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	<title>hoverflies &#8211; Science</title>
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	<title>hoverflies &#8211; Science</title>
	<link>https://scienmag.com</link>
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		<title>Rare Alpine hoverflies use mountaintops for mating above 3,000 metres</title>
		<link>https://scienmag.com/rare-alpine-hoverflies-use-mountaintops-for-mating-above-3000-metres/</link>
		
		<dc:creator><![CDATA[Gavin Prescott]]></dc:creator>
		<pubDate>Tue, 20 Oct 2026 14:47:44 +0000</pubDate>
				<category><![CDATA[Biology]]></category>
		<category><![CDATA[Science News]]></category>
		<category><![CDATA[Alpine ecology]]></category>
		<category><![CDATA[Alpine hoverfly distribution]]></category>
		<category><![CDATA[Alpine insect biodiversity]]></category>
		<category><![CDATA[description]]></category>
		<category><![CDATA[female]]></category>
		<category><![CDATA[first female description of P. altomontis]]></category>
		<category><![CDATA[French Alps]]></category>
		<category><![CDATA[high elevation insect sampling methods]]></category>
		<category><![CDATA[High-altitude hoverfly species]]></category>
		<category><![CDATA[high-altitude insects]]></category>
		<category><![CDATA[hilltopping]]></category>
		<category><![CDATA[hoverflies]]></category>
		<category><![CDATA[impact of elevation on insect diversity]]></category>
		<category><![CDATA[mountain summit insect habitat]]></category>
		<category><![CDATA[mountaintop mating behavior]]></category>
		<category><![CDATA[mountaintop pollinator ecology]]></category>
		<category><![CDATA[Platycheirus]]></category>
		<category><![CDATA[Platycheirus altomontis]]></category>
		<category><![CDATA[Pyrenean and Ardèche high-altitude surveys]]></category>
		<category><![CDATA[rare Platycheirus altomontis discovery]]></category>
		<category><![CDATA[Rohdendorfia alpina]]></category>
		<category><![CDATA[Rohdendorfia alpina record France]]></category>
		<category><![CDATA[species description]]></category>
		<category><![CDATA[Syrphidae]]></category>
		<guid isPermaLink="false">https://scienmag.com/?p=319473</guid>

					<description><![CDATA[A French field survey documented rare hoverflies hilltopping at elevations above 3,000 metres and supplied the first description of the previously unknown female of Platycheirus altomontis.]]></description>
										<content:encoded><![CDATA[<p>A focused survey of high-altitude sites in the French Alps found hoverfly species aggregating at mountaintops as high as 3,142 metres above sea level, including the rarely recorded Platycheirus altomontis and Rohdendorfia alpina, a species newly recorded for France. Fieldwork conducted between 2019 and 2021 also produced the first formal description of the female P. altomontis, based on three females collected in 2020. The observations indicate that the Alpine habitat above 2,800 metres remains poorly sampled and that searching high summits can reveal both undescribed morphology and new national records.</p>
<p>The field study was conducted by F. Van de Meutter during excursions to the French Alps, the French Pyrenees and Ardèche. Visits to Vars, Villar-d’Arêne, Freissinières and Molines-en-Queyras in the Alps covered elevations from 770 to 3,140 metres, with particular attention to the highest accessible points in July.</p>
<p>Additional Pyrenean localities ranged from 930 to 1,950 metres, while the Ardèche survey covered 550 to 1,250 metres. Hilltops were searched by sight and selected specimens were collected with a hand net. The collected hoverflies were preserved in the author’s personal collection in Tessenderlo, Belgium.</p>
<p>Because the French Alps had already been investigated extensively over many years, the study focused on a less explored component of the available habitat: the full elevational and seasonal range, especially high elevations during summer. The 2020 Alpine expeditions therefore targeted hilltops and prominent landmarks, with the highest accessible points sought particularly in July. Weather was favourable on all survey days, with long sunny spells and wind speed never exceeding 4 Bf.</p>
<p>Specimens were examined under a stereomicroscope and identified using a combination of identification works by Barkalov and Ståhls, Nielsen, van Veen, Šašić and colleagues, Ståhls and Barkalov, and Speight and Sarthou. Across all expeditions, the author observed 205 hoverfly species in French mountains. Two were new to the French fauna, while 26 occurred in five or fewer French departments according to the distribution information available to the study and could therefore be considered rare in the French context.</p>
<p>The lower montane and Alpine meadows between 1,200 and 2,400 metres contained numerous Cheilosia, Platycheirus, Pipizella and Sphaerophoria species, but no new species was found in that elevational band. By contrast, the narrow zone above 2,800 metres yielded a striking concentration of uncommon and newly recorded taxa, including many tens of R. alpina and multiple P. altomontis. Rohdendorfia alpina was recorded for the first time in France.</p>
<p>The species, associated with bare scree at high elevation, occurred in large numbers near Pain de Sucre at 2,780 metres and around La Mortrice, including the summit at 3,142 metres. The listed sample included 17 males and 11 females near Pain de Sucre, seven females near La Mortrice, and three males and one female at the summit. The numbers seen in the field were substantially higher than the numbers collected.</p>
<p>At La Mortrice, a male appeared to perform hilltopping behaviour. The species was found at both high mountain summits visited in July 2020, and the study noted that it may occur at other French Alpine summits as well, although that wider presence was not directly sampled. Platycheirus altomontis was also found at both mountain tops visited in July 2020.</p>
<p>One female was collected near Pain de Sucre at 2,780 metres, where it was feeding on small white flowers, while three males and two females were observed at La Mortrice at 3,142 metres. Females visited small flowers, whereas males fed or sat on stones and made short flights, behaviour described as suggestive of hilltopping. Until this study, the female of P. altomontis had not been formally described.</p>
<p>The description based on the three females established a body length of 6–7 millimetres. Females have bare eyes and a frons at antennal level that is distinctly broader than an eye. The third antennal segment is dark grey-brown, narrowly orange below at the base, while the scape and pedicel are black and the arista is relatively short and thick, slightly longer than the flagellum.</p>
<p>The face carries very long white pilosity, mainly at the sides, and is completely covered with thin grey pollinosity. The frons and vertex are undusted apart from narrow paired triangular dust spots. The scutum and scutellum are shining metallic blue-black with long white pilosity, and the pleurae and humerus have thin grey pollinosity with relatively long white hairs.</p>
<p>The wings have a light-yellow stigma and are covered with microtrichia apart from specified bare areas in cells bm, br and cua. The calypter is yellow-white and the haltere yellow-brown. All legs are dark and carry thin grey pollinosity, with narrow yellow tibial bases and yellow distal portions of the femora.</p>
<p>The relatively short, broad abdomen is dark grey-black and largely matt, apart from large shining areas at the sides of all tergites. Tergites 3 and 4 bear large, semi-rectangular white-grey pollinose spots with rounded inner corners. Abdominal pilosity is pale, sparse, short and appressed centrally, and long and erect laterally.</p>
<p>The female description nevertheless has a clear limitation. In Nielsen’s key to females, P. altomontis would run to P. lundbecki, but no female P. lundbecki was available for direct comparison, so the study did not provide a differential diagnosis between the two. Geographic context may help separate them: P. lundbecki is associated with Nordic countries, whereas P. altomontis is known from high Alpine summits.</p>
<p>From other known species in the P. ambiguus group, the newly described female was distinguished by its small, compact form, short and broad black abdomen with grey dust spots, and very dark legs. The female was also broadly similar to the male apart from the usual sexual dimorphism found within Platycheirus. Eight of the 23 species in the P. ambiguus group still lacked described females at the time of the study.</p>
<p>Thirteen species were observed hilltopping in the French Alps. At 3,142 metres, the highest site with confirmed observations, the group included P. altomontis, R. alpina, Epistrophe leiophthalma, Eupeodes flaviceps and Eristalis tenax. Lower Alpine sites produced concentrations of more than 25 males in loose swarms or around individual landmarks.</p>
<p>These assemblages included Platycheirus tatricus, Cheilosia melanura, Didea alneti, Pipizella calabra, P. nigriana and P. pennina, alongside hoverflies identified only provisionally as Parasyrphus kirgizorum or P. tarsatus. One Parasyrphus group was found at the last larch above the treeline at 2,320 metres, where more than 25 males sat on the tree or hovered nearby. The observations show that this strategy was not restricted to one taxonomic group or to species that are universally scarce.</p>
<p>The very common Cheilosia melanura hilltopped, and its summit-associated males were smaller than larger males of the same species observed hovering in lower forest clearings. The author suggested that hilltopping may be one mating strategy among several within a species and could be related to particular phenotypes, while emphasizing that further research is required to establish which species use the behaviour and how and why it evolved.</p>
<p><strong>Subject of Research:</strong> High-altitude hoverfly records, female morphology and hilltopping behaviour in French mountains</p>
<p><strong>Article Title:</strong> ﻿Description of the female of Platycheirus altomontis Merlin &amp; Nielsen in Nielsen, 2004 ( Diptera , Syrphidae ) with notes on the occurrence and hilltopping behaviour of rare French montane and Alpine Syrphidae</p>
<p><strong>Article References:</strong> Van de Meutter, F. (2022). ﻿Description of the female of Platycheirus altomontis Merlin &amp;amp; Nielsen in Nielsen, 2004 (Diptera, Syrphidae) with notes on the occurrence and hilltopping behaviour of rare French montane and Alpine Syrphidae. <em>Alpine Entomology, 6</em>, 65-76. <a href="https://doi.org/10.3897/alpento.6.81676" rel="noopener noreferrer">https://doi.org/10.3897/alpento.6.81676</a></p>
<p><strong>Image Credits:</strong> AI Generated</p>
<p><strong>DOI:</strong> <a href="https://doi.org/10.3897/alpento.6.81676" rel="noopener noreferrer">10.3897/alpento.6.81676</a></p>
<p><strong>Keywords:</strong> hoverflies, Syrphidae, Platycheirus altomontis, Rohdendorfia alpina, hilltopping, French Alps, high-altitude insects, species description, Alpine ecology, Description, female, Platycheirus</p>
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		<post-id xmlns="com-wordpress:feed-additions:1">319473</post-id>	</item>
		<item>
		<title>Czech survey maps warning colours in bees, wasps and mimic insects</title>
		<link>https://scienmag.com/czech-survey-maps-warning-colours-in-bees-wasps-and-mimic-insects/</link>
		
