Emerald Bay State Park – Vikingsholm and Rubicon Trails

I had attempted to hike the Eagle Falls Trail two days ago, but deep snow stopped us just below the Upper Falls before reaching the lake. I had noticed, however, that the lower elevations on the west shore of Emerald Bay looked fairly free of snow, and a conversation the following morning with an extraordinarily helpful staff member at the USDA Forest Service’s Lake Tahoe Basin Management Unit headquarters in South Lake Tahoe confirmed that the entire Vikingsholm Trail in Emerald Bay State Park and much of the Rubicon Trail in Emerald Bay State Park and D. L. Bliss State Park immediately to the north should be passable. My objectives were two-fold – hiking and botanizing. I wanted to get in at least 6 miles, and up to 10 would be even better; and I also wanted to locate and identify as many of the woody plants known from the area as possible. I probed the incredibly helpful USDA representative about the subtleties of distinguishing ponderosa pine from the ubiquitous but very similar Jeffrey’s pine, where I might see magnificently mature specimens of sugar pine and the grotesquely beautiful Sierra juniper, how to recognize the moisture loving lodgepole pine, and the slim chance of seeing western white pine due to its preference for higher altitudes. I commented about how I looked forward to seeing stately red firs and wind-swept whitebark pine when I went skiing later in the week – maybe I would be fortunate enough to find western white pine amongst them. I purchased three books: Conifers of California by Ronald Lanner, Discovering Sierra Trees by Stephen Arno, Plants of the Tahoe Basin by Michael Graf and National Geographic’s Trails Illustrated Map™ for Lake Tahoe Basin (my souvenirs for the trip), thanked the wonderfully knowledgeable USDA representative for her help, and bolted up to Emerald Bay. On an extraordinarly warm and delightful mountain day in spring, I hiked down the Vikingsholm Trail to Vikingsholm Castle, stopping frequently to sample and photograph plants, then hiked the Rubicon Trail all the way to Emerald Point at the mouth of Emerald Bay. I hopped on rocks out into the point until I could not go any further and turned around to admire a view that few people have experienced by foot. I lost the trail along the way due to snow, but I did not get lost – I could not get lost with a lake on one side of me and a mountain on the other. Going beyond Emerald Point the snow got too deep – a few steps where I sunk up to my hip confirmed that further passage without snow shoes would be impossible. I bushwhacked back until I found the trail and chose alternate paths the rest of the way. By the time I returned to my car, I had hiked 7 miles in 5½ hours (yes, I’m pokey), encountered only a handful of people (all within a quarter mile of the parking lot) and taken 110 photographs. I share seven of them with you here:

East shore (lateral glacial morraine) of Emerald Bay from Vikingsholm Trail.  Heavenly Ski Resort and the southeast shore of Lake Tahoe can be seen in the distance.

East shore (lateral glacial morraine) of Emerald Bay from Vikingsholm Trail. Heavenly Ski Resort and the southeast shore of Lake Tahoe can be seen in the distance.

Mt. Tallac (L) and Maggie's Peaks (R) from Vikingsholm Trail

Mt. Tallac (L) and Maggie's Peaks (R) from Vikingsholm Trail

Fannette Island from Vikingsholm Castle

Fannette Island from Vikingsholm Castle

Emerald Point from the west shore of Emerald Bay

Emerald Point from the west shore of Emerald Bay

Emerald Bay and Maggie's Peaks (L) from Emerald Point

Emerald Bay and Maggie's Peaks (L) from Emerald Point

West shore of Emerald Bay from Emerald Point

West shore of Emerald Bay from Emerald Point

Zoom view of Emerald Bay from Emerald Point

Zoom view of Emerald Bay from Emerald Point

Copyright © Ted C. MacRae 2009

Add to FacebookAdd to NewsvineAdd to DiggAdd to Del.icio.usAdd to StumbleuponAdd to RedditAdd to BlinklistAdd to Ma.gnoliaAdd to TechnoratiAdd to Furl

Answers to “Winter botany quiz #2”

Finally, I present to you the answers to “Winter botany quiz #2 “. The delay in providing these answers was two-fold. Firstly, I knew this would be a hard test, so I wanted to give people plenty of time to figure out the answers. Secondly, the answers were delayed an extra day due because of some debate that arose among the experts I consulted about #3 – more on that below. I thank all those who participated, and while there was no clear-cut “winner”, several honorable mentions are deserved:

  • Doug Taron, who was the first to properly deduce the South African nature of these plants.
  • James C. Trager, a myrmecologist (yet still my friend!) who correctly identified the genus of #1.
  • Everyone, for guessing that #2 was “an orchid” – although Tom @ Ohio Nature was the only one to use the formal scientific name for the family, and Doug Taron was the only one to attempt a generic identification (and came close – Oncidium and Ansellia are both assigned to the tribe Cymbidieae in the subfamily Epidendroideae).

#1.  Ornithogalum seineri (family Hyacinthaceae)
Ornithogalum is a large genus occurring mostly in the drier habitats of southern Africa and around the Mediterranean.  The genus and its relatives were formerly included in the Liliaceae (as many of the participants guessed), but the group is now given familial status as the Hyacinthaceae.  This genus contains numerous species of horticultural note.  One is (as James noted) O. umbellatum, or  “star of Bethlehem”, which in North America has escaped cultivation as a garden ornamental and gained status as an invasive weed.  Another is O. longibracteatum (syn. caudatum), a popular houseplant with the common name “pregnant onion”.  This species, native to the Cape and Natal Provinces of South Africa, is easily recognized by its bulb that “gives birth” to tiny replicas of itself just beneath a thin, transparent ‘onion’ skin (as shown in the photo at right from Trans-Pacific Nursery).  At flowering, a long spike grows from the center of the green strap leaves, eventually giving rise to a spearhead of tiny white flowers situated at the end.

