Petrochelidon pyrrhonotacliff swallow

Ge­o­graphic Range

Cliff swal­lows (Petroche­li­don pyrrhonota) oc­cupy areas of North Amer­ica and Cen­tral Amer­ica based on whether it is breed­ing sea­son or the mi­gra­tion sea­son. The breed­ing range be­gins as far north­west as Alaska, and ex­tends south down the west­ern coast of the United States through Cal­i­for­nia into cen­tral Mex­ico (Mex­i­can plateau south to cen­tral Oax­aca). The breed­ing range ex­tends east­ward through the Rocky Moun­tains and mid­west sec­tions of Canada and the United States and stops in east­ern Texas. This range in­cludes parts of Ten­nessee, west­ern North Car­olina, Vir­ginia, and West Vir­ginia. The breed­ing range ex­tends back north­ward through the north­east­ern states of the United States north­ward into On­tario and Que­bec. The north­ern limit of the breed­ing range roughly ends where at the tree­line's edge (around el­e­va­tion 3050m), but colonies have been found fur­ther north.

The win­ter range ex­tends south along the west­ern coast of Mex­ico, to the boarder of Colom­bia and ex­tends north­ward along the east coast of Mex­ico. The mi­gra­tion range also ex­tends through­out the south­east­ern United States with colonies in Florida, Geor­gia, Al­abama, Mis­sis­sippi, Louisiana, east­ern Texas. They are also found through­out parts of Ten­nessee, Ken­tucky, South Car­olina, North Car­olina, and parts of Vir­ginia, West Vir­ginia, and Ohio. Cliff swal­lows also mi­grate south­ward into Cuba, Puerto Rico and the Ba­hamas. There have also been mul­ti­ple sight­ings of the birds mi­grat­ing into South Amer­ica, south through Paraguay, Ar­gentina, and Bo­livia mainly, but the def­i­nite range is un­known.

Va­grants of cliff swal­lows have also been found on Wrangel Is­land, Green­lad, Siberia, and the British Isles, but find­ings have been rare and few. (Brown and Brown, 1995; ; Brown and Brown, 2000a; Brown, 2010; Brown, et al., 2015a; BirdLife In­ter­na­tional, 2012; Mc­Nair, 2013; Sother­land, et al., 1980; Tum­li­son, 2009)

Habi­tat

Cliff swal­low breed­ing habi­tat in­cludes canyons, hills, val­leys, and cliff faces. Man-made build­ings and struc­tures also pro­vide shel­ter for nest­ing areas; any areas that have build­ings or bridges serve as pos­si­ble nest­ing sites, ex­pand­ing their breed­ing areas to grass­lands and towns. Any nest­ing areas with ac­cess to water/mud spots are ben­e­fi­cial, be­cause of the avail­abil­ity of food and nest­ing ma­te­ri­als. Nest­ing typ­i­cally takes place from sea level to 2770m, but can be as high as 3200 m.

Habi­tats dur­ing the win­ter in­clude coast­lines and other in­land bod­ies of water. Very lit­tle in­for­ma­tion is avail­able on the habi­tat of cliff swal­lows dur­ing mi­gra­tion. Cliff swal­lows may tar­get wa­ter­bod­ies while mi­grat­ing, as a source of in­sect prey.

Very lit­tle is known about their habi­tat dur­ing the win­ter, but cliff swal­lows are known to use grass­lands, agri­cul­tural areas, towns, and marshes. (Brown and Brown, 1995; Brown and Brown, 2000a)

  • Aquatic Biomes
  • lakes and ponds
  • rivers and streams
  • coastal
  • Range elevation
    0 to 3200 m
    0.00 to 10498.69 ft

Phys­i­cal De­scrip­tion

Cliff swal­lows have square tails with an or­ange rump, and their throats have a chest­nut hue. Adults have chins, throats, and sides of the neck that are tipped with a chest­nut color. Their breasts are white or cream-col­ored. Some birds will have a cream or white tri­an­gu­lar-shaped fore­head patch, and a black or blue-ish crown. The birds' rumps can be pink. The bill of cliff swal­lows is black. The legs and feet are both brown in adults while ju­ve­niles are pink with a slight cin­na­mon hue.

The av­er­age mass of these birds ranges from 22.22 to 24.15 g. Length of cliff swal­low ranges from 127 to 152.4 mm, and wingspans range from 279.4 to 299.72 mm. They ex­hibit lit­tle sex­ual di­mor­phism, as the only dif­fer­ence is a larger dark blue patch on the throat of males.

Plumage for ju­ve­niles is duller than the plumage of adults. The col­ors on their throats and fore­heads vary con­sid­er­ably among in­di­vid­u­als of this age. Nestlings have a slight bit of yel­low, with brown irises.

