Thermogenic responses in Eurasian Tree Sparrow (<i>Passer montanus</i>) to seasonal acclimatization and temperature-photoperiod acclimation

Lin Li; Jingru Ge; Sangyu Zheng; Lihong Hong; Xini Zhang; Ming Li; Jinsong Liu

doi:10.1186/s40657-020-00222-9

Volume 11 Issue 1

Apr. 2020

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Avian Research > 2020 > 11(1): 35. > DOI: 10.1186/s40657-020-00222-9

Lin Li, Jingru Ge, Sangyu Zheng, Lihong Hong, Xini Zhang, Ming Li, Jinsong Liu. 2020: Thermogenic responses in Eurasian Tree Sparrow (Passer montanus) to seasonal acclimatization and temperature-photoperiod acclimation. Avian Research, 11(1): 35. DOI: 10.1186/s40657-020-00222-9

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Thermogenic responses in Eurasian Tree Sparrow (Passer montanus) to seasonal acclimatization and temperature-photoperiod acclimation

College of Life and Environmental Sciences, Wenzhou University, Wenzhou 325035, China

Funds:

grants from the National Natural Science Foundation of China 31470472

grants from the National Natural Science Foundation of China 31971420

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Corresponding author:
Ming Li, limingjinwen@126.com

Jinsong Liu, ljs@wzu.edu.cn
^†Lin Li and Jingru Ge contributed equally to this work
Received Date: 02 Jul 2020
Accepted Date: 07 Sep 2020
Available Online: 24 Apr 2022
Published Date: 12 Sep 2020

Abstract

Abstract

Background
Small birds in temperate habitats must either migrate, or adjust aspects of their morphology, physiology and behavior to cope with seasonal change in temperature and photoperiod. It is, however, difficult to accurately measure how seasonal changes in temperature and photoperiod affect physiological processes such as basal metabolic rate (BMR) and metabolic activity. To address this problem, we collected data in each month of the year on body mass (M_b) and BMR, and conducted a series of experiments to determine the effect of temperature and photoperiod on M_b, BMR and physiological markers of metabolic activity, in the Eurasian Tree Sparrow (Passer montanus).
Methods
In one experiment, we measured monthly change in M_b and BMR in a captive group of birds over a year. In another experiment, we examined the effects of acclimating birds to two different temperatures, 10 and 30 ℃, and a long and a short photoperiod (16 h light:8 h dark and 8 h light:16 h dark, respectively) for 4 weeks.
Results
We found that these treatments induced sparrows to adjust their M_b and metabolic rate processes. Acclimation to 30 ℃ for 4 weeks significantly decreased sparrows' M_b, BMR, and energy intake, including both gross energy intake and digestible energy intake, compared to birds acclimated to 10 ℃. The dry mass of the liver, kidneys and digestive tract of birds acclimated to 30 ℃ also significantly decreased, although their heart and skeletal muscle mass did not change significantly relative to those acclimated to 10 ℃. Birds acclimated to 30 ℃ also had lower mitochondrial state-4 respiration (S4R) and cytochrome c oxidase (COX) activity in their liver and skeletal muscle, compared to those acclimated to 10 ℃. Birds acclimated to the long photoperiod also had lower mitochondrial S4R and COX activity in their liver, compared to those acclimated to the short photoperiod.
Conclusions
These results illustrate the changes in morphology, physiology, and enzyme activity induced by seasonal change in temperature and photoperiod in a small temperate passerine. Both temperature and photoperiod probably have a strong effect on seasonal variation in metabolic heat production in small birds in temperate regions. The effect of temperature is, however, stronger than that of photoperiod.
- Acclimation,
- Acclimatization,
- Basal metabolic rate,
- Body mass,
- Eurasian tree sparrow (passer montanus)

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Background

Strigiformes, the bird order known commonly as owls, comprise cryptically colored nocturnal birds that can be notoriously hard to identify in the field. Their mysterious nature is typified by the Brown Hawk Owl or Brown Boobook complex (Ninox [scutulata] sp.), an assemblage widely distributed across Asia with populations in various regions exhibiting differentiation with respect to phenology, vocalizations and plumage. This differentiation has led to confusion about the taxonomic status of these populations. Some authors suggest that the complex is a single species comprising as many as 13 subspecies (König et al. 2009). However, King (2002) analyzed bioacoustic and morphometric data and determined that the complex comprises three biological species: the Northern Boobook (Ninox japonica), which breeds from southeast Siberia to Taiwan and adjacent mainland China, and winters across Southeast Asia, the Chocolate Boobook (Ninox randi), which is endemic to the main Philippines (i.e. the Philippine archipelago with the exclusion of Palawan and satellite islands), and the Brown Boobook (Ninox scutulata), which is distributed across South and Southeast Asia to the Greater Sundas and Palawan (Fig. 1).

