Abstracts
Honeydew foraging by birds has been extensively documented in recent years. However, this interaction has been poorly documented in Brazil, with predominance of few species of birds foraging only in Mimosa scabrella trees. With the objective of describing the behavior of birds interacting with scale insects associated with trees, we conducted a study at the Serra de São José, Tiradentes, in the State of Minas Gerais, Brazil. Observations were recorded from June to July 2012. We observed 13 species of birds feeding on honeydew scale insects, eight never previously recorded. We observed individuals using aerial and surface maneuvers to collect the honeydew on the branches or reaching the droppings below the branches. These species were observed foraging individually, in pairs and also in large groups. Our results suggest that honeydew excretion from scale insects associated with Pseudopiptadenia leptostachya trees represents an important energy source for local birds as observed in fragments of Atlantic Forest in the Minas Gerais State, southeast region of Brazil.
trophic connections; excretion; insects; behavior maneuvers; Serra de São José
O uso de excreções líquidas açucaradas por aves tem sido amplamente divulgado nos últimos anos. No entanto, estudos acerca desta interação são escassos no Brasil, sendo que os poucos existentes relatam apenas algumas espécies de aves forrageando a excreção de insetos presentes em uma única espécie de árvore (Mimosa scabrella). Com o objetivo de descrever o comportamento de aves interagindo com insetos excretores de líquidos açucarados associados com árvores, nós conduzimos um estudo na Serra de São José, município de Tiradentes em Minas Gerais, Brasil. Nossas observações foram feitas de Junho a Julho de 2012 e 13 espécies de aves foram registradas forrageando a excreção, sendo que oito delas nunca haviam sido anteriormente registradas envolvidas neste tipo de interação. Nós observamos indivíduos usando manobras aéreas e na superfície das árvores para coletar a excreção nos galhos ou alcançar gotículas debaixo dos troncos. Estas espécies foram observadas forrageando individualmente, em pares ou em grandes grupos. Nossos resultados sugerem que a excreção açucarada excretada por insetos associados com árvores mamica-de-porca (Pseudopiptadenia leptostachya), representa uma importante fonte de energia para as aves, conforme observado em fragmentos de mata Atlântica no Estado de Minas Gerais, sudeste do Brasil.
conexões tróficas; excreção; insetos; manobras comportamentais; Serra de São José
Introduction
Honeydew foraging by birds has been extensively documented as a result of an important interaction with scale insects (Hemiptera, Coccoidea) (Gamper & Koptur 2010GAMPER, H.A. & KOPTUR, S. 2010. Honeydew foraging by birds in tropical montane forests and pastures of Mexico. J. Trop. Ecol. 26:335-41. http://dx.doi.org/10.1017/S0266467409990654
http://dx.doi.org/10.1017/S0266467409990...
, Beggs 2001BEGGS, J.R. 2001. The ecological consequences of social wasps (Vespula spp.) invading an ecosystem that has an abundant carbohydrate resource. Biol. Conserv. 99:17-28. http://dx.doi.org/10.1016/S0006-3207(00)00185-3
http://dx.doi.org/10.1016/S0006-3207(00)...
, Gaze & Clout 1983GAZE, P.D. & CLOUT, M.N. 1983. Honeydew and its importance to birds in beech forest of the South Island, New Zealand. New Zeal. J. Ecol.6:33-37., Greenberg et al. 1993GREENBERG, R., MACIAS, C.C. & BICHIER, P. 1993. Defense of homopteran honeydew by birds in the Mexican highlands and other warm temperate forests. Oikos 68:519-524. http://dx.doi.org/10.2307/3544920
http://dx.doi.org/10.2307/3544920...
, Jirón & Salas 1975JIRÓN, L. & SALAS, S. 1975. Simbiosis entre “cochinillas de cola” (Coccidoidea: Margarodidae) y otros insectos. I. Los componentes del sistema simbiótico en la tierra alta de Costa Rica. Brenesia 5:67-71., Koster & Stoewesand 1973KOSTER, F. & STOEWESAND, H. 1973. Schildläuse als Honigtaulieferanten für Kolibris und Insekten. Bonn. Zool. Beitr. 24:15-23., Latta et al. 2001LATTA, S.C., GAMPER, H.A. & TIETZ, J.R. 2001. Revising the convergence hypothesis of avian use of honeydew: evidence from Dominican subtropical dry forest. Oikos 93:250-259. http://dx.doi.org/10.1034/j.1600-0706.2001.930208.x
http://dx.doi.org/10.1034/j.1600-0706.20...
