2024 Caterpillar Season – Spotted Apatelodes

Spotted Apatelodes
Apatelodes torrefacta fam. Apatelodidae
Host plant: Found on white oak (Quercus alba)
Date found: 02, Sep, 2024
Location Found: Hawn State Park, Ste. Genevieve County, MO
Notes: Adults of this species are as unique and fantastic as the larvae.

2024 Caterpillar Season – Harvey’s Prominent Moth

Harvey’s Prominent Moth
Litodonta hydromeli fam. Notodontidae
Host plant: Found on gum bumelia (Sideroxylon lanuginosum)
Date found: 24, Aug, 2024
Location Found: Washington State Park, Washington County, MO
Notes: Beating Sideroxylon lanuginosum trees within the glades of Washington SP proved fruitful in finding several of these fascinating caterpillars. Using Weller, 1987 these can be identified as a third instar and fifth instar larvae. Last year we found a forth instar of this species.

Third instar Litodonta hydromeli.

Fifth/final instar Litodonta hydromeli

Orgyia leucostigma (white-marked tussock moth)

This autumn I was fortunate to have this really interesting experience with a common but fascinating moth species. I invite you to read about it and see the photography.

New documented host plant (Nymphaeaceae) and life history documentation for the highly polyphagous moth, Orgyia leucostigma (Lepidoptera: Erebidae), in eastern Missouri.

Orgyia leucostigma Smith, 1797 is a moth species in the family Erebidae that is found throughout eastern North America and is known to be extremely polyphagous. Commonly known as the white-marked tussock moth, O. leucostigma has been recorded using 166 plant species in 55 families as hosts, mostly consisting of deciduous plants, but coniferous and herbaceous plants have also been recorded (Robinson et al. 2023).

Larvae of Orgyia leucostigma feeding on Nymphaea odorata.

In early September 2024, I observed six mid- to late-instar larvae of O. leucostigma, each feeding on the leaves of Nymphaea odorata (Nymphaeaceae) that were growing in a small artificial “pond” in my St. Louis County, MO suburban yard. Unfortunately, these insects consumed every available leaf of N. odorata in the pond before they could pupate. The only other species in the pond available to them was the exotic Pontederia crassipes (water hyacinth), which they did not readily consume. I was able to locate and remove five final-instar larvae from the remnants of the original host leaves and placed them in an outdoor cage where they successfully switched to feeding on leaves of Quercus muehlenbergii and Q. imbricaria (both Fagaceae). Within seven days, all five larvae built cocoons to pupate within.

Larvae of Orgyia leucostigma running out of leaf. Leaves of exotic Pontederia crassipes (water hyacinth) seen surrounding hostplant leaf.

To my knowledge, this is the first documentation of a nymphaeaceous host plant for O. leucostigma, which expands the host range of this already highly polyphagous species by another family. Unfortunately, the caterpillars did not reach pupation feeding on N. odorata alone, so the ability of O. leucostigma to reach adulthood on this host cannot be confirmed yet. However, the fact that five larvae of O. leucostigma were able to reach the final larval instar feeding solely on N. odorata makes this highly likely.

Larvae of Orgyia leucostigma finishing its larval stage on leaves of Quercus imbricaria (shingle oak).

Life history of Orgyia leucostigma
The lifecycle of O. leucostigma begins as an egg, typically laid in masses by the adult female. Eggs are laid in late summer or early fall on tree bark, branches, or other surfaces. A single female can lay anywhere between 100 to 600 eggs. These eggs are small, round, and white to pale yellow in color, and are coated in a protective frothy substance produced by the female to safeguard them from predators and environmental factors.

Two of five cocoons of Orgyia leucostigma that were raised primarily on the leaves of Nymphaea odorata.

Lepidopterans use a variety of strategies in overwintering. In the case of O. leucostigma, the eggs remain dormant over the winter, entering a state of diapause, a period of suspended development that allows them to withstand harsh winter conditions. They hatch in the spring when the weather warms, typically around late April or early May, coinciding with the budding of trees that will serve as food for the larvae.

