Browse > Article

Floral Visitors and Nectar Secretion of the Japanese Camellia, Camellia Japonica L.  

Rho, Jeong-Rae (School of Biological Sciences, Seoul National University)
Choe, Chun-Choe (School of Biological Sciences, Seoul National University)
Publication Information
Animal cells and systems / v.7, no.2, 2003 , pp. 123-125 More about this Journal
Abstract
We studied the nectar secretion of the Japanese Camellia (Camellia japonica L.), an evergreen tree and observed its floral visitors during the day. The mean volume of nectar secreted, during daylight (08:31 to 16:30 h) was 30.26$\pm8,29ml$ (SD) (n = 27). During the late afternoon and overnight (16:31 to 08:30 following day), 100.54$\pm54.85$(n = 27) of nectar was secreted. Total volume measured when flowers were sampled once every two hours for an eight-hour period was approximately one-half the volume which was measured when the flowers were sampled only once after eight hours. The mean nectar volume secreted was 8.55$\pm8.3ml$(n = 30) between 08:31 to 10:30, 4.38$\pm$6.1 ml (n = 30) between 10:31 to 12:30, 4.6$\pm5.4ml$(n = 30) between 12;31 to 14:30, and 4.02$\pm3.5ml$(n = 30) between 14:31 to 16:30 hours. During the day, Japanese Camellia flowers were principally visited by the Japanese white-eye (Zosterops erythropleura erythropleura 5.), a native bird, although insects and squirrels also visited to a lesser degree.
Keywords
Bird and mammal pollination; Japanese white-eye; Nectar production; Squirrel;
Citations & Related Records
연도 인용수 순위
  • Reference
1 Cruden RW, Hermann SM, and Peterson S (1983) Patterns of nectar production and plant-pollinator coevolution, In:Bentley B and Elias BT(eds), The Biology of Nectarines. Columbia University Press, New York, pp 82-125
2 Kakutani T, Inoue T, and Kato M (1989) Nectar secretion pattern of the dish-shaped flower, Cayratia japonica (Vitaceae), and nectar utilization patterns by insect visitors. Res Popul Ecol 31: 381-400   DOI
3 Kwok KK and Corlett RC (2000) The bird communities of a natural secondary forest and a Lophostemon confertus plantation in Hong Kong, South China. Forest Ecol Manag 130: 227-234   DOI   ScienceOn
4 Law BS, Lean M (1999) Common blossom bats (Syconycteris australis) as pollinators in fragmented Australian tropical rainforest. Biol Conserv 91: 201-212   DOI   ScienceOn
5 Pattersson S and Knudsen AJ (2001) Floral scent and nectar production in Parkia biglobosa Jacq. (Leguminosae: Mimosoideae). Bot J Linean Soc 135: 97-106   DOI   ScienceOn
6 Proctor M, Yeo P, and Lack A (1996) The Natural History of Pollination. Timber Press, Oregon, pp 130-133 and 225-265
7 Rathcke BJ (1992) Nectar distribution, pollinator behavior, and plant reproductive success, In: Hunter MD, Ohgushi T and Price PW(eds), Effect of Resource Distribution on Animal-plant Interactions. Academic Press, San Diego, pp. 113-138
8 Varassin IG, Trigo JR, and Sazima M (2001) The role of nectar production, flower pigments and odour in the pollination of four species of Passiflora (Passifloraceae) in south-eastern Brazil. Bot J Linean Soc 136: 139-152   DOI   ScienceOn
9 Yumoto T (1987) Pollination systems in a warm temperate evergreen broad-leaved forest on Yaku Island. Ecol Res 2: 133-145   DOI
10 Yumoto T (2000) Bird-pollination of three Durio species (Bombacaceae) in a tropical rainforest in Sarawak, Malaysia. Am J Bot 87: 1181-1188   DOI
11 Stiles FG (1975) Ecology, flowering phenology, and hummingbird pollination of some Costa Rican Heliconia species. Ecology 6: 285-301   DOI   ScienceOn
12 Sutherland GD and Gass CL (1995) Learning and remembering of spatial patterns by hummingbirds. Anim Behav 50: 1273-1286   DOI   ScienceOn