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Data Descriptor

A Dataset Trichoptera (Insecta) in Selected Regions of European Russia

by
Alexander B. Ruchin
1,*,
Natalia V. Borisova
2,
Leonid V. Egorov
1,3,
Mikhail N. Esin
1,
Evgeniy A. Lobachev
1,
Sergei V. Lukiyanov
1,
Gennadiy B. Semishin
1,
Irina G. Esina
1 and
Anna M. Nikolaeva
4
1
Joint Directorate of the Mordovia State Nature Reserve and National Park “Smolny”, 430005 Saransk, Russia
2
Chuvash Branch of the Russian Entomological Society, 428034 Cheboksary, Russia
3
Prisursky State Nature Reserve, 428034 Cheboksary, Russia
4
Oka State Nature Biosphere Reserve, 391072 Brykin Bor, Russia
*
Author to whom correspondence should be addressed.
Limnol. Rev. 2026, 26(3), 31; https://doi.org/10.3390/limnolrev26030031
Submission received: 18 May 2026 / Revised: 23 June 2026 / Accepted: 24 June 2026 / Published: 25 June 2026

Abstract

The study of aquatic biota is of particular interest in view of the considerable anthropogenic impact on freshwater ecosystems in recent decades. Information on regional Trichoptera faunas remains fragmented and scattered in many areas. The present paper provides data from a dataset that includes results of Trichoptera studies conducted since 1981 (primarily during 2018–2025) in 15 regions of European Russia. In total, the dataset contains records from 295 localities. The database includes information on 7759 specimens representing 134 species from 15 families. Eleven Trichoptera species are reported for the first time from the Nizhny Novgorod Region, seven species from the Penza Region, five species each from the Vladimir and Ryazan regions, three species each from the Samara Region, the Republic of Mordovia, and the Volgograd Region, and one species each from the Voronezh, Tambov, and Lipetsk regions, as well as the Chuvash Republic. Hydroptila angulata is recorded for the first time in the Middle Volga Region. The most abundant taxa in the collections belong to the families Limnephilidae, Phryganeidae, and Leptoceridae. Eight species are represented in the dataset by more than 300 specimens each. Hand-held sweep nets were used at 109 localities and yielded 109 species and 3308 specimens. The use of light traps at 45 localities resulted in the collection of 90 species represented by 2651 specimens.

1. Introduction

Aquatic ecosystems play a crucial role in the global environment. They are essential for maintaining the biodiversity of both aquatic ecosystems themselves and adjacent terrestrial ecosystems, regulating climate, sustaining ecological productivity, and many other ecosystem functions [1,2,3]. Along with terrestrial ecosystems, aquatic ecosystems have increasingly faced growing anthropogenic threats in recent years, associated with both direct and indirect human activities. The major concerns are linked to rising global temperatures. For example, reductions in snow cover depth and glacier volume decrease water input into rivers and lakes [4,5]. The duration of droughts, monsoon intensity, frequency of wildfires, and pollution of water bodies by livestock effluents and agrochemicals are also increasing [6,7,8,9]. All these factors lead to acidification of water bodies, alterations in hydrological and biological cycles, habitat degradation, declines in biodiversity, and the extinction of species and populations [10,11,12,13,14]. In order to preserve freshwater biodiversity and ecosystem quality, it is necessary to investigate these impacts and develop measures to mitigate them [1,15].
One of the most well-known groups of freshwater organisms is the order Trichoptera. The study of regional Trichoptera faunas is an important component of biodiversity monitoring. Caddisflies are ecologically significant and serve as valuable biological indicators of the condition of aquatic ecosystems. Trichoptera species exhibit a wide range of life-history strategies and play key roles in freshwater ecosystems, including the regulation of organic matter dynamics, nutrient cycling, and predation [16,17,18]. A total of 235 caddisfly species have been reported from the European part of Russia [19]. At the same time, this list is not final and may be expanded through the discovery of species previously unrecorded from this macroregion. In addition, regional Trichoptera faunas remain poorly known, and available information is usually fragmented and scattered. The compilation of dispersed information from various sources together with unpublished data and the development of integrated databases have become increasingly relevant in recent years. Digital biodiversity data and analytical tools available through various electronic platforms are now widely used to address biological questions. Currently, one of the largest databases on species distributions is the Global Biodiversity Information Facility (GBIF), which contains extensive lists and occurrence records of taxa from all regions of the world [20,21,22].
The main objective of our study was to compile a biodiversity database of Trichoptera in selected regions of European Russia. The specific aims were: (1) to analyse the biodiversity of individual regions, and (2) number and diversity of Trichoptera collected by different methods.