Cliff swal­lows dif­fer mor­pho­log­i­cally from other North Amer­i­can swal­lows in that their heads and necks are thicker. Color pat­terns also dis­tin­guish these cliff swal­lows. (Brown and Brown, 1995; ; Brown and Brown, 2000b; Brown and Brown, 2011)

  • Sexual Dimorphism
  • male more colorful
  • Range mass
    22.22 to 24.15 g
    0.78 to 0.85 oz
  • Range length
    127 to 152.4 mm
    5.00 to 6.00 in
  • Range wingspan
    279.4 to 299.72 mm
    11.00 to 11.80 in

Re­pro­duc­tion

Birds are so­cially monog­a­mous and ge­net­i­cally polyg­a­mous. Cliff swal­lows will choose a mate with which to raise nestlings, but both the males and fe­males will mate with other birds.

Cliff swal­lows will began pair for­ma­tion when nest own­er­ship and build­ing starts. Males and fe­males both con­tribute to­wards build­ing the nest dur­ing the breed­ing pe­riod, but males may get a head-start and begin build­ing be­fore fe­males ar­rive for the sea­son. The nests are mud-based and have a domed shape, typ­i­cally 1.5-10 above the ground or water's sur­face. It's not un­com­mon for nests from the pre­vi­ous year to be re­fur­bished and reused by a new pair.

These birds gen­er­ally have an in­for­mal courtship based on the twit­ter-squeak song to find mates. No vi­sual dis­plays or ad­di­tional courtship ef­forts are part of courtship. Singing by males de­clines after eggs are laid and in­cu­ba­tion starts.

Cop­u­la­tion can start in un­fin­ished nests, as the pair works to­gether to com­plete it. Males use the "churr" call to start cop­u­la­tion and at­tract the fe­males to the back of the nests. Cop­u­la­tion may be at­tempted mul­ti­ple times by the males. One brood per sea­son is com­pleted. (Brown and Brown, 1995; ; Brown and Brown, 2000b; Brown, et al., 2015b; Brown, et al., 2015a)

The breed­ing sea­son lasts from mid-April until mid-June, and egg-lay­ing may begin be­fore nests are fin­ished. Lay­ing oc­curs in the morn­ings at or be­fore 0800, and one egg per day is laid. The range per brood is 1-6 eggs, and the av­er­age is 4. The pairs need to guard the nests be­cause con­specifics may in­vade and ei­ther brood par­a­sitize (lay eggs for other pairs to raise) or force­fully re­move eggs from the nest. If a nest com­pletely fails, the pair may at­tempt a sec­ond, smaller brood of about 3 eggs, on av­er­age.

In­cu­ba­tion starts within three days after the first egg is laid and will con­tinue until the last one is laid. The pe­riod of in­cu­ba­tion varies de­pend­ing on lat­i­tude (north­ern colonies take longer), but typ­i­cally is 13.5 days (range 10-19 days).

Hatch­lings will lack plumage at the time of hatch­ing and will have a mass of 1.6 to 2.2 g (av­er­age 2.0 g). It takes the young typ­i­cally 20-26 days (av­er­age 22 days) to fledge and be­come fully grown. The birds will be­come fully in­de­pen­dent and began trav­el­ing at around 6 weeks old (range 5-8 weeks). Sex­ual ma­tu­rity for fe­males is reached in 42 to 50 days (av­er­age 45), 40 to 48 days in males (av­er­age 43). (Brown and Brown, 1995; Brown and Brown, 2000b; Brown, et al., 2015b; Brown, et al., 2015a; Weaver and Brown, 2004)

  • Breeding interval
    Cliff swallows will breed once per breeding season.
  • Breeding season
    Breeding occurs from mid-April to mid-June.
  • Range eggs per season
    1 to 6
  • Average eggs per season
    4
  • Range time to hatching
    10 to 19 days
  • Average time to hatching
    13.5 days
  • Range fledging age
    20 to 26 days
  • Average fledging age
    22 days
  • Range time to independence
    5 to 8 weeks
  • Average time to independence
    6 weeks
  • Range age at sexual or reproductive maturity (female)
    42 to 50 days
  • Average age at sexual or reproductive maturity (female)
    45 days
  • Range age at sexual or reproductive maturity (male)
    40 to 48 days
  • Average age at sexual or reproductive maturity (male)
    43 days

Par­ents are in­volved greatly be­fore the eggs hatch and gen­er­ally be­come less in­volved after fledg­ing. Males and fe­males both share the re­spon­si­bil­i­ties of pro­tect­ing eggs dur­ing in­cu­ba­tion. They will in­cu­bate the eggs while the other sex is out of the nest. Nest-guard­ing is a nec­es­sary ac­tion, as other cliff swal­lows may at­tempt to add or re­move eggs from neigh­bor­ing nests,.

