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Wilson’s Phalarope
The Wilson’s Phalarope breeds over a large area of the western U.S. and Canada, and after the breeding season the adults gather in huge flocks to molt before migrating to South America for the winter. The Wilson’s Phalarope’s migration take place at night, and if birds have sufficient fat they can fly from California to Ecuador nonstop.
Wilson’s Phalaropes are very social year-round, and do not establish nesting territories. Surprisingly, there are several records of nest parasitism by Brown-headed Cowbirds. Such cowbird eggs are doomed to failure because young shorebirds leave the nest very rapidly and forage for their own food, something cowbird young can not do.
Description of the Wilson’s Phalarope
BREEDING MALE
The Wilson’s Phalarope is a small shorebird with a long, needle-like bill. It is slender, with an upright posture. The plumage varies considerably by gender and season.
Color pattern is reversed from trypical. Females being brightly colored and males much more subdued. Breeding males have a white throat, pale reddish hind neck, white underparts, grayish upperparts, and black legs. They resemble the female shonw below but less strongly marked. Length: 9 in. Wingspan: 17 in.
Female
Breeding females are boldly marked, with a wide black stripe running through the eyes and down the sides of the neck, a white throat, reddish neck, grayish upperparts with black and reddish stripes, and black legs.
Seasonal change in appearance
Winter birds are pale grayish above and white below, with yellow legs.
Juvenile
Juveniles are similar to winter adults, but have darker brown upperparts and a brown cap.
Habitat
Wilson’s Phalaropes inhabit shallow lakes and marshes, as well as water treatment ponds.
Diet
Aquatic insects and crustaceans.
Behavior
Wilson’s Phalaropes forage by swimming, often spinning rapidly in a circle to stir up prey. They also probe in mud or pick along shorelines.
Range
Wilson’s Phalaropes breed in western Canada and the northern U.S. They winter primarily in South America, with a few wintering in southern California and southern Texas. They can be seen in migration across much of the U.S., though they are more common in the west. The population appears to be declining.
More information:
Bent Life History
Visit the Bent Life History for extensive additional information on the Wilson’s Phalarope.
Wing Shape
The shape of a bird’s wing is often an indication of its habits and behavior. Fast flying birds have long, pointed wings. Soaring birds have long, broad wings. Different songbirds will have a slightly different wing shape. Some species look so much alike (Empidonax flycatchers) that scientists sometimes use the length of specific feathers to confirm a species’ identification.
Wing images from the University of Puget Sound, Slater Museum of Natural History
Fun Facts
Male Wilson’s Phalaropes incubate the eggs and care for the young, and females may mate with more than one male.
The Wilson’s Phalarope is the only phalarope that breeds in the lower 48 states.
Unlike most other shorebirds, phalaropes have lobed toes.
Vocalizations
The flight call is a grunt or moan.
Similar Species
- Wilson’s Phalaropes are more erratic and active in foraging than yellowlegs or Stilt Sandpipers.
- Red Phalarope
Red Phalaropes have shorter, thicker bills. Breeding plumaged Red Phalaropes can not be confused with other species. Primarily winters at sea. - Red-necked Phalarope
Red-necked Phalaropes have more patterened back in breeding plumage, wide, dark line through and behind the eye in non-breeding plumage.
Nesting
The nest is a depression lined with grass, and is placed near water.
Number: 4.
Color: Buffy in color with darker markings.
Incubation and fledging:
The young hatch at about 18-27 days, and leave the nest shortly after hatching, though associating with the adult male for some time.
Bent Life History of the Wilson’s Phalarope
STEGANOPUS TRICOLOR VielliotHABITS
Spring: The spring migration seems to be directly northward from the west coasts of South America, through Central America, to the Mississippi Valley on one hand and to California on the other. Although it usually arrives in Manitoba during the first week in May, sometimes as early as April 27, I have found it common in Texas as late as May 17. Wilson phalarope are often associated with northern phalaropes on migrations, sometimes in considerable flocks, frequenting the temporary ponds made by heavy spring rains on the grassy meadows, rather than the larger ponds and lakes. The first arrivals are usually females, followed later by mixed flocks of both sexes, which soon scatter and separate into small parties of two or three pairs.