2. Data Description

2.1. Dataset Description

Data from the dataset can be uploaded as a single XLSX file to GBIF (https://doi.org/10.15468/z28m3x (accessed on 23 June 2026)). It contains 2014 rows, and each row represents a set of data. The columns contained in it are as follows (Table 1) [23].

2.2. Species Diversity

The database contains information on 7759 specimens representing 134 species from 15 families (Appendix A). Hydroptila angulata Mosely, 1922 is recorded for the first time in the Middle Volga Region. This species inhabits standing and slow-flowing waters of lakes, streams, and rivers, including brackish waters, as well as ponds [24,25,26]. Its case is a laterally flattened, seed-like structure constructed from sand particles. Most Hydroptilidae larvae feed by piercing and sucking the protoplasm of algal filaments [27]. Adult flight activity occurs from May to October. Hydroptila angulata is distributed across most of Europe but is absent from Scotland, Iceland, Norway, and Eastern Europe [24]. In European Russia, its distribution is sporadic (Karelia, Leningrad Region, Astrakhan Region, and the Urals) [19].
The distribution of Trichoptera species across the 15 regions was uneven, which is associated with differences in sampling intensity among regions. The most thoroughly surveyed regions were the Republic of Mordovia and the Chuvash Republic, where 98 and 86 species were recorded, respectively (Appendix A). In the remaining regions, species richness was considerably lower. The number of regions in which individual species were recorded also varied from 1 to 15. The most widespread species were Agrypnia varia (Fabricius, 1793), occurring in 13 regions, Limnephilus flavicornis (Fabricius, 1787), occurring in 14 regions, and Phryganea grandis Linnaeus, 1758, occurring in all 15 regions. In contrast, 36 species were found in only one of the fifteen regions.
As a result of our own sampling efforts, new Trichoptera species were recorded for several regions. Eleven species are reported for the first time from the fauna of the Nizhny Novgorod Region (Hagenella clathrata (Kolenati, 1848), Oligostomis reticulata (Linnaeus, 1761), Trichostegia minor (Curtis, 1834), Anabolia brevipennis (Curtis, 1834), Anabolia concentrica (Zetterstedt, 1840), Anabolia furcata Brauer, 1857, Limnephilus decipiens (Kolenati, 1848), Limnephilus dispar McLachlan, 1875, Limnephilus externus Hagen, 1861, Limnephilus ignavus McLachlan, 1865, Nemotaulius punctatolineatus (Retzius, 1783)). Seven species are newly recorded for the fauna of the Penza Region (Hydropsyche angustipennis (Curtis, 1834), H. contubernalis McLachlan, 1865, Anabolia furcata Brauer, 1857, Glyphotaelius pellucidus (Retzius, 1783), Grammotaulius nigropunctatus (Retzius, 1783), Ironoquia dubia (Stephens, 1837), Limnephilus bipunctatus Curtis, 1834). Five species are newly reported from the Vladimir Region (Psychomyia pusilla (Fabricius, 1781), Limnephilus fuscicornis (Rambur, 1842), Limnephilus griseus (Linnaeus, 1758), Limnephilus sparsus Curtis, 1834, Stenophylax lateralis (Stephens, 1837)). Five species are newly recorded from the Ryazan Region (Oligostomis reticulata (Linnaeus, 1761), Stenophylax lateralis, Molanna albicans (Zetterstedt, 1840), Ceraclea albimacula (Rambur, 1842), Oecetis furva (Rambur, 1842)). Three species are newly reported from the Samara Region (Agraylea sexmaculata Curtis, 1834, Agrypnia varia, Phryganea grandis). Three species are newly recorded from the Volgograd Region (Phryganea grandis, Anabolia furcata Brauer, 1857, Grammotaulius nitidus (Müller, 1764)). One species is newly reported from each of the following regions: Voronezh Region (Limnephilus dispar), Tambov Region (Agrypnia varia), Lipetsk Region (Stenophylax lateralis), and the Chuvash Republic (Oligotricha striata (Linnaeus, 1758)). In the Republic of Mordovia, compared with a recent publication [28], three species are newly recorded (Ithytrichia lamellaris Eaton, 1873, Cheumatopsyche lepida (Pictet, 1834), Hydroptila angulata). In the caddisfly fauna of the Moscow Region, the presence of five previously known species was confirmed, and in the Saratov Region fauna, four species were confirmed.
The most abundant families in the samples were Limnephilidae, Phryganeidae, and Leptoceridae. The highest number of specimens (more than 300 individuals) in the dataset was recorded for eight species: Anabolia brevipennis, Hydropsyche contubernalis, Hydropsyche pellucidula, Limnephilus flavicornis, Limnephilus rhombicus, Limnephilus sparsus, Phryganea grandis, and Potamophylax latipennis. These same species were also most frequently recorded across multiple localities. In particular, Phryganea grandis stands out, being recorded in 136 localities (46.1%) of the dataset (Figure 1).
Seventeen Trichoptera species are represented in the dataset by a single specimen: Agrypnia picta, Hydropsyche modesta, Hydroptila sparsa, Leptocerus interruptus, Limnephilus centralis, Oecetis nigropunctata, Orthotrichia costalis, Paduniella uralensis, Parasetodes respersellus, Philarctus bergrothi, Philopotamus montanus, Polycentropus irroratus, Rhadicoleptus alpestris, Rhyacophila obliterata, Setodes punctatus, Silo pallipes, and Tricholeiochiton fagesii. Accordingly, these species were each recorded in only one locality. In addition, six more species (Apatania zonella, Cyrnus crenaticornis, Hydroptila angulata, Limnephilus externus, Limnephilus femoratus, Odontocerum albicorne) were also recorded from a single locality each.
Most of the species in our dataset were collected with hand-held sweep net, which was used in 298 samples correspondent to 109 localities and yielded 109 species and 3308 specimens (Figure 2). The second with most species was the light trap (270 samples in 45 localities, 90 species, 2651 specimens). Malaise traps were used in 24 localities and yielded 48 species. The effectiveness of these sampling methods for studying Trichoptera has been highlighted by other researchers. Sweep-net sampling is particularly effective for collecting larvae in aquatic habitats [29,30]. Light traps are also highly effective for collecting adult Trichoptera, especially near or at some distance from water bodies [31,32]. Malaise traps can also provide good results, especially when operated continuously throughout the season, additionally offering phenological information [33,34].
The use of beer traps yielded notable results (26 species), despite being applied at a relatively large number of localities (156). In terms of abundance, Phryganea grandis dominated in beer traps. Adults of this species are characterized by active feeding behavior. Specialized receptors enable them to detect chemical compounds in solution and respond to sucrose [35,36]. Their antennae are sensitive to various volatile substances, making the bait odor attractive to them [37]. Agrypnia varia, Hagenella clathrata, Trichostegia minor, Anabolia brevipennis, and Glyphotaelius pellucidus were also frequently attracted to beer traps. These are typical forest-dwelling species. Baits based on fermented beer with sugar attract adult caddisflies of the families Phryganeidae and Limnephilidae, which is associated with the active feeding behavior of these species [38]. Other sampling methods collected fewer species (Figure 2).

