Friday Flower: Red Buckeye

Beetles, spiders, and snakes were not the only delights that Rich and I saw as we hiked the lower stretch of the Ozark Trail’s Wappapello Section in early April.  Entering the rich, moist, east-facing slopes overlooking the Black River valley, the oaks and hickories were still in the early stages of bud break. A lush, green understory, however, spread out before us, punctuated by the striking inflorescences of red buckeye, Aesculus pavia (family Hippocastanaceae). Among the first trees to bloom in spring, red buckeye is unmistakable in the field due to its red flowers and palmately divided leaves.

Red buckeye is native to the southeastern U.S., just reaching Missouri in the southeastern Ozarks (though cultivated further north). This makes it less well-known than the more widely distributed Ohio buckeye, Aesculus glabra (absent only from the southeastern lowlands and northwestern corner of the state, and easily distinguished by its white inflorescences, larger size, and spreading growth habit).  Like that species, the seeds and young foliage especially are poisonous if eaten due to glycosidic alkaloids and saponins.  Native Americans roasted, peeled and mashed the nuts into a meal called “Hetuck.”

I first encountered this species in 2001 along Fox Creek in the White River Hills of extreme southwestern Missouri.  It was one of several species that I had selectively “cut” and left in situ for a season to allow infestation by wood boring beetles.  I retrieved the wood the following spring and reared five species of longhorned beetles (family Cerambycidae) from the dead branches, including Astyleiopus variegatus, Hyperplatys maculata, Leptostylus transversus, Lepturges angulatus, and the prize – the very uncommonly encountered Lepturges regularis. All of these represented new larval host records; however, it was not until after I published those records (MacRae and Rice 2007) that I realized the plant itself was not known by Steyermark (1963) to occur naturally outside of the southeastern Ozark Highlands.

Speaking of early spring flowers, many such delights can be found at Berry Go Round #27 which is now up at Mary Farmer’s A Neotropical Savanna. It’s not just spring ephemerals, however, as another Missouri blogger and I show that winter has it’s own botanical charms. Stop by and enjoy the feast!

REFERENCES:

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

Steyermark, J. A. 1963. Flora of Missouri.  The Iowa State University Press, Ames, 1728 pp.

Copyright © Ted C. MacRae 2010

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Lake Tahoe – 2010 Preview

How does an entomologist/wannabe botanist-ecologist-geologist-cyclist-nature photographer spend his time on a family vacation?

  • Thursday evening to Saturday late afternoon:
    - Drive from St. Louis to Lake Tahoe.  In between driving shifts:
    - Complete manuscript on Cylindera cursitans surveys
    - Complete manuscript on Dromochorus pruinina surveys.
    - Arrive late afternoon, quick 1-hr bike ride before dark.
  • Sunday:
    - Cross-country skiing with the family: Spooner Lake (~6 miles).
    - Sight-seeing: Sand Harbor Overlook on the east shore.
    - Hang out at the hot tub with the family and a glass of wine.
  • Monday:
    - Drive to Sacramento with the family.
    - Visit buprestid-colleagues Chuck Bellamy (CDFA) and Mark Volkovitsh (Russian Academy of Science).
    - Private lesson from Mark on how to dissect buprestid larvae for taxonomic description.
    - Dinner with my favorite brothers-in-law.
    - Drive back to Lake Tahoe.
  • Tuesday:
    - Snowshoe hike with the family: Emerald Bay to Eagle Lake and back (2 miles, 1,900′ of climbing).
    - Bike ride: South Lake Tahoe to Bliss State Park and back (33 miles, 1,100′ of climbing).
  • Wednesday:
    - Bike ride: all the way around Lake Tahoe (72 miles, 3,500′ of climbing).
    - Hang out at the hot tub with the family and a glass of wine.
  • Thursday:
    - Botanizing and hiking with daughter Madison at Mt. Rose (4 miles, 1,300′ feet of climbing).
    - Hang out at the hot tub with the family and a glass of wine.
  • Friday:
    - Alpine skiing with the family at Heavenly Ski Resort.
    - Join a 2-hour ski tour with US Forest Service rangers discussing natural and cultural history of Lake Tahoe.
    - Hang out at the hot tub with the family and a glass of wine.
  • Saturday morning to Sunday night:
    - Drive from Lake Tahoe back to St. Louis.  In between driving shifts:
    - Process/file photographs from trip (~250).
    - Complete reports for 2009 collecting permits.
    - Complete new applications for 2010 permits.
    - Begin manuscript on Cylindera celeripes conservation status.
  • Monday:
    - Return to work mentally refreshed!

I’ve already shared a bit of the trip with a view of Mt. Rose from 7,000′ and ensuing pismire quagmire.  Today I share some views of one of the most scenic of lakeside spots on the east shore – Sand Harbor Overlook.  I featured this spot in this post from last year’s trip due to its stunning beauty, and this year I was no less impressed.  I still had that same, annoying, afternoon sun to deal with (next year I’ve resolved to get here during the morning) but managed to get some passable photographs.  The one above is my favorite, and I hope you enjoy the following as well. (p.s. if someone knows how to fix a sun-blown sky in Photoshop Elements, please let me know).

Copyright © Ted C. MacRae 2010

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Hawn State Park – Winter Hiking at its Finest

Two weekends ago we received another wave in what has been an unusually frequent series of snow events. I’m sure my northern (and Patagonian) friends are not impressed, but at our middlin’ latitudes snow falls rather infrequently and rarely sticks around for long when it does. This winter has been different, with snowfall almost every week, it seems like, and temperatures that have remained cold enough to keep it around for awhile. While this latest snowfall measured only a modest 1-2 inches here in the St. Louis area, a 7-inch blanket (as measured by my hiking stick) fell in the Ozark Highlands just south of here. Coming as it did at the start of the weekend, I welcomed the opportunity to go for a hike — among my favorite wintertime activities — in a landscape that is rarely seen covered in deep, newly-fallen snow. My daughter Madison loves hiking as much as I do (even in deep snow), so the two of us headed off to perhaps my favorite of Missouri’s public areas, Hawn State Park.  I have long adored Hawn for its premier hiking, facinating geology, and unusual flora, and everytime I visit Hawn I find something new to love about it.  

