RAPTORS IN THE CITY

One of the surprises in studies of urban wildlife in recent years is the invasion of our cities and suburbs by predatory birds such as hawks and owls. Perhaps "invasion" is too active a word, and a better word is "acceptance." More and more raptors are apparently becoming comfortable with living in the cities of the Pacific Northwest and, in fact, all across North America.

Bird feeders have become a dependable part of the urban/suburban environment, and many small birds are attracted to them. The juncos and finches and sparrows that abound at feeders attract Sharp-shinned Hawks in winter, but the hawks leave for the mountains in spring. However, their larger relatives Cooper's Hawks are year-round residents, feeding on pigeons, jays, and flickers and nesting in wooded areas that give them a sense of security. The males are conspicuous in spring, with display flights and vocalizations, so more and more of them are being detected living among us.

Merlins too are in the process of becoming city dwellers. These small falcons nest in forests near open country, where they usually capture their prey (small birds). Wintering Merlins probably moved into cities to take advantage of local concentrations of small birds, and eventually pairs remained throughout the year and nested because of that prey abundance. Their nesting efforts have been successful, and the population of urban-nesting Merlins has slowly risen.

Barred Owls have moved into the Pacific Northwest from the north, and they too appear to be comfortable in wooded parts of our cities. Preferred prey include the gray squirrels and rats that have been introduced into the region, and our bird feeders attract and concentrate these mammals as well. There are now pairs of Barred Owls, Cooper's Hawks, and Merlins nesting in wooded areas near my house in Seattle that weren't there 10 years ago.

Red-tailed Hawks do not live around dense housing developments, but large parks and open spaces furnish adequate hunting grounds for rats and squirrels, and if any trees in their territory are large enough to support their nests, they may nest in our cities. Many more of them appear in winter to hunt in open areas around parks and airports.

The Great Horned Owl is a top predator surprisingly willing to live in cities, mostly in relatively large parks. It is large enough and fierce enough to handle mid-sized mammals such as raccoons, opossums, and domestic cats that thrive in cities. Crows and pigeons furnish abundant prey populations as well. Nest sites (usually old Red-tailed Hawk nests) may be limiting, however.

Even more surprisingly, after a long period of decline during the DDT era, Bald Eagle populations have rebounded in the Northwest, and they not only visit but even nest in the cities, often in large parks near water where prey species such as waterfowl and fish are available. They need large trees for their huge stick nests.

Whenever a shift like this occurs, it is worth trying to distinguish between behavioral adaptation and genetic adaptation. Have these birds "learned" that cities are OK? Or are there genes for city living that have become favored? Are there genes for increased tameness, recognition of bird feeders as sources of bird concentrations, resistance to being mobbed by crows? Actually, cities aren't bad places to live for mobile predators such as these, as there may be local sources of abundant food and some of their own potential predators may be absent. Also, the first individuals to accept life in the cities have no competition from others of their species!

Dennis Paulson

BLACK-TAILED GULL IN COMMENCEMENT BAY

In the fall of 2009, a Black-tailed Gull (Larus crassirostris) showed up roosting on a log boom on the east side of Commencement Bay, near Tacoma. It was found on October 13 by Charlie Wright and remained for about a month, seen almost daily until November 7. I remember that date well, as it was seen that morning. That afternoon, Netta Smith and I were finally able to accompany Shep Thorp in his boat, the best way to see the gull, but we were unable to find it. It had presumably headed south with the large numbers of California Gulls that had been present until that time.

In the fall of 2011, presumably the same bird showed up at the same spot. First seen by Shep on September 14, it was still present as of November 4 but may have departed soon after that. During both of its visits, this bird was seen by many enthusiastic observers, mostly at a distance of several hundred yards, spotting-scope range. By far the best way to see it was to go out in a small boat and circle the big log boom on which it roosted daily with hundreds of other gulls.