One of five Orgyia leucostigma females that eclosed in late September and early October.

After hatching, the larvae emerge as small, hairy caterpillars. This larval stage is perhaps the most recognizable and distinctive phase of O. leucostigma. The caterpillars are known for their colorful and tufted appearance, with a series of tufts (or tussocks) of hair along their backs and two long black “pencils” of hair protruding from both the front and back ends. The body is primarily yellow or cream-colored, with a pattern of red and black markings.

One of approximately two-dozen male Orgyia leucostigma that were attracted to our screen porch, presumably by the pheromones released by the females.

As discussed above, the larvae feed on a wide variety of trees and shrubs, including both deciduous and coniferous species. In our area, oak, maple, and willow, are among the most common hosts. The larvae are voracious feeders and can cause significant defoliation when present in large numbers, which can lead to tree stress, although healthy trees typically recover without long-term damage.

The males found the stationary Orgyia leucostigma females once placed in their enclosure.

Once the larva has reached its final instar, it will spin a cocoon in a sheltered location, often on the trunk or branches of trees, beneath loose bark, or on the sides of buildings. The cocoon is made from silk and incorporates most of the caterpillar’s own urticating body hairs, offering added protection from predators.

Inside the cocoon, the caterpillar transforms into a pupa, a resting stage during which the most dramatic metamorphosis occurs. The pupal stage typically lasts 10-14 days, during which time the organism undergoes a complete transformation from a larva into an adult moth.

Upon completion of the pupal stage, the adult moth emerges. The adult form of O. leucostigma exhibits strong sexual dimorphism. The males are small, grayish-brown moths with a wingspan of about 25-35 mm. They have feathered antennae that they use to detect pheromones released by females from a considerable distance.

Within minutes of a presumed successful copulation, a female Orgyia leucostigma begins oviposition, forming a large foam-encapsulated egg mass.

In contrast, the females are wingless and remain on or near their cocoons after emerging. They are larger than the males and have a plump, cylindrical body covered with dense hairs. Since they are flightless, females rely on releasing pheromones to attract males for mating. After mating, the female lays eggs near the cocoon, starting the cycle again. The female typically dies shortly after laying her eggs, while the male lives a few days longer in search of other mates.

Due to the stationary habit of the females, it is fascinating that all dispersal is dependent on the larvae in this species. To do this efficiently, early-instar larvae will often “balloon,” letting out an amount of silk to catch the wind, thus allowing them to move to new areas much quicker than by crawling. This dispersal mechanism is also practiced by many spiders.

A worn male Orgyia leucostigma rests nearby as the female continues to oviposition.

In this specific case, all five of the pupa that I reared produced female adults and each of these eclosed exactly 10 days after cocoons/pupa were formed. At dawn of each morning following the females emergence, I walked the outside perimeter of our screened porch wherein the screened moth enclosure was contained. Each morning I found up to six male adult O. leucostigma that I captured and placed in the enclosure containing the females.

The extent of the egg masses of Orgyia leucostigma was astounding. The females were mostly eggs!

Mating appeared to be very brief and within minutes of contact by a male, each female began ovipositing. It was quite shocking observing the differences in size of the females before and after their egg masses where completed. See photos below that I attempted to document these changes.

A nearly completed Orgyia leucostigma egg mass along with her larger and older sister and a potential mate.

While observing and photographing these activities, I happened to notice that a jumping spider (F. Salticidae) was attacking one of the females prior to her ovipositing. The spider must have come from the oak branches that I placed in the enclosure to finish rearing the caterpillars. I took enough time to take a few photos of this and then removed the spider with a pair of forceps. I noticed a drop of hemolymph on the back of the female after removing the spider. However, the female did not seem too bothered by this and created her egg mass within a couple of hours of this incident.

A female Orgyia leucostigma that was attacked by a jumping spider (fam. Salticidae) that must have been hiding within the oak branches. The spider was removed and although it is likely the moth received a wound, she later completed ovipositioning.