Lamotte sandstone outcrops on the White Oaks Trail


Such was the case on this visit, when Madison and I decided to explore the White Oaks Trail, a newer trail that I had not yet hiked.  I was a little concered whether we would even be able to get to the park, as the road leading into it had only been partially plowed (and we had already seen one car off the road, causing me to reach down and switch on the 4-wheel drive).  Most of the park was snowed in, but we were able to reach the uppermost parking area, leaving our snow-covered trail-finding abilities as the last obstacle to overcome.  After studying the trail map and looking at different route options, I asked Madison if she wanted to hike 2 miles, 4 miles, or 6 miles.  She immediately blurted out “6 miles!”, so off we went.  I was disappointed to see that we were not the first persons to have the idea, as we entered the trail only to find two sets of footprints (one human, one canid) leading off in front of us.  It did, however, make following the trail easier, and in fact I’ve had enough experience finding trails through the Ozark Highlands that I never felt like I needed the footprints in front of us to point the direction.  

Madison next to the root wad of an 83-yr old wind-thrown oak tree.


The White Oaks Trail followed nicely up-and-down terrain through mature white oak (Querucs alba) (appropriately) upland forest dissected by small riparian valleys before settling into relatively mild terrain through monotonous black oak forest.  Just when I thought the trail wouldn’t match the splendor of Hawn’s Whispering Pines and Pickle Creek Trails, it wrapped around to the south at the far end and passed by a beautiful hoo-doo complex of Lamotte sandstone outcroppingss supporting majestic, widely-spaced, mature shortleaf pines (Pinus echinata).  The rock outcrops provided a perfect spot to break for lunch while looking out on the deep, snow-covered valley in front of us.  

More Lamotte sandstone exposures along Pickle Creek, Whispering Pines Trail.


After counting a cut, wind-thrown black oak (Quercus velutinus) and determining a lifespan of 83 years, we took a connector trail down to the Whispering Pines Trail where it ran alonside the incomparably beautiful Pickle Creek.  Our hope was to hike down to the igneous shut-ins, where hard, pink rhyolites channeled the creek’s clear, spring-fed waters through narrow chutes and miniature gorges.  Upstream from the shut-ins, Pickle Creek runs lazily through the softer Lamotte sandstones that overlay those ancient rhyolites, combining with the snow cover to create a scene as peaceful and serene as any I’ve ever witnessed.

Pickle Creek meanders lazily through Whispering Pines Wild Area.

  
Just above the shut-ins, Pickle Creek bends to the west, carving deeply into the soft sandstone.  The porous nature of the rock allows moisture to trickle through and between the strata from the hillside above, creating seep zones that weaken underlying layers and lead to their collapse.  The abundant moisture this winter and continuous cycles of daytime thawing and nighttime freezes have resulted in extraordinary ice formations along the bluff face and underneath the overhanging layers, the likes of which are rarely seen in our normally more open winters.  Compare the scene in the first photo below with that in the second, taken at almost exactly the same spot one year ago in February 2009.  

Icicle formations along Pickle Creek, Whispering Pines Trail.


Same place as above in February 2009.


Ice rarely forms over the small ponds and lakes that dot the Ozark Highlands, much less its creeks and other moving waters.   The scene below of Pickle Creek as it exits the sandstone gorge is a testament to the slowness of its movements and the unusually consistent cold temperatures experienced during the past several weeks.  Only a short distance downstream, however, these lazy waters reach the bottommost layers of the erodable sandstones and encounter the hard rhyolites below.  These half-a-billion year old layers of igneous rock are much more resistant to the wearing action of water, which rushes noisily through narrowly-carved chutes before fanning out in broad sheets over smooth, steep slopes below.  

Pickle Creek along Whispering Pines Trail.


Sadly, there would not be time to visit the shut-ins.  The short February day conspired with our snow-slowed pace to leave us with a too-low-sun by the time we reached the fork in the trail that led to the shut-ins, a mile in one direction, and our car, a mile in the other.  Although we (both) had thought to carry flashlights (just in case), the last thing I really wanted to do was find myself stumbling over snow-covered trails through the dark with my 10-yr old daughter. Even had we survived the nighttime winter woods, I might not have survived the inevitable maternal reaction to such an escapade.

Arriving back at White Oaks Trailhead with a few minutes to spare.


Copyright © Ted C. MacRae 2010  

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Tiger Beetles Agree—It’s Hot in Florida!

Florida is known for its rich assemblage of tiger beetles—27 species in all, including four endemics (Choate 2003).  However, late summer is generally considered not the best time of year for seeing this diversity, since adult populations of most species begin to wane as the intensity of the summer heat reaches its peak.  I knew the timing of my family vacation in early August might be a bit off; however, considering I had never looked for tiger beetles in Florida before, I remained optimistic that I still might encounter some interesting species.  My optimism was quickly rewarded—in one afternoon of exploring the small coastal preserve just outside the back door of my sister-in-law’s condo, I found Ellipsoptera marginata (Margined Tiger Beetle), its sibling species E. hamata lacerata (Gulf Beach Tiger Beetle), and several 3rd-instar larvae in their burrows that proved to be the Florida endemic Tetracha floridana (Florida Metallic Tiger Beetle).  Good fortune would continue when I made a one-day trip to the interior highlands in a successful bid to find Florida’s rarest endemic, Cicindela highlandensis (Highlands Tiger Beetle), finding also as a bonus the splendidly camouflaged and also endemic Ellipsoptera hirtilabris (Moustached Tiger Beetle).  Five species, including three endemics, in just over a day of searching!  I had one more day to sneak off and do what I love most, and I wanted to make the most of it. 

