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Rosalia: An experimental research site to study hydrological processes in a forest catchment - data repository
<p>This repository is a supplement to the paper <strong>Fürst, J., et al. (2021). “Rosalia: an experimental research site to study hydrological processes in a forest catchment.” Earth Syst. Sci. Data 13(8): 4019-4034.</strong></p> <p>Experimental watersheds have a long tradition as research sites in hydrology and have been used as far back as the late 19<sup>th</sup> and early 20<sup>th</sup> century. The University of Natural Resources and Life Sciences Vienna (BOKU) has been operating the experimental research forest site called “Rosalia” with an area of 950 ha since 1875 to support and facilitate research and education. Recently, BOKU researchers from various disciplines extended the “Rosalia” instrumentation towards a full ecological-hydrological experimental watershed. The overall objective is to implement a multi-scale, multi-disciplinary observation system that facilitates the study of water, energy and solute transport processes in the soil-plant-atmosphere continuum.</p> <p>This repository contains the datasets collected by a monitoring network of 4 discharge gauging stations, 7 rain-gauges, together with observations of air and water temperature, relative humidity and conductivity. In four profiles, soil water content and temperature are recorded in different depths. In 2019, additionally a program to collect isotopic data in precipitation and discharge was started. On one site, also Nitrate, TOC and turbidity are monitored. All data collected since 2015, including in total 56 high resolution time series data (10 min sampling interval), are provided to the scientific community.</p>
Fig. 1 in New population of Rosalia longicorn, Rosalia alpina, in Calabria (southern Italy) (Coleoptera: Cerambycidae)
Fig. 1 – Green areas: National Parks where Rosalia alpina is present; dotted blue line: Catena Costiera as an ecological corridor; red star: discovery point of the new population of R. alpina. Fig. 2 – SCI-SAC present in the study area (Image reworked from the maps downloadable from: http://retenatura2000. regione.calabria.it/).
Fig. 3 in New population of Rosalia longicorn, Rosalia alpina, in Calabria (southern Italy) (Coleoptera: Cerambycidae)
Fig. 3 – Individual of Rosalia alpina photographed on a rotting beech trunk on the ground covered with moss into the new Calabrian site.
Рис. 1. ЧешуекрыΛые, обнаруженные в Амурской обΛасти: внешний виΑ гусеницы посΛеΑнего возраста (A) и имаго (B–O): A — Sphecodina caudata; B — Mirina christophi, самец; C — Paracolax fentoni, самка; D — Pangrapta costaemacula, самка; E — P. suaveola, самец; F — Araeopteron amoena, самец; G — Sinocharis korbae, самец; H — Nacna malachitis, самец; I — Sarbanissa venusta, самец; J — Plusilla rosalia, самец; K — Xylopolia bellula, самец; L — Xestia efflorescens, самец; M — Orthosia satoi, самец; N, O — O. ariuna (N — самец, O — самка). Места сбора: A, F, H, J, N, O — окрестности БΛаговещенска; B, G, L — Архаринский район, окрестности станции Тарманчукан; C, M — окрестности станции Рачи; D, E, I – окрестности с. Грибовка; K — БΛаговещенский район, окрестности с. Новопетровка. Масштабная Λинейка 5 мм Fig. 1. Lepidoptera species from Amur Oblast: habitus of last