, Murphy & Kelly 2003MURPHY, D.J. & KELLY, D. 2003. Seasonal variation in the honeydew, invertebrate, fruit and nectar resource for bellbirds in a New Zealand mountain beech forest. New Zeal. J. Ecol.27:11-23., Paton 1980PATON, D.C. 1980. The importance of manna, honeydew, and lerp in the diets of honeyeaters. Emu 80:213-226., Woinarski 1984WOINARSKI, J.C.Z. 1984. Small birds, lerp-feeding and the problem of honeyeaters. Emu 84:137-141. http://dx.doi.org/10.1071/MU9840137
http://dx.doi.org/10.1071/MU9840137...
). Scale insects need large amounts of phloem to fulfill their nutrient demands and therefore excrete large amounts of honeydew, which is sugary waste rich in carbohydrates and amino acids. The excretion is done through small drops of honeydew at the end of a long anal filament (Williams & Williams 1980WILLIAMS, J.R. & WILLIAMS, D.J. 1980. Excretory behaviour in soft scales (Hemiptera: Coccoidae). B. Entomol. Res. 70:253-257. http://dx.doi.org/10.1017/S0007485300007513
http://dx.doi.org/10.1017/S0007485300007...
). In some ecosystems, the use of honeydew by ants, wasps and bees has been recorded (Bach 1991BACH, C.E. 1991. Direct and indirect interactions between ants (Pheidole megacephala), scales (Coccus viridis) and plants (Pluchea indica). Oecologia 87:233-239. http://dx.doi.org/10.1007/BF00325261
http://dx.doi.org/10.1007/BF00325261...
, Moller & Tilley 1989MOLLER, H. & TILLEY, J.A.V. 1989. Beech honeydew: seasonal variation and use by wasps, honey bees, and other insects. New Zeal. J. Zool. 16: 289-302. http://dx.doi.org/10.1080/03014223.1989.10422894
http://dx.doi.org/10.1080/03014223.1989....
, Didham 1993DIDHAM, R.K. 1993. The influence of honeydew on arthropods associated with beech trees in New Zealand. New Zeal. Nat. Sci. 20:47-53.). The use of honeydew may represent the primary source of carbohydrates to a large array of wildlife and may improve trophic connections (Grant & Beggs 1989GRANT, W.D. & BEGGS, J.R. 1989. Carbohydrate analysis of beech honeydew. New Zeal. J. Zool. 16:283-288. http://dx.doi.org/10.1080/03014223.1989.10422893
http://dx.doi.org/10.1080/03014223.1989....
).
In Brazil honeydew foraging by birds has been poorly documented, with predominance of scale insects associated with bracatinga trees (Mimosa scabrella Benth). Species of hummingbirds such as Leucochloris albicollis (Vieillot, 1818) and Chlorostilbon lucidus (Shaw, 1812) have been recorded foraging on scale insects mostly in the Santa Catarina State, south region of the country (Reichholf & Reichholf 1973REICHHOLF, H. & REICHHOLF, J. 1973. “Honigtau” der BracatingaSchildlaus als Winternahrung von Kolibris (Trochilidae) in Sud-Brasilien. Bonn. Zool. Beitr. 24:7-14.). Besides hummingbirds, groups of other species of birds, such as L. albicollis, Parula pitiayumi (Vieillot, 1817), Tangara peruviana (Desmarest, 1806), Stephanophorus diadematus (Temminck, 1823), Tachyphonus coronatus (Vieillot, 1822), Saltator similis (d'Orbigny & Lafresnaye, 1837) and Zonotrichia capensis (Müller, 1776) have been recorded foraging in one bracatinga tree of approximately 12 meters, in the northern area of Santa Catarina State (Sick 1988SICK, H. 1988. Ornitologia brasileira, uma introdução, v. 1. Editora Universidade de Brasília, Brasília, 827p., L.A. Rosário pers. comm.). In another occasion, a group comprised of eight maroon-bellied parakeets (Pyrrhura frontalis, Vieillot, 1817), was also recorded in one Mimosa scabrella tree in the highland forests of the same State (Rosário 1996ROSÁRIO, L.A. 1996. As aves em Santa Catarina: distribuição geográfica e meio ambiente. Editora FATMA, Florianópolis, 326p.). Our objective was to describe the behavior of birds interacting with scale insects associated with trees in the southeastern region of Brazil and discuss the importance of this interaction.
