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Diet composition of the Pharaoh eagle owl, Bubo ascalaphus, across agricultural and natural areas in Saudi Arabia

Composição da dieta da coruja bufo-real, Bubo ascalaphus, em áreas agrícolas e naturais em Arábia Saudita

Abstract

The diet of the Pharaoh eagle owl, Bubo ascalaphus, inhabiting agricultural and natural areas in Saudi Arabia, was studied. Pellet analysis for B. ascalaphus in the agricultural area contained a high percentage (61.3%) of the house mouse, Mus musculus, while pellets collected from natural habitats were void of M. musculus, however, with a high proportion of wild rodents (Meriones crassus (28.6%) and Jaculus loftusi (41.6%). This suggests the importance of this owl as a biological control agent in agricultural areas.

Keywords:
owls; biological control; feeding behaviour; Saudi Arabia

Resumo

Foi estudada a dieta da coruja bufo-real, Bubo ascalaphus, que habita áreas agrícolas e naturais em Arábia Saudita. A análise de pellets para a B. ascalaphus na área agrícola continha uma alta porcentagem (61,3%) de camundongos domésticos Mus musculus, enquanto os pellets coletados em habitats naturais não continham M. musculus, apresentando, no entanto, uma alta proporção de roedores selvagens (28,6% de Meriones crassus e 41,6% de Jaculus loftusi), o que sugere a importância desta coruja como agente de controle biológico em áreas agrícolas.

Palavras-chave:
corujas; controle biológico; comportamento alimentar; Arábia Saudita

1. Introduction

Feeding behaviour and diet composition of owls in agricultural and natural areas were investigated in several parts of the world. Saufi et al. (2020)SAUFI, S., RAVINDRAN, S., HAMID, N.H., ZAINAL ABIDIN, C.M.R., AHMAD, H., AHMAD, A-H. and SALIM, H., 2020. Diet composition of introduced barn owls (Tyto alba javanica) in urban area in comparison with agriculture settings. Journal of Urban Ecology, vol. 6, no. 1, pp. 1-8. https://doi.org/10.1093/jue/juz025.
https://doi.org/10.1093/jue/juz025...
compared the diet of the Barn Owl, Tyto alba javanica, in urban and agricultural areas in Malaysia. They showed that Rattus norvegicus and Rattus argentiventer were the most consumed prey items in urban and agricultural areas respectively. Diet of the Barn Owl in agricultural landscapes in Greece included Mus domesticus (26.3%) and Rattus spp. (11%), whereas rats constituted the highest biomass (Bontzorlos et al., 2005BONTZORLOS, V.A., PERIS, S.J., VLACHOS, C.G. and BAKALOUDIS, D.E., 2005. The diet of barn owl in the agricultural landscapes of central Greece. Folia Zoologica, vol. 54, no. 1-2, pp. 99-110.).

In central South Africa, Stenkewitz et al. (2010)STENKEWITZ, U., WILSON, B. and KAMLER, J.F., 2010. Seasonal comparisons of barn owl diets in an agricultural and natural area in Central South Africa. The Ostrich, vol. 81, no. 2, pp. 163-166. http://dx.doi.org/10.2989/00306525.2010.488423.
http://dx.doi.org/10.2989/00306525.2010....
showed that small mammals constituted most of the biomass in the diet of Tyto alba in both natural and agricultural areas. Analysis of pellets of western Burrowing Owls (Athene cunicularia hypugaea) in Idaho, USA, inhabiting agricultural areas showed greater species richness, while pellets from non-agricultural areas showed greater species evenness and broader food-niche breadths (Moulton et al., 2005MOULTON, C.E., BRADY, R.S. and BELTHOFF, J.R., 2005. A comparison of breeding season food habits of burrowing owls nesting in agricultural and nonagricultural habitat in Idaho. The Journal of Raptor Research, vol. 39, no. 4, pp. 429-438.). The Ural owl, Strix uralensis, reduced populations of voles in orchards by 63% compared to other natural habitats (Murano et al., 2019MURANO, C., KASAHARA, S., KUDO, S., INADA, A., SATO, S., WATANABE, K. and AZUMA, N., 2019. Effectiveness of vole control by owls in apple orchards. Journal of Applied Ecology, vol. 56, no. 3, pp. 677-687. http://dx.doi.org/10.1111/1365-2664.13295.
http://dx.doi.org/10.1111/1365-2664.1329...
).

