Video Surveillance of Bumble Bee- and Lepidopteran-Plant Interactions on a Reconstructed Missouri Prairie
Aracely A. Newton1*, Teghan Wilson1, and Carlie Burandt1
14525 Downs Drive, Biology Dept., St. Joseph, MO 64507 Missouri Western State University, Saint Joseph, MO 64507 *Corresponding Author.
Prairie Naturalist, Volume 56 (2024):42–55
Abstract
Pollinator biodiversity is important for the health of ecosystems. Many pollinator species, including bumble bees and butterflies, are experiencing population declines and reduced habitat availability. To better manage land for at-risk pollinator communities, it is becoming increasingly important to be able to identify pollinators at the species taxonomic level. Here, we assessed the use of inexpensive video monitoring equipment to gather information about bumble bees and Lepidoptera on a recently reconstructed prairie. We identified 6 Bombus and 17 lepidopteran species with information about plant visitation and plant visit durations. Our findings indicate that video surveillance can be used as a management or research tool to identify large pollinators and study their plant interactions.
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A.A. Newton, T. Wilson, and C. Burandt
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2024 PRAIRIE NATURALIST 56:42–55
Video Surveillance of Bumble Bee- and Lepidopteran-Plant
Interactions on a Reconstructed Missouri Prairie
Aracely A. Newton*, Teghan Wilson, and Carlie Burandt
Abstract–Pollinator biodiversity is important for the health of ecosystems. Many pollinator species,
including bumble bees and butterflies, are experiencing population declines and reduced habitat
availability. To better manage land for at-risk pollinator communities, it is becoming increasingly important
to be able to identify pollinators at the species taxonomic level. Here, we assessed the use of
inexpensive video monitoring equipment to gather information about bumble bees and Lepidoptera on
a recently reconstructed prairie. We identified 6 Bombus and 17 lepidopteran species with information
about plant visitation and plant visit durations. Our findings indicate that video surveillance can be
used as a management or research tool to identify large pollinators and study their plant interactions.
Introduction
Pollinators are essential for the reproductive success of many flowering plants, including
dozens of crops worldwide (Kevan et al. 2003, Klein et al. 2007). High pollinator species
richness is important for the health of an ecosystem (Peterson et al. 1998). Pollinator diversity
also positively correlates with fruit production (Albrecht et al. 2012), benefiting frugivores.
Among pollinators, bumble bees (Bombus spp.)—which comprise approximately
260 species worldwide (Cameron et al. 2020)—are relatively effective, partly due to the
differential placement of interspecific pollen on their bodies (Huang et al. 2015) and their
ability to buzz pollinate certain flowers (Buchmann 1985). Other well-known pollinators
are the butterflies and moths (order Lepidoptera), the most speciose group of pollinators
(Ollerton 2017, Wardhaugh 2015). Though generally not considered as effective at pollinating
as bumble bees (Barrios et al. 2015), these conspicuous insects are often viewed by the
general public as important symbols of healthy ecosystems (Ghaz anfar et al. 2016).
Pollinator species are facing population declines in many areas, including the Midwestern
United States. Several Bombus species native to the Midwest have faced a reduction in
habitat over the past 100 years (Cameron et al. 2011, Colla 2012, Grixti et al. 2009). In 2017
Bombus affinis Cresson, the Rusty patched bumble bee, was listed as endangered by the U.S.
Fish and Wildlife Service (USFWS 2017), and the International Union for Conservation of
Nature (IUCN) listed Bombus fraternus Smith, the Southern Plains bumble bee, as endangered
in 2014 (Hatfield et al. 2014). Other bumble bees, such as B. pensylvanicus De Geer
and B. auricomus Robertson, have been reported to be declining in population (Cameron et
al. 2011, Wood et al. 2019). Within Lepidoptera, the migratory Monarch butterfly, Danaus
plexippus spp. plexippus (L.), is listed as vulnerable by the IUCN (Normile 2023), and many
other lepidopterans native to the Midwest have been reported to be in decline, including the
Black swallowtail (Papilio polyxenes Fabricius) and the Common sootywing (Pholisora
catullus Fabricius, Wepprich et al. 2019).