After hatch­ing, both sexes will pro­tect the young for 2-3 days. The par­ents gen­er­ally con­tinue to feed fledg­lings but start to lessen their in­vest­ment in pro­tect­ing them as fledg­ing con­tin­ues. (Brown and Brown, 1995; ; Brown, et al., 2015a; Weaver and Brown, 2004)

  • Parental Investment
  • pre-fertilization
    • protecting
      • male
      • female
  • pre-hatching/birth
    • provisioning
      • male
      • female
    • protecting
      • male
      • female
  • pre-weaning/fledging
    • provisioning
      • male
      • female
    • protecting
      • male
      • female

Lifes­pan/Longevity

The high­est recorded lifes­pan for a cliff swal­low was 11 years, as was ob­served from two birds in Ne­braska. There is nei­ther recorded av­er­age lifes­pan nor any in­for­ma­tion col­lected for cliff swal­lows in cap­tiv­ity. These birds typ­i­cally are not kept in cap­tiv­ity.

The prob­a­bil­ity of sur­vival of birds was recorded dur­ing their pe­ri­ods of growth. Cliff swal­lows have an an­nual prob­a­bil­ity of sur­vival of 0.17 dur­ing their first year of growth, Brown and Brown (1995). This prob­a­bil­ity in­creases in the fol­low­ing years, up to 0.57 an­nu­ally. There is no dif­fer­ence be­tween male pop­u­la­tions or fe­male pop­u­la­tions for sur­vival. But, there is yearly vari­a­tion in adult pop­u­la­tions rang­ing from 0.47-0.64. (Brown and Brown, 1995; ; Brown, et al., 2008; Brown, et al., 2015b)

  • Range lifespan
    Status: wild
    11 (high) years

Be­hav­ior

Cliff swal­lows hold the largest colony sizes among all species of swal­lows. Colony size can range from 200-3700 total nests in the area (Brown and Brown 1995). Soli­tary nest­ing is rare, and typ­i­cally oc­curs in close prox­im­ity to an­other large colony. These birds prac­tice brood par­a­sitism in their colony, lay­ing eggs in the nests of neigh­bors. This lessens the re­pro­duc­tive ef­fort for the layer and max­i­mizes re­pro­duc­tive out­put. This has the op­po­site ef­fect on the oc­cu­pants of the nest. When de­fend­ing nests, the birds will puff out feath­ers to ap­pear larger. The white patches on cliff swal­lows' fore­heads may be used as a dis­play of own­er­ship of a nest.

Cliff swal­lows fight when se­lect­ing nest­ing areas. Many nests are ex­ist­ing ones from pre­vi­ous years, so re­pair and restora­tion is all that's needed. Birds use both their beaks and wings to at­tack one an­other and fights can last up to 15 min­utes.

Not all cliff swal­low in­ter­ac­tions are neg­a­tive. These birds may play while perched on high wires. Birds will at­tempt to knock one an­other off the wire and take their spots on the wire. This type of play will hap­pen for a short pe­riod of time and then nor­mal perch­ing oc­curs again. Birds also will al­lo­preen (clean one an­other) on high sur­faces like pow­er­lines close to the colonies, in large groups. The birds on the outer perime­ter of preen­ing groups will spend most of the time watch­ing for preda­tors. Preen­ing gen­er­ally hap­pens in the mid-end of sum­mer dur­ing pe­ri­ods of sun­rise and sun­down. Al­lo­preen­ing birds also will at­tack one an­other for un­known causes.

Birds also will chase one an­other in spring which could be part of their mat­ing be­hav­iors, be­cause the twit­ter-squeak song is usu­ally ac­com­pa­ny­ing these chases.

Cliff swal­lows will sun­bathe by rolling to one side and ex­pos­ing the ma­jor­ity of their bod­ies to the sun­light. This mainly oc­curs when al­lo­preen­ing is tak­ing place. They gen­er­ally don't swim and ac­tual bathing is un­com­mon.

Cliff swal­lows are speedy, ef­fi­cient fliers. Flight al­ti­tudes range for birds from ground level to 60 m above ground. Flap speed will in­crease when mak­ing ma­neu­vers or climb­ing in al­ti­tude. The tail is also out­spread dur­ing turns. Cliff swal­lows will make these fast ma­neu­vers when chas­ing their prey and flare tails after catch­ing prey.

Mi­gra­tion takes place in late sum­mer, and birds will mi­grate south­ward into South Amer­ica along the coast­lines. Cliff swal­lows will re­main in large groups dur­ing the non-breed­ing sea­sons. Birds may also be no­madic dur­ing the win­ter times. Cliff swal­lows then mi­grate back into North Amer­ica in early April. (Blake, 1948; ; Brown and Brown, 2002; Brown, 2010; Brown, et al., 2015b; John­son and Freed­berg, 2014; With­ers, 1977)

  • Average territory size
    <1 m^2

Home Range

Colonies in the spring gen­er­ally range from 2-15 km for males and 9-14km for fe­males. For­ag­ing gen­er­ally hap­pens in a 1.5 km ra­dius around the colony. For­ag­ing out­side this area some­times hap­pens up to 6km out­side the re­gion.

