Life at 8X—soybean aphid

Although my first attempt at adding extension tubes to my Canon MP-E 65mm macro lens, effectively converting it from a 1–5X to a 1.7–8.0X lens, was nearly a year ago, it has only been recently that I’ve actually started experimenting with this combination to obtain high-mag photographs of very small insects in the field. The first example that I showed of such a photograph was a tiny seed weevil (Althaeus sp.) on its hibiscus host plant. I’ve since photographed a number of other insect subjects at high-mag using this setup and am getting a better feel for the capabilities—and limitations—inherent in using it. First, here is what the setup actually looks like:

Canon 50D body, MP-E 65mm macro lens on 68mm extension, MT-24EX twin flash w/ DIY diffuser.

Not the normal photo quality for this site (just a quick field setup photographed with my I-Phone), but it shows just how long the lens component becomes when fully extended to achieve 8X magnification. The camera is quite front-heavy, making the camera difficult to use hand-held, and the very shallow DOF (depth of field) due to the extreme level of magnification makes precise focusing difficult and magnifies the effect of any motion between the camera and subject. Obviously, one solution for these problems is to mount the camera on a tripod and place the subject on a stable surface; however, for reasons I’ve mentioned elsewhere, it is unlikely that I will ever take to bringing a tripod into the field, and the whole point of this exercise is to develop the capability for getting usable hand-held field photographs no matter what level of magnification they may require. As an alternative, I use a number of other techniques, discussed in my prior post on the subject, to stabilize the camera without using a tripod.

One of the recent subjects I photographed with this setup is the soybean aphid, Aphis glycines (order Hemiptera, family Aphididae). This distinctive Asian species has recently established in the U.S. as invasive pest of soybeans; adult females measure only 1–2 mm in length (and the nymphs are even smaller) and can quickly develop very high densities on the leaves and upper stems of soybean plants. The following photograph was taken at the camera setup’s minimum magnification of 1.7X and provides a typical view of adult aphids and their progeny:

Aphis glycines (soybean aphid) | Warren Co., Illinois

While the above photograph does a very good job of showing the colonial appearance of infestations by these aphids on soybean foliage, what about the aphids themselves? It would be nice to get a better look at individual aphids. The following photographs were all taken with the lens fully extended to achieve 8X magnification (and completely hand-held):

Adult female aphid—note the eye spots of the unborn nymphs visible within the body.

Another adult female navigates the hairs on the surface of the soybean leaf (I never knew soybean leaves were so hairy!).

A mother surrounded by her progeny. As above, eye spots of unborn nymphs can be seen inside her body.

These photographs are not without their problems—they are a bit soft, probably due to motion blur that results from the camera being hand-held and the extremely thin DOF that makes it difficult to get all of the desired components of the photos equally in focus. Lighting also is a challenge, as the very small subject-to-lens distance forces light from the flash to come from directly above or even behind the subject while minimizing front lighting (especially evident in the last photo with its straight down view). Nevertheless, these are decent, usable photographs that provide an uncommon view of these exceedingly tiny insects—without the encumbrance of carrying a tripod in the field, the time investment of studio photography and/or focus-stacking, or the expense of a microscope-mounted camera system (for those of us without access to such systems).

Copyright © Ted C. MacRae 2012

Sea Grape Flatid – Petrusa epilepsis

The argid sawfly Sericoceros krugii wasn’t the only insect I saw associated with seagrape (Coccoloba uvifera) during my May trip to Puerto Rico. While exploring the magnificent coastal sand dune system near Isabela (northwestern Puerto Rico), I encountered a tree with literally dozens of frosty, white “homopterans” on the reddish lower surface of its newly expanded leaves (the photo below shows them at only about half the density that I saw initially, as many became disturbed and left when I tried to photograph them). Clearly they were planthoppers in the superfamily Fulgoroidea, with their general shape wings held tent-like suggesting either the family Acanaloniidae or its close relatives in the family Flatidae.