Caterpillars of this species are often found during my caterpillar hunts. Sometimes they are so plentiful as to be annoying when hoping for rarer quarry. I had read about the stationary eggbound females of this species but had little hope of ever actually seeing one in person. I very much enjoyed documenting these activities and I will try my best at overwintering these egg masses to fruition.

Literature Cited

Robinson, G. S., P. R. Ackery, I. Kitching, G. W Beccaloni and L. M. Hernández (2023). HOSTS (from HOSTS – a Database of the World’s Lepidopteran Hostplants) [Data set resource]. Natural History Museum. Available from https://data.nhm.ac.uk/dataset/hosts/resource/877f387a-36a3-486c-a0c1-b8d5fb69f85a (last accessed 16 Sep 2024).

Photographing the Comet of the 21st Century

Comet background
Hopefully you were aware that the astronomy gods gifted us with another incredible wonder in 2024–a bright comet that was naked-eye visible for several weeks. To date, this has been the brightest comet of the century.

The long-period comet, named C/2023 A3 (Tsuchinshan-ATLAS) (from hereon referred to as Comet A3), last visited this close to earth around 80,000 years ago, during a period of heavy glaciation in North America and when Homo sapiens were first beginning their epic migration from Africa. First discovered in January 2023, Comet A3 made its closest approach to earth on October 12th, 2024, at a distance of 0.275 AU, or 41.1 million km, where it reached a magnitude of -4.9. During the month of October, astronomy enthusiasts and astrophotographers found themselves at their favorite dark sky sites to observe the comet. Above the western horizon, it was naked-eye visible for short periods of time after sunset. Following its closest orbital intersection with earth, it then began to grow fainter as it climbed the sky night after night.

Perihelion, the point in which the comet was closest to the sun, occurred on September 27th, 2024 at a distance of 0.391 AU. Current projections are that, due to Comet A3’s hyperbolic trajectory, it will likely be ejected from the solar system after this pass.

Being an amateur astrophotographer and a comet enthusiast, I made a few attempts at photographing Comet A3 during its relatively close pass to earth. We were fortunate in having mostly clear skies during this period of time but unfortunate in that this period coincided with the a full moon, providing plenty of unwelcome light that hindered clear observation and photography of the comet.

Photography details

Dates and location
Comet A3 was photographed on 15-October (composition 1) and 20-October (composition 2). Data for both images were collected at Danville Conservation Area in Montgomery County, MO.

Equipment
For these images I used a Canon 7D mkii camera connected to the specific lenses described below. In order to compensate for the earth’s rotation and keep stars as pinpoint as possible, I used a Fornax LighTrack II tracking mount set on a William Optics Vixen Wedge Mount. A QHYCCD Polemaster was used to assist with obtaining polar alignment. This equipment sat on a Gitzo carbon fiber tripod. I also utilized a shutter release cable, a laser pointer to help find Polaris and sky targets, a lens warmer to prevent dew and frost on lens, and a dummy battery connected to an external power source to power the camera. A lithium battery generator was used to provide power to the camera, dew heater and the laptop computer.

Composition 1 was taken with an Askar ACL200 200mm f/4 lens (260mm focal length equivalent). Composition 2 was taken with a Canon 90mm f/2.8 macro tilt-shift lens (144mm focal length equivalent).

Imaging Details
Composition 1:
Sub-exposures taken (ISO 640, f/4, 25 second exposure): 73
Sub-exposures after cull due to tracker error, wind, bumps, clouds, etc.: 73
Used best 90% of remaining sub-exposures based on scores from stacking software in stack for a total of 66 subs (27 min. 30 sec.) used for integration
Calibration frames: none

Composition 2:
Sub-exposures taken (ISO 1600, f/2.8, 30 second exposure): 80
Sub-exposures after cull due to tracker error, wind, bumps, clouds, etc.: 79
Used best 90% of remaining sub-exposures based on scores from stacking software in stack for a total of 72 subs (36 min.) used for integration
Calibration frames: none

Processing
RAW files stacked in Deep Sky Stacker using comet stacking mode, GraXpert for gradient removal, Affinity Photo 2 for stretching and other cosmetic adjustments.

