Lijun Chen, Lei Zhu, Yunbiao Hu, Pengfei Liu, Nan Lyu, Yuehua Sun. 2018: The breeding biology of endemic Spectacled Parrotbill (Sinosuthora conspicillatus) in Lianhuashan National Nature Reserve, Gansu Province, China. Avian Research, 9(1): 5. DOI: 10.1186/s40657-018-0097-6
Citation: Lijun Chen, Lei Zhu, Yunbiao Hu, Pengfei Liu, Nan Lyu, Yuehua Sun. 2018: The breeding biology of endemic Spectacled Parrotbill (Sinosuthora conspicillatus) in Lianhuashan National Nature Reserve, Gansu Province, China. Avian Research, 9(1): 5. DOI: 10.1186/s40657-018-0097-6

The breeding biology of endemic Spectacled Parrotbill (Sinosuthora conspicillatus) in Lianhuashan National Nature Reserve, Gansu Province, China

Funds: 

the National Natural Science Foundation of China 31472012

the National Natural Science Foundation of China 31270468

More Information
  • Corresponding author:

    Sun Yuehua, sunyh@ioz.ac.cn

  • Received Date: 07 Aug 2017
  • Accepted Date: 23 Jan 2018
  • Available Online: 24 Apr 2022
  • Publish Date: 07 Feb 2018
  • Background 

    Life history traits play critical roles in population survival and evolution. Breeding information should be particularly detailed in order to provide significant insights into the population status and the evolution of other traits. To our knowledge, there is still no information about the breeding biology of Spectacled Parrotbill (Sinosuthora conspicillatus), an endemic parrotbill in China.

    Methods 

    We searched the nests, checked all nests found and recorded the information of eggs, nestlings and nest sites of the Spectacled Parrotbill from 2013 to 2015 at Lianhuashan National Nature Reserve in Gansu Province, China.

    Results 

    A total of 16 nests were found. Nest trees were artificial young spruces and honeysuckles. Mean nest height was 0.89 ± 0.47 m (n = 16) above the ground level. All nests were cup-shaped and constructed using leaves, fine strips of barks and grasses by both parents. The mean clutch size was 4.42 ± 0.79 (n = 12). The eggs were oval in pale blue without speckles, and the mean egg mass was 1.25 ± 0.07 g (n = 27). The egg length was 15.56 ± 0.46 mm (n = 27) and the width was 12.46 ± 0.29 mm (n = 27). Incubation period was 13 days and nestling period was 13–14 days. The breeding success rate was 46%, and among those failed nest, 71% were depredated and 29% were deserted.

    Conclusion 

    Detailed life history information about parrotbill is still limited. The breeding biology of Spectacled Parrotbill reported in the present study should be helpful for further research about population, breeding behavior and conservation of this bird.

  • Among the four species of ground jays (Podoces) in the world, two are found in the west of China (Qian et al., 1965; Cheng, 1987): the Xinjiang Ground Jay (P. biddulphi) (Fig. 1) and the Mongolian Ground Jay (P. hendersoni). Xinjiang Ground Jays occur only in the Taklimakan Desert, the southern part of Xinjiang. Since the species was established by A. Hume in 1874, little has been known of its status and ecology. The current essay describes such information based on a long-term field survey.

    Figure  1.  The Xinjiang Ground Jay in the Lopnur Desert (Photo by Ming Ma)

    The ground jays are residents at the center of the Taklimakan Desert (37–42°N, 77–94°E, 790–1500 m elevations; Fig. 2). Most of distribution range of the species falls within Xinjiang, with a few extending to the east, e.g. the Qaidam Basin in Qinghai Province and Dunhuang in Gansu Province (Collar et al., 2001; Sun and Li, 2009). Interestingly, Mongolian Ground Jays are distributed around the range of Xinjiang Ground Jays (Fig. 2). Such a pattern should be a result of inter-species competition. There is evidence showing that the ground jays are expanding their range from west to east during recent decades (Ma, 2010).

    Figure  2.  Distribution of the Xinjiang Ground Jay and the Mongolian Ground Jay in the Taklimakan Desert

    Ground jays are well adapted to desert and semi-desert regions (Ludlow and Kinnear, 1933). Compared with crows or choughs, ground jays are sandy in plumage, presumably providing protection from desert predators (Londei, 2004). As their names indicate, ground jays spend much of their time on the ground. The strong legs should be adaptive to the habit. However, ground jays nest in shrubs and trees, a characteristic similar to that followed by the Corvids species.

