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Foraging and pollination behavior of Apis mellifera adansonii Latreille (Hymenoptera: Apidae) on Glycine max L. (Fabaceae) flowers at Maroua

To assess the impact of Apis mellifera adansonii on pod and seed yields of Glycine max, its foraging and pollinating activities were studied in Maroua, during the two season seasons (August-September 2010 and 2011). Observations were made on 51 to 17866 flowers per treatment. Treatment 1 represented by free flowers; treatment 2 bagged flowers and treatment 3 flowers visited only by A. m. adansonii. In addition, all flower visitors were recorded. The abundance of bee, duration of visits, impact of activity of A. m. adansonii on fruiting percentage, the influence of this bee on formation of pods, number of seeds in each pods and average of normal seeds (well developed) were recorded. Individuals from 28 species of insects were recorded on the flowers of G. max, after two years of observations. Apis mellifera adansonii with 23.18% of 954 visits was the most frequent, followed by Polyrachis sp. 1 (14.77%), Macronomia vulpina (14.22%), Lipotriches collaris (11.07%). This honey bee intensely and exclusively foraged for nectar. The mean foraging speed was 12.56 ± 5.79 flowers per minute. Flowers visited by insects had higher fruiting rate compared with the others while those bagged had the lowest. Apis mellifera adansonii foraging resulted to a significant increment in fruiting rate by 14.14 and 11.98%, as well as the number of seeds per pod by 36.95 and 35.65%, and the percentage of normal seeds by 32.61 and 29.26% respectively in 2010 and 2011. The installation of A. m. adansonii colonies in G. max plantations is recommended to improve pod and seeds production of this species.

To assess the impact of Apis mellifera adansonii on pod and seed yields of Glycine max, its foraging and pollinating activities were studied in Maroua, during the two season seasons (August-September 2010 and 2011). Observations were made on 51 to 17866 flowers per treatment. Treatment 1 represented by free flowers; treatment 2 bagged flowers and treatment 3 flowers visited only by A. m. adansonii. In addition, all flower visitors were recorded. The abundance of bee, duration of visits, impact of activity of A. m. adansonii on fruiting percentage, the influence of this bee on formation of pods, number of seeds in each pods and average of normal seeds (well developed) were recorded. Individuals from 28 species of insects were recorded on the flowers of G. max, after two years of observations. Apis mellifera adansonii with 23.18% of 954 visits was the most frequent, followed by Polyrachis sp. 1 (14.77%), Macronomia vulpina (14.22%), Lipotriches collaris (11.07%). This honey bee intensely and exclusively foraged for nectar. The mean foraging speed was 12.56 ± 5.79 flowers per minute. Flowers visited by insects had higher fruiting rate compared with the others while those bagged had the lowest. Apis mellifera adansonii foraging resulted to a significant increment in fruiting rate by 14.14 and 11.98%, as well as the number of seeds per pod by 36.95 and 35.65%, and the percentage of normal seeds by 32.61 and 29.26% respectively in 2010 and 2011. The installation of A. m. adansonii colonies in G. max plantations is recommended to improve pod and seeds production of this species.

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Fohouo <str<strong>on</strong>g>and</str<strong>on</strong>g> Dounia, 2014<br />

nectar, A. m. <str<strong>on</strong>g>adans<strong>on</strong>ii</str<strong>on</strong>g> foragers regularly come into<br />

c<strong>on</strong>tact with the stigma <str<strong>on</strong>g>and</str<strong>on</strong>g> carry the pollen to the anthers<br />

for stigma. The weight <str<strong>on</strong>g>of</str<strong>on</strong>g> A. m. <str<strong>on</strong>g>adans<strong>on</strong>ii</str<strong>on</strong>g> shoot the<br />

fl owers <str<strong>on</strong>g>of</str<strong>on</strong>g> G. <strong>max</strong> during nectar collecti<strong>on</strong> <str<strong>on</strong>g>and</str<strong>on</strong>g> this<br />

movement played a positive role in liber<strong>at</strong>i<strong>on</strong> <str<strong>on</strong>g>of</str<strong>on</strong>g> pollen<br />

by anthers for the optimal occup<strong>at</strong>i<strong>on</strong> <str<strong>on</strong>g>of</str<strong>on</strong>g> the stigma.<br />

This phenomen<strong>on</strong> was also reported by Ahrent <str<strong>on</strong>g>and</str<strong>on</strong>g><br />

Caviness (1994) <str<strong>on</strong>g>and</str<strong>on</strong>g> Rortais et al., (2005) <strong>on</strong> G. <strong>max</strong>.<br />

Thus in additi<strong>on</strong> to their direct <str<strong>on</strong>g>pollin<strong>at</strong>i<strong>on</strong></str<strong>on</strong>g> role,<br />

A. m. <str<strong>on</strong>g>adans<strong>on</strong>ii</str<strong>on</strong>g> foragers also indirectly effected self<str<strong>on</strong>g>pollin<strong>at</strong>i<strong>on</strong></str<strong>on</strong>g><br />