Petrusa epilepsis adults on seagrape (Coccoloba uvifera) | vic. Isabela, Puerto Rico

A better look at the adults in the photos revealed the presence of numerous parallel cross-veins along the costal margin of the forewings, placing them squarely within the family Flatidae (species of Acanaloniidae have reticulate forewing venation without the parallel cross-veins). Wolcott (1948) lists a dozen or so species of flatids from Puerto Rico, roughly half of which belong to the subfamily Flatinae (wings held tent-like) and the other half belonging to the Flatoidinae (more flattened insects with wings held almost horizontal). The likeliest candidate seemed to be Ormenis marginata, which Wolcott describes as occurring in the “millions, vast clouds of them flying up from seagrape plants that one may disturb around Isabela…” I can’t say I saw “millions” of them, but certainly they were abundant on this one plant. My identification was kindly confirmed by Neotropical fulgoroid Lois O’Brien, who also noted that this species now goes under the name Petrusa epilepsis Kirkaldy.


This seems to be a species that could cause considerable problems should it ever find it’s way to the mainland U.S. Many flatids are famously infidel when it comes to host plants—Metcalfa pruinosa (citrus flatid planthopper) being perhaps the best known example. Petrusa epilepsis not only feeds on seagrape but has also become a pest of coffee (Coffea arabica), coco-plum (Chrysobalanus icaco), jasmin (Jasminum spp. ) and black mangrove (Avicennia germinans), with damage resulting not only from direct feeding but also the development of sooty mold that colonize the honeydew excreted by the bugs that covers the foliage of the plants they infest (Nieves-Rivera et al. 2002).

A particularly amusing passage by Wolcott was his observation that adults “with care may be chased around a stem by gentle pursuit with a lead pencil.” I can add that a finger works equally well, as I used precisely this technique to get the adults in these last two photos positioned precisely where I wanted them for the photographs. Let’s hope they are as easily kept within their current West Indies distribution and are not eventually unleashed as yet another exotic pest for agricultural producers in tropical and subtropical mainland America to deal with.

REFERENCES:

Nieves-Rivera, Á. M., T. A. Tattar & E. H. Williams, Jr. 2002. Sooty mould-planthopper association on leaves of the black mangrove, Avicennia germinans (L.) Stearn in southwestern Puerto Rico.  Journal 26:141–155.

Wolcott, G. N. 1948. Insects of Puerto Rico. The Journal of Agriculture of the University of Puerto Rico 32(1):1–223.

Copyright © Ted C. MacRae 2012

Crazy Eyes

Spissistilus festinus | Stoneville, Mississippi

Spissistilus festinus (three-cornered alfalfa hopper) is one of the few truly economic pests in the otherwise bizarre and innocuous family Membracidae (treehoppers).  Its common name alludes to one of the crops it affects, but my encounters with this species are most often in soybean (I am, after all, a soybean entomologist).  Damage in this crop is caused by both adults and nymphs, whose piercing/sucking mouthparts cause girdling and breakage of the stem—often just a few inches above the soil.  This individual was seen during my travels last week in a soybean field in Stoneville, Mississippi, where numbers throughout the season were especially high this year.  Although I have seen innumerable S. festinus adults, I have never noticed their crazy, zig-zag patterned red and white eyes until I managed this closeup face shot (click on photo for best view).

This slightly cropped photo was taken with a 100mm macro lens and full extension tube set, resulting in slightly more than 2X magnification.  One of the lessons I took from was the need to pay more attention to background and value contrast.  By placing the subject a few inches in front of the dark green soybean foliage I was able to achieve a much more pleasing background than the typical black background one gets with full flash photos at high magnification.  Although both the subject and the background are green, there is still sufficient difference in shade to create contrast between them.  Light-green is one of the more difficult colors to work with when full flash is used with high shutter speeds and small apertures to maximize crispness and detail (in this case, 1/250 sec and f/16).  However, increasing ISO to 400 and lowering flash exposure compensation to -2/3 can reduce the amount of flash needed to illuminate the subject with such settings, making it easier to achieve a properly exposed and true-colored subject.