Ter­ri­to­ries are re­stricted to the ac­tual nest site that pairs will de­fend in the breed­ing sea­son. These nests are mud domes, and pairs will at­tack neigh­bors who try to build nests within 8-12 cm from their nest open­ing. There­fore, ter­ri­tory sizes are neg­li­gi­ble. (Brown and Brown, 1995; ; Brown and Brown, 2002; Brown, 2010; Brown, et al., 2015b; John­son and Freed­berg, 2014)

Com­mu­ni­ca­tion and Per­cep­tion

Vo­cal­iza­tion is the main route of com­mu­ni­ca­tion for cliff swal­lows. Nestlings can vo­cal­ize at 5-6 days old. These swal­lows' vocal range con­sists of five main vocal calls. These are: beg­ging call, purr call (alarm), chur call (mul­ti­ple uses), twit­ter-squeak song (courtship and nest­ing), and squeak call (for­ag­ing). Males most likely only make the twit­ter-squeak call, but both sexes make the other four. Each bird has a dis­tinc­tive call that is dis­tin­guish­able by 15-18 days old, and, for ge­netic rea­sons, sib­lings ex­press sim­i­lar calls. The beg­ging call of youths be­comes the "chur" call once adult­hood is reached. Cliff swal­lows are also able to make their alarm call by week 6.

Vo­cal­iza­tion also varies by sea­sons. Vo­cal­iza­tion is at its low­est for these birds dur­ing the win­ter. There ap­pears to be no ef­fect on vo­cal­iza­tion due to time of day. How­ever, lo­ca­tion is in­flu­en­tial, as three of the calls (beg­ging, chur, twit­ter-squeak) occur only in­side the next.

The purr and chur calls are used dur­ing the nest­ing and breed­ing sea­son. The twit­ter-squeak call is mainly used in spring and de­clines once mates are found, but is used again in late sum­mer when de­fend­ing nests. The squeak call is used dur­ing breed­ing in mid­sum­mer. The beg­ging call is used pri­mar­ily from youth to par­ents for food and recog­ni­tion of the youth. Brown and Brown (1995) re­ported that cliff swal­lows in Wash­ing­ton will evict young that are not theirs from nests, while those in Ne­braska do not. Adult birds dis­tin­guish which young is theirs based on the beg­ging call. The purr call is used for when preda­tors are threat­en­ing. Though di­rected at the preda­tor, it may cause other colony mem­bers to come out of their nests in re­sponse. When the purr call is in the ab­sence of preda­tors, its goal may be to allow the caller to in­trude upon oth­ers' nests. The chur call ap­pears to have mul­ti­ple uses be­tween pairs, par­ents, off­spring, or nearby nests.

Vi­sion and tac­tile senses are im­por­tant in the colo­nial group, and they al­lo­preen, fly to avoid one an­other, and play peck­ing games on high­wires. Their sense of hear­ing also is im­por­tant, es­pe­cially for par­ents to rec­og­nize the calls of their young. (Brown and Brown, 1995; ; John­son and Freed­berg, 2014; Weaver and Brown, 2004)

Food Habits

Cliff swal­lows' main source of food is fly­ing in­sects. It ap­pears that in­sects are taken op­por­tunis­ti­cally, with­out pref­er­ence for cer­tain or­ders or fam­i­lies. How­ever, cliff swal­lows' diets may in­clude more swarm­ing species than not, do to the na­ture of ef­fi­ciently con­sum­ing large vol­umes of in­sects.

Oc­ca­sional in­ges­tion of seeds and gravel has been re­ported, as these could help break up food dur­ing di­ges­tion. Dur­ing for­ag­ing, cliff swal­lows feed from 50m and above from ground level. Gen­eral for­ag­ing areas are grassy areas, but lakes, ponds, and rivers are also sources of food when the in­sect pop­u­la­tion is low in the area. Some pop­u­la­tions have in­di­vid­u­als that will for­age on the ground, con­sum­ing ter­res­trial in­ver­te­brates, like ants.