While I couldn’t find much information about O. seineri, I did find this spectacular photo of numerous blooming plants in bushveld habitat amongst grazing zebra (photo by ingrid1968 in this post at SANParks.org Forum).  My view of this species was not quite so spectacular, as I saw only the lone plant in the photographs posted earlier.

#2.  Ansellia africana (family Orchidaceae)
Ansellia is an African genus of orchid commonly called Leopard Orchid or African Ansellia.  There is some degree of morphological, geographical and ecological variation in Ansellia populations, with the result that several species, subspecies and varieties have been described.  Flower color varies from pure yellow to variably splotched with brown to almost completely black with finely indicated yellow divisions.  Recent taxonomic work has concluded that there are no discontinuities within the spectra of variations exhibited and the populations are thus attributable to the single, polytopic species, A. africana (Khayota 1999).

Ansellia africana is a large, perennial, epiphytic species that usually grows attached to the branches of tall trees but is sometimes found growing on rocks.  This genus is immediately recognizable by its large, cane-like pseudobulbs that arise from a basal rhizome and is notable for the white, needle-like, upward pointing aerial roots that form a sort of “trash basket” around the clump.  The term is surprisingly appropriate, since the root basket seems to function in catching dropping leaves, flowers and detritus which provide nutrients for the plant as they decay.  This species can grow to enormous size and often forms spectacular clumps, some of which have an estimated weight of more than one ton.

Of the three plants featured in the quiz, this was the one I expected someone would guess, since the species is popularly cultivated by orchid enthusiasts.  Unfortunately, the pressures of wild collection for commercial purposes has caused declines in its population.  The problem is exacerbated by the unsustainable methods use to harvest, transport, and cultivate wild-born plants.  Host trees are usually cut down and sections with the orchid removed, resulting in wholesale destruction of both orchids and hosts. After harvesting, plants are cut up and transported slowly in open handcarts, to be sold along roadsides where they may sit exposed to full sun for days or weeks.  Cutting the clumps damages the roots, and exposure results in dessication, making it difficult for harvested plants to recover once in cultivation.  Plants that do survive harvest and transplant suffer high mortality rates in cultivation due to improper attention to light and moisture regimes.

#3. Adenia sp., poss. glauca (family Passifloraceae)
To be completely honest, not only did I not expect anyone to guess this one, I didn’t think I was even going to be able to provide an answer. I sent the photos to my friend and colleague, George Yatskievych, director of the Flora of Missouri Project (and author of the recently published Steyermark’s Flora of Missouri, 1999 and 2006), who forwarded the photographs to several more colleagues, and at the same time I posted the photos on SANParks.org Forum (a fantastic resource, which I just recently discovered myself, for those interested in South Africa National Parks and their natural history). It took some time for these sources to weigh in with their opinion, which in the end were in agreement that it represented a species of African passion flower in the genus Adenia of the family Passifloraceae (not to be confused with Adenium, a genus of flowering plants in the family Apocynaceae – also occurring in Africa). As for which species, the choices had been narrowed down to either A. glauca or A. fruticosa. According to Imberbe, a photo of the leaves would have been diagnostic, and the flowers are also different (A. glauca has yellow flowers while those of A. fruticosa are green). Fred Dortort, in an article on the University of California at Berkely Botanical Garden website titled, “Passion and Poison“, notes that A. fruticosa has a tall, spindle-shaped caudex topped with a few thin, sparsely-leafed, arching branches, while in A. glauca the caudex is roughly globose and can become quite large. This description seems to favor A. glauca, which Imberbe also noted was known to occur in the area where I took the photographs.

Species identification aside, the genus Adenia is notable for its bizarre adaptations for water storage. Most of the 100 or so species in this Afrotropical and Indomalaysian genus have underground tubers. Those of species adapted to drier environments have grown proportionately larger, with some turning into above ground caudices that can take several different forms and that, in some species, may reach up to eight feet in diameter and height. Even more notable than these succulent adaptations are the poisonous properties that many plants in the genus possess. Not all species have been analyzed (and I found little or conflicting information about A. glauca and A. fruticosa), but one species in the genus – A. digitata – has gained notoriety as perhaps the most poisonous plant in the world. Two different toxins are found within its tuber, one a cyanogenic glycoside, the other a particularly potent toxin called modeccin. The latter is a 57kD protein that resembles ricin and acts a powerful inhibitor of protein synthesis by binding to ribosomes (Gasperi-Campani et al. 1978). Imberbe, in her comments about the photos I posted on SANParks.org Forum, noted the following about plants in this group:

…take heed of the Afrikaans name “Bobbejaangif” (Baboon poison)… It has been used as a fish poison, as well as in suicide and murder. It causes nausea, fits and liver and kidney damage.

REFERENCES:

Gasperi-Campani, A., L. Barbieri, E. Lorenzoni, L. Montanaro, S. Sperti, E. Bonetti, & F. Stirpe. 1978. Modeccin, the toxin of Adenia digitata. Biochemistry Journal 174:491-496.

Khayota, B. N. 1999. Notes on systematics, ecology and conservation of Ansellia (Orchidaceae), pp. 423-425. In: J. Timberlake & S. Kativu (eds.), African Plants: Biodiversity, Taxonomy and Uses, Royal Botanic Gardens, Kew.

Copyright © Ted C. MacRae 2009

Add to FacebookAdd to NewsvineAdd to DiggAdd to Del.icio.usAdd to StumbleuponAdd to RedditAdd to BlinklistAdd to Ma.gnoliaAdd to TechnoratiAdd to Furl

Winter botany quiz #2

In the first winter botany quiz, I learned that I have some rather astute botanists amongst my readership. They were not only able to quickly identify to species every plant I had pictured but also identify their commonality, sometimes from quite afar. As a result, this one is harder.  I use the term “winter botany quiz” in the broadest possible sense – just because it’s winter here doesn’t mean it’s cold everywhere! All of the photos were taken in the same general (for now unspecified) locality during late November and early December (this paragraph simply reeks of clues!).