Courtship: The pursuit courtship is thus described by Rev. P. B. Peabody (1903):
For some three weeks after their arrival, these birds gladden landscape and water scape, in care-free abandon. They are ever on the move, afoot or awing; and during these three weeks of junketing, the unique courtship is carried on. There is no more laughable sight, to one endowed with a modicum of the sense of humor, than that of a couple, or even three, of the brightly colored females, ardently chasing a single somber-plumaged male, who turns and darts, here and there, in arrowy flights apparently much bored by the whole performance. Meanwhile, the sometimes dangling feet and the ever tremulous wings of the amorous females bespeak an ardor that would be ridiculous, under the circumastances, were it not so desperately in earnest.
Dr. E. W. Nelson (1877), on the other hand, writes:
At these times the nearest aproach to pursuit is in a habit they have of suddenly darting off for a short distance at right angles to their general course, hut this appears to be in mere sport, for nearly the same relative positions are kept by the birds, and this erratic course is rarely pursued beyond a few rods. In fact, throughout the pairing season I have always found the phalaropes very undemonstrative toward each other, the choice of mates being conducted in a quiet, unobtrusive way, quite unlike the usual manner among birds. The only demonstrations I have observed during the pairing time consist of a kind of solema bowing of the head and body; but sometimes, with the head lowered and thrust forward, they wiU run back and forth in front of the object of their regard, or again a pair may often be seen to salute each other by alternately bowing or lowering their heads; hut their courtship is characterized by a lack of rivalry and vehemence usuafly exhibited by birds. A male is often accompanied by two females at first, but as soon as his choice is made the rejected bird joins her fortunes with some more impressible swain.
During my various seasons spent on the western plains I have frequently seen these phalaropes flying about in trios, consisting of one male and two females, the male always in the lead, as if pursued. Females apparently outnumber the males; and, as nest building and incubation are entirely performed by the male, many of the females must remain unattached and unable to breed. I have actually seen the male building the nest and have never been able to flush a female from a set of eggs or a brood of young.
W. Leon Dawson (1923) writes:
We have already acknowledged that Mrs. Wilson wears the breeches and that she is more inclined to club life than she is to household cares. The case is, however, much more serious than we had at first suspected. I owe the original intimation of the true state of affairs to Mr. A. 0. Treganza, the veteran oologist of Salt Lake City; and subsequent investigation of my own has abundantly confirmed his claims. Mrs. Wilson is a bigamist. Not occasionally, and of course not invariably, but very usually she maintains two establishments. Now that attention is called to It, we see that our notebooks are full of references to female phalaropes seen In company with two males. The association can not be accidental, for we are in the very midst of the breeding season. The males, frightened by our presence in the swamp, and not daring to remain longer upon their eggs, have sought the comforting presence of the head of their house. The three take counsel together, and it is only when the redoubtable lady announces that the way is clear that the dutiful cuckolds trail off to their nests. On the 6th and 7th of June, 1922, our M. C. 0. party of three members gave close attention to a swamp in Long Valley, southern Mono County, at an altitude of 7,000 feeL We took 11 sets, of four eggs each, of the Wilson phalaropes, and we noted a distinct tendency of the nests to group themselves in pairs. In only one instance, however, were we able to trace clearly a connection between two occupied nests. These two, containing heavily incubated eggs, were situated only 42 feet apart, and the two males who were flushed from them by a surprise coup of ours joined themselves immediately to the only female who had shown any solicitude concerning this section of the swamp.
Neating: The Wilson phalarope is regarded by some egg collectors as an exasperating bird, because they have some difficulty in finding its nest. The nest is surprisingly well concealed, often in what seems to be scanty vegetation; and the eggs are good examples of protective coloration. I remember once crossing a moist meadow, covered with short grass which had been mowed the previous season; a male phalarope flushed from almost under foot, I threw down my hat to mark the spot and started hunting for the nest. I hunted in vain, until I gave it up and picked up my hat; there was the nest, with four eggs in it, under the hat and in plain sight.
In southwestern Saskatchewan in 1905 and 1906, we found some half dozen or more nests of this species, between June 8 and July 13. The nests were on the wet or moist meadows about the lakes and sloughs or on marshy islands; some of the nests were in practically plain sight in short grass; others were more or less well concealed in longer grass, which was sometimes arched over them; they were always difficult to find unless the incubating male was flushed. The nests were merely hollows in the damp ground, three or four inches in diameter, either scantily or well lined with dry grass.
Doctor Nelson (1877) gives a very good description of the behavior of these birds on their nesting grounds, as follows: Incubation is attended to by the male alone. The female, however, keeps near, and is quick to give the alarm upon the approach of danger. The females are frequently found at this time in smaU parties of six or eight; and should their breeding ground be approached, exhibit great anxiety, coming from every part of the marsh to meet the intruder, and, hovering over his head, utter a weak nasal note, which can be heard to only a short distance.