In the Middle East, the role of owls in controlling pest rodents in agricultural areas was studied in Syria. Both Mus musculus and Rattus rattus were found among the main prey items of Tyto alba (Shehab et al., 2004). Very little is known about the role of the Pharaoh eagle owl, Bubo ascalaphus, in controlling rodent pests in Saudi Arabia. Abi Said et al. (2020) showed that this owl diet consisted of 11.82% of R. rattus and 1.48% M. musculus in an urban area around Riyadh. In Qatar, Mohedano et al. (2014)MOHEDANO, I., ABU BAKER, M.A., HUNTER, B., BUCHAN, J., MICHAELS, C.J. and YAMAGUCHI, N., 2014. On the diet of the Pharaoh Eagle Owl, Bubo ascalaphus (Savigny, 1809), in Qatar, with an overview of its feeding habits. Zoology in the Middle East, vol. 60, no. 2, pp. 111-119. http://dx.doi.org/10.1080/09397140.2014.914713.
http://dx.doi.org/10.1080/09397140.2014....
showed that the diet of B. ascalaphus was mainly comprised (89.7% and 97.7% in frequency and biomass of wild rodents Jaculus jaculus and Meriones crassus respectively)

Other studies on the diet composition of B. ascalaphus in natural habitats showed that this owl fed on a variety of wild small and medium-sized mammals, reptiles, birds, and arthropods (Rifai et al., 2000RIFAI, L.B., AL-MELHIM, W.N., GHARAIBEH, B.M. and AMR, Z., 2000. The diet of the Desert Eagle Owl, Bubo bubo ascalaphus, in the Eastern Desert of Jordan. Journal of Arid Environments, vol. 44, no. 3, pp. 369-372. http://dx.doi.org/10.1006/jare.1999.0601.
http://dx.doi.org/10.1006/jare.1999.0601...
; Al Ghamdi et al., 2023AL GHAMDI, A.R., ALSHAMMARY, T., AL GETHAMI, F., AL BOUG, A., AL JBOUR, S., ABU BAKER, M.M. and AMR, Z.S., 2023. Diet of Pharaoh Eagle-Owl, Bubo ascalaphus, from Ara’r region, northeastern Saudi Arabia. Ornis Hungarica, vol. 31, no. 2, pp. 226-235. http://dx.doi.org/10.2478/orhu-2023-0032.
http://dx.doi.org/10.2478/orhu-2023-0032...
).

To this end, this is the first comparative study on the prey selection of the Pharaoh eagle owl, Bubo ascalaphus, in agricultural and natural habitats in Saudi Arabia to assess its role as a biological control agent.

2. Materials and Methods

2.1. Study sites

A total of 106 regurgitated pellets for the Pharaoh eagle owl were collected from two sites; 40 from Bsitah in Al Jouf Province (30° 44' 20.4” N 38° 31' 1.5” E), and 66 from Al Daba’ah in Tabuk Province (28° 44' 03” N, 37° 58' 23” E) during December of 2022 and March 2023. Two B. ascalaphus were observed in Bsitah perching on a eucalyptus tree (Figure 1).

Figure 1
Two individuals of B. ascalaphus perching on a Eucalyptus tree in Bsitah site.

2.2. Pellets processing

The length and width of the collected 39 (19 from Bsitah and 20 from Al Daba’ah) intact pellets were measured by a digital caliper. Each pellet was soaked in warm water and teased using a pair of forceps and a needle to separate prey remains for identification. Recovered items from each pellet were placed in a Petri dish. For each species, the lower and upper jaws were cleaned and preserved. Prey remains were identified using distinctive morphological characteristics of body and/or skull parts (e.g. mandibles and maxillae) described based on previous collections from the region (Amr, 2012AMR, Z.S., 2012. Mammal of Jordan. 2nd ed. Amman: Al Rai Press, 308 p.) as well as Iyad Nader small mammals collection kept at the NCW. Arthropod remains were identified up to the family level.