		<dc:creator><![CDATA[Gavin Prescott]]></dc:creator>
		<pubDate>Tue, 20 Oct 2026 08:21:25 +0000</pubDate>
				<category><![CDATA[Science News]]></category>
		<category><![CDATA[aposematic]]></category>
		<category><![CDATA[aposematic patterns in insects]]></category>
		<category><![CDATA[aposematism]]></category>
		<category><![CDATA[bees]]></category>
		<category><![CDATA[bees and wasps warning coloration]]></category>
		<category><![CDATA[black-and-yellow warning signals]]></category>
		<category><![CDATA[clearwing moths]]></category>
		<category><![CDATA[Czech Republic]]></category>
		<category><![CDATA[European bee and wasp species]]></category>
		<category><![CDATA[hoverflies]]></category>
		<category><![CDATA[insect colouration]]></category>
		<category><![CDATA[insect defense mechanisms]]></category>
		<category><![CDATA[insect mimicry in Czech Republic]]></category>
		<category><![CDATA[longhorn beetles]]></category>
		<category><![CDATA[metallic insect coloration]]></category>
		<category><![CDATA[mimicry]]></category>
		<category><![CDATA[mimicry in hoverflies and beetles]]></category>
		<category><![CDATA[proportions]]></category>
		<category><![CDATA[survey of aposematic insects]]></category>
		<category><![CDATA[toxic and unpalatable insect markings]]></category>
		<category><![CDATA[visual signals in Hymenoptera]]></category>
		<category><![CDATA[warning color evolution in insects]]></category>
		<category><![CDATA[warning colouration]]></category>
		<category><![CDATA[wasps]]></category>
		<guid isPermaLink="false">https://scienmag.com/?p=317098</guid>

					<description><![CDATA[A survey of 1,221 Czech bee and wasp species found aposematic colouration in 73.83%, with black-and-yellow patterns dominant across bees, wasps and three major mimic groups.]]></description>
										<content:encoded><![CDATA[<p>A museum-based and photographic survey of the Czech Republic found conspicuous warning colouration in 900 of 1,221 species of bees and wasps examined, or 73.83%. The analysis also identified similar aposematic patterns in three major groups of bee and wasp mimics: 36 of 43 clearwing moth species, 322 of 424 hoverfly species and 104 of 205 longhorn beetle species. Black-and-yellow, a category that also included white or creamy-white markings, was the dominant pattern among the aposematically coloured species in all four groups surveyed.</p>
<p>Aposematic colouration is associated with animals that are unpalatable, toxic or otherwise dangerous, and can take the form of conspicuous contrasting colours such as black with yellow or red. Among bees and wasps, aposematic signals are associated with the sting, although some non-stinging groups can also display warning-like coloration. The survey classified patterns into four categories: black-and-yellow, including white or creamy white; black-and-red; black-yellow-red; and metallic. The first three were pigment-based, whereas metallic coloration arose through physical effects within the insect cuticle.</p>
<p>The study examined the fauna of the Czech Republic, which the authors described as rich in the groups considered and representative of the European fauna for them. Its principal subject was Hymenoptera: Aculeata, or bees and wasps, with the families Bethylidae, Dryinidae, Embolemidae and Formicidae excluded because they have different life strategies. The three main mimic groups were clearwing moths in Lepidoptera, hoverflies in Diptera and longhorn beetles in Coleoptera. Species lists were drawn from established regional faunas for bees, wasps and each mimic group.</p>
<p>Colouration was assessed separately for males and females using the first author’s private collection, the National Museum in Prague and major online photographic resources, including iNaturalist, Flickr and Biolib. A species was recorded as aposematic when it possessed one of the four designated pattern types, with records made for body colour and body hairs. Bands of yellow or white hairs counted as aposematic patterns, as did combinations of black and red body colour with white hairy spots or bands. When males and females differed in colouration, the researchers entered half of each pattern for that species in the dataset.</p>
<p>Clearwing moths had the highest proportional representation of aposematic species in the comparison, with 36 of 43 species, or 83.72%. Hoverflies followed with 322 of 424 species, or 75.94%. Longhorn beetles had a lower overall prevalence, with 104 of 205 species, approximately 50.73%, displaying aposematic coloration. Despite these differences, black-and-yellow was the most frequent pattern in each of the four groups. It appeared in 271 of the 322 aposematic hoverflies, or 84% of that aposematic subset, and in 51% of the aposematic longhorn beetles recorded in the analysis.</p>
<p>The other patterns were less common overall but had distinctive distributions. Black-and-red coloration accounted for 23% of aposematic longhorn beetles, the highest proportion among the groups, compared with 8% of aposematic hoverflies. Metallic coloration was also relatively prominent in longhorn beetles, reaching 22% of their aposematic species. Among the bees and wasps, bees included 433 aposematic species, representing 71% of the bee species analyzed, and black-and-yellow was especially prominent among non-parasitic bees. In many of those species, the pale component of the pattern was produced by bands or spots of body hairs rather than pigmented skin.</p>
<p>Family-level comparisons revealed still greater concentrations of particular signals. Every cuckoo wasp in the family Chrysididae had metallic coloration and no other recorded aposematic type. Black-and-red was strongly represented in spider wasps, Pompilidae, while black-and-yellow predominated in Vespidae. Black-yellow-red coloration was more prevalent in Mutillidae. On average, the aposematic share of species in Chrysididae was only slightly above half that of Apoid wasps, which comprised 165 of 281 species, or 58%. These contrasts show that a broad survey category can conceal sharply different colour patterns among related insect lineages.</p>
<p>Foraging strategy also corresponded with differences in warning coloration. Nesting predators and nesting herbivores had similar proportions of aposematic representatives, while 96% of the parasitic species examined used aposematic signals frequently. Almost 87% of breeding herbivores had black-and-yellow coloration, whereas that pattern occurred in only 21% of parasites. Metallic coloration was the most common pattern among parasites at 34%, but the authors noted that this result was driven by cuckoo wasps. With Chrysididae excluded, metallic coloration was absent from the other parasitic species, and the three pigment-based patterns were approximately equally common, each accounting for between 32% and 40%.</p>
<p>Males and females differed in coloration in 67 of the 1,221 bee and wasp species, or 5.49%. One recurring arrangement involved females with white hair bands that were absent or less pronounced in males, as in several Andrena and Eucera species. More pronounced differences appeared in the cuckoo bees Ammobatoides abdominalis and Epeoloides coecutiens, whose males were cryptically coloured while their females had aposematic black-and-red patterns with white markings. Several Mutillidae and Pompilidae also combined aposematic females with entirely black males. In some Mutillidae, the difference coincided with wingless females and winged males, although the survey did not experimentally test the function of the dimorphism.</p>
<p>Sex-related differences also appeared among the mimics. Twenty-six hoverfly species showed some distinction between the sexes, usually the absence or reduction of yellow or red markings in males. Eight longhorn beetle species differed, and in most of them males were cryptically coloured while females were aposematic. Tetropium castaneum showed the reverse pattern, while the male Oxymirus cursor was black and the female metallic. No sex-based colour difference was recorded among the clearwing moth species examined, although Synanthedon culiciformis combined black-red with metallic coloration and S. cephiformis combined black-yellow with metallic coloration. Some mimics also reproduced behaviour as well as appearance: certain clearwing moths imitate the flight and buzzing of their models, while Plagionotus arcuatus resembles a wasp most strongly when moving.</p>
<p>The survey identifies a regional pattern of widely shared warning signals, but it does not directly measure predator responses, attack rates or survival benefits. Its authors interpret the abundance of aposematism among bees and wasps as compatible with protective mutual resemblance, while clearwing moths and other similarly coloured insects may gain protection through Batesian mimicry of defended models. They also note that coloration can serve purposes beyond defence, including thermoregulation, and that chemical communication may mediate some interactions between parasitic insects and their hosts. The analysis is geographically limited to the Czech fauna, relies on visual records from collections and photographs, and condenses varied patterns into four broad categories. Within those limits, it shows that nearly three-quarters of the bee and wasp species examined carried aposematic patterns and that clearwing moths, hoverflies and longhorn beetles displayed many of the same combinations.</p>
<p><strong>Subject of Research:</strong> Comparative survey of aposematic colour patterns in Czech bees, wasps and their principal mimic groups</p>
<p><strong>Article Title:</strong> ﻿Proportions of aposematic colouration in bees and wasps ( Hymenoptera , Aculeata ) and their main mimics – hoverflies, clearwing moths and longhorn beetles</p>
<p><strong>Article References:</strong> Bogusch, P., &amp; Zahradníková, A. (2025). Proportions of aposematic colouration in bees and wasps (Hymenoptera, Aculeata) and their main mimics – hoverflies, clearwing moths and longhorn beetles. <em>Journal of Hymenoptera Research, 98</em>, 325-338. <a href="https://doi.org/10.3897/jhr.98.141208" rel="noopener noreferrer">https://doi.org/10.3897/jhr.98.141208</a></p>
<p><strong>Image Credits:</strong> AI Generated</p>
<p><strong>DOI:</strong> <a href="https://doi.org/10.3897/jhr.98.141208" rel="noopener noreferrer">10.3897/jhr.98.141208</a></p>
<p><strong>Keywords:</strong> aposematism, warning colouration, bees, wasps, hoverflies, clearwing moths, longhorn beetles, mimicry, Czech Republic, insect colouration, Proportions, aposematic</p>
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		<post-id xmlns="com-wordpress:feed-additions:1">317098</post-id>	</item>
		<item>
		<title>New stingless bee mimic: spectacular hoverfly species discovered in Ecuadorian Amazon</title>
		<link>https://scienmag.com/new-stingless-bee-mimic-spectacular-hoverfly-species-discovered-in-ecuadorian-amazon/</link>
		