The movements of the birds usually render it an easy matter to decide whether or not they have nests in the immediate vicinity. After the first alarm, those having nests at a distance disperse, while the others take their course in the form of an ellipse, sometimes several hundred yards in length, with the object of their suspicion in the center; and, with long strokes of their wings, much like the flight of a kilideer, they move back and forth. As their nests are approached the length of their flight is gradually lessened, until at last they are joined by the males, when the whole party hover low over the intruder’s head, uttering their peculiar note of alarm. At this time they have an ingenious mode of misleading the novice, by flying off to a short distance and hovering anxiously over a particular spot in the marsh, as though there were concealed the objects of their solicitation. Should they be followed, however, and a search be there made, the maneuver is repeated in another place still farther from the real location of the nest. But should this ruse prove unavalllng, they return and seem to become fairly desperate, flying about one’s head almost within reach, manifesting great distress.
Aretas A. Saunders writes to me that, in Teton County, Mont., they nest in small colonies in grassy marshes, where alkaline soil prevents the grass, mainly species of Caret~o and .1u7wu8, from growing tall.
Eggs: The Wilson phalarope almost invariably lays four eggs, rarely only three. The shapes vary from ovate pyriform to ovate and there is a slight gloss. The ground colors vary from “cartridge buff” to “cream buff,” rarely “chamois.” The ground color is generally well concealed by numerous markings, more or less evenly distributed. Some eggs are uniformly covered with small spots and dots, but more often these are mixed with a few larger, irregular blotches. An occasional handsome set is boldly and very heavily blotched, sometimes almost concealing the ground color. The markings are usually in very dark, brownish black or blackish brown. In some handsome sets these dark markings are mixed with “bay” and “auburn” markings. The measurements of 57 eggs average 33 by 23.4 millimeters; the eggs showing the four extremes measure 36.2 by 23.7, 33 by 25.1, 30 by 22.5 and 30.5 by 22 millimeters.
Young: The period of incubation does not seem to be known. I can find no evidence that the female ever takes any part in it, but that abe does not lose interest in her family is plainly shown by her demonstrations of anxiety when the nest is approached; probably she feels responsible for the faithful performance of his duties by her demure spouse. The male broods over the newly hatched young, protecting them from rain, or excessive heat or cold. But they are soon able to run about in a lively manner and care for themselves. Doctor Nelson (1877) writes that “the young have a fine, wiry peep, inaudible beyond a few feet.” I believe that the young remain in the grassy meadows, where they can hide in safety, and do not take to the water until tbey are fully fledged.
Plumages: In its natal down the young Wilson phalarope is entirely unlike the other phalaropes and quite different from any other young wader. The slender bill and long slender legs and feet are characteristic. It is prettily and distinctively colored also. The prevailing color of the upper parts and of a band across the chest is “ochraceous buff,” deepening on the crown, wings, and mantle almost to “ochraceous orange,” and paling to buffy or grayish white on the belly and to pure white on the chin and throat. There is a narrow, median, black line on the crown extending nearly or quite to the bill; this is continued in a broad, more or less broken, black stripe down the center of the back to a large black patch on the rump; a black spot on each side of the crown, one on the occiput and several more on wings, thighs, and sides of the back, sometimes run together to form stripes.
In fresh juvenal plumage, in July, the feathers of the crown,back, scapulars, tertials, and all wing coverts are dusky or nearly black, ,, ” broadly edged with “light pinkish cinnamon or cinnamon buff,” broadest and brightest on the scapulars; the under parts are white, but the throat, sides of the breast and flanks are washed with “pinkish buff,” and the last two are mottled with dusky; the central tail feathers are broadly edged with “pinkish buff,” bordered inwardly with a broad dusky band, surrounding a white area, with a dusky central streak invading it; the other tail feathers are similarly marked, but less completely patterned.
This plumage is worn for only a short time, as the body plumage and tail are molted during the last half of July and in August. By September young birds are in first winter plumage, which is like that of the adult, except that the entire juvenal wing is retained with the buff edgings faded out to white. The sexes are alike in juvenal and all winter plumages. A partial prenuptial molt in the spring, involving the body plumage and most, if not all, of the wing coverts and scapulars, makes the young bird practically adult.