Cliff swal­lows are di­ur­nal for­agers and feed in groups of 2-1000 birds at times. They use the pres­ence of other in­sect eaters as a sig­nal of where to feed, then swarm the feed­ing area for in­sects. Ther­mals (up­ward wind cur­rents) also are lo­ca­tions where in­sects con­cen­trate, so the birds often tar­get these. Feed­ing is gen­er­ally in­tense be­fore the nest­ing sea­son and lasts all day long dur­ing the nest­ing sea­son. The birds will travel out of the colonies to feed in shorter but more fre­quent bursts dur­ing the nest­ing sea­son. (Brown and Brown, 1995; ; Brown and Brown, 2002)

  • Animal Foods
  • insects
  • Plant Foods
  • seeds, grains, and nuts

Pre­da­tion

Birds and snakes are the major preda­tors of cliff swal­lows. The birds and that are preda­tors of cliff swal­lows are sharp-shinned hawks (Ac­cip­iter stria­tus), Amer­i­can kestrels (Falco sparverius), barn owls (Tyto alba), great horned owls (Bubo vir­gini­anus), black-billed mag­pies (Pica pica), log­ger­head shrikes (La­nius lu­dovi­cianus), com­mon grack­les (Quisalus quis­cula), pere­grine fal­cons (Falco pere­gri­nus), prairie fal­cons (Falco mex­i­canus), and Mis­sis­sippi kites (Ic­tinia mis­sis­sip­pi­en­sis). The snakes that are preda­tors are bull snakes (Pituophis catenifer) and rat­tlesnakes (Cro­talus).

Amer­i­can minks (Neo­vi­son vison) and red im­ported fire ants (Solenop­sis in­victa) also can be preda­tors of these birds.

House spar­rows (Passer do­mes­ti­cus), acorn wood­peck­ers (Melan­er­pes formi­civorus), red-headed wood­peck­ers (Melan­er­pes ery­thro­cephalus), and deer mice (Per­omyscus man­ic­u­la­tus) will prey on eggs of cliff swal­lows.

The cliff swal­lows re­sponse to preda­tors is warn­ing other birds in the colony with the purr call. They will exit the colony, when fal­cons or hawks at­tack, in a mass flock to evade them. Preda­tors un­der­stand that they are de­tected when this oc­curs and will leave. Cliff swal­lows use the purr call for ground preda­tors as well.

Large colonies are a ben­e­fit to cliff swal­lows be­cause, with the larger size comes the ben­e­fit of de­tectabil­ity. More nests and colony size makes it eas­ier for the birds to de­tect in­com­ing preda­tors from the out­side. (Brown and Brown, 1995; Fajer, et al., 1987; Jones, 1883; Tum­li­son, 2009)

Ecosys­tem Roles

Cliff swal­lows may spread plant seeds dur­ing nest­ing and mi­gra­tion. Birds will com­pete for nests with barn swal­lows (Hirundo rus­tica) and con­vert them to the cliff swal­low style nest. Cliff swal­lows are also brood par­a­sites within their colonies.

A study by Brown and Sethi (2002) also found that mos­quito abun­dance was pos­i­tively re­lated to colony size. The au­thors could find no weather con­nec­tions or Ju­lian date is­sues to in­flu­ence this trend, and hy­poth­e­sized that mos­quito species were drawn to the large mud colonies in some way.

The par­a­sites that af­fect cliff swal­lows range from cimi­cid bugs Oe­ci­a­cus vic­ar­ius, ticks, fleas, dipter­ans, der­mestid bee­tles, lice, mites, ne­ma­todes, ces­todes, trema­todes, acan­tho­cepha­lans, and pro­to­zoans.

The ec­topar­a­sitic ticks ob­served are: Ixodes baergi, Ixodes how­elli, Argas coo­leyi, Car­ios con­ca­nen­sis, Or­nithodoros turi­cata. Ec­toparas­tic fleas ob­served are: Cer­ato­phyl­lus cel­sus, Cer­ato­phyl­lus petroche­li­doni, Cer­ato­phyl­lus ar­cue­gens, Cer­ato­phyl­lus calder­woodi, Cer­ato­phyl­lus coahuilen­sis, Cer­ato­phyl­lus idius, Cer­ato­phyl­lus scop­u­lo­rum, and Hec­top­sylla psittaci. Dipter­ans, specif­i­cally blowflies, ob­served are: Pro­to­cal­liphora hirundo, Pro­to­cal­liphora asiovora, Pro­to­cal­liphora braueri, and Pro­to­cal­liphora sialia. Der­mestid bee­tles were ob­served af­fect­ing cliff swal­lows, but no spe­cific ge­nius or species has been listed. Feather lice ob­served are: Machaer­i­lae­mus malleus, Brueelia longa, Philopterus ex­cisus, and Mysidea dis­sim­ilis. Mites ob­served are: Der­manys­sus gal­li­nae, Der­manys­sus hirun­di­nis, Der­manys­sus triscu­ta­tus, Cheyle­tus, Or­nithocheyla, Hirstio­soma, Eu­tro­mibcula al­fre­du­ge­sia, Der­matophagoides evansi, Proc­to­phyl­lodes, and Ptilonys­sus echi­na­tus. Ne­ma­todes ob­served are: Had­jelia pyrrhonota, Acuaria, Mi­crote­trameres in­er­mis, Splen­did­ofi­laria, and Diplo­tri­aena. Ces­todes ob­served are: An­gu­larella audubo­nen­sis, An­gu­larella beema, Anon­chotae­nia glo­bata, Vitta mag­ni­un­ci­nata, Vitta parvi­rostris, Vitta ri­paria, and May­hewia aba­bili. Trema­todes seen are: Col­lyri­clum faba, Concin­num minor, Brachylecithum mar­in­ho­lutzi, Pla­giorchis mac­u­lo­sus, and Sto­my­lotrema gra­tio­sus. Acan­tho­cepha­lans in­clude: Mediorhynchus gran­dis and Mediorhynchus pa­pil­lo­sus. Pro­to­zoan blood par­a­sites that were also spot­ted in­clude: He­pa­to­zoon, Try­panosoma, Haemo­pro­teus, Leu­co­cy­to­zoon, and Isospara petroche­li­don. (Brown and Brown, 1995)