		<dc:creator><![CDATA[Gavin Prescott]]></dc:creator>
		<pubDate>Sat, 17 Oct 2026 07:03:02 +0000</pubDate>
				<category><![CDATA[Biology]]></category>
		<category><![CDATA[Science News]]></category>
		<category><![CDATA[Amazon rainforest]]></category>
		<category><![CDATA[biodiversity in Napo Province rainforest]]></category>
		<category><![CDATA[DNA barcoding]]></category>
		<category><![CDATA[DNA barcoding of Syrphidae]]></category>
		<category><![CDATA[Ecuador]]></category>
		<category><![CDATA[Ecuadorian Amazon hoverfly discovery]]></category>
		<category><![CDATA[evolutionary significance of bee mimicry in flies]]></category>
		<category><![CDATA[hoverflies]]></category>
		<category><![CDATA[implications for pollination and ecological interactions]]></category>
		<category><![CDATA[insect mimicry and evolutionary strategies]]></category>
		<category><![CDATA[Microdontinae]]></category>
		<category><![CDATA[Microdontinae larval behavior inside ant nests]]></category>
		<category><![CDATA[mimicry]]></category>
		<category><![CDATA[mirabilissimus]]></category>
		<category><![CDATA[Neotropical stingless bee mimicry adaptations]]></category>
		<category><![CDATA[new species]]></category>
		<category><![CDATA[rare and poorly understood hoverfly species]]></category>
		<category><![CDATA[stingless]]></category>
		<category><![CDATA[stingless bee mimicry]]></category>
		<category><![CDATA[Syrphidae]]></category>
		<category><![CDATA[taxonomy]]></category>
		<category><![CDATA[tropical hoverfly diversity]]></category>
		<category><![CDATA[Ubristes]]></category>
		<category><![CDATA[Ubristes mirabilissimus new species]]></category>
		<guid isPermaLink="false">https://scienmag.com/?p=295054</guid>

					<description><![CDATA[A spectacular new hoverfly species from Ecuador's Napo Province, Ubristes mirabilissimus, mimics stingless bees and represents the first DNA barcodes ever obtained for its rare genus.]]></description>
										<content:encoded><![CDATA[<p>Deep in the lowland rainforest of Ecuador&#8217;s Napo Province, a fly with an uncanny resemblance to a stingless bee has turned out to be something entirely new to science. Researchers describing the insect have named it Ubristes mirabilissimus, a superlative form of the Latin word mirabilis, meaning wonderful or strange. The authors chose the name deliberately: in their view, it is the most wonderful species of the genus Ubristes known so far. The discovery, published in the journal Evolutionary Systematics, raises the number of recognized Ubristes species to five and delivers the first DNA barcodes ever obtained for this elusive group of hoverflies.</p>
<p>Ubristes belongs to the hoverfly family Syrphidae, but it is no ordinary flower visitor. The genus sits within the subfamily Microdontinae, an unusual lineage whose larvae are known to live inside ant nests. Adult microdontines are among the rarest and most poorly understood hoverflies in the tropics, with most species known from only one or two specimens. What makes Ubristes particularly striking is its strong resemblance to Neotropical stingless bees of the genus Trigona. The mimicry is built from a combination of long antennae, thickened hind legs armed with corbicula-like brushes on the tibiae, and a matching abdominal shape and colouration, a package that allows the fly to pass among the bees it imitates.</p>
<p>The new species was collected by hand-net along rainforest trails near Grand Selva Lodge and the Campo Cocha Community, at elevations of roughly 500 to 590 metres. The holotype and two paratype males were captured in September 2023 and September 2024, and an additional historical specimen from near Tena, collected in 1976 and held at the Natural History Museum in London, was also studied. The specimens are deposited in the Instituto Nacional de Biodiversidad in Quito, the Natural History Museum in London, and Museum Koenig in Bonn. Observers noted that the flies flew very low, close to the ground, with an erratic, zig-zag-like flight quite unlike the typical flight of most hoverflies, which may partly explain why the species had escaped detection for so long.</p>
<p>Morphologically, Ubristes mirabilissimus is a medium-sized to large hoverfly, measuring 12 to 14 millimetres in body length. Species of Ubristes are diagnosed by a scutellum without calcars and long, brush-like pilosity on the metatibia and metabasitarsomere, with hairs longer than the width of the tibia. Among the genera sharing this hind-leg pilosity, Ubristes alone bears a pair of lateral tubercles on the second abdominal segment at approximately half its length. The male genitalia are unique among all Microdontinae because of well-delimited, oval pits on both sides of the epandrium, structures named lateral fenestrae. These features, together with detailed differences in the cercus and surstylus, allowed the authors to separate the new species from its four known relatives.</p>
<p>What truly sets the new species apart, however, is its wing venation. In all previously described Ubristes species, the wing vein R4+5 carries a posterior appendix, a spur or additional vein extending into cell r4+5, a character also found in many other microdontine genera. In Ubristes mirabilissimus this appendix is entirely absent. As a consequence, the species would probably key out to the genus Hypselosyrphus in existing identification keys, since all Ubristes species differ from Hypselosyrphus and every other microdontine genus only by the presence of the lateral tubercles on tergite 2. The absence of the vein appendix, combined with the elongated abdomen, which is approximately 1.5 times as long as the head and thorax together, and the larger body size distinguishes the new species most notably from its closest relative, the black-bodied Ubristes flavitibia.</p>
<p>To document the species in full, the team applied a combination of classical and modern techniques. Male genitalia were dissected after softening the specimens in a wet chamber for 24 hours, then macerated in lactic acid at room temperature for another day before rinsing and storage in microvials with glycerine. Measurements were taken with an ocular micrometer in a stereo microscope, and high-quality images were produced through a Zeiss Stereo Discovery v12 microscope and processed by focus stacking with Axiovision software. A distribution map of all Ubristes species was drawn in Adobe Illustrator based on published locality information, with symbols placed by approximation because locality data for these rare flies is often imprecise.</p>
<p>The molecular component of the study marks a genuine milestone. One leg of each sequenced specimen was used for DNA extraction following established barcoding protocols, and the remnants were preserved and labelled as DNA voucher specimens. All new sequences were submitted to GenBank via the Barcode of Life Data System. The holotype and paratype males were successfully sequenced, and the resulting DNA barcodes are identical, constituting the first molecular data ever obtained for the genus Ubristes. A quick comparison against other sequences using BLAST showed that the new species&#8217; barcodes share less than 85 percent similarity with other microdontine genera, underscoring how genetically distinct this lineage is and how much of the group&#8217;s diversity remains unsampled.</p>
<p>The known distribution of Ubristes mirabilissimus is confined to two localities in Napo Province, in the Amazonian part of Ecuador, approximately 35 kilometres apart. Both sites lie within lowland tropical rainforest, consistent with the ecology of the other Ubristes species, which appear to be rainforest inhabitants. The number of known localities per species across the entire genus is very low, two at maximum, so the true distribution patterns are undoubtedly very incomplete. Ecuador is now the second country from which two Ubristes species are recorded, as Ubristes ictericus was previously described from the same country.</p>
<p>Rarity or easy overcollection seems to be the norm for tropical Microdontinae. Besides the four specimens of the new species, only about ten Ubristes specimens are known to science in total: five of U. flavitibia, three of U. ictericus, one of U. jaguarinus, and one of U. rex. The authors suggest several possible explanations. Unlike most other hoverflies, for which visiting flowers is a characteristic habit, microdontines are rarely observed at flowers, so they escape the standard survey methods. Another possibility is an association with rare species of ants, or with ants that build their nests in forest canopies, keeping the adult flies out of reach. The larvae of Ubristes remain entirely unknown, although microdontine larvae are generally associated with ants.</p>
<p>The female of Ubristes mirabilissimus is unknown, and so is the male of Ubristes rex, raising the theoretical possibility that these two taxa could belong to the same species. The authors reject this on the basis of clear differences in wing venation, the absence versus presence of the spur on vein R4+5, and body colouration. For those Ubristes species where both sexes are known, namely U. flavitibia and U. ictericus, only minor differences in colour and morphology exist between males and females, so a similarly low degree of sexual dimorphism is expected in the two incompletely known species. With an identification key now provided for all five known Ubristes species, together with the first molecular data for the genus, the stage is set for future work to uncover more of the hidden diversity of these remarkable bee mimics in the Neotropical rainforest.</p>
<p><strong>Subject of Research:</strong> Taxonomy and molecular characterization of a new stingless bee mimicking hoverfly species from the Ecuadorian Amazon</p>
<p><strong>Article Title:</strong> Ubristes mirabilissimus sp. nov., a new stingless bee mimicking hoverfly from the Ecuadorian Amazon ( Diptera , Syrphidae , Microdontinae )</p>
<p><strong>Article References:</strong> Reemer, M., &amp; Mengual, X. (2026). Ubristes mirabilissimus sp. nov., a new stingless bee mimicking hoverfly from the Ecuadorian Amazon (Diptera, Syrphidae, Microdontinae). <em>Evolutionary Systematics, 10</em>(1), 47-54. <a href="https://doi.org/10.3897/evolsyst.10.185722" rel="noopener noreferrer">https://doi.org/10.3897/evolsyst.10.185722</a></p>
<p><strong>Image Credits:</strong> AI Generated</p>
<p><strong>DOI:</strong> <a href="https://doi.org/10.3897/evolsyst.10.185722" rel="noopener noreferrer">10.3897/evolsyst.10.185722</a></p>
<p><strong>Keywords:</strong> hoverflies, Syrphidae, Microdontinae, Ubristes, new species, Ecuador, Amazon rainforest, mimicry, DNA barcoding, taxonomy, mirabilissimus, stingless</p>
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		<post-id xmlns="com-wordpress:feed-additions:1">295054</post-id>	</item>
		<item>
		<title>Hidden Japanese Hoverfly Revealed as New Species After 150 Years of Mistaken Identity</title>
		<link>https://scienmag.com/hidden-japanese-hoverfly-revealed-as-new-species-after-150-years-of-mistaken-identity/</link>
		