To give everyone a fair chance, I’ve turned on comment moderation so people can submit their answers without seeing what has already been submitted.  I’ll remove moderation after a couple days or so.  First one with all the right answers wins the admiration and jealousy of their peers!

424046-r1-e018_018_21

#1A

424046-r1-e019_019_21

#1B - closeup of flowers in #1A

424046-r1-e020_020_2

#2A

424046-r1-e021_021_2

#2B - closeup of flowers of #2A

424046-r1-e022_022_2

#3A - the vine, not the trees

424046-r1-e023_023_2

#3B - closeup of vine base

Copyright © Ted C. MacRae 2009

Add to FacebookAdd to NewsvineAdd to DiggAdd to Del.icio.usAdd to StumbleuponAdd to RedditAdd to BlinklistAdd to Ma.gnoliaAdd to TechnoratiAdd to Furl

Sanctuary for the Betulaceae

Nestled on the eastern side of the St. Francois Mountains, where the craggy exposures of the Ozarks most ancient rocks begin to subside underneath the Cambrian sandstones laid down over them, lies Hawn State Park – considered by many to be the loveliest of Missouri’s state parks. I have written previously about Hawn – in fact, it was the subject of my very first post on this blog. I have long treasured Hawn for its excellent insect collecting, diversity of plants and habitats, and unbridled beauty. I have hiked the incomparable Pickle Creek and Whispering Pine Trails many times – far more than any other trail in the state, and each time I fall more deeply in love with what, to me, represents the essence of the Missouri Ozarks in their most pristine state.

Lamotte sandstone cutThe charm of Hawn results from a unique combination of geological features. The Lamotte sandstone outcrops that dominate Hawn’s landscape are the oldest sedimentary rocks in the state, formed from coarse sand deposits that were laid down over the Precambrian rhyolites and granites that form the core of the St. Francois Mountains. These sand deposits were themselves buried under limestone and dolomite layers formed at the bottom of vast seas that later covered much of the interior of the continent. Subsequent periods of uplift and erosion once again exposed these sandstones, whose unique ability to hold groundwater has resulted in the formation of spring-fed streams that have cut deep into their soft layers to create canyon-rimmed valleys with tall vertical cliffs. rhyolite shut-ins One of these streams is Pickle Creek, which is fed throughout the year by Pickle Spring and has in some places cut all the way down to the underlying igneous rock to form “shut-ins.” In contrast to the slow, sandy bottomed stretches where Pickle Creek is still cutting through sandstones, the water in these igneous shut-ins rushes through narrow openings in the highly resistant rock. The igneous and sandstone exposures found in Hawn are spectacularly beautiful and support a unique flora due to the acid soils they produce. One group of plants that have taken sanctuary in these moist, acid soils is the Betulaceae, or birch family. Missouri is home to five native species of Betulaceae¹, and while none of them are extraordinarily uncommon they are limited in their occurrence to natural communities with sufficient moisture and exhibit a clear preference for acidic soils. This confluence of conditions occurs perfectly along Pickle Creek, allowing all five native species to grow here side-by-side – a betulaceous “hot spot” that represents not only the full diversity of the family in Missouri, but also the total generic diversity of the family in North America. In fact, only one other genus (Ostryopsis, shrubs related to Corylus and restricted to China) is assigned to the family on a global basis (Furlow 2004).

¹ Dr. George Yatskievych, in his recently published Steyermark’s Flora of Missouri (2006), regarded the presence of Corylus cornuta in Missouri as unlikely despite earlier reports of such. Dr. Yatskievych also recorded a single escape of the European species Alnus glutinosa from Springfield, Missouri.

The Betulaceae are deciduous trees and shrubs that occur primarily in the boreal and cool temperate zones of the Northern Hemisphere, although outposts are also known from high elevations in the Neotropics and, as mentioned above, China. Fossils of this ancient lineage of flowering plants are traceable to the late Mesozoic (upper Cretaceous), and the family appears to form a clade with hamamelidaceous plants. As would be expected from a group with boreal affinities, most species exhibit adaptations for survival in cold climates, such as small stature, shrubby growth habits, and small leaves. Several of Missouri’s species have performed well and gained acceptance as ornamental trees and shrubs, while others are important as sources of hazelnuts (genus Corylus) or ecologically for their ability to fix nitrogen (genus Alnus). My interest in these plants has nothing to do with their economic importance, but rather in their role as host plants for several rarely encountered species of woodboring beetles. Often, insects in this group may be collected on foliage of their hosts during the summer, making host identification fairly easy due to the presence of leaves. This is not always possible, however, due to limited periods of adult activity or low population densities. Rearing these insects from their hosts provides additional opportunity to document their occurrence, and winter is often the best time to collect the dead branches in which they breed, since by that time they have nearly completed their development and will be ready to emerge as soon as temperatures rise during spring. Identifying woody plants without foliage can be a challenge, but the ability to distinguish host plants by non-foliage characters such as bark, growth habit, bud shape, etc. greatly facilitates studies of wood boring beetles through rearing. In the past I have relied heavily on Cliburn and Klomps’ (1980), A Key to Missouri Trees in Winter, which utilizes mostly details of the twigs and buds to discriminate among Missouri’s 160+ species of trees. However, after a certain level of familiarity is gained, one eventually learns to recognize winter trees and even downed logs or fallen branches simply by their “look”.

