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769 results for “scale insects”

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zenodo52/100

Data for: "Continental-scale patterns in diel flight timing of high-altitude migratory insects"

<p>This dataset contains the proportional migratory insect intensity and traffic data used in Haest&nbsp;<em>et al.</em> (2024) to quantify patterns in diel flight periodicity of migratory insects between 50-500m above ground level during March-October 2021 using a network of seventeen vertical-looking radars across Europe. Please see the Materials and Methods section in Haest <em>et al.</em> (2024) for more details on the dataset.&nbsp;</p>

opencc-by-4.0May 2024View details →
zenodo44/100

Data and code from: Insect biomass decline scaled to species diversity: General patterns derived from a hoverfly community

<p>To study changes in&nbsp;flying insect communities, and hoverflies in particular, malaise trap samples from a German site&nbsp;were compared between two years (Hallmann et al. 2020).&nbsp;The data files deposited here&nbsp;contain&nbsp;data obtained from six malaise traps in the Wahnbachtal (North Rhine-Westphalia, Germany, 50.851944N, 7.320833E) that were deployed in 1989 and again in 2014, at the exact same locations. Traps were situated in wet meadows as well as tall perennial meadows, in close proximity to shrub corridors, to forest&ndash;grassland borders, and to the Wahnbach River and surrounded by agricultural land, essentially a rather heterogeneous habitat. The Wahnbach River and the greater part of the valley&nbsp;are protected for watershed purposes and are subject to nature conservation management by the Wahnbach Talperrenverband. Hence, several restrictions apply to safeguard against water contamination.</p> <p>Total insect biomass collected with these traps was already included in Hallmann et al. (2017), but here we focus on additional information: the abundance and richness of hoverflies (Syrphidae) in each of the collected samples (pots). Methodologies of collection are described in Sorg (1990), Schwan et al. (1993), Sorg et al. (2013), Hallmann et al. (2017), and Ssymank et al. (2018). &nbsp;In brief, malaise traps were deployed throughout the growing season and operated continuously (day and night). Malaise trap construction (e.g., size, material, colouring, and ground sealing) and placing (e.g., positioning, orientation, and slope of the locations) were standardised in all aspects. Insect samples were preserved in 80% ethanol solution. Catches of the six&nbsp;traps investigated in the present study were emptied regularly: On average exposure intervals were 7.0 d (SD = 0.5) in 1989 and 16.7 d (SD = 5.6) in 2014. Across the six traps in 2014 the total exposure time (in number of days) was 42% higher compared to 1989. All collected samples (n = 196) were used in the present analysis with in total 19,604 individual&nbsp;hoverflies counted, distributed over 162 species and 59 genera.</p> <p>To assess how environmental conditions have changed over the 25 year, several additional datasets were assembled. Climatic<br> data were obtained from 169 climatic stations and were used to interpolate daily weather variables to each trap location, using spatiotemporal kriging. These steps are described in detail in Hallmann et al. (2017).</p> <p>Our analysis (see R code)&nbsp;consists of three components. First, we&nbsp;considered total abundance, species richness, and species diversity, at two&nbsp;temporal scales: pooled per year, i.e., across the sampling season, and seasonally&nbsp;(i.e., per day), and we compared these metrics between 1989 and&nbsp;2014. Second, we examined how total flying biomass (i.e., the weight of all&nbsp;trapped insects, of which hoverflies are only a small proportion) related to&nbsp;total abundance as well as species richness of hoverflies. Third, we derived&nbsp;persistence probabilities and population growth rate trends per species, to&nbsp;examine interspecific variation in these parameters.</p> <p>Descriptions of the deposited files:</p> <p><strong>Groups.csv</strong><br> MF_NR&nbsp;= identifier of each of the six malaise trap locations<br> yrf&nbsp;= year of sampling<br> pot&nbsp;= sample identifier<br> dt = number of sampling days<br> from.dnr = day-of-the-year on which a pot was attached to a malaise trap<br> to.dnr = day-of-the-year on which a pot was collected from a malaise trap<br> mean.daynr = mean day-of-the-year of the sampling period<br> Nspec = number of different hoverfly species found in a pot<br> Nind = number of hoverfly individuals found in a pot</p> <p><strong>Counts.csv</strong><br> A matrix of counts of individual hoverflies per pot per species. The 196 rows represent the pots in the same order as in the file &#39;Groups.csv&#39;. The columns represent the 162 different hoverfly species found. The scientific species names are indicated in the column headers.</p> <p><strong>PairedData.csv</strong><br> pot =&nbsp;sample identifier<br> JAHR&nbsp;= year of sampling<br> MF_NR&nbsp;= identifier of each of the six malaise trap locations<br> dt = number of sampling days<br> from.dnr = day-of-the-year on which a pot was attached to a malaise trap<br> to.dnr = day-of-the-year on which a pot was collected from a malaise trap<br> NI&nbsp;= number of hoverfly individuals found in a potbiomass.daily<br> NSP&nbsp;= number of different hoverfly species found in a pot<br> biomass.daily = daily fresh weight [gram]&nbsp;of flying insects: total fresh weight in a&nbsp;pot&nbsp;divided by the number of sampling days.</p> <p><strong>ModelFrame.csv</strong><br> MF_NR&nbsp;= identifier of each of the six malaise trap locations<br> yrf = year of sampling<br> pot =&nbsp;sample identifier<br> dt = number of sampling days<br> from.dnr = day-of-the-year on which a pot was attached to a malaise trap<br> to.dnr = day-of-the-year on which a pot was collected from a malaise trap<br> mean.daynr = mean day-of-the-year of the sampling period<br> plot = identifier of each of the six malaise trap locations<br> date = date for which the weather variables are interpolated<br> daynr = day-of-the-year&nbsp;for which the weather variables are interpolated<br> altitude = altitude [m] of the malaise trap locations<br> year = year of sampling<br> temperature = interpolated temperature [degrees Celsius]<br> precipitation = interpolated precipitation [mm per day]<br> wind.speed = interpolated wind speed [m/s]</p> <p><strong>Data_Rcode.pdf</strong><br> This pdf&nbsp;provides the R-code behind the analysis of&nbsp;the Hoverfly data. Three datasets are provided along with this R-code document, namely &quot;Counts.csv&quot;,&nbsp;&quot;Groups.csv&quot;, &quot;PairedData.csv&quot; and &quot;ModelFrame.csv&quot;. Additionally, the BUGS-code &quot;&quot;syrphidModel.jag&quot;&nbsp;is required for running the daily-activity model in JAGS.</p> <p><strong>syrphidModel.jag</strong><br> This&nbsp;BUGS-code is required for running the daily-activity model in JAGS.</p>

