BEN |
BOTANICAL ELECTRONIC NEWS |
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ISSN 1188-603X |
No. 484 November 25, 2014 | aceska@telus.net | Victoria, B.C. |
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Crepis acuminata is among the most morphologically distinct species in the North American Crepis agamic complex; however, morphological confusion arises in parts of British Columbia, Washington State, Idaho, Oregon and California because Crepis acuminata and C. atribarba morphologically intergrade with each other. Allopolyploidy is the likely cause of this morphological disarray (Babcock & Stebbins 1938; Sears 2011). The types of C. intermedia (Bolander 4930) and C. angustata (Carl F. Baker 92) occupy this morphological spectrum between C. acuminata and C. atribraba, which is why I have placed them in synonymy with C. acuminata below. Part of this morphological continuum extends into the Flathead Basin in southeastern British Columbia. Some individuals collected in this area (e.g. Lomer 94-113) lean towards the C. acuminata end of the morphologically spectrum, while others (e.g. Polster 125) are well within it. Indeed, if Polster 125 is considered in isolation it is easily assigned to C. acuminata based on morphology alone. I propose that Crepis acuminata be added to the Canadian flora. A key to the native Crepis known to Canada and adjacent regions of the United States can be found below. Maximum and minimum character values are indicated in the key as well as means and ± one standard deviations.
Crepis acuminata Nutt. subsp. acuminata = Crepis acuminata subsp. typica Babc. and Stebbins, Carn. Inst. Washing. Publs. 504:170. 1938. TYPE U.S.A. Plains of the Upper Platte, Nuttall s.n. (SYNTYPES: BM-1010043!, HUH-6258!, HUH-6257!, PH-1025896!)
= Crepis angustata Rydb., Bull. Torr. Bot. Club 32:135. 1905. TYPE: U.S.A. Colorado: North Park, 8000 ft., July 28, 1896, Carl F. Baker 92 (HOLOTYPE: NY-167780!; ISOTYPE: NY-167781!, NDG- 48956!)
= Crepis acuminata subsp. pluriflora Babc. & Stebbins, Carn. Inst. Wash. Publ. 504:178-179. 1938. = Psilochenia acuminata subsp. pluriflora (Babc. and Stebbins) W. A. Weber, Phytologica 53(3):188. 1983. TYPE: U.S.A. Colorado: Delta Co., Cedar Edge, alt. 7000 ft., June 24, 1901, Baker 243 (HOLOTYPE: UC-91870; ISOTYPE: RM-33306! and 160594!)
= Crepis intermedia A. Gray, Syn. Fl. N. Amer. 1(2):432. 1884, Hieraciodes intermedium (A. Gray) Kuntze, Revis. Gen. Pl. 1:346. 1891, C. acuminata var. intermedia (A. Gray) Jepson Man. Fl. Pl. Calif. 1011. 1925, Psilochenia intermedia (A. Gray) W. A. Weber, Phytologica 53(3):189. 1983. TYPE: U.S.A. California: Yosemite Valley, sandy soil, 1866, Bolander 4930 (EPITYPE: GH-!)
Etymology. From the Latin word "acuminatus", meaning "narrowing gradually to a point". This is likely in reference to the terminal midlobe of the basal leaves, which are acuminate.
Key to the native Crepis s.s of Canada and adjacent regions of the United
States of America
Canada. BRITISH COLUMBIA: Lomer 94-113, 7-Jul-1994, Open mountainside,
Kishinena Creek, Flathead Basin, UBC (49.0621 -114.281, 4400 ft.); Polster
125, 12-Aug-1976, South facing ridge, Festubert Mountain, V (49.071861
-114.153, 5780 ft.); USA. Nuttall s.n., Plains of the Upper Platte
[River], BM, HUH, PH; CALIFORNIA: Bolander 4930, 1866, Sandy soil,
Yosemite Valley GH; COLORADO, Jackson County: Baker 92, 28 July 1896,
North Park (SE), NDH (40.853 -106.299, 7916 ft.); Delta County: Baker 243
(in part), Cedar Edge (Cedaredge), UC, RM (38.9016, -107.926, 6225 ft.)