3. Methods

3.1. Study Area

The study area where the authors conducted field research covers 15 regions of European Russia. The total area of the study exceeds 1.2 million km2 (Figure 3). Trichoptera samples were collected in European Russia (the Russian Plain) across 15 regions. Part of the study area lies within the Volga Upland (eastern part of the Republic of Mordovia, Chuvash Republic, Penza Region, Samara Region, Saratov Region, Nizhny Novgorod Region, Ulyanovsk Region, Republic of Tatarstan, Volgograd Region). Another part of the study area is located within the Oka–Don Lowland (western part of the Republic of Mordovia, Moscow Region, Tambov Region, Ryazan Region, Lipetsk Region, Penza Region, Voronezh Region, Vladimir Region). In these regions, the relief is predominantly hilly. Elevations above sea level range from 200 to 300 m in the Volga Upland. The Oka–Don Lowland is characterized by lower elevations and a more subdued topography. The climate is temperate continental, becoming warmer in southern regions compared to northern ones. The onset of positive temperatures occurs later in eastern regions than in western ones, which are influenced by warmer Atlantic air masses. Maps in Figure 3 were created using QGIS (version 3.22). Sampling localities were imported as a vector point layer from a CSV file containing geographic coordinates. To improve visualization and avoid overlapping records, occurrences located within a distance of 3–4 km from each other were merged and displayed as a single point. Administrative boundaries of the studied regions were obtained from the OSM Boundaries database (https://osm-boundaries.com (accessed on 23 June 2026)).
Forest and forest-steppe landscapes dominate the study area. In southern regions, forests are mainly of an island type, often without gradual transitions between stands. Large continuous forest tracts are characteristic only of northern regions [39]. The main rivers in the study area are the Volga and the Don, along with their tributaries of various orders. Numerous lakes occur in river floodplains. Tributaries of the Volga and Don are characterized by relatively high flow velocity in small 4th- and 5th-order streams, whereas larger tributaries do not exhibit such flow conditions. In recent years, river discharge in these basins has changed significantly and has become more regulated, with a general decrease in total runoff. It is believed that climate change recorded in recent decades has substantially altered the spatiotemporal variability of runoff characteristics [40,41].