Com­men­sal/Par­a­sitic Species

Eco­nomic Im­por­tance for Hu­mans: Pos­i­tive

Like many other song­birds and other mi­gra­tory birds, cliff swal­lows con­tribute to­wards bird-watch­ing in many re­gions. (Brown and Brown, 1995; ; Brown and Sethi, 2002)

Eco­nomic Im­por­tance for Hu­mans: Neg­a­tive

There are no re­ported neg­a­tive ef­fects of cliff swal­lows on hu­mans.

Con­ser­va­tion Sta­tus

Cliff swal­lows are listed as species of "Least Con­cern" under The IUCN Red List and are pro­tected under the US Mi­gra­tory Bird Act. The US Mi­gra­tory Bird Act pro­hibits any hunt­ing of cliff swal­lows. This species, be­cause it's the edge of its range, is listed as "Threat­ened" in Penn­syl­va­nia and New Jer­sey. They are not listed on the CITES ap­pen­dices or on the US Fed­eral List.

Cliff swal­lows con­tract the Fort Mor­gan Virus, but it ap­pears to have no ad­verse ef­fects dur­ing the fledg­ing process. An­other un­known virus also af­fected mul­ti­ple birds in Ok­la­homa that also has no wit­nessed ef­fects on birds.

As a species that can ben­e­fit from human in­ter­ac­tion, cliff swal­low pop­u­la­tions have been re­port­edly in­creas­ing. Habi­tats for cliff swal­lows are en­hanced by man-made struc­tures such as bridges and build­ings as pos­si­ble nest­ing sites. Be­cause the birds are very tol­er­ant of human dis­tur­bance, human ex­pan­sion does not neg­a­tively im­pact cliff swal­lows.

There are state- and lo­cal­ity-based con­ser­va­tion ef­forts that have at­tempted to in­crease the pop­u­la­tion of cliff swal­lows in cer­tain areas. Ef­forts in­clude man-made nests being put up to at­tract cliff swal­lows to col­o­nize in cer­tain areas and help in­crease the cliff swal­low pop­u­la­tions in lo­cal­i­ties. Con­trol or elim­i­na­tion of com­pet­ing, in­va­sive house spar­rows Passer do­mes­ti­cus also has shown to have pos­i­tive im­pacts on cliff swal­lows. (Brown and Brown, 1995; ; BirdLife In­ter­na­tional, 2012)

Con­trib­u­tors

Joshua Tulppo (au­thor), Rad­ford Uni­ver­sity, Alex At­wood (ed­i­tor), Rad­ford Uni­ver­sity, Marisa Dameron (ed­i­tor), Rad­ford Uni­ver­sity, Karen Pow­ers (ed­i­tor), Rad­ford Uni­ver­sity, Tanya Dewey (ed­i­tor), Uni­ver­sity of Michi­gan-Ann Arbor.

Glossary

Nearctic

living in the Nearctic biogeographic province, the northern part of the New World. This includes Greenland, the Canadian Arctic islands, and all of the North American as far south as the highlands of central Mexico.

World Map

Neotropical

living in the southern part of the New World. In other words, Central and South America.

World Map

Palearctic

living in the northern part of the Old World. In otherwords, Europe and Asia and northern Africa.

