Conventional and network analyses of song organization and complexity in northern House Wrens ( Troglodytes aedon parkmanii )

2020 ◽  
Vol 91 (4) ◽  
pp. 375-392
Author(s):  
Chinthaka Kaluthota ◽  
David Logue ◽  
Drew Rendall
Behaviour ◽  
1996 ◽  
Vol 133 (5-6) ◽  
pp. 357-366 ◽  
Author(s):  
William A. Searcy ◽  
L. Scott Johnson

AbstractThis study tested the hypothesis that the song of male birds can function to attract mates. At 11 different locations on our Wyoming study area, we broadcast the song of male house wrens (Troglodytes aedon) from a loudspeaker mounted next to an empty nest box in an unoccupied wren territory. The number of female wrens attracted to the 'speaker box' was compared to the number visiting a silent, control box on another, unoccupied territory nearby. Females visited speaker boxes at a significantly higher rate than they visited control boxes. Ten females visited speaker boxes in six different trials during periods when no male was associated with either the speaker or control box (total time = 45.5 h; visit rate = 0.22/h). In contrast, only one female visited a control box during these same periods (= 0.02 visits/h), and she did so after first visiting the speaker box. Two females visited the speaker box simultaneously in some trials and chasing or fighting always ensued. Many females showed signs of settling permanently at speaker boxes, remaining at speaker boxes from their arrival to the end of the trial (> 5 h in two cases), and most began constructing nests in boxes, despite the absence of a male. In summary, this study provides strong experimental evidence that the song of male house wrens can function to attract mates for breeding.


2019 ◽  
Vol 97 (1) ◽  
pp. 50-56
Author(s):  
C.L. Gable ◽  
T.J. Underwood ◽  
G.P. Setliff

House Wrens (Troglodytes aedon Vieillot, 1809) regularly add spider egg cases (Arachnida: Araneae) to their nests, which may be an example of heterospecific cleaning. This behavior involves one animal employing another to remove parasites from their nests. In House Wren nests, juvenile spiders hatching from egg cases may facilitate the reduction of mites that feed on nestlings. We tested this ectoparasite reduction hypothesis by monitoring House Wren nests for spider egg cases and by collecting completed nests to compare the number of spider egg cases and Dermanyssus hirundinis (Hermann, 1804) mites. No significant relationship was found between the number of spider egg cases and number of D. hirundinis mites in nests. We also found no significant relationship between the number of D. hirundinis mites in nests and the body condition of nestlings. Finally, no significant difference was found between the number of D. hirundinis mites in early versus late season nests, but significantly more spider egg cases were added to late season nests. Of a subsample of spider egg cases dissected, we found that 28% contained spider eggs or embryos. We also identified three species of juvenile spiders from House Wren nests using DNA barcoding. Overall, we found no evidence that spider egg cases reduce the number of D. hirundinis mites or engender better quality offspring in House Wren nests.


The Auk ◽  
1988 ◽  
Vol 105 (3) ◽  
pp. 480-491 ◽  
Author(s):  
Nancy E. Drilling ◽  
Charles F. Thompson

Abstract We studied the natal and breeding dispersal of yearling and adult House Wrens (Troglodytes aedon) for 7 yr in central Illinois. The forested study areas contained 910 identical nest boxes placed in a grid pattern. On average 38.1% (n = 643) of the adult males and 23.3% (n = 1,468) of the adult females present in one year returned the next; 2.8% (n = 6,299) of the nestlings that survived to leave the nest returned each year. Adult male (median distance = 67 m) and adult female (median = 134 m) breeding dispersal was less than yearling male (median = 607.5 m) and yearling female (median = 674 m) natal dispersal. Females that returned had produced more offspring the previous season than had nonreturning females, and females that successfully produced at least one chick in their last nesting attempt of the previous season moved shorter distances than did unsuccessful females. There were, however, no consistent differences between returning and nonreturning females in two other measures of reproductive success. Females that were unsuccessful in their last breeding attempt of the previous year were more likely to be successful in their next attempt if they moved two or more territories than if they did not move. Reproductive success did not affect the likelihood that a male would return nor the distance that he moved. The success of subsequent nesting attempts by males was also not related to the distance moved. Inbreeding avoidance may explain differences between breeding and natal dispersal, but it does not explain the lack of difference in dispersal of yearling females and males. Differences between adult and yearling dispersal are best explained by advantages accruing to adults that remain near former breeding sites and by the necessity for yearlings to move farther because of their late return from the wintering grounds. The advantages for adults to reoccupy previous breeding sites are counterbalanced, especially in females, by advantages associated with moving after breeding failure.


2008 ◽  
Vol 17 (16) ◽  
pp. 3697-3706 ◽  
Author(s):  
ANNA M.  FORSMAN ◽  
LAURA A.  VOGEL ◽  
SCOTT K.  SAKALUK ◽  
BONNIE G.  JOHNSON ◽  
BRIAN S.  MASTERS ◽  
...  

1997 ◽  
Vol 75 (2) ◽  
pp. 302-307 ◽  
Author(s):  
Stanislav Pribil ◽  
Jaroslav Picman

We tested five hypotheses that may explain why House Wren (Troglodytes aedon) nests are rarely parasitized by Brown-headed Cowbirds (Molothrus ater). House Wrens may prevent parasitism in five ways: (1) by choosing to nest in cavities with small entrances (inaccessible-entrance hypothesis), (2) by restricting the size of the entrance with nest material (nest-structure hypothesis), (3) by puncturing and ejecting parasitic eggs (puncture–ejection hypothesis), (4) by burying the parasitized clutch under a new nest (egg-burial hypothesis), or (5) by abandoning the parasitized nest altogether (nest-desertion hypothesis). We tested these hypotheses in field experiments and found that (i) female cowbirds cannot enter circular entrances smaller than 38 mm in diameter, (ii) wrens prefer cavities with small entrances (inaccessible to cowbirds) to those with large entrances (accessible to cowbirds), (iii) when forced to breed in cavities with large entrances, wrens do not reduce the entrance size with nest material, (iv) despite the unusual strength of cowbird eggs, wrens are physically capable of puncture–ejecting them, (v) wrens do not puncture–eject cowbird eggs from their own nests, (vi) wrens do not abandon parasitized nests or bury the parasitized clutches under new nests. These results are consistent with the inaccessible-entrance hypothesis. We propose that additional nesting adaptations, as well as active cowbird avoidance of House Wrens, may contribute to the low frequency of cowbird parasitism.


1991 ◽  
Vol 69 (6) ◽  
pp. 1441-1446 ◽  
Author(s):  
L. Scott Johnson ◽  
Marjorie D. Eastman ◽  
L. Henry Kermott

We investigated the effect of ectoparasitism by hematophagous larvae of the blow fly Protocalliphora parorum on nestling House Wrens (Troglodytes aedon) over 2 years in north-central Wyoming, U.S.A. Approximately 85% of wren nests contained P. parorum larvae. Mean parasite load was approximately 10 larvae per nestling. Nestling tarsus length, primary feather length, and hematocrit measured just before fledging did not differ significantly with parasite load. However, parasitized birds weighed approximately 8% more than unparasitized birds just prior to fledging. Parasites possibly delay the recession in weight that normally occurs as tissues mature late in the nestling stage. Delayed development may result in increased nestling or fledgling mortality.


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