Bon appétit!

I collected this larva in northwest Nebraska during last year’s Fall Tiger Beetle Trip.  I collected an adult Cicindela lengi (blowout tiger beetle) at the spot – a species that greatly resembles but is much less common than the ubiquitous C. formosa (big sand tiger beetle – see my post Cicindela lengi vs. Cicindela formosa for a comparison of the two species).  Before finally finding that adult, however, I had fished out several larvae from the site in the hopes that they represented that uncommon species (see how I did this in my post Goin’ fishin’).  After collecting the larvae and placing them in a small terrarium with native sandy soil, they burrowed in but then closed up shop – I wasn’t sure whether they had survived or not.  In early December I put the terrarium in a 10°C incubator for the winter and brought it back out earlier this month.  Yesterday, happily, this larva and one other opened up their burrows again, so with any luck I’ll feed them well and they’ll complete their development.  While I do hope they represent C. lengi, other possibilities include C. scutellaris (festive tiger beetle), which would not be exciting, and C. nebraskana (prairie long-lipped tiger beetle), which would be VERY exciting.  One species I do not have to worry about it being is C. formosa, as the larvae of that species make very unique excavations in the sand with the burrow opening directed towards the excavation (I don’t believe I’ve posted photos of that here, yet – I’ll have to do so soon).

In the meantime, here is a closeup of the larva in the video prior to feeding. Those of you who have ever reared or photographed tiger beetle larvae will know just how easily “spooked” these larvae can be – any sudden movement will cause the larva to “drop” into its burrow and sit there for awhile. As a result, it was a real challenge to go through the whole process of taking first the photos and then the video while feeding it without causing it to drop.

cicindela_sp_larva_p1020936

Coming soon – lunchtime for adults!

Copyright © Ted C. MacRae 2009

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I Brake for Dung Beetles!

A few days ago I learned of a new campaign by The WILD Foundation called “Make a Big Impact with Small Change.” Founded in 1974, WILD seeks to protect intact wilderness areas and the wildlife and people who depend upon them. Their new campaign pays homage to dung beetles – usually overlooked by conservationists in favor of the so-called “charismatic megafauna,” but who nevertheless provide an important ecological service by tirelessly processing megafaunal dung. From the WILD website:

Here at The WILD Foundation, we realize that it is not just those large, charismatic animals that inspire conservation – it is often the small, typically unnoticed and vastly under-appreciated ones that inspire us the most….and that are an indispensible part of the ecosystem!

As a way of generating support for their work, WILD is giving away bumper stickers like the one pictured above. I have got to have one of these bumper stickers! It is the best entomology bumper sticker I’ve seen since “I fear no weevil!” The WILD website also features this amusing little video that shows some dung beetles in action:

Vodpod videos no longer available.

more about “I Brake for Dung Beetles!“, posted with vodpod

The website doesn’t provide any clues as to the species of dung beetle or where it was recorded, but judging by its large size I’m guessing that it might have been recorded in Africa, perhaps representing a species of the genus Scarabaeus.  My most memorable dung beetle experiences occurred in Africa, which is blessed with a dizzying diversity of “dungers.”  Following is an excerpt from an article I wrote that appeared in the December 2008 issue of the SCARABS Newsletter, in which I discussed some of these marvelous beetles:

Chafers were not the only scarabs I encountered in abundance at Borakalalo [National Park], and I’ll give you one guess as to what other scarab group I encountered in abundance at this mammal game reserve. That’s right, dung beetles. Never before have I seen such an abundance and diversity of dung beetles in one spot, but then again, never before have I seen such an abundance of dung!  The ground was littered with the stuff – antelope such as gemsbok  and impala, warthogs, giraffes, and a host of other mammals thrive in the protected confines of the park, and the seasonally dry climate allows their dung to dry quickly and accumulate rather than breaking down and disappearing. It did, however, take a few days before I became aware of the area’s dung beetle diversity. Prior to our arrival in the park, the weather had been dry for some time, and so it remained for the first few days we were there. I collected a smattering of different dung beetles during that time, but it seemed like they should be more abundant considering the abundance of available resource. Our third day in the park was interrupted by heavy thundershowers that moved through during the afternoon. The next morning, as we arose and begin wandering away from the camp, the air seemed literally abuzz with dung beetles. They were flying everywhere and crawling all over the ground, frantically rolling and fighting over the reconstituted pieces of dung. Big, black scarabaeines proper such as Kheper clericus (Boheman) and Scarabaeus galenus Westwood (Photo 4), the small metallic

scarabaeus-galenus_1

Photo 4: Scarabaeus galenus (Westwood).