Figure 1. Map of East and Southeast Asia depicting the breeding range of the Brown Boobook (N. scutulata) (a) and the breeding and known wintering ranges of both the japonica lineage and the undetermined mitochondrial lineage (Lin et al. 2013) of the Northern Boobook (N. japonica) (b). Also included are sighting records from Bangkok (b(i)), Laem Phak Bia (b(ii)) (Round 2011; Upton 2014), and a 1963 specimen record from Trang (b(iii)) (Round 2011) in Thailand, as well as the recent specimen records from Singapore described in this study (b(iv)). The main Asian landmass stretching from mainland China to Russia, inclusive of Sakhalin island, is separately labelled owing to uncertainty over the exact breeding lineage within that range. Question marks refer to areas where the Northern Boobook are likely to winter but are presently under-surveyed with no confirmed records. Breeding and range maps were obtained and modified from the IUCN Red List of Threatened Species (BirdLife International and NatureServe 2014), and basemap and Thailand sightings were generated using QGIS v2.8.2-Wien (Quantum GIS Development Team, 2015) and edited on Adobe PhotoShop CS5 (Adobe, 2010)

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At present knowledge, Ninox japonica occurs as two mitochondrially distinct populations—a nominate population that occurs in both Japan (including Ryukyu) and little islands off of Taiwan (e.g. Lanyu), and a resident population on the Taiwanese mainland said to be non-migratory due to year-round records of the taxon on the island (Lin et al. 2013). While the latter lineage has been identified based on DNA samples from the island of Taiwan only, unsampled breeding populations in mainland China and Russia may well be closely related or identical to this lineage. Lin et al. (2013) refer to this as an unnamed population, but it may well have a taxonomic name already if mainland populations are shown to belong with it: based on morphological considerations, many treatises nowadays refer to mainland populations as N. j. florensis (del Hoyo et al. 2015), a name based on type material from the wintering range in East Indonesia that may extend to Taiwan if future research can verify the connection between the type of florensis and mainland Chinese breeding populations. For the purposes of clarity and brevity, we will refer to this mitochondrial lineage as the "undetermined lineage" henceforth.

The wintering range of the migratory nominate form is unclear; there have been confirmed records from Wallacea, Borneo and Java, but the limits of its winter range further west remain unknown (Fig. 1). Additionally, morphological similarity between Northern and Brown Boobooks makes it difficult to confirm identification in the field where their ranges potentially overlap.

Recent advances in identification between Brown and Northern Boobooks based on wing: tail ratios, wing formulas (King 2002) and ventral markings (Round 2011) have led to new Northern Boobook winter records in mainland Southeast Asia, with several reports of the species in Thailand and a single new record from Kedah in peninsular Malaysia (Table 1). However, the range of variation in ventral patterning is not fully understood, which has led to some confusion with regards to distinguishing the two species in the field. For instance, individuals displaying ventral markings typical of Brown Boobooks (sensu Round 2011) have been photographed breeding across Japan (e.g., Morlan 2012), over 3000 km away from the nearest confirmed breeding locality of Brown Boobooks, indicating that Northern Boobooks, especially from Japan, may display similar ventral markings.

