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A
chapter from the electronic book:
Life Histories of Familiar North American
Birds
Pine Siskin
Carduelis pinus
Contributed by Ralph S. Palmer
[Published in 1968:
Smithsonian Institution United States National Museum Bulletin 237
(Part 1): 424-447]
The pine siskin is a social bird the year round. Breeding
individuals join in social flocks away from the nesting territory,
and they sometimes feed in the tree where the nest is situated.
These social groups are small, up to a half dozen birds, not the
large flocks commonly seen outside the breeding season. From late
summer to late winter the pine siskin associates, roughly in
descending order of frequency, with the redpolls, the goldfinches,
the two crossbills, the purple finch, the cedar waxwing, and, very
occasionally, the juncos. Except for the first two mentioned, the
association usually is brief and may break off whenever a mixed
flock takes flight. A common situation is to find the few siskins
in the flocks of the other species, especially when goldfinches or
redpolls are plentiful and the siskins few.
The siskin is a relatively high and swift flier, often crossing
from ridge to ridge or peak to peak in direct flight far above the
trees in the intervening area. The flocks are compact, and all
members execute long undulating sweeps in unison. Usually the
birds fly silently, but now and again one or many may utter a
sharp lisping call-note that carries well.
The decision to alight seems to come abruptly, and the flock
drops down into the trees to rest or feed. It is common for the
birds to be more vocal on alighting, and again as they depart.
Often when feeding, there are no birds in flight; at other times
part of the flock may take wing and pass over those still feeding
to other food trees. As the birds thus go
"leapfrogging," the entire mass of the flock of busy,
lisping birds appears to flow through the forest. Then all of a
sudden the lisping ceases and the flock is silent; it takes flight
with a very audible whirring of wings and flies rapidly away.
By observing alders in Strawberry Canyon at Berkeley, Calif.,
in February, T. L. Rodgers (1937) provides a description of siskin
habits that applies generally:
It began to appear as if the regular procedure of the birds
was to alight in the top of a tree, forage down to the lower
limbs, never spreading over an area more than 12 or 15 feet
across, and then by means of a circular flight move to the top of
another tree and forage down it. Although this was the commonest
method, they were also seen to forage in a nearly horizontal line
through a group of trees without foraging through any of them
completely; they foraged up through a tree, and then moved by a
direct route, at times even "flowing" from one tree to
the next after the manner of a flock of Bush-tits. The direct
flights of the flocks were either to trees far away or to those
ten or fifteen feet off. This seems to bear out the idea that
"circle flights" are survey flights.
The siskin's gait seems much better adapted to climbing about
tree tops than to ground feeding. On the ground it walks with very
short steps interspersed with occasional little hops, and its body
almost seems to cling to the ground.
Many authors have commented on the siskin's tameness and
boldness in its relations with human beings. Brooding females
usually can be approached within inches before they leave the
nest. Exceptional, however, was the experience of F. H. Allen
(1888) at Newton Mass., in late April. He observed two siskins
near a heap of hops by the roadside. One flew away on his
approach; the other, though able-bodied and in good condition,
allowed itself to be approached closely, stroked, and caught in
the hand. Allen queried: "Was this bird affected by the hops.
. .?" E. R. Davis (1926) reported siskins at Leominster,
Mass., to be remarkably tame in late fall. He says:
In a short time the birds came to regard me as their friend,
and in the days that followed grew to be exceedingly sociable and
to lose every vestige of fear. Whenever I would appear at the
window, or step outside the door, down they would come and,
settling upon my head, shoulders, and arms, would peer anxiously
about for the food that they had learned to know I held concealed
from them in a box, dish, or other receptacle. The moment I
removed the cover or exposed the food, they would make a dash for
it and the usual scrapping program would be on. Nor was it at all
necessary for me to go outside the door. . . . In a short time the
siskins discovered this opening [in a window pane], and it
was only necessary for me to draw the slide when one after another
would come right into my kitchen, and soon one or more of them
would be perched on my head or shoulder, or hopping around on the
desk where I was writing, looking for the handful of seeds that
they all knew was forthcoming. . . . Now and then some members of
the flock would elect to spend the night in the warm room,
sleeping on the clothes-line, stretched across the room a little
below the ceiling. On such occasions they seemed to be without
fear and totally oblivious to people moving about the room, often
within a few inches of them, turning on or snapping off electric
lights.
The interested reader may want to read all of the above quoted
article by E. R. Davis. He carried out a series of conditioned
reflex experiments. Only a paragraph about one of these is quoted
here; it concerns a button rigged to release a small batch of
seeds when pushed:
For quite a while the thing remained a puzzle to them.
Finally, one of them happened to notice that push-button, which
was a different colored wood from the rest of the contraption. He
sidled up to it, looked it over for a moment, then gave it a
"biff." This released the catch on the other side and
down at his feet came a little handful of seeds. This frightened
him, of course, and he flew away, only to return a minute later,
eat the seeds that had fallen down the chute, and then tried the
"press the button" arrangement again. It was not long
before several of the flock learned the secret, but it was quite a
while before they became used to the seeds falling down at their
feet, so that they were not afraid, and would proceed to eat them
without first flying away a few inches.
A siskin's life is not always easy. During severe weather in
March and April, 1939, many siskins died on Mount Desert Island,
Maine (R. S. Palmer, 1949). Winter deaths, presumably from eating
a poisonous chloride are discussed under food. Various authors
have reported destruction of nests, eggs, or young by wind, sleet,
and rain. Heavy rains have killed young after they departed from
the nest. Several observers, on finding nests empty and sometimes
damaged, have suspected predation by the red squirrel and the blue
jay. The domestic cat is a known predator. The cowbird, too, is a
hazard, since its egg or chick in a siskin nest is detrimental to
the siskin's nesting success. Both parent siskins treat the young
cowbird as one of their own. At Wenatchee, Wash., R. T. Congdon
found a young siskin that had died after a foot became entangled
in the nest lining.
E. R. Davis (1926) described siskin actions at the sight of a
northern shrike at Leominster, Mass., in winter:
It was wonderful how quickly they would detect one of these
birds in the vicinity, or even at a great distance. Instantly, if
one of them appeared in the sky or on a distant tree, all activity
ceased among the Siskins, and each bird, intently watching the
enemy, would literally "freeze" to the spot where he was
sitting, hardly moving a feather until the enemy had disappeared.