On November 4, Netta and I brought our kayak down from Seattle and launched it from the Gilmur access point on the bay. Very quickly we found the Black-tailed Gull and captured a few mediocre photos. Then something spooked them, and a bunch of the gulls took off. We saw our bird head across the bay and disappear in the distance, very disappointing. But we weren't discouraged, as the day, although threatening rain, had turned beautiful, with the low afternoon sun illuminating the maple-covered hillside in front of us.

We maneuvered the kayak around the log boom and found a place to enter it, giving us better light for photography. The boom was covered with gulls over much of its length, with photo ops abounding. Double-crested Cormorants roosting on it didn't like us at all, and they took off when we were a hundred yards away. Harbor Seals watched us but stayed put until, in a few cases, we got too close for their comfort level. The gulls just mostly sat and watched us paddle or drift past as close as 30 feet from them. They are surely used to curious kayakers by this time.

The most abundant gulls on the boom were Bonaparte's and Mew, at least several hundred of each. Among them were dozens of California and a few Thayer's and Glaucous-winged. We scrutinized the flock carefully and were able to find no other species. While slowly moving around the boom, we found to our delight that the Black-tailed had returned. We were able to get photo after photo of it as it watched us; it often rested with eyes closed, comfortably napping. When we got a little too close several times, it hopped onto another log, giving us the opportunity to photograph it with a different species.

Among the hundreds of gulls, the lack of immatures was noteworthy. There were no immature Bonaparte's and only a few immature Mew and California, a far lower proportion than would have been in their populations. Obviously immature gulls were not using Commencement Bay, or perhaps they weren't roosting. Do they have a harder time finding enough food and therefore have to continue foraging for a longer time? That makes sense, and the timing of mature vs. immature gulls at roost sites would be an interesting research project.

Another point of interest was the variation in leg color in the adult gulls. We noted such variation in Bonaparte's, Mew, California, and Thayer's, usually from duller to brighter. Bonaparte's varied from pale pink to red-orange, California from yellow-green to blue-gray. Thayer's are supposed to have rather bright red-pink legs, but one adult had very pale whitish-pink legs.

In any case, my luck had changed; it turned out that this was probably the last time the gull was seen!

Dennis Paulson

ODONATE OVIPOSITION

Egg laying is a very important part of the life of an insect, as the number and placement of the eggs influences where the larvae that hatch from them will live and how many of its own species it will have to compete with. The presence of other animals that are potential predators on the eggs must also be taken into consideration. Oviposition occurs in two quite different fashions in the dragonflies and damselflies, order Odonata.

Exophytic egg-layers extrude fertilized eggs, often in a clump, through the genital opening in their eighth abdominal segment. The female flies over the water, stopping at intervals to descend to the surface and tap the abdomen in the water, releasing the cluster of eggs. This mode is characteristic of most dragonfly families, for example skimmers (Libellulidae), emeralds (Corduliidae), and clubtails (Gomphidae).

There are several variations on this theme. Numerous species splash eggs onto the adjacent bank in drops of water, perhaps to make the eggs safer from aquatic predators. The larva will find its way to the water upon hatching. Some members of the skimmer family drop single eggs one at a time onto dry land in basins that fill up with winter rains. Their larvae develop during the spring and emerge as adults in midsummer, then hanging around as the pond dries up to lay eggs in the pond basin after it dries up in the heat of late summer.

Others actually deposit their egg masses on leaves and stems above the water, and the larvae drop into the water when the eggs hatch.

Dragonflies of the darner family (Aeshnidae) and all damselflies are endoophytic egg layers, utilizing a quite different oviposition strategy. These odonates have well-developed ovipositors at the end of the abdomen, and they insert eggs singly or in pairs into plant tissues. These eggs are much better protected against predation than the exophytically laid eggs, placed precisely rather than scattered, and fewer of them are laid.