Pine sandhill habitat, Withlachoochee State Forest—Citrus Tract

Among the suggestions given to me by my colleagues, the most promising-sounding was the “end of the road,” a Gulf Coast salt marsh near Steinhatchee in Dixie County where I was told as many as 6-10 species of tiger beetles could be seen at once.  I didn’t know it at the time, but this particular location has achieved legendary status among tiger beetle enthusiasts (Doug Taron recently wrote about his experience, calling it the Road to Nowhere).  A 200+ mile drive from my base near St. Petersburg, it would take the better part of 5 hours to drive there, and not wanting to put all of my eggs in one basket, I looked for potential stops along the way.  About midway along the drive was Withlacoochee State Forest, where one of my colleagues had told me I might still find the fairly widespread Cicindela abdominalis (Eastern Pinebarrens Tiger Beetle) and its close relative, C. scabrosa (Scabrous Tiger Beetle)—the fourth Florida endemic.  My plan was to leave early in the morning and spend a few hours at Withlacoochee before driving the rest of the way to finish out the day at Steinhatchee. 

"Stilting" by Cicindela abdominalis (Eastern Pinebarrens Tiger Beetle)

It took some time to find my bearings upon arriving, but after some discussion with the decidedly forestry-oriented staff at the headquarters, it seemed that the Citrus Tract was where I wanted to be.  I was looking for the sand barren and pine sandhill habitats that these species require, and the staff’s description of the northern edge of the tract as having lots of sand and “not very good for growing trees” suggested this might be the place.  Pine sandhill (also called “high pine”) is a pyrophytic (fire-dependent) plant community characterized by sandy, well-drained soils, a widely-spaced longleaf pine (Pinus palustris) and turkey oak (Quercus laevis) canopy, and an herbaceous layer dominated by wiregrass (Aristida stricta).  I quickly found such habitat in the area suggested, and it wasn’t long before I found the first of the two species—C. abdominalis—rather commonly along a sandy 2-track leading through the area.  For those of you who see a distinct resemblance of this species to the rare C. highlandensis that I highlighted from my trip to the central highlands, this is no coincidence.  Cicindela abdominalis is very closely related to that species, the latter distinquished by an absence of flattened, white setae on the sides of the prothorax and the abdomen and by the highly reduced or absent elytral maculations (Choate 1984).  Dense white setae and distinct apical elytral maculations are clearly visible in the individuals shown in these photographs. 

Stilting is often accompanied by "sun-facing" for additional thermoregulation

It was a blistering hot day (just as every other day on the trip had been so far), and it wasn’t only me who felt that way.  Tiger beetles, of course, are ectothermic and rely upon their environment for their body temperature.  Despite this, they are able to regulate body temperatures to some degree by using a range of behavioral adaptations intended to mitigate the effects of high surface temperatures and intense sunlight.  The photos above show one of these behaviors, known as stilting.  In this behavior, the adult stands tall on its long legs to elevate its body above the thin layer of hotter air right next to the soil surface and as far off the sand as possible (Pearson et al. 2006).  As the heat of the day intensifies and the zone of hot air at the soil surface broadens, stilting alone may be insufficient to prevent overheating. When this happens, the beetles combine stilting with sun-facing, a behavior in which the front part of the body is elevated with the head oriented towards the sun. This position exposes only the front of the head to the sun’s direct rays, thus minimizing the body surface area exposed to incident radiation.

Stilting and sun-facing by Ellipsoptera hirtilabris (Moustached Tiger Beetle)

I was also fortunate to have another chance at photographing the beautiful and marvelously-camouflaged Ellipsoptera hirtilabris (Moustached Tiger Beetle), which, in similar fashion to C. highlandensis, I found co-occurring with C. abdominalis in rather low numbers. As before, they were extremely wary and difficult to approach, especially in the extreme heat of the day, and all of my best efforts to get a good shot of the species in its “classic” pose were frustrated. The photo above was about as close as I could get to any of these beetles when they were out in the open before they would flee; however, it nicely demonstrates the use of stilting combined with sun-facing during the hottest part of the day.

"Shade seeking" is another behavioral response to intense heat.

Another behavioral response to extreme heat is shade-seeking—adults may either remain active, shuttling in and out of shaded areas, or avoid exposed areas altogether and become inactive.  One thermoregulatory behavior for extreme heat that I did not observe was daytime-burrowing, in which adults construct temporary shallow burrows during the hottest hours of the day. Although I did not observe this behavior by either species at Withlacoochee, I have seen it commonly among several species in sandy habitats here in Missouri and in the Sandhills of Nebraska (e.g., Cicindela formosa, Cicindela limbata, Cicindela repanda, Cicindela scutellaris, Cicindela tranquebarica, Ellipsoptera lepida).

There was one disappointment on the day—I did not see C. scabrosa.  However, I still had the “end of the road” to explore, so I remained happy with the now six species I had encountered and optimistic about finding additional species later in the day… 

Photo Details: Canon EOS 50D, ISO 100.
Habitat: Canon 17-85mm zoom lens (landscape, 17mm), 1/100 sec, f/10, natural light.
Insects: Canon 100mm macro lens (manual), 1/250 sec, f/16–18 (C. abdominalis) or f/20–22 (E. hirtilabris), MT-24EX flash w/ Sto-Fen diffusers.

REFERENCES: 

Choate, P. M., Jr.  1984.  A new species of Cicindela Linnaeus (Coleoptera: Cicindelidae) from Florida, and elevation of C. abdominalis scabrosa Shaupp to species level.  Entomological News 95:73–82.

Choate, P. M., Jr. 2003. A Field Guide and Identification Manual for Florida and Eastern U.S. Tiger Beetles.  University Press of Florida, Gainesville, 224 pp.

Pearson, D. L., C. B. Knisley and C. J. Kazilek. 2006. A Field Guide to the Tiger Beetles of the United States and Canada. Oxford University Press, New York, 227 pp.