On more than one occasion I have had them "freeze" in my
hand, where they had been sitting when the danger threatened.
Aggressiveness is a marked siskin trait at feeding stations.
Davis (1926) placed food on a shelf 3 feet square and found that
"the bird that first reached the place seemed to consider
himself the sole owner of the entire stand, and woe to the
individual that dared dispute his claim." When feeding with
purple finches the siskins are bold and usually hold their own.
Generally they feed together peaceably, but now and again a siskin
takes the offensive and darts at a purple finch, scaring it away.
Perhaps the siskin's sharp bill gives it authority. In feeding
with evening grosbeaks, the siskins keep their distance and show
pugnaciousness only among themselves.
Territory.--Siskins go in flocks
containing a few to well over a thousand individuals. Flocks of 50
to 200 are common. At the close of the breeding season--usually
early summer--the birds generally leave the breeding localities,
although the extent and often direction of this movement is
unknown. The birds may occur in or pass through the nesting area
again in autumn. Large-scale incursions in the postbreeding period
have not been noted as frequently as autumn and winter invasions.
However, in Alberta beginning in mid-June and lasting into August,
1921, large numbers of siskins moved into the park country of the
prairie where no evergreens occur except for small patches along
river bottoms. F. L. Farley (1921) reports that at almost any hour
of the day one could see large flocks, "whirling here and
there" in redpoll fashion. They would feed, then take flight
suddenly.
In parts of the siskin's range near and along the Pacific
coast, the species occurs in many localities all year, but a
goodly share of the population moves altitudinally to the lowlands
in autumn and to higher elevations to breed in spring. The highest
altitudinal record is for a siskin that Taylor and Shaw (1927)
found dead at approximately 11,000 feet on Mount Ranier, Wash.
The siskin's center of abundance is from the Rocky Mountains
westward. Part of the population in the interior of the continent
shows a more or less northwest-southeast movement in autumn and
the reverse in spring. Thus it seems likely that the species may
have spread eastward, as the evening grosbeak did at a later
period, but before the event could be chronicled. M. H. Swenk
(1929) wrote:
Judging from the fact that in various falls that they have
occurred in Nebraska the Pine Siskins usually have been seen first
in the more westerly and northerly parts of the state, and later
in the more southeastern localities, and also from the further
fact that they may reach western or central Nebraska commonly in
seasons when they are uncommon or absent in extreme southeastern
Nebraska, it is probable our Pine Siskin winter visitors are birds
that summer in the Black Hills and those parts of the Rocky
Mountains at a corresponding latitude, or northward.
The fall and winter
wanderings, especially in the East, are so irregular in occurrence
and so variable in extent that it is difficult to define the
species' usual range as compared to its total range. At any rate
there is usually some movement--vertical migration in mountains,
horizontal elsewhere, both unpredictable regarding the amount or
direction. In some years these movements become southward
incursions of vast extent. Dorothy Mierow (1946) summarized as
follows:
Some years are marked by exceptional flights of these birds
southward. In 1896, enormous flocks were found in Louisiana, South
Carolina, Missouri, and Illinois. Again in the year 1907, notable
for its cold spring, flocks were observed in Florida, Tennessee,
Ohio, Michigan and Missouri. This year they nested in Nebraska.
The season of 1922-23 was characterized by an abundant crop of
beech nuts and wild fruits, and again the siskins appeared in
large numbers in Alabama, Virginia, Ohio, Wisconsin, North Dakota,
and Nebraska. They were conspicuous by their absence from Yosemite
National Park, California, in the fall of 1923. In 1925, they were
seen in Kentucky and Michigan, and they nested in North Dakota and
also at Ithaca, New York. There were abundant spruce, fir, and
hemlock seeds in the Great Smokies of Tennessee in 1937. Siskins,
usually rare in Tennessee, appeared in thousands during November.
In other years, too, there were great flights at one place or
another, but in these particular years the movement was most
marked.
During an incursion into the southeast in winter of 1946-47, R.
L. Weaver (1948) saw five birds in Orange Park, Clay County, Fla.,
probably the southeasternmost record.
The pine siskin is commonly stated to wander continually
throughout the nonbreeding season, especially during fall and
winter. But when food is plentiful, many observers have noted that
siskins will remain in one particular area over a long span of
time. At Northampton, Mass., B. M. Shaub (1951a) analyzed his
banding data for early 1947 as follows:
An examination of this record will show at once that the
birds with which we were working were not, in all probability,
wandering winter visitors or transients as they generally have
been described. On the other hand they more-or-less settled down
in Northampton and vicinity for the winter and spring. . . . [Seven
banded individuals] were with us rather regularly over a period
of 2 1/2 months, although it is possible that they could have made
visits to other localities nearby and as often returned.
Courtship.--The pine siskin
probably begins breeding when a year old, but data from banded
birds to prove this are scant. Richard Harlow (1951) states that
there is abundant evidence that the crossbills and siskin have no
definite breeding ranges. He writes: "I do not know of any
locality in our northeastern and northern forests where one can
say, 'We will find the pine siskin here this year.'"
M. H. Swenk (1929), in his study of this species in Nebraska,
correlated breeding records with temperatures of the months of
March, April, and May. If the mean temperatures for April were
subnormal, the siskins might remain and breed; the same might
happen if supernormal April temperatures were followed by
subnormal May temperatures. Nebraska is, of course, outside the
area where the siskin ordinarily may be expected to breed. Usually
the birds are numerous--often abundant--in areas where food is
plentiful. The flocks contain both sexes. Scattered flocks tend to
join, forming larger ones. By late January of most years, in
localities all across the continent, the thin lispy calls of the
siskin are augmented by a warbled song. At this time the flocks
break up into smaller ones, then into groups of three to five
birds, then into pairs.
There is considerable fighting and chasing when the flocks
start to disintegrate. At Rutherglen, Ontario, Mrs. Lawrence
notes: "In the midst of all this sweet singing, two birds
swing into the air in an extensive 'cloud chase,' their movements
tightly synchronized as they alternate in the roles of pursuer and
pursued."