Phalops ardea Klug, the attractive green iridescent species Garetta nitens (Olivier) and Gymnopleurus virens Erichson, their darkened relative Allogymnopleurus thalassinum (Klug) (Photo 5),
Photo 5: Allogymnopleurus thalassinum (Klug) individuals fighting over a mammal dung ball.

Photo 5: Allogymnopleurus thalassinum (Klug) individuals fighting over a mammal dung ball.

and the tiny little Sisyphus costatus (Thunberg),  standing tall on its elongated hind legs while pushing dung with its forward pairs of legs (opposite of what I’ve seen in any other dung beetle), all made their sudden appearance. I spent some time  watching one S. galenus individual excavating a burrow for the prized piece of poop it had snatched (Photo 6).
Photo 6: Scarabaeus galenus (Westwood) excavating a burrow.

Photo 6: Scarabaeus galenus (Westwood) excavating a burrow.

The most impressive dunger that I saw, however, was the enormous, flattened Pachylomera femoralis Kirby (Photo 7).
Photo 7: Pachylomera femorata Kirby.

Photo 7: Pachylomera femorata Kirby.

Looking like flying Tonka trucks and sounding like diesel engines from real trucks, their low-pitched, rumbling buzz filled the air as they searched among the freshly moistened turds. So loud was the noise caused by the beating of their wings that several times I ducked thinking one was about to collide with me. This sudden dunger super-diversity continued into the night, as Anachalcos convexus Boheman, Catharsius sp., Copris elphenor Klug, Metacatharsius sp., Pedaria sp., Scarabaeus goryi (Laporte), three species of Onitis, Caccobius ferrugineus (Fåhraeus), Digitonthophagus gazella (Fabricius), and nearly a dozen species of Onthophagus flew to our ultraviolet light-illuminated sheet.

REFERENCE:

MacRae, T. C. 2008. Dungers and chafers: A trip to South Africa. SCARABS 34:1-9.

Copyright © Ted C. MacRae 2009

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Coral Pink Sand Dunes tiger beetle – range map

Those of you on RSS feed might be interested in revisiting my previous post, Coral Pink Sand Dunes tiger beetle on ARKive.  I’ve added a Google screen shot to the post that shows a visual perspective of the entire range of Cicindela albissima within a tiny inset of the state of Utah.  The image provides a sobering reminder of just how vanishingly small the range of this species is.  If we, as a society, cannot take the steps required to ensure the survival of a beautiful little species such as this one – living on only the tiniest sliver of the lands under our stewardship, it speaks ill of our ability to do so for other species with much greater habitat requirements.

Copyright © Ted C. MacRae 2009

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Coral Pink Sand Dunes tiger beetle on ARKive

I’ve been meaning to write about ARKive for awhile now. ARKive is a unique collection of videos, images and fact-files assembled from among the world’s very best wildlife videographers and photographers in an attempt to create a centralized digital library of life on Earth. Their short to mid-term priority is the completion of audio-visual profiles for the 16,300-plus species on The IUCN Red List of Threatened Species, before moving on to profiling all species that have ever been filmed or photographed. With backing from many of the world’s leading conservation organizations, ARKive hopes to “promote public understanding and appreciation of the world’s biodiversity and the need for its conservation, through the power of wildlife imagery.”

With tiger beetle season almost now upon us, it seems appropriate to highlight the media collection that ARKive has assembled for one of North America’s most spectacularly beautiful and critically imperiled tiger beetles, Cicindela albissima (Coral Pink Sand Dune tiger beetle). This amazing species is not only stunning in appearance, with its nearly pure white elytra, but has perhaps the most restricted habitat of any tiger beetle species in North America – the entire population being restricted to 400 hectares within coral-pink-sand-dunes_3Utah’s Coral Pink Sand Dunes State Park and the adjacent Bureau of Land Management (BLM) dune management area (Pearson et al. 2006). The Google screen shot at right shows the entire range of this species as a light pink swath (inset shown on larger map of the state of Utah).  Regarded initially as a subspecies of the widespread C. limbata (sandy tiger beetle), recent molecular studies showed this beetle to be only distantly related to that species and, thus, deserving of full species status (Morgan et al. 2000).

