Saturday, January 15, 2011

Crooked Foot Lily: aka Foetid adders tongue, later Slink Pods


Scoliopus bigelovii


In flower, the common name Fetid Adders tongue is used, whereas in fruit Slink Pod applies, one of the very few plants who changes its common name through the year. This coastal lily is endemic to California, ranging from Humboldt County southward. Etymology: Greek skolios (crooked) and pous (foot). Sciopolis bigelovii flowers very early in coastal central California. The photograph shown is at Aptos, Nisene Marks SP, January 14, 2011.


One of the interesting aspects of flowering progression through the season in S. bigelovii is the delayed development of leaf area, and the sequential, progressive production of flowers from within a basal vase formed by the developing leaves. At flowering, the vase is often filled with water.


The southerly distributional record for this lily is uncertain: there is no CCH specimen record for Monterey County. Moreover, both Matthews (1997) and Yadon (1995) fail to list it for their region. Ostensible, the southerly limit thus may be the large colony along Aptos Creek in the Forest of Nisene Marks state park. However, one CCH specimen is labeled from San Luis Obispo, but this lily was not known to Hoover (1970). Field verification of any record south of Santa Cruz County along the Big Sur Coast and southward is thus worthy of mention.


Hoover, R.F. 1970. Vascular Plants of San Luis Obispo County, California. UC Press.


Matthews, M.A. 1997. An illustrated field key to the Flowering Plants of Monterey County. CNPS, 401 p.


Yadon, V. 1995. A Checklist of the vascular plants of Monterey County, California. Monterey Bay Chapter, CNPS. 85 pp.

Friday, January 14, 2011

Maytennus magellanica in California?









This post pertains to UC1755439, my number 21,098, collected 28 October 2010. The report may be the first detection of a second non-native Maytenus for California.






Maytenus magellanica (Lam.) Hook. f. (Celastraceae) is a large shrub native to the southern portion of South America (Argentina and Chile). Enciclopedia de la Flora Chilena (2010) attributes it to south of 36oS. The genus Maytenus consists of about 225 species, according to Maberly, topical to warm Old World and Australasian distribution, with only Maytenus phyllanthoides Benth. being native to the se U.S.






I have had this putative taxon of Maytenus under observation for many years. A small colony, consisting of multiple age cohort plants, grows in Aptos, Santa Cruz County. The plants are tall shrubs to ca. 4 meters tall and with multiple branched stems to ca. 15 cm basal diameter.






Photographs of authentic Chilean material show a taxon with bright red flowers, whereas the plants under discussion here have greenish and less showy flowers. In this respect, the Aptos plants of Maytenus are more similar in appearance to the USDA Plants database photo of Maytenus cymosa Krug & Urb., which is native to the Caribbean. Maytenus boaria Molina is a commonly seen plant in coastal California gardens, known for its distinctive pendant branches; it is now sparingly naturalized in California. Clearly, our plant is not this taxon.






The taxonomic assignment of UC1755439 DWT#21098 requires assessment of a monographer, and awaits treatment of Celastraceae for FNA. Regardless, the report herein is an early detection and requires monitoring and assessment for invasibility.













Wednesday, January 12, 2011

What is the magnitude of introduction of non-native plants in California?

here is the calculus I use:


 

1. there are on the order of 450,000 species of vascular plants


 

2. perhaps half of those are adapted to places that are too warm or too cold to grow in California, that leaves 225,000


 

3. let us for sake of sanity, cut 225,000 in half and we will sleep better


 

4. in California we have ca. 2000 non native plants and 7000 natives, total ca. 9000


 

5. Subtract 9000 from 125,000 and we get 116,000 plants that might some day come hither


 

6. the challenge of introductions is daunting. Which become invasive, if only 1% of those might be invasive, that is far too many: amongst the 1160 of the 1% there are going to be a host of horror stories. Halloween and botany do not mix well (except for the requirement of fully ripe pepos). Early detection and eradication is the most economical solution to the problem. Detect the zebra mussel early – after all it had stripes – and you save a bundle. Fail to provide botanists whom can make detections, fail to allow the detection botanists to roam, and you guarantee the next star-thistle will be on our doorstep.


 

The problem seems daunting but daunting problems are a fun element of challenge.

Wednesday, January 5, 2011

Red Berries coastal California, winter it is not, coincidence neither





An obvious feature of coastal central California settings at the turn of the new year is the presence of both native and introduced shrubs and trees with fully ripe, red fruits. Red fruit = bird dispersal. At this time of year in coastal central California it is hardly winter for many vascular plants, as temperature is suitable for growth and moisture is no longer limiting. In the Santa Cruz Mountains we have toyon (Heteromeles arbutifolia) as the sole native red berried shrub. Close by one finds madrone (Arbutus menziesii) which in some regions this year are very heavily laden with ripe pendant clusters of fruit. One of the common names of toyon is Christmas berry.