Betula nigra - habit

Betula nigra - habit

Betula nigra - old bark

Betula nigra - old bark

Betula nigra - sapling

Betula nigra - sapling

Betula nigra (river birch) is the only member of this largely boreal genus found in the middle and southern latitudes of the U.S. and, thus, cannot be confused with any of Missouri’s other betulaceous species². It is the largest of the five and, along with the following species, is the most demanding in terms of keeping its “feet” wet. Trees are usually encountered right at the water’s edge, with tall, slender, often twisted or leaning trunks. Young trees and large branches on older trees exhibit gorgeous reddish brown bark peeling in thin, papery sheets, becoming thick and scaly on the main trunks of older trees. Small branches are dark, purplish brown in color with smooth bark and distinctly horizontal lenticels.  I have reared a small jewel beetle from fallen, dead branches of this tree collected at several locations in Missouri – this beetle turned out to be new to science, which I described and named Agrilus betulanigrae in reference to its (then) only known host (MacRae 2003).  I have also reared tremendous series of another jewel beetle, Anthaxia cyanella, which at the time was not known to utilize this host and was considered uncommon.  As it turns out, Betula nigra is its preferred host, and the rearing of large series from many locations resulted in improved knowledge about color forms and variability in this species (MacRae & Nelson 2003).

² The widely planted but dreadfully non-adapted Betula pendula (European white birch) and B. papyrifera (paper birch) can be recognized by their distinctly white bark. These species are limited to urban landscapes where they rarely achieve significant stature before declining and eventually succumbing to insect pests such as Agrilus anxius (bronze birch borer). River birch provides an equally attractive and much more durable choice!

Alnus serrulata - habit

Alnus serrulata - habit

Alnus serrulata - sapling

Alnus serrulata - sapling

Alnus serrulata - old cones

Alnus serrulata - old cones

Alnus serrulata (common alder, hazel alder, smooth alder, tag alder…) also demands to be next to (or even in) the water.  Unlike B. nigra, however, this species rarely reaches true tree status, instead usually forming shrubby thickets along the water’s edge.  Saplings can resemble those of B. nigra due to their smooth brownish bark, but the latter is usually more purplish, and the lenticels of A. serrulata are not distinctly horizontal as in B. nigra. The large purple-red buds also differ from the small brown buds of B. nigra, and during winter A. serrulata is adorned with numerous staminate catkins.  The persistent woody cones also cannot be mistaken for those of any other species of Betulaceae in Missouri. Associated with this plant is the longhorned beetle, Saperda obliqua, which reaches its southwesternmost distributional limit in Missouri on the basis of a single specimen collected some 25 years ago right here along Pickle Creek and given to me by lepidopterist George Balogh. Numerous attempts to find this species here since then have not (yet!) been successful.

Carpinus caroliniana - habit

Carpinus caroliniana - habit

Carpinus caroliniana (blue beech, hornbeam, musclewood) is one of my favorite betulaceous species. The beautifully fluted trunks and smooth, light gray bark are remniscent of the limbs of a sinewy, muscular person – every time I see this tree I cannot resist the temptation to grab and stroke the hard limbs (should I be admitting this?). This character begins to show even in very young trees, making its identification during winter quite easy. These trees also like to be near water, but they are not so demanding to be right at the water’s edge as are the previous two species. They usually form small trees, often in clumps with multiple trunks.  There are some notable insect associations that I’ve found with this plant.  One is a small jewel beetle, Agrilus ohioensis, which I reared from dead branches of this plant collected along Pickle Creek (Nelson & MacRae 1990), and which after more than 20 years still remain the only known Missouri specimens of this species.  Another is the longhorned beetle, Trachysida mutabilis, a single adult of which I reared from a dead (almost rotting) branch of this plant collected not too far from Pickle Creek in Iron Co.  This beetle also is the only representative of its species known from Missouri (MacRae & Rice 2007).

Ostrya virginiana - habit

Ostrya virginiana - habit

Ostrya virginiana - trunk

Ostrya virginiana - trunk

Ostrya virginiana (hop hornbean, American hornbeam) has a form and growth habit very similar to C. caroliniana, but its leaves that persist through the winter make it instantly recognizable from afar.  In Missouri, this habit is most often seen with the oaks (Quercus spp.).  This species can be found even further away from the water than the previous species, and its small stature combines with the orangish, persistent leaves to form a distinctive understory layer during winter.  Also, in contrast to the smooth gray bark of Carpinus, this species exhibits scaly, light reddish brown to brownish gray bark.  I have succeeded in rearing one of the two known Missouri specimens of another jewel beetle, Agrilus champlaini, from O. virginiana collected along Pickle Creek (the other specimen was reared from wood collected at Graham Cave State Park, another site where sandstone bedrocks favor an O. virginiana understory).  Unlike most other jewel beetles, A. champlaini forms galls in small living branches of its host.  I have collected the distinctive swellings during winter on many occasions but managed to rear only these two individuals (plus one ichneumonid parasitoid).  I have also noted similar swellings on Carpinus but have not yet managed to definitely associated them with this beetle.

Corylus americana (hazelnut, American hazelnut) is the smallest of Missouri’s five betulaceous species, always forming shrubs, sometimes in thickets, and never assuming the form of a tree. Its staminate catkins present during winter immediately identify plants of this species as Betulaceae, but the small, globe-shaped buds are unlike the more pointed buds of Ostrya and the elongated, reddish buds of Alnus. This species is the least demanding in terms of being near water and can be found even in upland prairies and glades. I haven’t yet associated any woodboring beetles with this plant in Missouri, but there are several jewel beetles known from the eastern U.S. that utilize Corylus (Agrilus corylicola, A. fulgens, and A. pseudocoryli) and could occur in Missouri.

pine savanna - fire managementThe upland habitats at Hawn are of interest as well. Lamotte sandstones are the dominant bedrock, creating acid soils that support a canopy dominated by Missouri’s only native species of pine, Pinus echinata (shortleaf pine), several species of oak, and a diversity of acid-loving shrubs primarily in the family Ericaceae (including the stunningly beautiful Rhododendron prinophyllum, or wild azalea). Historically, so-called “pine savanna” was prevalent in this area, a natural community in which periodic fires maintained an open structure amongst the fire-adapted pines and allowed a diverse herbaceous layer beneath the open canopy. Much of Hawn has closed up after decades of fire suppression; trail through pine savannahowever, the Department of Natural Resources has implemented a rotational burn management regime to recreate pine savanna habitat within Hawn’s Whispering Pines Wild Area. Evidence of what appeared to be very recent burns could be seen at several places as I hiked along the Whispering Pines Trail, and while many visitors might have been alarmed at the apparent “damage” they were observing, my heart sang with the prospect of seeing mature pine savanna communities taking hold throughout my beloved Hawn. As I stood atop this ridge and looked back down from where I had come, I could almost see Henry Schoolcraft and Levi Pettibone in the distance on horseback, perhaps pausing to gaze at an elk.