C/2023 A3 (Tsuchinshan-ATLAS)–Composition 1. Comet, including anti-tail, alongside extrasolar neighbor–Messier 5 globular star cluster, to the right (north) of comet.
C/2023 A3 (Tsuchinshan-ATLAS)–Composition 2. Comet alongside extrasolar neighbors–Messier 12 and Messier 10 star clusters, to the left (south) of comet.

2024 Caterpillar Season – Beautiful Wood Nymph

Beautiful Wood Nymph
Eudryas grata fam. Notctuidae
Host plant: grape species (Vitis sp)
Dates found: 24, Aug, 2024; 07, Sep, 2024
Locations Found: Schoolcraft Prairie, Washington County, MO; Kaintuck Hollow, Phelps County, MO
Notes: The adult moth is a beautiful bird dropping mimic.

2024 Caterpillar Season – Morning-glory Prominent

Morning-glory Prominent
Schizura ipomoeae fam. Notodontidae
Host plant: Oak species (Quercus sp)
Date found: 24, Aug, 2024
Location Found: Schoolcraft Prairie, Washington County, MO
Notes: Despite both its common and scientific names, it is highly unlikely this species ever feeds on morning glories (Ipomoea spp.).

2024 Caterpillar Season – Calico Paint

Calico paint aka brown-hooded owlet (adult)
Cucullia convexipennis fam. Noctuidae
Host plant: Found on goldenrod (Solidago sp.)
Date found: 24, Aug, 2024
Location Found: Schoolcraft Prairie, Washington County, MO

It’s a Thin Line Between Love and Hate

The year 2024 was a very notable year in our area. No, I’m not talking about the circus joke of an election coming up. Of course, I’m referring to the year of the Brood XIX periodical cicada emergence. Brood XIX, also known as the “Great Southern Brood,” holds a special place as a natural marvel. These periodical cicadas are a part of the Magicicada genus, known for their unique life cycle, which spans 13 years, culminating in a synchronized mass emergence.

A newly emerged Magicicada tredecassini photographed on May-11

Unlike annual cicadas, which appear every year, periodical cicadas have a distinctive life cycle, emerging in massive numbers after spending 13 or 17 years underground. These insects belong to three distinct species groups, with Brood XIX being part of the 13-year group that is comprised of four species: Magicicada tredecimMtredecassiniMtredecula, and Mneotredecim. Cicada broods are geographically isolated populations that emerge in synchrony, making their appearance not only rare but region-specific. Brood XIX has a vast range, covering at least portions of 11 states across much of the southeastern United States.

A newly emerged Magicicada tredecassini photographed on May-18

Life Cycle of Brood XIX
The life of a Brood XIX cicada is primarily hidden underground, where they live as nymphs, feeding on sap from tree roots. For 13 years, they remain underground, quietly developing and maturing. Then, seemingly overnight, millions emerge from the soil in an overwhelming display of nature’s rhythm. Once they emerge, their primary purpose is reproduction.

Adult cicadas live only for a few weeks. During this time, males produce loud, buzzing mating calls using specialized structures called tymbals. These mating calls fill the air, creating a chorus that can reach deafening levels in regions with high cicada density. After mating, females lay eggs in tree branches, and once the eggs hatch, the nymphs fall to the ground and burrow into the soil, starting the 13-year cycle anew.

Magicicada tredecassini

The Mystery of Synchronized Emergence
One of the most intriguing aspects of Brood XIX is the synchronized nature of their emergence. The question remains: how do they know it’s time to come out? Scientists believe cicadas track environmental clues, such as soil temperature, to time their appearance. When the soil reaches about 64°F (18°C), it signals that it is time for the cicadas to surface.

