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101 results for “Saproxylic beetles”
Supplementary material 2 from: Maurizi E, Campanaro A, Chiari S, Maura M, Mosconi F, Sabatelli S, Zauli A, Audisio P, Carpaneto GM (2017) Guidelines for the monitoring of Osmoderma eremita and closely related species. In: Carpaneto GM, Audisio P, Bologna MA, Roversi PF, Mason F (Eds) Guidelines for the Monitoring of the Saproxylic Beetles protected in Europe. Nature Conservation 20: 79-128. https://doi.org/10.3897/natureconservation.20.12658
Field sheet to fill during each survey and its legend :
Supplementary material 1 from: Hardersen S, Bardiani M, Chiari S, Maura M, Maurizi E, Roversi PF, Mason F, Bologna MA (2017) Guidelines for the monitoring of Morimus asper funereus and Morimus asper asper. In: Carpaneto GM, Audisio P, Bologna MA, Roversi PF, Mason F (Eds) Guidelines for the Monitoring of the Saproxylic Beetles protected in Europe. Nature Conservation 20: 205-236. https://doi.org/10.3897/natureconservation.20.12676
Excel sheet, Volume of log piles :
Supplementary material 1 from: Della Rocca F, Bogliani G, Milanesi P (2017) Patterns of distribution and landscape connectivity of the stag beetle in a human-dominated landscape. In: Campanaro A, Hardersen S, Sabbatini Peverieri G, Carpaneto GM (Eds) Monitoring of saproxylic beetles and other insects protected in the European Union. Nature Conservation 19: 19-37. https://doi.org/10.3897/natureconservation.19.12457
Additional information :
Supplementary material 1 from: Thomaes A, Verschelde P, Mader D, Sprecher-Uebersax E, Fremlin M, Onkelinx T, Méndez M (2017) Can we successfully monitor a population density decline of elusive invertebrates? A statistical power analysis on Lucanus cervus. In: Campanaro A, Hardersen S, Sabbatini Peverieri G, Carpaneto GМ (Eds) Monitoring of saproxylic beetles and other insects protected in the European Union. Nature Conservation 19: 1-18. https://doi.org/10.3897/natureconservation.19.11761
Figures of statistical support : Data type: statistical data
Supplementary material 2 from: Kadej M, Zając K, Smolis A, Tarnawski D, Tyszecka K, Malkiewicz A, Pietraszko M, Warchałowski M, Gil R (2017) The great capricorn beetle Cerambyx cerdo L. in south-western Poland – the current state and perspectives of conservation in one of the recent distribution centres in Central Europe. In: Campanaro A, Hardersen S, Sabbatini Peverieri G, Carpaneto GM (Eds) Monitoring of saproxylic beetles and other insects protected in the European Union. Nature Conservation 19: 111-134. https://doi.org/10.3897/natureconservation.19.11838
Distribution data of Cerambyx cerdo : Data type: occurence
Fig. 3 in Saproxylic weevils and edaphic beetles as indicators of environmental quality of relict forests in Piedmont lowlands (Coleoptera)
Fig. 3 – Scatter graph of study areas, relative to abundance data; × = sampling plots of Vaj (v), △ = sampling plots of Partecipanza (p), ○ = sampling plots of Merlino (m), + = sampling plots of Stupinigi (s).
Figure 1 in First record of the saproxylic beetle Corticeus (= Hypophloeus) unicolor Piller & Mitterpacher, 1783 in Montenegro (Coleoptera: Tenebrionidae) with comments on old-growth forests conservation in the Country
Figure 1. Location of discovery of C. unicolor in Montenegro in the Dinaric Alps (Biogradska Gora National Park) (from Parisi, 2023).
Data from: Trophic level, successional age and trait matching determine specialization of deadwood-based interaction networks of saproxylic beetles
The specialization of ecological networks provides important insights into possible consequences of biodiversity loss for ecosystem functioning. However, mostly mutualistic and antagonistic interactions of living organisms have been studied, whereas detritivore networks and their successional changes are largely unexplored. We studied the interactions of saproxylic (deadwood-dependent) beetles with their dead host trees. In a large-scale experiment, 764 logs of 13 tree species were exposed to analyse network structure of three trophic groups of saproxylic beetles over 3 successional years. We found remarkably high specialization of deadwood-feeding xylophages and lower specialization of fungivorous and predatory species. During deadwood succession, community composition, network specialization and network robustness changed differently for the functional groups. To reveal potential drivers of network specialization, we linked species' functional traits to their network roles, and tested for trait matching between plant (i.e. chemical compounds) and beetle (i.e. body size) traits. We found that both plant and animal traits are major drivers of species specialization, and that trait matching can be more important in explaining interactions than neutral processes reflecting species abundance distributions. High network specialization in the early successional stage and decreasing network robustness during succession indicate vulnerability of detritivore networks to reduced tree species diversity and beetle extinctions, with unknown consequences for wood decomposition and nutrient cycling.