REFERENCES:

Cliburn, J. and G. Klomps. 1980. A Key to Missouri Trees in Winter, 2nd edition. Missouri Department of Conservation, Jefferson City, 43 pp. (subsequently revised)

Furlow, J. J.  2004. Betulaceae in Flora of North America @ efloras.org. http://www.efloras.org/florataxon.aspx?flora_id=1&taxon_id=10101.

MacRae, T. C. 2003. Agrilus (s. str.) betulanigrae MacRae (Coleoptera: Buprestidae: Agrilini), a new species from North America, with comments on subgeneric placement and a key to the otiosus species-group in North America. Zootaxa 380:1–9.

MacRae, T. C., and G. H. Nelson. 2003. Distributional and biological notes on Buprestidae (Coleoptera) in North and Central America and the West Indies, with validation of one species. The Coleopterists Bulletin 57(1):57–70.

MacRae, T. C. and M. E. Rice. 2007. Distributional and biological observations on North American Cerambycidae (Coleoptera). The Coleopterists Bulletin 61(2):227–263.

Nelson, G. H. and T. C. MacRae. 1990. Additional notes on the biology and distribution of Buprestidae (Coleoptera) in North America, III. The Coleopterists Bulletin 44(3):349–354.

Yatskievych, G. 2006. Steyermark’s Flora of Missouri, Volume 2. The Missouri Botanical Garden Press, St. Louis, 1181 pp.

Copyright © Ted C. MacRae 2009

Add to FacebookAdd to NewsvineAdd to DiggAdd to Del.icio.usAdd to StumbleuponAdd to RedditAdd to BlinklistAdd to Ma.gnoliaAdd to TechnoratiAdd to Furl

Top Ten of 2008

For the first post of 2009, I begin with a look back at some of my favorite photos from 2008 (idea stolen from Alex Wild and others).  I initially hesitated to do a “best photos” post since I’m not really a photographer – just an entomologist with a camera.  Nevertheless, and with that caveat in mind, I offer ten photos that represent some of my favorites from this past year. To force some diversity in my picks, I’ve created “winning” categories (otherwise you might just see ten tiger beetles!). Click on the photos to see larger versions, and feel free to vote for your favorite. If so, what did you like about it? Was there a photo I didn’t pick that you liked better?  Enjoy!

Best tiger beetle

Cicindela formosa generosa

From “All the better to see you with, my dear!” (September 2008).  Picking a top tiger beetle photo was tough with so many to choose from.  Ultimately, I decided I really like these face-on shots, and of the several I’ve posted this one of Cicindela formosa generosa has the overall best composition, balance and symmetry.  I considered this one of Cicindela formosa formosa – with its half-cocked jaws, it probably has better personality.  However, the one above got the final nod because it is a true field shot of an unconfined, unmanipulated individual.

Best jewel beetle

Aegelia petelii

From Buppies in the bush(veld) (December 2008).  Although taken back in 1999, I just recently scanned and posted this photo of Agelia petelii from South Africa.  I like the bold, contrasting colors of the beetle combined with the soft colors of the host foliage.  Runners up included these photos of Evides pubiventris with its sumptuous iridescent green blending beautifully with the green background (but suffering slightly from shallow depth of field) and Chrysobothris femorata with its intricate surface sculpturing.

Best longhorned beetle

Tetraopes femoratus

From Rattled in the Black Hills (September 2008).  This was an easy choice – none of the other longhorned beetle photos that I posted during 2008 matched this photo of Tetraopes femoratus for clarity, composition, and the striking contrast between the red color of the beetle and the green color of the host plant.  I especially like the detailing of the body pubescence.

Best non-beetle insect

Proctacanthus milbertii

From Magnificently Monstrous Muscomorphs (November 2008).  I do like other insect besides beetles, and robber flies are hard to beat for their charisma.  This photo of Proctacanthus milbertii (which, as Chris Taylor pointed out, literally translates to “Milbert’s spiny butt”), has great composition and nice, complimentary colors.  I like contrast between the fine detail of the fly and the soft background.

Best non-insect arthropod

Argiope aurantia

From Happy Halloween! (October 2008). I didn’t have many non-insect arthropod photos to choose from, but this photo of a female Argiope aurantia (yellow garden spider) would be deserving of recognition no matter how many I had to choose from. I like the bold, contrasting colors and symmetry of the spider in front of the dappled background of this photo.

Best non-arthropod animal

Prairie rattlesnake (Crotolus viridis)

Another one from Rattled in the Black Hills (September 2008).  This is admittedly not the best photo from a purely technical perspective – it’s a little out of focus, and the color is a bit off.  However, no photo could better convey the moment – confronted with a live, angry prairie rattlesnake (Crotalus viridis) (among the more aggressive species in the genus).  The forked tongue and rattle – blurred in motion – were icing on the cake.

Best wildflower

Victoria Glades

From Glades of Jefferson County (July 2008).  I had several wildflower closeups to choose from, but I kept coming back to this field shot of pale purple coneflower (Echincea simulata) and Missouri evening primrose (Oenethera macrocarpa).  The eastern redcedars (Juniperus virginiana) in the background are at once indicative of their preferred habitat (limestone/dolomite glades) and also testament to their threatening encroachment.