A contributing factor to pollinator declines is habitat loss, such as the loss of prairie systems
(Hanberry et al. 2021, Spiesman et al. 2013). Prairies once dominated the Midwest and
were a vast supply of grasses and forbs (herbaceous flowering plants) for pollinators and other
14525 Downs Drive, Biology Dept., St. Joseph, MO 64507 Missouri Western State University, Saint Joseph, MO 64507
*Corresponding Author: anewton4@missouriwestern.edu
Associate Editor: C.K. Pei, University of North Dakota Aerospace, Grand Forks, ND
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animals. In Missouri and nearby states, less than 1% of prairie ecosystems remain (Samson et
al. 1994), highlighting a need for prairie restorations and reconstructions as a land management
tool to preserve declining pollinators. An important aspect of habitat reconstruction is
identifying realistic goals that can be measured (Ehrenfeld 2000). For example, if a goal is to
provide habitat for declining bumble bee species, then a survey of bumble bee species would
be an appropriate assessment tool. Additional reconstruction goals could include removal and
monitoring of invasive species. Management goals could also include behavioral analysis
of at-risk pollinators to better understand their behaviors such as plant visitation and flower
visit duration, both of which are positively correlated with the amount of pollen picked up
by bumble bees (Thøstesen et al. 1996). In controlled experimental setups, visit duration can
indicate a preference for a certain flower (Vaudo et al. 2014).
Monitoring pollinators can be challenging for a number of reasons. Accurate identification
of morphologically similar insects can be difficult in the field, leading to aggregation of
species such as B. pensylvanicus and B. auricomus (Novotny et al. 2023). Time constraints
and lack of manpower can influence the quality of field surveys. Human observation is also
confined to the time in which the observer is present, which may not coincide with a pollinator’s
visitation patterns (Majetic 2015). Additionally, some species may be more likely
to avoid human observers, resulting in data bias.
In response to these and other challenges, the use of video surveillance for observing
insects has been increasing. Video monitoring can be beneficial for understanding pollinator
ecology for several reasons. For example, the experimental setup can easily be
performed by non-experts. Surveillance videos can also be used in the training of novices
because animal identity can be verified later by experts. Another advantage of video surveillance
is that it allows for repeated reviewing and the potential for in-depth behavioral
analysis (Steen 2017). Video monitoring can also help eliminate biases caused by human
interference in the field. Video surveillance methods range from continuous video to motion-
activated recordings (Pegoraro et al. 2020, Weinstein 2015). The small size of insects
and wind-driven motion of prairie plants can create issues when using motion-activation.
A recent study compared motion-activated cameras with scheduled 60-s-long videos and
determined that the scheduled cameras detected more insects because the insects were too
small to consistently activate the motion sensor (Naqvi et al. 2022). Pairing continuous
or scheduled recording with deep learning systems may prove to be the most powerful
combination for pollinator ecology, as it enables specific and automated filtering of vast
amounts of data (Weinstein 2018).
Here, we investigated whether a relatively inexpensive videography surveillance method
could be used to classify large insect pollinators to the species taxonomic level on a reconstructed
prairie in northwest Missouri. Our goal was to identify bumble bee and Lepidoptera
species and their behaviors. We conducted our studies using inexpensive portable video
camera setups that were arranged near flowering plants, most of which were native and one
that is a noxious invasive weed, Musk thistle (Carduus nutans Linnaeus), which appeared
to be attracting numerous pollinators. We wanted to determine if the cameras would allow
us to confidently identify lepidopterans and bumble bees to the species taxonomic level.
We measured visit duration on various prairie plants and Musk thistle to determine if any
differences could be detected between plant species. We investigated whether differences in
visit duration could be observed between Bombus species or Lepidoptera families. Finally,
we used our camera setups to calculate visitation rates between plant species. Such video
surveillance methodology can be useful towards monitoring pollinators and pollinator-plant
interactions to address a variety of conservation-related quest ions.