instar larva (A) and adult (B–O): A — Sphecodina caudata; B — Mirina christophi, male; C — Paracolax fentoni, female; D — Pangrapta costaemacula, female; E — P. suaveola, male; F — Araeopteron amoena, male; G — Sinocharis korbae, male; H — Nacna malachitis, male; I — Sarbanissa venusta, male; J — Plusilla rosalia, male; K — Xylopolia bellula, male; L — Xestia efflorescens, male; M —Orthosia satoi, male; N, O — O. ariuna (N — male, O — female). Localities: A, F, H, J, N, O — environs of Blagoveshchensk; B, G, L — Arkhara District, vicinity of Tarmanchukan; C, M — vicinity of Rachi; D, E, I — vicinity of Gribovka; K — Blagoveshchensk District, vicinity of Novopetrovka. Scale bar 5 mm in New species of moths (Lepidoptera, Macroheterocera) in the fauna of Amur Oblast, Russian Far East
Рис. 1. ЧешуекрыΛые, обнаруженные в Амурской обΛасти: внешний виΑ гусеницы посΛеΑнего возраста (A) и имаго (B–O): A — Sphecodina caudata; B — Mirina christophi, самец; C — Paracolax fentoni, самка; D — Pangrapta costaemacula, самка; E — P. suaveola, самец; F — Araeopteron amoena, самец; G — Sinocharis korbae, самец; H — Nacna malachitis, самец; I — Sarbanissa venusta, самец; J — Plusilla rosalia, самец; K — Xylopolia bellula, самец; L — Xestia efflorescens, самец; M — Orthosia satoi, самец; N, O — O. ariuna (N — самец, O — самка). Места сбора: A, F, H, J, N, O — окрестности БΛаговещенска; B, G, L — Архаринский район, окрестности станции Тарманчукан; C, M — окрестности станции Рачи; D, E, I – окрестности с. Грибовка; K — БΛаговещенский район, окрестности с. Новопетровка. Масштабная Λинейка 5 мм Fig. 1. Lepidoptera species from Amur Oblast: habitus of last instar larva (A) and adult (B–O): A — Sphecodina caudata; B — Mirina christophi, male; C — Paracolax fentoni, female; D — Pangrapta costaemacula, female; E — P. suaveola, male; F — Araeopteron amoena, male; G — Sinocharis korbae, male; H — Nacna malachitis, male; I — Sarbanissa venusta, male; J — Plusilla rosalia, male; K — Xylopolia bellula, male; L — Xestia efflorescens, male; M —Orthosia satoi, male; N, O — O. ariuna (N — male, O — female). Localities: A, F, H, J, N, O — environs of Blagoveshchensk; B, G, L — Arkhara District, vicinity of Tarmanchukan; C, M — vicinity of Rachi; D, E, I — vicinity of Gribovka; K — Blagoveshchensk District, vicinity of Novopetrovka. Scale bar 5 mm
Un des individus de Rosalia alpina découverts sur un tronc de hêtre mort sur pied lors de l'excursion de juillet au-dessus de Fully. (Photo Pierre Bornand) in Groupe Entomologique De La Murithienne (VS)
Un des individus de Rosalia alpina découverts sur un tronc de hêtre mort sur pied lors de l'excursion de juillet au-dessus de Fully. (Photo Pierre Bornand)
Un mâle (Fig. 1a) et une femelle ont ainsi été capturés au moyen de deux pièges d'interception (selon le modèle de Brustel 2012). Le premier piège était suspendu sur un chêne mort sur pied dans une chênaie thermophile de plaine, à une altitude de 499 m (Fig. 1b). Outre cette découverte, ce piège a permis de mettre en évidence d'autres espèces rares telles Clytus tropicus (Panzer, 1795) (Cerambycidae) et Camptorhinus simplex Seidlitz, 1867 (Curculionidae). Le second piège, situé à près de 5 km du premier, était placé sur un hêtre mort sur pied à 869 m d'altitude. Cet arbre était notamment colonisé par Rosalia alpina (Linnaeus, 