Adults have a partial p’renuptial molt in April and May, involving the tail, the wing coverts and all the body plumage, which produces the well-known brilliant plumage of the female and the duller plumage of the male. The complete postnuptial molt in summer produces the gray winter plumage in both sexes, in which the crown, back, and scapulars are “light drab” or “drab-gray,” with narrow white edgings, and the upper tail coverts, as well as the under parts, are white. The sexes can be recognized in adult winter plumage by size only.
Food: The other two species of phalaropes feed mainly on the water, but the Wilson phalarope is more of a shore bird and obtains most of its food while walking about on muddyï shores or wading in shallow water. It does, however, adopt the whirling tactics of the others occasionally, concerning which Mr. Dawson (1923) says:
Instead of swinging from side to side with a rhythmical motion, as do the reds and northerns, the Wilson whirls all the way around. Moreover, he keeps on whirling, and though he pauses for the fraction of a second to inspect his chances, he goes on and on again like an industrious, mad clock. One bird which I had under the binoculars turned complctcly around 247 times in one spot, without stopping save for instantaneous dabs at prey. These dabs were directed forward or backward, I. e., with or against the direction of the body motion. A single gyration normally contains two. such minute pauses, accompanied by a hitching motion of the head; and these are evidently the periods of maximum attention, since they are followed by, or rather flow into, the prey stroke, if game is sighted. “Game” is not always abundant nor certain, and I have seen a bird whirl a dozen times without a single stroke.
The method of feeding on mud flats or in shallow water is well described by Roland C. Ross (1924), as follows:
When feeding along the shallows with least, western, and red-hacked sandpipers, they differed from them not only in size and color, but in their habit of steady, energetic walking and the constant “side sweeping” with the bill. Occasionally they picked objects from the surface with their needle hills, but this was not very actively pursued. In deeper water they fed among the northern phalaropes, knots, and dowitchers, wading along until they swam in places. However, they were able to wade where the northern swam. At such depths they feed with the head clear under and the energy of the feeding operation was indicated by the motion of the tail. They commonly walked steadily hack and forth through the deeper sections of the ponds, and in such deep places they moved as headless bodies, evidently feeding as usual in the surface mud. From the vigorous side moves of the tail it would seem they were feeding in their usual manner as well; that is, “side sweeping.” When the birds were standing to feed in the deeper places the tail was again much in evidence, and indicated the manner of feeding. This would seem to be a probing motion performed with some rapid vibration which was communicated to the tail as a series of quivers. It is rather a droll sight, and arresting as well, to see a certain area marked out by headless gray bodies buried in the water up to the bend of the wing, the vibrating tail indicating the vigorous operations being carried on down below. It seemed their best feeding was in the deeper waters.
The feeding habits of this and the other phalaropes are almost wholly beneficial. They live very largely on the larvae of mosquitoes. They also eat crane-fly larvae, which are often very destructive in grass lands and wheat fields. Predaceous diving beetles, which are a nuisance in fish hatcheries, are eaten by them. Dr. Alexander Wetinore’s (1925) analysis of the contents of 106 stomachs showed that the food of the Wilson phalarope is mainly insects, of which various flies made up 43.1 per cent, aquatic bugs 24.4 per cent and beetles 20.1 per cent. The remainder of the food included brine shrimps, amphipods, eggs of water fleas, and seeds of various aquatic plants.
Behavior: Much of the interesting behavior of the Wilson phala. ropes has been described under different headings above. In all its movements it is light, airy and graceful. Its flight is much like that of the lesser yellow legs, with which it is often associated; but. when suddenly alarmed, it sometimes flies hurriedly away in a zigzag fashion. On its breeding grounds it often hovers, almost motionless in the air, as the upland plover sometimes does. It swims lightly and buoyantly, but apparently does not dive. It walks about on land actively and daintly, where it is said to resemble the solitary sandpiper. It mingles freely on its feeding grounds with various other species of shore birds. Toward the close of the nesting season the females become very gregarious; as early as June 18, in southern Alberta, we saw them in large flocks, mixed with lesser yellow legs, flying about the marshy lakes.
Voice: The only note I have recorded is a soft, nasal grunt or subdued quack. Dr. Walter P. Taylor (1912) describes a peculiar nuptial ( ?) call note “as oit, oit, oit, somewhat resembling the croak of a toad during the breeding season. At the instant of utterance of the note the bird which is calling raises its head somewhat, pauses momentarily in its flight, and its throat bulges slightly.” Mr. Saunders calls it a low note sounding like cr00, cr00, croo.