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Materials and Methods
Site description
The John Rushin Teaching and Research Prairie (Fig. 1A) is a 36-acre (14.4 ha) urban
prairie-savanna located on Missouri Western State University’s campus in St. Joseph, Missouri.
It is located east of most of the university buildings. It is comprised primarily of
prairie habitat reconstruction with a connecting 5-acre (2 ha) savanna habitat. The area of
land that comprises actively growing prairie vegetation totals approximately 25 acres (10
ha). The prairie reconstruction began in 2019 with two rounds of herbicide application followed
by seeding in 2020 with over 200 species of forbs, grasses, sedges, and rushes that
were collected as part of a partnership with the Missouri Department of Conservation and
The Nature Conservancy (Supplemental Table 1).
Figure 1. (A) The John Rushin Teaching and Research Prairie totals 36 acres (14.4 ha) and is located
on the eastern side of Missouri Western State University’s campus within the city limits of St. Joseph,
Missouri 39.760833, -94.775556 (Google Earth Pro 7.3 July 2022). B) Examples of the camera
surveillance setup to record Goldenrod (left, Solidago spp.) and native thistle (right, Cirsium spp.).
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Video collection
We used Polaroid Cube HD 1080p cameras to capture footage of different plants in the
prairie from June to October 2022. Each camera contains a magnetic bottom which was
used to attach it to a 2.5 cm x 3.8 cm piece of 1.25 cm welded wire mesh after the mesh was
slipped over and attached to a 1.2 m metal fence post with a binder paper clip (Fig. 1B).
The pole was placed ~15–20 cm away from a flower of interest and the height of the wire
mesh was adjusted to match the height of the flower. The camera was then placed on top
of the wire mesh. In the case of tall plants, two metal fence posts were often attached with
hose clamps to add height. Occasionally, a nearby tall plant was used as an attachment point.
Cameras were always oriented in the same direction as the sun to maximize light exposure;
pointing the camera into the sun yielded dark videos that made identification very difficult.
Twice weekly (weather permitting), we deployed 5 cameras for approximately 50 min.
Recordings began in the morning between 10 AM to noon on summer days and later in the
afternoon on autumn days when temperatures were favorable for insect sightings. Each day,
we aimed to record visitations at 3 different floral species with observed pollinator activity.
Once the filming was complete, the cameras were collected, and the files were downloaded
for analysis. Videos of poor quality and those that had technical difficulties (for example,
a plant that was blown over by the wind) were excluded from the analysis. All plants were
native to the Midwest with the exception of Musk thistle because we wanted to compare its
pollinator demographic with that of surrounding native plants.
Video analysis
All videos were manually analyzed using VLC media player, version 3.0.17. Pollinators
and corresponding timestamps were documented in a spreadsheet from each video. An insect
was manually documented when it physically touched a flower of interest. Next, we identified
each animal to the appropriate taxonomic level for which we were confident. For this study,
we report Bombus and Lepidoptera data only. The subset of bumble bees and lepidopterans
that were confidently identified to the species taxonomic level were included in our analysis.
We used identification guides for areas that included the state of Missouri (Cameron 2009,
Cameron et al. 2016) and online resources including iNaturalist (2022-2023, www.inaturalist.
org) and Insect Identification (Missouri Insects 2022-2023, www.insectidentification.org).
Bombus auricomus and B. pensylvanicus females were distinguished from each other based
on the presence or absence of yellow on the head. Flower visit duration (in seconds) was defined
as the time from which a pollinator touched a flower head until it moved off, except in
the case Common milkweed (Asclepias syriaca Linnaeus) and Bee balm (Monarda fistulosa
Linnaeus), which were measured by inflorescence and Goldenrod (Solidago spp.), which was
measured by branch (Fig. 2B). If an insect flew out of the camera’s field of view and then flew
back into view, it was counted as a new observation.
Declining vs stable species designation
A pollinator species was designated as “declining” in our study if it had USFWS or IUCN
status as endangered or vulnerable, or if populations have been reported to be declining in
scientific studies. An absence of such information led to a species to be labeled a s “stable”.
Statistical analysis
All data were calculated as mean ± standard error of the mean. For visit duration, plants
containing fewer than 10 bumble bee or Lepidoptera visitors were removed from analysis.