Copyright © Ted C. MacRae 2009

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Ant-like Tiger Beetle

Fig. 1.  Adult female Cylindera cursitans

Fig. 1. Adult female Cylindera cursitans

One of the more recent of the 24 species of tiger beetles that we’ve collected in Missouri is Cylindera cursitans (Ant-like Tiger Beetle).  Although not yet formally recorded from the state, we’ve known about its occurrence here for some time now based on a single specimen deposited in the Enns Entomology Museum (University of Missouri).  With no more locality information to go on than the frustratingly vague “nr. Portageville,” my colleague Chris Brown and I made several attempts over the years to look for this species – eventually deciding that one particular spot where the highway stretched east of Portageville and dead-ended at the Mississippi River was the most likely collection site.  This locality, which we would come to call the “end of the hiway” spot (I suspect that every state with at least one tiger beetle aficionado has one or more so-named spots), proved to be a true tiger beetle “hot-spot,” with no less than 8 species of tiger beetles found along its sandy banks in our first few surveys.  However, C. cursitans was not among them, and success would only come with a little bit of serendipity when I received an email in 2007 from Kent Fothergill.  Kent explained that he had learned of me from my Missouri Tigers article (MacRae and Brown 2001), offered some comments about the tiger beetles that he had been finding since his recent move to southeast Missouri, and included full label data from the tiger beetles in the small collection of the Delta Research Center where his then-fianceé had secured a position as a research entomologist.  I wrote Kent back, thanked him for the data, and added this plea for assistance:

There is a single specimen of Cicindela cursitans in the UMC collection, it was collected in “nr. Portageville” on July 7, 1991.  We have tried several times without success to locate this species in Missouri – it’s the only species that we have not relocated.  If you have any interest in looking for it that would be great.  Attached is a pdf of recent paper describing its habits and biology in Nebraska.

Fig. 2.  Adult female Cylindera cursitans ovipositing into substrate.

Fig. 2. Adult female Cylindera cursitans ovipositing in moist sand/loam substrate.

Little did I know how catalytic that comment would be – the very next day I received an email from Kent not only stating that he found it, but that he found it at the “end of the hiway” spot where we thought it might be.  A digital photo confirmed its identity, and the that weekend I blasted down to meet Kent and see the beetle for myself.  I would see just two beetles that day, but both were at a new locality about one mile south of where Kent had originally spotted them.  Kent would later find them at yet another locality further north along the Mississippi River, and in 2008 the three of us (Kent, Chris, and myself) conducted an intensive survey of potential habitats in southeastern Missouri that identified additional populations both north and south of the original localities.  We concluded that populations of C. cursitans, were restricted in southeast Missouri to the ribbons of wet bottomland forest that occupy the narrow corridor between the Mississippi River and the levees that confine it. However, the populations appeared secure and likely did not require any immediate conservation measures to ensure their long-term survival within the state. 

Fig. 3.  Adult male Cylindera cursitans.

Fig. 3. Adult male Cylindera cursitans.

The bottomland forests that harbor C. cursitans in southeast Missouri (Fig. 3) contrast sharply with the wet meadow habitats reported for populations in Nebraska (Brust et al. 2005a). Within these habitats, the beetles themselves are very easily overlooked because of their small size and rapid running capabilities.  In addition, adult activity peaks in June and begin to wane in July.  The combination of these factors explains our initial difficulty in finding the beetle; however, with a proper search image and better understanding of its temporal occurrence and habitat preference, we have since found the beetles to be rather easily located.  A lingering question from last year’s survey is, how far north along the Mississippi River does C. cursitans occur? Furthermore, might the species also occur in northeast Missouri due to its proximity to the Nebraska populations?  Most of Missouri straddles a curious distributional gap that separates the bottomland forest dwelling populations in the southeast from the wet meadow dwelling populations in the upper Great Plains (Hoback and Riggins 2001). This has led some authors to suggest that the observed distribution represents two disjunct forms and potentially two species (Ron Huber, pers. comm.). Additional surveys of potential habitat further north along the Mississippi River and in northwest Missouri along the Missouri River could prove useful in confirming or refuting that suggestion. 

Fig. 3.  Habitat for Cylindera cursitans, along Mississippi River, vic. Donaldson Point Conservation Area, New Madrid Co., Missouri.

Fig. 4. Habitat for Cylindera cursitans, along Mississippi River, vic. Donaldson Point Conservation Area, New Madrid Co., Missouri.

While such surveys were not possible this year, long-time fieldmate Rich Thoma and I were able to visit the Southeastern Lowlands in June to examine a few habitats along the Mississippi River found a little further north of the northernmost extent of our 2008 survey area. We succeeded in finding another population at one of these sites near the northern limit of the Southeastern Lowlands.  The individuals shown here (Figs. 1-3) were collected from that location (extreme northeastern Mississippi Co.), confined on local sand/loam substrate, and photographed a few days later.  In one of the photos (Fig. 2), a female can be seen in the act of ovipositing into a hole dug into the substrate with her ovipositor.  The more observant readers might notice a strong resemblance between this species and another species to which I have devoted several posts, Cylindera celeripes (Swift Tiger Beetle).  These two species are, in fact, quite closely related and can be distinguished by characters of the elytra (posterior portion not or only slightly expanded and lateral white maculations complete in cursitans, distinctly expanded and maculations reduced in celeripes) (Pearson et al. 2006), habitat (cursitans in moist lowland sites, celeripes in dry upland sites), and distribution (southeast Nebraska/southwest Iowa is the only area where the distributions of these two species overlap, although C. celeripes has not been seen in Nebraska for nearly 100 years! (Brust et al. 2005b)).

Photo details:
Figs. 1-3: Canon 100mm macro lens with Kenco extension tubes (68mm) on Canon EOS 50D (manual mode), ISO-100, 1/250 sec, f/18, MT-24EX flash 1/2 power through diffuser caps.
Fig. 4: Panasonic DMC-FX3 (landscape mode), ISO-100, 1/25 sec, f/2.8, natural light.

REFERENCES:

Brust, M., W. Hoback and C. B. Knisley.  2005a.  Biology, habitat preference, and larval description of Cicindela cursitans LeConte (Coleoptera: Carabidae: Cicindelinae).  The Coleopterists Bulletin 59(3):379-390.

Brust, M. L., S. M. Spomer and W. W. Hoback.  2005b.  Tiger Beetles of Nebraska.  University of Nebraska at Kearney.  http://www.unk.edu (Version 5APR2005).