    Information on breeding ecology of Xinjiang Ground Jays is very limited. A total of 20 ground jay nests were recorded in Niya and Qarqan from 2003 to 2004. The birds placed their nests on the small desert-poplar tree Populus diversifolia and Tamarix spp. bushes, averaging 1.09 ± 0.15 m (range = 0–2.30 m, n = 18) above the ground (Fig. 3). The nests were composed of sheep wool, camel's wool, horse's hair, dead leaves, dry grass, and the soft cottony growth of reeds, with poplar skin, twigs and small sticks being lined at the base. The external diameter of the nest is 35.75 ± 2.30 cm (range = 16–55 cm, n = 16), the internal diameter of the nest is 12.82 ± 0.85 cm (range = 9–20 cm, n = 14), and depth of the nest is 9.50 ± 1.00 cm (range = 5–16 cm, n = 13) and the height is 20.88 ± 1.33 cm (range = 12–35 cm, n = 16) (Fig. 4a). Clutch size varied between 1 and 3 eggs (1.89 ± 0.31 eggs, n = 9), the diameters of the eggs are 32.88 ± 0.83 mm × 23.48 ± 0.09 mm, and the weight of egg is 8.33 ± 0.88 g (n = 4). The color of egg is pale green and grayish white with brown spots scattered all over the surface, rather more densely at the broad end (Fig. 4b). The parents fed the young (Fig. 4c) more than 42 times during one day for one nest located in the middle March (Ma, 2004). After fledging, family flocks of 4 to 6 birds were encountered between early May and July. These data suggested that the ground jays laid eggs from late February to April.

    Figure  3.  Nest height above the ground in relation to nesting bush height of the Xinjiang Ground Jays
    Figure  4.  Breeding ecoloty of the Xinjiang Ground Jay. (a) The local guide in the field work, showing the nest built on a Tamarix bush; (b) The egg; (c) Feeding the chicks; (d) Nearly fledging chicks (photos by Ming Ma).

    Based on the transect counting conducted from 1988 to 2011, the density of ground jays was to be 3–5 pairs per 100 km2. It was estimated to have 4100–6700 pairs of ground jays over the species' range of 135000 km2.

    The ground jay populations seemed to drop during recent decades (Grimmett, 1991; Madge and Burn, 1994; Ma, 1998). However, with the intensified desertification in western China, the jays have a tendency to expand to the east.For example, there were some of new records in Gansu and Qinghai provinces (Collar et al., 2001; Sun and Li, 2009; Ma, 2010). Arguably, this bird is an indicator species of desertification and climate change.

    Human activities such as oil industry, ecotourism, land exploitation and overgrazing should be responsible for the population decline (Ma, 2001; Ma and Kwok, 2004). The restricted range and special requirements for nesting habitats suggest an urgent conservation need for this species. Now, although the bird is classified as "near-threatened" (Collar et al., 2001), no protection measures have been in practice (Zheng and Wang, 1998).

    The research is supported by the Science Supporting Project of National Ministry of Science and Technology (2008BAC39B04) and the National Natural Science Foundation of China (30270211, 30470262, 30970340). Sincere thanks are due to all participants in the field work, especially to Jinghe Gu, Kwok Hon Kai, Zexin Jia, Batuerhan, Eugene Potapov, Chuanbo Wang, Feng Xu, Yiqun Wu, Mike Kilburn, Geoff Carey, Richard Lewthwaite, Sebastien Lepetz and Paul Leader. Gratitudes are also given to Prof. Xin Lu from Wuhan University who helps revise the earlier manuscript very carefully.

