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Flowers and insect visitors of Calanthe izuinsularis. (a) Photoscotosia lucicolens; (b) Odontopera arida melanchonica; (c) Noctuidae sp.; (d) Geometridae sp.; (e) Trichoplusia intermixta; (f) Diarsia deparca; (g) Paliga minnehaha; (h) Serrodes campanus; (i) Lasioglossum apristum; (j) Lasioglossum occidens; (k) Lasioglossum occidens. The pollinaria indicated by white arrows can be seen attached to the bee's mesothorax.  

Flowers and insect visitors of Calanthe izuinsularis. (a) Photoscotosia lucicolens; (b) Odontopera arida melanchonica; (c) Noctuidae sp.; (d) Geometridae sp.; (e) Trichoplusia intermixta; (f) Diarsia deparca; (g) Paliga minnehaha; (h) Serrodes campanus; (i) Lasioglossum apristum; (j) Lasioglossum occidens; (k) Lasioglossum occidens. The pollinaria indicated by white arrows can be seen attached to the bee's mesothorax.  

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Calanthe izuinsularis is a rare, beautiful and fragrant orchid endemic to the Izu archipelago. Although it is known that mainland populations of closely related Calanthe species are pollinated by medium- to large-sized bees, it is likely that C. izuinsularis has been forced to alter its floral biology to attract alternative pollinators, as large-si...

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... intensive nighttime observation covering 89 hours of time-lapse photography detected no nocturnal moth visitors to the flowers of C. discolor, even in the sympatric population of the present investigation (Suetsugu et al. unpublished data). However, although most of the nocturnal moths exhibited typical pollinator behaviour, inserting their proboscises into the spur of the C. izuinsularis flowers, no images of moths with C. izuinsularis pollinaria attached to their proboscises were captured (Figure 1). In some cases this might be have been expected, as moth species such as Paliga minnehaha (Crambidae) are too small to carry the C. izuinsularis pollinaria. ...
Context 2
... nocturnal moths were the most frequent visitors, there were also a significant number of hymenopteran visitors, and in terms of the number of times visited (8/38), they are the second-most frequent functional group of C. izuinsularis floral visitors. All of the bee species observed visiting the flowers of C. izuinsularis exhibited typical pollinator behaviour, crawling deep into the chamber formed between the column and labellum to forage for nectar (Figure 1). Although the smaller bees (Lasioglossum (Evylaeus) sp.) were unable to carry pollinaria, the sweat bee Lasioglossum occidens was observed with pollinaria attached to its thorax (Figure 1). ...
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... of the bee species observed visiting the flowers of C. izuinsularis exhibited typical pollinator behaviour, crawling deep into the chamber formed between the column and labellum to forage for nectar (Figure 1). Although the smaller bees (Lasioglossum (Evylaeus) sp.) were unable to carry pollinaria, the sweat bee Lasioglossum occidens was observed with pollinaria attached to its thorax (Figure 1). Consecutive before and after photographs indicated the bee had not been carrying any pollinaria when it arrived at the flower, and thus indicated that the attached pollinaria were truly derived from C. izuinsularis, even though it cannot be absolutely certain how the pollinaria became attached to its mesothorax. ...
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... been found on the islands of Kohzu, Nii and Hachijo, as well as the hybrids of C. izuinsularis and C. aristulifera found on Mikura Island, the site of the current study (Cribb and Bailes 2001). Indeed, a previous study of a sympatric C. aristulifera population at the current study site found that C. aristulifera was also pollinated by L. occidens (Suetsugu et al. Forthcoming 2016). Given that C. aristulifera and C. discolor are rarely visited by nocturnal moths (Suhara 1993;Sugiura 2013;Suetsugu and Fukushima 2014), the weight of evidence suggests that pollination by hymenopteran floral visitors is the most likely mechanism of hybridisation between C. izuinsularis, C. discolor and C. ...