Table 1. Winter records of Ninox japonica in mainland Southeast Asia

Location	Date	Record type and status	Source
Chiang Mai: Mae Rim:Ban Khi Lek	24/11/1970	Specimen: TISTR53- 1848; wing measurements and ventral plumage intermediate between scutulata and japonica; identification unconfirmed	Round (2011)
Samut Prakan: Suan Sri Nakhon Kheaun Khan, Phra Pradaeng	2/10/2008	Photograph; unconfirmed identification merely based on ventral spotting (see text)	Round (2011)
Bangkok: Suan Rotfai (Railway Park; Suan Venchirabhas)	5/4/2010	Photograph; unconfirmed identification merely based on ventral spotting (see text)	http://bangkokcitybirding.blogspot.com/2010_04_01_archive.html
Malaysia: Kedah State: coast between Kuala Kedah and Kuala Sanglang	5/12/2010	Photograph; unconfirmed identification merely based on ventral spotting (see text)	David Bakewell (pers. comm.)
Nakhon Pathom: Phutthamonthol, Salaya	7/2/2011	Photograph; unconfirmed identification merely based on ventral spotting (see text)	Round (2011)
Bangkok: Suan Rotfai (Railway Park; Suan Venchirabhas)	9/1/2014–8/2/2014	Photograph; unconfirmed identification merely based on ventral spotting (see text)	Limparungpattanakij (pers. comm.)
Bangkok: Sammakorn Village, Ramkhamhaeng	11/10/2014	Photograph; unconfirmed identification merely based on ventral spotting (see text)	https://www.facebook.com/photo.php?fbid=10205116649379611&set=a.1196106546563.2030022.1345440622&type=1&fref=nf
Phetchaburi: Laem Phak Bia, Ban Laem	30/3/2015	Trapped; ring no 8A0 1825; measurements confirm identification	Round ( 2011 )
Confirmed identifications in italic. All records are from Thailand unless otherwise specified

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On 23 March 2014, the carcass of a Ninox owl (ID CR059) was found near the Tanglin Halt estate in Singapore (01.3009500°N, 103.7930667°E). Close inspection of the bird revealed its ventral patterning to be indicative of the Northern Boobook (sensu Round 2011). This potentially represents the first country record of the Northern Boobook and extends the mainland wintering range of the species considerably further south. If substantiated with molecular methods, this record would constitute the first corroboration that Northern Boobooks winter on or just off the southern part of mainland Southeast Asia. We here present morphological measurements and cytochrome-b (cytb) sequences of this bird and additional specimens collected throughout the region to confirm their identity and to discuss Ninox taxonomy and field identification.

Methods

Tissue was sampled from the carcass as well as three presumable Brown Boobooks collected in Singapore that had been deposited in the Lee Kong Chian Natural History Museum (Additional file 1: Table S1). DNA extractions were carried out with GeneAll^® DNA Purification kits as per the protocol for animal tissue. Polymerase chain reactions (PCR) were carried out in a C1000™ Thermal Cycler and cytb was amplified as per Cibois et al. (1999) and Dong et al. (2010) using the conditions stated in Sorenson et al. (1999). PCR amplifications were done in 20 μL reaction volumes, which comprised 2 μL 10 × Taq PCR buffer, 1.2 μL MgCl₂ (25 mM), 1 μL of each primer (10 μm), 0.4 μL Fermentas Taq polymeras, 2 μL mtDNA template and 11.6 μL MilliQ water. PCR product clean up was carried out using ExoSAP-IT^® and the BigDye^® Terminator v3.1 Cycle Sequencing Kit (Applied Biosystems Inc., Foster City, CA, USA) was used to cycle-sequence samples. Sequences were obtained by capillary electrophoresis using an Applied Biosystems 3130 × l Genetic Analyzer.

DNA sequences were assembled with CodonCode Aligner version 4.1 (CodonCode Corporation, http://www.codoncode.com) and aligned with MEGA 6.06 using ClustalW (Larkin et al. 2007; Tamura et al. 2013). The final alignment was 923 base pairs in length and contained no indels. We compared our four novel sequences with those of 32 individuals of the nominate form of Ninox japonica from Japan and Lanyu, 48 individuals of the presumably resident undetermined lineage from the main island of Taiwan and a single novel sequence of Ninox japonica from Brunei for a total sample size of 85 (Additional file 1: Table S1; Lin et al. 2013). Sequences were easily aligned, therefore unlikely to be paralogs. MEGA 6.06 was employed to construct phylogenetic trees using Neighbor-Joining (NJ), Maximum Parsimony (MP) and Maximum Likelihood (ML). For each analysis, 1000 bootstrap replicates were run. MP was run with all sites used for gap treatment, Tree-Bisection-Reconnection as the tree search method and other settings in default mode. The program jModelTest 2.1.4 (Darriba et al. 2012) was used to determine the best evolutionary model for ML. The results identified the Hasegawa, Kishino, and Yano model with parameters for gamma distribution (HKY + G) as the most suitable model for ML analysis. The outgroup for tree analyses was a cytb sequence of the Powerful Owl (Ninox strenua) downloaded from GenBank. DnaSP v5.10.01 (Librado and Rozas 2009) was used to calculate raw sequence divergence and nucleotide diversity between and within taxa.