Material and Methods
This study was conducted at the Serra de São José, a mountain range near the town of Tiradentes, in the State of Minas Gerais, Brazil. The region is located in the ecotone of the Cerrado and semi-deciduous portions of the Atlantic Forest (Oliveira-Filho & Machado 1993OLIVEIRA-FILHO, A.T. & MACHADO, J.N.M. 1993. Composição florística de uma floresta semidecídua montana, na Serra de São José, Tiradentes, MG. Acta Bot. Bras. 7:71-88. http://dx.doi.org/10.1590/S0102-33061993000200004
http://dx.doi.org/10.1590/S0102-33061993...
). The vegetation is very diversified (Carvalho et al. 1994CARVALHO, M.M., EVANGELHISTA, A.R. & CURI, N. 1994. Desenvolvimento fisiográfico de pastagens na zona fisiográfica Campos das Vertentes, MG. Empresa Brasileira de Pesquisa Agropecuária, Escola Superior de Agricultura de Lavras, Coronel Pacheco, 127p.), originally comprised by a complex mosaic of forest patches, Cerrado and opens fields of campos rupestres (Eiten 1982EITEN, G. 1982. Brazilian savannas. In: HUNTLEY, B.J. & WALKER, B.H. (Eds.). Ecology of tropical savannas. Springer-Verlag, Berlin, p.25-47. http://dx.doi.org/10.1007/978-3-642-68786-0_3
http://dx.doi.org/10.1007/978-3-642-6878...
). The tropical climate of the region is characterized by rainy summers and dry winters. Mean annual precipitation and temperature at the base of the mountain range were 1.514-1.588 mm and 19,3- 20,1 °C respectively, whereas at the upper montane area were 1.536-1.605 mm and 14,8-18,6 °C (Pereira et al. 2007PEREIRA, J.A.A., OLIVEIRA FILHO, A.T. & LEMOS-FILHO, J.P. 2007. Environmental heterogeneity and disturbance by humans control much of the tree species diversity of fragments of tropical montane seasonal forests in SE Brazil. Biol. Conserv. (16):1761-1784. http://dx.doi.org/10.1007/s10531-006-9063-4
http://dx.doi.org/10.1007/s10531-006-906...
). Approximately 70% of the rains occur between November and February.
The fragment where observations were recorded was located at an altitude of approximately 1000 meters (21° 6′ 6.79″ S and 44° 10′ 53.30″ W) in a semi-deciduous fragment of forest along the southern border of the study area. The fragment was comprised by medium-sized trees of approximately 16 meters in the interior portion of the semi-deciduous forest.
Observations were recorded from June (15th, 17th, 18th, 19th and 26th) to July (7th), 2012. The number of birds visiting the trees, species and total time spent in the tree by each bird, were recorded during 3 hours observation periods. Observations were made using binoculars (Bushnell 8×40 mm) during the first hours of the morning (7:00-10:30 hours) and between 15:00-17:30 hours in the afternoon. All the birds visiting the trees were followed visually to determine whether they were feeding on scale insect honeydew or performing another sort of behavior. Feeding behaviors or intraspecific interactions (chasing behavior or physical contact) not direct related to honeydew feeding were recorded by taking photographs (Canon Powershot SX30) of birds. We assumed that each picture corresponded to one independent event of feeding behavior since individual identification of birds was not accomplished visually. To guide our interpretation of different behaviors performed by the birds, we use descriptions suggested by Volpato & Mendonça-Lima (2002)VOLPATO, G.H. & MENDONÇA-LIMA, A. 2002. Estratégias de forrageamento: proposta de termos para a língua Portuguesa. Ararajuba 10:101-105., based on Remsen & Robinson (1990)REMSEN, J.V. & ROBINSON, S. K. 1990. A classification scheme for foraging behavior of birds in terrestrial habitats. Stud. Avian Biol. 13:144-160..