Endophytic ovipositors typically have a clutch size (the number of eggs matured in one batch) of one to two hundred eggs and typically lay only a few clutches. However, long-lived females may lay more clutches, eventually totaling in the low thousands of eggs in their lifetime. Exophytic ovipositors lay smaller eggs more quickly (up to 300/minute in some species), and their clutch sizes are larger, in the thousands, but with lifetime totals perhaps no higher than the longer-lived endophytic species.

Oviposition sites are presumably chosen as good larval habitats, and several egg-laying females will often collect at the same spot, presumably attracted by the ones already there.

Because female dragonflies are a scarce resource at the water, males will always try to mate with them, and in many species, the male stays hooked up to the female with which he has mated through the oviposition process to keep other males away from her. Thus both exophytic and endophytic ovipositors may be seen doing so in tandem.

Dennis Paulson

A HALLOWEEN TREAT

A spooky Halloween story or chilling thriller film is incomplete without the appropriate array of creepy nighttime animal sounds. Unfortunately, many an evening stroll has been transformed into a terrifying, heart-pounding experience thanks to these bloodcurdling calls. In fact, we can encounter a variety of these sounds right here in the Pacific Northwest! And because we only fear what we don't understand, here is a brief guide to the spookiest of our local animal sounds to help you learn more about these relatively harmless creatures.

Barred Owl - Strix varia   L: 21"
Common, year-round resident of the Puget Sound region. Often found in mixed coniferous-deciduous forests and seen during daytime hours near roosts. Calls include very loud hooting/barking, often described as monkey-like sounds. Individuals may also hiss or cackle.

Listen

Boreal Owl - Aegolius funereus   L: 10"
Uncommonly seen inhabitant of montane forests in Eastern Washington. Found in mixed coniferous-deciduous northern forests. Call is a series of low, piping hoots that rise and fall in pitch and intensity. Also gives a low, nasal hooAh as well as short screeches.

Listen

Great Horned Owl - Bubo virginianus   L: 22"
Fairly common and widespread, inhabiting a variety of habitats including forests, deserts, tundra, and urban areas. Often seen perched at dusk or mobbed by small birds in the daytime. Call is an iconic series of rhythmic hoots associated with most midwinter forest settings.

Listen

Western Screech-owl - Megascops kennicottii   L: 8.5"
Common in wooded to sparsely wooded areas including urban parks, native woodland, and deserts. Generally roosts in very dense, dark areas and is difficult to see in the daytime. Call is a series of accelerating, abrupt whistled hoots that ends slightly lower in pitch.

Listen
(Can you hear the coyote in the background?)

Barn Owl - Tyto alba   L: 16"
Extremely widespread species common to Western Washington. Prefers open grassland habitat and roosts in cavities or human-made structures. Populations may be in decline. These birds do not "hoot" like other owls. Calls generally only a shrieking screech. Very commonly thought to be a frightening, ghostly critter, but its silent flight and phenomenal hearing make it one of nature's best mouse-exterminators.

Listen

Northern Pygmy-owl - Glaucidium gnoma   L: 6.75"
Widespread in coniferous forests throughout Washington. Some may migrate to lower elevations in winter months. Call is a regular, repeating series of tooting hoots. Listen for these distinctive calls at dawn and dusk.

Listen

Coyote - Canis latrans   L: 45"   H: 24"

Common throughout a variety of habitats, especially open areas and clearings. They have adapted well to the presence of humans and have expanded their ranges since the disappearance of the Gray Wolf. Sounds include yips, yaps, whines, barks and bone-chilling howls.

Listen (yips, yaps, barks, howls)
Listen ("moonlight howl")

 
Red Fox - Vulpes vulpes   L: 40"   H: 15"
Prefers brushy open habitats throughout Washington, but generally avoids densely forested areas and higher elevations. Varies in color from black to gray-brown. Sounds include barks, whines, wails and a fairly frightening scream (see video below).
 
Listen
 








-Robert Niese
Education and Outreach Coordinator

WOULD YOU BELIEVE A MILLION MEADOWHAWKS?