1) New version 2.2 of MatchMaker - Mushrooms of the Pacific Northwest
MatchMaker (http://www.matchmakermushrooms.com/) is the free Pacific Northwest
Mushroom Identification application for the PC or MAC, developed by Ian
Gibson, Danny Miller and a host of other contributing authors and
photographers. Over 4,000 species are fully described, many of them with
photos, including a synoptic key. This is not like reading a paper key that
asks you questions you might not know the answer to, but it involves telling
the computer what you do know about the mushroom. It includes dozens of
other features and learning opportunities, as well as a quiz.
2) Pictorial Key and Tables
MatchMaker now includes a Pictorial Key to 1,500 of the most common PNW
Mushrooms. This Pictorial Key is also available as a self-standing
application outside of MatchMaker (http://www.alpental.com/psms/) for use on
a smart phone, where no internet or cell reception is necessary.
Pictures of similar mushrooms are shown side by side (not in alphabetical
order) where you will see a concise summary of their differences, with the
most important points highlighted in bold, so that you can quickly see the
features that make a species unique.
Amanitaceae journal (ISSN [online] 2331-7612, R. E. Tulloss, publisher)
is an open access e-journal with the sole purpose of formally publishing
results of research of those actively working in Herbarium Rooseveltensis
Amanitarum. This journal is a means of meeting part of the requirement for
on-line treatments in the continuously updated monograph of the Amanitaceae
family. This was discussed informally during the initial meeting concerning
a proposed North American Mycoflora project (New Haven, Connecticut, June
2012). At that meeting, several speakers recognized the need for periodic
publication as a stable state version of a continuously updated on-line
monograph.
Amanitaceae journal will satisfy that proposal through the creation of
(1) the e-journal that will meet the requirements of valid and effective
Publication of the ICN and (2) a mechanism for creating snapshots of the site
on a regular basis and storing those snapshots for open access. Clearly,
both approaches require archival storage. For the e-journal, ISO certified
digital repositories (as described in the ICN) already exist.
Articles for this journal are peer reviewed. Authors of manuscripts will
advise the publisher with regard to reviewers with suitable knowledge of the
subject matter of a given manuscript.
The inaugural issue of Amanitaceae contains the description of a new
species of Amanita from California and Oregon, i.e., Amanita pruittii
A. H. Sm. ex Tulloss, J. Lindgr. & Arora:
Amanita pruittii is a new Amanita species, recently known from sites
in California and Oregon. Morphologically the species is a member of
Amanita
subsect. Vittadiniae and is assignable to stirpus Vittadinii of Bas.
Amanita pruittii belongs to a small group of saprophytic members of
otherwise mostly mycorrhizal genus Amanita and occurs commonly without an obvious,
woody, ectomycorrhizal symbiont. It grows in grassland habitats with
standing water part of the year, and is often found submerged or partially submerged in water:
http://mushroomobserver.org/185950 or
http://mushroomobserver.org/185959
available on Mushroom Observer web site: http://mushroomobserver.org/name/show_name/15254
Amanita pruittii is also included in the Trial key to the species of
AMANITA in the Pacific Northwest prepared for the Pacific Northwest Key
Council by J. Lindgren in 2014: http://www.svims.ca/council/Amanit.htm
The search is on to find additional locations for A. pruittii, previously
also known as Arora's Anonymous Amanita. The known sites are separated by
about 600 miles and we are interested in finding other locations between
these sites and to extend the range along the Pacific Coast. In October/November,
these amanitas are fruiting in good numbers at Fern Ridge Reservoir in Oregon
and one should look for them in wet meadows and lowlands along rivers.
Please sent your reports of new locations to Jan Lindgren
(jlindg@centurylink.net), ideally supported by dried herbarium specimens and
photographs.