Unfortunately, the beetle’s highly restricted habitat continues to be adversely affected by ongoing, recreational off-road vehicle use, especially in the interdunal swales used by the larvae. Impacts occur not only by direct run-over mortality, but also through disruption of normal adult and larval activity, damage to vegetation, reduction of arthropod prey of C. albissima, and mixing of the upper soil layer which increases desiccation of the larval microhabitat (Knisley and Hill 2001). The species was nominated for federal protection under the Endangered Species Act in 1996 (when it was still considered a subspecies of C. limbata), and two years later a Conservation Agreement between BLM, U.S. Fish and Wildlife Service, Utah Department of Parks and Recreation and Kane County was established in an effort to protect the critically sensitive habitats in which this species lives. Despite these conservation measures, ongoing monitoring and research within the protected areas has documented a continuing decline in the population, suggesting that these areas may not be of sufficient size to enable the population to increase, and off-road vehicle use continues outside of the protected areas (U.S. Department of Interior, Fish and Wildlife Service (FWS) 2008). While still only a candidate for federal listing as an endangered or threatened species, the FWS now considers the magnitude of the threat from off-road vehicles, in view of these recent findings, to be high and imminent. As a result, the FWS has increased the priority of the species’ candidacy from 8 to 2 (1 being the highest priority a candidate species can receive).

While I would dearly have loved to embed one of ARKive’s extraordinary videos or photographs of C. albissima within this post, copyright considerations do not allow that.  What I can do is provide hyperlinks directly to the site, and I encourage everyone to visit ARKive and see their images of this gorgeous species.

Photos by Christine Breton: adult beetle, dorsal view, adult beetle, adults mating, habitat

Videos by Ganglion Films: overview, adults mating, adult burrowing in sand, OHVs threatening protected habit.

In addition to the ARKive images, Chris Wirth, author of the blog Cicindela, has taken photographs of this species and presents stunning examples of both the larva and the adult in his post Cicindela albissima (Re-post). I myself am making plans to visit Coral Pink Sand Dunes – perhaps this season – to find and photograph this species for myself. When I succeed, rest assured those photographs will appear on this site.

REFERENCES:

Knisley, C. B., and J. M. Hill. 2001. Biology and conservation of the Coral Pink Sand Dunes tiger beetle, Cicindela limbata albissima Rumpp. Unpublished report.

Morgan, M., C. B. Knisley and A. Vogler. 2000. New taxonomic status of the endangered tiger beetle Cicindela limbata albissima (Coleoptera: Cicindelidae): evidence from mtDNA. Annals of the Entomological Society of America 93(5):1108-1115.

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.

U.S. Department of Interior, Fish and Wildlife Service. 2008. 50 CFR Part 17. Endangered and threatened wildlife and plants; review of native species that are candidates for listing as endangered or threatened; annual notice of findings on resubmitted petitions; annual description of progress on listing actions; proposed rule. Federal Register 73(238) (December 10, 2008):75176-75244.

Copyright © Ted C. MacRae 2009

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Tiger Beetle Safari

In looking back at my posts over the past few weeks, I realized that it has been far too long since I’ve actually talked about beetles.  Perhaps “Petals In The Bush” would be a better name for this blog!  I still have some botanical thoughts to get off my chest before the insect season starts in earnest, but until then, and in anticipation of the upcoming summer’s hunts, I offer this fun, light-hearted introduction to collecting and keeping tiger beetles by Peter Schriemer.  Pay particular attention to the method he uses to capture these elusive little creatures:

Tiger Beetles are my favorite type of beetle! Entomologist John Acorn got me hooked on these little guys. They live across the country in various habitats, so you may not need to travel far to go on a Tiger Beetle Safari of your own!

Vodpod videos no longer available.

more about “Tiger Beetle Safari“, posted with vodpod

Capturing tiger beetle adults can a little (lot) more difficult than implied by this video. Adults have excellent eyesight, and many species are extremely wary. It takes practice, patience, and lots of second chances. The collecting method shown in the video is what I refer to as the “stalk and slap” method – the beetle is slowly stalked until within net reach, and the net bag is slapped over the beetle.  This method works well enough, but it has its limitations.  If there are any gaps between the ground and the net rim, the beetle will quickly dart through them and fly away.  This is easy to prevent on sandy and soft clay substrates, as the net rim can be sealed against the ground by kneeling quickly on each side of the rim to embed it slightly and using the hands to hold up the net bag and locate the beetle.  Still, there are a few things I don’t like about this method – the beetle may hide against the inside of the rim and be difficult to locate, and once found it may be difficult to grab the beetle through the net if it is against the ground (don’t even try lifting the rim and reaching under – the beetle will zip out and be gone).  This method can also be taxing on the legs, as each attempted capture involves kneeling and standing back up (getting harder and harder for these 50+ year old knees to do).

