-0.683
|
0.395-0.4955
|
slope PDA 25 °C1
|
0.522-0.5405
|
0.603-0.6085
|
0.695-0.7214
|
0.332-0.3895
|
0.610-0.6175
|
0.608-0.6245
|
(0.547-)0.544-0.706(-0.829)
|
(0.558-)0.550-0.742(-0.815)
|
0.551-0.8565
|
(0.562-)0.586-0.622(-0.629)
|
(0.585-)0.602-0.674(-0.724)
|
(0.631-)0.673-0.823(-0.848)
|
0.625-0.6335
|
slope PDA 30 °C1
|
0.055-0.5395
|
0.593-0.6015
|
0.108-0.1504
|
5
|
0.261-0.4865
|
0.547-0.6315
|
(0.540-)0.556-0.606(-0.618)
|
(0.269-)0455-0.735(-0.807)
|
0.519-0.7935
|
(0.214-)0.362-0.648
|
(0.550-)0.587-0.629(-0.641)
|
(0.650-)0.659-0.749(-0.782)
|
0.592-0.6295
|
slope PDA 35 °C1
|
0
|
0
|
0
|
0
|
0
|
0
|
0
|
(0.003-0.063(-0.111)
|
0.007-0.333
|
0
|
0
|
0
|
0
|
Colony radius and slope of growth curve on SNA after 72h
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Colony radius SNA 15 °C1
|
6.0-7.05
|
8-95
|
8-154
|
8-175
|
7-105
|
8-155
|
(5-)7-13
|
(5.3-)8-12(-14)
|
(5.0-)5.0-10.0
|
(6-)7-12(-13)
|
(1.5-)3.0-8.0(-10)
|
(2-)3-11(-12)
|
6-85
|
Colony radius SNA 20 °C1
|
17-205
|
22-245
|
20-274
|
14-225
|
17-215
|
20-275
|
(14-)18-23
|
(16-)22-31(-43)
|
(25-)19-27
|
(19-)20-24
|
(10-)13-19(-21)
|
(13-)17-27(-30)
|
16-255
|
Colony radius SNA 25 °C1
|
27-345
|
41-425
|
31-334
|
22-305
|
19-285
|
31-335
|
(25-)29-35
|
(32-)37-47(-51)
|
40-48
|
(27-)31-35
|
(15-)21-31(-33)
|
(22-)28-49(-41)
|
27-485
|
Colony radius SNA 30 °C1
|
25-315
|
36-465
|
224
|
1-25
|
12-155
|
65-705
|
(20-)21-27(-28)
|
(15-)32-54(-64)
|
39-41(-51)
|
(22-)26-31(-34)
|
(12-)14-28(-35)
|
(25-)30-43(-45)
|
30-505
|
Colony radius SNA 35 °C1
|
0-15
|
0.5-1.0
|
0
|
0-1
|
0-1
|
0
|
(0.5-)1.0-1.8(-2.0)
|
(0-)1.5-6.2(-14)
|
4-7
|
(0-)0.2-1.5(-2)
|
0-3.2
|
0-1
|
0-25
|
Colony slope SNA 15 °C1
|
0.119-0.1465
|
0.156-0.1825
|
0.167-0.1834
|
0.156-0.1895
|
0.134-0.1865
|
0.057-0.0855
|
(0.057-)0.110-0.202(-0.226)
|
(0.085-)0.121-0.201(-0.232)
|
0.164-0.2365
|
(0.115-)0.124-0.214(-0.232)
|
(0.054-)0.064-0.148(-0.190)
|
0.087-0.199
|
0.104-0.1145
|
Colony slope SNA 20 °C1
|
0.236-0.3405
|
0.397-0.4065
|
0.341-0.4134
|
0.385-0.4425
|
0.253-0.3965
|
0.200-0.3675
|
(0.200-)0.272-0.444(-0.482)
|
(0.161-)0.290-0.462(-0.518)
|
0.401-0.5545
|
(0.311-)0.313-0.419(-0.461)
|
(0.213-)0.248-0.318(-0.321)
|
0.227-0.381
|
0.220-0.3835
|
Colony slope SNA 25 °C1
|
0.460-0.5575
|
0.451-0.5945
|
0.495-0.5504
|
0.603-0.6335
|
0.275-0.6145
|
0.424-0.6405
|
(0.275-)0.328-0.618(-0.712)
|
(0.215-)0.453-0.675(-0.779)
|
0.504-0.7895
|
(0.465-)0.486-0.554(-0.520)
|
(0.354-)0.392-0.482(-0.485)
|
0.264-0.574
|
0.371-0.6505
|
Colony slope SNA 30 °C1
|
0.371-0.4515
|
0.160-0.4035
|
0.3254
|
0.321-0.6195
|
0.075-0.6195
|
0.457-0.6535
|
(0.014-)0.100-0.558(-0.654)
|
(0.004-)0.296-0.676(-0.782)
|
0.297-0.7695
|
(0.206-)0.290-0.450(-0.483)
|
(0.200-)0.229-0.391(-0.461)
|
0.038-0.537
|
0.354-0.5675
|
Colony slope SNA 35 °C1
|
0
|
0
|
0
|
0
|
0
|
0.168
|
0
|
0
|
0
|
0
|
0
|
0
|
0-0.0045
|
Colony morphology on PDA
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Colony type after 96 h in light
|
growth slow; conidia formed abundantly in two concentric rings
|
fast; faint concentric rings; few conidia
|
growth slow; abundant conidia in concentric rings
|
growth slow; mycelium uniform or abundant in faint concentric rings; sterile
|
growth slow; mycelium uniform or abundant in faint concentric rings; sterile or not
|
fast; faint concentric rings; few conidia
|
growth fast; faint to pronounced concentric rings, conidia typically abundant
|
growth fast; faint to pronounced concentric rings, conidia typically abundant
|
growth fast; faint to pronounced concentric rings, conidia typically abundant
|
growth slow; conspicuous concentric rings; conidia abundant, lacking any yellow color
|
growth slow; few faint concentric rings; conidia formed abundantly in the center of the colony
|
growth slow, abundant conidial production in 3 or 4 broad concentric rings. Some yellow pigment in developing conidia and PDA reverse
|
growth slow, few conidia in concentric rings
|
| Time of appearance of green conidia on PDA in darkness1 |
48 |
72-96 |
48 |
>96 |
72-96 |
>96 |
72 |
48 |
48 |
48-72 |
24(-48) |
48(-72) |
48 |
hours
|
|
|
|
|
|
|
|
|
|
|
|
|
|
| Temperature of appearance of green conidia on PDA in darkness1 |
25 |
20 |
25-30 |
25 |
20-25 |
25 |
25-30 |
(20-)25-30 |
20 |
20-25 |
25-30 |
25-30 |
25 |
°C
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
1 Characters used in PCO analysis.
2 Number of collections.
3 Only two asci could be measured from three collections.
4 Continuous measurements from SNA. All measurements pertaining to growth rate report the range observed in three, independent trials.
5 maximum and minimum of all cultures studied.
6 Total range of two isolates.
7 Measured from pustules.