Perhaps anticipatory to courtship- and nest-feeding is a
performance observed in late April in Everett, Wash., by M. R.
Thayer (1911): "Our attention was called to three birds on a
[trellis] cross-bar about seven feet from where we stood. Two were
close together and the third a little apart, and all three were
opening and closing their bills, stretching them wide as if
yawning and closing them with a snap. Before we had time to
consider what it might mean, the two turned toward each other and
touched their bills in a most lover-like manner. They were quiet a
moment, then one opened his bill wide again and they both flew
away followed by the third. . . ."
Courtship feeding begins while the birds are still in flocks or
small groups. On Feb. 5, 1948, at Rutherglen, Ontario, Mrs.
Lawrence noted: "The female sat on a twig. Presently the male
alighted on the same twig, hopped up to her and offered her a
small particle, of what I could not see. She crouched and, with
trembling wings, accepted the offering."
The birds are still in flocks or groups when courtship flight
with song reaches its fullest development. Two paragraphs from
Mrs. Lawrence's notes describe it well: "With a beam of
sunshine illuminating his golden flashes, the male rose into the
air with tail spread wide and wings in a blur of rapid motion. To
the accompaniment of a flight song which seemed to express far
more musical adoration than could be contained in so small a body,
he described circle after circle around his chosen mate. That the
female reflected none of her partner's emotion in no way seemed to
dampen his ardor and, after he dropped on to a twig from pure
exhaustion to catch his breath, a few moments later he rose again
in a repeat performance no less ecstatic than the first.
"None of the flight song performances I saw ended in
copulation. When that took place in my presence, it was an
anticlimax to what I had previously seen. Two birds came to the
salt lick and one of them perched in a bush. That very instant the
male alighted directly upon the first bird by the pouncing
technique without any sort of preliminaries. Copulation took place
with both birds trembling violently. When it was over, the female
begged and the male, with nothing in the bill, performed a token
feeding. The female shook herself and both birds hopped down on
the ground where the male strutted a little with raised head
feathers."
Formation of the pair bond involves symbolic feeding, sexual
flight, and song, and it occurs while the birds are in social
groups. Single brood monogamy is certain, but how much longer the
pair bond lasts is not known.
Nesting.--At times Siskins nest as
isolated pairs. More usually, nesting is somewhat a colonial
affair, with the nests rods apart. Adults join in social flocks
away from the nests.
Typically, the nest is at middle height in a conifer, well out,
and concealed on a densely foliaged horizontal limb. The most
frequent departure from this pattern is for the nest to be located
lower down, but when this happens it is still usually above 8 feet
from the ground. Commonest choices for nesting are hemlock, pines,
spruces, firs, cedars, redwood, cypress, and wild lilac.
Introduced conifers, also transplantings of native trees, are
occupied in addition to natural stands. Deciduous trees are used
for nesting occasionally. For example, the siskin has nested in
box elder in New Mexico (F. M. Bailey, 1928) and North Dakota (R.
Reid, 1929), in maples and oaks in Oregon (C. Keller, 1891), in
maple in Washington (R. T. Congdon), in the very top of a 50-foot
eucalyptus in California (Carriger and Pemberton, 1907), among
cottonwoods in Montana (A. A. Saunders, 1912, 1921), and two nests
in lilacs in Colorado (F. M. Dille, 1900). The highest nests are
at about 45 to 50 feet. In manuscript notes, S. F. Rathbun
recorded a nest in Washington only 4 1/2 feet above ground in a
stunted cedar. The lowest record at hand is of a nest in Iowa,
recorded by Dales and Bennett (1929) as only 3 feet up in a 4
1/2-foot cedar on a lawn. During resting periods the birds go to
tree tops.
The female chooses the nest site and is accompanied by the male
as she brings nesting material. At times the birds return to
social life in flocks; also, other siskins occasionally accompany
the nesters on flights to the nest tree. As C. W. Bowles (1903)
puts it, several paris may be "superintending" when one
is building. The small nesting territory is used for
copulation--although this occurs elsewhere, too--and nesting; in
addition, the male feeds his mate there during incubation and the
period until the young attain flight. The defense of territory is
developed slowly, being weak until after the nest is built. Weaver
and West (1943) write:
During nest building the male had been quite attentive to
the female and never left the nesting area for very long periods,
and he did not seem to be very closely associated with any of the
other siskins or flocks which fed near the nest tree. After the
eggs were laid, he would leave the area for short periods, which
became longer as incubation progressed. He frequently returned in
company with one of several other siskins. The female would chase
these birds, as would the male, if they came too close to the
nest. On several occasions, he flew off with these birds after
feeding her on the nest. Other birds would enter the general
nesting area and feed with one or both of the mated birds,
unmolested.
As is common with a number of early nesters, the structure that
the siskin builds is rather large in proportion to the size of the
builder and usually well concealed in foliage. It is fairly well
put together, generally somewhat flat, and often not very securely
fastened to the branch. The foundation and sides consist of such
materials as twigs, rootlets, and grass; the lining consists of
fine rootlets, hair, fur, feathers, and other fine-textured
material. The finer material, at least, is often gathered on the
ground. Dales and Bennett (1929) saw a siskin dismantling an old
goldfinch nest and using the materials in new construction.
Numerous photographs and descriptions of nests have been
published. A good example of the latter is C. H. Morrell's (1899)
of one found in March in Nova Scotia:
It was saddled on the limb and radiating twigs but not
attached to them. Considering the size of the bird, it is quite
large, rather flat, and bears no resemblance to. . . [Goldfinch
nests], measuring as follows: height, 1.63 inches; depth, .75;
outside top diameter, 4 inches; inside top diameter, 2 inches. It
is constructed mainly of dark pendulous tree-moss, with some
fulvous bark from weed-stalks, plant-down, usnea, and other
mosses. About the bottom of the nest is [sic] woven a few
spruce twigs. The lining is entirely the pendulous moss.
From Eureka, Calif., R. R. Talmadge writes of two nests that he
considered distinct from all others he had found. The first was
composed of fine grayish rootlets with a minimum of plant fiber
and lined with black horsehair. The other was similar, but was
lined with red hair from cattle that were in the immediate area.