<str<strong>on</strong>g>and</str<strong>on</strong>g> cross-<str<strong>on</strong>g>pollin<strong>at</strong>i<strong>on</strong></str<strong>on</strong>g> <str<strong>on</strong>g>of</str<strong>on</strong>g> G. <strong>max</strong> <strong>flowers</strong>. The<br />

positive <str<strong>on</strong>g>and</str<strong>on</strong>g> significant c<strong>on</strong>tributi<strong>on</strong> <str<strong>on</strong>g>of</str<strong>on</strong>g> A. m. <str<strong>on</strong>g>adans<strong>on</strong>ii</str<strong>on</strong>g><br />

in pods, seed yields <str<strong>on</strong>g>and</str<strong>on</strong>g> percentage <str<strong>on</strong>g>of</str<strong>on</strong>g> normal seeds <str<strong>on</strong>g>of</str<strong>on</strong>g><br />

G. <strong>max</strong> is justified by the acti<strong>on</strong> <str<strong>on</strong>g>of</str<strong>on</strong>g> this bee <strong>on</strong><br />

<str<strong>on</strong>g>pollin<strong>at</strong>i<strong>on</strong></str<strong>on</strong>g>. The similar have been obtain in Britain<br />

(Kendall <str<strong>on</strong>g>and</str<strong>on</strong>g> Smith, 1976) <strong>on</strong> Phaseolus coccineus<br />

(<strong>Fabaceae</strong>), USA (Ibarra-Perez et al., 1999) <strong>on</strong><br />

Phaseolus coccineus (<strong>Fabaceae</strong>), Ngaoundéré<br />

(Camero<strong>on</strong>) (Kingha et al., 2012) <strong>on</strong> Phaseolus vulgaris<br />

(<strong>Fabaceae</strong>), <strong>Maroua</strong> (Camero<strong>on</strong>) (Douka <str<strong>on</strong>g>and</str<strong>on</strong>g><br />

Tchuenguem, 2013) <strong>on</strong> Phaseolus vulgaris (<strong>Fabaceae</strong>)<br />

<str<strong>on</strong>g>and</str<strong>on</strong>g> Brazil (Milf<strong>on</strong>t et al., 2013) <strong>on</strong> G. <strong>max</strong> who showed<br />

th<strong>at</strong> these plants species produce fewer seeds per pod in<br />

the absence <str<strong>on</strong>g>of</str<strong>on</strong>g> efficient pollin<strong>at</strong>ors. The higher<br />

percentage <str<strong>on</strong>g>of</str<strong>on</strong>g> pods, seeds <str<strong>on</strong>g>and</str<strong>on</strong>g> normal seeds in the<br />

tre<strong>at</strong>ment with unlimited visits or tre<strong>at</strong>ment visiting<br />

exclusively by A. m. <str<strong>on</strong>g>adans<strong>on</strong>ii</str<strong>on</strong>g> compared to tre<strong>at</strong>ment<br />

with protected, showing th<strong>at</strong> insect visits were effective<br />

in increasing cross-<str<strong>on</strong>g>pollin<strong>at</strong>i<strong>on</strong></str<strong>on</strong>g> or self- <str<strong>on</strong>g>pollin<strong>at</strong>i<strong>on</strong></str<strong>on</strong>g>.<br />

Our results c<strong>on</strong>firmed those <str<strong>on</strong>g>of</str<strong>on</strong>g> Caviness (1970), Ahrent<br />

<str<strong>on</strong>g>and</str<strong>on</strong>g> Caviness (1994), Rortais et al., (2005) <str<strong>on</strong>g>and</str<strong>on</strong>g> Milf<strong>on</strong>t<br />

et al., (2013) who revealed th<strong>at</strong> G. <strong>max</strong> <strong>flowers</strong> set little<br />

pods in the absence <str<strong>on</strong>g>of</str<strong>on</strong>g> insect pollin<strong>at</strong>ors. Similar<br />

experiments <strong>on</strong> cr op sp e ci es r ea l i zed in Engl<str<strong>on</strong>g>and</str<strong>on</strong>g><br />

(Free, 1966) <str<strong>on</strong>g>and</str<strong>on</strong>g> in Brazil (Free, 1993) have shown th<strong>at</strong><br />

<str<strong>on</strong>g>pollin<strong>at</strong>i<strong>on</strong></str<strong>on</strong>g> by insects was not always needed.<br />

Woodworth (1922) showed th<strong>at</strong> self-<str<strong>on</strong>g>pollin<strong>at</strong>i<strong>on</strong></str<strong>on</strong>g> <str<strong>on</strong>g>of</str<strong>on</strong>g><br />

G. <strong>max</strong> <strong>flowers</strong> produced as many pods <str<strong>on</strong>g>and</str<strong>on</strong>g> seeds as<br />

exposed plants. Thus, <str<strong>on</strong>g>pollin<strong>at</strong>i<strong>on</strong></str<strong>on</strong>g> requirements may<br />

differ between plant varieties <str<strong>on</strong>g>and</str<strong>on</strong>g> /or regi<strong>on</strong>.<br />

