Hymanoptera: A Look at Some Bees, Wasps, Hornets, and Ants

What’s all this buzz about bees?  And what’s a hymanopteran?  Well, let’s see.

Hymanoptera—our bees, wasps, hornets and ants—are generally considered to be our most evolved insects.  Some form complex social colonies.  Others lead solitary lives.  Many are essential pollinators of flowering plants, including cultivars that provide food for people around the world.  There are those with stingers for disabling prey and defending themselves and their nests.  And then there are those without stingers.  The predatory species are frequently regarded to be the most significant biological controls of the insects that might otherwise become destructive pests.  The vast majority of the Hymanoptera show no aggression toward humans, a demeanor that is seldom reciprocated.

Late summer and early autumn is a critical time for the Hymanoptera.  Most species are at their peak of abundance during this time of year, but many of the adult insects face certain death with the coming of freezing weather.  Those that will perish are busy, either individually or as members of a colony, creating shelter and gathering food to nourish the larvae that will repopulate the environs with a new generation of adults next year.  Without abundant sources of protein and carbohydrates, these efforts can quickly fail.  Protein is stored for use by the larval insects upon hatching from their eggs.  Because the eggs are typically deposited in a cell directly upon the cache of protein, the larvae can begin feeding and growing immediately.  To provide energy for collecting protein and nesting materials, and in some cases excavating nest chambers, Hymanoptera seek out sources of carbohydrates.  Species that remain active during cold weather must store up enough of a carbohydrate reserve to make it through the winter.  Honey Bees make honey for this purpose.  As you are about to see, members of this suborder rely predominately upon pollen or insect prey for protein, and upon nectar and/or honeydew for carbohydrates.

We’ve assembled here a collection of images and some short commentary describing nearly two dozen kinds of Hymanoptera found in the Lower Susquehanna River Watershed, the majority photographed as they busily collected provisions during recent weeks.  Let’s see what some of these fascinating hymanopterans are up to…

SOLITARY WASPS

Great Black Wasp on goldenrod (Solidago species)
A Great Black Wasp on goldenrod (Solidago species).  Like other solitary wasps, a female  Great Black Wasp will sting and paralyze a host insect upon which she’ll deposit her eggs.  After hatching, the larvae will begin consuming the host’s body as a source of protein.  The parasitized insects are often katydids or grasshoppers.
A Great Black Wasp.
A Great Black Wasp feeding on nectar, a source of carbohydrates.  Unlike social bees and wasps, solitary wasps are equipped with a stinger solely used for immobilizing prey, not defending a nest.  They are therefore quite docile and pose little threat to humans.
A Great Black Wasp powdered with pollen.
A Great Black Wasp powdered with pollen.  Hymanopterans that gather nectar and/or pollen are tremendously important pollinators of hundreds of species of plants.
Thread-waisted Wasp
A female Thread-waisted wasp (Ammophilia species, probably A. nigricans) drags a paralyzed caterpillar to her excavated nest where she’ll deposit an egg on the body.  After hatching, the larval wasp will feed on the disabled caterpillar.  The protein will enable the larvae to grow, pupate, and later emerge as an adult wasp.
The female Eastern Cicada Killer (Sphecius speciosus) excavates an underground nest with branch tunnels connecting a dozen chambers or more.  As the common name suggests, the female wasp paralyzes a cicada, then makes a strenuous effort to fly and drag it back to the nest for placement in a cell.  Each male wasp egg is deposited upon just one immobilized cicada, but a female egg is provided with a cache of several cicadas to provide adequate protein for growth to a larger size.  Nest cells are sealed with soil, then the larvae hatch in just a couple of days.  Within about two weeks, they have consumed the cicada protein and are fully grown.  Wrapped in a cocoon, they spend the winter in the nest, then pupate in the spring before emerging as a new generation of adults.
The Black-and-yellow Mud Dauber
The Black-and-yellow Mud Dauber (Sceliphron caementarium) builds a mud-ball nest within which it packs paralyzed spiders to function as a source of protein for its larvae.
Black-and-yellow Mud Dauber at nest.
A Black-and-yellow Mud Dauber at nest.
Pipe Organ Mud Dauber Nest
The Pipe Organ Mud Dauber builds this elaborate nest in which their eggs and paralyzed spiders are deposited in cells sealed with mud partitions.  After consuming the spiders, the larvae pupate, overwinter, then emerge from their cells as adults during the following spring.  To escape the protection of the nest, the new generation of adults bore through the mud walls.  Adult Pipe Organ Mud Daubers resemble the Great Black Wasp, but have a white or yellow distal segment on their rear legs resembling a pair of light-colored socks.
A closeup of the previous image with the lengths of the nest tubes compressed to show four scavenger flies (Miltogramminae), possibly two species, that have invaded this Pipe Organ Mud Dauber nest.  Scavenger flies are kleptoparasites that victimize various solitary bees and wasps, depositing larvae directly into the host species’ nest cells to consume the protein cache stored therein.

CUCKOO WASPS

Cuckoo Wasp
Cuckoo Wasps (Chrysididae), also known as Emerald Wasps, parasitize the nests of other species of wasps.  Females lay their eggs inside the host’s nest, then flee the scene.  Upon hatching, larval Cuckoo Wasps feed on stockpiles of prey intended for the host species’ offspring.  Like the adult mud daubers that have already matured and departed this nest by digging a hole through the wall of the cell within which they were hatched, the metallic green Cuckoo Wasp in the upper left has just emerged in much the same way.