Most of the nests discovered were similar in composition, but the
lining was mixed, not distinct as in these two.
According to Weaver and West (1943), at Hanover, N.H.:
Three days were required to complete the outer layers and
bottom of the nest. On the fourth day, lining materials were
added. Several attempts to break off small twigs from the nest
branch were observed. After the fifth day, materials were added to
the nest sporadically until the eggs were laid. On the seventh day
the female began making trips to the nest without materials and
sitting on it for short periods. This procedure continued with the
trips to the nest becoming more frequent and the time spent on the
nest increasing to as much as fifty minutes before the tenth day,
April 18, when the first of the two eggs was laid. The second egg
was laid on the following day.
Eggs.--The data summarized from
Mierow (1946) plus other available published and unpublished
information through 1954, indicate that three-egg clutches
predominate, about two-thirds as many have four eggs, a third as
many have two, that clutches of five are rare but occur more often
than those presumed complete with a single egg. C. W. Bowles
(1903), for example, mentions sets of one (complete?), three, and
four in Washington, and stated that three seemed most common.
Carriger and Pemberton (1907), writing of San Mateo and San
Francisco Counties, Calif., states that the "average set
seems to be three eggs, but four is also a common number. Several
sets of two eggs were taken in advanced states of incubation, and
also two sets of five, but these are rare." There seems to be
no geographic variation in clutch size, but it is difficult to
assess the data since most sets observed were from Pacific coastal
states.
Carriger and Pemberton (1907) write: "The eggs are a pale
greenish blue several shades lighter than the eggs of Astragalinus
[goldfinches], and are marked with chocolate spots and irregular
blotches, with a number of pale lavender blotches which appear to
be beneath the surface of the shell. Eggs vary from very nearly
unmarked, to well marked about the larger end and sparingly over
the whole surface. The average size of all eggs at hand is .63 X
.48 inches."
In a manuscript note, Robert R. Talmadge of Eureka, Calif.,
states: "Several sets which I have found had one or two
unmarked eggs. The markings vary from small blackish spots to
semi-elaborate scrolling of dark sepia and lavender."
All egg data at hand indicate that complete sets of fresh eggs
usually are to be found in the United States and Canada from early
April to early May. Eggs in March, or indications of their
probable occurrence then, are as follows: young nearly ready
to leave the nest March 19 at Woodstock, Vt. (E. H. Forbush,
1929); nest nearly completed March 15 (had three eggs on the 31st)
and another started March 18, at Lincoln, Nebr. (M. H. Swenk,
1929); siskin gathering nesting material March 16 in San Francisco
County, Calif. (M. S. Ray, 1916); nest completed March 11 had
three eggs on March 18, also nest with two nearly fledged young on
April 13, in Lewis County, N.Y. (C. H. Merriam, 1878); nest with
two eggs and two newly hatched young March 28 or 29, at Tacoma,
Wash. (J. H. Bowles, 1924); clutch of four on March 29 in Nova
Scotia (C. H. Morrell, 1899); nest with two eggs taken on unstated
March day in Ontario (Baillie and Harrington, 1937); and unstated
number of eggs the last of the month in Vermont (Tracy in
Mierow, 1946). Fresh eggs in May and early June are common but why
many fresh clutches have been found in California in early June is
a matter for speculation.
The set of eggs of the pine siskin varies from three to six;
sets of four and five are most frequent. They are ovate with some
tendency toward short-ovate and have very little lustre. The
ground color is greenish-white or bluish-white, delicately
speckled and spotted with "light cinnamon drab,"
"cinnamon drab," "warm sepia," or "Verona
brown," with a few thin scrawls of black. In general, the
markings are concentrated somewhat toward the large end where they
often form a loose wreath; rarely an egg is found that is almost
immaculate.
The measurements of 50 eggs average 16.6 by 12.4 millimeters;
the eggs showing the four extremes measure 18.08 by 13.1,
and 14.3 by 11.3 millimeters.
Eggs are laid on successive days. Weaver and West (1943) say
that at Hanover, N.H., both eggs of a two-egg clutch "were
laid before nine o'clock in the morning. Incubation
began upon the laying of the first egg and the young hatched
thirteen days later, one day apart. . . . The danger from freezing
of the eggs would appear to be lessened with incubation beginning
upon the laying of the eggs."
Only the female has an incubation patch and she alone
incubates. Weaver and West (1943) write: "During incubation,
the female stayed very close to the nest. The longest observed
period that the female was off the nest for the entire period of
incubation was eight minutes. She was fed by the male during
incubation, and this permitted long uninterrupted periods on the
nest; in fact, he began feeding her on the nest the day before the
first egg was laid and in one instance was observed to feed her
while she was off the nest before the eggs were laid."
Hatching is described by the same authors (1943) as follows:
"Just prior to hatching, the female stood up on the edge of
the nest and looked at the eggs a great many times. Hatching
occurred early in the morning, before 7:30 a.m., or possibly
during the night. There was no sign of the egg shell in the nest,
but later a small piece was found under the tree.
Young.--In the above-mentioned nest,
"feeding of the young began very soon after hatching,
possibly within the hour." Weaver and West reported that,
during the first few days after hatching, the female fed the young
about every 10 to 15 minutes, but near the end of the nesting
period feedings were about an hour apart. For the first 7 or 8
days the male fed the female on the nest and she fed the young; he
increased his trips with food to twice an hour, and made even
three or four trips per hour toward evening.On the 7th or 8th day
he began to feed the young directly. After the 10th day, the male
was not seen to feed the female and she began to forage for
herself and the young.
The usual method of male feeding female when the young are
small has been reported from Berkeley, Calif., by T. L. Rodgers.
The bird on the nest hears ti-er, ti-er from the mate in
another tree, and replies ti-er. They call back and forth
three or four to a dozen times, and the food bearer flies to a
position a few feet from the nest and utters one or more plaintive
pseee notes. Then, while both are silent, it hops quietly
toward the brooding bird. She flutters her wings and begs and the
feeder regurgitates. Rodgers (1937) states: "The feeding
process continued by the clasping of the bills of the two birds,
the upper and lower mandibles of one just closing the complete
gape of the other. Three or four such contacts were made, and,
between each, the bird doing the feeding gulped as if bringing
more food into its mouth. The bird then flew away, and the
brooding bird sat quietly for eight or ten seconds before
proceeding to feed the young."