3.2. Data Collection

The authors conducted their own field research starting in 1981, with the most intensive sampling carried out during 2018–2025. A wide range of conventional and non-conventional sampling methods was used to obtain specimens: hand-held sweep net, light traps, Malaise traps, beer traps, window traps, yellow pan traps, and pitfall traps [42,43,44,45]. The hand-held sweep net was used both for collecting adults (sweep sampling) and for collecting larvae from various types of water bodies. It was the only method that included larvae. As light traps, a standard TDM Electric lamp (DRV 250 W, 4200 K, 4700 lm, E40) was used. This method was typically applied at forest edges near human structures such as small isolated houses or settlements surrounded by forest and located near water bodies. Malaise traps were used in both commercially produced and homemade versions. The collecting container was filled with 70% ethanol. One trap was installed per locality, usually at forest edges or slightly inside forest stands near water bodies. In many habitats, Malaise traps operated from April to October, with samples collected every 3–12 days. Beer traps were constructed from 5 L or 1.5 L containers filled to one quarter with beer mixed with sugar and left to ferment. The traps were suspended from branches of trees and shrubs at a height of 1.5–12 m. Samples were retrieved every 7–15 days after filtering the liquid. Window traps were made of transparent plastic and consisted of intersecting panels with a funnel at the bottom. A collecting container filled with ethanol was placed beneath the funnel. These traps were suspended from large tree branches at heights above 2 m and were used both at forest edges and within forest stands. Yellow pan traps consisted of yellow plastic bowls with a volume of 1 L. They were filled halfway with water and a detergent was added as a surfactant. Traps were placed on the ground in different habitats in linear transects of 10–12 units, with 1–3 m spacing between traps. Exposure time ranged from 3 to 7 days. Pitfall traps consisted of standard 0.5 L plastic cups inserted into the soil so that the rim was level with the ground surface. A 4% formalin solution (approximately 150 mL per trap) was used as a preservative. These traps were used across a range of habitats. Other collection methods were used to collect adult insects. The collection methods were not standardized and the amount of effort varies in all cases. However, species diversity can be easily accounted for when collecting in a variety of ways.
During our own field studies, we recorded coordinates, dates, habitat type, and the original name of each locality. These data were entered into a database. We also used published sources (see dataset) containing reliable information on sampling locations and timing of studies conducted by the authors, which are included in the dataset [23]. Some sections of the dataset were not filled in, as these publications lacked the necessary information. Data on the life cycle stage was not included in the dataset. During data processing, results obtained using different sampling methods were pooled, combining all available records. Statistical analyses were performed using Microsoft Office Professional Plus 2019 software packages.

3.3. Taxonomic Analysis

Most of the collected specimens were preserved in ethanol for subsequent processing. A portion of the material was mounted on entomological pins. All specimens obtained using different types of traps were rinsed each time and stored in 90% ethanol. In the laboratory, all specimens were identified under an MBS-10 stereomicroscope. Larval identification was carried out using the keys by S.G. Lepneva [42,43] and V.D. Ivanov et al. [46], while adults were identified using the keys by T.T. Macan [47], H. Malicky [48], and J. Salokannel & K. Mattila [49]. In total, the dataset includes records from 295 localities. The studied material is stored in the Mordovia State Nature Reserve, Voronezh State University and the Zoological Institute of the Russian Academy of Sciences (St. Petersburg).

4. Conclusions

A biodiversity analysis of Trichoptera was conducted across 15 regions. The most thoroughly surveyed regions were the Republic of Mordovia and the Chuvash Republic, where 98 and 86 species were recorded (including newly added records), respectively. In total, 36 species were recorded in only one of the fifteen regions. Eleven species are newly reported for the fauna of the Nizhny Novgorod Region, seven for the Penza Region, five for the Vladimir Region, five for the Ryazan Region, three for the Samara Region, three for the Republic of Mordovia, three for the Volgograd Region, and one species each for the Voronezh, Tambov, Lipetsk Regions and the Chuvash Republic. The most abundant families in the samples were Limnephilidae, Phryganeidae, and Leptoceridae. Eight species were represented by more than 300 specimens in the dataset. The most widespread species across regions were Agrypnia varia (recorded in 13 regions), Limnephilus flavicornis (14 regions), and Phryganea grandis (15 regions). Most species were collected through hand-held sweep net (mostly larvae), followed by the light trap (adult specimens). In practice, these two methods together provided the most complete representation of regional Trichoptera fauna.

