scholarly journals Honey Bee Pollination Requirements for Triploid Watermelon

HortScience ◽  
2005 ◽  
Vol 40 (5) ◽  
pp. 1268-1270 ◽  
Author(s):  
S. Alan Walters

Honey bees (Apis mellifera L.) are important pollinators of triploid watermelon [Citrullus lanatus (Thunb.) Matsum & Nakai]. Pistillate (or female) watermelon flowers require multiple honey bee or other wild bee visitations after visiting staminate (or male) flowers for fruit set, and pollination is even more of a concern in triploid watermelon production since staminate flowers contain mostly nonviable pollen. Six honey bee visitation treatments—1) no visitation control, 2) two visits, 3) four visits, 4) eight visits, 5) 16 visits, and 6) open-pollinated control—were evaluated to determine the effectiveness of honey bee pollination on `Millionaire' triploid watermelon fruit set, yield, and quality utilizing `Crimson Sweet' at a 33% pollenizer frequency. `Millionaire' quality characters (hollow heart disorder or percent soluble solids) did not differ (P > 0.05) between honey bee pollination treatments. The open-pollinated control provided the highest fruit set rate (80%) and the greatest triploid watermelon numbers and weights per plot compared to all other honey bee visitation treatments. Fruit set, and fruit numbers and weights per plot increased linearly as number of honey bee visits to pistillate flowers increased from 0 (no visit control) to the open-pollinated control (about 24 visits). This study indicated that between 16 and 24 honey bee visits are required to achieve maximum triploid watermelon fruit set and yields at a 33% pollenizer frequency, which is twice the number of honey bee visits required by seeded watermelons to achieve similar results. This is probably due to many honey bees visiting staminate triploid watermelon flowers (that are in close proximity) before visiting pistillate flowers thus providing mostly nonviable pollen that is useless for fruit set and development. Therefore, more honey bee visits to pistillate triploid watermelon flowers would be required to achieve maximum fruit set and subsequent development compared to seeded watermelons.

HortScience ◽  
2005 ◽  
Vol 40 (4) ◽  
pp. 1118C-1118
Author(s):  
S. Alan Walters

Cucurbit vegetable crops, such as watermelon (Citrullus lanatus), require insect pollination for fruit set, which is usually achieved by placing honey bee (Apismellifera) colonies in a field or relying upon natural bee populations. Pistillate (or female) watermelon flowers require multiple honey bee (or other bee) visitations after visiting staminate (or male) flowers for fruit set, and pollination is even more of a concern in triploid watermelon production since staminate flowers contain mostly nonviable pollen. Six honey bee visitation treatments, 1) no visitation control, 2) two visits, 3) four visits, 4) eight visits, 5) 16 visits, and 6) open-pollinated control, were evaluated to determine the effect of honey bee pollination on `Millionaire' triploid watermelon fruit set, yield, and quality utilizing `Crimson Sweet' at a 33% pollinizer frequency. No differences (P> 0.05) between honey bee pollination treatments were observed for `Millionaire' quality characters (hollow heart disorder or percent soluble solids). The lowest pistillate flower abortion rate (20%) and subsequently the greatest triploid watermelon yields (fruit numbers and weights per hectare) occurred with the openpollinated control compared to all other honey bee visitation treatments. Fruit abortion rates decreased linearly, while fruit numbers and weights per hectare increased linearly as number of honey bee visits to pistillate flowers increased from 0 (no visit control) to the open-pollinated control (≈24 visits). This study indicated that >16 honey bee visits are required to achieve maximum triploid watermelon fruit set and yields, which is twice the number of honey bee visits required by diploid watermelons to achieve similar results.


2003 ◽  
Vol 13 (1) ◽  
pp. 58-61 ◽  
Author(s):  
Dena C. Fiacchino ◽  
S. Alan Walters

