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SOYBEAN and BEES

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• Nectar secretion via trichomes excludes an apoplastic transport for the respective species,<br />

owing to apoplastic barriers in the external cells walls in the stalk <strong>and</strong> intermediate<br />

cells of the trichomes (Fahn, 1988; Kuo <strong>and</strong> Pate et al., 1985);<br />

• Vesicles are common in nectariferous tissues (Fahn, 1988; Kuo <strong>and</strong> Pate et al., 1985);<br />

• Secreted nectars are characterized by a wide range of concentrations <strong>and</strong> sucrose: hexose<br />

ratios (Baker <strong>and</strong> Baker, 1975; Baker <strong>and</strong> Baker, 1982) <strong>and</strong>, therefore, cannot be<br />

produced only by a passive flow or transport mechanisms exclusively driven by sucrosecleaving<br />

enzymes;<br />

• Non-carbohydrates such as lipids <strong>and</strong> proteins are likely to be synthesized in the<br />

nectariferous tissue <strong>and</strong> then must enter the prenectar before its secretion (Nicolson et<br />

al., 2007; Kram et al., 2008);<br />

• Nectar secretion depends on several fast-acting control mechanisms, which cannot result<br />

solely from passive source sink relationships.<br />

Bee general orientation<br />

Generally speaking, when approaching blossoms, honeybees are firstly attracted by their<br />

color <strong>and</strong>/or the form. These cues are then used for successful revisits. According to Hsu <strong>and</strong><br />

Young (2012), the bees receives visual cues through two types of parallel channels located<br />

behind the retina. The first channel is used for colors; the other is a monochrome channel<br />

directed to the orientation <strong>and</strong> edge of an item in their visual field. In the integration process<br />

of these channels, the priority <strong>and</strong> interaction between them are significant, as these chromatic<br />

<strong>and</strong> achromatic signals coexist naturally.<br />

Hsu <strong>and</strong> Young (2012) trained bees to detect form <strong>and</strong> color, afterwards tested for its ability<br />

to differentiate combinations of opposite patterns. The bees choose the correct color but the<br />

wrong form pattern in the above experiment as well as for other manipulations. The effect of<br />

the color training for the blue reward pattern differed from that of the green reward pattern.<br />

The color pattern choices tended to be more correct if blue was the target during the training<br />

process, indicating that the chromatic signal was the main cue in pattern discrimination.<br />

The authors concluded that color tended to be the decisive factor in a conflicting situation.<br />

In addition, the color blue was preferred over green, indicating that color preference was<br />

involved in bees’ visual recognition.<br />

Honeybee visitation to a flower can be considered a two stage process. At first involves<br />

orientation from a larger distance <strong>and</strong> then, secondarily, close-range orientation during<br />

which the bee alights <strong>and</strong> probes for nectar. Von Frisch (1967) established that bees are<br />

66 SoybeAn <strong>and</strong> bees

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