Author Contributions

Conceptualization, A.B.R.; methodology, A.B.R. and N.V.B.; software, M.N.E.; validation, A.B.R. and M.N.E.; formal analysis, A.B.R. and M.N.E.; investigation, A.B.R., N.V.B., M.N.E., E.A.L., S.V.L. and G.B.S.; resources, A.B.R., M.N.E., L.V.E., A.M.N. and I.G.E.; data curation, A.B.R. and M.N.E.; writing—original draft preparation, A.B.R. and N.V.B.; writing—review and editing, A.B.R.; visualization, A.B.R.; supervision, A.B.R.; project administration, A.B.R.; funding acquisition, A.B.R. and M.N.E. All authors have read and agreed to the published version of the manuscript.

Funding

This research was funded by Russian Science Foundation, grant number 22-14-00026-П.

Institutional Review Board Statement

Not applicable.

Data Availability Statement

Creative Commons Attribution (CC BY-NC) 4.0 License. https://doi.org/10.15468/z28m3x (accessed on 23 June 2026).

Acknowledgments

The authors thank K.P. Tomkovich, M.A. Shestov, G.F. Suleymanova, D.A. Sidorov, A.V. Melnikova, S.N. Bochenkov, M.V. Maresev, and M.K. Ryzhov (Russia) for providing materials for the study.

Conflicts of Interest

The authors declare no conflicts of interest.