2.3. Data analysis

Diet composition was expressed by the number of individuals (minimum number of individuals, MNI) and percentage (number of individuals divided by the total number of prey individuals). The total number of prey individuals in a pellet was determined using the total number of mandibles and/or skulls found (Yalden and Morris, 1990YALDEN, D.W. and MORRIS, P.A., 1990. The analysis of owl pellets. Occasional Publication of the Mammal Society, vol. 13, pp. 1-24.). Dietary composition was estimated in terms of diversity using Simpson’s diversity index (Simpson, 1949SIMPSON, E.H., 1949. Measurement of diversity. Nature, vol. 163, no. 4148, p. 688. http://dx.doi.org/10.1038/163688a0.
http://dx.doi.org/10.1038/163688a0...
):

Pi is the relative representation of the “i” the prey category in the sample. To test for differences in diet composition between the two sites, we conducted a chi-square test of independence using the number of prey items consumed from every prey category.

3. Results

Pellets collected from both sites were cylindrical with an average of 56.36± 9.98 mm (mean ± standard deviation) in length (ranging from 32.43 and 75.2 mm in length), and 27.22± 2.62 mm in width (ranging from 22.38 and 38.29 mm in width) for Bsitah pellets, and 52.21± 15.33 mm in length (ranging from 37.44 and 86.6 mm in length), and 24.72±2.23 mm in width (18.57 and 21.04 mm in width) for Al Daba’ah pellets.

A total of 80 prey items were recovered from Bsitah pellets. The House Mouse, Mus musculus was the most dominant prey item (61.3%), followed by birds (16.3%). Prey items found in pellets from Al Daba’ah included remains of 84 individuals, with the Arabian Jerboa, Jaculus loftusi, being the most common accounting for 41.6% of the total prey items, followed by Sundevall's Jird, Meriones crassus (28.6%).

By species number, seven and nine species were found in Bsitah and Al Daba’ah pellets respectively. Animals recovered from Al Daba’ah pellets contained five native rodent species (Acomys dimidiatus, Meriones crassus, Jaculus loftusi, Gerbillus dasyurus, and Gerbillus sp.), while those from Bsitah included five species, one invasive (M. musculus), and four native species (Meriones crassus, Jaculus loftusi, Gerbillus sp. and Paraechinus aethiopicus). Furthermore, diet composition was more diverse in the Al Daba’ah site (3.62) compared to Bsitah (2.5) based on Simpson’s diversity estimates (Table 1). The diet composition of the owls from the two sites appeared to be independent in terms of the dietary composition as suggested by the significant value of the chi-square test (χ2 = 136.4; df 13; P < 0.05).

Table 1
Food composition of the Pharaoh eagle owl, Bubo ascalaphus in terms of frequencies and percentages of prey items from Bsitah and Al Daba’ah.