Context 5
... pollinaria can only be transferred when the bee crawls deep into the spur and the anthers make contact with the mesothorax. It is also likely that this alternative mechanism of pollination in both C. izuinsularis and C. aristulifera arose on Mikura Island by convergent evolution in response to the lack of bumblebees and other relatively large bees, such as the genus Eucera (Fukasawa and Miyano 2010). ...

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... In addition to the above observations, I opportunistically collected flower visitors of J. osense during this study. I also attempted to photograph flower visitors using time-lapse photography (Suetsugu et al. 2017). Digital cameras (WG-30 and WG-70, RICHO, Tokyo, Japan) were mounted on tripodsGorillapod (Gorillapod, Joby, San Francisco, USA) and placed in front of the inflorescences of J. osense to photograph flower visitors. ...
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... Calanthe species are evergreen or deciduous terrestrial herbs with thick roots, small oval pseudobulbs, and large corrugated leaves . The flowers of Calanthe species are usually bright-colored, with an empty spur, and are often pollinated by bees (Sugiura, 2013;Ren et al., 2014;Sakata et al., 2014;Suetsugu et al., 2017), although butterflies and hoverflies (Ren et al., 2014) were also recorded as effective pollinators for a few Calanthe species. China is one of the diversity centers for both Habenaria and Calanthe, with high proportion of endemism. ...
... There is an urgent need to protect Calanthe species accounting for their deceptive pollination system. Without containing rewarding nectar in their spurs, Calanthe populations usually threatened from pollinator limitation and extremely low levels of fruit sets (Sugiura, 2013;Ren et al., 2014;Sakata et al., 2014;Suetsugu et al., 2017;Luo et al., 2020; Fig. S8). Non-rewarding orchids are poorer competitors for pollinator visitation than rewarding orchids in plant communities (Pellissier et al., 2010). ...
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... Camera monitoring has a big potential in supplementing human observations in the field as it is time-efficient and at the same time accumulates valuable ecological data (Bjerge et al., 2023;Hofmeester et al., 2020). Recently, insects visiting mushrooms on the forest floor have been monitored by the use of time-lapse cameras (Schmid et al., 2019) and similar techniques have also been used to observe insects visiting flowers (Alison et al., 2022;Bjerge et al., 2023;Suetsugu et al., 2017). In this study, we use time-lapse cameras to better understand the importance of fungal fruit bodies for forest invertebrates. ...
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... Photographs and videos can keep recording for longer time without getting tired and can be reviewed repeatedly in order to record precise data of each flower visitation event. Successive observations using these devices have helped identify effective pollinator taxa [31][32][33] or changes in pollinators' activity with the time of day 21,22,34,35 . By using several cameras, they can also observe the patterns of pollinator visitation among several www.nature.com/scientificreports/ ...
... Another problem with the application of our system to other plant species is that pollinator detection rates may be dropped in flowers with complex spatial structure 74 or for mass tiny insect pollinators. For those species, multiple cameras from different angles may be required for each target flower 33 . Methods for pollinator species identification must also be improved. ...
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... There is also substantial evidence that some calanthe species are pollinated by bees (Sugiura, 2013;Ren et al., 2014;Sakata et al., 2014;Suetsugu and Fukushima, 2014;Suetsugu et al., 2016Suetsugu et al., , 2017. For example, calanthe striata is exclusively pollinated by the carpenter bee, Xylocopa appendiculata circumvolans (Sugiura, 2013). ...
... Our study showed that the bee E. nipponensis is a potential pollinator of calanthe discolor × c. striata. It can be assumed that Eucera visits to calanthe discolor × c. striata are rare, as we observed only a single visitation during our study; however, even rare pollination events can contribute to hybridization events in nature (Cozzolino et al., 2006;Suetsugu et al., 2017). Interestingly, Suetsugu and Fukushima (2014) reported that E. nipponensis is the main polli-nator of calanthe discolor; this study was conducted in a different population, but these results in combination with the results of the present study strongly suggest that the hybrid and parental species share pollinators. ...