Non-native shrubs, largely Rosaceae, are juxtaposed against the natives: cotoneaster (C. franchetii and C. pannosa) and pyrracantha (P. angustifolia). Often one can see mixed stands of both native and non-native red berried shrubs. One can, and I do, also point to a non-rosaceous, but relatively rarely encountered red fruited shrub, Ilex aquifolium, English holly (Aquifoliaceae), an asterid eudicot contrasts to the others, which are rosids. Coincidence of red fruits? No. Clearly selection for bird dispersal which has produced this syndrome in unrelated lineages.


Interesting, there are known genetic variants of both native and non-native rosaceae with orange rather than red fruit. The photo is such a variant of pyrracantha, perhaps P. fortuneana. A named race of toyon, H. arbutifolia var. cerina (Jepson) E. Murry with yellow fruits is a similar genetic variant. In the case of the pyrracantha in the photo, the variant is orange vs. red


Plant taxonomists are a wishy-washy bunch, as if they do not want to be ever caught with their names in parenthesis, so the yellow variant of toyon is not considered a 'taxon'. Get real folks, it is genetically based, is it not? Ought names be coined to facilitate our use, and ought not those names, when used, be taken to refer to specific genome features? Taxonomists: recognize H. arbutifolia var. cerina please, and get over species denial.

Tuesday, December 28, 2010

Branching in Camissonia seedlings


Branching in Camissonia lacustris begins at the cotyledonary node (at red arrow, the cotyledons at yellow arrows, 80 day old seedlings). At this age, the cotyledons are still fully functional and are, after post germination maturation, identical to the first formed foliage leaves. Precious branching is not uncommon throughout angiosperms, indicating that the feature is adaptive in specific environments, and can be selected out of a genome again and again. In Onagraceae, within Camissonia as delimited by Raven (1969), the differences in growth features between rosette annuals (now treated within Chylisma and Eremothera) and Camissonia sensu stricto are manifold, and support the dismemberment of the Raven genus concept. Done. Remember, Raven dismembered the Munz' genus Oenothera with the occasional raised eye-brow typical of the pre-DNA era of systematics. In thinking about the expression of branching control in Camissonia seedlings, the feature of flowers at basal nodes in Gayophytum, where G. diffusum, which branches distally and is very common, contrasts to G. decipiens and its basal branching and relative rarity comes to mind: perhaps the grazing lips of a herbivore ought to be brought into the mix: lateral gene transfer? {by that I mean that there is a distance above the ground surface which grazing influence does not penetrate, the lip-o-the-grazer distance. Branch below that distance, and survive.

Plants are cool!







Wednesday, November 24, 2010






Top: Camissonia sierrae ssp. alticola from Little Yosemite Valley, DWT #20938 16 July 2010 Bottom: Camissonia lacustris Wawona (vouchered by DWT 18082, JEPS109727)

There are distinct differences in the seedlings of two species of Camissonia in the Yosemite Region. In Camissonia sierrae ssp. alticola Little Yosemite Valley, the colytedons are of quite different shape from those in C. laucustris Wawona, as pictured (red arrow in each photo).

In C. sierrae, the cotyledons are initially rhombic in shape, but later become lanceolate; they lack ciliate margins which can be seen on the first foliage leaves, and are entire margined. The plants at 7 weeks of age form a distinct rosette.

By contrast, C. laucustris Wawona produces cotyledons which are linear and distinctly emarginate. Moreover, during development, their cotyledons elongate markedly, becoming 15-20 mm long and are similar to the first foliage leaves.

The differences in early development of these two species makes their seedlings relatively easy to identify, if one could find them in the field.

More species need to be grown out to ascertain if these differences form morphological classes within the genus, and if the morphological differences have classificatory and/or phylogenetic value.

































































central Sierra Camissonia seedlings






Top:
Camissonia sierrae ssp. alticola
Little Yosemite Valley
DWT #20938 (JEPS, YM) 16 July 2010
Bottom:
Camissonia sierrae ssp. alticola
Little Yosemite Valley
DWT #20938 (JEPS, YM)

There are distinct differences in the seedlings of two species of Camissonia in the Yosemite Region. In Camissonia sierrae ssp. alticola Little Yosemite Valley, the colytedons are of quite different shape from those in C. laucustris Wawona, as pictured (red arrow in each photo).

In C. sierrae, the cotyledons are initially rhombic in shape, but later become lanceolate; they lack ciliate margins which can be seen on the first foliage leaves, and are entire margined. The plants at 7 weeks of age form a distinct rosette.



By contrast, C. laucustris Wawona produces cotyledons which are linear and distinctly emarginate. Moreover, during development, their cotyledons elongate markedly, becoming 15-20 mm long and are similar to the first foliage leaves.



The differences in early development of these two species makes their seedlings relatively easy to identify, if one could find them in the field.



More species need to be grown out to ascertain if these differences form morphological classes within the genus, and if the morphological differences have classificatory and/or phylogenetic value.



























































Camissonia lacustris