 

Hoback, W. W. and J. L. Riggins.  2001.  Tiger beetles of the United States.  Jamestown, ND: Northern Prairie Wildlife Research Center Online.  http://www.npwrc.usgs.gov/resource/distr/insects/tigb/index.htm (Version 12DEC2003).

MacRae, T. C., and C. R. Brown. 2001. Missouri Tigers. Missouri Conservationist 62(6):14–19.

Pearson, D. L., C. B. Knisley and C. J. Kazilek. 2006. A Field Guide to the Tiger Beetles of the United States and Canada. Oxford University Press, New York, 227 pp.

Copyright © Ted C. MacRae 2009

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Typocerus deceptus in Missouri

It has been fifteen years now since I published an annotated checklist of the longhorned beetles (families Cerambycidae and Disteniidae) of Missouri (MacRae 1994).  That publication (and a similar one on Buprestidae) was the product of eight years of collecting – of specimens in the field and of data in any other public or private collection I could find that contained Missouri specimens – during my stint as a field entomologist with the Missouri Department of Agriculture.  I collected during the week while on my rounds.  I collected on weekends as well.  I visited every college and university in the state that had an insect collection of any size, and a few in neighboring states as well.  I made the acquaintance of private collectors with significant Missouri material – most notably Richard Heitzman, Marlin Rice, and the late Gayle Nelson.  By the time I left Missouri for a new position in Sacramento, I had documented 219 species and subspecies of longhorned beetles from the state – 66 of which were new state records.

Typocerus deceptus on flower of Hydrangea arborescens

Typocerus deceptus on flower of Hydrangea arborescens

Despite my best efforts, however, I knew the list was not complete – they never are.  In the years since returning to Missouri, I’ve documented an additional 10 species and subspecies in the state (MacRae and Rice 2007), and in a newly published paper (McDowell and MacRae 2009) the rare species, Typocerus deceptus, is documented from Missouri for the first time.  I cannot take credit for this discovery – that honor goes to the paper’s lead author, Tom McDowell of Carbondale, Illinois.  Tom first encountered this species in 2005 at Trail of Tears State Park in southeastern Missouri near Cape Girardeau while conducting routine insect surveys.  After seeing additional individuals on a subsequent visit to the park the following year, Tom contacted me to tell me of his find and graciously invited me to join him on further studies of this rarely encountered species.  I readily agreed, and in July of last year I met up with Tom at Trail of Tears to see the beetle for myself.

Typocerus deceptus on flower of Hydrangea arborescens

Typocerus deceptus on flower of Hydrangea arborescens

Typocerus deceptus has been recorded sporadically from across the eastern U.S.  Nothing is known of its biology other than adult flower hosts and activity periods, and the larva and larval host(s) remain completely unknown.  The species is aptly named, as its appearance is deceptively similar to the common and widespread species, T. velutinus.  Both of these species belong to the so-called “flower longhorn” group (subfamily Lepturinae), characterized by adults that are largely diurnal (active during the day) and attracted to a great variety of flowers upon which they feed.  Tom had found T. deceptus feeding on flowers of wild hydrangea (Hydrangea arborescens) in the company of several other flower longhorns, including T. velutinus.  The similarity of T. deceptus to T. velutinus makes distinguishing individuals amongst the vastly more abundant T. velutinus quite difficult.  However, Tom was able to recognize the species during his surveys as a result of prior experience with it in Illinois.  As Tom and I searched the wild hydrangea plants growing along an intermittent drainage between the road and the park’s unique mesic forest, we succeeded in picking out a total of four individuals of this species amongst the dozens of T. velutinus and other lepturines also feeding on the flowers.

Typocerus velutinus on flower of Hydrangea arborescens

Typocerus velutinus on flower of Hydrangea arborescens

I gradually developed a sense of the subtle differences that distinguish this species from T. velutinus and that allow its recognition in the field.  Typocerus deceptus is slightly more robust than T. velutinus, and whereas the transverse yellow elytral bands of the latter are distinct and well delimited, they are weaker and often interrupted at the middle in T. deceptus, giving the beetle a slightly darker brownish appearance.  The lateral margins of the elytra are also more strongly emarginated near the apices, giving the beetle a more distinctly tapered appearance.  Finally, while both species possess a distinct band of dense, yellow pubescence along the basal margin of the pronotum, this band is interrupted at the middle in T. deceptus. My ability to recognize this species in the field was confirmed a few weeks ago when I returned to Trail of Tears (with longtime field companion Rich Thoma) to attempt what seemed to be an impossible task – photograph these active and flighty insects in the field on their host plants.  Conditions were brutally humid, and I only saw two individuals that day – the first I immediately captured and kept alive as a backup for studio photographs should I fail to achieve my goal in the field, but the second individual (not seen until almost two hours later!) posed just long enough for me to whip off a series of frames, two of which turned out well enough to share with you here.  The first photo clearly shows the interrupted basal pubescent band, and both photos show the distinctly emarginate lateral elytral margins and weak transverse yellow bands (compare to the uninterrupted pronotal pubescent band and well developed transverse elytral bands of T. velutinus in the third photo).

Me with the discoverer of Typocerus deceptus in Missouri Trail of Tears State Park, July 2008

TCM with the discoverer of Typocerus deceptus in Missouri at Trail of Tears State Park, July 2008

It is possible that T. deceptus is not as rare as it appears and is simply overlooked due to its great resemblance to another much more abundant species. However, I believe this is unlikely given its rarity in collections of eastern U.S. Cerambycidae by casual and expert collectors alike.  Moreover, T. deceptus is not the only “rare” longhorned beetle to have been documented at Trail of Tears State Park – a number of other species have also been found there but not or only rarely elsewhere in Missouri (e.g., Enaphalodes cortiphagus, Hesperandra polita, Metacmaeops vittata, and Trigonarthris minnesotana).  This may be due to the unique, mesic forest found at Trail of Tears, being one of only a few sites in southeastern Missouri that support more typically eastern tree species such as American beech (Fagus grandifolia), tulip poplar (Liriodendron tulipifera), and cucumbertree (Magnolia acuminata).  Whether one of these trees serves as a larval host for T. deceptus is unknown.  Nevertheless, I will be returning to Trail of Tears in the future to see what other treasures remain hidden within its unique forests.