		<dc:creator><![CDATA[Gavin Prescott]]></dc:creator>
		<pubDate>Fri, 16 Oct 2026 18:32:10 +0000</pubDate>
				<category><![CDATA[Biology]]></category>
		<category><![CDATA[Science News]]></category>
		<category><![CDATA[DNA barcoding]]></category>
		<category><![CDATA[DNA barcoding in entomology]]></category>
		<category><![CDATA[European and Asian hoverfly species]]></category>
		<category><![CDATA[Evolutionary Systematics]]></category>
		<category><![CDATA[Ferdinandea]]></category>
		<category><![CDATA[Ferdinandea cuprea]]></category>
		<category><![CDATA[Ferdinandea harusawai]]></category>
		<category><![CDATA[forest ecosystem pollinators]]></category>
		<category><![CDATA[hoverflies]]></category>
		<category><![CDATA[hoverfly taxonomy revision]]></category>
		<category><![CDATA[insect species misidentification]]></category>
		<category><![CDATA[Japan]]></category>
		<category><![CDATA[Japanese hoverfly]]></category>
		<category><![CDATA[lectotype]]></category>
		<category><![CDATA[long-term insect taxonomy correction]]></category>
		<category><![CDATA[new species]]></category>
		<category><![CDATA[new species discovery]]></category>
		<category><![CDATA[novel insect species discovery]]></category>
		<category><![CDATA[Palaearctic]]></category>
		<category><![CDATA[Palaearctic hoverfly species]]></category>
		<category><![CDATA[saproxylic larvae habitat]]></category>
		<category><![CDATA[Syrphidae]]></category>
		<category><![CDATA[Syrphidae family identification]]></category>
		<category><![CDATA[taxonomy]]></category>
		<guid isPermaLink="false">https://scienmag.com/?p=288238</guid>

					<description><![CDATA[An integrative taxonomic revision of the hoverfly genus Ferdinandea in the Palaearctic Realm describes a new Japanese species and synonymizes the long-misapplied name Ferdinandea nigrifrons with Ferdinandea cuprea.]]></description>
										<content:encoded><![CDATA[<p>A coppery gleam in the forests of Japan has finally been given a name of its own. A new study revising the hoverfly genus Ferdinandea across the Palaearctic Realm describes Ferdinandea harusawai, a species new to science that had spent decades hiding in plain sight under a borrowed European name. The work, published in the journal Evolutionary Systematics, combines classical morphology with DNA barcoding to untangle a taxonomic knot that has confused entomologists on two continents for more than a century and a half.</p>
<p>Ferdinandea is a genus of medium-sized hoverflies in the family Syrphidae, instantly recognizable to specialists by the strong black bristles on the thorax, the powdery pruinose stripes running along the scutum, dark markings on the wings, and a black abdomen that in some species shimmers with a metallic, copper-coloured iridescence. The adults patrol forest edges, particularly deciduous woods with over-mature trees, and are sometimes seen visiting orchids. Their larvae are saproxylic, living in sap runs on trees where they filter bacteria, making the genus a quiet but genuine component of forest nutrient cycling. Seventeen species were previously known worldwide, distributed across the Holarctic and Indomalayan Realms but absent from the Americas, Australasia and Africa.</p>
<p>The heart of the confusion lies with a name coined in Vienna. In 1861, the Austrian dipterist Johann Nepomuk Georg Egger described Chrysochlamys nigrifrons from material collected around his home city. For generations afterwards, hoverflies in the eastern Palaearctic bearing a dark abdomen and dark wing tips were labelled Ferdinandea nigrifrons, including specimens recorded from South Korea, northern China&#8217;s Gansu Province, Sichuan, and throughout Japan, where the name entered the literature as early as the work of Shiraki in 1968. Meanwhile, some European authors had already suspected that nigrifrons was nothing more than a dark variant of the widespread copper-backed species Ferdinandea cuprea, described all the way back by Scopoli in 1763, but nobody had ever formally checked Egger&#8217;s type specimens.</p>
<p>The research team did exactly that. Digging into the Naturhistorisches Museum Wien, they located specimens identified by Egger himself in his private collection, acquired by the museum after his death in 1866, along with additional material from the museum&#8217;s historic Old Collection. One male from Egger&#8217;s own collection was designated as the lectotype, a specimen that permanently anchors the meaning of the name nigrifrons for future taxonomists. The verdict was unambiguous: every Egger-identified specimen belonged to Ferdinandea cuprea. The name nigrifrons, which had cast a long shadow over Asian hoverfly taxonomy, was formally synonymized with cuprea, erasing a 150-year-old misidentification at its source.</p>
<p>That left the Asian insects formerly called nigrifrons without any valid name, and the Japanese material turned out to represent something genuinely undescribed. The new species, Ferdinandea harusawai, is distinguished from its closest relatives by a suite of concrete characters. Its wings show dark infuscation along the margin at the tips of cells r2+3 and r4+5, whereas the wings of its relatives are clear. The second abdominal tergum carries black hairs on its posterior half, where the similar Ferdinandea ruficornis usually bears only pale yellow pile, and the black hairs on the third tergum lie flat and recumbent rather than standing erect. The middle third of its scutum carries black pile exclusively, and the front protibia and first tarsal segment are black rather than yellow.</p>
<p>Male genitalia provided the decisive confirmation. In hoverflies, the shape of the distiphallus, the terminal structure of the male reproductive apparatus, is often species-specific, and in Ferdinandea it reliably separates every Palaearctic species. In the new species, the distal lobes of the distiphallus are longer than the basal lobes, forming an L-shaped profile in lateral view and converging into a V-shape when seen from below, a configuration distinct from the C-shaped, O-shaped and U-shaped architectures found in its congeners. Specimens were prepared by macerating dissected genitalia in potassium hydroxide solution, then drawing and photographing them under compound and focus-stacking setups to document every diagnostic detail.</p>
<p>DNA barcodes added a molecular dimension to the case. The team compiled mitochondrial cytochrome c oxidase subunit I sequences, the standard 658-base-pair animal barcode, for seven of the eight Palaearctic species, building a Neighbour-Joining tree with bootstrap support from a thousand replicates. All twelve barcodes of the new species clustered together with very high support at 99.8 percent, and the species grouped with Ferdinandea ruficornis in a well-supported larger cluster. Notably, ruficornis itself showed weak internal resolution at only 57.1 percent, hinting at a genetically diverse but morphologically coherent species spanning two continents. For some other pairs, such as Ferdinandea luteola and the resurrected Ferdinandea suzukii, barcodes clustered together without a clear barcoding gap, a reminder that DNA barcoding alone cannot always deliver species identifications and must be weighed alongside morphology.</p>
<p>The species name honours Keitaro Harusawa, a Japanese entomologist who died in 2024 and was a founding member of the Dipterist&#8217;s Club of Japan, the country&#8217;s only amateur research group devoted to flies, where he served for many years on the board. The holotype, a male collected in April 2024 on Mount Nantai-san in Ibaraki Prefecture at 654 metres elevation, is deposited at the Museum Koenig in Bonn, Germany, alongside dozens of paratypes spanning Hokkaido to Kyushu, including specimens caught in malaise traps in Nagano&#8217;s Sugadaira forests and individuals collected as far back as 1953 that had languished in museum drawers mislabelled as nigrifrons.</p>
<p>With the revision complete, the Palaearctic fauna now includes eight Ferdinandea species, and a striking biogeographic pattern emerges. Ferdinandea aurea, cuprea and fumipennis are confined to the western Palaearctic, while suzukii, luteola and the new harusawai are exclusive to the east. Only Ferdinandea ruficornis straddles both sides of the realm, showing a remarkable colour polymorphism: copper-bodied, yellow-pilose individuals in central and southern Europe versus shiny black, blue-tinged individuals with dark abdominal patches in northern Europe and eastern Asia. The authors argue these are one species, unified by their shared genital morphology despite their divergent appearance, a textbook example of why colour alone is a treacherous guide in fly taxonomy.</p>
<p>Large gaps remain on the map. Between the Ural Mountains and longitude 122 degrees east, only a handful of unidentified Ferdinandea records exist in public databases, and Ferdinandea volkovae, described from Tajikistan in 2022, is still known from a single male holotype for which no DNA barcode exists. The authors suspect that Chinese records of cuprea actually represent suzukii, based on barcode matches and published genitalia drawings, and they call for intensified fieldwork across the central Palaearctic to resolve which species truly live there. Their broader message resonates far beyond one genus: European type material and eastern Asian lookalikes bearing the same name deserve systematic re-examination, because, as this study demonstrates, a name applied faithfully for 150 years can conceal an entirely unknown species waiting in the drawers.</p>
<p><strong>Subject of Research:</strong> Taxonomic revision of the Palaearctic hoverfly genus Ferdinandea, including DNA barcoding and the description of a new species from Japan</p>
<p><strong>Article Title:</strong> The genus Ferdinandea Rondani, 1844 ( Diptera , Syrphidae ) in the Palaearctic Realm, with description of a new species from Japan</p>
<p><strong>Article References:</strong> Mengual, X., &amp; Ichige, K. (2026). The genus Ferdinandea Rondani, 1844 (Diptera, Syrphidae) in the Palaearctic Realm, with description of a new species from Japan. <em>Evolutionary Systematics, 10</em>(2), 383-402. <a href="https://doi.org/10.3897/evolsyst.10.210478" rel="noopener noreferrer">https://doi.org/10.3897/evolsyst.10.210478</a></p>
<p><strong>Image Credits:</strong> AI Generated</p>
<p><strong>DOI:</strong> <a href="https://doi.org/10.3897/evolsyst.10.210478" rel="noopener noreferrer">10.3897/evolsyst.10.210478</a></p>
<p><strong>Keywords:</strong> Ferdinandea, Syrphidae, hoverflies, taxonomy, new species, Japan, DNA barcoding, Palaearctic, lectotype, Ferdinandea cuprea, Ferdinandea harusawai, Evolutionary Systematics</p>
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		<post-id xmlns="com-wordpress:feed-additions:1">288238</post-id>	</item>
		<item>
		<title>Invasive goldenrod reshuffles pollinator communities in suburban landscapes, study finds</title>
		<link>https://scienmag.com/invasive-goldenrod-reshuffles-pollinator-communities-in-suburban-landscapes-study-finds/</link>
		