4. Discussion

The Pharaoh eagle owl is the most common species of owls in Saudi Arabia (Jennings, 2010JENNINGS, M.C., 2010. Atlas of the breeding birds of Arabia. Fauna of Arabia, vol. 25, pp. 1-751.). It was found to inhabit a wide range of habitats of arid rocky deserts. Recently, we conducted studies on the feeding behavior of this species (Al Ghamdi et al., 2023AL GHAMDI, A.R., ALSHAMMARY, T., AL GETHAMI, F., AL BOUG, A., AL JBOUR, S., ABU BAKER, M.M. and AMR, Z.S., 2023. Diet of Pharaoh Eagle-Owl, Bubo ascalaphus, from Ara’r region, northeastern Saudi Arabia. Ornis Hungarica, vol. 31, no. 2, pp. 226-235. http://dx.doi.org/10.2478/orhu-2023-0032.
http://dx.doi.org/10.2478/orhu-2023-0032...
) along with other owls (Al Ahmary et al., 2023AL AHMARY, A., AL OBAID, A., AL GHAMDI, A.-R., SHURAIM, F., AL JBOUR, S., AL BOUG, A. and AMR, Z.S., 2023. Diet of the Barn Owl, Tyto alba, from As Saqid Island, Farasan Archipelago, Saudi Arabia. Sandgrouse, vol. 45, pp. 79-83.). B. ascalaphus, is an opportunistic species that has a wide range of prey items depending on their availability in a particular habitat. For instance, it was found to feed on R. rattus and M. musculus in urban areas around Riyadh (Abi Said et al., 2020) and six species of wild rodents in Ara’ar region (Al Ghamdi et al., 2023AL GHAMDI, A.R., ALSHAMMARY, T., AL GETHAMI, F., AL BOUG, A., AL JBOUR, S., ABU BAKER, M.M. and AMR, Z.S., 2023. Diet of Pharaoh Eagle-Owl, Bubo ascalaphus, from Ara’r region, northeastern Saudi Arabia. Ornis Hungarica, vol. 31, no. 2, pp. 226-235. http://dx.doi.org/10.2478/orhu-2023-0032.
http://dx.doi.org/10.2478/orhu-2023-0032...
).

Elsewhere, Saufi et al. (2020)SAUFI, S., RAVINDRAN, S., HAMID, N.H., ZAINAL ABIDIN, C.M.R., AHMAD, H., AHMAD, A-H. and SALIM, H., 2020. Diet composition of introduced barn owls (Tyto alba javanica) in urban area in comparison with agriculture settings. Journal of Urban Ecology, vol. 6, no. 1, pp. 1-8. https://doi.org/10.1093/jue/juz025.
https://doi.org/10.1093/jue/juz025...
showed that the Barn Owl, T. a. javanica fed on R. norvegicus in urban areas, while hunted R. argentiventer in agricultural areas in Malaysia. Reduction of damage in palm plantations in Malaysia was observed after the introduction of the Barn Owl, where 98% of its diet consisted of rats (Duckett, 1991DUCKETT, J.E., 1991. Management of the barn owl (Tyto alba javanica) as a predator of rats in oil palm (Elaeis quineensis) plantations in Malaysia. Birds of Prey Bulletin, vol. 4, pp. 11-24.). Owl boxes for the Barn Owl were used in agricultural areas in the Jordan Valley to increase its population as a mean of biological control (Meyrom et al., 2009MEYROM, K., MOTRO, Y., LESHEM, Y., AVIEL, S., IZHAKI, I., ARGYLE, F. and CHARTER, M., 2009. Nest-box use by the Barn Owl Tyto alba in a biological pest control program in the Beit She’an valley, Israel. Ardea, vol. 97, no. 4, pp. 463-467. http://dx.doi.org/10.5253/078.097.0410.
http://dx.doi.org/10.5253/078.097.0410...
).

The results demonstrated that the B. ascalaphus owls have varied niche breadths and limited food-niche overlap between the two areas, suggesting opportunistic feeding habits that are likely influenced by prey availability, in the agricultural area of Bsitah, the owls fed more often on M. musculus which is small and thus required more than one individual to satisfy its nutritional needs hence more than one item per pellet were found, whereas in Al Daba’ah, high proportion of larger, wild rodents were eaten (M. crassus and J. loftusi), resulting mostly in one item per pellet (Figure 2).

Figure 2
Number of prey items per pellet from the two sites.