For visitors per hour analysis, plants that consisted of one observational video and plants
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for which no bumble bee or Lepidoptera pollinators were observed were removed from
analysis. Statistical analyses were conducted using R, version 4.3.0 (R Core Team 2023).
Mean visit duration and mean visitors per hour were analyzed using a Kruskal-Wallis test
because the data were not normally distributed. Post-hoc Dunn’s test was completed using
the FSA and rcompanion packages with a Bonferroni adjustment (Mangiafico 2023, Ogle et
al. 2023). We accepted significant differences at p < 0.05.
Results
We accumulated 123 hours of video footage from 3 June 2022 to 28 October 2022.
Most of our footage (78.1%) was comprised of native plant flowers (Fig. 2A) and approximately
21.9% came from flowers of Musk thistle, a noxious invasive weed that was
located on the prairie and appeared to be attracting numerous visitors. The plants with the
lowest number of footage hours were Prairie rosinweed (Silphium integrifolium Michx)
with 0.98 hr, Bee balm with 1.03 hr, and Ironweed (Vernonia fasciculata Michx) with 1.29
hr. Some plants were not recorded as much because they were not in bloom for very long
during our analysis window (for example, Bee balm) compared with other plants, such
as Purple coneflower (Echinacea purpurea [L.] Moench). A few morphologically similar
species were categorized by genus, such as Coreopsis and Goldenrod. Similarly, white
asters were grouped by genus and collectively labeled Symphyotrichum spp. to distinguish
them from New England aster (Symphyotrichum novae-angliae [L.] G.L. Nesom). Field
Figure 2. (A) Total amount of time that each plant was recorded. A total of 123 hours of footage was
collected. (B) Examples of different plants analyzed in this study: i. Flowering head of a Field Thistle
(Cirsium discolor), ii. Bee Balm (Monarda fistulosa) with inflorescence circled, iii. Goldenrod (Solidago)
spp. with branch circled, and iv. Common Milkweed (Asclepias syriaca) with inflorescence circled.
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thistle (Cirsium discolor [Muhl. ex Willd.] Spreng.) was the sole native species in our
study that was not part of the seed mix used in the reconstruction process. Examples of
flowers that were recorded are shown in Figure 2B.
Of the bumble bees that were observed in our footage and landed on a flower, we were
able to confidently identify 76.1% (648 of 852) to the species taxonomic level, which included
6 different species (Table 1). The stable species B. impatiens Cresson was the most
frequently observed bumble bee (n = 447). Likewise, the second and third most observed
Bombus Species Common Name Count
B. auricomus Robertson Black and Gold Bumble Bee 23
B. bimaculatus Cresson Two-Spotted Bumble Bee 72
B. fraternus Smith Southern Plains Bumble Bee 1
B. griseocollis De Geer Brown-Belted Bumble Bee 76
B. impatiens Cresson Common Eastern Bumble Bee 447
B. pensylvanicus De Geer American Bumble Bee 29
Total identified 648
Total Bombus count (identified and unidentified species) 852
Lepidoptera Species Common Name Count
Atalopedes campestris Boisduval Sachem Skipper 55
Danaus plexippus Linnaeus Monarch 28
Epargyreus clarus Cramer Silver-Spotted Skipper 17
Erynnis horatius Scudder and Burgess Horace’s Duskywing 3
Euphyes vestris Boisduval Dun Skipper 1
Euptoieta claudia Cramer Variegated Fritillary 1
Hemaris diffinis Boisduval Snowberry Clearwing 27
Hylephila phyleus Drury Fiery Skipper 1
Junonia coenia Hübner Common Buckeye 4
Lerema accius Smith Clouded Skipper 2
Papilio glaucus Linnaeus Eastern Tiger Swallowtail 4
Papilio polyxenes Fabricius Black Swallowtail 5
Phoebis sennae Linnaeus Cloudless Sulphur 2
Pholisora catullus Fabricius Common Sootywing 1
Polites peckius Kirby Peck’s Skipper 8
Speyeria cybele Fabricius Great Spangled Fritillary 5
Vanessa cardui Linnaeus Painted Lady 13
Total identified 177
Total Lepidoptera count (identified and unidentified species) 267
Table 1. Counts of Bombus and Lepidoptera species identified in the recordings.