Results
We recorded a total of 16 bird species visiting trees during our six different observation periods (four periods during the mornings of 15, 17, 26 of June, and 07 of July, and two in the afternoons of 18 and 19 of June). Of those 16 bird species, 13 (81%) were observed feeding on honeydew scale insects (Table 1). All individual observation trees were determined to be Pseudopiptadenia leptostachya (Benth). The other three species were visiting the trees to either feed on other species of insects (Florisuga fusca Vieillot, 1817, and Sittasomus griseicapillus Vieillot, 1818) or just resting (Amazilia versicolor Vieillot, 1818). All bird species were considered resident to the study area.
Bird species visits to scale insects on mamica-de-porca trees in a semi-deciduous fragment of forest at the Serra de São José, Minas Gerais State, Brazil (June to July, 2012). The use of honeydew is indicated by Y = yes, N = no. Behavior status (A = aerial, S= surface).
Honeydew feeding behavior differed among observed birds. On four periods (15, 17, 18 and 26 of June) we observed single individuals of five species (Leucochloris albicollis, Amazilia lacteal, Lesson, 1832, Thalurania glaucopis Gmelin, 1788, Tangara cyanoventris Vieillot, 1819, and Chlorostilbon lucidus) using sally-hover aerial maneuvers for feeding on honeydew. Among these species, only Leucochloris albicollis was observed foraging in large numbers of approximately twelve individuals.
Other eight species of birds were observed foraging honeydew using surface maneuvers either gleaning to collect the honeydew on the branches or reaching the droppings below the branches. These species were observed on three periods (17 and 26 of June and 07 of July) foraging individually (Tangara palmarum Wied, 1823, Dacnis cayana Linnaeus, 1766, Tachyphonus coronatus, Parula pitiayumi,Tangara cayana Linnaeus, 1766, and Coereba flaveola Linnaeus, 1758), in pairs (Tangara sayaca Linnaeus, 1766, and Hemithraupis ruficapilla Vieillot, 1818), in groups of three individuals being two adults and one young (Tangara sayaca) or groups of approximately ten individuals (Tangara cyanoventris).
Three other species were observed foraging insects either on the canopy (Florisuga fusca, Sittasomus griseicapillus) or on the understory (Amazilia versicolor) of Pseudopiptadenia leptostachya trees. However we could not confirm the foraging of honeydew by these species. In addition to bird species, we observed a large amount of bees (Trigona sp.) feeding on honeydew on the 18 of June. During this observation period, we did not record birds foraging on honeydew while bees were present at the trees.
Discussion
Our results show high incidence of movement among local birds towards Pseudopiptadenia leptostachya trees for foraging honeydew. These results suggest that honeydew excretion represents an important energy source for local birds. This fact seems to be supported by our observations of approximately 12 birds of the same species feeding at the same time and a total of 13 different species foraging along six different observation periods.
Honeydew excretion is considered an important carbohydrate source for several animals (Gaze & Clout 1983GAZE, P.D. & CLOUT, M.N. 1983. Honeydew and its importance to birds in beech forest of the South Island, New Zealand. New Zeal. J. Ecol.6:33-37., Grant & Beggs 1989GRANT, W.D. & BEGGS, J.R. 1989. Carbohydrate analysis of beech honeydew. New Zeal. J. Zool. 16:283-288. http://dx.doi.org/10.1080/03014223.1989.10422893
http://dx.doi.org/10.1080/03014223.1989....
