Nectar robbing is a foraging behavior utilized by some organisms that feed on floral nectar. "Nectar robbers" usually feed from holes bitten in flowers, rather than by entering through the flowers' natural openings. Often, nectar robbers avoid contact with the floral reproductive structures, and therefore do not facilitate plant reproduction via pollination. Because many species that act as pollinators also act as nectar robbers, nectar robbing is considered to be a form of exploitation of plant-pollinator mutualism.
Nectar robbers vary greatly in species diversity and include species of carpenter bees, bumblebees, stingless Trigona bees, solitary bees, wasps, ants, hummingbirds, passerine birds, and flowerpiercer birds. Nectar robbing mammals include a fruit bat and a squirrel which robs nectar from the ginger plant.
Records of nectar robbing in nature date back at least to 1793 when German naturalist Christian Konrad Sprengel observed bumblebees perforating flowers. Charles Darwin observed bumblebees stealing nectar from flowers in 1859.
Forms of floral larceny
Nectar robbing is specifically the behavior of consuming nectar from a perforation (robbing hole) in the floral tissue rather than from the floral opening. There are two main types of nectar robbing: primary robbing, which requires that the nectar forager perforates the floral tissues itself, and secondary robbing, which is foraging from a robbing hole created by a primary robber. The term "floral larceny" has been proposed to include the entire suite of foraging behaviors for floral rewards that can potentially disrupt pollination. They include "nectar theft" (floral visits that remove nectar from the floral opening without pollinating the flower), and "base working" (removing nectar from in between petals, which generally bypasses floral reproductive structures).
Effects on plant fitness
Pollination systems are mostly mutualistic, meaning that the plant benefits from the pollinator's transport of male gametes and the pollinator benefits from a reward, such as pollen or nectar. As nectar robbers receive the rewards without direct contact with the reproductive parts of the flower, their behaviour is easily assumed to be cheating. However, the effect of robbery on the plant is sometimes neutral or even positive. For example, the proboscis of E. elvina does not come in contact with the reproductive parts of the flower in C. ovandensis, but this does not lead to significant reduction in fruit-set of the plant. In another example, when 80 percent of the flowers in a study site were robbed and the robbers did not pollinate, neither the seed nor fruit set were negatively affected.
The effect of floral-nectar robbing on plant fitness depends on several issues. Firstly, nectar robbers such as carpenter bees, bumble bees and some birds can pollinate flowers. Pollination may take place when the body of the robber contacts the reproductive parts of the plant while it robs, or during pollen collection which some bees practice in concert with nectar robbing. The impact of Trigona bees (e.g. Trigona ferricauda) on a plant is almost always negative, probably because their aggressive territorial behaviour effectively evicts legitimate pollinators. Nectar robbers may change the behaviour of legitimate pollinators in other ways, such as by reducing the amount of nectar available. This may force pollinators to visit more flowers in their nectar foraging. The increased number of flowers visited and longer flight distances increase pollen flow and outcrossing, which is beneficial for the plant because it lessens inbreeding depression. This requires a robber's not completely consuming all of a flower's nectar. When a robber consumes all of a flower's nectar, legitimate pollinators may avoid the flower, resulting in a negative effect on plant fitness.
The response of different species of legitimate pollinators also varies. Some species, like the bumble bees Bombus appositus or B. occidentalis and many species of nectar-feeding birds can distinguish between robbed and unrobbed plants and minimize their energy cost of foraging by avoiding heavily robbed flowers. Pollinating birds may be better at this than insects, because of their higher sensory capability. The ways that bees distinguish between robbed and unrobbed flowers have not been studied, but they have been thought to be related to the damage on petal tissue after robbery or changes in nectar quality. Xylocopa varipuncta steals nectar through a slit they make in the base of the petals. If nectar robbing severely reduces the success of legitimate pollinators they may be able to switch to other nectar sources.
Nectar robbing, especially by birds, can damage the reproductive parts of a flower and thus diminish the fitness of a plant. In this case, the effect of robbery on a plant is direct. A good example of an indirect effect is the change in the behaviour of a legitimate pollinator, which either increases or decreases the fitness of a plant. There are both primary and secondary nectar robbers. Secondary robbers are those (e.g. flies and bees) that take advantage of the holes made by primary robbers.