opencc-by-4.0Nov 2020View details →
zenodo40/100

GC-MS data set for Generation of a chromosome-scale genome assembly of the insect-repellant terpenoid-producing Lamiaceae species, Callicarpa americana

<p>RAW GC/MS data set for characterization of class II terpene synthases from <em>Callicarpa americana&nbsp;</em></p>

opencc-by-4.0Feb 2020View details →
zenodo40/100

Figure 2 in Taxonomic study and population variation of scale insects (Hemiptera: Coccidae and Diaspididae) and associated parasitoids (Hymenoptera: Chalcidoidea) in an olive grove at Rio Grande do Sul, Brazil

Figure 2. Population variation of Hemiberlesia lataniae (Hemiptera: Diaspididae) on different varieties of Olea europaea (Arbequina, Arbosana and Koroneiki), at different times of sampling, in Barra do Ribeiro (30°30′54.95″S, 51°30′20.84″W), Rio Grande do Sul, Brazil.

opencc-by-4.0Nov 2018View details →
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Figure 1 in Taxonomic study and population variation of scale insects (Hemiptera: Coccidae and Diaspididae) and associated parasitoids (Hymenoptera: Chalcidoidea) in an olive grove at Rio Grande do Sul, Brazil

Figure 1. Population variation of Hemiberlesia lataniae (Hemiptera: Diaspididae) in an Olea europaea multivarietal olive grove (Arbequina, Arbosana and Koroneiki), at different sampling times, considering different phases and stage of development in Barra do Ribeiro (30°30′54.95″S, 51°30′20.84″W), Rio Grande do Sul, Brazil.