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species, B. griseocollis De Geer (n = 76) and B. bimaculatus Cresson (n = 72), are stable
species as well. We observed 3 declining Bombus species: B. auricomus (n = 23), B. pensylvanicus
(n = 29), and B. fraternus (n = 1).
We were able to confidently identify 66.3% (177 of 267) of lepidopterans to the species
taxonomic level. A total of 17 different species were recorded, including 9 skippers (Hesperiidae)
and the Snowberry clearwing sphinx moth (Hemaris diffinis Boisduval). The Sachem
skipper (Atalopedes campestris Boisduval) was the most frequently observed lepidopteran
(n = 55). The Monarch butterfly was the second most observed (n = 28) and the Snowberry
clearwing was third (n = 27). Four species were identified once: the Dun skipper (Euphyes
vestris Boisduval), the Variegated fritillary (Euptoieta claudia Cramer), the Fiery skipper
(Hylephila phyleus Drury), and the Common sootywing. Of the Lepidoptera observed, 3
have been reported to be declining in population: the Monarch, the Black swallowtail, and
the Common sootywing (Wepprich et al. 2019). Because the Monarch butterfly is a species
of concern, we documented the plants on which it was observed (Supplemental Table 2).
Monarchs were seen from June 6 through October 10, peaking in September. They were
observed predominantly on Tickseed sunflower, Bidens aristosa (Michx) Britton, and New
England aster but also seen on Field thistle, Common milkweed, Musk thistle, Cup plant
(Silphium perfoliatum L.), Goldenrod, and Symphyotrichum spp.
We first wanted to determine if flower visit duration by pollinators differed between
plants and began by evaluating bumble bee visit durations (Fig. 3A). A Kruskal-Wallis
analysis revealed significant differences between samples (H[8] = 135.19, p < 0.001). Mean
visit durations were highest on Common milkweed (36.4 ± 5.88 s), Musk thistle (40.1 ±
6.08 s), and Field thistle (44.4 ± 10.1 s). On these plants, bees had a significantly longer
mean visitation time (p < 0.05) than on Tickseed sunflower, Bee balm, Goldenrod spp., New
England aster, and Symphyotrichum spp. Within Lepidoptera, a Kruskal-Wallis analysis also
revealed significant differences in visit duration between plants (H[4] = 30.605, p < 0.001)
The longest mean visitation was seen on Field thistle (Fig. 3B, 100.0 ± 35.6 s), which had a
significantly longer visit duration than Tickseed sunflower (15.1 ± 5.20 s) and New England
aster (17.6 ± 2.50 s, p < 0.05).
Individual Bombus species showed no significant differences in visit duration within a
plant species (Fig. 4A). Notably, Musk thistle, Cup plant, and Field thistle were visited by
a higher proportion of declining bumble bee species compared to other plant species that
we observed. Symphyotrichum spp., including New England aster, Goldenrod spp., and
Tickseed sunflower were predominantly visited by B. impatiens. A Kruskal-Wallis analysis
for each plant revealed no significant differences in visit duration between Bombus species.
Evaluating the 5 Lepidoptera families in our study (Fig. 4B), Kruskal-Wallis analysis
revealed significant differences between families for Musk thistle (H[3] = 13.799, p =
0.003) and New England Aster (H[1] = 6.924, p = 0.009). On Musk thistle, Hesperiidae had
significantly longer visit durations (67.4 ± 19.1 s) compared with the Snowberry clearwing
(Sphingidae, 17.8±4.77 s). On New England aster, Nymphalidae displayed significantly
longer visit durations (22.0 ± 3.39 s) compared with Hesperiida e (9.9 ± 2.10 s).