) because it is more easily metabolized (almost totally) in comparison with other types of food, like invertebrates (approximately 70% of metabolization) (Bell 1990BELL, G.P. 1990. Birds and mammals on an insect diet: a primer on diet composition analysis in relation to ecological energetics. In: MORRISON, M.L., RALPH, C.J., VERNER, J. & JEHL, J.R. (Eds.). Avian foraging: theory, methodology and applications. Cooper Ornithological Society, Lawrence, Kansas, p.416-422.). Moreover, the cost of foraging on honeydew is lower than foraging for invertebrates, particularly those more difficult to find and capture (Murphy & Kelly 2003MURPHY, D.J. & KELLY, D. 2003. Seasonal variation in the honeydew, invertebrate, fruit and nectar resource for bellbirds in a New Zealand mountain beech forest. New Zeal. J. Ecol.27:11-23.).
Hierarchy of dominance and spatial segregation have already been reported among Trochilidae (Antunes 2003ANTUNES, A.Z. 2003. Partilha de néctar de Eucalyptus spp., territorialidade e hierarquia de dominância em beija-flores (Aves: Trochilidae) no sudeste do Brasil. Ararajuba 11(1):39-44.). Indeed, larger individuals seem to dominate over areas with higher resource availability (Camfield 2006CAMFIELD, A.F. 2006. Resource value affects territorial defense by broad-tailed and rufous hummingbirds. J Field Ornithol. 77:120-125. http://dx.doi.org/10.1111/j.1557-9263.2006.00031.x
http://dx.doi.org/10.1111/j.1557-9263.20...
, Lara et al. 2009LARA, C., LUMBRERAS, K. & GONZÁLEZ, M. 2009. Niche partitioning among hummingbirds foraging on Penstemon roseus (Plantaginaceae) in central Mexico. Ornitol. Neotrop. 20:73-83., 2011LARA, C., MARTINEZ-GARCIA, V., ORTIZ-PULIDO, R., BRAVO-CADENA, J. & CORDOBA-AGUILAR, A. 2011. Temporal-spatial segregation among hummingbirds foraging on honeydew in a temperate forest in Mexico. Current Zool. 57:56-62.), while smaller species feed either on the top of the canopy or near to bottom of the trees' bark (Lara et al. 2009LARA, C., LUMBRERAS, K. & GONZÁLEZ, M. 2009. Niche partitioning among hummingbirds foraging on Penstemon roseus (Plantaginaceae) in central Mexico. Ornitol. Neotrop. 20:73-83., 2011LARA, C., MARTINEZ-GARCIA, V., ORTIZ-PULIDO, R., BRAVO-CADENA, J. & CORDOBA-AGUILAR, A. 2011. Temporal-spatial segregation among hummingbirds foraging on honeydew in a temperate forest in Mexico. Current Zool. 57:56-62.). However, our results suggest that Thalurania glaucopis, which is a larger species than Leucochloris albicollis and Amazilia lactea (Sick 1988SICK, H. 1988. Ornitologia brasileira, uma introdução, v. 1. Editora Universidade de Brasília, Brasília, 827p.), was less abundant and fed only on the bottom portion of the trees bark. Although considered an aggressive species that dominate food resources (Persegona et al. 2009), it is commonly found inhabiting the understory or medium strata of the forest, while other species occupy the canopy (Parker III et al. 1996PARKER III, T. A., STOTZ, D.F. & FITZPATRICK, J.W. 1996. Ecological and distributional databases. In: STOTZ, D. F., FITZPATRICK, J.W., PARKER III, T.A. & MOSKOVITS, D.K. (Eds.). Neotropical birds: ecology and conservation. Univ. Chicago Press, Chicago, 478p.). This might explain the minimum contact among Trochilidae species during our study.
Our results show that birds presented two different types of behavior while foraging on honeydew. Birds either used aerial maneuvers or surface maneuvers. In the first case, birds normally performed sally-hover movements for foraging while in the second case they gleaned to collect the honeydew on the branches or reached the droppings below the branches. While the Apodiformes performed only aerial maneuvers to forage on honeydew available on the branches or below them, all the Passeriformes but Tangara cyanoventris, fed exclusively through surface maneuvers. Therefore it seems that Passeriformes had a wider array of spatial behavior strategies while exploring honeydew.