This regurgitative feeding of the brooding female by the male
was observed at close range at Sioux City, Iowa, by Dales and
Bennett (1929), who pointed out that the process is a
comparatively long one. Their description of a feeding ends thus:
"Toward the end of the feeding as the male withdrew his beak
from the female's mouth a string of saliva-like substance
stretched between the two bills; this was immediately sucked in by
the female. There must have been considerable of it, for there
seemed to be a flow of it for nearly fifteen seconds. Then the
male flew away."
The food-bearing male sometimes is accompanied by other siskins
who do not trespass in the small defended area around the nest.
They perch in the nest tree, or in nearby trees; they also
accompany the male when he departs, as several observers have
noted. The female also joins social groups.
Weaver and West state that the young never were left
unprotected more than 11 minutes, that during the first week the
female's usual duration of absence was 3 minutes. She kept the
nest clean by eating all excreta for the first 7 or 8 days; later
it became fouled because neither parent removed the droppings. T.
L. Rodgers (1937) observed the eating of the droppings. He states
that the nest was kept clean during the first 8 days and, from the
9th day on, no droppings were taken from the nest and they
accumulated there.
Data on the growth and development of young siskins have not
been published in detail. In New Hampshire, Weaver and West (1943)
report that the brood of two young they studied showed their first
fear reactions about in their 6th day. The young became very
active during the last 4 days of nest life and the female then
spent little time brooding them. They took turns exercising and
stretching their wings, also walking on the nest rim. In their
haste to be fed, they sometimes fell over the side and grasped the
outer structure and pulled themselves back again. They say that
"The adults seemed to approach the nest rather deliberately
during the last 2 days, seemingly coaxing the young to such daring
feats."
Both young left the nest 15 days after the first hatched; thus
one was a nestling 14 days (it probably departed prematurely) and
the other 15, which may be the usual initial flight age. One young
was seen being fed in the nest tree an hour or so after both had
left the nest. Other observers have indicated that the young are
with the parents and fed several days, or longer, but the span of
time from nest-leaving to independence remains unknown.
Whether our bird, like the Old World siskin, Spinus spinus,
is double-brooded is still a moot point. There is a strong
probability that it is--at least in some years--and that the birds
may change localities between nestings. E. H. Forbush (1929),
without direct support, says: "One brood yearly, probably two
in many cases." Suggestive is a single sentence by William
Brewster (1938) relative to the siskin on Aug. 9, 1873, at Lake
Umbagog on the Maine-New Hampshire boundary: "A male shot
this morning was unmistakably breeding and yet full-grown young
are about in considerable numbers." As already shown, the
siskin is an early nester; also, fresh eggs are fairly common as
late as early June in some localities and seasons, especially
Pacific coastal states, and eggs or nestlings in July have been
recorded for a number of localities widely spaced geographically.
Here are some late breeding records: set of five eggs July 22 in
Ontario (Baillie and Harrington, 1937); pair of siskins seen
copulating July 30 on Forrester Island, Alaska (Willett, in Mierow,
1946); nest with young August 4 in Faith Valley, Calif. (Bassett,
in Mierow, 1946); birds in breeding condition carrying nesting
material, July 15 - August 14, in the Porcupine Mountains, Mich.
(W. B. Barrows, 1912); four young left the nest August 19 at
Bozeman, Mont. (A. A. Saunders, 1921); clutch of three fresh eggs
August 14 at Tacoma, Wash. (C. W. Bowles, 1903); and nests
"containing young in early September," also at Tacoma
(J. H. Bowles, 1924). Omitted are various late dates for adults
reported as seen "feeding young"; it is assumed they are
for young that have been flying, and for an unknown length of
time.
It seems that the very long span of breeding dates can hardly
be explained in terms of replacement layings after a loss of an
earlier clutch or brood. More likely, either some birds breed
twice in some years or different parts of the population breed at
different times.
Plumages.--There is little sexual
dimorphism although, after the juvenal stage, and presumably among
birds of equal age and state of plumage wear, males are usually
more brilliantly colored. This applies especially to the yellow
portions of the wing and tail.
Breeding adults are grayish brown above, heavily streaked with
dusky; the paler rump is often tinged with yellow. Wings and tail
are mainly dusky. The basal portions of the flight feathers are
yellow, and are conspicuous in flight but almost entirely
concealed when the birds are at rest. There are two narrow whitish
wing bars. Underparts are whitish, heavily streaked with dusky
except from the abdomen posteriorly when it is often plain. The
bill is brownish or dusky at the tip, becoming paler (flesh
colored or bluish) toward the base, especially the lower mandible.
The iris is brown. Legs and feet vary greatly in color, but
usually are medium light to a darker shade of brown. This breeding
condition is a result of wear and fading of the plumage acquired
months beforehand by a partial post-juvenal molt in the case of
young birds and a complete post-nuptial molt in the case of
adults.
At Rutherglen, Ontario, 1948, siskins were plentiful and
nested. Mrs. Louise de Kiriline Lawrence saw the first flying
young on May 10. On May 22 females with incubation patches were
noted going into molt and, in general, acquiring fat--first on the
abdomen, then on the axilla, and last on the fulcrum. The birds
then left the area, the last seen on June 3.
After the postnuptial molt--details of it have been described
by T. and E. McCabe (1928)--the new fresh plumage has these
characteristics: orange-buff wing bars; strong dusky markings and
yellowish edges on back feathers; buffy or yellowish tint on
abdomen (which may be either heavily or lightly streaked or
plain); and buffy chest and flanks.
Although the natal down has been observed quite often,
apparently no description of it has been published. The
photographs in the article by T. L. Rodgers (1937) indicate a well
developed nestling down exists.
The development of the juvenal plumage has not been described;
it is developed to the point that initial flight occurs at 15 days
of age. This plumage is more buffy and warmer in general tone than
the worn breeding plumage of the adults it associates with, so the
two age groups then can be distinguished afield. After wear and
fading, it is very similar in general aspect to that of worn adult
plumage.