World Map

acoustic

uses sound to communicate

agricultural

living in landscapes dominated by human agriculture.

arboreal

Referring to an animal that lives in trees; tree-climbing.

bilateral symmetry

having body symmetry such that the animal can be divided in one plane into two mirror-image halves. Animals with bilateral symmetry have dorsal and ventral sides, as well as anterior and posterior ends. Synapomorphy of the Bilateria.

carnivore

an animal that mainly eats meat

chemical

uses smells or other chemicals to communicate

coastal

the nearshore aquatic habitats near a coast, or shoreline.

colonial

used loosely to describe any group of organisms living together or in close proximity to each other - for example nesting shorebirds that live in large colonies. More specifically refers to a group of organisms in which members act as specialized subunits (a continuous, modular society) - as in clonal organisms.

crepuscular

active at dawn and dusk

diurnal
  1. active during the day, 2. lasting for one day.
ecotourism

humans benefit economically by promoting tourism that focuses on the appreciation of natural areas or animals. Ecotourism implies that there are existing programs that profit from the appreciation of natural areas or animals.

endothermic

animals that use metabolically generated heat to regulate body temperature independently of ambient temperature. Endothermy is a synapomorphy of the Mammalia, although it may have arisen in a (now extinct) synapsid ancestor; the fossil record does not distinguish these possibilities. Convergent in birds.

forest

forest biomes are dominated by trees, otherwise forest biomes can vary widely in amount of precipitation and seasonality.

freshwater

mainly lives in water that is not salty.

insectivore

An animal that eats mainly insects or spiders.

iteroparous

offspring are produced in more than one group (litters, clutches, etc.) and across multiple seasons (or other periods hospitable to reproduction). Iteroparous animals must, by definition, survive over multiple seasons (or periodic condition changes).

marsh

marshes are wetland areas often dominated by grasses and reeds.

migratory

makes seasonal movements between breeding and wintering grounds

monogamous

Having one mate at a time.

motile

having the capacity to move from one place to another.

native range

the area in which the animal is naturally found, the region in which it is endemic.

oviparous

reproduction in which eggs are released by the female; development of offspring occurs outside the mother's body.

polygynandrous

the kind of polygamy in which a female pairs with several males, each of which also pairs with several different females.

seasonal breeding

breeding is confined to a particular season

sexual

reproduction that includes combining the genetic contribution of two individuals, a male and a female

suburban

living in residential areas on the outskirts of large cities or towns.

tactile

uses touch to communicate

temperate

that region of the Earth between 23.5 degrees North and 60 degrees North (between the Tropic of Cancer and the Arctic Circle) and between 23.5 degrees South and 60 degrees South (between the Tropic of Capricorn and the Antarctic Circle).

tropical

the region of the earth that surrounds the equator, from 23.5 degrees north to 23.5 degrees south.

tropical savanna and grassland

A terrestrial biome. Savannas are grasslands with scattered individual trees that do not form a closed canopy. Extensive savannas are found in parts of subtropical and tropical Africa and South America, and in Australia.

savanna

A grassland with scattered trees or scattered clumps of trees, a type of community intermediate between grassland and forest. See also Tropical savanna and grassland biome.

temperate grassland

A terrestrial biome found in temperate latitudes (>23.5° N or S latitude). Vegetation is made up mostly of grasses, the height and species diversity of which depend largely on the amount of moisture available. Fire and grazing are important in the long-term maintenance of grasslands.

visual

uses sight to communicate

Ref­er­ences

Bent, I. 1942. A man­aged cliff swal­low colony in south­ern Wis­con­sin. Wil­son Bul­letin, 54: 153-161.

BirdLife In­ter­na­tional, 2012. "Petroche­li­don pyrrhonota" (On-line). The IUCN Red List of Threat­ened Species 2012: e.T22712427A38672463. Ac­cessed Sep­tem­ber 15, 2016 at http://​dx.​doi.​org/​10.​2305/​IUCN.​UK.​2012-1.​RLTS.​T22712427A38672463.​en.

Blake, C. 1948. The flight of swal­lows. Auk, 65: 54-62.

Brown, C., M. Brown. 1996. Colo­nial­ity in the Cliff Swal­low: The Ef­fect of Group Size on So­cial Be­hav­ior. Chicago, Illi­nois: Uni­ver­sity of Chicago Press.

Brown, C., M. Brown. 2000. Weather-me­di­ated nat­ural se­lec­tion on ar­rival time in cliff swal­lows (Petroche­li­don pyrrhonota). Be­hav­ioral Ecol­ogy and So­cio­bi­ol­ogy, 47/5: 339-345.

Brown, C. 2010. How cliff swal­lows choose where to live. Phi Kappa Phi Forum, 90/1: 4-7.

Brown, C., M. Brown. 2002. Does in­ter­colony com­pe­ti­tion for food af­fect colony choice in cliff swal­lows?. The Con­dor, 104/1: 117-128.

Brown, C., M. Brown. 2000. Her­i­ta­ble basis for choice of group size in a colo­nial bird. Pro­ceed­ings of the Na­tional Acad­emy of Sci­ences, 97/26: 14825–14830.

Brown, C., M. Brown, K. Brazeal. 2008. Fa­mil­iar­ity with breed­ing habi­tat im­proves daily sur­vival in colo­nial cliff swal­lows. An­i­mal Be­hav­iour, 76/4: 1201-1210.