Photo details (insects): Canon 100mm macro lens on Canon EOS 50D, ISO 100, 1/250 sec, f/18-20, MT-24EX flash 1/4 power through diffuser caps.

REFERENCES:

MacRae, T. C. 1994. Annotated checklist of the longhorned beetles (Coleoptera: Cerambycidae and Disteniidae) known to occur in Missouri. Insecta Mundi 7(4) (1993):223–252.

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

McDowell, W. T. and T. C. MacRae. 2008. First record of Typocerus deceptus Knull, 1929 (Coleoptera: Cerambycidae) in Missouri, with notes on additional species from the state. The Pan-Pacific Entomologist 84(4):341-343 DOI: 10.3956/2008-23.1

Copyright © Ted C. MacRae 2009

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Trees of Lake Tahoe – The Deciduous Trees

Alder, Maple, and Nuttall’s Flowering Dogwood make beautiful bowers over swift, cool streams at an elevation of from 3000 to 5000 feet, mixed more or less with willows and cottonwood; and above these in lake basins the aspen forms fine ornamental groves, and lets its light shine gloriously in the autumn months.–John Muir, The Mountains of California (1894).

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This is the third installment of a “Trees of Lake Tahoe” series summarizing the trees of Tahoe Basin. The basin forests are, of course, dominated by a diverse assemblage of conifers – eleven species in all.  These were covered in parts 1 (Trees of Lake Tahoe – The Pines) and 2 (Trees of Lake Tahoe – The “Other” Conifers ) of this series.  Yet, despite this coniferous domination, the 14 species of deciduous trees¹ that occur in the Tahoe Basin is three more than the number of coniferous tree species.  These deciduous tree species will be covered in this third and final part, including the nine species I was able to locate on my recent visit to the area back in mid-March.  Because of the timing of that trip, the trees will be discussed from a decidedly wintertime perspective that makes species identifications a little more challenging compared to the coniferous species.

¹ Admittedly, I use the term “tree” in the broadest sense, since many of these species might better be described as “tree-like shrubs” or “shrubby trees,” often representing only the largest examples of genera whose members include a number of true shrubs.  Only a handful of these species routinely form large, unmistakably tree-like forms, the largest of which still pale in comparison to the coniferous giants that dominate the basin.

Family SALICACEAE

This family of dioecious plants (male and female flowers on separate plants) is represented in the Tahoe Basin by two genera.  Two species of Populus occur here, and both decidedly trees in form.  Most of the nine species of Salix that grow in the basin grow only as shrubs, while two of them sometimes form distinct trees.

Quaking aspen (Populus tremuloides)

…in winter, after every leaf has fallen, the white bark of the boles and branches seen in mass seems like a cloud of mist that has settled close down on the mountain, conforming to all its hollows and ridges like a mantle, yet roughened on the surface with innumerable ascending spires.–John Muir, Steep Trails (1918).

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Quaking aspen is one of the most unmistakable trees of the Tahoe Basin – regardless of the season.  Famous for its shimmering foliage during summer and blazing fall colors, it is equally distinctive during winter when its smooth, creamy, greenish-white trunks stand in stark, leafless contrast to the dark green coniferous foliage that cloaks the landscape.  Thick stands of this species are common in moist meadows and stream margins, with stands typically representing clonal colonies of genetically identical trees sprouting from a common root mat.  Although another species of Populus does occur in the basin (black cottonwood – see below), that species is not nearly as abundant as quaking aspen and lacks its distinctive smooth bark.

The second photo above shows some of the few, still-clinging leaves that I found, unremarkable in senescence but showing the flattened petioles that cause to summertime leaves to flutter and quiver incessantly with the summer breezes, alternately flashing their bright green upper surface and silvery underside.

Black cottonwood (Populus balsamifera ssp. trichocarpa)

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Black cottonwood is the largest American Populus and the tallest non-conifer in western North America.  Growing throughout the cool, moist Pacific Northwest, it is at its elevational limit in the Sierra Nevada along moist streams and lakeside habitats in the lower Tahoe Basin. The wonderfully knowledgeable Forest Service worker, who helped me greatly in my quest to locate all of the basin’s conifers, was skeptical about my chances of finding this species; however, while hiking the Rubicon Trail at Emerald Bay State Park I spotted the unmistakable, deeply furrowed, gray bark of this close relative of our own eastern cottonwood (Populus deltoides).  Examining the twigs revealed the large, pointed buds, sticky with resin, and a few clinging leaves whose wide, ovate shape confirmed the species’ identity.  It was the only black cottonwood I saw in the basin, although surely others exist throughout the basin at lakeside elevations.

Willows (Salix spp.)

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As a group, willows are easily distinguished from the other deciduous trees and shrubs that occur in the Tahoe Basin.  However, discriminating among the several species can be quite difficult, even for trained botanists.  Winter is not the best time to try to identify willows, as many species are distinguished by characters of the foliage and flowers.  In some cases, examination of both male and female flowers is required – frustrating since they are borne on separate plants!  Wintertime characters normally useful for other plants such as bark and twig color are rarely informative for different species of willow, and even growth habit as trees or shrubs can vary greatly within species depending on elevation and available moisture.  All of this is a long-winded way of saying I don’t know which or how many species of willow I observed in the Tahoe Basin.

p1020705_2p1020707_2According to Graf (1999), there are nine species of willow in the Tahoe Basin; however, only two of them are trees – the abundant shining willow (S. lucida spp. lasiandra), and the more drought-tolerant Scouler’s willow (S. scouleriana).  The remaining seven species are shrubs that rarely exceed 10-12 feet in height.  Indeed, one of them – arctic willow (Salix arctica) – grows no more than 4 inches tall, occurring in seepy slopes and along lake and stream margins in the subalpine zone at Carson Pass.  Most of the willows I observed were at lower elevation along the shore of Emerald Bay and in the wet meadows around South Lake Tahoe and Spooner Lake and were growing as large shrubs or small trees and exhibited either bright yellow or red bark on the year-old branches, turning to smooth gray on older branches.  I don’t know whether these represent one or more species, or if they even represent one of the two arborescent species, but I suspect the yellow-twigged species may represent Lemmon’s willow (S. lemmonii), one of the shub species and Tahoe’s most common willow.  Perhaps a stretch goal for next year’s trip could be to find and distinguish all nine Tahoe Basin willow species, but realistically I would settle for knowing for sure what species the plants in these photographs represent (although I definitely would like to find the diminutive arctic willow).