opencc-by-4.0Nov 2018View details →
zenodo40/100

Fig. 4 in A new genus and two new species of soft scale insect (Sternorrhyncha, Coccoidea, Coccidae) from Africa

Fig. 4. Hemilecanium cedrelus Hodgson, sp. n., female 2nd-instyar nymph. For lettering, see Figs 1 &amp; 2, but also where 3rd = position of dorsal tubercles on pharate 3rd-instar nymph.

opencc-by-4.0Sep 2008View details →
zenodo40/100

Fig. 3 in A new genus and two new species of soft scale insect (Sternorrhyncha, Coccoidea, Coccidae) from Africa

Fig. 3. Hemilecanium cedrelus Hodgson, sp. n., female 3rd- instar nymph. For lettering, see Figs 1 &amp; 2, but where scar = position of scars left by dorsal tubercles of 2nd-instar nymph.

opencc-by-4.0Sep 2008View details →
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Fig. 2 in A new genus and two new species of soft scale insect (Sternorrhyncha, Coccoidea, Coccidae) from Africa

Fig. 2. Hemilecanium cedrelus Hodgson, sp. n., adult female. For lettering, see Fig. 1, but also where B = dorsal tubercle; E = preopercular pore; J = marginal seta and J 1 = marginal seta on anal lobe; K = stigmatic spines; P = tubular ducts; and scars = scars showing position of dorsal tubercles of 3rd-instar nymph.

opencc-by-4.0Sep 2008View details →
zenodo40/100

Fig. 1 in A new genus and two new species of soft scale insect (Sternorrhyncha, Coccoidea, Coccidae) from Africa

Fig. 1. Sterculicoccus tafoensis Hodgson, sp. n., adult female. Where: A = dorsal setae; C = dorsal microductule; D = dorsal simple porte; F = dorsal view of anal plates; G = ventral view of anal plates; H = microridges on dorsal surface of anal plate; J = marginal seta; L = pregenital disc-pore; M = spiracular disc-pore; N = ventral microduct; P = larger ventral tubular duct; Q = smaller ventral tubular duct; R = antenna; S = claw, and T = ventral setae.

opencc-by-4.0Sep 2008View details →
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Fig. 5 in A new genus and two new species of soft scale insect (Sternorrhyncha, Coccoidea, Coccidae) from Africa

Fig. 5. Hemilecanium cedrelus Hodgson, sp. n., 1st-instar nymph (sex unknown). For lettering, see Figs 1 &amp; 2, but where E = dorsal trilocular pore; L =dorsal protuberances, and H = tibio-tarsal articulation with microspines.

opencc-by-4.0Sep 2008View details →
zenodo40/100

Fig. 1 in New scale insects (Homoptera: Coccinea) from the Cape Floristic Region

Fig. 1. South Africa, Western Cape Prov., banks of the Lower Palmiet River, the type locality of the new species.

opencc-by-3.0Nov 2017View details →
zenodo40/100

Figures 10-12 in A new genus and species of armored scale insect (Hemiptera: Diaspididae) from Australia found in the historic Koebele Collection of the California Academy of Sciences John W. Dooley III

Figures 10-12. Diaspididae spp., habitus, detail of venter of L1 lobes, and pygidium ventral (left) and dorsal (right). 10) Dichosoma convexa (after Brimblecombe 1957). 11) Duplaspidiotus claviger (after Ferris 1937). 12) Eulaingia stenophyllae (after Borchsenius and Williams 1963).

opencc-by-4.0Mar 2012View details →
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Figure 3 in A new genus and species of armored scale insect (Hemiptera: Diaspididae) from Australia found in the historic Koebele Collection of the California Academy of Sciences John W. Dooley III

Figure 3. Protomorgania koebelei adult female (pygidium). A) L1 lobes fused ventrally, appressed dorsally; B) single simple plate between L1 and position of L2 seta; C) anal pore; D) sclerotized arch; E) chitinized and finely stippled cuticle around vulva.