Best tree

Calocedrus decurrens

From the very simply and aptly named Lake Tahoe, California (March 2008).  Incense cedar (Calocedrus decurrens), with its reddish, deeply furrowed bark and great height, is one of the most majestic of western conifers.  I was captivated by this tree – beautiful even in death and contrasting nicely with the surrounding green foliage.

Best rockscape

Pipestone National Monument, Old Stone Face

From Pipestone National Monument (April 2008).  “Old Stone Face” is one of Pipestone’s most recognizable geologic features, and the short angle of the sun on this early spring day provided nice detail to the cracks and fissures of the rock – almost appropriately adding a weathered “age” to this old man.

Best landscape

Emerald Isle, Lake Tahoe

Another one from Lake Tahoe, California (March 2008).  Few places on earth are more photogenic than Lake Tahoe, and this perspective overlooking Emerald Bay is among the finest views I’ve seen.  Brilliant blue skies and majestic snow covered mountains reflected perfectly from the still surface, with Fannette Island providing a perfect focal point for the photo.

Best miscellaneous

Water drops, Ozark Trail, Trace Creek SectionFrom Ozark Trail, lower Trace Creek Section (December 2007).  While technically not a 2008 photo, it’s close enough.  This was one of the first macro photographs I took with my camera, and it remains one of my favorites.  A chance occurence of an unlikely subject, created by cold temperatures and heavy moisture-laden air. I like the contrast between the water drops – sharp, round, and clear – with the vertical shapes of the leaf petioles and background trees.  Viewing the image full-sized reveals the reflection of the photographer in the leftmost water drop.

Subsequent edit: Okay, so after I put this post together, I realized I actually featured eleven photos – too much difficulty choosing, I guess. Let’s call it a baker’s ten.

Two new species of Agrilus from Mexico

ResearchBlogging.orgThe enormous, cosmopolitan genus Agrilus (family Buprestidae – commonly called jewel beetles or metallic woodboring beetles) contains nearly 4,000 described species (Bellamy 2008). With many more still awaiting description, it is perhaps the largest genus in the entire animal kingdom (Bellamy 2003). Agrilus species are primarily twig and branch borers, utilizing recently dead wood for larval development – although there are notable exceptions, e.g. Agrilus anxius (bronze birch borer), A. bilineatus (twolined chestnut borer), and A. planipennis (emerald ash borer), which attack the trunks of living trees and, thus, are of significant economic importance in forest and ornamental landscapes. Host specificity among Agrilus species ranges from highly monophagous – associated exclusively with a single plant species – to rather oliphagous – utilizing several, usually related, plant genera. Adults of Agrilus species are most often found on the foliage of their larval hosts and do not generally visit flowers, as is common in some other genera (e.g., Acmaeodera and Anthaxia). Interestingly, despite the diversity and worldwide distribution of the genus, no species of Agrilus are known to be associated with coniferous plants – a fact that has limited their expansion into the vast northern boreal forests.

Texas, Bexar Co., San Antonio, nr. Fort Sam Houston, em. 25.iv-14.v.1997 ex Phoradendron tomentosum coll. ii.1997, D. Heffern & D. W. SundbergAs can be imagined by its enormity, a comprehensive understanding of the genus will remain a distant goal for many years. Progress will come incrementally, as formal descriptions of new species gradually improve our knowledge of the fauna that exists in each of the world’s main biogeographic provinces. In a recent issue of the online journal Zootaxa, Dr. Henry Hespenheide (UCLA) describes two new species of Agrilus from Mexico. These two species are interesting because of their association with ‘mistletoe’ plants in the genus Phoradendron (family Viscaceae1), obligate hemiparasites that attach to branches and stems of various woody trees and shrubs in tropical and warm temperate regions of the New World. Plants in this genus are known to support a variety of host-restricted insect herbivores, principally in the orders Hemiptera, Coleoptera and Lepidoptera. A single buprestid species has been associated with Phoradendron to this point – Agrilus turnbowi, recently described from specimens reared from dead stems of Phoradendron tomentosum attached to mesquite (Prosopis glandulosa) in southern Texas (Nelson 1990) and pictured here from a specimen in my collection that was reared from dead mistletoe collected at the type locality. At the time of its description, this species was not relatable to any of the other known species in the genus.

1 The Angiosperm Phylogeny Group (2003) includes the Viscaceae in a broader circumscription of the family Santalaceae. However, recent molecular studies suggest the Santalaceae are polyphyletic, with strong support for Viscaceae as a distinct, monophyletic clade (Der & Nickrent 2008).

The two new Mexican species – A. andersoni from Guerrero and Puebla (Figs. 1-3), and A. howdenorum from Oaxaca (Figs. 4-6) – are apparently related to A. turnbowi, which they resemble by their purplish-red coloration and complex pattern of golden setae on the elytra. They are also superficially very similar to each other but differ most notably in size and the overall color and pattern of setae on the elytra.

Figures 1–3. Agrilus andersoni Hespenheide: 1. dorsal habitus; 2. lateral habitus (scale bar indicates 2.0 mm); 3. genitalia of male (scale bar indicates 0.5 mm) (from Hespenheide 2008).

Figures 4–6. Agrilus howdenorum Hespenheide: 4. dorsal habitus; 5. lateral habitus (scale bar indicates 2.0 mm); 6. genitalia of male (scale bar indicates 0.5 mm) (from Hespenheide 2008).

Hespenheide speculates that the color and pattern of the golden setae on the elytra may serve to make the beetles less conspicuous by disruptive coloration, noting the similar coloration of the setae to the leaves of Phoradendron as seen in the photograph of Agrilus howdenorum on its host plant (Fig. 7). This form of crypsis may also be enhanced by the purplish-red ground coloration of the adult, which resembles that of the small, darkened blemishes often observed on the foliage of these plants.

