These are interesting observations regarding the issue of pollination in Haskap flowers. It is possible that pollination of Haskap flowers also occurs in the evening.
https://pollinationecology.org/index.php/jpe/article/download/370/138/1470
cit: DISCUSSION
The timing of commencement of anthesis in Haskap is staggered; flowers open throughout the day, and likely during the night as well. The majority of flowers were first observed to be open by 9 AM; since observations were not made overnight, it is possible that many of the flowers observed at this time actually opened earlier, as anthesis appeared quite advanced in some of these flowers. Although this should be confirmed by future studies, it could indicate that nocturnal insects such as moths may be important contributors to Haskap pollination, in addition to diurnal bees and flies. This is further supported by our observation that roughly 20% of Haskap flowers also open in the evening. The average duration of anthesis of the un-pollinated flowers is 83 hours (3.5 days; Fig. 2); however, pollination will significantly shorten this, triggering senescence of the flowers on an average of 34 hours following the pollination event. Our findings are slightly shorter than those of Bożek & Wieniarska (2006) who found that flowers of Lonicera caerulea var. kamtschatica lived 4-5 days, but they also noted that flowers excluded from pollinators were longer lived. This extended floral period may result in more opportunities for visitation by insects and increased pollination success, while senescence in response to pollination reduces the occurrence of repeat visits to flowers that are already pollinated, and may also reduce damage to the flowers, which can reduce seed set (Young 1988; Burquez & Corbet 1991). Our observation that emasculation has no effect on floral longevity in Haskap suggests it is completely selfincompatible, and self-pollination does not shorten the lifespan of the flower, nor does it result in significant stigma clogging that may prevent cross pollination. However, although we did not quantify actual levels of self-pollination in this study, field studies have shown significant self-pollination of the stigma (Frier et al. 2016). It is possible that in greenhouse conditions very little selfpollination actually occurs, and in more realistic settings (with vigorous disruption by wind and handling by insect visitors) these factors may be more significant. This is made more likely by the fact that the anthers dehisce almost immediately following the onset of anthesis (Fig. 3), leaving little or no prior opportunity for cross-pollination. This strategy could maximize the chance that pollen is picked up by a floral visitor, but it also could increase the chance of self-pollen interfering with cross-pollination of the stigma and reducing reproductive success (Bertin & Sullivan 1988; Galen et al. 1989; Waser & Price 1991; Broyles & Wyatt 1993; Barrett 2002), especially because the anthers and stigma exist in very close proximity to one another. If this type of stigma clogging is common, this could suggest some competition or trade-off between male and female reproductive success in Haskap. It may be worthwhile to explore differences in style length among Haskap cultivars, as well as compared to wild varieties, as longer styles may be less likely to experience self-pollination. Nectar production begins as soon as the flowers open, perhaps even slightly before, during the bud stage. We have observed bumble bees visiting Haskap flowers before they are entirely open, and our results suggest that the stigma is receptive at this stage as well. Early nectar production and stigma receptivity may have evolved to take advantage of these early visitors and increase the chance of successful pollination. Nectar production peaks between 8-16 hours of anthesis and is maintained throughout the lifetime of the inflorescence. Considerable variation in the amount of nectar is consistent with findings that variability in nectar production is correlated with large floral displays (Biernaskie & Cartar 2004), as risk-averse pollinators pay shorter visits to a single bush when nectar is variable (Biernaskie et al. 2002). As Haskap produces many flowers simultaneously and is self-incompatible, this strategy would help decrease the instance of geitonogamy and promote cross-pollination. We found no evidence of nectar resorption, and the corolla abscised from the ovaries with the nectar load intact. However, we only analyzed nectar dynamics in un-pollinated flowers; in some flowers, reabsorption is triggered by pollination, presumably to reuse the energy resources in berry development (Luyt & Johnson 2002). However, Burquez and Corbet (1991) suggest that if the nectary is lost when the corolla dehisces, as in Lonicera, reabsorption is unlikely. Additionally, the entire nectar volume can be replaced several times throughout anthesis. This may be an adaptation to nectar robbers or ineffective pollinators, increasing the possibility of repeat visits to a single flower. We have commonly observed both honey bees and bumble bees nectar robbing the flowers, and there is evidence that many legitimate pollinator visits do not deposit sufficient pollen grains for full fertilization of the ovaries (Frier et al. 2016).
The results of this study suggest that Haskap flowers are likely generalized in their pollinator attraction strategy and may be pollinated by a wide variety of insect species and functional groups. Haskap flowering occurs very early in the year when few pollinators are active, and the characteristics described here may reflect adaptations to capitalize on every opportunity to receive a successful pollination visit. The flowers, which open throughout the day (and perhaps the night as well), remain open for up to four days, but successful pollination triggers early senescence. Nectar is produced immediately upon anthesis, potentially beginning in the large bud stage. After initial nectar production the volume is held relatively constant until senescence and any nectar removed during this period is replaced. The anthers begin to dehisce immediately after the flower opens and continue over the first day. The stigma appears receptive in the bud stage, and could potentially be pollinated before the flower opens. As a plant with polyphilic flowers, Haskap is less likely to be pollinator limited than more specialized species, and it may be effectively pollinated by a wide variety of managed and wild insects. This means that Haskap could be successfully cultivated in many habitats and geographic locations, and not be limited to distributions or commercial use of specific pollinators. As the flowers are observed to open in the evening, it is likely that nocturnal insects such as moths are important pollinators of this crop, not just diurnal bees and flies. Haskap growers should take advantage of this generalist system by developing and maintaining healthy pollinator habitat in and around Haskap orchards, as species rich pollinator populations may be essential to realizing optimum fruit yields from this crop (Frier et al. 2016).