opencc-by-4.0Mar 2012View details →
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Figure 2 in A new genus and species of armored scale insect (Hemiptera: Diaspididae) from Australia found in the historic Koebele Collection of the California Academy of Sciences John W. Dooley III

Figure 2. Protomorgania koebelei adult female (thorax and Abdomen). A) anterior perispiracular pores; B) dorsal microducts; C) dorsal microducts, magnified; D) roughened cuticle.

opencc-by-4.0Mar 2012View details →
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Figure 19 in A new genus and species of armored scale insect (Hemiptera: Diaspididae) from Australia found in the historic Koebele Collection of the California Academy of Sciences John W. Dooley III

Figure 19. Pseudotargionia glandulosa, habitus, detail of venter of L1 lobes, and pygidium ventral (left) and dorsal (right) (after Ferris 1937).

opencc-by-4.0Mar 2012View details →
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Figure 1. Protomorgania koebelei adult female. A in A new genus and species of armored scale insect (Hemiptera: Diaspididae) from Australia found in the historic Koebele Collection of the California Academy of Sciences John W. Dooley III

Figure 1. Protomorgania koebelei adult female. A) habitus; B) tubercle; C) anterior spiracle; D) posterior spiracle; E) pygidial lobes; F) slide mounted female habitus; G) habitus on host; H) close-up of habitus on host

opencc-by-4.0Mar 2012View details →
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Figures 7-9 in A new genus and species of armored scale insect (Hemiptera: Diaspididae) from Australia found in the historic Koebele Collection of the California Academy of Sciences John W. Dooley III

Figures 7-9. Diaspididae spp., habitus, detail of venter of L1 lobes, and pygidium ventral (left) and dorsal (right) (after Brimblecombe 1957). 7) Diaphoraspis orbata. 8) Diaspidopus distinctus. 9) Diastolaspis novata.

opencc-by-4.0Mar 2012View details →
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Figures 4-6 in A new genus and species of armored scale insect (Hemiptera: Diaspididae) from Australia found in the historic Koebele Collection of the California Academy of Sciences John W. Dooley III

Figures 4-6. Diaspididae spp., habitus, detail of venter of L1 lobes, and pygidium ventral (left) and dorsal (right) (after Brimblecombe 1957). 4) Achorphora obliqua. 5) Acontonidia triangulari. 6) Aspidonymus woodwardi.

opencc-by-4.0Mar 2012View details →
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Figures 16-18 in A new genus and species of armored scale insect (Hemiptera: Diaspididae) from Australia found in the historic Koebele Collection of the California Academy of Sciences John W. Dooley III

Figures 16-18. Diaspididae spp., habitus, detail of venter of L1 lobes, and pygidium ventral (left) and dorsal (right). 16) Neoleonardia extensa (after Ferris 1938). 17) Neomorgania eucalypti (after Ferris 1937). 18) Pseudaonidia duplex (after Ferris 1937).

opencc-by-4.0Mar 2012View details →
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Fig. 5 in Nestedness of stream insects in Subtropical region: importance of inter-annual temporal scale

Fig. 5. NODF nestedness of Chironomidae (Diptera) assemblages in streams of southern Brazil in the summer and winter of 2010, 2011 and 2012. (A) Each line represents a stream independent of intra- and inter-annual factor. (B, C, D) Dotted lines represent winter data and continuous lines represent summer data. In these graphs, the individual information for each stream was grouped to assess intra-annual nestedness.

opencc-by-4.0Mar 2021View details →

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Allen Brain Atlas

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allen-brain-atlas
neuroscienceopenDocumentation, web resources, and API references are available online.
Last verified 2026-04-30Open record

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abode-home-cage
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Last verified 2026-04-30Open record

DANDI Archive for NWB datasets

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dandi-nwb
electrophysiologyopenPublished Dandiset metadata and archive endpoints are available through the production DANDI API.
Last verified 2026-04-30Open record

International Brain Laboratory public data

The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.

ibl
behavioral-neuroscienceopenPublic sessions can be searched and loaded from the IBL public data server through ONE.
Last verified 2026-04-29Open record

OpenNeuro

OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.

openneuro
neuroscienceopenPublished datasets are available on demand over the internet.
Last verified 2026-04-29Open record