Family BETULACEAE

Like the Salicaceae, plants in this family have male and female flowers on separate structures called catkins, but the plants themselves are monoecious (both sexes on the same plant).  Two genera – Alnus and Betula – occur in the basin, each represented by one species.

Mountain alder (Alnus incana ssp. tenuifolia)

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Like the willows, mountain alder is another deciduous plant that straddles the line between tree and shrub, and as is typical of most species in these two plant families (Salicaceae and Betulaceae) the species shows a high affinity for moist sites along stream and lake margins and on seepy north- and east-facing slopes.  The largest specimens I saw, as pictured above left, were found growing on the granite sand beaches along the Rubicon Trail on the western shore of Emerald Bay in Emerald Bay State Park.  Like alders anywhere, this species is immediately recognizeable in winter due to the persistent woody cones that represent the previous year’s female catkins.  Another larger species of alder, white alder (A. rhombifolia), occurs in the Sierra Nevada, but it is not clear to me whether this species actually occurs in the Tahoe Basin proper.  Graf (1999) does not include it in his rather comprehensive treatment of Tahoe Basin plants, but Peterson & Peterson (1975) and Quinn (2006) both list it from the basin (although rare). 

Water birch (Betula occidentalis)

I did not observe this species, which Graf (1999) records from Carson Pass.  The only birch occurring in the Sierra Nevada, it is more common outside the basin proper on the eastern slopes above the burning sagebrush plains.  Like alder, separate male and female catkins are borne on the same tree; however, the female catkins of birch are solitary rather than clustered and disintegrate when ripe rather than persisting as woody cones.

Family FAGACEAE

This family contains the über diverse genus Quercus – represented in California by 20 species.  However, of the five arborescent oaks that occur in the Sierra Nevada, only one has successfully penetrated the high elevations of the Tahoe Basin. A second species of Quercus also inhabits this montane region but grows exclusively as a low shrub, and another shrub in the related genus Chrysolepis also grows here – these two latter species will be treated more fully in a future post.

Canyon live oak (Quercus chrysolepis)

The trunk was all knots and buttresses, gray like granite, and about as angular and irregular as the boulders on which it was growing—a type of steadfast, unwedgeable strength.–John Muir, The Mountains of California (1894).

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This is one of North America’s most variable oaks, exhibiting extreme variability in leaves and fruit and developing as either a tree or a shrub, depending upon the site where it grows. Slow growing and solid, it does best in sheltered locations, where it can develop an impressive, spreading crown and live a hundred years or more. On exposed slopes, it takes on a shorter, shrubbier aspect (above left) or forms dense thickets (above right).  I saw most of this species at lower elevations within the basin – along the Vikingsholm Trail in Emerald Bay State park leading down to the west shore of Emerald Bay.

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The leaves of this evergreen species are bluish green with numerous golden glandular hairs when young and becoming dull gray and smooth with age. Although there are no other arborescent oaks at this elevation with which it can be confused, I did find growing alongside it the strictly montane and shrubby huckleberry oak (Q. vaccinifolia).  The somewhat smaller, mostly entire leaves were the only indication it was not merely a shrub form of canyon live oak, and further study revealed that the two species can be distinguished by the presence of multiradiate glandular hairs on both leaf surfaces of canyon live oak.  These two species are closely related (both are in the Protobalanus – or “golden oak” – section of the genus), and widespread hybridization has apparently been documented in this part of the Sierra Nevada where the two species’ distributions overlap (Nixon 2002).

Family ROSACEAE

This large family of dioecious plants with usually pentamerous radial flowers is represented in the Tahoe Basin by nearly three dozen mostly perennial shrubs.  Six of these species, representing the genera Amelanchier, Cercocarpus, Prunus and Sorbus, sometimes develop a tree form.

Cherry (Prunus sp.)

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Two species of Prunus – bitter cherry (P. emarginata) and western chokecherry (P. virginiana var. demissa) – occur in the Tahoe Basin, both growing as either shrubs or small trees.  I cannot say for sure which species is represented in these photographs (taken on the slopes above Emerald Bay at Emerald Bay State Park), as the two species are best distinguished by subtle differences in their flowers and foliage.  Bitter cherry is apparently common in the Tahoe Basin and has bark that is smooth and dark brown, while chokecherry is more of a foothill species that is uncommon on the western shore (where these photos were taken) and has more grayish brown and somewhat scaly bark.  I can go either way with bark color based on these photos, so I’ll forgo an ID for the time being and seek to follow up during my next visit.  A third species of Prunus, the strictly shrubby desert peach (P. andersonii), formerly occurred at low elevations around the south shore, but it is now considered to be extirpated from the basin.

Mountain ash (Sorbus californica)

While hiking the Rubicon Trail in Emerald Bay State Park, I spotted a single, small tree with distinctive, large winter buds that reminded me immediately of the ornamental species mountain ash (Sorbus aucuparia) from my former days as a nursery inspector.  This thought seemed to be confirmed when I found a senesced but still attached leaf, pinnately compound with nine ovate, toothed leaflets.  However, my pocket copy of Native Trees of the Sierra Nevada (Peterson & Peterson 1975) included no species of Sorbus, and I concluded it must be something else.  This lone tree was located in deep shade within the white fir forest near the western shore of Emerald Bay, so I opted to find another tree in better lit conditions for taking photos – unfortunately, no other trees of this species were found.  Once I got back home, I was happy to find Sorbus californica listed in my just purchased copy of Graf (1999).  This species has attractive white flowers in small panicles during the summer that give rise to bright red berries during fall and is apparently common in mid- to higher-elevation riparian communities around the lake.