Copyright © Ted C. MacRae 2011

BugShot 2011 – Lesson 2

Most of my insect photography is done up close using fast shutter speeds (to prevent motion blur) and small apertures (to maximize depth of field).  This necessitates the use of full flash – the amount of light reaching the camera sensor at f/16 and 1/250 sec is not enough to show any image at all, much less one properly exposed.  Full flash photography has its own set of challenges, but for the most part it can be used to produce excellent closeup photographs of insects, even very small ones.  One thing that has always bothered me about full flash photography, however, is the “black background” effect when photographing an insect sitting up on a plant without something else in the immediate background to reflect light.  Not that I don’t like black backgrounds—they can be used to stunning effect with the right subject.  I just don’t want it to be my only option for insects that I photograph up off the ground. Of course, it is rather a simple matter to place something in the background that is close enough to reflect light but far enough away to remain out of focus, but what I really want to be able to do sometimes is have a blue sky.  I always thought this meant natural light, with its low f stops, slow shutter speeds, and the resulting motion blur and loss of depth of field. 

Of the many things I learned today, how to include a blue sky background in a closeup photograph at f/16 was my favorite.  This is accomplished by bumping up the ISO to 400 (to make the camera sensor more receptive to light) and decreasing the shutter speed to 1/60 sec.  Keeping the f stop high maintains the depth of field, but the increased ISO and decreased shutter speed allows sufficient light from a sky background to register on the sensor.  By themselves, however, these setting will still result in an underexposed subject, which is illuminated instead by fill flash.  Despite the slower shutter speed, there is no motion blur because the “effective” shutter speed for the subject is the duration of the flash pulse rather than the camera shutter speed—it’s like combining two exposure speeds in a single photograph, one for the background and another for the subject.

The following three photographs illustrate this principle—again, they are not technically perfect photos, but rather the result of quick experimentation to understand the principles involved.  Photo 1 is from yesterday’s post and illustrates what my typical settings have always been: ISO 160, f/16, and 1/250 sec.  It’s a decent photo of the treehopper, Acutalis tartarea; however, black is perhaps the least appropriate background to choose for this black species. Until now, it would have been my only option unless I tried arranging foliage in its background.  Photos 2 and 3 are of another individual of this species that I found today (fortunately in similar orientation to the individual photographed yesterday).  In both photos I kept the flash unit set to ETTL (adjusting FEC as appropriate for the shots).  In Photo 2 I bumped up the ISO to 400 but kept the shutter speed fast (1/200 sec)—you can see some effect in that the background is not truly black, having received some light from the blue sky.  It’s not enough, however, because the shutter speed was still too fast.  In Photo 3 the ISO remained at 400 but the shutter speed was also decreased to 1/60 sec.  The shutter staying open that long allows enough light from the sky to register on the sensor and, Voila!, we have a blue sky background that creates nice value contrast with the black subject.  The subject these photos is not terribly sharp, but that is just lack of focus—not motion blur from a slow shutter (sorry, I was just practicing settings rather than going for a perfect shot). All three photos were shot with the Canon 100mm macro lens + 68 mm of extension tube (total magnification ~2X).

''Typical'' insect macro settings: ISO 160, 1/250 sec, f/16

ISO increased to 400 (1/200 sec, f/16)

Shutter speed decreased to 1/60 (ISO 400, f/16)


Copyright © Ted C. MacRae 2011

Stink Bugs on Soybean in Argentina

Despite the natural history and taxonomic focus on beetles and other insects I have adopted for this blog, I am by day an agricultural research entomologist.  For the past 15 years soybean entomology has been my focus, and there is no better nexus for soybeans and entomology than South America.  Cultivated hectares have increased dramatically in Argentina and Brazil over the past several decades, now totaling nearly 80 million acres in those two countries alone (roughly the same area as in the US, by far the world’s largest producer of soybean).  Unlike the US, however, where insect pressure is minor outside of a small number of acres in the southeast, significant pressure occurs in nearly 100% of South America’s soybean acres.  Lepidopterans, primarily species in the family Noctuidae such as velvetbean caterpillar (Anticarsia gemmatalis) and soybean looper (Pseudoplusia includens), are the most important pests, followed closely by stink bugs.  This latter group is especially problematic for growers to deal with.  Stink bugs feed on the developing seeds, causing direct yield impacts through reductions in weight and quality, and because they are a guild of insects rather than a single species, differences in product efficacy against the different species can lead to ineffective or inconsistent control.  I’m involved in trying to do something about this, and while I hate to be deliberately coy, suffice it to say that there is an awful lot of insecticide being sprayed on an awful lot of acres and that the world really would be better off if this weren’t the case.