The juvenal plumage is worn a long time, probably two months
according to Dwight (1900), but the exact time is hard to
determine because of the irregular breeding season. Rockwell and
Wetmore (1914) state that immature birds were still in molt in
Colorado the first week in October. They mention young out of the
nest July 18, but since the duration of molt is not known, one
cannot estimate the time lapse before it began. Winter flocks of
incursion visitants usually are preponderantly birds of the year,
but this is hardly a clue in interpreting A. T. Wayne's (1906)
comment for the period Dec. 12, 1896, to the following mid-March
in South Carolina: "Between these dates many of the birds
taken seemed to be in a state of perpetual molt."
According to Dwight (1900), there is a partial post-juvenal
molt in August in eastern Canada involving body plumage but not
wings and tail. The first nuptial stage, therefore, is this
combination in worn condition.
Food.--The pine siskin is a tree- and
ground-foraging finch. Like the crossbill, it often hangs upside
down when feeding in vegetation, but it is a more generalized
feeder, not tied closely to cone feeding and hence independent of
the varying extent of the cone crop.
The results of food habits analyses were summarized by W. L.
McAtee (1926): "The food of the siskin is principally the
seeds of coniferous trees, alder, birch, ragweed, and other weeds.
About one-sixth of the total food is animal, consisting chiefly of
caterpillars, plant lice, scale insects, and grasshoppers. No
doubt the siskin pays, in the destruction of these pests, for the
forest seeds it consumes."
Two decades later Dorothy Mierow (1946), having more published
information to summarize, wrote:
They feed their young mainly on aphids and seem quite
content with alder, birch, and willow seeds. As they wander
farther south and over the plains, their main items of diet may
become weed seeds. Farther east, seeds of sweet gum, maple, and
elm, as well as buds and insects, form part of their diet. In
California, where they seem to be most numerous, they often feed
almost entirely on the seeds of eucalyptus, extracting them from
the pods either on the trees or on the ground. They also seek
after the sweet liquid in the eucalyptus flowers.
The following information elaborates on the taking of some of
the items already mentioned. Also, in some measure, it indicates
seasonal and geographical variation in food habits, plus
mentioning some items taken that might not be readily identified
in analysis of contents of digestive tracts.
In early April in Ohio, examination of a siskin revealed it had
been feeding on flower buds of the slippery elm (Kemsies, 1948).
In June in West Virginia, Maurice Brooks (1943) saw siskins avidly
eating the coated carpels of young spruces. Mr. R. E. Mumford
writes of seeing birds feeding on Jack pine cones (Pinus
banksiana) during an invasion of Indiana during the winter of
1952-1953.
After Oct. 4, 1889, at Lake Umbagog, Maine, they were feeding
exclusively on the seeds of birches (Brewster, 1938). John F.
Ferry (1907) writes that, in winter in northeastern Illinois,
"they were observed to feed industriously on coneless
branches of pines and spruces. The object sought was probably the
dry resinous aments of these conifers. They frequent patches of
thistle and seed-bearing weeds and work very actively in perfect
silence."
In South Carolina in the winter of 1896-97, a time of siskin
abundance there, Arthur Wayne (1906) observed them "feeding
on the seeds of sweet gum (Liquidamber styraciflua), and
shortleaf pine (Pinus mitis)."
During a winter and spring when siskins were common at San
Diego, Calif., F. F. Gander (1929b) noted that their food was
almost entirely seeds of various species of eucalyptus, which they
obtained from pods on the trees and also among fallen leaves.
In Flathead County, Mont., on Aug. 7, 1915, A. D. DuBois
recorded pine siskins eating thistle seeds along the railway.
"I watched one for some time. He would fly up to a thistle
head and, clinging to it, sometimes nearly upside down, would pull
out the cottony tufts one or two at a time, very dexterously and
rather rapidly, working his bill along to the seed which he
removed and then threw the fluff to the breeze, immediately
working out another tuft. He pulled them part way out, a bunch at
a time, afterward slipping them along until they came out one at a
time or sometimes two." In North Dakota, O. A. Stevens
wondered how the siskins got dandelion seeds. On investigation he
found that they did not wait for the heads to open, but pulled off
some of the bracts and took the seeds before they were fully ripe.
In two areas, on opposite sides of the continent, the siskin
has reportedly done extensive damage to vegetable and flower
gardens. From Independence Lake, British Columbia, T. and E.
McCabe (1929) write regarding areas recently opened to farming:
None of us who have vegetable gardens have been spared by
the siskins. Our own case is the most extreme, as we have
attracted the species by means of amazingly effective salt and
clay baits for banding purposes. It is now impossible to raise
most vegetables except under wire. In rather long experience of
gardens and their pests we have seen nothing to rival the
instantaneous devastation which an unobtrusive flock of siskins
can inflict, often before their presence in a garden has been
noticed. Not once, but season after season, and time after time
within the same season, we have seen long rows of seedling beets,
chard, lettuce, radishes, and onions, cut neatly to the ground. .
. . Peas and cole crops, as far as we know, are not taken, but we
hear of the destruction of turnips. . . .
The farmers nearer the Fraser [River] suffer as much
as we do and, in spite of being further from the mountains, more
than most of our nearer neighbors. We know of one ranch where for
years a barn door has been used as a deadfall, and the birds fed
to hogs by the bucketfuls. In another case great numbers are shot,
and as many as thirty-five have been picked up as the result of
enfilading a row of vegetables with a single charge of shot. As
the typical associations of the Canadian Zone are left behind, and
the greater drouth and summer heat of the river flats approached,
the nuisance decreases. From the immediate vicinity of Quesnel we
hear a few scattered complaints of moderate losses, but a short
distance southward, within touch of the long arm of Transition
Zone conditions, which stretches so far up the valley, all
knowledge of the trouble seems to disappear, though we do not know
where it may recur.
In Maine, siskins occurred in thousands in the spring and
summer of 1925. Forbush (1929) states that they "invaded
gardens, stripped beets, beans and other plants of their leaves,
and ate the blossoms of many flowering plants." A
correspondent in Patten, Maine, wrote Forbush that he had seen
"as many as a thousand birds on a half acre."