CONCLUSION<br />

This study reveals th<strong>at</strong> th e var i et y <str<strong>on</strong>g>of</str<strong>on</strong>g> G. <strong>max</strong><br />

studied is a nectariferous bee plant th<strong>at</strong> obtained<br />

benefits from the <str<strong>on</strong>g>pollin<strong>at</strong>i<strong>on</strong></str<strong>on</strong>g> by insects am<strong>on</strong>g which A.<br />

m. <str<strong>on</strong>g>adans<strong>on</strong>ii</str<strong>on</strong>g> is the must important. The comparis<strong>on</strong> <str<strong>on</strong>g>of</str<strong>on</strong>g><br />

pods <str<strong>on</strong>g>and</str<strong>on</strong>g> seeds set <str<strong>on</strong>g>of</str<strong>on</strong>g> unprotected <strong>flowers</strong> with th<strong>at</strong> <str<strong>on</strong>g>of</str<strong>on</strong>g><br />

<strong>flowers</strong> visited exclusively by A. m. <str<strong>on</strong>g>adans<strong>on</strong>ii</str<strong>on</strong>g><br />

underscores the value <str<strong>on</strong>g>of</str<strong>on</strong>g> this bee in increasing pods <str<strong>on</strong>g>and</str<strong>on</strong>g><br />

seed yields as well as seed quality. The install<strong>at</strong>i<strong>on</strong> <str<strong>on</strong>g>of</str<strong>on</strong>g><br />

A. m. <str<strong>on</strong>g>adans<strong>on</strong>ii</str<strong>on</strong>g> col <strong>on</strong> i es to G. <strong>max</strong> fields should<br />

be recommended for the increase <str<strong>on</strong>g>of</str<strong>on</strong>g> pod <str<strong>on</strong>g>and</str<strong>on</strong>g> seeds<br />

yields <str<strong>on</strong>g>of</str<strong>on</strong>g> this valuable crop.<br />

REFERENCES<br />

Ahrent DK, Caviness CE. 1994. N<strong>at</strong>ural cross<str<strong>on</strong>g>pollin<strong>at</strong>i<strong>on</strong></str<strong>on</strong>g><br />

<str<strong>on</strong>g>of</str<strong>on</strong>g> twelve soybean cultivars in Arkansas.<br />

Crop. Sci. 34 (2): 376-378.<br />

Borror DJ, White RE. 1991. Les insectes de<br />

l’Amérique du Nord (au nord du Mexique). Broquet<br />

(ed.), Laprairie. p. 408.<br />

Boyeldieu J. 1991. Produire des grains oléagineux et<br />

protéagineux. Ed. Tec et Doc/Lavoisier Col. Agriculture<br />

d’aujourd’hui. 115 - 152<br />

Caviness CE. 1970. Cross-<str<strong>on</strong>g>pollin<strong>at</strong>i<strong>on</strong></str<strong>on</strong>g> in the soybean.<br />

In : The indispensable pollin<strong>at</strong>ors, Ark. Agr. Ext. Serv.<br />

Misc. Pub. 127: 33-36.<br />

Demarly Y. 1977. Genetic <str<strong>on</strong>g>and</str<strong>on</strong>g> amelior<strong>at</strong>i<strong>on</strong> <str<strong>on</strong>g>of</str<strong>on</strong>g> plants.<br />

Mass<strong>on</strong>, Paris. p. 577.<br />

Douka C, Tchuenguem FF-N. 2013. <str<strong>on</strong>g>Foraging</str<strong>on</strong>g> <str<strong>on</strong>g>and</str<strong>on</strong>g><br />

<str<strong>on</strong>g>pollin<strong>at</strong>i<strong>on</strong></str<strong>on</strong>g> <str<strong>on</strong>g>behavior</str<strong>on</strong>g> <str<strong>on</strong>g>of</str<strong>on</strong>g> <str<strong>on</strong>g>Apis</str<strong>on</strong>g> <str<strong>on</strong>g>mellifera</str<strong>on</strong>g> <str<strong>on</strong>g>adans<strong>on</strong>ii</str<strong>on</strong>g> L.<br />

(<str<strong>on</strong>g>Hymenoptera</str<strong>on</strong>g>, <str<strong>on</strong>g>Apidae</str<strong>on</strong>g>) <strong>on</strong> Phaseolus vulgaris<br />

(<strong>Fabaceae</strong>) <strong>flowers</strong> <strong>at</strong> <strong>Maroua</strong> (Camero<strong>on</strong>). Intern<strong>at</strong>i<strong>on</strong>al<br />

Research Journal <str<strong>on</strong>g>of</str<strong>on</strong>g> Plant Science 4(2): 45-54.<br />

Journal <str<strong>on</strong>g>of</str<strong>on</strong>g> Research in Biology (2014) 4(1): 1209-1219 1217

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