SWEAT BEES

A Sweat Bee (Lasioglossum species).
A Sweat Bee (Lasioglossum species) collecting nectar and pollen on White Snakeroot (Ageratina altissima).
A Sweat Bee (Lasioglossum species).
Sweat Bees (Lasioglossum species) visit human skin to lick up the electrolytes left behind by evaporating perspiration.
A Sweat Bee (Lasioglossum species).
Sweat Bees  in the genus Lasioglossum demonstrate various social behaviors ranging from species that are solitary nesters to those that create colonies with work forces ranging in size from as few as four to as many as hundreds of bees.  Some Lasioglossum practice kleptoparasitism, while others are quite accomplished foragers.
An Augochlorine Green Sweat Bee (Augochlorini).
A female Augochlorine Green Sweat Bee (Augochlorini) collecting nectar on White Snakeroot.  Notice the pollen “baskets” on the rear leg.
An Augochlorine Green Sweat Bee (Augochlorini).
An Augochlorine Green Sweat Bee (Augochlorini).  Sweat bees nest in subterranean cavities and in hollowed out sections of trees.
An Augochlorine Green Sweat Bee (Augochlorini).
A copper-colored Augochlorine Green Sweat Bee (Augochlorini) collecting nectar and dusted with pollen.

LEAFCUTTER AND MASON BEES

Leafcutter Bee
A Leafcutter Bee (Megachile species).  Like Mason Bees, female Mason Bees deposit each of their eggs on a “pollen loaf” within an individual cell inside a preexisting tunnel-like cavity in wood, stone, or in the ground.  Unlike Mason Bees, female Leafcutter Bees cut a circular piece of leaf to create each of the cells in their nest.  After hatching, the larval bee feeds on the pollen loaf, pupates, then emerges from the shelter of the nest to start a new generation, usually during the following year.
A Leafcutter Bee (Megachile species).
A Leafcutter Bee (Megachile species) visiting Wild Bergamot.  Female Leafcutter and Mason Bees lack pollen “baskets” on their rear legs but instead have pollen “brushes” on the underside of the abdomen to gather the protein they need to create a “pollen loaf” for each nest cell.
Leafcutter Bee
A Leafcutter Bee (Megachile species) collecting nectar from White Snakeroot.
A Mason Bee (Osmia species) emerging from a nest cell in spring.
A Mason Bee (Osmia species) emerging from a nest in spring.  Mason Bees create nesting cells within preexisting cavities in wood, stone, and other other supporting structures.  Within the nest cavity, each egg is deposited atop a cache of pollen and nectar, a pollen loaf, then enclosed behind a partition of mud.  The female Mason Bee will usually repeat this process until an entire cavity is filled with cells.  During the following spring, a new generation of adult Mason Bees digs its way through the cell walls to emerge and repeat the process.  These bees readily use paper straws or holes drilled in blocks of wood for nesting.
A mason bee nest box with holes drilled into blocks of wood.
A mason bee nest box with holes drilled into blocks of wood.
Parasitized Mason Bee Nest
Mason Bees seal each cell and the outer end of their nest cavity with mud.  These outer nest cells can been parasitized by a variety of wasps.  Here, the outer cell of a Mason Bee nest has been victimized by a tiny chalcid wasp (looks like another one to the lower left).  Several species of female chalcid wasps (native Monodontomerus species or non-native Pteromalus venustus) enlarge weak points in the outer partition of a mason bee nest, then sting and paralyze the larval bee inside before depositing their eggs.  Within the cell. the wasp larvae consume the larval Mason Bee and the “pollen loaf” provided for its growth.  These same parasitic wasps prey upon Leafcutter Bees as well.

BUMBLE BEES, CARPENTER BEES, HONEY BEES, AND DIGGER BEES

Common Eastern Bumble Bee
A Common Eastern Bumble Bee (Bombus impatiens) collecting nectar and pollen on goldenrod.  Bumble bees are our sole native group of social bees.  Their wax nests are built in a burrow or other shelter.  The eggs are deposited in cells along with a supply of pollen for nourishing the larvae upon hatching.  Honey is stored in “honey pots” within the nest.  New queens are produced along with male bees during the late-summer and fall.  Only the new generation of fertilized queens survive the winter to lay eggs and produce workers to construct a new nest.
Common Eastern Bumble Bees
A pair of Common Eastern Bumble Bees collecting nectar and becoming dusted with pollen.  Their fuzzy coats and semi-warm-blooded metabolism allows them to be active in cooler weather than is tolerated by other bees.
A Common Eastern Bumble Bee pollinating a Great Rhododendron flower.
Flowering plants including the Great Rhododendron find success attracting pollinators to their reproductive blossoms by offering carbohydrate-rich nectar to insects like this Eastern Bumble Bee.  The yellow spots on the flower’s upper petal help to guide visitors toward their sweet treat.
Eastern Carpenter Bee
An Eastern Carpenter Bee feeding on goldenrod nectar.  Compare the almost hairless abdomen to that of the bumble bees.  Carpenter bees are semi-social insects.  Females lay their eggs in cells within galleries bored into wood.  These nests are completed with great precision, avoiding creation of any second entrance by mistakenly breaching the outer surface of the excavated wood.  Each egg/larvae is provided with a supply of protein-rich pollen.  Males often hover outside their mate’s nest to prevent competing males from entering the area.
A Honey Bee visiting goldenrod alongside Common Eastern Bumble Bees.
A worker Honey Bee, a female member of a sisterhood of foragers from a nearby hive, visits goldenrod alongside Common Eastern Bumble Bees.  Honey Bees were brought to North America during the 1620s, the earliest years of the trans-Atlantic migration of European colonists, to pollinate cultivated plants and to provide a reliable source of honey and beeswax.  Within the Honey Bee’s social structure, the queen of each hive lays the eggs to produce the female worker bees.  Once each year, male drones are produced along with a new generation of queens.
Honey Bee Hive
In nature, Honey Bees build hives in tree cavities.  Recently, this colony constructed a hive in a screech owl nest box at susquehannawildlife.net headquarters.  To provide protein for the hatching larvae, worker bees collect pollen and deposit it within the hexagonal cells of the vertically aligned beeswax combs.  After an egg is deposited upon the pollen cache, each cell is sealed with more beeswax.  Young females tend these nest combs before maturing and becoming foraging worker bees.
Bee Hive Display
In apiculture, Honey Bees are raised in man-made hives.  This Pennsylvania Association of Beekeepers display gives visitors to the Pennsylvania Farm Show in Harrisburg a look at the inner workings of a live bee hive.  Nectar collected by worker bees is turned into honey to provide the supply of carbohydrates needed to fuel the colony through the winter.  Note the honeycombs on the glass.
A possible Small Carpenter Bee Ceratina species).
A possible Small Carpenter Bee (Ceratina species) visiting White Snakeroot.  Small Carpenter Bees nest inside hollow stems and twigs.  Some species are eusocial, with a queen’s daughters and sisters sharing responsibility for finding food and rearing the young.  Females overwinter inside a one of the excavated stems and begin a new nest there in the spring.
A Digger Bee (possibly Melissodes species).
A Digger Bee (possibly Melissodes species) with “pollen baskets” full of pollen collected from nearby flowers.  Digger Bees in the genus Melissodes are often known as the Long-horned Bees.  These social insects excavate underground nests and many species practice communal living.