Figure 7. Agrilus howdenorum adult on mistletoe host plant near Diaz Ordaz, Oaxaca, México. The golden setae on the elytra are similar in color to the leaves of the mistletoe and may function as a disruptive color pattern. Photograph by C.L. Bellamy (from Hespenheide 2008).

REFERENCES

Angiosperm Phylogeny Group. 2003. An update of the Angiosperm Phylogeny Group classification for the orders and families of flowering plants: APG II. Botanical Journal of the Linnean Society, 141: 399-436.

Bellamy, C. L. 2003. The stunning world of jewel beetles. Wings, Essays on Invertebrate Conservation, 26(2): 13-17.

Bellamy, C. L. 2008. A World Catalogue and Bibliography of the Jewel Beetles (Coleoptera: Buprestoidea), Volume 4: Agrilinae: Agrilina through Trachyini. Pensoft Series Faunistica No. 79, 722 pp.

Der, J. P. & D. L. Nickrent. 2008. A Molecular Phylogeny of Santalaceae (Santalales). Systematic Botany, 33(1):107-116.

Hespenheide, H. A. (2008). New Agrilus Curtis species from mistletoe in México (Coleoptera: Buprestidae) Zootaxa, 1879, 52-56

Nelson, G. H. 1990. A new species of Agrilus reared from mistletoe in Texas (Coleoptera: Buprestidae). The Coleopterists Bulletin, 44(3):374-376.

A sand prairie autumn

Splitbeard bluestem seed headsAsk any astronomer when autumn begins, and they will likely tell you it begins at the autumnal equinox – when shortening days and lengthening nights become equal as the sun crosses over the celestial equator. According to them, fall began this year on September 22 – at 11:44:18 A.M. EDT, to be precise. I agree that autumn begins at a precise moment, but it is not at the equinox. Rather, it is that unpredictable moment when a sudden crispness in the air is felt, when the sky somehow seems bluer and shadows seem sharper, and hints of yellow – ever so subtle – start to appear in the landscape. Butterfly pea blossomIn Missouri, with its middle latitudes, this usually happens a few weeks before the equinox, as August is waning into September. It is a moment that goes unnoticed by many, especially those whose lives and livelihoods have lost all connection with the natural world. To plants and animals, however, it is a clear signal – a signal to begin making preparations for the long cold months of winter that lie ahead. Plants that have not yet flowered begin to do so in earnest, while those that have shift energy reserves into developing seeds. Animals take advantage of their final opportunities to feed before enduring the scarcities of winter, digging in to sleep through them, or abandoning altogether and migrating to warmer climes. Insects begin hastily provisioning nests for their broods or laying eggs – tiny capsules of life that survive the harsh winter before hatching in spring and beginning the cycle anew.

Sand prairie in early September.Sand prairie in early October.  Note abundance of splitbeard bluestem seed heads.Across much of Missouri, in the Ozark Highlands and in riparian ribbons dissecting the northern Plains, autumn brings an increasingly intense display of reds, purples, oranges, and yellows, as the leaves of deciduous hardwoods begin breaking down their chlorophyll to unmask underlying anthocyanins and other pigments. Small southern jointweedIn Missouri’s remnant prairies, seas of verdant green morph to muted shades of amber, tawny, and beige. This subtle transformation is even more spectacular in the critically imperiled sand prairies of the Southeast Lowlands, where stands of splitbeard bluestem (Andropogon ternaries – above) turn a rich russet color while fluffy, white seed heads (1st paragraph, 1st photo) appear along the length of each stem, evoking images of shooting fireworks. Small southern jointweed (Polygonella americana – right) finds a home at the northern extent of its distribution in these prairie remnants and in similar habitats in nearby Crowley’s Ridge, blooming in profusion once the cooler nights arrive. Butterfly pea (Clitoria mariana – 1st paragraph, 2nd photo) blooms add a gorgeous splash of soft purple in contrast to the muted colors of the plants around them.

Kent Fothergill, Ted MacRae, and Rich ThomaAfter first becoming acquainted with Missouri’s sand prairies this past summer, I knew a fall trip (or two) would be in order. The extensive deep, dry sand barrens were ideal habitat for sand-loving insects, including certain spring/fall species of tiger beetles that would not be active during the summer months. The cooler nights and crisp air of early fall make insect collecting extraordinarily pleasurable, so it took little effort to convince friends and colleagues Kent and Rich to join me on another excursion to these extraordinary remnant habitats, along with my (then 8 yr-old) daughter Madison (who would likely characterize this as “tallgrass” prairie). Madison MacRae, age 9 (almost)I was, as ever, on the lookout for tiger beetles; however, temperatures were cool, skies were overcast, and the fall season was just beginning, greatly limiting tiger beetle activity during this first fall visit. We did see one Cicindela formosa (big sand tiger beetle), which cooperated fully for a nice series of photographs. We also found single specimens of the annoyingly ubiquitous C. punctulata (punctured tiger beetle) and a curiously out-of-place C. duodecimguttata (12-spotted tiger beetle), which must have flown some distance from the nearest dark, muddy streambank that it surely prefers. Of greatest interest, we found two specimens of C. scutellaris (festive tiger beetle), which in this part of Missouri is represented by a population presenting a curious mix of influences from two different subspecies (more on this in a later post…). Despite the scarcity of tiger beetles, other insects were present in great diversity, some of which I share with you here.