This poor guy was not able to emerge from its final larval form

The reason for their long, synchronized life cycles is believed to be a survival strategy known as predator satiation. By emerging in overwhelming numbers all at once, they reduce the likelihood of being completely eaten by predators. There are simply too many cicadas for predators to consume, ensuring that enough survive to reproduce.

Additionally, 13 and 17 are both prime numbers and this is not likely a mere coincidence. Because these intervals are in prime-numbered years, it is nearly impossible for these patterns to overlap with the breeding strategies of would-be predators.

Periodical cicada (Magicicada spp.) exuviae

The Ecological Importance of Cicadas
Though their emergence may seem disruptive, periodical cicadas play a vital role in the ecosystem. Their sheer numbers provide a feast for predators, from birds to mammals, and their death leaves behind nutrient-rich carcasses that fertilize the soil.

While some may find them a nuisance due to their loud calls and vast numbers, these insects do not pose a significant threat to crops or forests. Their presence is fleeting, and they leave behind a healthier environment in their wake.

Of the millions of cicadas that emerged in our neighborhood, many had issues with expanding their wings as shown here. These individuals become likely calories for others and will not be able to pass on their genes to the next generation.

That thin line…
I’m sure you’ll agree that anyone with a shred of curiosity about the natural world would find what I shared here of immense interest. As a naturalist, I am still overwhelmed by what I observed for a few weeks in May in our suburban St. Louis County neighborhood. I spent many hours in amazed observation, watching them climb as freshly emerged adults, listening to their midday chorus and observing as my watch counted more than 100 decibels standing in our front yard.

Mating Magicicada tredecassini

As mentioned above, it is true that in the grand scheme of ecology, these creatures provide nothing but benefit – except, if you are a young woody plant. This is where I found my my awe and fascination becoming replaced with a red, searing rage. For those who may not know, I have spent considerable time, effort, and money over the past four years planting approximately 50 trees and bushes in our once florally depauperate yard. The spring and early summer of 2024 were turning out to be absolutely perfect in regards to establishing woody plants. Temperatures were mild and rains were plentiful.

Although the periodical cicadas did not use my potted fig tree in the backyard for ovipositing, this pair of Magicicada tredecassini found it a fine place for “making babies.”

Then I slowly realized the numbers of cicadas emerging in our neighborhood and the pressure my plants were soon to receive from the thousands of ovipositing females that were looking for just what my yard provided. The ovipositors of the female cicada are sharp and literally metal-studded. These guys are as apt as beavers when working with wood. Heavy pressures from swarming periodical cicadas can and do kill young trees. Cicadas love young trees for depositing their eggs because there are plenty of branches that are the perfect size — about the diameter of a pencil. They especially love young trees that are exposed to the full sun. This makes tremendous evolutionary sense. A young tree that is in full-sun will typically have all the advantages for growing and will therefore more likely be around for the full 13 years that it knows its offspring will need to feed on its host’s roots. I will never forget shaking young dogwood trees in the front yard and watching as hundreds of cicadas swarmed off of them, most simply flying for 50 feet or so and turning right around to land in the same tree.

An example of the pressures of the Brood XIX cicadas on the young and establishing trees in our suburban yard.

Over the next month or so I watched as limb after limb on most of my trees browned and succumbed to the damage done by the heavy onslaught of ovipositing females. I filled several trash cans with limbs that were either self-pruned or that I removed once they were certainly dead. No tree in my yard has died at the time of my writing this, but most plants were significantly set back in their efforts in becoming established. I will have to wait and hope that most will make it through the coming winter season.

Magicicada neotredecim ovipositing on branches of Cotinus obovatus (American smoke tree).

I made a list of the 26 plants I recorded that were used for ovipositing by the Magicicada cicadas in our yard. With a couple of exceptions, this list comprises every woody species in the yard. I even recorded them ovipositing in the herbaceous forb, Penstemon digitalis.