Appendix A

Species richness and abundance of Trichoptera across different regions (from the dataset).
SpeciesVlRVgRVrRLRRMMRNNRPRRRSmRSrRTRRTURRChTotal of Specimens
Rhyacophilidae
1.Rhyacophila fasciata Hagen, 1859 1 1314
2.Rhyacophila nubila Zetterstedt, 1840 2 13
3.Rhyacophila obliterata McLachlan, 1863 11
Glossosomatidae
4.Agapetus ochripes Curtis, 1834 5 5
Hydroptilidae
5.Agraylea multipunctata Curtis, 1834 7 2 31720
6.Agraylea sexmaculata Curtis, 1834 1 24 12 1938
7.Hydroptila angulata Mosely, 1922 * 2 2
8.Hydroptila dampfi Ulmer, 1929 4 4
9.Hydroptila sparsa Curtis, 1834 1 1
10.Hydroptila tineoides Dalman, 1819 3 2 16
11.Ithytrichia lamellaris Eaton, 1873 109 1 22 114
12.Orthotrichia costalis (Curtis, 1834) 1 1
13.Orthotrichia tragetti Mosely, 1930 27 936
14.Oxyethira flavicornis (Pictet, 1834) 3 1 1 5
15.Oxyethira tristella Klapalek, 1895
16.Tricholeiochiton fagesii (Guinard, 1879) 1 1
Philopotamidae
17.Philopotamus montanus (Donovan, 1813) 1 1
Psychomyiidae
18.Lype phaeopa (Stephens, 1836) 3 137
19.Paduniella uralensis Martynov, 1914 1 1
20.Psychomyia pusilla (Fabricius, 1781)1 2 1 1 179184
21.Tinodes waeneri (Linnaeus, 1758) 4 66 373
Ecnomidae
22.Ecnomus tenellus (Rambur, 1842) 1 20 10 12153
Polycentropodidae
23.Cyrnus crenaticornis (Kolenati, 1859) 22
24.Cyrnus flavidus McLachlan, 1864 7 1 1 1515
25.Cyrnus trimaculatus (Curtis, 1834) 1 4 5
26.Holocentropus dubius (Rambur, 1842) 75 1 76
27.Holocentropus insignis Martynov, 1924 3 1 4
28.Holocentropus picicornis (Stephens, 1836) 11 2
29.Neureclipsis bimaculata (Linnaeus, 1758) 1 7 4 921
30.Plectrocnemia conspersa (Curtis, 1834) 1 1 9 11729
31.Polycentropus flavomaculatus (Pictet, 1834) 30 3 21339
32.Polycentropus irroratus Curtis, 1835 1 1
Hydropsychidae
33.Cheumatopsyche lepida (Pictet, 1834) 2 4 1 18
34.Hydropsyche angustipennis (Curtis, 1834) 82 2113 3132233
35.Hydropsyche bulgaromanorum Malicky, 1977 1 7 6 14
36.Hydropsyche contubernalis Mclachlan, 1865 163 167 56129 4 151571
37.Hydropsyche ornatula McLachlan, 1878 + 1 214
38.Hydropsyche pellucidula (Curtis, 1834) 103 2 1 2234342
39.Hydropsyche siltalai Doehler, 1963 77
Phryganeidae
40.Agrypnia crassicornis (McLachlan, 1876) 4 15
41.Agrypnia obsoleta (Hagen, 1864) 12 1 922
42.Agrypnia pagetana Curtis, 1835 1 5 3 150159
43.Agrypnia picta Kolenati, 1848 1 1
44.Agrypnia varia (Fabricius, 1793) 1 1 2813542844537103
45.Hagenella clathrata (Kolenati, 1848) 65 9 579
46.Oligostomis reticulata (Linnaeus, 1761) 6 4 1 718
47.Oligotricha striata (Linnaeus, 1758) 12 1114
48.Phryganea bipunctata Retzius, 1783 2 35 1 5 11550
49.Phryganea grandis Linnaeus, 1758 19231615522342232128332911126533
50.Semblis phalaenoides (Linnaeus, 1758) 6 28
51.Trichostegia minor (Curtis, 1834) 108 351131 7 511172
Brachycentridae
52.Brachycentrus subnubilus Curtis, 1834 7 21 10
Odontoceridae
53.Odontocerum albicorne (Scopoli, 1763) 4 4
Lepidostomatidae
54.Lepidostoma hirtum (Fabricius, 1775) 1 1 2
Apataniidae
55.Apatania zonella (Zetterstedt, 1840) 66
Limnephilidae
56.Anabolia brevipennis (Curtis, 1834) 32 566 42315 166707
57.Anabolia concentrica (Zetterstedt, 1840) 7 1 5 1023
58.Anabolia furcata Brauer, 1857 31 4 111 15 1339
59.Anabolia laevis (Zetterstedt, 1840) 35 1045
60.Chaetopteryx villosa (Fabricius, 1798) 2 46
61.Colpotaulius incisus (Curtis, 1834) 1 5 2 8
62.Colpotaulius major Martynov, 1909 2 2
63.Glyphotaelius pellucidus (Retzius, 1783)9 1 52 94 32 119100
64.Grammotaulius nigropunctatus (Retzius, 1783) 2 13
65.Grammotaulius nitidus (Müller, 1764) 1 2 1 7 1719
66.Halesus digitatus (Schrank, 1781) 31 6 845
67.Halesus radiatus (Curtis, 1834) 63 164
68.Halesus tesselatus (Rambur, 1842) 1 63 42106
69.Ironoquia dubia (Stephens,1837) 3 1 711
70.Lenarchus bicornis (McLachlan, 1880) +
71.Limnephilus affinis Curtis, 1834 2 13
72.Limnephilus auricula Curtis, 18341 4 712
73.Limnephilus bipunctatus Curtis, 1834 3 22 1219
74.Limnephilus borealis (Zetterstedt, 1840)1 + 1 1 3
75.Limnephilus centralis Brauer, 1857 11
76.Limnephilus decipiens (Kolenati, 1848) 4 1 11 3 2039
77.Limnephilus dispar McLachlan, 1875 1 1 2 4
78.Limnephilus elegans Curtis, 1834 1 1 3 5
79.Limnephilus externus Hagen, 1861 6 6
80.Limnephilus extricatus McLachlan, 1865 9 2 1 1619
81.Limnephilus femoratus (Zetterstedt, 1840) 4 4
82.Limnephilus flavicornis (Fabricius, 1787) 4219175156623 6754183428
83.Limnephilus fuscicornis (Rambur, 1842)30 52 2816 4112
84.Limnephilus fuscinervis (Zetterstedt, 1840) 1 5 6
85.Limnephilus griseus (Linnaeus, 1758) 1 45 4 45 67162
86.Limnephilus ignavus Mclachlan, 1865 2 8 111 2 1631
87.Limnephilus lunatus Curtis, 1834 1 3 5 2 415
88.Limnephilus nigriceps (Zetterstedt, 1840) 5 3 1523
89.Limnephilus politus McLachlan, 1865 26 6 77109
90.Limnephilus rhombicus (Linnaeus, 1758) 199 3062 2 1 108348
91.Limnephilus sericeus (Say, 1824) 125 10 22 13170
92.Limnephilus sparsus Curtis, 1834 46 111 16469 33 25367
93.Limnephilus stigma Curtis, 1834 6 28 1 6398
94.Limnephilus vittatus (Fabricius, 1798) 8 5 5 3048
95.Limnephilus xanthodes McLachlan, 1873 3 115
96.Nemotaulius punctatolineatus (Retzius, 1783) 2 5 11110
97.Philarctus bergrothi McLachlan, 1880 1 1
98.Potamophylax latipennis (Curtis, 1834) 551 12 2114580
99.Potamophylax nigricornis (Pictet, 1834) 5 2 1210
100.Potamophylax rotundipennis (Brauer, 1857) 9 5160
101.Rhadicoleptus alpestris (Kolenati, 1848) 1 1
102.Stenophylax lateralis (Stephens, 1837)1 19 513 1 829
103.Stenophylax sequax (Mclachlan, 1875) 2 158
Goeridae
104.Goera pilosa (Fabricius, 1775) 2 2
105.Silo pallipes (Fabricius, 1781) 1 1
Sericostomatidae
106.Sericostoma personatum (Kirby & Spence, 1826) 1 3 15
Molannidae
107.Molanna albicans (Zetterstedt, 1840) 21 9 1444
108.Molanna angustata Curtis, 1834 2 1 1 15
109.Molannodes tinctus (Zetterstedt, 1840) 2 2
Leptoceridae
110.Athripsodes aterrimus (Stephens, 1836) 1 7 3846
111.Athripsodes cinereus (Curtis, 1834) 4 1 5
112.Ceraclea albimacula (Rambur, 1842) 2 2 4
113.Ceraclea annulicornis (Stephens, 1836) 3 28 31
114.Ceraclea dissimilis (Stephens, 1836) 19 1 12950
115.Ceraclea excisa (Morton 1904) 3 2528
116.Ceraclea fulva (Rambur, 1842) 3 3
117.Ceraclea nigronervosa (Retzius, 1783) 1 89
118.Ceraclea senilis (Burmeister, 1839) 5 5
119.Leptocerus interruptus (Fabricius, 1775) 1 1
120.Leptocerus tineiformis Curtis, 1834 60 31 6 130128
121.Mystacides azureus (Linnaeus, 1761) 8 11212
122.Mystacides longicornis (Linnaeus, 1758) 2 5 2 11214225
123.Mystacides niger (Linnaeus, 1758) 1 21610
124.Oecetis furva (Rambur, 1842) 1 9 717
125.Oecetis intima McLachlan, 1877 7 7
126.Oecetis lacustris (P. J. Pictet, 1834) 1 1 1 1215
127.Oecetis nigropunctata Ulmer, 1908 1 1
128.Oecetis ochracea (Curtis, 1825) 1 3 5 91 3325
129.Parasetodes respersellus (Rambur, 1842) 1 1
130.Setodes punctatus (Fabricius, 1793) 1 1
131.Setodes viridis (Fourcroy, 1785) 2 1 1 4
132.Triaenodes bicolor (Curtis, 1834) 5 1 1824
133.Triaenodes unanimis McLachlan, 1877 2 2
134.Triaenodes conspersus (Rambur, 1842) 3 3
Total specimens in dataset29717192183368172972755502420051957922797759
Total species17141239852321353557284986134
Note: VlR—Vladimir Region; VgR—Volgograd Region; VrR—Voronezh Region; LR—Lipetsk Region; RM—Republic of Mordovia («+»—literature data); MR—Moscow Region; NNR—Nizhny Novgorod Region; PR—Penza Region; RR—Ryazan Region; SmR—Samara Region; SrR—Saratov Region; TR—Tambov Region; RT—Republic of Tatarstan; UR—Ulyanovsk region; RCh—Republic of Chuvashia. The sign “*” marks the first record of the species for the Middle Volga region.