SCOLIID WASPS

Two-spotted Scoliid Wasp
The Two-spotted Scoliid Wasp (Scolia dubia), also known as the Blue-winged Scoliid Wasp, is most frequently observed feeding on nectar.  Scoliid wasps are solitary nesters, though they may assemble into groups while visiting flowers.  They often ignore the presence of humans and are seldom disturbed by their presence.  Females seek out the burrowing grubs of beetles including the Green June Bug (Cotinis nitida) and possibly the Japanese Beetle.  After stinging a grub to paralyze it, the wasp will deposit her egg on its body, then bury it.  Upon hatching, the larval wasp will feed on the grub for nourishment as it grows.
June Bugs eating watermelon.
Don’t like having your watermelon overrun by Green June Bugs while you’re eating?  Then you ought to go out of your way to be nice to the Two-spotted Scoliid Wasp.
The Double-banded Scoliid
The Double-banded Scoliid (Scolia bicincta) parasitizes beetle larvae as hosts for its larvae.  For carbohydrates it relishes flower nectar.

PAPER WASPS

Northern Paper Wasp
A Northern Paper Wasp (Polistes fuscatus).  Paper wasps prey upon numerous garden pests, particularly caterpillars, to collect protein.  Though they are social insects equipped with stingers to subdue their victims and defend their nests, paper wasps are surprisingly docile.
The Northern Paper Wasp
A Northern Paper Wasp (Polistes fuscatus) feeding on nectar from a goldenrod flower.
A Northern Paper Wasp harvesting wood pulp
A Northern Paper Wasp harvesting wood pulp from the side of a mason bee nest box at susquehannawildlife.net headquarters.  The pulp is chewed in the wasp’s saliva to create the paper used to construct the colony’s open-cell nest.
Guinea Paper Wasps (Polistes exclamans) at their nest.
Common Paper Wasps (Polistes exclamans), also known as Guinea Paper Wasps, at their open-cell nest.  This and the nests of most other paper wasps are suspended on a filament or a pedicle.  Many paper wasps can excrete an ant repellent on this section of the nest in an effort to prevent invasion.  Like many other social hymenopterans, a defending wasp can secrete a pheromone venom during the stinging process to warn the colony of danger at the nest.  In winter, Common Paper Wasps seek shelter in stumps and other locations to hibernate.
European Paper Wasp
The European Paper Wasp (Polistes dominula) is a non-native species which builds nests in man-made structures including bird houses.  To collect protein, they prey on a wide selection of insects and other invertebrates.  As such, European Paper Wasps are widespread and successful here in North America.