Fig. 1 in The Saproxylic Beetle Corticaria bella Redtenbacher, 1847 (Coleoptera: Cucujoidea: Latridiidae) in Europe: Distribution and Habitats
Fig. 1. Corticaria bella, habitus. Body length:
Fig. 2. Corticaria bella, aedeagus. A in The Saproxylic Beetle Corticaria bella Redtenbacher, 1847 (Coleoptera: Cucujoidea: Latridiidae) in Europe: Distribution and Habitats
Fig. 2. Corticaria bella, aedeagus. A) Ventral view, B) Lateral view. Drawing by W. H. Rücker.
Figures 24-35 from: Bonacci T, Mazzei A, Horak J, Brandmayr P (2012) Cucujus tulliae sp. n. – an endemic Mediterranean saproxylic beetle from genus Cucujus Fabricius, 1775 (Coleoptera, Cucujidae), and keys for identification of adults and larvae native to Europe. ZooKeys 212: 63-79. https://doi.org/10.3897/zookeys.212.3254
Figures 24-35 - The three European Cucujus species, larvae. 24–27 Cucujus cinnaberinus 24 Head, dorsal view 25 Head, ventral view 26 Tergum IX and urogomphi, dorsal view 27 Tergum IX and urogomphi, ventral view 28–31 Cucujus haematodes 28 Head, dorsal view 29 Head, ventral view 30 Tergum IX and urogomphi, dorsal view 31 Tergum IX and urogomphi, ventral view 32–35 Cucujus tulliae 32 Head, dorsal view 33 Head, ventral view 34 Tergum IX and urogomphi, dorsal view 35 Tergum IX and urogomphi, ventral view.
Figure 23 from: Bonacci T, Mazzei A, Horak J, Brandmayr P (2012) Cucujus tulliae sp. n. – an endemic Mediterranean saproxylic beetle from genus Cucujus Fabricius, 1775 (Coleoptera, Cucujidae), and keys for identification of adults and larvae native to Europe. ZooKeys 212: 63-79. https://doi.org/10.3897/zookeys.212.3254
Figure 23 - Cucujus haematodes caucasicus stat. nov.: dorsal view of male specimen. Locality: Kaukasus, N. W. – Kuban – lg. C. Rost, Berlin.
Figures 13-22 from: Bonacci T, Mazzei A, Horak J, Brandmayr P (2012) Cucujus tulliae sp. n. – an endemic Mediterranean saproxylic beetle from genus Cucujus Fabricius, 1775 (Coleoptera, Cucujidae), and keys for identification of adults and larvae native to Europe. ZooKeys 212: 63-79. https://doi.org/10.3897/zookeys.212.3254
Figures 13-22 - Male genitalia of four Cucujus species/subspecies. 13–15 Cucujus cinnaberinus (Sila N. Park) 13 Median lobe and median strut with flagellum, dorsal view 14 Median lobe 15 flagellum "ball" inside the endophallus 16–18 Cucujus haematodes (Sila N. Park) 16 Median lobe and median strut with flagellum, dorsal view 17 Median lobe 18 Abdominal end of flagellum, with the basal part of the endophallus and genital duct 19–20 Cucujus tulliae (Sila N. Park) 19 Median lobe and median strut with flagellum removed 20 Median lobe 21–22 Cucujus caucasicus ("Caucasus") 21 Median lobe and median strut with flagellum, dorsal view 22 Median lobe.
Figures 1-12 from: Bonacci T, Mazzei A, Horak J, Brandmayr P (2012) Cucujus tulliae sp. n. – an endemic Mediterranean saproxylic beetle from genus Cucujus Fabricius, 1775 (Coleoptera, Cucujidae), and keys for identification of adults and larvae native to Europe. ZooKeys 212: 63-79. https://doi.org/10.3897/zookeys.212.3254
Figures 1-12 - The three European Cucujus species, adults. 1–4 Cucujus cinnaberinus 1 Total body, dorsal view 2 Head 3 Pronotum 4 Prosternal apophysis 5–8 Cucujus haematodes 5 Total body, dorsal view 6 Head 7 Pronotum 8 Prosternal apophysis 9–12 Cucujus tulliae 9 Total body, dorsal view 10 Head 11 Pronotum 12 Prosternal apophysis.