Our results show a spatial interaction between birds and honeybees at least in one of our observation periods. While no antagonistic interactions between nectarivorous birds and insects such as wasps have been reported in previous studies (Gaze & Clout 1983GAZE, P.D. & CLOUT, M.N. 1983. Honeydew and its importance to birds in beech forest of the South Island, New Zealand. New Zeal. J. Ecol.6:33-37.), this bee species seems to represent an annoyance to humming bird species (Sick 1988SICK, H. 1988. Ornitologia brasileira, uma introdução, v. 1. Editora Universidade de Brasília, Brasília, 827p.).
Of the thirteen bird species recorded by this study, eight had not been previously recorded foraging on honeydew. There has been a known interaction between Coereba flaveola and scale insects (Coccoidea) in the subtropical dry forests at Dominican Republic (Latta et al. 2001LATTA, S.C., GAMPER, H.A. & TIETZ, J.R. 2001. Revising the convergence hypothesis of avian use of honeydew: evidence from Dominican subtropical dry forest. Oikos 93:250-259. http://dx.doi.org/10.1034/j.1600-0706.2001.930208.x
http://dx.doi.org/10.1034/j.1600-0706.20...
). However, this is the first report recording the use of honeydew by this species in Brazil. For the species recorded in our study, previous reports indicate the use of honeydew by only Leucochloris albicollis, Chlorostilbon lucidus (Reichholf & Reichholf 1973REICHHOLF, H. & REICHHOLF, J. 1973. “Honigtau” der BracatingaSchildlaus als Winternahrung von Kolibris (Trochilidae) in Sud-Brasilien. Bonn. Zool. Beitr. 24:7-14., Sick 1988SICK, H. 1988. Ornitologia brasileira, uma introdução, v. 1. Editora Universidade de Brasília, Brasília, 827p.), Parula pitiayumi and Tachyphonus coronatus (Sick 1988SICK, H. 1988. Ornitologia brasileira, uma introdução, v. 1. Editora Universidade de Brasília, Brasília, 827p.). Moreover, all reports have occurred in the Santa Catarina State, in the south of Brazil and only in the Mimosa scabrella trees. Our results suggest that honeydew excretion associated with Pseudopiptadenia leptostachya trees represents an important energy source for local birds as observed in fragments of Atlantic Forest in the Minas Gerais State, southeastern region of Brazil.
Despite the apparent importance and relevance of the behaviors herein documented, studies about the use of honeydew by birds in Brazil are scant. Some aspects such as seasonality of honeydew foraging, identification of other insects involved in the interactions and behavioral aspects of the foraging are unknown and more studies should be performed to elucidate the importance of such resource for birds.
We would like to thank Lenir Rosário for her contribution to this manuscript. We thank Fundação de Amparo à Pesquisa do Estado de Minas Gerais (FAPEMIG) for the financial support and the Instituto Estadual de Florestas de Minas Gerais (IEF) for license to conduct this project and for institutional support.
References
- ANTUNES, A.Z. 2003. Partilha de néctar de Eucalyptus spp., territorialidade e hierarquia de dominância em beija-flores (Aves: Trochilidae) no sudeste do Brasil. Ararajuba 11(1):39-44.
- BACH, C.E. 1991. Direct and indirect interactions between ants (Pheidole megacephala), scales (Coccus viridis) and plants (Pluchea indica). Oecologia 87:233-239. http://dx.doi.org/10.1007/BF00325261
» http://dx.doi.org/10.1007/BF00325261 - BEGGS, J.R. 2001. The ecological consequences of social wasps (Vespula spp.) invading an ecosystem that has an abundant carbohydrate resource. Biol. Conserv. 99:17-28. http://dx.doi.org/10.1016/S0006-3207(00)00185-3
» http://dx.doi.org/10.1016/S0006-3207(00)00185-3 - BELL, G.P. 1990. Birds and mammals on an insect diet: a primer on diet composition analysis in relation to ecological energetics. In: MORRISON, M.L., RALPH, C.J., VERNER, J. & JEHL, J.R. (Eds.). Avian foraging: theory, methodology and applications. Cooper Ornithological Society, Lawrence, Kansas, p.416-422.