Ululodes macleayanusThis bizarre creature, sitting on the stem of plains snakecotton (Froelichia floridana), is actually a neuropteran insect called an owlfly (family Ascalaphidae). Looking like a cross between a dragonfly and a butterfly due to its overly large eyes and many-veined wings but with long, clubbed antennae, this individual is demonstrating the cryptic resting posture they often assume with the abdomen projecting from the perch and resembling a twig. The divided eyes identify this individual as belonging to the genus Ululodes, and Dr. John D. Oswald (Texas A&M University) has kindly identified the species as U. macleayanus. As is true of many groups of insects, their taxonomy is far from completely understood. Larvae of these basal holometabolans are predaceous, lying on the ground with their large trap-jaws held wide open and often camouflaging themselves with sand and debris while waiting for prey. The slightest contact with the jaws springs them shut, and within a few minutes the prey is paralyzed and can be sucked dry at the larva’s leisure.

Ant lion, possibly in the genus Myrmeleon.Another family of neuropteran insects closely related to owlflies are antlions (family Myrmeleontidae, sometimes misspelled “Myrmeleonidae”). This individual (resting lower down on the very same F. floridana stem) may be in the genus Myrmeleon, but my wanting expertise doesn’t allow a more conclusive identification [edit 4/12/09 – John D. Oswald has identified the species as Myrmeleon immaculatus]. Strictly speaking, the term “antlion” applies to the larval form of the members of this family, all of whom create pits in sandy soils to trap ants and other small insects, thus, it’s occurrence in the sand prairie is not surprising. Larvae lie in wait beneath the sand at the bottom of the pit, flipping sand on the hapless prey to prevent it from escaping until they can impale it with their large, sickle-shaped jaws, inject digestive enzymes that ‘pre-digest’ the prey’s tissues, and suck out the liquifying contents. Finding larvae is not easy – even when pits are located and dug up, the larvae lie motionless and are often covered with a layer of sand that makes them almost impossible to detect. I’ve tried digging up pits several times and have failed as yet to find one. Larvae are also sometimes referred to as “doodlebugs” in reference to the winding, spiralling trails that the larvae leave in the sand while searching for a good trap location – these trails look like someone has doodled in the sand.

Bembix americanaThis digger wasp, Bembix americana (ID confirmed by Matthias Buck), was common on the barren sand exposures, where they dig burrows into the loose sand. Formerly included in the family Sphecidae (containing the better-known “cicada killer”), members of this group are now placed in their own family (Crabronidae). Adult females provision their nest with flies, which they catch and sting to paralyze before dragging it down into the burrow. As is common with the social hymenoptera such as bees and paper wasps, these solitary wasps engage in active parental care by providing greater number of prey as the larva grows. As many as twenty flies might be needed for a single larva. I found the burrows of these wasps at first difficult to distinguish from those created by adults of the tiger beetles I so desired, but eventually learned to distinguish them by their rounder shape and coarser, “pile” rather than “fanned” diggings (see this post for more on this subject).

Stichopogon trifasciatusRobber flies (family Asilidae) are a favorite group of mine (or, at least, as favorite as a non-coleopteran group can be). This small species, Stichopogon trifasciatus (ID confirmed by Herschel Raney), was also common on the barren sandy surface. The specific epithet refers to the three bands of alternating light and dark bands on the abdomen. Many species in this family are broadly distributed but have fairly restrictive ecological requirements, resulting in rather localized occurrences within their distribution. Stichopogon trifasciatus occurs throughout North America and south into the Neotropics wherever barren, sandy or gravely areas near water can be found. Adults are deadly predators, swooping down on spiders, flies and other small insects and “stabbing” them with their stout beak.

Chelinidea vittigerPrickly pear cactus (Opuntia humifusa) grows abundantly in the sandy soil amongst the clumps of bluestem, and on the pads were these nymphs of Chelinidea vittiger (cactus bug, family Coreidae). This wide-ranging species occurs across the U.S. and southward to northern Mexico wherever prickly pear hosts can be found. This species can either be considered a beneficial or a pest, depending upon perspective. On the one hand, it serves as a minor component in a pest complex that prevents prickly pear from aggressively overtaking rangelands in North America; however, prickly pear is used by ranchers as emergency forage, and fruits and spineless pads are also sometimes harvested for produce. In Missouri, O. humifusa is a non-aggressive component of glades, prairies, and sand and gravel washes, making C. vittiger an interesting member of the states natural diversity.

Ammophila sp., possibly A. proceraThis wasp in the genus Ammophila (perhaps A. procera as suggested by Herschel Raney) was found clinging by its jaws to a bluestem stem in the cool morning, where it presumably spent the night. One of the true sphecid (or “thread-waist”) wasps, A. procera is a widespread and common species in eastern North America. One of the largest members of the genus, its distinctive, bold silver dashes on the thorax distinguish it from most other sympatric congeners. Similar to the habits of most other aculeate wasp groups, this species captures and paralyzes sawfly or lepidopteran caterpillars to serve as food for its developing brood. Females dig burrows and lay eggs on the paralyzed hosts with which the nests have been provisioned. Adults are also found commonly on flowers, presumably to feed on nectar and/or pollen.

Dusty hog-nosed snakeRich is a bit of herpatologist, so when he brought this hog-nosed snake to our attention we all had a good time pestering it to try to get it to turn upside down and play dead. I had never seen a hog-nosed snake before but knew of its habit of rolling over and opening its mouth with its tongue hanging out when disturbed, even flopping right back over when turned rightside up or staying limp when picked up. We succeeded in getting it to emit its foul musky smell, but much to our disappointment it never did play dead, instead using its shovel-shaped snout to dig into the sand. Dusty hog-nosed snake - head closeupWe had assumed this was the common and widespread eastern hog-nosed snake (Heterodon platirhinos); however, in our attempts to turn it over I noticed its black and orange checker patterned belly. I later learned this to be characteristic of the dusky hog-nosed snake (H. nasicus gloydi), only recently discovered in the sand prairies of southeast Missouri and regarded as critically imperiled in the state due to the near complete destruction of such habitats. Disjunct from the main population further west, its continued survival in Missouri depends upon the survival of these small sand prairie remnants in the Southeast Lowlands.