		<dc:creator><![CDATA[Julie Wynn]]></dc:creator>
		<pubDate>Fri, 16 Oct 2026 04:55:37 +0000</pubDate>
				<category><![CDATA[Science News]]></category>
		<category><![CDATA[biodiversity]]></category>
		<category><![CDATA[butterflies]]></category>
		<category><![CDATA[community composition]]></category>
		<category><![CDATA[ecological consequences of invasive goldenrod in Europe]]></category>
		<category><![CDATA[effects of invasive species on pollinator diversity]]></category>
		<category><![CDATA[effects of Solidago canadensis invasion on native and honey bee populations]]></category>
		<category><![CDATA[goldenrod's role in reshaping pollination networks]]></category>
		<category><![CDATA[honey bees]]></category>
		<category><![CDATA[hoverflies]]></category>
		<category><![CDATA[impact of invasive plants on native wild bees and butterflies]]></category>
		<category><![CDATA[Invasive goldenrod impact on pollinator communities]]></category>
		<category><![CDATA[invasive plant dispersal and reproductive strategies]]></category>
		<category><![CDATA[Invasive Species]]></category>
		<category><![CDATA[NeoBiota]]></category>
		<category><![CDATA[plant-pollinator interactions in invaded habitats]]></category>
		<category><![CDATA[Poland]]></category>
		<category><![CDATA[pollinator community restructuring by invasive species]]></category>
		<category><![CDATA[pollinators]]></category>
		<category><![CDATA[Solidago canadensis]]></category>
		<category><![CDATA[suburban habitat changes due to invasive plants]]></category>
		<category><![CDATA[suburban landscape invasive]]></category>
		<category><![CDATA[Urbanization]]></category>
		<category><![CDATA[wild bees]]></category>
		<guid isPermaLink="false">https://scienmag.com/?p=281838</guid>

					<description><![CDATA[A two-year Polish field study shows flowering Canadian goldenrod attracts honey bees and hoverflies while reducing wild bee and butterfly visitation, reshaping pollinator communities before full landscape invasion.]]></description>
										<content:encoded><![CDATA[<p>A late-summer spectacle familiar across Central Europe — dense stands of Canadian goldenrod glowing yellow at the field edge — is doing more than feeding hungry honey bees. New research published in the journal NeoBiota shows that when the invasive Solidago canadensis reaches local dominance in suburban habitats, it visibly reorganizes which pollinators show up at flowers, boosting honey bees and hoverflies while thinning out wild bees and butterflies. Crucially, the study captured this shift at an intermediate stage of invasion, before the goldenrod had swallowed the entire landscape mosaic.</p>
<p>Canadian goldenrod arrived in Europe in the seventeenth century as an ornamental garden plant and has since spread from Spain to Scandinavia and from northern Italy deep into Eastern Europe. It is now regarded as one of the continent&#8217;s most aggressive invasive plants. The species thrives in human-altered habitats, forming extensive, dense stands that displace native flora through rapid growth, vast numbers of light wind-dispersed seeds, easy vegetative reproduction, tolerance of a wide range of conditions, and the absence of natural enemies outside its native range. Allelopathic chemicals that suppress neighboring plants may add to its competitive arsenal.</p>
<p>For pollinators, goldenrod presents a paradox. On one hand, its mass flowering late in the season delivers a flood of nectar and pollen at a time when most other blooms have faded, potentially extending the foraging window for honey bee colonies preparing for winter. On the other hand, invasive plants can disrupt plant-pollinator mutualisms and simplify plant communities, narrowing the dietary options available to insects that depend on complementary resources across their life cycles. Whether goldenrod acts as a seasonal lifeline or an ecological trap depends heavily on which pollinators are considered — a question the new study set out to answer directly.</p>
<p>Researchers working in the metropolitan area of Poznań in western Poland selected twenty sites of ruderal vegetation, each dominated or co-dominated by goldenrod, with cover ranging from thirty percent to nearly complete. Within 200 meters of each goldenrod stand, they established a paired control plot of diverse non-goldenrod vegetation, so that both plots sat inside the same suburban landscape already containing the invader. This design defines what the authors call an intermediate stage of invasion: goldenrod dominates focal patches, but heterogeneous co-flowering vegetation persists nearby. Across two flowering seasons in August and September, the team netted pollinators for twenty minutes per plot per visit, sampling each site three times per season under standardized warm, sunny conditions.</p>
<p>The haul was substantial: 1,245 pollinators representing 63 species across wild bees, butterflies, and hoverflies. Honey bees dominated numerically, accounting for 66 percent of all individuals, with 577 recorded in goldenrod plots versus 254 in controls. The white butterfly Pieris rapae and the drone fly Eristalis tenax followed far behind. Among wild bees, the red-tailed bumblebee Bombus lapidarius, the common carder bee Bombus pascuorum, and the mining bee Colletes similis led the counts. Notably, the survey also documented six taxa from the Polish Red List, including the vulnerable bumblebee Bombus veteranus, and Halictus scabiosae, a species first recorded in Poland only shortly before the study began.</p>
<p>Statistical analysis revealed a clear compositional divide. Non-metric multidimensional scaling of community data separated goldenrod plots from control plots, a result confirmed by permutational analysis of variance that attributed roughly nineteen percent of compositional variation to plot type. Twenty-six species appeared in both plot types, but nineteen were recorded only in goldenrod stands and eighteen only in the diverse control vegetation. The goldenrod-only species included several small ground-nesting sweat bees of the genus Lasioglossum and their cleptoparasites in the genus Sphecodes, while control plots hosted a few Asteraceae specialists such as the mason bee Osmia spinulosa and the plasterer bee Colletes daviesanus.</p>
<p>The group-specific responses were striking. Honey bee abundance rose sharply in goldenrod plots and increased further with the proportion of goldenrod cover at each site, consistent with a resource-concentration effect comparable to the way honey bees exploit mass-flowering crops. Hoverflies also became more abundant in goldenrod stands, echoing earlier European studies, likely reflecting their flexible adult foraging and larval independence from living plants. Wild bees, by contrast, were significantly less abundant in goldenrod plots even though their species richness and Shannon diversity remained statistically unchanged — a pattern suggesting reduced patch use rather than outright local extinction. Butterflies fared worst, with both abundance and species richness significantly lower in goldenrod-dominated vegetation, plausibly because dense near-monospecific stands lack the larval host plants and structural heterogeneity butterflies need across life stages.</p>
<p>Perhaps the most intriguing finding was a reversal in the relationship between honey bees and wild bees depending on habitat context. In control plots, honey bee abundance and wild bee metrics rose together; in goldenrod plots, the association turned negative. This context-dependent co-occurrence suggests that flowering goldenrod alters local patterns of pollinator interaction around concentrated floral resources, although the authors caution that observational data cannot distinguish direct competition from differential attraction to contrasting patch types. Urbanization, measured as impervious surface area within 250 meters using Copernicus satellite data, showed no consistent main effects, and site-level goldenrod cover predicted only honey bee abundance, not the metrics of any wild group.</p>
<p>The authors frame these results as evidence of community reassembly rather than uniform decline. Goldenrod dominance redistributes pollinator activity among floral patches, concentrating managed and generalist visitors while underrepresenting guilds with more specialized requirements. Because sampling captured only the late-season flowering pulse, the study cannot assess whether goldenrod&#8217;s displacement of diverse earlier-season blooms creates net forage imbalances across the full beekeeping season — a concern raised by prior laboratory work showing reduced bee survival on goldenrod-dominant honey diets. The findings also stop short of demonstrating population-level consequences, since flower-visitation data reflect local activity rather than demographic performance.</p>
<p>For conservation, the message is practical. Retaining and restoring floristically diverse late-season vegetation within suburban mosaics may prevent the biotic homogenization that could follow if goldenrod progressively replaces heterogeneous plant communities. Because the invader can continue expanding if unmanaged, the window in which contrasting floral patches coexist — the very intermediate stage this study documented — may be the most valuable moment for intervention, sustaining pollinator diversity before landscape saturation locks in a simplified late-summer flora.</p>
<p><strong>Subject of Research:</strong> Effects of invasive Canadian goldenrod flowering on pollinator community composition in suburban landscapes</p>
<p><strong>Article Title:</strong> Flowering Solidago canadensis restructures pollinator patch use and assemblage composition at an intermediate stage of invasion in urbanizing landscapes</p>
<p><strong>Article References:</strong> Banaszak-Cibicka, W., Stanisławska, I., Dylewski, Ł., Białas, J. T., &amp; Langowska, A. (2026). Flowering Solidago canadensis restructures pollinator patch use and assemblage composition at an intermediate stage of invasion in urbanizing landscapes. <em>NeoBiota, 109</em>, 85-105. <a href="https://doi.org/10.3897/neobiota.109.191683" rel="noopener noreferrer">https://doi.org/10.3897/neobiota.109.191683</a></p>
<p><strong>Image Credits:</strong> AI Generated</p>
<p><strong>DOI:</strong> <a href="https://doi.org/10.3897/neobiota.109.191683" rel="noopener noreferrer">10.3897/neobiota.109.191683</a></p>
<p><strong>Keywords:</strong> invasive species, Solidago canadensis, pollinators, wild bees, honey bees, butterflies, hoverflies, urbanization, biodiversity, community composition, NeoBiota, Poland</p>
]]></content:encoded>
					
		
		