During my recent visit to Argentina this past March, I took advantage of the opportunity while touring soybeanland to photograph a number of these stink bug species.  Proper identification of stink bugs in a crop is the first step towards controlling them, thus I present here my own photographic guide to some of the more important stink bug species found on soybean in Argentina.

Nezara viridula (chinche verde), adult | Pergamino, Argentina

Nezara viridula, 5th instar nymph | San Pedro, Argentina

Nezara viridula, 1st instar nymphs on egg mass | Oliveros, Argentina

Piezodorus guildinii (chinche de las leguminosas), adult | Pergamino, Argentina

Piezodorus guildinii, 1st instar nymphs on egg mass | Acevedo, Argentina

Edessa meditabunda (alquiche chico), adult | Acevedo, Argentina

Edessa meditabunda, 1st instar nymphs on egg mass | San Pedro, Argentina

Edessa meditabunda, eggs nearing eclosion (note eye spots) | Oliveros, Argentina

Euschistus heros (chinche marrón), adult | Oliveros, Argentina

Dichelops furcatus (chinche de los cuernos - note two ''horns'' in front), adult | Inés Indart, Argentina

Copyright © Ted C. MacRae 2011

Bichos Argentinos #12 – Lace Bugs

Corythaica cyathicollis on upper leaf surface of Solanum granuloso-leprosum.

Shortly after entering La Reserva Ecológica Costanera Sur (Buenos Aires, Argentina) during my early March visit, I noticed a fairly large patch of solanaceous-looking shrubs.  Even from a distance, I could see patterns of white stippling on the foliage immediately identifiable as signs of lace bugs, true bugs (order Hemiptera) in the family Tingidae.  As the only arborescent solanaceous plant recorded from the reserve, I was quickly able to identify the plant as Solanum granuloso-leprosum (Haene and Aparicio 2007), but I expected an identification of the bug to be much more difficult to come by.  Afterall, 84 species of tingids distributed in 25 genera have been recorded from Argentina (Montemayor and Cascarón 2005), and lace bug photos aren’t very frequently encountered in the variety of web sites that I visit when trying to get a lead on the identity of insects outside my area of expertise.

Corythaica cyathicollis adult. The black spots either represent frass or protective egg coverings.

Still, I had a clue—the association of the species with Solanum. Lace bugs are predominantly specialist feeders, with many species showing fidelity to a particular plant genus or group of related genera. The genus Solanum contains a number of economically important species, thus, it was a good bet that this species has at some point been considered an economic pest. With this in mind, I opened my volume of Heteroptera of Economic Importance (Schaefer and Panizzi 2000) to the chapter on lace bugs (Neal and Schaefer 2000) and began looking through the species accounts for South American species recorded on Solanum or other species in the family Solanaceae. I only had to reach the second species account before finding Corythaica cyathicollis and the statement “This Neotropical species is a pest on many solanaceous crops…” The identification was confirmed when I found a rather complete description of the species’ systematics, biology, and economic importance (Kogan 1960), complete with line drawings of the adults and all immature stages. Comparison of my photos with these drawings leaves little doubt that this is, indeed, C. cyathicollis.  (Interestingly, Montemayor and Cascarón (2005) list 28 species of Solanum as recorded hosts for C. cyathicollis in their Argentina checklist; however, S. granuloso-leprosum is not among them…)

Corythaica cyathicollis late-instar nymphs.

The bristles of needle-like setae exhibited by the nymphs may be useful for species identification by entomologists (and even phylogenetic analyses—see Guilbert 2005), but for the nymphs themselves it seems fairly obvious that they serve some adaptive function for protection. Neal and Schaefer (2000) note that nymphs of many species of Tingidae seem to be protected by a wide variety of other adaptive mechanisms as well, including maternal care, the production of alarm pheromones and possibly the secretion of noxious compounds. Indeed, most tingids occur in multiple aggregations with large numbers of nymphs of the same species on a single host plant relatively free of predation and parasitism—it is difficult to imagine that such aggregations could exist without employing a strong arsenal of multiple defense mechanisms.

A presumably teneral adult Corythaica cyathicollis.