YELLOWJACKETS AND HORNETS

An Eastern Yellowjacket
An Eastern Yellowjacket feeding on lanternfly honeydew.  Eastern Yellowjackets derive much of their success from being generalists, collecting carbohydrates from nearly any sweet source, natural or man made.  They are quite fond of ripe fruits, flower nectar, and sugary snacks and drinks, especially soda.  Protein for nourishing their larvae is derived from the wide variety invertebrates upon which they prey and from carrion.  These foods are chewed into a paste form in preparation for placement into the brood cells.
An Eastern Yellowjacket.
A subterranean colony of Eastern Yellowjackets is started anew each spring by a young queen that has survived winter hibernation in diapause, a state of interrupted development.  She constructs the new nest’s first cells using pulp made by chewing rotting wood.  The first brood of workers scales up construction while the queen continues producing eggs.  At the nest, these social insects will viciously attack anyone or anything perceived to be a threat, so give them their space and leave them alone.  Many yellowjacket infestations of homes and other buildings are the work of non-native German Yellowjacket (Vespula germanica) [not shown], an invasive species that constructs paper nests in void spaces including walls and attics.
Robber Fly consuming an Eastern Yellowjacket
Yellowjackets may be moody and aggressive, but they do fall victim to a number of predators.  A Robber Fly (Promachus species) has taken down and is devouring this Eastern Yellowjacket.
A Bald-faced Hornet (Dolichovespula maculata) feeding on Spotted Lanternfly honeydew deposits
A Bald-faced Hornet (Dolichovespula maculata) feeding on Spotted Lanternfly honeydew on a Tree-of-heaven (Ailanthus altissima).  In the absence of nectar-producing flowers, many bees, yellowjackets, and hornets have turned to the invasive lanternfly and Ailanthus combo to turn the sun’s energy into the carbohydrates they need.  For protein, they prey upon spiders, flies, caterpillars, and a variety of other insects.
A Bald-faced Hornet collecting wood pulp from the surface of a weathered picnic table.
To create paper for nest construction, this Bald-faced Hornet is collecting wood pulp from the surface of a weathered picnic table.  Away from the nest, these hornets demonstrate a calm, carefree demeanor and can be closely observed.
Bald-faced Hornet Nest
A Bald-faced Hornet nest in a pine tree.  These hives are strictly temporary.  Within the nest, a generation of drones (males) and new queens are produced late each year.  These wasps leave the colony to mate.  With the arrival of freezing weather, all inhabitants within the nest, including the old queen, perish, as do the drones that departed to breed.  Only the new queens survive winter hibernation to propagate the next generation of wasps,  starting with the workers needed to construct a fresh nest and reestablish the colony.
Bald-faced Hornets Peering from Nest
Did you ever get the feeling you’re being watched?  Don’t go messing around with Bald-faced Hornet nests.  The occupants therein, like other social bees, wasps, and hornets, are equipped with stingers and venom for defending their colony.  This is an adaptation that has developed over time to assure the survival of populations of these insects.  Think about it this way, a solitary wasp that loses a nest loses only their individual brood of offspring.  There is minimal impact on the wider local population of such insects.  Conversely, a social wasp or hornet that loses a nest loses an entire colony, possibly negating the benefits of their cooperative behavior and threatening the survival of the species.  Insects that cooperate to build societies for survival can be more vulnerable to the catastrophic impacts of certain circumstances like disease, weather, and invasion of their colonies.  Therefore, natural selection has provided them with contingencies for these dangers, for example, the instinct to construct protective shelters and the adaptation of stingers and venom for defense against intruders and would-be predators.  Oh, and by the way, the Bald-faced Hornet can spray venom, often aiming for the eyes, so keep your distance.
European Hornets
European Hornets (Vespa crabro), an introduced species, are predatory on a variety of flying insects for protein.  For carbohydrates they are attracted to sweets like this lanternfly honeydew on Tree-of-heaven.
European Hornets constructing a nest in a tree cavity.
European Hornets constructing a paper nest in a tree cavity.

POTTER WASPS

A Potter Wasp (Eumenes species, probably E. fraturnus) hovering near a European Paper Wasp.
A potter wasp (Eumenes species), probably a Fraternal Potter Wasp (E. fraternus), hovering near a European Paper Wasp on Partridge Pea.  The female potter wasp builds a small mud nest resembling a tiny clay pot.  One of her eggs is inserted and left hanging on a thin thread.  Then a paralyzed caterpillar is deposited as a source of protein to nourish the larva upon hatching.  Lastly, the pot is sealed with a lid made of wet mud.  Upon maturing, the new generation of adult wasps perform a pottery breaking to emerge and take flight.

ANTS

Field Ants (Formica species, possibly Formica pallidefulva) clearing the entrance to their underground nest.
Field Ants (Formica species, possibly Formica pallidefulva) clear the entrance to their underground nest.  Field ants are eusocial insects, they work in concert to build, maintain, and defend the nest, rear young, and find food.  There is no social caste system.  Field Ants are predators and scavengers when collecting protein.  For carbohydrates they often rely on the honeydew produced by aphids.  As a method of improving and sustaining the production of honeydew, some ant species will tend colonies of aphids by moving the younger individuals from depleted portions of plants to more healthy tissue.  Field Ant nests contain chambers used for a variety of functions including raising young and storing food.  Some nests include multiple queens and some colonies consist of more than one nest.   Ants in the genus Formica are weaponized; they can spray formic acid to repel intruders and defend their colony.

We hope this brief but fascinating look at some of our more common bees, wasps, hornets, and ants has provided the reader with an appreciation for the complexity with which their food webs and ecology have developed over time.  It should be no great mystery why bees and other insects, particularly native species, are becoming scarce or absent in areas of the Lower Susquehanna River Watershed where the landscape is paved, hyper-cultivated, sprayed, mowed, and devoid of native vegetation, particularly nectar-producing plants.  Late-summer and autumn can be an especially difficult time for hymanopterans seeking the sources of proteins and carbohydrates needed to complete preparations for next year’s generations of these valuable insects.  An absence of these staples during this critical time of year quickly diminishes the diversity of species and begins to tear at the fabric of the food web.  This degradation of a regional ecosystem can have unforeseen impacts that become increasingly widespread and in many cases permanent.

A farmland desert.

A farmland desert.
How can anyone be surprised by the absence of bees and other pollinators in farmland? Manicured and cultivated ground offers little in the way of year-round shelter and food sources for insects and other wildlife.
A savanna-like habitat.
This savanna-like habitat on a south-facing slope provides the abundance of nectar-producing, pollen-rich wildflowers needed to nourish a diverse population of insects including bees, wasps, hornets, and ants.  Goldenrods, asters, and White Snakeroot are some of their late-season favorites.

Editor’s Note: No bees, wasp, hornets, or ants were harmed during this production.  Neither was the editor swarmed, attacked, or stung.  Remember, don’t panic, just observe.

SOURCES

Eaton, Eric R., and Kenn Kaufman.  2007.  Kaufman Field Guide to Insects of North America.  Houghton Mifflin Company.  New York, NY.

(If you’re interested in insects, get this book!)

Photo of the Day

An "Annual Cicada" (Neotibicen) dries its wings after emerging from its exuvia.
The Eastern Scissor Grinder (Neotibicen winnemanna), a species of “Annual Cicada” or “Dog-day Cicada”, dries its wings after emerging from its exoskeleton (exuvia).  After two to five years of subterranean life as a nymph, this adult will soon be ready to fly into the treetops in search of a mate.  There is a sense of urgency.  Summer’s end will bring its life to an end as well.