1758) (Cerambycidae). Ce second piège a permis de capturer en outre plusieurs spécimens de Stictoleptura scutellata (Fabricius, 1781) (Cerambycidae) et un de Mesosa curculionoides (Linnaeus, 1760) (Cerambycidae), deux espèces rares. À noter toutefois que de nombreux chênes étaient présents à proximité de ce hêtre. Malgré le long intervalle entre les deux relevés, l'excellent état de conservation des deux spécimens capturés laisse supposer une date tardive de capture (plutôt en novembre qu'en septembre ou octobre). in Tetratoma desmarestii Latreille, 1807, un Tetratomidae nouveau pour la faune de Suisse (Coleoptera)
Un mâle (Fig. 1a) et une femelle ont ainsi été capturés au moyen de deux pièges d'interception (selon le modèle de Brustel 2012). Le premier piège était suspendu sur un chêne mort sur pied dans une chênaie thermophile de plaine, à une altitude de 499 m (Fig. 1b). Outre cette découverte, ce piège a permis de mettre en évidence d'autres espèces rares telles Clytus tropicus (Panzer, 1795) (Cerambycidae) et Camptorhinus simplex Seidlitz, 1867 (Curculionidae). Le second piège, situé à près de 5 km du premier, était placé sur un hêtre mort sur pied à 869 m d'altitude. Cet arbre était notamment colonisé par Rosalia alpina (Linnaeus, 1758) (Cerambycidae). Ce second piège a permis de capturer en outre plusieurs spécimens de Stictoleptura scutellata (Fabricius, 1781) (Cerambycidae) et un de Mesosa curculionoides (Linnaeus, 1760) (Cerambycidae), deux espèces rares. À noter toutefois que de nombreux chênes étaient présents à proximité de ce hêtre. Malgré le long intervalle entre les deux relevés, l'excellent état de conservation des deux spécimens capturés laisse supposer une date tardive de capture (plutôt en novembre qu'en septembre ou octobre).
Supplementary Material for publication "Bifidobacteria Define Gut Microbiome Profiles of Golden Lion Tamarin (Leontopithecus rosalia} and Marmoset Callithrix sp. Metagenomic Shotgun Pools
<p>Supplementary Tables and Figure for the publication "Bifidobacteria Define Gut Microbiome Profiles of Golden Lion Tamarin <em>Leontopithecus rosalia</em> and Marmoset <em>Callithrix</em> sp. Metagenomic Shotgun Pools"</p>
Abb. 2 in Der Alpenbockkäfer Rosalia alpina (L.) (Coleoptera: Cerambycidae) im Steirischen Salzkammergut (Österreich)
Abb. 2: Fundorte und Lebensraumflächen von Rosalia alpina.
Abb. 1 in Der Alpenbockkäfer Rosalia alpina (L.) (Coleoptera: Cerambycidae) im Steirischen Salzkammergut (Österreich)
Abb. 1: Übersicht zur Lage der Untersuchungsflächen.
Hl. Rosalia
Figure of St. Rosalia on the grounds of the parish church of Maria-Lanzendorf. Source: Objaverse 1.0 / Sketchfab
On following pages: 473. Senegal Striped Grass Mouse (Lemniscomys linulus); 474. Mittendorf's Striped Grass Mouse (Lemniscomys mittendorfi); 475. Hoogstraal's Striped Grass Mouse (Lemniscomys hoogstraali), 476. Buffoon Striped Grass Mouse (Lemniscomys macculus); 477. Griselda Striped Grass Mouse (Lemniscomys griselda); 478. Single-striped Grass Mouse (Lemniscomys rosalia); 479. Rosevear's Striped Grass Mouse (Lemniscomys roseveari); 480. West African Rufous-nosed Rat (Oenomys ornatus); 481. Common Rufous-nosed Rat (Oenomys hypoxanthus); 482. East African Groove-toothed Swamp Rat (Pelomys fallax); 483. Hopkins's Groove-toothed Swamp Rat (Pelomys hopkinsi); 484. Lake Victoria Groove-toothed Swamp