E. S. Cameron (1907) writes:
The Wilson’s phalaropes, both when feeding and when disturbed and circling on the wing, constantly uttered a low croaking, which at close quarters might he compared to the much louder note of the sandhiil cranes, or, at a distance, to the faintly heard barking of a dog. On the other hand, I have heard them give a shrill and totally different call of indecision or satisfaction on their first arrival when hovering over a pool.
Field marks: The Wilson is larger than the other phalaropes and has a longer bill, neck, and legs. It can be distinguished from other shore birds by its needlelike bill and small head and by the absence of white in its wings. Its spring plumage is, of course, well marked and very beautiful. John T. Nichols gives me the following field characters:
Very rare, but apparently regular on the south shore of Long Island in southward migration; those that I have known of have all beea in pale gray and white plumage occurring singly about the marshes in flocks of the lesser yellow legs. Little smaller than that species, they are to be picked out in a flock of same at once by their much paler color. In alighting such a bird may swim on puddles of water between the stubble where the others are wading. At short range the long, straight, very slender bill and indications of a curved “phalarope” mark on the neck, backward and downward from the eye, are to be looked for. Large size and long, very slender bill should prevent confusion of this with other phainropes in the field in any plumage.
Fall: As soon as the young are able to care for themselves the males join the flocks of females and they all depart on their fall migration in August. Some individuals wander eastward to the Atlantic coast, but the main flight is southward along both coasts of Mexico to their winter home in Argentina, Chile, and Patagonia.
Breeding range: The breeding range of Wilson’s phalarope extends north to Washington (Bumping Lake); Alberta (Alix, Buffalo Lake, and Edmonton); Saskatchewan (Osler, Quill Lake, and Indian Head); Manitoba (Moose Mountain, Brandon, and Shoal Lake); North Dakota (Pembina); Minnesota (probably Leech Lake); Michigan (St. Clair Flats) ; and southern Ontario (Dunnville). East to southern Ontario (Dunnville); northern Indiana (Lake County); northern Illinois (West Nortlifield, Fox River, and Calumet Marshes) ; and formerly Missouri (Pierce). South to Indiana (Whiting); Missouri (formerly Pierce) ; rarely southern Kansas (Meade County); Colorado (Sterling, Barr, and San Luis Valley) ; southwestern ‘Wyoming (Fort Bridger); northern Utah (Salt Lake City); Nevada (Washoe Lake); and California (Tahoe Lake and Los Banos). West to California (Los Banos, Lassen County, and Tule Lake); Oregon (Klamath Lake); and Washington (Conconully and Bumping Lake). It also has been reported in summer from southern California (Furnace Creek and Tulare Lake) and from central Mexico (Lerma).
Winter range: The winter range of the Wilson phalarope is very imperfectly known. The few records available come chiefly from South America, but it also has been reported as wintering in Mexico (Mayorazgo, Ixtapalapa, and the City of Mexico); rarely southern Texas (Corpus Christi) ; and in southern California (Riverside). South American specimens have been taken or observed at this season in the Falkland Islands; Patagonia (Chupat) ; Argentina (Mendoza, Buenos Aires, Tucuman, Barracas al Sud, and Missiones); Chile (Valdivia); Bolivia (Alto Paraguay); Peru (Ingapirca); and Brazil (Caicara).