Brown, C., m. Brown, M. Shaf­fer. 1991. Food-shar­ing sig­nals among so­cially for­ag­ing cliff swal­lows. An­i­mal Be­hav­iour, 42/4: 551-564.

Brown, C., M. Brown. 1995. Cliff swal­low (Petroche­li­don pyrrhonota). Pp. None in P Rode­wald, ed. Birds of North Amer­ica, Vol. None. Ithaca, New York: Cor­nell Lab of Or­nithol­ogy. Ac­cessed No­vem­ber 27, 2016 at https://​birdsna.​org/​Species-Account/​bna/​species/​cliswa.

Brown, C., E. Roche, M. Brown. 2015. Par­ent-off­spring re­sem­blance in colony-spe­cific adult sur­vival of cliff swal­lows. Evo­lu­tion­ary Ecol­ogy, 29/4: 537-550.

Brown, C., E. Roche, V. O'Brien. 2015. Costs and ben­e­fits of late nest­ing in cliff swal­lows. Oeo­colo­gia, 177/2: 413-421.

Brown, C., R. Sethi. 2002. Mos­quito abun­dance is cor­re­lated with cliff swal­low (Petroche­li­don pyrrhonota) colony size. Jour­nal of Med­ical En­to­mol­ogy, 39/1: 115-120.

Brown, M., C. Brown. 2011. In­tense nat­ural se­lec­tion on mor­phol­ogy of cliff swal­lows (Petroche­li­don pyrrhonota) a decade later: Did the pop­u­la­tion move be­tween adap­tive peaks?. The Auk, 128/1: 69-77.

Bullard, R. 1963. Band­ing notes on the Nick­a­jack cliff swal­lows (Petroche­li­don pyrrhonota). East­ern Bird-Band­ing As­so­ci­a­tion News, 26: 191-203.

Byard, M., R. Free­man, G. Pester. 1979. Pere­grine fal­cons sighted in Texas County, Ok­la­homa. Bul­letin of the Ok­la­homa Or­nitho­log­i­cal So­ci­ety, 12/2: 13-14.

Dugas, M. 2010. Nestling birds put their best flange for­ward. Jour­nal of Avian Bi­ol­ogy, 41/3: 336-341.

Fajer, E., K. Schmidt, J. Es­chler. 1987. Acorn wood­pecker pre­da­tion on cliff swal­low nests. Con­dor, 89: 177-178.

John­son, A., S. Freed­berg. 2014. Vari­able fa­cial plumage in ju­ve­nile cliff swal­lows: A po­ten­tial off­spring recog­ni­tion cue?. The Auk, 131/2: 121-128.

Jones, H. 1883. An un­recorded habit of the Red-headed Wood­pecker. Or­nithol­o­gist and Ool­o­gist, 8: 56.

Kirby, R. 1978. Roost­ing of passer­ines over open water at night.. North Amer­i­can Bird Ban­der, 3: 104-105.

Mc­Nair, D. 2013. Cliff swal­low breed­ing range ex­pan­sion along the Great Pee Dee River cor­ri­dor in the Car­oli­nas. South­east­ern Nat­u­ral­ist, 12/3: 500-513.

Oliver, G. 1970. Black rat­snake pre­da­tion upon nest­ing Barn and Cliff swal­lows. Ok­la­homa Or­nitho­log­i­cal So­ci­ety, 3: 17-20.

Sikes, P., K. Arnold. 1986. Red im­ported fire ant (Solenop­sis in­victa) pre­da­tion on cliff swal­low (Hirundo pyrrhonota) nestlings in east-cen­tral Texas. South­west­ern Nat­u­ral­ist, 31: 105-106.

Sother­land, P., G. Packard, T. Taigen, T. Board­man. 1980. An al­ti­tu­di­nal cline in con­duc­tance of cliff swal­low (Petroche­li­don pyrrhonota) eggs to water vapor. The Auk, 971: 177-185.

Thomp­son, B., C. Turner. 1980. Bull snake pre­da­tion at a cliff swal­low nest. Mur­relet, 61: 35-36.

Tum­li­son, R. 2009. Breed­ing by cliff swal­lows (Petroche­li­don pyrrhonota) in south­ern Arkansas. South­west­ern Nat­u­ral­ist, 54/2: 208-210.

Weaver, H., C. Brown. 2004. Brood par­a­sitism and egg trans­fer in cave swal­lows (Petroche­li­don fulva) and cliff swal­lows (Petroche­li­don pyrrhonota) in south Texas. The Auk, 121/4: 1122-1129.

Wilkin­son, G., G. Eng­lish-Loeb. 1982. Pre­da­tion and colo­nial­ity in cliff swal­lows (Petroche­li­don pyrrhonota). Auk, 99: 459-467.

With­ers, P. 1977. En­er­getic as­pects of re­pro­duc­tion by the cliff swal­low. Auk, 94: 718-725.