Be on the Lookout for Mississippi Kites

Common sense tells us that Brood X Periodical Cicada emergence begins in the southern part of the population zone, where the ground temperatures reach 64° first, then progresses to the north as the weather warms.  In the forested hills where the lower Piedmont falls away onto the flat landscape of the Atlantic Coastal Plain in Maryland’s Cecil and Harford Counties, the hum of seventeen-year-old insects saturates a listener’s ears from all directions—the climax nears.

Periodical Cicadas, mostly Magicicada  septendecim, are well into their breeding cycle along the Piedmont-Atlantic Coastal Plain border right now.  Love is in the air.

With all that food flying around, you just knew something unusual was going to show up to eat it.  It’s a buffet.  It’s a smorgasbord.  It’s free, it’s all-you-can-eat, and it seems, at least for the moment, like it’s going to last forever.  You know it’ll draw a crowd.

The Mississippi Kite (Ictinia mississippiensis), a trim long-winged bird of prey, is a Neotropical migrant, an insect-eating friend of the farmer, and, as the name “kite” suggests, a buoyant flier.  It experiences no winter—breeding in the southern United States from April to July, then heading to South America for the remainder of the year.  Its diet consists mostly of large flying insects including beetles, leafhoppers, grasshoppers, dragonflies, and, you guessed it, cicadas.  Mississippi Kites frequently hunt in groups—usually catching and devouring their food while on the wing.  Pairs nest in woodlands, swamps, and in urban areas with ample prey.  They are well known for harmlessly swooping at people who happen to get too close to their nest.

Mississippi Kites nest regularly as far north as southernmost Virginia.  For at least three decades now, non-breeding second-year birds known as immatures have been noted as wanderers in the Mid-Atlantic States, particularly in late May and early June.  They are seen annually at Cape May, New Jersey.  They are rare, but usually seen at least once every year, along the Piedmont-Atlantic Coastal Plain border in northern Delaware, northeastern Maryland, and/or southeastern Pennsylvania.  Then came the Brood X Periodical Cicadas of 2021.

During the last week of May and these first days of June, there have been dozens of sightings of cicada-eating Mississippi Kites in locations along the lower Piedmont slope in Harford and Cecil Counties in Maryland, at “Bucktoe Creek Preserve” in southern Chester County, Pennsylvania, and in and near Newark in New Castle County, Delaware.  They are being seen daily right on the lower Susquehanna watershed’s doorstep.

Today, we journeyed just south of Mason’s and Dixon’s Delaware-Maryland-Pennsylvania triangle to White Clay Creek State Park along Route 896 north of Newark, Delaware.  Once there, we took a short bicycle ride into a wooded neighborhood across the street in Maryland to search for the Mississippi Kites that have been reported there in recent days.

Periodical Cicadas filled the treetops and the airspace just above them.
It wasn’t long before Mississippi Kites appeared over the trees along a hilltop clearing to snatch up cicadas for a morning meal.
This kite glides on autopilot as it holds a captured cicada in its talons and tears it apart with its hook-shaped bill.
At least ten Mississippi Kites have been seen simultaneously at this site or in nearby Newark during recent days. This morning, we saw six.
All the Mississippi Kites we saw today were second-year birds.  The banded tail is characteristic of both hatch-year (juvenile) and second-year (immature) Mississippi Kites.  Of course, at this time of year, hatch-year birds are still in the nest and not flying around pigging out on Periodical Cicadas.
The banded tail, gray underside, and white head of a second-year Mississippi Kite.  Though known as immature or subadult birds during their second year, there are records of Mississippi Kites successfully breeding at this age.  Recent wanderings into the Mid-Atlantic States and New England have led to a spotty expansion of the nesting range there.
Mississippi Kites in their second year undergo molt of their flight feathers. The timing can vary greatly among individual birds with diet among the factors affecting the process.  This bird is just beginning the replacement of its juvenile remiges and rectrices.
Tail molt beginning on this second-year Mississippi Kite.  These banded juvenile tail feathers will be replaced by a set of all-dark adult rectrices.
A second-year Mississippi Kite with an all-dark adult tail feather (rectrix).  An abundance of protein-rich cicadas should provide ample nutrition to keep the molt process going for this maturing bird, at least for another couple of weeks.  Relocating inland on the Piedmont could keep this and other kites well-nourished for even longer.

Will groups of Mississippi Kites develop a taste for our seventeen-year cicadas and move north into the Lower Susquehanna River Watershed?  Ah, to be young and a nomad—that’s the life.  Wandering on a whim with one goal in mind—food.  It could very well be that now’s the time to be on the lookout for Mississippi Kites, especially where Brood X Periodical Cicadas are abundant.

Identification of the Three Species of Brood X Periodical Cicadas

The emergence of Brood X Periodical Cicadas is now in full swing.  If you visit a forested area, you may hear the distant drone of very large concentrations of one or more of the three species that make up the Brood X event.   The increasing volume of a chorus tends to attract exponentially greater numbers of male cicadas from within an expanding radius, causing a swarm to grow larger and louder—attracting more and more females to the breeding site.

Holes in the ground where emerging Brood X Periodical Cicadas have come to the surface.
The exuvia of Periodical Cicadas that, following emergence from the soil, have ascended the trunk of an Eastern White Pine.  The exuvia is the exoskeletal remains of the cicada’s final molt from a nymph into a flying adult.

Each Periodical Cicada species has a distinctive song.  This song concentrates males of the same species at breeding sites—then draws in an abundance of females of the same species to complete the mating process.  Large gatherings of Periodical Cicadas can include all three species, but a close look at swarms on State Game Lands 145 in Lebanon County and State Game Lands 46 (Middle Creek Wildlife Management Area) in Lancaster County during recent days found marked separation by two of the three.  Most swarms were dominated by Magicicada septendecim, the largest, most widespread, and most common species.  However, nearly mono-specific swarms of M. cassinii, the second most numerous species, were found as well.  An exceptionally large one was northwest of the village of Colebrook on State Game Lands 145.  It was isolated by a tenth of a mile or more from numerous large gatherings of M. septendecim cicadas in the vicinity.  These M. cassinii cicadas, with a chorus so loud that it outdistanced the songs made by the nearby swarms of M. septendecim, seized the opportunity to separate both audibly and physically from the more dominant species, thus providing better likelihood of maximizing their breeding success.