Spring migration: Early dates of spring arrival are: Missouri, St. Louis, April 22, Corning, April 23, Independence, May 1, and Marionville, May 2; Illinois, Quincy. April 20, Chicago, April 21, Liter, April 27, Fernwood, May 1, and South Englewood, May 3; Indiana, Waterloo, April 27, and Kouts, April 30; Michigan, Ann Arbor, April 1, Detroit, May 1, and Iron Mountain, May 2; Ontario, Toronto, May 25; Iowa, Emmetsburg, April 24, Gilbert Station, April 27, Marshalltown, May 2, Sioux City, May 5, and Keokuk, May 6; Wisconsin, Delavan, April 26, North Freedom, April 29, and Whitewater, May 6; Minnesota, Heron Lake, May 8, Wilder, May 8, Hallock, May 9. and Waseca, May 12; northern Texas, Gainesville, May 0, and Huntsville, May 7; Kansas, Emporia, April 23, Paola, April 28, Onaga, April 29, and Wichita, April 30; Nebraska, Dunbar, April 5, Badger, April 18, Callaway, April 19, Lincoln, April 22, and Valentine, May 1; South Dakota, Harrison, April 29, Vermilion, April 29, Forestburg, May 1, Pitrodie, May 3, and Huron, May 4; North Dakota, Menoken, May 1, Bismarck, May 3, Charlson, May 4, Antler, May 10, Cando, May 17, and Westhope, May 18; Manitoba, Oak Lake, April 27, Shoal Lake, May 7, Reaburn, May 10, and Winnipeg, May 22; Saskatchewan, Indian Head, May 12, Dinsmore, May 13, and Osler, May 19; New Mexico, Albuquerque, April 20, and Aragon, April 21; Arizona, Tucson, April 12; Colorado, Denver, April 25, Durango, April 25, Loveland, April 27, Boulder, May 3, and Salida, May 4; Wyoming, Lake Como, May 6, near Cokeville, May 7, Yellowstone Park; May 11, and Cheyenne, May 19; Idaho, Meridian, May 14; Montana, Billings, April 30, Great Falls, May 9, Fort Keogh, May 10, Big Sandy, May 14, and Terry, May 21; Alberta, Beaverhill Lake, May 7, Alliance, May 18, Veteran, May 22, and Stony Plain, May 23; California, Santa Barbara, April 20, Unlucky Lake, April 28, and Stockton, May 2; Nevada, Steptoe Valley, May 12, Washoe Lake, May 19, and Quinn River, May 20; and Oregon, Klamath Lake, April 30, Narrows. May 1, and Lawen, May 20.
Fall rnigration: Late dates of fall departure are: Oregon, Malheur Lake, September 5; California, Santa Barbara, September 8, and near San Francisco, September 9; Montana, Milk River, July 21, and Great Falls, August 15; Utah, Great Salt Lake, September 16; Wyoming, Seven-mile Lake, September 14, and Yellowstone Park, September 27; Colorado, Denver, September 12; Arizona, Fort Verde, September 7; Saskatchewan, Ravine Bank, August 25; North Dakota, Grafton, September 11, and Westhope, September 24; South Dakota, Forestburg, August 13, Harrison, September 12, and Sioux Falls, October 14; Nebraska, Badger, August 30, and Gresham, September 1; Kansas, Emporia, August 31; Texas, Tivoli, September 14, and Corsicana, September 12; Minnesota, Lanesboro, September 13; Michigan, Kalamazoo County, September 8; and Ontario, near Toronto, September 23.
Casual records: Although essentially a western species the Wilson phalarope has many times been detected in eastern localities. Among these are: Alabama, Bayou la Batre, September 5, 1911; South Carolina, Sullivans Island, September 7, 1910; North Carolina, near Church Island, August 25, 1910, and Currituck Light House, September 14, 1911; New Jersey, Ocean City, May 19, 1898, and Cape May, May 4, 1909; New York, Mastic, September 21, 1918, and August 28, 1920, Shinnecock, August 20, 1883, and August 15, 1885, Far Rockaway, October 10, 1874, East River, October 15, 1879, Onondaga Lake, September 2, 1886, Oneida Lake, October 6,1883, Ithaca, fall of 1892, Atlanticville, August 15, 1885, and June 1,1887, and Bronx Park, September 21, 1924; Connecticut, Bridgeport (Linsley); Rhode Island, Newport, August 2, 1880, August 20, 1883 and September 13, 1886, Sakonnet, August 24, 1899, and Quonochontaug, August 28, 1909; Massachusetts, Chatham, October 19, 1888, Nantucket, August 31, 1889, Nahant, May, 1874, Salisbury and Boston (Townsend) ; New Hampshire, Rye Beach, August 15, 1872; Maine, Sabattus Pond, September or October, 1906, and Scarborough, June 9, 1881; and Quebec, Montreal, August, 1869. It also has been taken in British Columbia, Chilliwack, September 9,1888, and Osoyoos Lake, May 15, 1922 and May 18, 1922. It has been detected a few times in Lower California, La Paz (date ?), and San Jose del Cabo, one in spring and another in August, 1887.
Egg dates: Saskatchewan and Alberta: 51 records, May 16 to June 24; 26 records, June 5 to 11. Dakotas: 23 records, May 25 to June 22; 12 records, June 3 to 12. Colorado and Utah: 20 records, May 15 to July 10; 10 records, May 25 to June 8. California: 50 records, May 21 to June 22; 25 records, June 2 to 7.