Rat (Pelomys isseli); 485. Angolan Groove-toothed Swamp Rat (Pelomys campanae); 486. Least Groove-toothed Swamp Rat (Pelomys minor); 487. Target Rat (Stochomys longicaudatus); 488. Kemp's Thicket Rat (Thamnomys kempi); 489. Hatt's Thicket Rat (Thamnomys majon; 490. Schouteden's Thicket Rat (Thamnomys schoutedeni); 491. Thomas's Thicket Rat (Thamnomys venustus); 492. Namaqua Rock Rat (Micaelamys namaquensis); 493. Grant's Rock Rat (Micaelamys granti); 494. Mesic Four-striped Grass Rat (Rhabdomys dilectus); 495. West-Central South African Fourstriped Grass Rat (Rhabdomys bechuanae); 496. KwaZulu Natal Four-striped Grass Rat (Rhabdomys chakae); 497. Karoo Four-striped Grass Rat (Rhabdomys intermedius); 498. Xeric Four-striped Grass Rat (Rhabdomys pumilio), 499. Loring's Thallomys (Thallomys loringi); 500. Black-tailed Thallomys (Thallomys nigricauda); 501. Sundevall's Thallomys (Thallomys paedulcus); 502. Shortridge's Thallomys (Thallomys shortridgei). in Muridae
On following pages: 473. Senegal Striped Grass Mouse (Lemniscomys linulus); 474. Mittendorf's Striped Grass Mouse (Lemniscomys mittendorfi); 475. Hoogstraal's Striped Grass Mouse (Lemniscomys hoogstraali), 476. Buffoon Striped Grass Mouse (Lemniscomys macculus); 477. Griselda Striped Grass Mouse (Lemniscomys griselda); 478. Single-striped Grass Mouse (Lemniscomys rosalia); 479. Rosevear's Striped Grass Mouse (Lemniscomys roseveari); 480. West African Rufous-nosed Rat (Oenomys ornatus); 481. Common Rufous-nosed Rat (Oenomys hypoxanthus); 482. East African Groove-toothed Swamp Rat (Pelomys fallax); 483. Hopkins's Groove-toothed Swamp Rat (Pelomys hopkinsi); 484. Lake Victoria Groove-toothed Swamp Rat (Pelomys isseli); 485. Angolan Groove-toothed Swamp Rat (Pelomys campanae); 486. Least Groove-toothed Swamp Rat (Pelomys minor); 487. Target Rat (Stochomys longicaudatus); 488. Kemp's Thicket Rat (Thamnomys kempi); 489. Hatt's Thicket Rat (Thamnomys majon; 490. Schouteden's Thicket Rat (Thamnomys schoutedeni); 491. Thomas's Thicket Rat (Thamnomys venustus); 492. Namaqua Rock Rat (Micaelamys namaquensis); 493. Grant's Rock Rat (Micaelamys granti); 494. Mesic Four-striped Grass Rat (Rhabdomys dilectus); 495. West-Central South African Fourstriped Grass Rat (Rhabdomys bechuanae); 496. KwaZulu Natal Four-striped Grass Rat (Rhabdomys chakae); 497. Karoo Four-striped Grass Rat (Rhabdomys intermedius); 498. Xeric Four-striped Grass Rat (Rhabdomys pumilio), 499. Loring's Thallomys (Thallomys loringi); 500. Black-tailed Thallomys (Thallomys nigricauda); 501. Sundevall's Thallomys (Thallomys paedulcus); 502. Shortridge's Thallomys (Thallomys shortridgei).
Hl. Rosalia
Statue of Saint Rosalia from the end of the 17th century next to the staircase to the parish church of St. James the Elder in Falkenstein. She is depicted with open hair, cross and skull. St. Rosalia was a virgin and hermit on Monte Pellegrino. She is venerated as a saint in the Roman Catholic Church. Source: Objaverse 1.0 / Sketchfab
Abb. 5 in Der Alpenbockkäfer Rosalia alpina (L.) (Coleoptera: Cerambycidae) im Steirischen Salzkammergut (Österreich)
Abb. 5: Mehrere Exemplare des Alpenbockkäfers konnten am 16.8.2016 nördlich des Altausseer Sees an diesen vier bewusst exponierten Totholzstrukturen, die unberindet und mit Trockenrissen versehen sind, beobachtet werden. Fotos: S. Aurenhammer.