Some of the tens of thousands of M. cassinii Periodical Cicadas in a concentration on State Game Lands 145 northwest of Colebrook in Lebanon County, Pennsylvania.  This swarm occupied deciduous and evergreen trees on several acres of a south-facing hillside.  To provide protection from predators and assure the chance of finding a mate “in the crowd”, lesser numbers of this and the rarer species, Magicicada septendecula, would need to merge into the swarms of the abundant M. septendecim Periodical Cicadas to breed.

The process of identifying Periodical Cicadas is best begun by listening to their choruses, songs, and calls.  After all, the sounds of cicadas will lead one to the locations where they are most abundant.  The two most common species, M. septendecim and M. cassinii, produce a buzzy chorus that, when consisting of hundreds or thousands of cicadas “singing” in unison, creates a droning wail that can carry for a quarter of a mile or more.  It’s a surreal humming sound that may remind one of a space ship from a science fiction film.

Listen to the songs of individual cicadas at close range and you’ll hear a difference between the widespread M. septendecim “Pharaoh Periodical Cicada” and the other two species.  M. septendecim‘s song is often characterized as a drawn out version of the word “Pharaoh”, hence the species’ unofficial common name.  As part of their courtship ritual, “Pharaoh Periodical Cicadas” sometimes make a purring or cooing sound, which is often extended to sound like kee-ow, then sometimes revved up further to pha-raohM. cassinii, often known as “Cassin’s Periodical Cicada”, and the least common species, M. septendecula, often make scratchy clicking or rattling calls as a lead-in to their song.  Most observers will find little difficulty locating the widespread M. septendecim “Pharaoh Periodical Cicada” by sound, so listening for something different—the clicking call—is an easy way to zero in on the two less common species.

To penetrate the droning choruses of large numbers of “Pharaoh” and/or “Cassin’s Periodical Cicadas”, sparingly distributed M. septendecula cicadas have a noise-penetrating song consisting of a series of quick raspy notes with a staccato rhythm reminiscent of a pulsating lawn sprinkler.   It can often be differentiated by a listener even in the presence of a roaring chorus of one or both of the commoner species.  However, a word of caution is due.  To call in others of their kind, “Cassin’s Periodical Cicadas” can produce a courtship song similar to that of M. septendecula so that they too can penetrate the choruses of the enormous numbers of “Pharaoh Periodical Cicadas” that concentrate in many areas.  To play it safe, it’s best to have a good look at the cicadas you’re trying to identify.

M. cassinii Periodical Cicadas “singing” from a treetop at Colebrook, Lebanon County, Pennsylvania.  Clicking phrases are sure sign of the presence of this species and/or M. septendecula, the least likely of the three species to be encountered.  When in close proximity to a swarm, a listener will often notice the rising and falling volume of a chorus in a cycle that repeats every few seconds, an effect caused by cicadas attempting to synchronize their songs in a harmony with others in the group.  When courtship and mating is complete, female Periodical Cicadas will begin laying eggs in slits made in fresh new growth at the ends of branches on deciduous trees like the one seen here.

Visually identifying Brood X Periodical Cicadas to the species level is best done by looking for two key field marks—first, the presence or absence of orange between the eye and the root of the wings, and second, the presence or absence of orange bands on the underside of the abdomen.  Seeing these field marks clearly requires in-hand examination of the cicada in question.

Observing a perched Brood X Periodical Cicada can sometimes provide a view of the key field marks needed for identification of the species.  On the M. septendecim “Pharaoh Periodical Cicada” seen here, the orange patch between the eye and wing root and the orange bands on the underside of the abdomen are visible.
The abdomen of this perched M. cassinii “Cassin’s Periodical Cicada” appears, when viewed through the wings, to have orange bands.  But, examination in hand would show an all-black abdomen with glossy surfaces shining in the sunlight.  For accuracy, the up-close-and-personal look is necessary.
In the hand, cicadas can be better studied for key field marks.  M. septendecim (top) is larger than M. cassini (bottom) and M. septendecula, but the difference is not always apparent, particularly when a direct comparison cannot be made.

To reliably separate Brood X Periodical Cicadas by species, it is necessary to get a closeup view of the section of the thorax between the eye and the root (insertion) of the wings, plus a look at the underside of the abdomen.  Here’s what you’ll see…

Magicicada septendecim—“Pharaoh Periodical Cicada”

M. septendecim has an orange patch between the eye and the root of the wings.
The underside of M. septendecim’s abdomen has orange bands or stripes along the trailing edge of each segment. The width of the bands can vary, but is typically wider on males (left) than on females (right).

Magicicada cassinii—“Cassin’s Periodical Cicada”

The thorax of M. cassinii is black between the eye and the wing insertion.
The underside of M. cassinii’s abdomen is all black without orange bands or stripes in both the male (left) and female (right).

Magicicada septendecula

M. septendecula’s thorax is black between the eye and root of the wings.
The underside of M. septendecula’s abdomen has narrow orange bands or stripes along the trailing edge of each segment.  The width of the bands can differ.  Those of this male (left) are minimal and the bands on this female (right) are near the maximum for the species.

There you have it.  Get out and take a closer look at the Brood X Periodical Cicadas near you.

The abundant and widespread “Pharaoh Periodical Cicada” (M. septendecim).
It’ll all be over before long.  Accumulating remains of M. cassinii “Cassin’s Periodical Cicadas” beneath an Eastern White Pine at the site of the Colebrook State Game Lands swarm.