[Editorial Comment: for R.E. Tulloss' profile see http://www.scientificamerican.com/article/the-mushroom-man/]
1a. Involucral bracts with glandular hairs ............................. 2
1b. Involucral bracts devoid of glandular hairs ........................ 4
2a. Glandular hairs present on the involucral bracts but not also on the
stems, and upper cauline and basal leaves .... C. occidentalis Nutt. (in part)
2b. Glandular hairs present on the involucral bracts, stems, upper cauline
and basal leaves ................................................... 3
3a. Involucral bracts of the outer series differ from each other by >= 2mm
in length; 12-45 (23 ± 7) flowers per head; midrib of basal leaves
always purple to red in living and herbarium material, and upper
peduncles weakly to strongly expanded below the heads ................
............ C. bakeri Greene (not currently known from Canada)
3b. Involucral bracts of the outer series differ from each other by < 2 mm
in length; 7-19 (14 ± 3) flowers per head; if midrib of basal leaves
are purple to red in living and herbarium material then the peduncles
are not expanded below the heads ... C. occidentalis Nutt. (in part)
4a. Involucral bracts with at least some non-glandular hairs ........... 5
4b. Involucral bracts glabrous ......................................... 8
5a. Inner involucral bracts with only pure white villous hairs, or yellow-
green crisped bristles ............................................. 6
5b. Inner involucral bracts with dark green to black, straight or villous
hairs .............................................................. 7
6a. Inner involucral bracts with pure white and villous hairs ............
..................................... C. modocensis Greene (in part)
(This form includes the diploids and the closely associate autotetra-
ploids. It is known from Canada)
6b. Inner involucral bracts with yellow to yellow/green crisped bristles
............. C. barbigera Leiberg (not currently known from Canada)
7a. Base of petioles or stem or both with stout yellow bristles; 18-47 (30
± 7) flowers per head; basal leaves with lanceolate, toothed to pinna-
tifid lobes, rarely falcate ......... C. modocensis Greene (in part)
7b. Base of the petioles and stem without bristles; 5-23 (13 ± 4) flowers
per head; basal leaves with deep lobes, lobes narrow and entire to
wide and toothed, often falcate and pointing towards the tips of the
leaves (antrorse) ................. C. atribarba A. Heller (in part)
8a. Leaves mostly in a basal rosette, cauline leaves much reduced or
absent; leaves runcinate and olive green; occurring on ultramafic
soils .... C. pleurocarpa A. Gray (not currently known from Canada)
8b. Plants with well-developed cauline leaves; leaf shape various and
green to grey/green; occurring on various soil types, sometimes also
including ultramafic soils ......................................... 9
9a. Leaves with minute papillae on their margins and largest heads with
4-10 (6 ± 1) flowers; margins of inner involucral bracts scarious
................................................. C. acuminata Nutt.
9b. Leaves rarely with minute papillae on the margins of the leaves and
largest heads with 8-47 (16 ± 4) flowers; margins of inner involucral
bracts tomentose .................................................. 10
10a. Basal leaves with deep, narrow and entire to wide and toothed, lobes,
often falcate and antrorse (but some populations in Washington and
British Columbia lacking lobes); leaves green and glabrate .........
.................................. C. atribarba A. Heller (in part)
10b. Basal leaves with lobes deeply cleft to shallowly lobed, lobes never
falcate or antrorse; leaves grayish-tomentose to densely canescent
................................... C. occidentalis Nutt. (in part)
Specimens mentioned in the text
Literature Cited
COMPUTER TOOLS FOR IDENTIFICATION OF THE PACIFIC NORTHWEST MACROFUNGI
From: Ian Gibson ig@islandnet.com and Danny Miller dannymi@alpental.com
TWO MYCOLOGICAL NOVELTIES: AMANITA PRUITTII N.SP. AND AMANITACEAE JOURNAL
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