Both the insect foods and ways of obtaining these are varied.
In Ohio during a "most unseasonable and heavy snow in early
October, these little birds surrounded our houses and literally
skimmed the outer walls of all insect life. From foundation to
eaves they hunted in every nook and corner, capturing spiders,
flies, cocoons. . ." (J. L. Parsons, 1906).
In February at Alameda, Calif., an oak (Quercus agrifolia)
was swarming with siskins. F. N. Bassett (1923) noted that the
birds were procuring their food from the lower surfaces of the
leaves. Many leaves were afflicted with the gall of a saw-fly, Callirhytis
bicornis. Bassett reports: "The galls were attached to
the midrib or a lateral vein on the lower surfaces of the leaves.
They were composed of leaf material, light green in color (lighter
than the leaf), from two to four millimeters long and shaped
somewhat like a miniature saddle, being depressed in the middle
and rising to an apex at both ends. Each contained a minute
milky-white grub and many close views revealed the birds
'shelling' the galls and devouring the contents exactly as a
domestic canary shells its seeds."
In February at Berkeley, Calif., T. L. Rodgers (1937) writes
about siskins feeding in Monterey cypress:
I was unable at first to determine by observation, exactly
what the birds were eating, so I collected one hundred cypress
tips, averaging three inches long and representative of places all
over the side of a tree on which I watched many siskins foraging.
Examination of the cypress tips showed many psocid-like insects,
many scale insects, a few small green caterpillars, and many
yellow larvae that were inside thin-walled cavities in enlarged
green vegetative tips. There were few indications of broken-off
vegetative tips, but some were damaged, which probably indicated
that some of the yellow larvae had been torn from their chambers.
The indication was quite definite that the siskins were taking
only insect food.
Rodgers also saw a siskin picking aphids which it fed to a
young bird just out of the nest. In April at Seattle, Wash., S. F.
Rathburn recorded this observation: "I noticed that, when
alighting on any older limb, the siskins would examine it closely
until its extremity was reached, and this was particularly the
case when any had the appearance of being dead. Then the bird
would clip or break off the twig's end. I examined one of the
twigs that fell and, in breaking it, I found deeply embedded
within a fat grayish-green grub, evidently the larva of a
twig-boring insect. This explained the siskins' actions."
The McCabes (1929) mention the attraction that salt and clay
have for siskins. In an earlier article (1928) they state:
"The attraction has always been some mineral food, relish, or
medicament, natural or artificial. Ashes, deep blue clay from a
cellar hole, salt, and newly-set Portland cement have all had
their periods of favor." The habit has been noted in
different seasons at widely separated points. Mierow (1946) made
the general statement that a "necessary item in the siskin's
diet, as well as in that of other boreal finches, is some kind of
mineral salt." D. S. Farner (1952) reported this habit in
Crater Lake National Park as follows: "Although to a much
lesser extent, siskins display 'salt-feeding habits' similar to
those of the Red Crossbills. Especially during the summer of 1951
it was possible to observe siskins pecking at the powdery crusts
on the andesite rocks."
In the first half of March 1941, between Saranac Lake and
Tupper Lake, N.Y., the road had been treated with a mixture of
sand and calcium chloride--the latter apparently added as a binder
for the former. G. M. Mead (1942) quotes an observer as follows:
For several days great numbers of White-winged Crossbills
and small numbers of Red Crossbills and Pine Siskins settled on
the road to eat the salt. The roadbed was covered with them and it
was almost impossible to scare them away even by using the horn.
They appeared to be too sick to rise and even though motorists
drove slowly they were killed in great numbers. The surface of the
snow-covered road was actually reddened by the blood and feathers
of the birds. My estimate is that there were at least a thousand
birds killed.
From Rutherglen, Ontario, it is clear from the following
observations for the winter of 1947-48 by Louise de Kiriline
Lawrence that salt in some form is a real desideratum of siskins.
She writes: "At this time, the birds were encountered chiefly
on the highway where they assembled in dense flocks, eating gravel
mixed with chloride. Soon after sun-up they began to appear in
these places with their numbers reaching a peak around midday,
followed by a slow decline until, just before sunset, the last
flock flew away to roost. Many of these birds apparently travelled
considerable distances to these cherished feeding places; I saw
birds winging their way to and from the highway from the woods at
least a mile away. When disturbed, the birds swung off the road as
of one accord, amid excited twitter, to alight in the trees
alongside and there continue their feeding on the seeds of the
evergreens, or on the buds of the white birches and aspen trees,
with the siskins showing particular liking for the seeds of the
alder-bushes. The siskins were a gregarious lot, associating
freely with all the other finches, especially the Goldfinches and
the Red Crossbills.
"The pine siskins were first attracted to my feeding place
under the pines, a little off the highway, by the coal ash pile.
One day they dropped down from the surrounding trees by the
dozens. I counted 92 before I got too mixed up by their numbers,
all clustered into a little space 10 inches by 10 inches in front
of my window. They ate the ash-dusted snow mixed with slop water.
On an old cedar stump I kept a block of salt. From rain and snow
and the humidity of the air, the salt had saturated the stump and
this saltlick became hereafter the number one attraction. The
birds crawled over the stump and picked the salt crystals from the
block itself as well as from the top and the underparts of the
stump, where the deposition of crystals was richest, and from the
gravel around it, where the snow had been melted away by the salt.
I put baited traps near the saltlick, hoping for some good
banding, but not until I changed the bait to dried cedar seeds did
my banding luck turn. These seeds proved irresistible to the
siskins and when my supply ran out I put small dishes of water in
the traps with the same excellent results. Thus, from January 7 to
May 29, I banded 337 pine siskins."
Siskins can be attracted to feeding stations by millet seed and
by chaff, and Forbush (1929) states that they are "extremely
fond of cracked butternuts." They eat many of the vegetable
foods commonly used at feeding or banding stations, and eat suet
occasionally. In winter at Leominster, Mass., E. R. Davis (1926)
notes that whenever "an Evening Grosbeak came to the
feeding-shelf and began cracking the seeds, he would be surrounded
by several of the siskins. As he cracked the seeds, some particles
of the kernel would scatter from his beak, and immediately the
siskins would rush in and gobble them up. This act was not much
relished by the Grosbeaks and they would often show their
displeasure by a vicious peck at the intruder. . . ."