Bombus plant visitation rates differed significantly by Kruskal-Wallis analysis (H[10] =
46.81, p < 0.001; Fig. 5A). New England aster was visited significantly more often (21.1 ±
3.49 bees/hr) than Tickseed sunflower (3.02 ± 1.14 bees/hr), Musk thistle (2.52 ± 0.66 bees/
hr), and Purple coneflower (0.67 ± 0.56 bees/hr) at p < 0.001; Field thistle (2.41 ± 1.51 bees/
hr), False sunflower (Heliopsis helianthoides (L.) Sweet; 0.52 ±0.33 bees/hr), and Goldenrod
spp. (2.61 ± 1.43 bees/hr) at p < 0.01; and Symphyotrichum spp. (2.16 ± 0.74 bees/hr) at
p < 0.05. All identified bumble bees on New England aster were B. impatiens, and it was also
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the sole or most frequently observed bumble bee on Tickseed sunflower (100%), Goldenrod
(95.7%), and Symphyotrichum spp. (100%). B. griseocollis was the most frequent visitor
on Common milkweed (89.2%) and Cup plant (46%). Cup plant was visited by the greatest
number of different bumble bee species (n = 5). The most frequent visitor of Musk thistle
(47.8%) and False sunflower (100%) was B. bimaculatus. Bombus pensylvanicus was identified
as the most common visitor of Field thistle (68.2%) and t he sole visitor of Ironweed.
Figure 3. Mean visit duration of (A) Bombus and (B) Lepidoptera on prairie plants. Vertical lines represent
SE. A Kruskal-Wallis analysis revealed significant differences between plant species. Samples
containing different letters were statistically different from each other (p < 0.05) using Dunn’ s test.
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A Kruskal-Wallis test revealed no significant differences in Lepidoptera visitors per
hour (± standard error, SE) between different plant species (H[10] = 15.14, p = 0.127;
Fig. 5B). Hesperiidae was the most frequent visitor to Tickseed sunflower (52.8%), Musk
Figure 4. Mean flower visit duration on prairie plants by (A) Bombus species and (B) Lepidoptera
families. Vertical lines represent SE. A Kruskal-Wallis analysis revealed no significant differences
between Bombus species within each plant. In Lepidoptera, a Kruskal-Wallis analysis revealed significant
differences within plant species. Families containing different letters within Musk Thistle
(Carduus nutans) and New England Aster (Symphyotrichum novae-angliae) were statistically different
from each other (p < 0.05) using Dunn’ s test.
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thistle (46.3%), Field thistle (75%), Purple coneflower (83.3%), and False sunflower
(100%). The Snowberry clearwing (family Sphingidae) was the most frequent visitor to
Common milkweed (75%), and Sphingidae and Hesperiidae visited Ironweed equally
(50%). The plants with visitors from the greatest number of families were Musk thistle
(Hesperiidae, Nymphalidae, Papilionidae, and Sphingidae) and Cup plant (Hesperiidae,
Nymphalidae, Papilionidae, and Pieridae).
Discussion
We demonstrate that bumble bee and Lepidoptera species can be identified at the species
taxonomic level using inexpensive video cameras. Video surveillance provides advantages
compared with in-person surveys. The videos allow us to revisit and slow footage to distinguish
between morphologically similar species such as B. pensylvanicus and B. auricomus. Videos
also add flexibility; if time is limited, identifications can be done at a later date. Video monitoring
also allowed us to easily assess other behaviors such as flower visits and flower visit durations,
which can serve as a proxy for pollen pickup in bumble bees (Thøstesen et al. 1996).
Our cameras allowed us to identify 6 different Bombus species on a reconstructed prairie.
We recorded a single observation of B. fraternus, listed as endangered by the IUCN
(Hatfield et al. 2014), on Goldenrod spp., indicating that at least one colony is located on
or near the prairie. Other observed Bombus species were consistent with those reported in
the region (Cameron et al. 2011, Larose et al. 2020). In our study the declining species B.
pensylvanicus and B. auricomus visited Field thistle (a native plant) and the closely related
noxious weed Musk thistle (Fig. 4A). This is consistent with Wood et al. (2019), who described
pollen found on the hind legs of B. pensylvanicus and B. auricomus museum specimens
dating as far back as 1912 and reported that both species carried a higher proportion
of Cirsium-type pollen than any other analyzed species. The declining Common sootywing
was also seen on Musk thistle. In our study, both native and non-native thistles appear to
be an important food source for declining pollinators. It has been proposed that non-native
plants can serve as important resources to native wildlife (Gleditsch et al. 2011). Therefore,
careful planning may be necessary when removing these plants to ensure that sufficient native
plants are in bloom to serve as food for declining pollinators.