The wing of the carcass retrieved in Singapore was measured by determining the distance between the foremost extremity of the carpus to the tip of the longest primary feather using the closed, flattened wing. Wing point measurements were determined by closing the wing and placing the tips of the primary feathers in order. The feathers were then splayed slightly and the primaries were measured in relation to the longest primary. The tail was measured by sliding a ruler between the retrices and the undertail coverts up to the base of the tail, and then flattening and measuring the longest tail feather. Wing and tail measurements were compared against those obtained for vouchered Brown and Northern Boobook specimens (King 2002).

Results

NJ, MP and ML analyses all yielded trees with identical topology. Three similar clades emerged from the phylogenetic analysis, with the first two clades representing the two genetically distinct Northern Boobook taxa (Lin et al. 2013). The first clade contained known Taiwanese breeders [the undetermined lineage identified by Lin et al. (2013)] and the second contained individuals from the migratory main population (Fig. 2). The Singaporean carcass and the Brunei sample were nested within the first clade, confirming that they are Northern Boobooks. Of the three tissue samples analyzed from the Lee Kong Chian Museum of Natural History, one sample (November 2000) also emerged within the undetermined lineage whilst the other two samples (July 2003; June 2004) formed a separate clade (Fig. 2). These latter two samples represent Brown Boobooks resident in Singapore as they were collected in summer months when no migrants are present.

Figure 2. Phylogram of Brown Boobook (N. scutulata) and Northern Boobook (N. japonica) samples. Annotated numbers are Neighbor-Joining, Maximum Likelihood and Maximum Parsimony bootstrap values, respectively. Only nodes with at least two bootstrap values > 90 are annotated. Black arrows indicate samples collected in Singapore and red arrow indicates sample from Brunei. Tree topology used is from NJ tree

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Analysis of raw sequence divergence between clades showed that Ninox scutulata exhibited a divergence of 2.1-2.6 % from the two Ninox japonica clades, whilst the nominate clade of Ninox japonica showed a smaller divergence of 1.6 % from the undetermined lineage (Table 2).

Table 2. Matrix of p-divergences between taxa (below diagonal) and p-divergences within each sampled taxon (along diagonal, italic)

	*Ninox japonica* [nominate form]	*Ninox japonica* [undetermined lineage]	*Ninox scutulata*
Ninox japonica [nominate form]	0.000–0.009
Ninox japonica [undetermined lineage]	0.016	0.000–0.004
Ninox scutulata	0.026	0.021	0.000

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The wing and tail measurements of the Singaporean carcass were 217 mm and 114 mm, respectively, giving a wing:tail ratio of 1.90 (Table 3). These results, combined with wing morphology measurements (Table 4) provided morphological confirmation that our specimen was a Northern Boobook as diagnosed by King (2002).

Table 3. Comparison of morphological measurements across Ninox sp. and the Singaporean carcass (in italic)

	Wing	Tail	Wing/tail ratio
Ninox japonica	220.8 (214.0–226.8)	115.8 (107.5–122.6)	1.91 (1.75–2.03)
Ninox scutulata	195.7 (182.4–213.3)	109.5 (100.3–115.0)	1.78 (1.69–1.87)
Singapore carcass CR059	217.0	114.0	1.90
Average values are provided in mm with range given in brackets. Values highlighted show instances where measurement range overlaps with values from Singapore carcass

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Table 4. Wing morphology; comparative length differences among five longest primary feathers in the following order: P9, P8, P7, P6, P5

	P9	P8	P7	P6	P5
Ninox japonica	15.6	0	3.9	19.6	46.1
Ninox scutulata	16.7	1.6	0	5.3	23.3
Singapore carcass CR059	16.0	0	1.0	15.0	43.0
Measurements start from wing tip, so zero stands for longest primary. Data for Ninox japonica and Ninox scutulata adapted from King (2002)

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Discussion

All previous records of Northern Boobooks in mainland Southeast Asia have relied on visual identification based on the ventral markings or measurements based on wing:tail ratios (Round 2011). However the full extent of intra-specific variation in ventral markings within Northern and Brown Boobooks is not well understood, making it difficult to distinguish the two species visually. Our molecular results constitute a considerable southward extension of the wintering range of > 1400 km from a previous winter record (Phetchaburi; Table 1) confirmed by measurements. It is possible that the wintering range of Northern Boobooks may even include Sumatra based on its proximity to Singapore. This discovery represents a new avian country record for Singapore. We show here that in cases where visual identification is challenging, genetic analysis is a handy tool for clarifying species identity.