Yes, I said a million. Or perhaps 10 million or 100 million. Netta Smith and I visited Harney County in south-central Oregon on 24-26 September 2011 to look for birds, which as usual were in great numbers. But we were struck even more by the numbers of odonates. Rather than diversity, we found abundance. Two species were there in prodigious numbers like I have never seen before.

Striped Meadowhawks (Sympetrum pallipes) were the most abundant and ubiquitous. Our first stop near water was at a big pond on the east side of Hines. As soon as we stopped, we saw there were Sympetrum everywhere. On our first afternoon, the temperature reached 92° F, what I would call very hot. We stopped several times along highway 205 south of Burns and saw that the barbed-wire fences were covered with meadowhawks. They clearly chose to perch on the barbs rather than the wire between them, and in some places there was a dragonfly on just about every barb.

We stopped at Wrights Point, a long rocky ridge that extends out into the Blitzen River basin, and were flabbergasted at the numbers of Striped Meadowhawks there, flushing from the road and shrubs and dead tree branches. In addition, there were hundreds of Spotted Spreadwings (Lestes congener) in the shrubbery, only visible at closer range, although occasionally one would just fly across in front of me, perhaps flushed by one of the meadowhawks we were scaring up.

We got back into Burns at about 6:30 pm, and I immediately noticed dragonflies going past, a real flight. In all directions there were meadowhawks heading just a little east of south, right into the face of a moderate breeze. We estimated at least 10/minute passing in front of us, and we walked 50 yards to the grass behind the station and saw the same numbers. If they were flying over a broad front, there were hundreds/minute.

The sky was clouding up, and the flight fell off after about 15 minutes. At 6:45, there were still a few dragonflies passing, and there were many perched in the bushes. The flight seemed exactly like a migratory flight, yet the species is not known to be migratory, and I presume this was a local flight, perhaps individuals dispersing to find new breeding areas. I wondered if the high density of individuals would lead to such a flight.

The second day dawned cool, cloudy, and windy, and odonate activity fell dramatically. Nevertheless, the high temperature reached about 60° F., and we still saw meadowhawks and spreadwings wherever we stopped. It was warm enough that they were well able to fly as we flushed them, and many of them were perched in the same situations as on the preceding and following sunny day. The third day dawned clear and cold, but it warmed up rapidly to a high in the low 70s before we left the area to head back to Seattle.

On all three days, we stopped at additional oases of trees and shrubs in the midst of the vast prairie, shrub-steppe and wetland habitats, and every one of them was full of both Sympetrum and Lestes. As we walked along dirt paths, the meadowhawks rose one after another and fluttered off. We could look up a path and see them all over the sunlit ground. A diversion into the edge of any patch of woodland would reveal spreadwings all over the branches and twigs.

In several areas both species were perched on rock walls and sidewalks, the Lestes alongside the Sympetrum. As we flushed them, many of them ended up landing again near another, which in turn would flush, a chain reaction of fluttering. All the odonates were sexually mature; I never saw one that I could call immature.

Perhaps the third day was the most surprising. As we drove along a road through open fields just east of Burns at 11:30 am, temperature around 70° F, we started seeing Sympetrum flying across the road as we had on the evening of the first day. But they were in copulating pairs, not individuals! They were moving in the same direction as before, just east of south but still into a light breeze. I speculated that the wind direction was setting the flight direction, but who knows? This flight lasted the half hour that we were in that area and extended across at least a mile of road. Clearly thousands of individuals were participating.

As we drove into Burns at about noon, the flight was still going, patchy because of large buildings and areas of dense trees, but whenever we were in the open, there they were, crossing busy highways, all in exactly the same direction. Perhaps 10% of the individuals were single, but all the rest were in the wheel position. It was a fantastic sight. We saw no evidence of oviposition anywhere, nor did we see any sign of breeding in the spreadwings, yet I have no doubt that it took place somewhere.