During the 1999 and 2000 growing seasons in Illinois, studies were conducted to determine the influence of two pollinizers (`Crimson Sweet' and `Fiesta') and three pollinizer frequencies (11%, 20%, and 33%) on `Millionaire' seedless watermelon (Citrullus lanatus) quality and yields. More large-sized [>16 lb (7.2 kg)] `Millionaire' watermelons were produced when `Crimson Sweet' was used as the pollinizer compared to `Fiesta', which resulted in `Crimson Sweet' leading to greater marketable and total `Millionaire' yields. Pollinizers responded similarly over the pollinizer frequencies for `Millionaire' watermelon yields as no pollinizer by pollinizer frequency interaction was observed. The 20% and 33% pollinizer frequencies produced similar `Millionaire' yields per acre and both resulted in greater yields compared to the 11% pollinizer frequency. Soluble solids in `Millionaire' fruits were not influenced by pollinizer or pollinizer frequency. However, hollow heart disorder followed a quadratic response with respect to pollinizer frequency with the lowest amount of hollow heart observed at the 33% pollinizer frequency and greatest at the 11% pollinizer frequency. No significant interaction (P ≤ 0.05) was observed for pollinizer by pollinizer frequency for hollow heart disorder in `Millionaire'; although, more hollow heart disorder in `Millionaire' was observed when `Fiesta' was used as the pollinizer.


2007 ◽  
Vol 17 (4) ◽  
pp. 518-522 ◽  
Author(s):  
Joshua H. Freeman ◽  
G.A. Miller ◽  
S.M. Olson ◽  
W.M. Stall

As triploid watermelons (Citrullus lanatus) increase in popularity, production has shifted away from seeded watermelons. To achieve successful fruit set in triploid watermelons, a diploid watermelon cultivar must be planted as a pollen source. Three diploid cultivars in 2005 and seven diploid cultivars in 2006 were evaluated at one and three locations, respectively, to determine their effectiveness as pollenizers. Each cultivar was planted within plots of the triploid watermelons ‘Tri-X 313’ (2005) and ‘Supercrisp’ (2006) with buffers on all sides of the plots to contain pollen flow within individual plots. Performance of pollenizers was based on triploid watermelon yield, soluble solids concentration, and incidence of hollowheart. In 2005, there were no significant differences in total weight, fruit per acre, average weight, or soluble solids concentration among pollenizers. In 2006, significant differences in yield were observed, and plots with ‘Sidekick’ as a pollenizer yielded the highest but were not significantly different from ‘Patron’, ‘SP-1’, ‘Jenny’, or ‘Mickylee’. In 2006, there were no significant differences in fruit per acre, soluble solids concentration, or incidence of hollowheart between pollenizers. The experimental design was successful in isolating pollenizers and there was minimal pollen flow outside of experimental plots as indicated by minimal fruit set in control plots.


HortScience ◽  
1991 ◽  
Vol 26 (5) ◽  
pp. 488g-489 ◽  
Author(s):  
G. W. Elmstrom ◽  
D. N. Maynard

Watermelon, Citrullus lanatus (Thunb.) Matsum. & Nakai, requires insects, most commonly honey bees, for pollination and fruit set. The transfer of an adequate amount of pollen is essential to ensure optimum fruit set, size, and shape. To encourage bee visits and the transfer of pollen, two applications of Bee-Scent*, a bee attractant, at 2.47 liter·ha-1 were made to watermelon on five farms in central and southwest Florida. Honey bee, Apis melifera L., activity was monitored for two days following each application and yield and fruit quality were determined. On only a few occasions was increased honey bee activity noted. Application of bee attractant increased total yield in one field in central Florida and resulted in an increase in early yield at all three locations in southwest Florida. Soluble solids content of mature fruit was not directly affected by treatment. Treatment increased the seed content of fruit from three of five farms.


HortScience ◽  
1999 ◽  
Vol 34 (3) ◽  
pp. 479C-479
Author(s):  
Laura C. Merrick ◽  
Frank Drummond ◽  
Constance Stubbs ◽  
Rhonda Weber

Managed and feral honey bee (Apis mellifera) colonies have declined dramatically in the past decade due largely to parasitic mites, pesticide contamination, and severe weather. Squash (Cucurbita spp.) is one of many agricultural crops whose production may be negatively effected by decline of these pollinators. A study was conducted on a set of nine farms in Maine to assess the relationship between bee abundance and fruit set of summer and winter squash. The organic and conventional farms targeted in the study included farms with and without the presence of honey bees. With winter squash, fields with more bees tended to exhibit higher fruit set. The average fruit set was slightly higher for farms with honey bees (42%) vs. those without (35%), but both types of farms were similar to that found in controlled hand pollinations (31% on average). In contrast, fruit set for summer squash averaged 95% to 96% for all farms, regardless of the relative abundance of censused bees. Bumble bees (Bombus spp.) were the most abundant wild bees found pollinating squash. Farms with honey bees on average had higher numbers of bees in squash flowers than farms without honey bees, although a difference in preference for floral sex type was detected for bee taxa. Honey bees were much more likely to be found in female flowers, while bumble bees were more abundant in male flowers. Significantly more native bees were found in squash flowers on farms without honey bee hives, although native bees were still present to some extent on farms that were dominated by Apis mellifera.