The major limitation of the slap method, however, is that it doesn’t really work on hard, uneven surfaces. Many species are found in glades and other habitats with exposed rock substrates. In these types of habitats, the net rim simply cannot be clamped tightly enough to eliminate the gaps (not to mention the added difficulties in kneeling on these surfaces).  Because of this, I have adopted a technique that I call the “tap and swipe” method.  Here again, the beetle is stalked until within net reach (made easier with a longer handle), but rather than slapping the net bag over the beetle, the rim of the net is tapped against the ground next to the beetle and then assertively swiped sideways to catch the beetle just as it starts flying.  A quick 180° flip of the net rim closes the opening to prevent the beetle from escaping, and it is easily seen in the hanging net bag, where it can be grabbed from outside the net bag with one hand to secure it before reaching into the net bag with the other hand.  With a little practice, one eventually learns to reach down into the open net bag and grab the beetle while preventing it from flying up and out.  All of this can be done while standing, so it’s easier on the knees.

The tap method does require more knowledge about the beetle’s escape behavior in order to anticipate how quickly and in which direction the beetle will fly – some species delay take off just slightly, thus requiring a slight “pause” between the tap and the swipe. However, once their behavior is learned I have found this method to be more consistently successful than the slap method – even on soft substrates.  For species that I haven’t encountered in the field before, I use the slap method at first (if I can) until I have a feel for their escape behavior. If I can’t, I use the tap method and hope for the best!

Copyright © Ted C. MacRae 2009

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Magodo – giant twig wilter

petascelis-remipes

In previous posts, I have highlighted some of the insects I observed on a trip to South Africa in November-December 1999.  All of the photos I have shown to this point were taken at Borakalalo National Park in North West Province or at the Geelhoutbos farm of Susan Strauss below the Waterberg Range in the formerly Northern, now Limpopo Province.  Both of these locations are deep inside the bushveld, providing ample opportunity to observe an incredible diversity of insect life.  This is not to say that insects, even spectacular ones, cannot be found in more urban areas.  During the weekend between those two mini-expeditions, I stayed with my friend and colleague, Chuck Bellamy, at his home in Pretoria, a beautiful city with lovely architecture, elegant gardens… and some very impressive bugs!  The bug in this photo was found on a tree in a shrubby enclave, and at well over 35 mm in length it is easily the largest leaf-footed bug (order Hemiptera, family Coreidae) that I have ever seen.  Its chunky build, velvety black coloration with thin yellow lines along the sides and down the center of the thorax, and greatly enlarged hind femora quickly led me to a provisional identification of a male Petascelis remipes, or giant twig wilter.  This ID was confirmed by my friend and colleague Harry Brailovsky, an entomologist at UNAM (Universidad Nacional Autónoma de México) and world expert on Coreidae (and who, incidentally, just recently published a review of this Afrotropical genus – Brailovsky 2008).

According to Picker et al. (2002), these insects are found on plants in the genus Combretum.  Like most species in the family, they have scent (“stink”) glands that provide defensive capabilities. Adults are gregarious and bold, walking towards intruders with antennae vibrating when disturbed, and they are apparently capable of squirting their defensive secretions for some distance.  The nymphs are black as well but futher advertise their noxiousness with warning coloration of red spots on a whitish background. Interestingly, and despite their powerful chemical defenses, this species is considered a delicacy in parts of Mozambique where it is known as Magodo.  In a post called Insects for Dinner (in a blog with the eerily similar title, Beating about the Bush), Bart Wursten of Gorongosa National Park in Mozambique describes how local folk burn small patches of the grassland in which these insects are found to smoke them out and catch them.  The Magodo hunters kill the bugs by breaking off the head and removing the scent glands, which releases a very strong almond-like smell.  In doing this, the locals are able to catch considerable quantities of the bugs, which they eat with supper.

Lest you believe such practices are an anomaly, van Huis (2003) has compiled a list of about 250 insect species used as food in sub-Saharan Africa.  Lepidoptera, Orthoptera and Coleoptera represented the bulk (78%) of species eaten, with Isoptera, Hemiptera, Hymenoptera, Diptera and Odonota making up the rest.  Several examples of toxic insects and the traditional methods used to remove the poisons were given.  It was noted that whether or not insects are eaten depends not only on taste and nutritional value, but also on customs and ethnic preferences or prohibitions.  I’m not one to shy away from the thought of eating insects – after all, shrimp are just bugs that live in water, and insects rank far lower in ‘slime factor’ than many other invertebrates (e.g., oysters) that enjoy great popularity in our culture.  I’ve eaten roasted beet armyworm (Spodoptera exigua) pupae and munched on chocolate covered ants, but that’s kid stuff – the armyworms tasted like the soy sauce in which they were roasted, and the ants tasted like, well… chocolate.  I did once eat a softshelled crab (alive!), and I actually hope to one day taste the enormous grub of the giant metallic ceiba borer, Euchroma gigantea, eaten by indigenous cultures in Central and South America.   Still, I think I’d need a lot of faith in my chef’s scent gland removal prowess before I started scarfing Magodo down like popcorn.