The house mouse was the most abundant prey item within the agricultural area of Bsitah. It is a commensal and invasive species that can establish colonies in remote agricultural areas in the desert. Previous studies have reported this mouse as the most frequent food item of the Barn Owl in the Middle East (Nader, 1968NADER, I., 1968. Animal remains in pellets of the Barn Owl, Tyto alba, from the vicinity of An-Najaf, Iraq. Bulletin of the Iraq Natural History Museum, vol. 4, pp. 1-7.; Abu Baker et al., 2005ABU BAKER, M., QARQAZ, M. and AMR, Z., 2005. Small mammal remains recovered from pellets of the Barn Owl (Tyto alba) at Shawmari Wildlife Reserve, eastern Jordan. Časopis Národního Muzea, Řada Přírodovědná, vol. 174, pp. 125-127.). Its high occurrence as the main prey item strongly suggests that owls have the potential to be an effective biological control agent against commensal small mammal pest populations therefore providing valuable pest control services in these areas. In the Bethlehem, the Palestinian Territories, Rattus rattus constituted 37% of the diet of the Eurasian Eagle Owl, Bubo bubo (Amr et al., 2016). Abi Said et al. (2020) showed that the Pharaoh Eagle Owl diet consisted of 11.82% R. rattus and 1.48% M. musculus in an urban area around Riyadh, thus a good candidate as a biological control agent. The same observation was made in suburbs of Hurghada, Egypt, whereas B. ascalaphus consumed a large proportion of both adults and juveniles of Rattus norvegicus by both number of consumed individuals (66.1%) and by biomass (89.1%), and M. musculus (Moldován and Sándor, 2009).

This study suggests the use of owl’s nest boxes for small-sized owls in agricultural areas in Saudi Arabia as an environmentally friendly method to reduce pest rodents in both open agricultural areas and palm plantations.

Acknowledgements

This study was supported by the National Center for Wildlife (NCW), Kingdom of Saudi Arabia. Our thanks are extended to Faisal Shuraim, Director of Department of Terrestrial Mammals for his encouragement and support. Authors wish to express their gratitude to Dr. Mohammed Qurban, Chief Executive Officer, NCW for his continuous support and guidance.