Serviceberry (Amelanchier spp.)
Curl-leaf mountain mahogany (Cercocarpus ledifolius)

I did not locate either of the two species of serviceberry that occur in the Tahoe Basin, the common serviceberry (Amelanchier utahensis) and the more localized glabrous serviceberry (A. alnifolia var. pumila).  Being highly familiar with our eastern species, A. arborea (just recently finished flowering), I suspect either of these species would be readily recognized, even in winter, by their smooth, silvery-gray bark and shrubby, small-tree form.  I also did not see curl-leaf mountain mahogany (Cercocarpus ledifolius), another species that barely qualifies as a small tree.  It is apparently more at home on the dry eastern flank of the Sierra Nevada but can be found within the basin proper sporadically in the southwest and along the southeastern lake shore and more commonly on dry slopes in the far north and south of the basin.  I have collected a number of woodboring beetles from mountain mahogany across the southwestern U.S. from the mountains of southern California to the Chisos Mountains of Texas.

Family ACERACEAE

The single North American genus, Acer, is represented in California by four species, three of which occur in the Sierra Nevada but only one occurring in the Tahoe Basin.  Plants in this family are closely related to the Hippocastanaceae, represented in the Sierra Nevada foothills by California buckeye (Aesculus californica).

Mountain maple (Acer glabrum var. torreyi)

As with mountain ash, I found a single small tree representing this species near the west shore of Emerald Bay while hiking the Rubicon Trail.  Despite lacking foliage, I recognized it immediately as a maple by its opposite, scaly buds.  Also like mountain ash, I assumed I would see more after finding the first one and thus didn’t photograph this particular tree growing in deep shade.  That’ll teach me.  This species sometimes grows as a multi-stemmed shrub in moist situations, and even when assuming tree form, as did the one I saw, it is at best a small tree with a maximum height of only around 15′.  With fall foliage in varying shades of pink to red, it must rather nicely compliment the blazing yellow cloak of the quaking aspen during September and October.  Tahoe Basin individuals are placed in var. torreyi due to their bright reddish twigs, while those on the eastern slope of the Sierra Nevada exhibit gray twigs and are placed in var. diffusum.

This concludes my “Trees of Lake Tahoe” series – at least until next year when I hope to locate some of the remaining species I did not find during this year’s visit.  However, I do have one more “flora of Lake Tahoe” post in preparation covering some of the many woody shrubs that occur within the basin.

REFERENCES:

Arno, S. F. 1973. Discovering Sierra Trees. Yosemite Association, Yosemite National Park, California, 89 pp.

Graf, M. 1999. Plants of the Tahoe Basin. Flowering Plants, Trees, and Ferns. A Photographic Guide. California Native Plant Society Press, Berkeley, 308 pp.

Muir, J. 1894. The Mountains of California. The Century Co., New York, xiii+381 pp.

Muir, J.  1918. Steep Trails. Houghton, Mifflin, Boston, ix+390 pp.

Nixon, K. C. 2002. The oak (Quercus) biodiversity of California and adjacent regions. USDA Forest Service General Technical Report PSW-GTR-184, 20 pp.

Peterson, P. V., and P. V. Peterson, Jr. 1975. Native Trees of the Sierra Nevada. University of California Press, Berkeley, 147 pp.

Quinn, C.  2006.  A Nature Guide to the Southwest Tahoe Basin: Including Desolation Wilderness and Fallen Leaf Lake: Trees, Shrubs, Ferns, Flowers, Birds, Amphibians, Reptiles, Mammals, and Fishes Inhabiting the Sierra Nevada Watershed Southwest of Lake Tahoe, California.  CraneDance Publications, Eugene, Oregon, 232 pp. 

Copyright © Ted C. MacRae 2009

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Winter botany quiz #5

This may be the last winter botany quiz for awhile, but I did come across this interesting little plant on my recent visit to Lake Tahoe that doesn’t fit neatly into any other category upon which I have (or will be) posting about. I was excited to see this plant, and I’ll be interested in seeing what others think about it. Hints: photograph taken on 03/17/2009 at Emerald Bay State Park, along Rubicon Trail, elev. 6,250′.  The host is ponderosa pine (Pinus ponderosa).

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The usual rules – I’ll leave the photo up for a couple days to give people time to research their answer, with comment moderation turned on during that time. Whoever gets it right (or is closest in case nobody gets it right) wins, and being first is always good in case of a tie-breaker!

EDIT 04/20/2009 - Wow, congratulations to, well… almost everyone, for getting this one right. I guess it was not as hard as I thought it would be, since I’d never heard of dwarf mistletoe until I ran into this plant.

To be exact (something I’m fond of being), this is western dwarf mistletoe (Arceuthobium campylopodum, arse-youth-OH-bee-um cam-pie-low-POE-dum). The term dwarf mistletoe refers to the genus as a whole, while ponderosa pine dwarf mistletoe generally refers to what is now called southwestern dwarf mistletoe (A. vaginatum) from AZ and NM. Accordingly, Kirk deserves special mention for being the first to get both the common name (spelled correctly with lower case) and the scientific name, while Doug was the first to properly italicize the scientific name. I know, I’m being really picky – it’s my nature. Also, Adrian added a nice tidbit of information regarding the impact these plants can have on their hosts.

I can be fairly certain about the ID, but not 100%. According to Hawksworth & Wiens (1998), four species of dwarf mistletoe occur within the Tahoe Basin. Of these, only western dwarf mistletoe utilizes ponderosa pine as a principal host.  There is a small chance it could be lodgepole pine dwarf mistletoe (A. americanum), which occasionally utlizes ponderosa pine but is most often (as the common names suggests) associated with lodgepole pine. The two remaining species, fir dwarf mistletoe (A. abietinum) and hemlock dwarf mistletoe (A. tsugense), are restricted in the Tahoe Basin to white/red fir and mountain hemlock, respectively.

REFERENCE:

Hawksworth, F. G., and D. Wiens. 1998. Dwarf Mistletoes: Biology, Pathology, and Systematics. Diane Publishing Company, Darby, Pennsylvania, 410 pp.

Copyright © Ted C. MacRae 2009

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