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Figure 1. Number of specimens and number of localities for the most represented Trichoptera species in the dataset.
Figure 1. Number of specimens and number of localities for the most represented Trichoptera species in the dataset.
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Figure 2. Number of Trichoptera species and specimens collected using different sampling methods. The number of sample events (data from different collection dates and geographic coordinates) is shown below each method.
Figure 2. Number of Trichoptera species and specimens collected using different sampling methods. The number of sample events (data from different collection dates and geographic coordinates) is shown below each method.
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Figure 3. Study sites and sampling locations (shown as red dots): (A) the regions of the study are indicated in light green; (B) 1—Moscow Region; 2—Vladimir Region; 3—Nizhny Novgorod Region; 4—Chuvash Republic; 5—Republic of Tatarstan; 6—Ryazan Region; 7—Republic of Mordovia; 8—Ulyanovsk region; 9—Samara Region; 10—Lipetsk Region; 11—Tambov Region; 12—Penza Region; 13—Saratov Region; 14—Voronezh Region; 15—Volgograd Region.
Figure 3. Study sites and sampling locations (shown as red dots): (A) the regions of the study are indicated in light green; (B) 1—Moscow Region; 2—Vladimir Region; 3—Nizhny Novgorod Region; 4—Chuvash Republic; 5—Republic of Tatarstan; 6—Ryazan Region; 7—Republic of Mordovia; 8—Ulyanovsk region; 9—Samara Region; 10—Lipetsk Region; 11—Tambov Region; 12—Penza Region; 13—Saratov Region; 14—Voronezh Region; 15—Volgograd Region.
Limnolrev 26 00031 g003
Table 1. Description of the data in the dataset.
Table 1. Description of the data in the dataset.
Column LabelColumn Description
occurrenceIDAn identifier for the occurrence (as opposed to a particular digital record of the occurrence)
basisOfRecordThe specific nature of the data record: HumanObservation
eventDateThe date when material from the trap was collected or the range of dates during which the trap collected material
scientificNamThe full scientific name including the genus name and the lowest level of taxonomic rank with the authority
kingdomThe full scientific name of the kingdom in which the taxon is classified
decimalLatitude The geographic latitude of location in decimal degrees
decimalLongitudeThe geographic longitude (in decimal degrees, using the spatial reference system given in dwc:geodeticDatum)
countryThe name of the country in which the location occurs
countryCodeThe standard code for the country in which the location occurs.
individualCountThe number of individuals represented present at the time of the occurrence
yearThe integer year in which the event occurred
monthThe ordinal month in which the event occurred
dayThe integer day of the month on which the event occurred
associatedReferencesA list (concatenated and separated) of identifiers (publication, bibliographic reference, global unique identifier, URI) of literature associated with the dwc:Occurrence.
recordedByA person, group, or organization responsible for recording the original occurrence
identifiedByA list of names of people who assigned the taxon to the subject
locality_originalThe specific description of the place. This term may contain information modified from the original to correct perceived errors or standardize the description
samplingProtocolThe names of the methods or protocols used during an event
georeferenceSourcesA list of maps, gazetteers, or other resources used to georeference the Location
coordinateUncertaintyInMetersThe maximum uncertainty distance in metres
geodeticDatumThe ellipsoid, geodetic datum, or spatial reference system (SRS) upon which the geographic coordinates given in decimalLatitude and decimalLongitude is based
stateProvinceThe name of the next smaller administrative region than country (state, province, canton, department, region, etc.) in which the dcterms:Location occurs.
habitatA category or description of the habitat in which the Event occurred
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MDPI and ACS Style