We had to leave and started west on highway 20 toward Bend. There were still pairs going across the road up to about 10 miles west of Burns, then we saw no more but a few singles. We stopped in a rest area 16 miles west of Burns, and there were Striped Meadowhawks and Spotted Spreadwings all over the open grass, perched on the ground and in shrubs. Still the same species in abundance, but there was no mating, no flight. We stopped again at Hampton Station, much farther west, and again saw a few meadowhawks, but nothing in the air.

These observations were of the greatest interest to me in several ways. (1) I have never seen so many individuals of an odonate species spread over so much landscape. Underestimating all the time, I decided there was a minimum of 100 individuals/acre, and I think it was more like 1000/acre in many places. I thought the dragonflies were distributed over an area at least 50 x 30 miles, or 150 square miles. 150 square miles = 96,000 acres. At 100/acre, there were 9.6 million meadowhawks. Or perhaps there were 10x that many.

(2) Where did they all come from? Both species oviposit over dry land, then the basin fills with water during the winter rains, and the eggs hatch that spring, the larvae develop over the summer, and the adults are present in fall. So these individuals came from whatever wetlands filled during the winter of 2010-2011 and contained their eggs. 2011 has been an especially wet year, on the other hand, with Malheur Lake filling a huge area, so the eggs that were there produced a lot of larvae, thus the numbers of adults we saw.

But just a year ago, in spring 2010, there was almost no water in Malheur Lake, and the whole basin was dry, dry, dry. That would have provided much habitat for widespread oviposition of meadowhawks and spreadwings. But if it was dry, where did those adults come from? The puzzling aspect of this is that eggs had to be there in the first place from some previous successful year, and 2010 should have been a poor one for these species, with little water and thus few eggs hatching and relatively few adults. Is it possible that the eggs of these species (and of course other odonates) can lie dormant for multiple years?

(3) The meadowhawks were active in the sun at shockingly low temperatures on the third day. I saw several in flight when our car thermometer (known to be accurate within a degree or two) read 39° and 42° F at two stops. I have no idea how much their body temperature could have been raised by basking, but I almost never see odonates when it is colder than 55° F.

(4) We were really surprised to see no other species at all, except for the very occasional Blue-eyed Darner (Rhionaeschna multicolor); about a half dozen were seen over the three days, usually foraging in the lee of a tree grove. We checked several ponds and found nothing at all flying at them. How could one see a million odonates and see only three species?

As is so often the case in nature, observations generate more questions than answers.

Dennis Paulson

MIGRATORY MONARCHS

The Monarch (Danaus plexippus) is surely the best known of North American butterflies. Occurring all across the continent, as well as on several other continents, this big orange butterfly with a vivid black-lined pattern delights all who see it. Like the swallowtails, it is the epitome of butterflyhood, bouncing across meadows and sipping nectar from a wide variety of flowers.

At this time of year, Monarchs all across North America head south for the winter. The vast majority acome from the eastern two-thirds of the continent. They fly south in trickles, then streams, then rivers converging on just a few areas in the mountains of central Mexico, wintering grounds not discovered by scientists until 1975. Many fewer (about 5% of the total population) head for the Pacific coast to winter in a few coastal groves in California.

Although many insects are migratory, this one is the most noteworthy in the US because of its large size, bright coloration, and great numbers of individuals on the move at once.

If you live near milkweed plants (Asclepias species), you may be very familiar with Monarchs. The beautiful flowers of milkweeds give no hint of their toxic nature. The plants have a milky sap full of cardiac glycosides, chemicals that affect the sodium-potassium pump in vertebrate cell membranes and can cause tachycardia and ventricular fibrillation, both very stressful to the human heart. The sap is also viscous and bitter tasting and caustic to our mucous membranes.

Monarchs breed on milkweeds, and their caterpillars are among the small number of insects that have evolved a resistance to the harmful effects of milkweed sap. They munch it with no worries throughout their development. The sap confers unpalatability and distastefulness on the larvae, and their bright aposematic coloration serves as a warning flag to potential predators.