List of plants used by ovipositing Magicicada Brood XIX cicadas in a St. Louis County yard in 2024 eruption.
Amelanchier arborea, Amorpha fruticosa, Aronia melanocarpa, Asimina triloba, Carpinus caroliniana, Cephalanthus occidentalis, Cercis canadensis, Cornus florida, Cotinus obovatus, Diospyros virginiana, Euonymus americanus, Euonymus atropurpureus, Gymnocladus dioicus, Hamamelis virginiana, H. vernalis, Lindera benzoin, Nyssa sylvatica, Penstemon digitalis, Physocarpus opulifolius, Prunus americana, P. serotina, Quercus bicolor, Q. muehlenbergii, Q. shumardii, Sassafras albidum, Viburnum dentatum

Of the plants listed above, particularly high preference seemed to be for the redbuds, dogwoods and oaks. I’m not sure if there is really some taxa preference or if these particular plants simply had more of the best sized limbs.

A Magicicada sp cicada ovipositing on a stem of the herbaceous Penstemon digitalis.

With hopes of photographing the full cicada lifecycle, I collected quite a few stems from trees that were dropped due to the damage they received or that I removed myself. Unfortunately, my insect rearing skills need some work and I never did see a newly emerged cicada nymph. I did cut into some branches and photographed the eggs.

Eggs from Magicicada sp cicada that were inserted into the pith of Amorpha fruticosa stems. Up to 30 eggs may be inserted in each incision the female makes in the plant and a single female may lay up to 600 eggs in her life.

The next generation…?
Despite the angst and dread this caused when wondering what would become of my woodies that I have spent so much time in watering and protecting from deer over the past several years, I was very pleased to live in a place that still had natural wonders such as this. If the damage caused to my trees indicates the potential success of the next Group XIX emergence, then I am happy and will look forward to the next time we see these guys, assuming I am fortunate enough to be here in 13 years. Hopefully enough of my trees will survive to help them on their way.

Don’t Skip Out on the Skippers: The How’s and Whys I Photograph the Overlooked Hesperiidae

Today I am featuring a guest post by my friend, Casey Galvin, who has spent ample time and efforts photographing rare skippers in recent years. Enjoy!

Butterflies through time have been written about more than any other insect. Their beauty and life cycle are a thing of wonder. Who doesn’t enjoy watching their flight on gossamer wings? Or, the idea to metamorphose from a crawling caterpillar into something that is not only colorful, but to be able to leisurely flutter? No wonder philosophers, artist and poets can’t stop from being in their thrall.

A spreadwing skipper that was once widely found, the mottled duskywing (Erynnis martialis) is now known from local and isolated populations. A species of concern in many states.

Unfortunately, not all members of the order Lepidoptera are given their just attention. Skippers, those brown moth-looking butterflies, which never seem to sit still and dart quickly from here to yon, are usually given a passing notice at best. Yes, they go through the same life cycle as other butterflies, egg to larva to pupa and then adult. They also serve the same important ecological functions that the rest of the order does. But it is hard for many to see their beauty in any of this when they look so small and often seem so drably colored.

Then there are those lucky enough to look closer and try to appreciate these creatures, opening up opportunities for exploration and adventure in finding and understanding this unique family – the Hesperiidae. If you would like to be in the latter group there are a few things to consider to help in this endeavor.

Duke’s skipper (Euphyes dukesi)

Skippers in the U.S.A. can be broken into three subfamilies within the family Hesperiidea. These are the Pyrginae (spreadwings skippers), Hesperiinae (Grass skippers) and the Heteropterinae (skipperlings). The first two groups have hooks at the terminal end of their antennae, whereas the skipperlings do not.

And now to the challenges which I call the three phonetic “F’s”. Finding them, Photographing them and then Figuring out what you have.

Dion skipper (Euphyes dion)

Finding them.
A key component of finding any living subject is to know their lifestyle. For many insects finding the host plant that the larval stage feeds on is critical. Without the host plant finding the adult can be difficult. The adult females need to lay her eggs on or near the host plant to allow the life cycle to begin. Knowing the flight time for adults is also important. Many of the most frequently seen skippers have two or more generations or broods (known as “polyvoltine”) within a single growing season. Others might have only one generation, or “univoltine,” making for short yearly adults periods. Rarer species usually have fewer annual flight periods.