Ruchin, A.B.; Borisova, N.V.; Egorov, L.V.; Esin, M.N.; Lobachev, E.A.; Lukiyanov, S.V.; Semishin, G.B.; Esina, I.G.; Nikolaeva, A.M. A Dataset Trichoptera (Insecta) in Selected Regions of European Russia. Limnol. Rev. 2026, 26, 31. https://doi.org/10.3390/limnolrev26030031

AMA Style

Ruchin AB, Borisova NV, Egorov LV, Esin MN, Lobachev EA, Lukiyanov SV, Semishin GB, Esina IG, Nikolaeva AM. A Dataset Trichoptera (Insecta) in Selected Regions of European Russia. Limnological Review. 2026; 26(3):31. https://doi.org/10.3390/limnolrev26030031

Chicago/Turabian Style

Ruchin, Alexander B., Natalia V. Borisova, Leonid V. Egorov, Mikhail N. Esin, Evgeniy A. Lobachev, Sergei V. Lukiyanov, Gennadiy B. Semishin, Irina G. Esina, and Anna M. Nikolaeva. 2026. "A Dataset Trichoptera (Insecta) in Selected Regions of European Russia" Limnological Review 26, no. 3: 31. https://doi.org/10.3390/limnolrev26030031

APA Style

Ruchin, A. B., Borisova, N. V., Egorov, L. V., Esin, M. N., Lobachev, E. A., Lukiyanov, S. V., Semishin, G. B., Esina, I. G., & Nikolaeva, A. M. (2026). A Dataset Trichoptera (Insecta) in Selected Regions of European Russia. Limnological Review, 26(3), 31. https://doi.org/10.3390/limnolrev26030031

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