HortScience ◽  
2006 ◽  
Vol 41 (2) ◽  
pp. 370-373 ◽  
Author(s):  
S. Alan Walters ◽  
Bradley H. Taylor

The objective of this study was to measure honey bee (Apis mellifera L.) impact on seed set, fruit set, and yield of jack-o-lantern (Cucurbita pepo L.), large-sized (C. maxima Duch.), and processing pumpkins (C. moschata Duch. ex Poir.) under field conditions. There were sufficient natural pollinators [including bumblebees (Bombus spp.), carpenter bees (Xylocopa spp.), honey bees, and squash bees (Peponapis pruinosa Say)] provided under field conditions to induce fruit set of jack-o-lantern pumpkins as fruit number obtained per hectare was not affected by the addition of a honey bee colony. However, the addition of honey bees did increase fruit number per hectare of the C. moschata and C. maxima cultivars evaluated. Honey bee pollination resulted in larger-sized fruit, increasing individual fruit size of all but small-sized pumpkins (<0.5 kg). Individual pumpkin fruit weights of the Cucurbita pepo, C. moschata, and C. maxima cultivars evaluated increased by about, 26%, 70%, and 78%, respectively, when honey bee colonies were included. Natural pollination was insufficient to stimulate maximum fruit size development and seed number and seed weight per fruit. Although pumpkin fruit set will occur with natural pollinators, the addition of honey bee colonies will ensure the presence of pollinators to maximize fruit size. Since pumpkins are generally sold on a weight basis, growers may generate greater revenues with the addition of honey bee colonies in pumpkin fields.


1987 ◽  
Vol 65 (9) ◽  
pp. 2168-2176 ◽  
Author(s):  
K. W. Richards

Diversity, density, efficiency, and effectiveness of pollinators of cicer milkvetch, Astragalus cicer L., grown at two locations in southern Alberta were studied from 1978 to 1983. Twenty-seven species of bees were identified as pollinators. At Lethbridge, honey bees (Apis mellifera) comprised 74% of the observations, bumble bees 16%, and leafcutter bees 10%, while at Spring Coulee, the proportions were honey bees 14%, bumble bees 69%, and leafcutter bees 17%. The rate of foraging by pollinator species from flower to flower varied; bumble bee species, especially Bombus nevadensis Cress., foraged consistently more efficiently than honey bees or alfalfa leafcutter bees, Megachile rotundata (F.). A theoretical approach used to predict the bee populations required to pollinate varying flower densities shows that the population of B. nevadensis required is about half those of Bombus huntii Greene and M. rotundata and less than one-quarter that of the honey bee. Pollination by B. nevadensis consistently resulted in more seeds per pod than with any other bumble bee species, the honey bee, or M. rotundata. Of the nine species of bumble bee that established colonies in artificial domiciles near the field, B. nevadensis established the most colonies each year. The number of workers and sexuals produced per colony varied considerably among bumble bee species with only 55% of the colony establishments producing workers and 31% producing sexuals. The propagation rate and quality of alfalfa leafcutter bees produced on cicer milkvetch was excellent.


1998 ◽  
Vol 8 (4) ◽  
pp. 590-594 ◽  
Author(s):  
M.S. Stanghellini ◽  
J.T. Ambrose ◽  
J.R. Schultheis