		<post-id xmlns="com-wordpress:feed-additions:1">281838</post-id>	</item>
		<item>
		<title>Virtual Hoverflies: New Agent-Based Model Puts a Two-Species Ecosystem Warrior on the Map</title>
		<link>https://scienmag.com/virtual-hoverflies-new-agent-based-model-puts-a-two-species-ecosystem-warrior-on-the-map/</link>
		
		<dc:creator><![CDATA[Gavin Prescott]]></dc:creator>
		<pubDate>Thu, 15 Oct 2026 19:02:35 +0000</pubDate>
				<category><![CDATA[Earth Science]]></category>
		<category><![CDATA[Science News]]></category>
		<category><![CDATA[agent-based model]]></category>
		<category><![CDATA[agrochemical impact assessment]]></category>
		<category><![CDATA[ALMaSS]]></category>
		<category><![CDATA[ALMaSS simulation framework]]></category>
		<category><![CDATA[aphid control biological agents]]></category>
		<category><![CDATA[aphids]]></category>
		<category><![CDATA[biological control]]></category>
		<category><![CDATA[European hoverfly species]]></category>
		<category><![CDATA[habitat and weather effects on insect populations]]></category>
		<category><![CDATA[hoverflies]]></category>
		<category><![CDATA[Hoverfly ecosystem modeling]]></category>
		<category><![CDATA[insect life cycle modeling]]></category>
		<category><![CDATA[insect pollinators in agriculture]]></category>
		<category><![CDATA[landscape ecology]]></category>
		<category><![CDATA[landscape-scale ecological modeling]]></category>
		<category><![CDATA[overwintering]]></category>
		<category><![CDATA[parasitoids]]></category>
		<category><![CDATA[pesticide exposure risk analysis]]></category>
		<category><![CDATA[pesticide risk assessment]]></category>
		<category><![CDATA[pollination]]></category>
		<category><![CDATA[pollination services in farmland]]></category>
		<category><![CDATA[species-specific population simulation]]></category>
		<category><![CDATA[Sphaerophoria scripta]]></category>
		<category><![CDATA[thermal development]]></category>
		<guid isPermaLink="false">https://scienmag.com/?p=277046</guid>

					<description><![CDATA[Scientists have built a detailed agent-based model of the marmalade hoverfly Sphaerophoria scripta within the ALMaSS landscape simulator, aiming to predict how pollination and aphid-control services respond to weather, farming and pesticides.]]></description>
										<content:encoded><![CDATA[<p>It is one of the unsung heroes of the European countryside: a slender, wasp-mimicking fly that spends its adult days sipping nectar from daisies and thistles, pollinating crops and wildflowers as it goes, and its larval days devouring aphids by the hundreds. Now scientists have taken a major step toward capturing that entire double life inside a computer. A team modelling the hoverfly Sphaerophoria scripta has published a formal, individual-based model designed to run within the Animal, Landscape and Man Simulation System (ALMaSS), a simulation framework that reconstructs agricultural landscapes at a resolution of just one square metre. The goal is ambitious: to predict how hoverfly populations respond to weather, landscape change and, crucially, pesticide exposure, with the model ultimately feeding into regulatory risk assessments for agrochemicals.</p>
<p>The choice of species is no accident. Sphaerophoria scripta is among the most common aphid-eating hoverflies in Central Europe, active from May to October with peaks in August, and found everywhere from open grasslands and flower-rich urban wastelands to the edges of farm fields. Adults are mixed feeders, spending roughly two-thirds of their daylight hours feeding on nectar and pollen, which makes them effective pollinators of crops and wild plants alike. Their larvae, meanwhile, are voracious generalist predators that attack more than thirty genera of aphids, including notorious crop pests such as the peach–potato aphid Myzus persicae, as well as thrips, spider mites and even caterpillars. Few other insects deliver pollination and biological pest control in a single package.</p>
<p>What sets the new model apart from earlier attempts is its level of spatial and ecological detail. Previous individual-based hoverfly models either simplified the landscape into just fields and margins, or focused narrowly on a single life stage such as overwintering females. The prototype Sphaerophoria model instead embeds every individual — egg, larva, pupa and adult female — within ALMaSS&#8217;s dynamic, one-metre-resolution landscape, complete with realistic crop rotations, pesticide application schedules, daily vegetation growth and simulated weather. Aphid prey can be supplied either by a parallel, already-published aphid model that simulates four pest species, allowing predator and prey to interact within the same simulated world. A companion model for the saprophagous drone fly Eristalis tenax is also under development, broadening coverage of the hoverfly guild&#8217;s functional diversity.</p>
<p>Temperature emerges as the master variable of hoverfly development. Drawing on decades of laboratory and field studies, the authors fitted thermal response curves for each immature stage. Eggs and pupae follow simple linear degree-day models: eggs need about 55.6 degree-days above a threshold of roughly 6 degrees Celsius, meaning development takes around twelve days at 10 degrees but barely two and a half days at 30. Pupae require about 146 degree-days, with emergence ceasing at or below 10 degrees. Larval development is trickier: it peaks at an intermediate optimum of about 20.6 degrees and falls off at both extremes, so the modellers used a Gaussian thermal performance curve rather than a straight line. Food complicates the picture further, because larval development slows measurably as aphid availability drops — a relationship the team captured with a scaling factor derived from experiments in which larvae developed in roughly fifteen days when offered just five aphids a day, but in under ten when given sixty.</p>
<p>Those feeding numbers matter because a hoverfly larva is essentially a small eating machine with a life-or-death deadline. Laboratory work shows that Sphaerophoria larvae consume on the order of 130 to 365 aphids in total during development, depending on aphid species, and that consumption rises steeply through mid-development before tapering just before pupation. First-instar larvae are the most fragile: the model assumes they die after a single day without food, while older larvae can survive two and three days of starvation respectively, assumptions borrowed from closely related species of similar size. The larvae also show a classic Holling Type II functional response — consumption rises quickly at low aphid densities then saturates as handling time becomes the bottleneck — with third instars out-eating second instars, and with an opportunistic streak that even extends to cannibalism when food runs short.</p>
<p>Adult females face their own energetic arithmetic, and the model reconstructs it with striking granularity. Since direct measurements of Sphaerophoria scripta energetics are scarce, the team used allometric scaling from better-studied relatives: estimated body masses between roughly 6.6 and 33 milligrams yielded predicted flight energy costs of about 0.001 to 0.004 watts, a gut capacity of one to three and a half microlitres of nectar, and a maximum starvation endurance of around five to six days. The energetic budget implies a female must refill her gut about twice a day on 50 percent sugar nectar just to keep going. Flight speeds are similarly scaled, with maximum dashes estimated near eight metres per second and typical foraging speeds of around one metre per second. Daily activity follows a thermally driven rhythm: flies stir only when temperatures pass roughly 16 degrees, peak in a 20-to-25-degree window, switch to a two-peaked pattern on hot days to avoid midday heat, and stop entirely in rain or strong wind.</p>
<p>Reproduction adds another layer of behavioural sophistication. Females cannot mature a single egg without pollen — sugar alone leaves them sterile and short-lived, with pollen-fed females surviving an average of 31 days versus nine and a half without. Under optimal greenhouse conditions, a female begins laying five to six days after emergence and produces 228 to 551 eggs over her lifetime, peaking about a third of the way through her oviposition period. The model encodes this as a fecundity function tied to female body mass, modulated by temperature and photoperiod, and gated by aphid availability: eggs are laid singly, and only where local aphid biomass exceeds a threshold calibrated so that hatching larvae will find enough prey. In a neat touch of behavioural realism, females in the model preferentially target dense, young aphid colonies, guided in reality by plant and aphid volatiles that the oviposition probability function abstracts into a logistic response.</p>
<p>Death, too, is modelled mechanistically. Immature mortality depends on temperature and humidity through polynomial functions fitted to data from the related species Sphaerophoria rueppellii, where dry conditions proved brutal — at 50 percent relative humidity, larval mortality hit 100 percent. Parasitoid wasps add a delayed, insidious threat: species such as Diplazon laetatorius lay eggs inside larvae, which keep feeding normally before dying at the pupal stage, sometimes wiping out 20 to 80 percent of hoverfly immatures in intensively managed crops. The model handles this with a two-step, landscape-modulated parasitism probability, and also simulates agricultural mortality, assigning probabilities that ploughing, harrowing and other soil-disturbing operations crush overwintering pupae, while mechanical weeding disturbs eggs and larvae on crop plants.</p>
<p>Overwintering and migration round out the life cycle. Sphaerophoria scripta survives winter mainly as fully grown larvae tucked into soil or leaf litter, entering a cold-induced quiescence that ends when spring days warm. The final autumn generation faces a fork: some females stay and produce the overwintering brood, while others — the model will eventually allow a probabilistic split — embark on the long migrations documented along mountain passes and coastlines, where females consistently dominate the migrant crowds, likely thanks to their larger fat reserves. For the first version aimed at pesticide risk assessment, the team deliberately sets migration to zero, keeping exposure effects local and interpretable.</p>
<p>The authors are candid about the gaps. Many parameters come from other Sphaerophoria species or allometric extrapolations, upper thermal limits could not be estimated from existing data, and several quantities — adult background mortality, overwintering survival, pollen intake rates — will be determined during calibration using pattern-oriented modelling against field observations. Yet even as a prototype, the framework represents a significant upgrade in how regulators and ecologists can interrogate the fate of a non-target beneficial insect: not as a static laboratory test species, but as a population of virtual individuals living out full lives across a simulated farm landscape, generation after generation, under whatever climate, crop and chemical futures we care to explore.</p>
<p><strong>Subject of Research:</strong> Agent-based modelling of the aphidophagous hoverfly Sphaerophoria scripta for pesticide risk assessment</p>
<p><strong>Article Title:</strong> The Formal Model for the hoverfly Sphaerophoria scripta ( Diptera , Syrphidae ) agent-based model in the Animal Landscape and Man Simulation System (ALMaSS)</p>
<p><strong>Article References:</strong> Ziółkowska, E., Sowa, G., Duan, X., &amp; Topping, C. J. (2026). The Formal Model for the hoverfly Sphaerophoria scripta (Diptera, Syrphidae) agent-based model in the Animal Landscape and Man Simulation System (ALMaSS). <em>Food and Ecological Systems Modelling Journal, 7</em>, Article e169793. <a href="https://doi.org/10.3897/fmj.7.169793" rel="noopener noreferrer">https://doi.org/10.3897/fmj.7.169793</a></p>
<p><strong>Image Credits:</strong> AI Generated</p>
<p><strong>DOI:</strong> <a href="https://doi.org/10.3897/fmj.7.169793" rel="noopener noreferrer">10.3897/fmj.7.169793</a></p>
<p><strong>Keywords:</strong> hoverflies, Sphaerophoria scripta, agent-based model, ALMaSS, biological control, pollination, pesticide risk assessment, aphids, thermal development, landscape ecology, overwintering, parasitoids</p>
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		<post-id xmlns="com-wordpress:feed-additions:1">277046</post-id>	</item>
		<item>
		<title>Honeybees bully wild rivals at flowers, two-year Cambridge study reveals</title>
		<link>https://scienmag.com/honeybees-bully-wild-rivals-at-flowers-two-year-cambridge-study-reveals/</link>
		