Of the three additional Singaporean tissue specimens used as a comparison, two were Brown Boobooks as expected, but surprisingly the third also emerged as a Northern Boobook. The fact that two out of four randomly collected boobooks in Singapore refer to Northern rather than Brown Boobooks suggests that the recently procured carcass is not an accidental stray, but that Northern Boobooks may be regular annual visitors to the island. Given that Singapore has one of the best-known national avifaunas in the world (Wang and Hails 2007; Chisholm et al. 2015), it seems that this seasonal visitor may have been overlooked due to confusion with the island's resident Brown Boobook. The procurement date of one specimen in November suggests that Northern Boobooks are not mere migrants but may overwinter on the island.

The Northern Boobooks identified from Singapore and Brunei were not of the migratory Japanese population but of the undetermined mitochondrial lineage. This lineage has been reported year-round in Taiwan including breeding in March (Lin et al. 2013)—the month of procurement of the carcass in Singapore. Our discovery suggests that some populations of the undetermined mitochondrial lineage are long-distance migratory, whereas others are not. While we cannot rule out that Taiwan harbors both migratory and non-migratory populations, we consider it more likely that the undetermined mitochondrial lineage extends to genetically unsampled parts of the breeding range of the Northern Boobook across the East Asian mainland from South China north all the way to Russia. If true, it is likely that the provenance of the migratory populations of this lineage lies in the more northerly parts of their distribution, such as northeast China (Heilongjiang Province) and eastern Siberian Russia.

The internal taxonomy of the Northern Boobook N. japonica is confused: subspecies florensis was described on the basis of a wintering specimen from the island of Flores (eastern Indonesia); it has been attributed to breeding populations from northern mainland Asia (such as eastern Siberian Russia and northeastern China) presumably because of its large size. If true, this name would apply to the undetermined mitochondrial lineage of Lin et al. (2013), of which Taiwanese birds would then be a resident subset. Additional genetic research including mainland breeding populations of Northern Boobooks is urgently needed to confirm this hypothesis. Further, the use of high resolution genome-wide SNP data will help provide a more comprehensive understanding of the taxonomy of these boobooks.

Conclusions

Analysis of mitochondrial DNA has extended the wintering range of Northern Boobooks in Southeast Asia and suggests that most winterers in the Sundaic region may refer to a mitochondrial lineage of uncertain taxonomic status that has previously been documented from Taiwan but may breed over large parts of mainland Eastern Asia. A genetic research into mainland breeders is urgently required to characterize the geographic distribution of this undetermined mitochondrial lineage. Future taxonomic research may show that the name florensis, based on a wintering individual from the island of Flores, refers to this lineage.

Additional file

Authors' contributions

FER conceived of and designed the study, KRS conducted molecular genetic and analytical work, KRS and FER wrote the manuscript, DJXT provided samples, KS provided sequences and PDR provided information on Ninox japonica records from across Southeast Asia. All authors read and approved the final manuscript.

Acknowledgements

We would like to thank David Bakewell for details on a potential record in Kedah, and Joe Morlan for making his photo of a Japanese breeder available online. We are grateful to the Lee Kong Chian Natural History Museum for providing us with samples. This research was funded by the National University of Singapore (NUS) Faculty of Science and Department of Biological Sciences through grants WBS R-154-000-570-133 and R-154-000-583-651, respectively.

Ethics statement

Lab work was conducted in accordance with NUS's Office of Safety, Health and Environment regulations.

Competing interests

The authors declare that they have no competing interests.

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Corresponding author: Jinsong Liu, ljs@wzu.edu.cn

College of Life and Environmental Sciences, Wenzhou University, Wenzhou 325035, China

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Thermogenic responses in Eurasian Tree Sparrow (Passer montanus) to seasonal acclimatization and temperature-photoperiod acclimation