The effect of robbing is positive if the robber also pollinates or increases the pollination by the legitimate pollinator, and negative if the robber damages the reproductive parts of a plant or reduces pollination success, either by competing with the legitimate pollinator or by lessening the attractiveness of the flower. Distinguishing between a legitimate pollinator and a nectar robber can be difficult.
Pollination systems cause coevolution, as in the close relationships between figs and fig wasps as well as yuccas and yucca moths. If nectar robbers have an effect (direct or indirect) on a plant or pollinator fitness, they are part of the coevolution process. Where nectar robbing is detrimental to the plant, a plant species might evolve to minimize the traits that attract the robbers or develop some type of protective mechanism to hinder them. Another option is to try to neutralize negative effects of nectar robbers. Nectar robbers are adapted for more efficient nectar robbing: for instance, hummingbirds and Diglossa flowerpiercers have serrated bills that are thought to aid them in incising flower tissue for nectar robbing.
Nectar robbers may only get food in illegitimate ways because of the mismatch between the morphologies of their mouthparts and the floral structure; or they may rob nectar as a more energy-saving way to get nectar from flowers.
It is not completely clear how pollination mutualisms persist in the presence of cheating nectar robbers. Nevertheless, as exploitation is not always harmful for the plant, the relationship may be able to endure some cheating. Mutualism may simply confer a higher payoff than nectar robbing.
Defences in flowering plants
Even though there has not been much research on the defences evolved in plants against nectar robbers, the adaptations have been assumed not to rise from traits used in interactions between plants and herbivores (especially florivores). Some defences may have evolved through traits originally referred to pollination. Defences against nectar robbers have been thought to include toxins and secondary compounds, escape in time or space, physical barriers and indirect defences.
Toxins and secondary compounds are likely to act as a defence against nectar robbing because they are often found in floral nectar or petal tissue. There is some evidence that secondary compounds in nectar only affect nectar robbers and not the pollinators. One example is a plant called Catalpa speciosa which produces nectar containing iridoid glycosides that deter nectar-thieving ants but not legitimate bee pollinators. Low sugar concentration in nectar may also deter nectar robbers without deterring pollinators because dilute nectar does not yield net energy profits for robbers.
If robbers and pollinators forage at different times of day, plants may produce nectar according to the active period of a legitimate pollinator. This is an example of a defence by escaping in time. Another way to use time in defence is to flower only for one day as a tropical shrub Pavonia dasypetala does to avoid the robbing Trigona bees. Escaping in space refers to a situation in which plant avoids being robbed by growing in a certain location like next to a plant which is more attractive to the robbers.
The last two methods of protection are physical barriers and indirect defence like symbionts. Tightly packed flowers and unfavourably sized corolla tubes, bract liquid moats and toughness of the corolla or sepal are barriers for some nectar robbers. A good example of an indirect defence is to attract symbiotic predators (like ants) by nectar or other rewards to scare away the robbers.
The term 'resistance' refers to the plant's ability to live and reproduce in spite of nectar robbers. This may happen, for example, by compensating the lost nectar by producing more. With the help of defence and resistance, mutualisms can persist even in the presence of cheaters.
- Maloof, J. E.; Inouye, D. W. (2000). "Are nectar robbers cheaters or mutualists?". Ecology. 81 (10): 2651–2661. doi:10.1890/0012-9658(2000)081[2651:ANRCOM]2.0.CO;2.
- Olmos, F.; Boulhosa, R. (2000). A meeting of opportunists: birds and other visitors to Mabea fistulifera (Euphorbiaceae) in florescences. Ararajuba 8(2):93–98.
- Deng, X.; Ren, P.; Gao, J.; Li, Q. (2004). The Striped Squirrel (Tamiops swinhoei hainanus) as a Nectar Robber of Ginger (Alpinia kwangsiensis). Biotropica. 36(4):633–636.