... Seven species have been reported to be autogamous (Suetsugu & Fukushima 2014). It has also been reported that medium-to-large bees, such as Xylocopa, Eucera, Bombus, and Apis could pollinate Calanthe (Sugiura 2013;Sakata et al. 2014;Suetsugu & Fukushima 2014;Suetsugu et al. 2016Suetsugu et al. , 2017. Furthermore, it was reported that the pollinator of Calanthe argenteostriata was Pieris rapae, in the national orchid conservation center of China (Zhang et al. 2010). ...
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... Calanthe discolor, which is widely distributed throughout the islands of Japan, including the Izu Islands (from Izuoshima Island to Hachijojima Island), is pollinated by medium-sized bees (Suetsugu & Fukushima, 2014). On the other hand, C. izu-insularis, endemic to Kozushima and Mikurajima Islands in the Izu Islands (Cribb & Bailes, 2001;Yukawa, 2015) is still somewhat dependent on bee pollination, although C. izu-insularis has also changed its floral coloration and scent to facilitate moth pollination because most floral visitors to this species were moths (Suetsugu et al., 2017). In addition, individuals hypothesized to have been derived from natural hybridization between C. discolor and C. izuinsularis have also been found in the Izu Islands (Cribb & Bailes, 2001). ...
... Owing to its use as an ornamental plant and the consequent excessive collection, its population size on the Izu Islands has declined to several hundred; thus, this species is classified as 'endangered' in the Japanese Red List (Ministry of the Environment, Japan, 2018). Although the predominant floral visitors to this species are nocturnal moths, pollination by the small bee species Lasioglossum occidens has been reported (Suetsugu et al., 2017). ...
... The results of PCA of flower morphology supported the grouping and detection of hybridization based on microsatellite markers developed by Nakahama et al. (2018) (Fig. 5). The reduced number of keels on the mid-lobe of the lip and long spur and dorsal sepal length, the pale coloration and the strong, fragrant scent might represent adaptations of C. izu-insularis for moth pollinators (Giménez-Benavides, Escudero & Iriondo, 2007;Suetsugu et al., 2017). On oceanic islands where social bee species are not distributed, flower traits evolve to adapt to pollination by other insects, such as species of Lepidoptera or Diptera (Mizusawa et al., 2014;Shrestha et al., 2016). ...
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... Modern photographic equipment can, to a certain extent, be automated allowing for capturing of relatively infrequent events such as pollination. For example, a waterproof camera with a timer was used in the habitat of the Calanthe izuinsularis orchid to capture the identity and behaviour of that species' pollinator [3]. It would have been difficult or impossible for the authors to take those photographs without potentially disturbing the pollinating insects. ...
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Calanthe amamiana is a terrestrial orchid that thrives on the shady forest floors of broad‐leaved forests on Amami Island, central Ryukyus, Japan. Here, I report on the floral and pollination biology of this critically endangered orchid based on a 7‐year study conducted in the species' natural habitats. As the nectarless flowers are probably self‐compatible but are unable to autonomously self‐pollinate, they need to attract pollen vectors by deceit for pollination. To advertise themselves, the flowering inflorescences, which comprise a few to dozens of flowers, use whitish floral colors that are comparatively conspicuous against the shaded background. The exclusive pollinator was the long‐horned bee Eucera okinawae , which nests in soils of the forest floor, although bee abundance varied considerably among study years. Natural fruit‐set ratios were generally low but showed interannual variation. The annual fruit‐set ratios were positively correlated with annual bee abundance, thereby suggesting that under natural conditions, the orchid is pollinator‐limited. Given that C . amamiana is dependent exclusively on E . okinawae for pollination and is also probably pollinator‐limited, conservation plans for this orchid should take into consideration the welfare of long‐horned bees. In particular, as nectariferous flowers were unavailable within broad‐leaved forests, to satisfy the foraging requirements of long‐horned bees, conservation managers should be cognizant of conservation values of flowering plants distributed in sun‐lit sites near orchid habitats, and manage those in an appropriate manner.