		<dc:creator><![CDATA[Julie Wynn]]></dc:creator>
		<pubDate>Wed, 14 Oct 2026 16:50:49 +0000</pubDate>
				<category><![CDATA[Athmospheric]]></category>
		<category><![CDATA[beekeeping]]></category>
		<category><![CDATA[behavioral observations of pollinator exclusion]]></category>
		<category><![CDATA[British countryside pollination dynamics]]></category>
		<category><![CDATA[bumblebees]]></category>
		<category><![CDATA[Cambridge]]></category>
		<category><![CDATA[climate change]]></category>
		<category><![CDATA[conservation of wild pollinators]]></category>
		<category><![CDATA[Ecological Entomology]]></category>
		<category><![CDATA[ecological impacts of managed honeybees]]></category>
		<category><![CDATA[ecological implications of honeybee dominance]]></category>
		<category><![CDATA[effects of honeybee management on wild insects]]></category>
		<category><![CDATA[floral resource competition]]></category>
		<category><![CDATA[heat stress]]></category>
		<category><![CDATA[Honeybee dominance in flower foraging]]></category>
		<category><![CDATA[honeybees]]></category>
		<category><![CDATA[hoverflies]]></category>
		<category><![CDATA[impact on bramble and ivy pollination]]></category>
		<category><![CDATA[interference competition]]></category>
		<category><![CDATA[ivy bee]]></category>
		<category><![CDATA[managed versus wild bee interactions]]></category>
		<category><![CDATA[nectar]]></category>
		<category><![CDATA[Pollination ecology]]></category>
		<category><![CDATA[wild pollinator competition]]></category>
		<category><![CDATA[wild pollinators]]></category>
		<guid isPermaLink="false">https://scienmag.com/?p=271539</guid>

					<description><![CDATA[A two-year Cambridge field study has documented how honeybees aggressively displace, chase and outcompete wild pollinators at shared flowers, with warming temperatures expected to intensify the conflict.]]></description>
										<content:encoded><![CDATA[<p>In the crowded world of flowers, the honeybee is not the gentle ambassador of spring that popular culture often imagines. A two-year field study conducted in and around Cambridge, England, has documented for the first time the full extent to which managed honeybees dominate shared foraging grounds, systematically excluding, displacing and even chasing away the wild insects that depend on the same nectar and pollen resources. The research, led by scientists at Anglia Ruskin University and published in the journal Ecological Entomology, provides some of the most detailed behavioural evidence yet that competition between managed and wild pollinators is not merely a theoretical concern but an observable, measurable and increasingly one-sided struggle playing out on bramble blossoms and ivy flowers across the British countryside.</p>
<p>The study focused on two plant species of exceptional importance to late-season pollinators: bramble (Rubus fruticosus) and ivy (Hedera helix). Both are prolific sources of nectar and pollen and both attract enormous numbers of flower-visiting insects when in bloom, making them natural arenas in which competitive dynamics can be observed at scale. The researchers selected five sites, all situated within 300 metres of known honeybee colonies, ensuring that honeybee presence at the flowers was substantial and consistent. Over 93 hours of direct observation spread across two years, the team recorded every instance in which one pollinator disrupted or prevented another from accessing a flower, categorising each encounter according to the species involved and its outcome.</p>
<p>The methodological framework was elegantly simple. Flower visitors were sorted into five categories: honeybees, bumblebees, solitary bees, hoverflies, and an &#8216;other&#8217; group that included butterflies, beetles and wasps. Each recorded interaction was scored either as a &#8216;win&#8217;, in which one insect gained access to a flower at the direct expense of another, or as a &#8216;share&#8217;, in which both insects fed without conflict. This binary scoring system allowed the researchers to quantify not just the frequency of competitive encounters but also which species consistently emerged victorious, and to correlate those outcomes with the local density of honeybees at each site.</p>
<p>The results were striking. Higher densities of honeybees were associated with both lower numbers of other pollinators and a greater frequency of competitive interactions, with honeybees claiming a disproportionately high share of &#8216;wins&#8217; in their encounters with other flower visitors. The effect was quantifiable in ways that carry real ecological weight. On bramble, a doubling of honeybee density was associated with a 14 per cent reduction in bumblebee abundance. On ivy, increases in honeybee numbers were linked to declines in solitary bees and hoverflies, two groups that include many species of conservation concern. These are correlational findings drawn from field observation, but their consistency across sites and plant species lends them considerable persuasive force.</p>
<p>What distinguishes this study from earlier work on pollinator competition is its behavioural granularity. Honeybees did not simply outcompete rivals by arriving earlier or in greater numbers; they actively instigated aggressive interactions, winning resources by physically displacing or chasing other insects away from flowers. Other pollinators appeared to recognise the threat: honeybees were actively avoided by their wild counterparts in 28 per cent of interactions on bramble and 36 per cent of interactions on ivy. In at least one in five of the honeybees&#8217; winning outcomes on both plant species, the victory involved physical displacement or pursuit. Crucially, the researchers recorded very few aggressive interactions that were not initiated by honeybees, underscoring the asymmetry of the conflict.</p>
<p>There was, however, one remarkable exception to honeybee dominance. The ivy bee, Colletes hederae, a solitary bee species that is itself a relatively recent arrival to Britain, having first been recorded there in 2001, was the only insect observed contesting encounters with honeybees and winning. Ivy bees were seen defending their food source by displacing and chasing honeybees, turning the usual hierarchy on its head. The study&#8217;s lead author, Victoria Buckle, a PhD student at Anglia Ruskin University, noted that this was the first time, to the researchers&#8217; knowledge, that such behaviours had been observed, and that ivy bees appear able to hold their own in direct confrontations with the otherwise dominant honeybee.</p>
<p>The findings arrive at a moment of rapid change in British beekeeping. The number of registered beekeepers in the United Kingdom has risen from approximately 19,000 in 2010 to 47,000 last year, a trajectory that implies a substantial and ongoing increase in managed honeybee hive density. Because honeybee colonies can contain tens of thousands of foragers, even modest increases in hive numbers translate into very large increases in the number of individual insects competing at local flowers. The Cambridge study suggests that this numerical advantage is compounded by a behavioural one: honeybees are not passive competitors but active aggressors that shape the foraging environment for every other species around them.</p>
<p>Climate change adds a further and potentially alarming layer to the picture. The researchers found that periods of higher temperature were associated with an increase in competitive interactions between flower visitors. One plausible mechanism lies in the physiology of the plants themselves: heat stress is known to cause flowers to produce less nectar, shrinking the total forage available and forcing pollinators into more frequent and more intense conflict over what remains. As UK summers warm, this mechanism could operate over ever wider areas and longer seasons, intensifying the very competition the study documents.</p>
<p>Temperature also acts directly on the insects, and here the asymmetry between species becomes starker. Low temperatures favour the foraging capacity of hoverflies and bumblebees, both of which are sensitive to heat, while the opposite holds for honeybees. A previous study cited by the researchers found that a 12°C increase in temperature led to a tenfold increase in the number of honeybees leaving their nests. In a warming climate, then, honeybees are likely to become more active foragers precisely when bumblebees and hoverflies are becoming less able to compete, a combination that the study&#8217;s authors warn is only likely to exacerbate interference competition from dominant honeybees under future predicted warming in the UK.</p>
<p>The research team is careful to frame the work not as an indictment of beekeeping but as a contribution to coexistence. Buckle emphasised that the aim of the study was not to discourage beekeeping but to better understand how competition unfolds between wild and managed pollinators, with the goal of helping to conserve wild species that play an essential ecological role in pollinating both crops and wild plants. The practical implications, however, are clear: in locations with high densities of hives, such as urban areas where hobbyist beekeeping has surged in popularity, the pressure on wild pollinators may be greatest. Finding ways to ensure that honeybees and wild pollinators can continue to share the landscape, whether through careful siting of hives, habitat restoration that increases total forage availability, or monitoring of wild pollinator populations near apiaries, will be a central challenge for pollinator conservation in the decades ahead. What this study makes unmistakably clear is that the flowers of Britain are contested ground, and that the contest is neither neutral nor gentle.</p>
<p><strong>Subject of Research:</strong> Interference competition between managed honeybees and wild pollinators on bramble and ivy flowers in the UK</p>
<p><strong>Article Title:</strong> Honeybees exert flower power over other species</p>
<p><strong>Article References:</strong> Honeybees exert flower power over other species. (n.d.). <a href="https://www.eurekalert.org/news-releases/1147684" rel="noopener noreferrer">Original publication</a></p>
<p><strong>Image Credits:</strong> AI Generated</p>
<p><strong>DOI:</strong> Not provided</p>
<p><strong>Keywords:</strong> honeybees, wild pollinators, bumblebees, hoverflies, ivy bee, interference competition, nectar, climate change, heat stress, beekeeping, Cambridge, Ecological Entomology</p>
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		<post-id xmlns="com-wordpress:feed-additions:1">271539</post-id>	</item>
		<item>
		<title>Himalayan Orchards Reveal a Hidden Pollinator Handover as Elevation Rises</title>
		<link>https://scienmag.com/himalayan-orchards-reveal-a-hidden-pollinator-handover-as-elevation-rises/</link>
		