The effectiveness of bumble bees, Bombus impatiens Cresson, and honey bees, Apis mellifera L., on the pollination of cucumber, Cucumis sativus L., and watermelon, Citrullus lanatus (Thunb.) Matsum. & Nakai, was compared under field conditions. Comparisons were based on fruit abortion rates and seed set as influenced by bee type (honey bee or bumble bee) and the number of bee visits to treatment flowers (1, 6, 12, and 18 bee visits), plus two controls: a no-visit treatment and an open-pollinated (unrestricted visitation) treatment. For both crops, an increased number of bee visits had a strong positive effect on fruit and seed set. All cucumber and watermelon flowers bagged to prevent insect visitation aborted, demonstrating the need for active transfer of pollen between staminate and pistillate flowers. Bumble bee-visited flowers consistently had lower abortion rates and higher seed sets in the cucumber and watermelon studies than did honey bee-visited flowers when compared at the same bee visitation level. Only slight differences in fruit abortion rates were detected between bee types in the watermelon study. However, abortion rates for bumble bee-visited flowers were consistently less than those for honey bee-visited flowers when compared at equal bee visitation levels, with one exception at the 12 bee visit level. As the number of honey bee colonies continues to decline due to parasitic mite pests and based on the data obtained, we conclude that bumble bees have a great potential to serve as a supplemental pollinator for cucumbers, watermelons, and possibly other vine crops, when honey bees available for rental are in limited supply.


HortScience ◽  
2008 ◽  
Vol 43 (1) ◽  
pp. 274-275 ◽  
Author(s):  
Josh H. Freeman ◽  
Stephen M. Olson ◽  
Eileen A. Kabelka

In the Spring and Fall 2006, the pollen viability of four diploid watermelon pollenizers was evaluated in Quincy, FL. Triploid watermelon plants [Citrullus lanatus (Thunb.) Matsum. & Nakai.] do not produce sufficient viable pollen to pollenize themselves and a diploid cultivar must be interplanted as a pollen source. Recent studies have illustrated differences in triploid watermelon yields as a result of the pollenizer cultivar used. The viability of the pollen produced by pollenizer cultivars may greatly influence the fruit set and fruit quality in the triploid watermelon crop. Pollen samples were taken from ‘Companion’, ‘Jenny’, ‘Mickylee’, and ‘SP-1’ and were stained to determine their viability. There were no significant differences in pollen viability among cultivars and all cultivars had high average viability. Pollen viability was never lower than 95% for any cultivar. This study indicates that pollen viability of the cultivars evaluated should not influence their effectiveness as pollenizers.


HortScience ◽  
2010 ◽  
Vol 45 (4) ◽  
pp. 541-545 ◽  
Author(s):  
Peter J. Dittmar ◽  
David W. Monks ◽  
Jonathan R. Schultheis

An experiment was conducted during 2005 and 2006 in Kinston, NC, with the objective of maximizing triploid watermelon [Citrullus lanatus (Thunb.) Matsum. and Nak.] fruit yield and quality by optimizing the choice and use of pollenizers. Treatments were pollenizer cultivars planted singly [‘Companion’, ‘Super Pollenizer 1’ (‘SP1’), ‘Summer Flavor 800’ (‘SF800’), and ‘Mickylee’] or in pairs (‘Companion’ + ‘SP1’, ‘Companion’ + ‘SF800’, and ‘SP1’ + ‘SF800’). All pollenizers from these seven treatments were interplanted with the triploid cultivar Tri-X-313. Planting arrangement was compared by establishing ‘SF800’ in a hill versus an interplanted field arrangement. Effect of pollenizer establishment timing on triploid fruit yields and quality was evaluated by establishing ‘SP1’ 3 weeks after planting and comparing it with the establishment of ‘SP1’ at the time of triploid plant establishment. Finally, a triploid planting with no pollenizer (control) was included to determine pollen movement. Fruit yield from the control was 22% or less of yield of the other treatments containing a pollenizer and less than 10% in the initial or early harvests. Pollen movement was minimal among plots and differences in yield and fruit quality could be attributed to pollenizer treatment. In 2005, the use of ‘Companion’, ‘SP1’, or ‘Mickylee’ as pollenizers produced similar total yields, whereas ‘SF800’ produced the lowest yield. In 2005, ‘Companion’ produced more large fruit than the other individual pollenizer treatments. Combining the pollenizers generally did not enhance triploid yields or quality. Interplanting of pollenizers consistently resulted in greater yield compared with the hill system. Late planting of ‘SP1’ increased the incidence of hollow heart in the marketable fruit and decreased yield compared with simultaneously planting ‘SP1’ and triploid plants. Thus, selection of pollenizer, planting arrangement, and time of pollenizer establishment are all important considerations to optimizing triploid yield and quality.


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