- CAMFIELD, A.F. 2006. Resource value affects territorial defense by broad-tailed and rufous hummingbirds. J Field Ornithol. 77:120-125. http://dx.doi.org/10.1111/j.1557-9263.2006.00031.x
» http://dx.doi.org/10.1111/j.1557-9263.2006.00031.x - CARVALHO, M.M., EVANGELHISTA, A.R. & CURI, N. 1994. Desenvolvimento fisiográfico de pastagens na zona fisiográfica Campos das Vertentes, MG. Empresa Brasileira de Pesquisa Agropecuária, Escola Superior de Agricultura de Lavras, Coronel Pacheco, 127p.
- DIDHAM, R.K. 1993. The influence of honeydew on arthropods associated with beech trees in New Zealand. New Zeal. Nat. Sci. 20:47-53.
- EITEN, G. 1982. Brazilian savannas. In: HUNTLEY, B.J. & WALKER, B.H. (Eds.). Ecology of tropical savannas. Springer-Verlag, Berlin, p.25-47. http://dx.doi.org/10.1007/978-3-642-68786-0_3
» http://dx.doi.org/10.1007/978-3-642-68786-0_3 - GAZE, P.D. & CLOUT, M.N. 1983. Honeydew and its importance to birds in beech forest of the South Island, New Zealand. New Zeal. J. Ecol.6:33-37.
- GAMPER, H.A. & KOPTUR, S. 2010. Honeydew foraging by birds in tropical montane forests and pastures of Mexico. J. Trop. Ecol. 26:335-41. http://dx.doi.org/10.1017/S0266467409990654
» http://dx.doi.org/10.1017/S0266467409990654 - GREENBERG, R., MACIAS, C.C. & BICHIER, P. 1993. Defense of homopteran honeydew by birds in the Mexican highlands and other warm temperate forests. Oikos 68:519-524. http://dx.doi.org/10.2307/3544920
» http://dx.doi.org/10.2307/3544920 - GRANT, W.D. & BEGGS, J.R. 1989. Carbohydrate analysis of beech honeydew. New Zeal. J. Zool. 16:283-288. http://dx.doi.org/10.1080/03014223.1989.10422893
» http://dx.doi.org/10.1080/03014223.1989.10422893 - JIRÓN, L. & SALAS, S. 1975. Simbiosis entre “cochinillas de cola” (Coccidoidea: Margarodidae) y otros insectos. I. Los componentes del sistema simbiótico en la tierra alta de Costa Rica. Brenesia 5:67-71.
- KOSTER, F. & STOEWESAND, H. 1973. Schildläuse als Honigtaulieferanten für Kolibris und Insekten. Bonn. Zool. Beitr. 24:15-23.
- LARA, C., LUMBRERAS, K. & GONZÁLEZ, M. 2009. Niche partitioning among hummingbirds foraging on Penstemon roseus (Plantaginaceae) in central Mexico. Ornitol. Neotrop. 20:73-83.
- LARA, C., MARTINEZ-GARCIA, V., ORTIZ-PULIDO, R., BRAVO-CADENA, J. & CORDOBA-AGUILAR, A. 2011. Temporal-spatial segregation among hummingbirds foraging on honeydew in a temperate forest in Mexico. Current Zool. 57:56-62.
- LATTA, S.C., GAMPER, H.A. & TIETZ, J.R. 2001. Revising the convergence hypothesis of avian use of honeydew: evidence from Dominican subtropical dry forest. Oikos 93:250-259. http://dx.doi.org/10.1034/j.1600-0706.2001.930208.x
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» http://dx.doi.org/10.1080/03014223.1989.10422894 - MURPHY, D.J. & KELLY, D. 2003. Seasonal variation in the honeydew, invertebrate, fruit and nectar resource for bellbirds in a New Zealand mountain beech forest. New Zeal. J. Ecol.27:11-23.
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Publication Dates
-
Publication in this collection
Dec 2013
History
-
Received
8 July 2013 -
Reviewed
30 Oct 2013 -
Accepted
7 Dec 2013