		<dc:creator><![CDATA[Julie Wynn]]></dc:creator>
		<pubDate>Sat, 12 Sep 2026 11:47:08 +0000</pubDate>
				<category><![CDATA[Climate]]></category>
		<category><![CDATA[altitude-dependent pollinator succession]]></category>
		<category><![CDATA[apple orchards]]></category>
		<category><![CDATA[apricot]]></category>
		<category><![CDATA[bees]]></category>
		<category><![CDATA[bionomics]]></category>
		<category><![CDATA[Doda]]></category>
		<category><![CDATA[ecological handover in pollinator communities]]></category>
		<category><![CDATA[elevational gradient]]></category>
		<category><![CDATA[elevational gradient pollination]]></category>
		<category><![CDATA[high-altitude pollination ecology]]></category>
		<category><![CDATA[Himalayan orchard pollinators]]></category>
		<category><![CDATA[Himalayas]]></category>
		<category><![CDATA[honey bees versus sweat bees]]></category>
		<category><![CDATA[hoverflies]]></category>
		<category><![CDATA[hoverflies as pollinators]]></category>
		<category><![CDATA[impact of elevation on pollinator species]]></category>
		<category><![CDATA[insect pollinator community shift]]></category>
		<category><![CDATA[niche overlap]]></category>
		<category><![CDATA[orchard biodiversity and climate change]]></category>
		<category><![CDATA[plant-pollinator networks]]></category>
		<category><![CDATA[pollination services in Himalayan fruit crops]]></category>
		<category><![CDATA[pollinator conservation]]></category>
		<category><![CDATA[pollinator diversity in Jammu and Kashmir]]></category>
		<category><![CDATA[pollinators]]></category>
		<guid isPermaLink="false">https://scienmag.com/?p=193890</guid>

					<description><![CDATA[A new survey of Himalayan orchards finds that honey bees give way to sweat bees and hoverflies as elevation rises, reshaping the pollination networks that sustain apple and apricot crops in Doda, India.]]></description>
										<content:encoded><![CDATA[<p>High in the western Himalayas, the apple and apricot orchards of Doda district in Jammu and Kashmir sustain the livelihoods of roughly two-thirds of local households, and their fruit depends almost entirely on insects moving pollen between blossoms. A new study published in Discover Ecology has now mapped, for the first time, how the pollinator communities serving these crops change across a steep elevational gradient, and the results reveal a dramatic ecological handover: as altitude climbs, honey bees and other social bees retreat, while sweat bees and hoverflies step forward to carry the pollination load.</p>
<p>Researchers Rohit Rohit and Anjali Dhar of the Department of Zoology at Central University of Jammu surveyed six orchard sites spanning 1,073 to 2,302 meters above sea level during the 2025 blooming season. Using a combination of passive pan trapping with ultraviolet-bright blue, yellow, and white bowls and nearly one hundred hours of timed focal observations at flowering trees, they recorded 847 individual floral visitors belonging to 13 species across 10 families and 4 orders. The assemblage included six bee species, four species of hoverflies, and three butterflies, with the western honey bee Apis mellifera, the sweat bee Lasioglossum moroi, the Asiatic honey bee Apis cerana indica, and the drone fly Eristalis tenax together dominating the counts.</p>
<p>The most striking finding is the strength of the relationship between elevation and diversity. Shannon diversity declined in an almost perfectly linear fashion with altitude, with elevation explaining 91.3 percent of the variation in the diversity index. Total abundance fell by 71.8 percent across the gradient, from 238 individuals at the lowest site to just 67 at the highest, while species richness dropped from 13 to 5. The authors caution that elevation and temperature were nearly perfectly collinear in their dataset, with temperatures falling roughly 9.5 degrees Celsius over the 1,229-meter span, so the pattern reflects the composite elevational thermal environment rather than either factor alone. Temporal sampling waves, in which high sites were visited later in the season, add a further phenological confound that the team explicitly acknowledges.</p>
<p>Beneath the aggregate decline lies a pronounced taxonomic reshuffling. Social Apid bees, which made up 39.7 percent of visitors at low elevations, fell to 22.2 percent at high elevations, an absolute decline of 76 percent driven by losses of both honey bee species. Halictidae, represented solely by the sweat bee Lasioglossum moroi, nearly doubled their relative share, rising from 18.1 to 38.2 percent while maintaining near-stable absolute numbers. Hoverflies also held their proportional ground, and the authors attribute this resilience to multivoltine life cycles, larvae that develop in aquatic or aphid-rich habitats decoupled from orchard flowers, and the ability of several species to forage at temperatures as low as 8 to 10 degrees Celsius.</p>
<p>Life-history traits appear to explain much of this filtering. Perennial honey bee colonies demand continuous forage across a long season, conditions that collapse as elevation compresses the bloom window and thins floral diversity. In contrast, Lasioglossum moroi combines flexible sociality with ground nesting, which buffers nests against cold, and can shift to a single generation per year at altitude. Strictly solitary, univoltine bees such as Osmia cornuta and Anthophora confusa vanished from the highest site, consistent with their narrow thermal requirements for emergence. Habitat measurements reinforced the story: bare ground cover, essential nesting substrate for ground-nesting sweat bees, increased with elevation and correlated strongly with L. moroi abundance, while declining non-crop floral richness tracked the disappearance of solitary bees that need diverse forage during their brief adult lives.</p>
<p>At the single site where apple and apricot co-flowered under identical conditions, the team uncovered a clear division of labor. Apid bees accounted for 43.9 percent of apple visits but only 27.1 percent of apricot visits, with both honey bee species showing statistically significant preferences for apple. Hoverflies showed the mirror-image pattern, contributing 42.2 percent of apricot visits against 24.5 percent on apple, with the drone fly Eristalis tenax displaying the strongest crop preference of any species. The generalist sweat bee visited both crops in equal measure. The authors suggest that apple&#8217;s larger flowers and higher nectar sugar concentrations suit energy-hungry social bees, while apricot&#8217;s nectar volume and volatile profile may better attract olfactory-guided hoverflies, though direct floral trait measurements will be needed to confirm the mechanism.</p>
<p>Behavioral effectiveness scores, combining visit duration with the frequency of stigma contact, pointed to functional complementarity between the two pollinator groups. Honey bees achieved their highest scores on apple, where they contacted stigmas in 78 percent of visits compared with 62 percent on apricot, while all four hoverfly species scored higher on apricot, with E. tenax recording 16.8 versus 10.2 on apple. Overall mean scores were higher on apricot, driven by the extended visits of syrphid flies. The researchers stress these are visitation-based behavioral proxies rather than measured pollen deposition, and confirming actual pollination efficiency would require single-visit pollen assays. Even so, the pattern implies that keeping both crops in the landscape sustains two complementary pollinator guilds.</p>
<p>Network analysis added a structural dimension to the elevational story. High-elevation interaction networks, built from just 8 pollinator and 6 plant species, were more modular and more specialized than their low-elevation counterparts, with modularity rising from 0.38 to 0.46 and network-level specialization from 0.39 to 0.61. Niche overlap among species, measured with Pianka&#8217;s index, was significantly lower at high elevations, 0.31 versus 0.58, consistent with intensified resource partitioning when few species share scarce flowers. Within these simplified networks, Lasioglossum moroi emerged as the critical connector, showing the highest degree and species strength and the lowest specialization of any taxon, bridging network modules that would otherwise remain isolated. The authors warn that losing this single species could disproportionately fragment high-altitude pollination webs.</p>
<p>The conservation implications are elevation-specific rather than uniform. At low elevations, the authors recommend wildflower strips to sustain non-crop forage, careful timing of pesticide applications away from peak morning visitation hours, and preservation of dead wood and hollow stems for cavity-nesting solitary bees. At mid-elevations, maintaining a mosaic of both apple and apricot may support transition-zone communities that could serve as refugia under warming. At high elevations, where barely five or six pollinator species persist, priorities include minimizing soil disturbance to protect sweat bee nesting substrate, retaining water features and leaf litter for hoverfly larvae, and ensuring at least one wildflower species blooms throughout the compressed growing season. The strong elevation-diversity relationship also offers a quantitative baseline: repeated surveys at the same six sites could detect the upward range shifts and community disassembly expected as Himalayan winters warm and apple cultivation itself climbs ever higher in search of suitable chill.</p>
<p><strong>Subject of Research:</strong> Elevational changes in insect pollinator communities and their interactions with apple and apricot trees in Himalayan orchards</p>
<p><strong>Article Title:</strong> Bionomics of insect pollinators and their interaction with host trees in the orchards of Doda, Indian Himalayas</p>
<p><strong>Article References:</strong> Rohit, R., &amp; Dhar, A. (2026). Bionomics of insect pollinators and their interaction with host trees in the orchards of Doda, Indian Himalayas. <em>Discover Ecology, 2</em>(1), Article 24. <a href="https://doi.org/10.1007/s44396-026-00040-1" rel="noopener noreferrer">https://doi.org/10.1007/s44396-026-00040-1</a></p>
<p><strong>Image Credits:</strong> AI Generated</p>
<p><strong>DOI:</strong> <a href="https://doi.org/10.1007/s44396-026-00040-1" rel="noopener noreferrer">10.1007/s44396-026-00040-1</a></p>
<p><strong>Keywords:</strong> pollinators, Himalayas, apple orchards, apricot, elevational gradient, bees, hoverflies, plant-pollinator networks, niche overlap, pollinator conservation, Doda, bionomics</p>
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		<post-id xmlns="com-wordpress:feed-additions:1">193890</post-id>	</item>
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