The poisonous qualities of the milkweed are carried through metamorphosis, and the butterflies are also distasteful, unpalatable, and probably warningly colored. They are left alone by vertebrate predators, although invertebrates such as dragonflies can handle them.

Monarchs are large and conspicuous, not especially fast flying, and if they weren't distasteful they would probably be the object of much predation during their migrations and certainly on their communal roosts. In fact, they probably roost communally to concentrate the warning to predators that they are not to be touched.

Monarchs are nowhere nearly as common in the West as in the East, and in Washington state they are downright uncommon. It's always thrilling to see an adult or larval Monarch in the Columbia Basin, where they are associated with the big milkweed Asclepias speciosa. Presumably our Monarchs head south to the California roosts.

After overwintering, Monarchs take off for the North. They move back into southern US and breed where they stop. Their larvae develop quickly in the spring and, as soon as they are out of the pupa, the adults head north like the previous generation. They are one-way migrants, and they will stop somewhere in the northern US or even southern Canada to breed. There may be as many as three northbound migrant generations, before their offspring head off in the other direction, back to the wintering ground.

Dennis Paulson

TIGERS OF THE SAND

Go to a sandy beach or an open patch of sandy soil just about anywhere in the summer and you are likely to see tiger beetles. You will at first see these diurnal insects running ahead of you. Their long, slender legs propel them over the ground at amazing speeds. If you get too close, they jump into the air, open their elytra (wing covers), and quickly fly away. They usually land nearby, and you may be able to follow individual beetles until one lets you get close enough for prolonged observation.

But look quickly, as they are likely to run and stop, run and stop as they hunt for prey. They have exceptionally long, sharply pointed, tooth-lined mandibles, with which they capture other insects and spiders. They make short work of their prey and move on to hunt again. Their vision is superb, both to find prey and avoid predators.

Even though they are alert and fast, they do have predators, including birds, lizards, and robber flies. Birds such as kestrels and flycatchers capture them in the air, shrikes on the ground. As well as their obvious adaptations, some tiger beetles secrete defensive chemicals that presumably protect them from some predators.

The cuticle of tiger beetles is somewhat iridescent, and although the majority of species are sort of a bronzy brown, many of them are brightly colored, usually green but sometimes purple or blue. Some species are polymorphic, coming in two or more of these colors. The undersides are often more metallic than the upper surfaces. Some species have red abdomens that show up when they fly. Most tiger beetles have a characteristic pattern of spots and lines on their elytra, and variations on that pattern are often what define different species.

Unlike many insects, when tiger beetles mate they both face the same way, so they can continue to run across the ground (but not to fly) when the male is perched on the female's back. This lessens the likelihood of predation when they are in this vulnerable state. A male may remain on the female's back after copulation to keep other males from mating with her. Females lay their eggs, one at a time, into the soil in places appropriate for the larva.

Tiger beetle larvae are just as predacious as the adults, but we don't see them at work. They live in burrows in the sand, covered except for a hard head capsule and a pair of mandibles. When another insect comes too close, they reach up from the surface and grab it, then pull it down into their burrow, to which they are anchored by hooks on top of the fifth abdominal segment. They have been known to capture dragonflies of much larger size that had the bad luck to land right at the mouth of a burrow.

There are 17 species of tiger beetles known from Washington state, all in the day-active, brightly colored genus Cicindela except for two nocturnal black species of Omus. Few of the species are statewide; most have limited ranges on one side of the Cascades, up in the mountains, or along the coast or big rivers.

Fortunately for aficionados of this group, there are two fine books available:

A Field Guide to the Tiger Beetles of the United States and Canada, by David L. Pearson, C. Barry Knisley, and Charles J. Kazilek, Oxford University Press, 2006.

Tiger Beetles: The Evolution, Ecology, and Diversity of the Cicindelids, by David L. Pearson and Alfried P. Vogler, Cornell University Press, 2001.

Dennis Paulson