Assuming you have found your subject, You are now ready to try and photograph them.
Like many insects, skippers are part of the food chain and are aware of their surroundings. Quick movements, casting your shadow across them, or disturbing the platform they are resting, feeding or searching for a mate on may cause them to flush, thus foiling your chances. To be successful, making yourself as small or low to the ground as possible helps tremendously. Walking on your knees or even crawling to get as close to the subject as possible is not out of the question. Also, paying attention to where your shadow is cast is important, as this sudden change may indicate a potential predator. Be aware of the platform the animal is on and how your movements might affect the platform helps in approaching the insect. Does this work all the time? No, but with patience and practice will come success.

The wild indigo duskywing (Erynnis baptisiae) uses wild indigo (Baptisia spp.) as hosts

Once in a close enough position, try your best to align the plane of focus of your camera’s sensor with that of the butterfly, making sure the subject’s eye is the sharpest part of the image. Try to take as many images of the subject as possible, and make sure to document the sides of both fore and hind wings in the closed (ventral) and open (dorsal) positions, if possible, looking for scale patterns. This will help tremendously in the next process.

For my skipper photography, I use a Nikon D500 attached to a Sigma 180mm f2.8 macro lens. My ISO is typically set to 400 and I use Aperture Priority mode, with my f stop set at f6.3-11 and with autofocus turned on. I will change to fully manual mode and change my ISO and f stop occasionally when necessary. I will also switch off my autofocus if I need to. I carry a flash, but rarely use it, preferring natural lighting. With this photography I usually hand hold my camera.

With the loss of prairie, the Ottoe skipper has disappeared from most states in which it was once found

Once you have accomplished your goals in the field of collecting as many great images as possible, you are now ready to head home and figure out what you might have. This is often the most challenging phase of this process.

How they hold their wings is the first way to know which group a skipper belongs to. When they land, the spreadwings group usually put both sets of wings in a flat plane. The grass skipper group normally keep their wings closed, but can also put one set flat and the other perpendicular to the flat wings giving them a fighter jet look. These butterflies can also flatten the wings like the spreadwing group and usually do this when they are trying to warm themselves in the morning sun before flying. Skipperlings usually spread their wings at a 45 degree angle at rest or keep them closed.

The location where subject was found, local plants (hopefully the host you were looking for) and the time of year will definitely help in identification. Scale patterns will certainly be needed also. It might take some time looking at reference books and online resources to get an identification. Several skippers may have nearly identical patterns. Looking at the details matter in this step.

One of the more colorful skippers, Leonard’s skippers prefer grasslands. Still widespread but losing populations with habitat loss.

If you are still stumped after using reference guides and online resources, you might consider taking the next step of seeking help. Web sites like iNaturalist and Butterflies and Moths of North America allow you to create an account and then upload your photographs to have experts in the field help with identifying the subject.

With practice and experience, all the above methods help to make this less stressful and increases your chances for success. Making new acquaintances also becomes rewarding. Many photographers choose new projects in order to improve upon existing or make new skills. This is the latest one I have chosen.

Many of my natural history friends had just two question when I took on this subject. Why? Or really Skippers?

Here are my some of my reasons: Many of the skipper species are not looked for at all. In many cases, there is little information on whether or not a species may still be found at historical location records. Grass skippers, in particular, seem to be disappearing widely, especially ones that have only one or two broods per year. Secondly, I personally like grasslands, tallgrass prairie in particular. This biome and its skipper inhabitants have pretty much disappeared from North America along with the rest of its flora and fauna. To find some parts of it still among us is rewarding. Finally, I like to travel and explore. Even returning to well-known haunts, allows me to look at these sites from a different perspective.

Linda’s roadside skipper (Amblyscirtes linda) is a species of conservation concern in every state that still contains populations.

There is still a small group of scientist and enthusiasts that want to keep these wonderful creatures around. We would like others to join our tribe. Why not become one also?