They’re Here

The Magi have arrived.   Emanating from the shadows of a nearby forest, you may hear the endless drone of what sounds like an extraterrestrial craft.  Then you get your first look at those beady red eyes set against a full suit of black armor—out of this world.  The Magicicada are here at last.

This exuvia, the leftover from a cicada’s final molt, tells us they are here.
A Brood X Periodical Cicada soon after emergence and final molt.
Not to worry, cicadas are harmless and docile when handled.  This is Magicicada septendecim, the largest and most common of our three species of Brood X seventeen-year cicadas.  They are currently emerging along south-facing borders of forests and wooded parks and lawns.
Magicicada septendecim can be recognized by the orange on the thorax behind each eye and in front of the wing insertions.  The smaller M. cassinii and M. septendecula have no orange coloration between the eye and wing.
Magicicada septendecim (seen here) has broad orange stripes on the abdomen.  M. cassinii has an all black abdomen and M. septendecula, the rarest species, has narrow well-defined orange stripes.

If you go out and about to observe Periodical Cicadas, keep an eye open for these species too…

Spotted Lanternflies, one of our most dreaded invasive species, have hatched.  These tiny nymphs about 5 millimetres in length were found feeding on a Virginia Creeper (Parthenocissus quinquefolia), a native vine in the grape family (Vitaceae).
Deer Ticks, also known as Black-legged Ticks, are hanging around on vegetation of all kinds looking to hitch a ride on a suitable host.  Don’t let it be you.  This adult female, less than 5 millimetres in length, was washed loose during an after-hike shower.

Seventeen Years Ago Today

Back in the spring of 2004, members of the Tri-County Conewago Creek Association (T.C.C.C.A.), a non-profit conservation group founded to improve water quality in Conewago Creek and its tributaries in Dauphin, Lancaster, and Lebanon Counties in Pennsylvania, were, in order to better understand the status of the flora and fauna in the watershed, frequently spending their weekends surveying the animal and plant life found in the drainage basin’s forests, streams, and farmlands.  This effort identified populations of several species of concern and helped supplement the more formal assessment that was used to determine the placement, scale, and scope of projects needed to reduce nutrient and erosion impairment in the Conewago’s waterways.

These regular outings happened to coincide with the Brood X Periodical Cicada emergence of 2004.  Back then, as the record keeper for the T.C.C.C.A.’s weekly survey forays, your editor decided to shade a map of the Conewago Creek Watershed showing where the group’s volunteers encountered choruses of the Brood X cicadas.  Fortunately, the map is still in the editor’s pile of stuff, and is reproduced here for you.

T.C.C.C.A.’s brochure map of the Conewago Creek Watershed (the Conewago east of the Susquehanna River), shaded with red ink in 2004 indicating locations where noisy choruses of Brood X Periodical Cicadas were found.  The range of the insects closely mirrors the forested areas of the watershed.  The nearly contiguous range along the southeast border includes the heavily wooded areas of Mount Gretna, State Game Lands 145, and the northwest slope of the diabase ridge that separates the Conewago from neighboring watersheds in Lancaster County.

A notation on the map (visible just above the cap on the pen) indicates May 16 as the emergence date for the cicadas in 2004—seventeen years ago today.

So why no seventeen-year cicadas yet in 2021?  The answer is ground temperature.  This year, by mid-April, Brood X Periodical Cicadas were just below the leaves and rocks, ready to break the surface.  But a cold month since then has stalled their emergence.  A thermometer pushed into the forest soil today showed readings of 60 degrees and less—at least four degrees below the temperature needed to get the nymphs crawling out of the dirt to climb rocks and vegetation where they’ll molt, dry, and take flight.

In the forested hills east of Conewago Falls, in the Conewago Creek Watershed, soil temperatures were as low as 54 degrees Fahrenheit today.

A warm week ahead with daytime temperatures in the eighties and nighttime lows in the fifties and sixties, instead of in the forties, should get the woodland soils warming.  Brood X Periodical Cicadas will be out and about in a jiffy—and you’ll hear all about it.

Coming up, The Great Eastern Brood.

Coming Soon, Very Soon: Brood X Periodical Cicadas

Yesterday, a hike through a peaceful ridgetop woods in the Furnace Hills of southern Lebanon County resulted in an interesting discovery.  It was extraordinarily quiet for a mid-April afternoon.  Bird life was sparse—just a pair of nesting White-breasted Nuthatches and a drumming Hairy Woodpecker.  A few deer scurried down the hillside.  There was little else to see or hear.  But if one were to have a look below the forest floor, they’d find out where the action is.

Not much action in the deer-browsed understory of this stand of hardwoods.
Upon discovery beneath a rock, this invertebrate quickly backed its way down the burrow, promptly seeking shelter in the underground section of the excavation.
A closeup of the same image reveals the red eyes of this Periodical Cicada (Magicicada species) nymph.  It has reached the end of seventeen years of slowly feeding upon the sap from a tree root to nourish its five instars (stages) of larval development.

2021 is an emergence year for Brood X, the “Great Eastern Brood”—the largest of the 15 surviving broods of Periodical Cicadas.  After seventeen years as subterranean larvae, the nymphs are presently positioned just below ground level, and they’re ready to see sunlight.  After tunneling upward from the deciduous tree roots from which they fed on small amounts of sap since 2004, they’re awaiting a steady ground temperature of about 64 degrees Fahrenheit before surfacing to climb a tree, shrub, or other object and undergo one last molt into an imago—a flying adult.