Of the plants analyzed, New England aster had a significantly higher total Bombus
visitation rate than Tickseed sunflower, both thistles, Purple coneflower, False sunflower,
Goldenrod, and white Symphyotrichum spp. This is likely because it was visited primarily
by B. impatiens, which was the most frequently recorded bumble bee and the only Bombus
visitor that we detected on the aster. In fact, B. impatiens was the only bumble bee observed
from September 26 until the end of our analysis period on October 28. New England aster
began blooming on approximately October 3. This is consistent with Novotny et al. (2023)
who saw a decrease in non-B. impatiens species, starting in August. Though no other bumble
bees were observed on New England aster, we noted that it is a food source for other
pollinators, such as butterflies (Fig. 3B) and other native bees, flies, and beetles (data not
shown). The abundance of B. impatiens on New England aster may be due to the fact that
the aster was one of the only remaining food sources in October. Bombus impatiens has been
reported to have a relatively wide dietary niche and has been regarded as a generalist feeder
(Novotny et al. 2023, Wood et al. 2019).
Overall, the advantages of video monitoring place it as a valuable complement to other
survey methods. The cameras we used were continuous-use cameras as opposed to motionactivated
camera traps. This was intentional, as the movement of the prairie plants due to
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wind would have activated the camera traps and generated false positive data. However,
modifications of this technique can be applied to better suit different research needs, such
as scheduled recordings to prolong camera life, connection to an external power source, or
anchoring of the plant to prevent its movement (Steen 2017). In the near future, the incorporation
of deep learning and automation in video monitoring research will greatly accelerate
the field (Pegoraro et al. 2020), which is fortuitous as it is becoming increasingly urgent to
identify at-risk species as part of land management goals.
We demonstrate that bumble bee and Lepidoptera species and their pollinator-plant
interactions can be evaluated using an inexpensive camera setup and free video software
Figure 5. (A) Mean Bombus visits per hour. Vertical lines represent SE. A Kruskal-Wallis analysis
revealed significant differences between plant species. Samples containing different letters were
statistically different from each other (p < 0.05) using Dunn’s test. (B) Mean Lepidoptera visits per
hour. Vertical lines represent SE. No significant differences were found between plant species using
a Kruskal-Wallis analysis.
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(VLC media player). Reconstruction and restoration goals may include surveying wildlife,
including pollinators. Traditional pollinator surveys can be time-constraining and
difficult and may require the capture of animals to correctly identify the species. The
videography method we described is a simple way to gather information about pollinatorplant
interactions, ranging from general, “What types of pollinators are present?” to specific
information, “Is species X found in our habitat?” It can inform management efforts
regarding noxious invasive weeds to determine if the plants are being used by declining
species. It could also help identify deficits in forb composition. For example, our study
emphasized the importance of late-blooming plants such as New England aster and Goldenrod
for at-risk species, including Monarchs and B. fraternus. However, the addition of
other late-blooming species to the reconstructed prairie would provide additional nectar
and pollen sources. Video surveillance as a management tool can be easily adapted to suit
the needs of land managers, as it can provide valuable information about the current status
of a habitat as well as implications for improvement.
Acknowledgments
We thank Nina Walker, Fidel Supnet Jr., Em Kretzer, and Carson Quick for their help during different
stages of this research. We are grateful to Dr. Csengele Barta for input on prairie vegetation,
and to Dr. Cary Chevalier and Dr. Carissa Ganong for reviewing this manuscript. We thank members
of the Biology Department at Missouri Western State University and members of the Saint Joseph,
MO community for their assistance in maintaining the John Rushi n Teaching and Research Prairie.
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