What insects have you eaten?

REFERENCES:

Brailovsky, H.  2008. Notes on the genus Petascelis Signoret and description of one new species (Hemiptera: Heteroptera: Coreidae: Coreinae: Petascelini).  Zootaxa 1749:18–26.

Picker, M., C. Griffiths and A. Weaving. 2002. Field Guide to Insects of South Africa. Struik Publishers, Cape Town, 444 pp.

van Huis, A. 2003. Insects as food in sub-Saharan Africa. Insect Science and Its Application 23(3):163-185.

Copyright © Ted C. MacRae 2009

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Ship-timber beetle

Atractocerus brevicornis

One of the more unusual, and enigmatic, beetles that I encountered in South Africa was this beetle in the pantropical genus Atractocerus.  Placed in the family Lymexylidae (ship-timber beetles), species in this genus look less like beetles than they do large flying ants or strange damselflies due to their highly reduced elytra that expose their greatly elongated abdomen and leave the hind wings uncovered.  The hind wings also are unusual in that they are held fan-like in repose rather than folded as in most other beetles.  Atractocerus brevicornis is the only species in the genus found in Africa (Scholtz & Holm 1985).

Adults are attracted to light at night, as was this individual that came to our ultraviolet light at Geelhoutbos farm below the Waterberg Range in Limpopo Province. Nothing is known about the biology of Atractocerus, but larvae of other genera are reported to bore into hardwoods and palm stems (Picker et al. 2002). Larvae of the genera Lymexylon and Melittomma are believed to form symbiotic associations with ambrosia fungi that grow on the walls of their galleries (Young, 2002).  Adult females deposit fungal spores in a sticky matrix when they lay their eggs, and the hatching larvae carry the spores into wood on their bodies.  The large eyes of Atractocerus, however, suggest a predatory lifestyle. The common name of the family originates from a northern European species that has in the past been a destructive pest of ship timbers.

Atractocerus species are rarely encountered and therefore, not well studied. Their evolutionary history is still unknown; however, the oldest known lymexylid fossil is a very primitive member of the genus Atractocerus preserved in 100 myo Burmese amber (Grimwold & Engel 2005). Thus, the lineage containing these beetles had already appeared by the mid-Cretaceous and may have originated as early as the Jurassic, a fact that has earned them the moniker “living fossils.” These beetles were once thought to be among the most primitive of all Coleoptera – their simple wing venation, almost undifferentiated antennae and tarsi, and naked abdomen being likened to a supposed neuropteran common ancestor. Most authors now consider the family to be most closely related to the cucujiform groups Cleroidea and Cucujoidea (Wheeler 1986, Young 2002), although some have placed it in the Elateriformia near the Lampyridae based on wing venation. Scholtz and Holm (1985) accepted a cucujiform placement but related the group to the Styopidae (twisted-winged parasites), apparently due to the similarity of their highly reduced forwings.  At the same time, they acknowledged the many morphological and behavioral differences between the two groups, the latter itself being the subject of much evolutionary debate due to disagreement about whether the reduced forwings of male stylopids are truly homologous to the elytra of Coleoptera (some have even suggested homology with the halteres of Diptera that were switched from the metathorax to the mesothorax as a result of homeotic mutation). Most authors now place this latter group in the separate order Strepsiptera.

REFERENCES:

Grimaldi, D. and M. S. Engel. 2005. Evolution of the Insects. Cambridge University Press, New York, xv + 755 pp.

Picker, M., C. Griffiths and A. Weaving. 2002. Field Guide to Insects of South Africa. Struik Publishers, Cape Town, 444 pp.

Scholtz, C. H. and E. Holm (eds.). 1985. Insects of Southern Africa. Butterworths, Durbin, South Africa, 502 pp.

Wheeler, Q. D. 1986. Revision of the genera of Lymexylidae (Coleoptera: Cucujiformia). Bulletin of the American Museum of Natural History 183:113-210.

Young, D. K.  2002. 71. Lymexylidae Fleming 1821, pp. 261-262.  In: R. H. Arnett and M. C. Thomas [eds.], American Beetles, Volume 2, Polyphaga: Scarabaeoidea Through Curculionoidea, CRC Press, Boca Raton,880 pp.

Copyright © Ted C. MacRae 2009

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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

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