Figures 36-44 from: Bonacci T, Mazzei A, Horak J, Brandmayr P (2012) Cucujus tulliae sp. n. – an endemic Mediterranean saproxylic beetle from genus Cucujus Fabricius, 1775 (Coleoptera, Cucujidae), and keys for identification of adults and larvae native to Europe. ZooKeys 212: 63-79. https://doi.org/10.3897/zookeys.212.3254
Figures 36-44 - The three European Cucujus species, larvae. 36–38 Cucujus cinnaberinus 36 Urogomphi, lateral view and conical appendage (black arrow) 36 Conical appendage 38 Lateral end of tergum IX, sclerotized thorn 39–41 Cucujus haematodes 39 Urogomphi, lateral view and conical appendage (white arrow) 40 Conical appendage 41 Lateral end of tergum IX, sclerotized thorn 42–44 Cucujus tulliae 42 Urogomphi, lateral view and conical appendage (black arrow) 43 Conical appendage 44 Lateral end of tergum IX, sclerotized thorn.
Data from: Forest age is a primary trait filter for saproxylic beetles in the southeastern United States
<p>Data from: Forest age is a primary trait filter for saproxylic beetles in the southeastern United States</p> <p>Clayton R. Traylor, Michael D. Ulyshen, Joseph V. McHugh, Ryan C. Burner</p> <p>Forest Ecology and Management 553: 121545. </p> <p><a title="Persistent link using digital object identifier" href="https://doi.org/10.1016/j.foreco.2023.121545" target="_blank" rel="noreferrer noopener"><span>https://doi.org/10.1016/j.foreco.2023.121545</span></a> </p> <p> </p> <p>Corresponding author: Clayton R. Traylor, <a href="mailto:clayton.r.traylor@gmail.com">clayton.r.traylor@gmail.com</a></p> <p> </p> <p> </p> <p><strong>Abstract</strong></p> <p>Many forests throughout the world consist of regenerating mature stands. Although these forests differ in many respects from old-growth (with a history of minimal human disturbance), they typically develop similar structural attributes over time. As a result, older mature forests may be of particular conservation value if they contain resources and microhabitats benefitting saproxylic (deadwood dependent) species. Species' response to forest age may be driven by traits that relate to ecological functions or habitat preferences, such that species with less compatible traits for a local forest environment are "filtered" out. Thus, forest age may influence species' distributions and the trait composition of assembled communities. </p> <p>The Piedmont region of the southeastern United States has experienced widespread forest regrowth over the past century due to agricultural abandonment. Today's landscapes are largely characterized by mature forests that are becoming increasingly fragmented by suburbanization. Here, we assessed the filtering effects of forest age, landscape forest cover (LFC), and deadwood volume on saproxylic beetles in northeastern Georgia. Using historic aerial imagery to distinguish forest age (young = regrown after 1938; old = mature in 1938), we sampled beetles in mature forests of both age classes occurring along an LFC gradient. We measured five traits with hypothesized functional roles (body length, body width, body roundness, antenna length, eye length) for the 472 species captured. Using a joint species distribution model (JSDM), we tested trait-niche relationships (i.e., how traits influence species' responses) and estimated community trait composition (mean and dispersion of trait values) along gradients of environmental filters.</p> <p>We found that forest age is a filter for several traits (six supported relationships with >95% posterior probability), but LFC and deadwood volume were less strongly related to fewer traits. Most notably, large species (typically having lower population sizes and requiring stable larval habitat) were filtered from young mature forests and low LFC. Thus, old mature forests with high LFC showed higher mean and dispersion of beetle body length. Sensory traits also showed responses, likely reflecting adult life under bark (eye length) or ability to detect resources or mates (antenna length). Body width and roundness showed inconsistent responses with regard to indicated functional roles. Our results show that forest age is a strong filter on saproxylic beetle communities in the southeastern United States. Old mature forests, despite their scarcity in the region, are important for species requiring habitat stability and for maintaining communities with diverse trait composition.</p> <p> </p>
Data from: Fine-scale vertical stratification and guild composition of saproxylic beetles in lowland and montane forests: similar patterns despite low faunal overlap
Open the record for dataset details and reuse information.
Data from: Trophic level, successional age and trait matching determine specialization of deadwood-based interaction networks of saproxylic beetles
Open the record for dataset details and reuse information.
Appendix 1 in Saproxylic beetle (Coleoptera) communities and forest management practices in coniferous stands in southwest Nova Scotia, Canada
Appendix 1. Species, trophic categories, and numbers of Coleoptera collected
Figure 1 in Saproxylic beetles (Coleoptera) and hoverflies (Diptera: Syrphidae) from a Mediterranean forest: towards a better understanding of their biology for species conservation
Figure 1. Biogeographical composition of the beetle and hoverfly saproxylic community of Cabañeros National Park, Spain. Species % is the percentage of beetles or hoverflies identified in Cabañeros known to inhabit each biogeographical region. The number of species is specified in square brackets. Abbreviations: NA, North Africa; CM, Central Mediterranean region; EM, Eastern Mediterranean region; CE, Central Europe; EE, Eastern Europe and Western Siberia; NE, Near East.
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