Occasional adults were seen within the aggregations that showed decidedly lighter coloration than the majority of adults seen. The aggregations were comprised primarily of adults and late-instar nymphs, so I presume these light-colored adults represented newly molted, teneral individuals that will eventually assume normal coloration once their new adult exoskeleton fully hardens.

Adult Gargaphia lunulata on lower leaf surface of Ricinus communis.

Later in the day, I encountered a different lace bug species on a different shrub—Ricinus communis.  This is the famous castor oil plant, a member of the Euphorbiaceae, native to the Old World and now widely distributed throughout tropical regions.  Despite castor oil’s reputed ability to heal wounds and cure ailments, the beans and other plant parts also contain ricin—a toxin with known insecticidal properties.  Apparently these lace bugs possess some mechanism that makes them immune from its effects.

Gargaphia lunulata 5th instar nymphs (and an apparent 1st instar in lower left corner).

This species was also fairly easy to identify—one of the species listed in Neal and Schaefer (2000) as feeding on Ricinus is Gargaphia lunulata, which they note feeds on several useful South American plants belonging to a number of families, including the Euphorbiaceae.  Photographs and drawings of this species can be found in Ajmat et al. (2003) and agree well with the adults and nymphs I found on this plant.  Unlike C. cyathicollis, which were found on the adaxial (upper) surface of the leaves, I found G. lunulata exclusively on the abaxial (lower) surfaces.  Nevertheless, the characteristic white stippling was easily visible on the leaves and gave immediate clue to their presence.

Photo Details: Canon 50D w/ MP-E 65mm 1-5X macro lens (ISO 100, 1/200 sec, f/13), Canon MT-24EX flash w/ Sto-Fen + GFPuffer diffusers. Typical post-processing (levels, minor cropping, unsharp mask). Photo 1 taken at 1X, photos 2 through 6 taken at or near 5X.

REFERENCES:

Ajmat, M. V., S. G. Bado, M. A. Coviella and M. J. Pannuzio. 2003. Aspectos morfológicos, biológicos y daño de Gargaphia lunulata (Mayr) 1865 (Heteroptera: Tingidae) sobre Passiflora caerulea L. (Passifloraceae). Boletin Sanidad Vegetal Plagas 29:339–346.

Guilbert, É. 2005. Morphology and evolution of larval outgrowths of Tingidae (Insecta, Heteroptera), with description of new larvae. Zoosystema27(1):95–113.

Haene, E. and G. Aparicio.  2007.  100 Trees of Argentina. Editorial Albatros, Buenos Aires, República Argentina, 128 pp.

Kogan, M.  1960.  Corythaica cyathicollis (Costa, 1864), aspectos sistemáticos, biológicos e econômicos (Hemiptera, Tingidae). Memorias Instituto Oswaldo Cruz 58(1):59–88.

Montemayor, S. and M. del Carmen Coscarón. 2005. List of Argentinian Tingidae Laporte (Heteroptera) with their host plants. Zootaxa 1065:29–50.

Neal, J. W., Jr. and C. W. Schaefer. 2000. Chapter 4. Lace Bugs (Tingidae), pp. 85–137. In:C. W. Schaefer and A. R. Panizzi (Eds.). Heteroptera of Economic Importance, CRC Press LLC, Boca Raton, 828 pp.

Copyright © Ted C. MacRae 2011

Bichos Argentinos #5 – Cyrtocoris egeris

Cyrtocoris egeris | 15 km S Reconquista, Pcia. Santa Fe, Argentina

Despite its obvious membership in the order Hemiptera, I knew the insect featured in ID Challenge #7 would be a difficult subject to identify.  This bizarre bug is Cyrtocoris egeris, a member of the small pentatmoid family Cytocoridae (congratulations to HBG Dave, who was the only commenter to correctly identify not only the family, but the genus).  While their relationship to Pentatomidae (stink bugs) and Scutellaridae (shield-backed bugs) is obvious, hemipterist-great Carl Schaefer thinks these insects might actually be most closely related to the Cydnidae (burrowing bugs).  I encountered this individual a couple of weeks ago in a soybean field in Santa Fe Province, Argentina.  Now, I have to be honest here – I did not figure this one out on my own. Instead, I assumed it must be some bizarre member of the Pentatomidae or Scutellaridae, and it was only after my repeated searches in either of those two families failed to turn up anything promising did I throw up my hands and call for hired help. This time it was USDA Research Entomologist Don Thomas, a pentatomid specialist (and former co-alumnus at the University of Missouri) who responded to my query with a genus-level ID. Once I had that bit of information in hand I was able to locate the recent revision of the family (Packhauskas and Schaefer 1998) and identify the species.