- Irwin, Rebecca E.; Bronstein, Judith L.; Manson, Jessamyn S.; Richardson, Leif (2010-11-02). "Nectar Robbing: Ecological and Evolutionary Perspectives". Annual Review of Ecology, Evolution, and Systematics. 41 (1): 271–292. doi:10.1146/annurev.ecolsys.110308.120330. ISSN 1543-592X.
- Inouye, David W. (1980). "The Terminology of Floral Larceny". Ecology. 61 (5): 1251–1253. doi:10.2307/1936841.
- Irwin, R. E., Adler, L. S.; Brody, A. K. (2004). "The dual role of floral traits: pollinator attraction and plant defence". Ecology. 85 (6): 1503–1511. doi:10.1890/03-0390.
- Morris, W. F. (1996). "Mutualism denied? Nectar-robbing bumble bees do not reduce female or male success of bluebells". Ecology. 77 (5): 1451–1462. doi:10.2307/2265542.
- Irwin, R. E. (2003). "Impact of nectar robbing on estimates of pollen flow: conceptual predictions and empirical outcomes". Ecology. 84 (2): 485–495. doi:10.1890/0012-9658(2003)084[0485:IONROE]2.0.CO;2.
- Navarro L (2000). "Pollination ecology of Anthyllis vulneraria subsp. vulgaris (Fabaceae): Nectar robbers as pollinators". American Journal of Botany. 87 (7): 980. doi:10.2307/2656997.
- Schemsk e, Douglas W.; Horvitz, Carol C. (1984). "Variation among Floral Visitors in Pollination Ability: A Precondition for Mutualism Specialization". Science. 225 (4661): 519–521. doi:10.1126/science.225.4661.519. JSTOR 1694004.
- Maloof J. E. (2001). "The effects of a bumble bee nectar robber on plant reproductive success and pollinator behavior". American Journal of Botany. 88 (11): 1960–1965. doi:10.2307/3558423.
- Irwin, R. E.; Brody, A. K. (1998). "Nectar Robbing in Ipomopsis aggregata: effects on pollinator behaviour and plant fitness". Oecologia. 116 (4): 519–527. doi:10.1007/s004420050617.
- Roubic, D. W. (1982). "The ecological impact of nectar robbing bees and pollinating humming birds on a tropical shrub". Ecology. 63 (2): 354–360. doi:10.2307/1938953.
- Bentley, Barbara; Elias, Thomas (1983). The Biology of Nectaries. Columbia University Press.[page needed]
- Traveset, A., Willson, M. F.; Sabag, C. (1998). "Effect of nectar robbing birds on fruit set of Fuchsia magellanica in Tierra Del Fuego: a disrupted mutualism". Functional Ecology. 12 (3): 459–464. doi:10.1046/j.1365-2435.1998.00212.x.
- Irwin R. E.; Brody A. K. (1999). "Nectar robbing bumble bees reduce the fitness of Ibomopsis aggregata (Polemoniaceae)". Ecology. 80 (5): 1703–1712. doi:10.2307/176558.
- Bronstein, J. L. (2001). "The exploitation of mutualisms". Ecology Letters. 4 (3): 277–287. doi:10.1046/j.1461-0248.2001.00218.x.
- Pellmyr O., Thompson J.N., Brown J.M., Harrison R.G. (1996). "Evolution of pollination and mutualism in the yucca moth lineage". American Naturalist. 148 (5): 827–847. doi:10.1086/285958.
- Anstett, M.C.; Hossaert, McKey M.; Kjellberg, F. (1997). "Figs and fig pollinators: Evolutionary conflicts in a coevolved mutualism". Trends in Ecology and Evolution. 12 (3): 94–99. doi:10.1016/s0169-5347(96)10064-1.
- Ornelas, J. F. (1994). "Serrate tomia: An adaptation for nectar robbing in hummingbirds?". The Auk. 111 (3): 703–713.
- Zhang Y., Wang Y., Guo Y. (2006). "The effects of nectar robbing on plant reproduction and evolution". Zhiwu Shengtai Xuebao. 30 (4): 695–702.
- Stephenson, A. G. (1981). "Toxic nectar deters nectar thieves of Catalpa speciosa". American Midland Naturalist. 105: 381–383. doi:10.2307/2424757.
|Wikimedia Commons has media related to Nectar robbing.|