Here, approximately one dozen Periodical Cicada nymphs have tunneled into pre-emergence positions beneath a rock.  Seventeen-year Periodical Cicadas, sometimes mistakenly called “seventeen-year locusts”, are the longest-lived of our insects.
Note the wings and red eyes beneath the exoskeleton of this Periodical Cicada nymph. Within weeks it will join billions of others in a brief emergence to molt, dry, fly, mate, and die.
Adult (imago) Periodical Cicadas.  Brood X includes all three species of seventeen-year Periodical Cicadas: Magicicada septendecim, M. cassinii, and M. septendecula.  All Periodical Cicadas in the United States are found east of the Great Plains, the lack of trees there prohibiting the expansion of their range further west.  Seventeen-year life cycles account for twelve of the fifteen broods of Periodical Cicadas; the balance live for thirteen years.  The range of Brood X includes the lower Susquehanna basin and parts of Delaware, Georgia, Illinois, Indiana, Kentucky, Maryland, Michigan, New Jersey, Ohio, Tennessee, Virginia, West Virginia, and the District of Columbia.  (United States Department of Agriculture/Agricultural Research Service image)
The flight of Periodical Cicadas peaks in late-May and June.  Shown here is the Eastern Scissor Grinder, an “Annual Cicada” that emerges later in the season, peaking yearly during July and August.

The woodlots of the Lower Susquehanna River Watershed won’t be quiet for long.  Loud choruses of male Periodical Cicadas will soon roar through forest and verdant suburbia.  They’re looking for love, and they’re gonna die trying to find it.  And dozens and dozens of animal species will take advantage of the swarms to feed themselves and their young.  Yep, the woods are gonna be a lively place real soon.

Did you say Periodical Cicadas?  We can hardly wait!

The Dungeon

There’s something frightening going on down there.  In the sand, beneath the plants on the shoreline, there’s a pile of soil next to a hole it’s been digging.  Now, it’s dragging something toward the tunnel it made.  What does it have?  Is that alive?

We know how the system works, the food chain that is.  The small stuff is eaten by the progressively bigger things, and there are fewer of the latter than there are of the former, thus the whole network keeps operating long-term.  Some things chew plants, others devour animals whole or in part, and then there are those, like us, that do both.  In the natural ecosystem, predators keep the numerous little critters from getting out of control and decimating certain other plant or animal populations and wrecking the whole business.  When man brings an invasive and potentially destructive species to a new area, occasionally we’re fortunate enough to have a native species adapt and begin to keep the invader under control by eating it.  It maintains the balance.  It’s easy enough to understand.

Japanese Beetles (Popillia japonica) seen here on Halberd-leaved Rose Mallow.  Without predation, exploding numbers of this invasive non-indigenous insect can defoliate and kill numerous species of plants in a given area.
The Song Sparrow (Melospiza melodia) is a generalist feeder, eating seeds and invertebrates including Japanese Beetles.  This species is the omnipresent year-round occupant of shoreline vegetation along the lower Susquehanna River.

Late summer days are marked by a change in the sounds coming from the forests surrounding the falls.  For birds, breeding season is ending, so the males cease their chorus of songs and insects take over the musical duties.  The buzzing calls of male “Annual Cicadas” (Neotibicen species) are the most familiar.  The female “Annual Cicada” lays her eggs in the twigs of trees.  After hatching, the nymphs drop to the ground and burrow into the soil to live and feed along tree roots for the next two to five years.  A dry exoskeleton clinging to a tree trunk is evidence that a nymph has emerged from its subterranean haunts and flown away as an adult to breed and soon thereafter die.  Flights of adult “Annual Cicadas” occur every year, but never come anywhere close to reaching the enormous numbers of “Periodical Cicadas” (Magicicada species).  The three species of “Periodical Cicadas” synchronize their life cycles throughout their combined regional populations to create broods that emerge as spectacular flights once every 13 or 17 years.

An “Annual Cicada” also known as a “Dog-day Cicada”, clings to the stem of a Halberd-leaved Rose Mallow at Conewago Falls.

For the adult cicada, there is danger, and that danger resembles an enormous bee.  It’s an Eastern Cicada Killer (Specius speciosus) wasp, and it will latch onto a cicada and begin stinging while both are in flight.  The stings soon paralyze the screeching, panicked cicada.  The Cicada Killer then begins the task of airlifting and/or dragging its victim to the lair it has prepared.  The cicada is placed in one of more than a dozen cells in the tunnel complex where it will serve as food for the wasp’s larvae.  The wasp lays an egg on the cicada, then leaves and pushes the hole closed.  The egg hatches in a several days and the larval grub is on its own to feast upon the hapless cicada.

An Eastern Cicada Killer (Sphecius speciosus) along the river shoreline. Despite their intimidating appearance, they do not sting humans and can be quite docile when approached.

Other species in the Solitary Wasp family (Sphecidae) have similar life cycles using specific prey which they incapacitate to serve as sustenance for their larvae.

A Solitary Wasp, one of the Thread-waisted Wasps (Ammophila species), drags a paralyzed moth caterpillar to its breeding dungeon in the sandy soil at Conewago Falls.  For the victim, there is no escape from the crypt.

The Solitary Wasps are an important control on the populations of their respective prey.  Additionally, the wasp’s bizarre life cycle ensures a greater survival rate for its own offspring by providing sufficient food for each of its progeny before the egg beginning its life is ever put in place.  It’s complete family planning.

The cicadas reproduce quickly and, as a species, seem to endure the assault by Cicada Killers, birds, and other predators.  The Periodical Cicadas (Magicicada), with adult flights occurring as a massive swarm of an entire population every thirteen or seventeen years, survive as species by providing predators with so ample a supply of food that most of the adults go unmolested to complete reproduction.  Stay tuned, 2021 is due to be the next Periodical Cicada year in the vicinity of Conewago Falls.

SOURCES

Eaton, Eric R., and Kenn Kaufman.  2007.  Kaufman Field Guide to Insects of North America.  Houghton Mifflin Company.  New York.