Looks stink bugish enough in this head on view...

In addition to the expanded scutellum bearing a broad-based spine or hump, members of this exclusively Neotropical family are characterized by flattened expansions of the anterior part of the head, the covering of flattened scalelike setae, and a mediodistal tubercle on at least the foretibiae. Packauskas and Schaefer (1998) recognize only three genera and 11 species in the family, its members occurring from Argentina north through central Mexico.

...but there's some crazy stuff going on at the back end.

My ID as C. egeris is based on the very well-developed scutellar crest and my interpretation of the humeral projections not extending forward of the anterior angles next to the head. Packauskas and Schaefer (1998) recorded this wide-ranging species from Mexico to Argentina, with the southernmost specimens in extreme northeastern Argentina (Pcia. Missiones), but Schaefer et al. (2005) later recorded it from Reconquista – also on soybean. Cyrtocoris gibber is very similar to C. egeris and is also widespread from Costa Rica to Argentina (and also with the southernmost record in Pcia. Missiones, Argentina), but in that species the humeral expansions project forward nearly as far as the anterior angles of pronotum (strongly surpassing a line drawn through the bases of these angles).  Besides soybean for C. egeris, the only other host records I am aware of for any species in the family are by Costa Lima (1940), who reported C. gibbus on the branches of Mimosa scabrella (Leguminosae), and Schaeffer et al. (2005), who reported C. tigrinus on Sida rhombifolia (Malvaceae) (although nymphs could not be reared to adulthood on this plant).

REFERENCES:

Costa Lima, A. 1940. Insetos do Brasil. 2° Tomo, Capitulo XXII. Hemipteros. Escola Nacional do Agronomia, Rio de Janeiro.

Packauskas, R. J. and C. W. Schaefer. 1998.  Revision of the Cyrtocoridae (Hemiptera: Pentatomoidea).  Annals of the Entomological Society of America 91(4):363–386;

Schaefer, C. W., A. R. Panizzi and M. C. Coscarón. 2005.  New records of plants fed upon by the uncommon heteropterans Cyrtocoris egeris Packauskas & Schaefer and C. trigonus (Germar) (Hemiptera: Cyrtocoridae) in South America.  Neotropical Entomology 34(1):127-129.



Brazil Bugs #16 – Outro Percevejo

Proxys sp. | Barão Geraldo, Campinas, Brazil

Another stink bug (family Pentatomidae) from my recent travels to South America, but this one from southeastern Brazil rather than Argentina.  Although the white spot at the apex of the scutellum is a common theme across the family, the jet black coloration and strongly acute clypeus (“nose”) immediately reminded me of Proxys punctulatus from eastern North America. Although that species does also occur south through Mexico and Central America into northern South America, the lack of distinctively black femoral apices (“knees”) on this individual suggest it is likely a different species.  I’ve not found much information on other species in this genus, as my old standby Flickr repeatedly proffers images of P. punctulatus in its Pentatomidae pages but not other species in the genus.  Grazla and Campos (2010) list P. hastator from “Cayenna” (likely French Guiana) and P. victor from “Brésil,” and an illustration of the latter in the monumental Biologia Centrali-Americana (Distant 1880-1893) agrees reasonably well (but not completely) with this individual.  For now, this will have to stand as Proxys sp.

REFERENCES:

Distant, W. L.  1880-1893.  Biologica Centrali-Americana. Insecta. Rhynchota. Hemiptera-Heteroptera. Volume I.  London: published for the editors by R. H. Porter, 462 pp.

Grazia, J. and L. A. Campos. 2010. Neotropical Pentatomidae (Insecta: Hemiptera: Heteroptera) of the collection of Massimiliano Spinola preserved in the “Museo Regionale de Scienze Naturali”, Turin, Italy. ZOOLOGIA 27(3):413–424.

Copyright © Ted C. MacRae 2011