  • Alström P, Ericson PGP, Olsson U, Sundberg P. Phylogeny and classification of the avian superfamily Sylvioidea. Mol Phylogenet Evol. 2006;38:381–97.
    Alström P, Olsson U, Lei FM. A review of the recent advances in the systematics of the avian superfamily Sylvioidea. Chin Birds. 2013;4:99–131.
    Boulord A, Wang TH, Wang XM, Song GX. Impact of reed harvesting and smooth cordgrass Spartina alterniflora invasion on nesting Reed Parrotbill Paradoxornis heudei. Bird Conserv Int. 2011;21:25–35.
    Chen LJ, Zhu L, Yang XN, Lyu N, Liu Y, Liang W, Sun YH. Are egg colors and patterns signs of phylogenetic relatedness in parrotbills? Ornithol Sci. 2016;15:119–25.
    Dong B, Wu D, Song GX, Xie YM, Pei EL, Wang TH. Research on the habitatselection of Reed Parrotbill (Paradoxornis heudei) during the winter in Chongming Dongtan, Shanghai. Acta Ecol Sin. 2010;30:4351–8 (in Chinese).
    Guo ZM, Chen W, Hu JC. Analysis on nest habitation factors and chick growth of Paradoxornis webbianus. Sichuan J Zool. 2006;25:858–61 (in Chinese).
    Hu YB, Hao G, Jiang YX, Pechacek P, Sun YH. Breeding ecology of the Fulvous Parrotbill (Paradoxornis fulvifrons) in Wawushan Nature Reserve, Sichuan, China. J Nat Hist. 2014;48:975–82.
    Hu YB, Zhao QS, Lou YQ, Chen LJ, González MA, Sun YH. Parental attendance of chestnut thrush reduces nest predation during the incubation period: compensation for low nest concealment? J Ornithol. 2017;158:1111–7.
    Jiang YX, Sun YH, Lu N, Bi ZL. Breeding biology of the Grey-hooded Parrotbill (Paradoxornis zappeyi) at Wawushan, Sichuan, China. Wilson J Ornithol. 2009;121:800–3.
    Julliard R, Clavel J, Devictor V, Jiguet F, Couvet D. Spatial segregation of specialists and generalists in bird communities. Ecol Lett. 2006;9:1237–44.
    Kim CH, Yamagishi S, Won PO. Egg-color dimorphism and breeding success in the crow tit (Paradoxornis webbiana). Auk. 1995;112:831–9.
    Lack D. The significance of clutch-size. Part ⅲ. Some interspecific comparisons. Ibis. 1948;90:25–45.
    Lee JW, Jabloński PG. Egg color polymorphism and morph-ratio variation in Korean populations of the Vinous-throated Parrotbill. Chin Birds. 2012;3:312–9.
    Lee JW, Kim HY, Hatchwell BJ. Parental provisioning behaviour in a flock-living passerine, the Vinous-throated Parrotbill Paradoxornis webbianus. J Ornithol. 2010;151:483–90.
    Lei FM, Lu TC. China endemic birds. Beijing: Science Press; 2006.
    Li S, Chen LM, Chen WL. First report on the nest and nesting habitat of rare Rusty-throated Parrotbill Paradoxiornis przewalskii, China. Chin J Zool. 2014;49:435–7 (in Chinese).
    Martin TE. A new view of avian life-history evolution tested on an incubation paradox. Proc Biol Sci. 2002;269:309–16.
    Martin TE. Avian life-history evolution has an eminent past: does it have a bright future? Auk. 2004;121:289–301.
    Martin TE. Age-related mortality explains life history strategies of tropical and temperate songbirds. Science. 2015;349:966–70.
    Martin TE, Geupel GR. Nest-monitoring plots: methods for locating nests and monitoring success. J Field Ornithol. 1993;64:507–19.
    Moreno J, Osorno JL. Avian egg colour and sexual selection: does eggshell pigmentation reflect female condition and genetic quality? Ecol Lett. 2003;6:803–6.
    Partridge L, Harvey PH. The ecological context of life history evolution. Science. 1988;241:1449–55.
    Robson C. Family Paradoxornithidae (Parrotbills). In: del Hoyo J, Elliott A, Sargatal J, Christie DA, de Juana E, editors. Handbook of the birds of the world alive. Barcelona: Lynx Edicions; 2014.
    Skutch AF. Do tropical birds rear as many young as they can nourish. Ibis. 1949;91:430–58.
    Sun YH, Fang Y, Klaus S, Martens J, Scherzinger W, Swenson JE. Nature of the Lianhuashan Nature Reserve. Liaoning: Liaoning Science and Technology Publishing House; 2008 (in Chinese).
    Underwood T, Sealy S. Adaptive significance of egg coloration. Oxf Ornithol Ser. 2002;13:280–98.
    Wang ZY, Zhou YS. Habitat and breeding of Chinese crowtit around Lianyungang. Zool Res. 1988;9:216 (in Chinese).
    Warren M, Hill J, Thomas J, Asher J, Fox R, Huntley B, Roy D, Telfer M, Jeffcoate S, Harding P. Rapid responses of British butterflies to opposing forces of climate and habitat change. Nature. 2001;414:65–9.
    Xiong LH, Lu JJ. Habitat specialization in the Reed Parrotbill Paradoxornis heudei–evidence from its distribution and habitat use. Forktail. 2013;29:64–70.
    Yang CC, Liang W, Cai Y, Shi SH, Takasu F, Moller AP, Antonov A, Fossoy F, Moksnes A, Roskaft E, Stokke BG. Coevolution in action: disruptive selection on egg colour in an avian brood parasite and its host. PLoS ONE. 2010;5:e10816.
    Yang CC, Cai Y, Liang W, Antonov A. Breeding biology of the Golden Parrotbill (Paradoxornis verreauxi) (Aves: Timaliidae) in southwestern China. J Nat Hist. 2011;45:1817–22.
    Yeung CKL, Lin RC, Lei FM, Robson C, Hung LM, Liang W, Zhou FS, Han LX, Li SH, Yang XJ. Beyond a morphological paradox: complicated phylogenetic relationships of the parrotbills (Paradoxornithidae, Aves). Mol Phylogenet Evol. 2011;61:192–202.
    Zhao ZJ. A handbook of the birds of China: passerines. Changchun: Jilin Science and Technology Press; 2001 (in Chinese).
    Zheng GM. A checklist on the classification and distribution of the birds of China. Beijing: Science Press; 2017 (in Chinese).
    Zhu L. Studies and conservation status on the breeding birds community of the Wawu plateau, Central Sichuan, China. Beijing: University of Chinese Academic of Science; 2014 (in Chinese).
  • Related Articles

Catalog

    Figures(2)  /  Tables(1)

    Article Metrics

    Article views (568) PDF downloads (7) Cited by()

    /

    DownLoad:  Full-Size Img  PowerPoint
    Return
    Return