Abb. 4 in Der Alpenbockkäfer Rosalia alpina (L.) (Coleoptera: Cerambycidae) im Steirischen Salzkammergut (Österreich)
Abb. 4: Die vitalste Population lebt nordwestlich des Altausseer Sees, vom Nordufer über die Seewiese bis zum Steinfeld. Der Lebensraum ist südorientiert, fels- und blockdurchsetzt, laubholzdominiert und lückig. Foto: S. Aurenhammer.
Data from: Revisiting Santa Rosalia to unfold a degeneracy of classic models of speciation
Many classic models of speciation incorporate assortative mating based on mating groups, such as plants with different flowering times, and they investigate whether an ecological trait under disruptive natural selection becomes genetically associated with the selectively neutral mating trait. It is well known that this genetic association is potently destroyed by recombination. In this note, we point out a more fundamental difficulty: if a "knife-edge" symmetry assumption of previous models is violated, then the mating trait is no longer neutral and sexual selection eliminates the polymorphism in the mating locus. This result strengthens the growing consensus that magic traits are the more likely route to nonallopatric speciation. We expand the model assuming also ecological selection on the mating trait and investigate the conditions for natural selection to overcome sexual selection and maintain mating polymorphism; we find that the combination of natural and sexual selection can cause also bistability of allele frequencies.
Supplementary material 1 from: Campanaro A, Redolfi De Zan L, Hardersen S, Antonini G, Chiari S, Cini A, Mancini E, Mosconi F, Rossi de Gasperis S, Solano E, Bologna MA, Sabbatini Peverieri G (2017) Guidelines for the monitoring of Rosalia alpina. 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: 165-203. https://doi.org/10.3897/natureconservation.20.12728
Monitoring of Rosalia alpina – field sheet : Data type: Field sheet
Abb. 1 in Erfolgreiche Larvalentwicklung des Alpenbocks Rosalia alpina (L.,1758) (Coleoptera: Cerambycidae) in einem Buchenholzast von 66 cm Länge
Abb. 1. In diesem Holzstück haben sich zwei Larven des Alpenbocks Rosalia alpina erfolgreich entwickelt.
Data from: Revisiting Santa Rosalia to unfold a degeneracy of classic models of speciation
Open the record for dataset details and reuse information.
Abb. 3 in Der Alpenbockkäfer Rosalia alpina (L.) (Coleoptera: Cerambycidae) im Steirischen Salzkammergut (Österreich)
Abb. 3: Rosalia alpina. Foto: W.E. Holzinger.
Rosalia Times Series Database
<p><strong>Rosalia Times Series Database</strong></p> <p>The BOKU (University of Natural Resources and Life Sciences Vienna) university demonstration forest Rosalia with an area of 950 ha has been used for research and education since 1875. In 2013 – upon an initiative of a group of researchers in various disciplines – it was decided to extend the so far mainly forestry oriented activities by implementing a hydrological experimental research watershed. The overall objective is to collect data that support the study of transport processes in the system of soil, water, plants and atmosphere. More specifically, emphasis is on bridging the gap between point related measurements and effective values and parameters required for modelling flow and transport processes in watersheds.</p> <p>2 Objectives</p> <p>The main objectives for the research watershed are</p> <ul> <li>to collect data that support the study of transport processes in the system of soil, water, plants and atmosphere</li> <li>emphasis is on bridging the gap between point related measurements and effective values and parameters for modelling watersheds of various sizes</li> <li>to generate comprehensive reference information for research projects on future management and climate change impacts</li> </ul> <p>Operation is planned for a period of at least 10 years using only internal resources of the university, to avoid potential interruptions due to project-based short-term availability of personal and financial resources.</p> <p>The objective of this article is to present the research watershed, the data collected and to make these data accessible to the research community.</p> <p> </p> <p> </p>
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