The contribution of a bee plant species to honey production depends on the plant's nectar secretion quality and quantity, which is mainly governed by biotic and abiotic factors. The aim of the current study, was to investigate the nectar secretion dynamics and honey production potential of 14 major bee plant species of the target area. We examined the quantity and dynamics of nectar sugar per flower five times a day using a nectar sugar washing technique and direct measuring of nectar with calibrated capillary tubes. The average nectar sugar amount of the species varied from 0.41 mg/flower to 7.7 mg/flower ( < 0.0001). The honey sugar per flower was used to extrapolate the honey production potential per plant and per hectare of land. Accordingly the honey production potential of the species observed to vary from 14 kg/hectare in to 829 kg/hectare in. The nectar secretion dynamics of the species generally showed an increasing trend early in the morning, peaking toward midday, followed by a decline but different species observed to have different peak nectar secretion times. Generally, the tree species secreted more nectar sugar/flower than the herbs. The nectar secretion amount of the species was positively correlated with the ambient temperature, indicating the adaptation of the species to hot climatic conditions. However, different species were observed to have a different optimum temperature for peak nectar secretion. Despite the limited rainfall and high temperature of the area, many plants were found to have good potential for honey production. The monetary value of honey per hectare of the studied honeybee plant species can be of equal or greater than the per-hectare monetary value of some cultivated crops that require numerous inputs. In addition, the information generated is believed to be useful in apiary site selection and to estimate the honey bee colony carrying capacity of an area.
Both climatic factors and bee forage characteristics affect the population size and productivity of honey bee colonies. To our knowledge, no scientific investigation has as yet considered the potential effect of nectar-rich bee forage exposed to drastic subtropical weather conditions on the performance of honey bee colonies. This study investigated the performance of the honey bee subspecies Apis mellifera jemenitica Ruttner (Yemeni) and Apis mellifera carnica Pollmann (Carniolan) in weather that was hot and dry and in an environment of nectar-rich flora.The brood production, food storage, bee population and honey yield of Yemeni (native) and Carniolan (imported) colonies on Talh trees (Acacia gerrardii Benth.), a nectar-rich, subtropical, and summer bee forage source in Central Arabia were evaluated. Owing to their structural and behavioral adaptations, the Yemeni bees constructed stronger (high population size) colonies than the Carniolan bees. Although both groups yielded similar amounts of Talh honey, the Yemeni bees consumed their stored honey rapidly if not timely harvested. A. m. jemenitica has a higher performance than A. m. carnica during extremely hot-dry conditions and A. gerrardii nectar-rich flow.
Hemolymph osmolarity has great effect on honey bee health, especially in arid and semi-arid zones. It regulates water and nutrients in stressed tissues. Osmotic concentration in three races (, and) of was tested in central Saudi Arabia during spring and summer seasons in 2015. Newly emerged bee workers were first marked and later their hemolymph was extracted after intervals of 1, 5, 10, 15, 20 and 25 days. A significant positive correlation between age and osmolarity was found in all three races during spring and summer seasons. The lowest combined osmotic concentration for all three races was found after 1 day interval, while the highest osmotic concentration was recorded after 25 days. Among all races, showed significantly high osmotic concentration after 25 days in spring and summer seasons as compared to the other two races. Only showed similar osmotic concentration after 10 and 15 days in both spring and summer seasons compared to other two races. Mean osmotic concentration of all three races was significantly different after 20 and 25 days in spring and summer seasons. Overall mean recorded during summer was significantly higher than the mean of spring season. Combined osmotic concentration in young drones of all races was significantly lower than that of old drones during spring and summer seasons.
The nectar secretion of Ziziphus flowers was studied by removing and measuring the nectar every four hours, for two consecutive days, from 88 flowers of four trees (‘repeated sampling’). In another 120 flowers from the same trees, the accumulated sugar was measured at the end of the flowering stage. The mass of the nectar sugar was determined following the washing technique. The total amount of sugar per tree was calculated by multiplying the number of flowers per tree by the average mass of nectar sugar secreted per flower. The average mass of sugar produced per flower in repeated sampling was 0.79±0.54 mg/flower (range 0.09 - 2.48 mg). The average mass of sugar per flower for each of the four investigated trees was 1.43±0.53 mg, 0.72±0.27 mg, 0.94±0.39 mg and 0.37±0.26 mg, respectively. The differences among trees was statistically significant. For accumulated nectar, the overall average mass of sugar per flower was 0.55±0.23 mg (range 0.06 - 1.29 mg) and the average values for flowers on the investigated trees of Z. spina-christi were 0.69±0.26 mg, 0.41±0.16 mg, 0.51±0.16 mg and 0.53±0.21 mg; these variations were statistically significant. The average mass of nectar sugar calculated for the flowers with accumulated nectar sampling was significantly lower than the average mass of sugar recorded for repeated nectar sugar samplings (0.79±0.54 mg). According to this study, one Ziziphus tree is estimated to produce 3.6 kg of honey (range 2.2 - 5.2 kg), equivalent to about 900 kg of honey/ha (range 550 - 1300 kg). These figures indicate the high potential value of the plant for honey production. Nectar secretion was positively correlated with temperature, indicating the adaptation of the tree to hot climates.
Talh trees (Acacia gerrardii Benth.) are acacias that are native to the arid and semiarid Africa and west Asia. We investigated the flowering biology, pod set and flower visitors of Talh and discussed the role of these visitors in pollen transfer. The Talh trees blossomed laterally on the nodes of one-year-old twigs. Each node produced 21 flower buds seasonally. Each flower bud opened to a flower head (FH) of 60 florets. The bagged FHs podded significantly (p ⩽ 0.05) less than did the unbagged FHs. The FHs were visited by 31 insect species (25 genera, 16 families and 5 orders). The major taxa were honeybees, megachilids, butterflies, ants, beetles and thrips. Each of honeybees, megachilids and beetles showed a significant (p ⩽ 0.05) hourly pattern, while each of butterflies, ants and thrips had no hourly pattern (p > 0.05). Furthermore, some birds and mammals touched the Talh FHs. Talh trees evolved a mass flowering behavior to face pre- and post-flowering obstacles. Megachilids seemed to play the major effort of zoophily because of their relatively high numbers of individuals and species and their effective movement behavior on the FH surface. Nevertheless, honeybees and other insects and vertebrate taxa also contributed to the pollen transfer. These results greatly contribute to our understanding of the pollination ecology of acacias, especially Arabian acacias.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
customersupport@researchsolutions.com
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply.
Copyright © 2025 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.