Dishes of water, for drinking and bathing, have been used to
bait siskins into traps for banding. At Sioux City, Iowa, a basin
of water was placed under a nesting tree and both parent siskins
came to drink and bathe (Hayward and Stephens, 1914). In March at
Berkeley, Calif., T. L. Rodgers (1937) observed:
Several times, I saw siskins approach [eucalyptus]
blossoms from above, lean over and reach into them. I had supposed
they were after insects attracted by the flowers, but twice I
noticed that after reaching into the blossoms, they raised their
heads after the manner of a chicken drinking. I gathered a large
bunch of the blossoms and in every one examined found several
drops of clear sweet liquid, with only a slight eucalyptus flavor.
Later, I saw more siskins drinking from flowers, also a junco.
At Macon, Ga., in late December, a siskin was observed at
borings made by a yellow-bellied sapsucker in the trunk of a sweet
gum. The sapsucker chased it away (H. L. Batts, 1953).
Field marks.--It is somewhat
difficult to distinguish at a distance between the pine siskin,
the goldfinches, and the redpolls. Not only do these various birds
mingle in flocks, but their size, manner of flight, call notes,
and general habits, are all quite similar. The siskin, however, is
characterized in all seasons by its dusky-streaked plumage (on
grayish brown base above, more or less whitish or buffy below) two
light wing bars, and, usually, considerable yellow on the basal
portions of its wing and tail flight feathers. It has no red on
its crown or black on its throat as the redpolls do. Siskins in
juvenal plumage have the adult pattern but, for some time after
they first fly, they are readily distinguished from their elders
at close range by the worn plumage of the latter, the young being
much buffier, their underparts often tinged with pale yellow, and
their overall appearance lighter. Our siskin at any age is fairly
similar in color and pattern to the female and juvenal Spinus
spinus, the siskin of the Old World--a species in which the
adult male is redpoll-like in having a crown patch (which is black
in the siskin) and a blackish chin.
Voice.--Various utterances
frequently are compared with those of the goldfinch, redpolls, and
canary. Call notes are given in chorus, especially when the birds
alight or rest. Descriptive words commonly used by describers of
siskin call notes are: weak, thin, lispy, buzzy, wheezy, and
churring. In general their calls are more husky than those of the
American goldfinch.
Ralph Hoffmann (1904) describes the common call notes as "chee-ee
given in a husky tone; when flying it utters a note like the
syllables tit-i-tit. Another very sweet call, often given
by a single bird to call back the flock, is identical with a note
of the American Goldfinch." In winter at Anniston, Ala., R.
H. Dean (1923) observes that, when siskins took flight, their
utterances were tit-i-te, tit-i-te, several times in
succession; sometimes notes were a smoother see-a-wee. On
March 22, a new note was recorded, z-z-z-z-z (a prolonged z),
weak, as are all the notes, but rather harsh. The z notes
seem to be part of the song, "a weak prolonged chittering
performance interspersed with the louder z-z-z-z
notes." A. A. Saunders (1935) points out that the siskin has
an "undulatory flight, calling tit-a-tit with each
undulation." He also mentions a "husky but sweet swi-sieee,
slurring upward at the end, much like the Goldfinch's similar
note, except for the huskiness. He says that the siskin's song is
uttered in choruses and that mixed choruses are heard when
goldfinches and siskins flock together. The latter's song much
resembles the former's, being a "long-continued series of
notes, groups of two-note phrases, or single notes and long
trills." The quality is "husky, and the trills fricative
and like a loud long whisper."
From Rutherglen, Ontario, Louise de Kiriline Lawrence sends
this observation: "From this day [January 29], the Pine
Siskin's singing became common all over the woods. It was
particularly intensive during the morning and early forenoon. The
birds sang from perches, sometimes from the top of a bush along
the road, at other times from the highest twig of the tallest
tree. Their song included some of their common notes, which seemed
to serve as punctuations between the more elaborate sentences and
a 'vireo' song, very like that of the Purple Finch, only with the
performance in keeping with the Siskin's smaller size. A 'churry'
(not 'burry') note was also interpolated often in the
singing, so like that of the Evening Grosbeak that I several times
mistakenly thought the Grosbeaks were present unseen amongst the
trees. The weather had no effect whatever on the Siskins' vocal
ardor, be the day dull and mild, or cold and clear with the
temperature far below zero."
From Camrose, Alberta, F. L. Farley writes me as follows of a
siskin found injured on November 29 and kept in a cage: "It
is now more than two months since we have had him and we are all
surprised with his musical ability. Between daylight and noon
every day he sings just as continuously as most of the tame
canaries, and the most interesting thing we have learned is that
he combines the well known notes of Goldfinch and Redpoll and the
rich ones of the tame Canary. Then, in between these songs come
the nasal squeez or issch so diagnostic of the
Siskin in its wild state. As I write now, he is singing quite
steadily, and in between songs he gives the Canary e-r-e.
His songs are on a low scale and cannot be heard more than a third
of the distance that a tame Canary's voice carries."
Enemies.--Friedmann (1963) writes:
"Generally, the pine siskin is ecologically allopatric with
the brown-headed cowbird, a fact which effectively protects it
from the attentions of the parasite. However, there are places
where the two species overlap and here the siskin is occasionally
imposed upon. Eleven such instances have come to my notice,
distributed among the following states: Iowa, Kansas, Nebraska,
South Dakota; and in Canada: Ontario and British Columbia."
To these may be added N. J. Ilnicky's (1963) observations of a
pair of siskins feeding a newly fledged cowbird in Marquette,
Michigan, on July 11, 1962.
Pine Siskin*
Carduelis pinus
Contributed by Ralph S.
Palmer
*Original Source: Bent,
Arthur Cleveland and collaborators (compiled and edited by Oliver
L. Austin, Jr.). 1968. Smithsonian Institution United States
National Museum Bulletin 237 (Part 1): 424-447. United States
Government Printing Office
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