References

  • ABI-SAID, M.R., AL ZEIN, M.S., ABU BAKER, M.A. and AMR, Z.S., 2020. Diet of the desert eagle owl, Bubo ascalaphus, Savigny 1809 in Eastern Saudi Arabia. Pakistan Journal of Zoology, vol. 52, no. 3, pp. 1169-1171. http://dx.doi.org/10.17582/journal.pjz/20190130180117
    » http://dx.doi.org/10.17582/journal.pjz/20190130180117
  • ABU BAKER, M., QARQAZ, M. and AMR, Z., 2005. Small mammal remains recovered from pellets of the Barn Owl (Tyto alba) at Shawmari Wildlife Reserve, eastern Jordan. Časopis Národního Muzea, Řada Přírodovědná, vol. 174, pp. 125-127.
  • AL AHMARY, A., AL OBAID, A., AL GHAMDI, A.-R., SHURAIM, F., AL JBOUR, S., AL BOUG, A. and AMR, Z.S., 2023. Diet of the Barn Owl, Tyto alba, from As Saqid Island, Farasan Archipelago, Saudi Arabia. Sandgrouse, vol. 45, pp. 79-83.
  • AL GHAMDI, A.R., ALSHAMMARY, T., AL GETHAMI, F., AL BOUG, A., AL JBOUR, S., ABU BAKER, M.M. and AMR, Z.S., 2023. Diet of Pharaoh Eagle-Owl, Bubo ascalaphus, from Ara’r region, northeastern Saudi Arabia. Ornis Hungarica, vol. 31, no. 2, pp. 226-235. http://dx.doi.org/10.2478/orhu-2023-0032
    » http://dx.doi.org/10.2478/orhu-2023-0032
  • AMR, Z.S., 2012. Mammal of Jordan 2nd ed. Amman: Al Rai Press, 308 p.
  • BONTZORLOS, V.A., PERIS, S.J., VLACHOS, C.G. and BAKALOUDIS, D.E., 2005. The diet of barn owl in the agricultural landscapes of central Greece. Folia Zoologica, vol. 54, no. 1-2, pp. 99-110.
  • DUCKETT, J.E., 1991. Management of the barn owl (Tyto alba javanica) as a predator of rats in oil palm (Elaeis quineensis) plantations in Malaysia. Birds of Prey Bulletin, vol. 4, pp. 11-24.
  • JENNINGS, M.C., 2010. Atlas of the breeding birds of Arabia. Fauna of Arabia, vol. 25, pp. 1-751.
  • MEYROM, K., MOTRO, Y., LESHEM, Y., AVIEL, S., IZHAKI, I., ARGYLE, F. and CHARTER, M., 2009. Nest-box use by the Barn Owl Tyto alba in a biological pest control program in the Beit She’an valley, Israel. Ardea, vol. 97, no. 4, pp. 463-467. http://dx.doi.org/10.5253/078.097.0410
    » http://dx.doi.org/10.5253/078.097.0410
  • MOHEDANO, I., ABU BAKER, M.A., HUNTER, B., BUCHAN, J., MICHAELS, C.J. and YAMAGUCHI, N., 2014. On the diet of the Pharaoh Eagle Owl, Bubo ascalaphus (Savigny, 1809), in Qatar, with an overview of its feeding habits. Zoology in the Middle East, vol. 60, no. 2, pp. 111-119. http://dx.doi.org/10.1080/09397140.2014.914713
    » http://dx.doi.org/10.1080/09397140.2014.914713
  • MOULTON, C.E., BRADY, R.S. and BELTHOFF, J.R., 2005. A comparison of breeding season food habits of burrowing owls nesting in agricultural and nonagricultural habitat in Idaho. The Journal of Raptor Research, vol. 39, no. 4, pp. 429-438.
  • MURANO, C., KASAHARA, S., KUDO, S., INADA, A., SATO, S., WATANABE, K. and AZUMA, N., 2019. Effectiveness of vole control by owls in apple orchards. Journal of Applied Ecology, vol. 56, no. 3, pp. 677-687. http://dx.doi.org/10.1111/1365-2664.13295
    » http://dx.doi.org/10.1111/1365-2664.13295
  • NADER, I., 1968. Animal remains in pellets of the Barn Owl, Tyto alba, from the vicinity of An-Najaf, Iraq. Bulletin of the Iraq Natural History Museum, vol. 4, pp. 1-7.
  • RIFAI, L.B., AL-MELHIM, W.N., GHARAIBEH, B.M. and AMR, Z., 2000. The diet of the Desert Eagle Owl, Bubo bubo ascalaphus, in the Eastern Desert of Jordan. Journal of Arid Environments, vol. 44, no. 3, pp. 369-372. http://dx.doi.org/10.1006/jare.1999.0601
    » http://dx.doi.org/10.1006/jare.1999.0601
  • SAUFI, S., RAVINDRAN, S., HAMID, N.H., ZAINAL ABIDIN, C.M.R., AHMAD, H., AHMAD, A-H. and SALIM, H., 2020. Diet composition of introduced barn owls (Tyto alba javanica) in urban area in comparison with agriculture settings. Journal of Urban Ecology, vol. 6, no. 1, pp. 1-8. https://doi.org/10.1093/jue/juz025
    » https://doi.org/10.1093/jue/juz025
  • SIMPSON, E.H., 1949. Measurement of diversity. Nature, vol. 163, no. 4148, p. 688. http://dx.doi.org/10.1038/163688a0
    » http://dx.doi.org/10.1038/163688a0
  • STENKEWITZ, U., WILSON, B. and KAMLER, J.F., 2010. Seasonal comparisons of barn owl diets in an agricultural and natural area in Central South Africa. The Ostrich, vol. 81, no. 2, pp. 163-166. http://dx.doi.org/10.2989/00306525.2010.488423
    » http://dx.doi.org/10.2989/00306525.2010.488423
  • YALDEN, D.W. and MORRIS, P.A., 1990. The analysis of owl pellets. Occasional Publication of the Mammal Society, vol. 13, pp. 1-24.

Publication Dates

  • Publication in this collection
    18 Dec 2023
  • Date of issue
    2023

History

  • Received
    30 June 2023
  • Accepted
    14 Nov 2023
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