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135 results for “functional strategy”
Supporting Material for "Enhancing Mental Health and Cognitive Function in Older Adults: A Swiss Perspective on Public Health Interventions and Stigma Mitigation Strategies Informed by a Desk Review"
<p>This dataset contains all supporting material for the paper "Enhancing Mental Health and Cognitive Function in Older Adults: A Swiss Perspective on Public Health Interventions and Stigma Mitigation Strategies Informed by a Desk Review", published in the journal Swiss Psychology Open:</p> <p><em>Mack, M., Scarampi, C., Joly-Burra, E., Zuber, S., de Freitas, C., Teixeira, R. and Kliegel, M. (2025) ‘Enhancing Mental Health and Cognitive Function in Older Adults: A Swiss Perspective on Public Health Interventions and Stigma Mitigation Strategies Informed by a Desk Review’, Swiss Psychology Open, 5(1), p. 2. Available at: <a href="https://doi.org/10.5334/spo.81.">https://doi.org/10.5334/spo.81</a>.</em></p> <p>It includes the following documents and files:</p> <p><strong>S1. Protocol:</strong> ADVANCE Protocol for desk reviews</p> <p><strong>S2. Search strategy</strong></p> <p><strong>S3. Guidelines for title and abstract screening:</strong> Guidelines for the selection of articles included in the desk review</p> <p><strong>S4. Guidelines full-text screening:</strong> Guidelines for the selection of articles included in the desk review</p> <p><strong>S5. Guidelines data extraction:</strong> ADVANCE Guidelines/codebook data extraction</p> <p><strong>data extraction_desk review_switzerland.xlsx</strong></p> <p>This desk review was conducted as part of the ADVANCE project, which aims to enhance our understanding of mental health promotion and prevention. This desk review evaluates the current state of interventions for mental health and cognitive functioning among older adults in Switzerland focusing on the features of these interventions as well as on Swiss-specific contextual factors that contribute to vulnerability and stigma. This results of the desk review has been submitted for publication to 'LIVES Working Papers' and 'Swiss Psychology Open' . The two versions of the desk review differ slightly. The version for LIVES Working Papers, included the results of the Delphi survey and the resulting intervention scenarios. The version for Swiss Psychology Open, did not include the Delphi survey results and the resulting intervention scenarios, but included a more detailed discussion of the review results.</p>
Data for: The function of stilt roots in the growth strategy of Socratea exorrhiza (Arecaceae) at two neotropical sites
<p>We provide the raw and processed data used in the following study: Goldsmith, G. R., & Zahawi, R. A. (2007). The function of stilt roots in the growth strategy of Socratea exorrhiza (Arecaceae) at two neotropical sites. <em>Revista de Biología Tropical</em>, <em>55</em>(3-4), 787-793.</p> <p><strong>Methods</strong> can be found in the file entitled "README-GoldsmithZahawi-SocrateaData-5Mar23F.txt," while metadata for data columns can be found in the file entitled: "GoldsmithZahawi-SocrateaMetaData-5March2023.csv."</p> <p><strong>Original Published Abstract</strong>: Arboreal palms have developed a variety of structural root modifications and systems to adapt to the<br> harsh abiotic conditions of tropical rain forests. Stilt roots have been proposed to serve a number of functions<br> including the facilitation of rapid vertical growth to the canopy and enhanced mechanical stability. To examine<br> whether stilt roots provide these functions, we compared stilt root characteristics of the neotropical palm tree<br> Socratea exorrhiza on sloped (>20º) and flat locations at two lowland neotropical sites. S. exorrhiza (n=80 trees)<br> did not demonstrate differences in number of roots, vertical stilt root height, root cone circumference, root cone<br> volume, or location of roots as related to slope. However, we found positive relationships between allocation<br> to vertical growth and stilt root architecture including root cone circumference, number of roots, and root cone<br> volume. Accordingly, stilt roots may allow S. exorrhiza to increase height and maintain mechanical stability<br> without having to concurrently invest in increased stem diameter and underground root structure. This strategy<br> likely increases the species ability to rapidly exploit light gaps as compared to non-stilt root palms and may also<br> enhance survival as mature trees approach the theoretical limits of their mechanical stability.</p>
Assessing the vulnerability of plant functional trait strategies to climate change
<p><strong><span>Aim: </span></strong><span>Our ability to understand how species may respond to changing climate conditions is hampered by a lack of high-quality data on the adaptive capacity of species. Plant functional traits are linked to many aspects of species life history and adaptation to environment, with different combinations of trait values reflecting alternate strategies for adapting to varied conditions. If the realised climate limits of species can be partially explained by plant functional trait combinations, then a new approach of using trait combinations to predict the expected climate limits of species trait combinations may offer considerable benefits. </span></p> <p><strong><span>Location:</span></strong><span> Australia.</span></p> <p><span><strong>Time period:</strong> </span><span>Current and future. </span></p> <p><strong><span>Methods:</span></strong><span><strong> </strong>Using trait data for leaf size, seed mass and plant height for 6,747 Australian native species from 27 plant families, we model the expected climate limits of trait combinations and use future climate scenarios to estimate climate change impacts based on plant functional trait strategies. </span></p> <p><strong><span>Results:</span></strong><span><strong> </strong>Functional trait combinations were a significant predictor of species climate niche metrics with potentially meaningful relationships with two rainfall variables (R<sup>2</sup> = 0.36 & 0.45) and three temperature variables (R<sup>2</sup> = 0.21, 0.28, 0.30). Using this method, the proportion of species exposed to conditions across their range that are beyond the expected climate limits of their trait strategies will increase under climate change. </span></p> <p><strong><span>Main conclusions:</span></strong><span><strong> </strong>Our new approach, called Trait Strategy Vulnerability, includes three new metrics. For example, the Climate Change Vulnerability (CCV) metric identified a small but important proportion of species (4.3%) that will on average be exposed to conditions beyond their expected limits for summer temperature in the future. These potentially vulnerable species could be high priority targets for deeper assessment of adaptive capacity at the genomic or physiological level. Our methods can be applied to any suite of co-occurring plants globally.</span></p>
Measuring platelet function: new strategies for precision medicine to prevent thrombosis - Prof Jon Gibbins (University of Reading)
<p>This video is the third talk from our two day Future Blood Testing: Challenges & Opportunities Event that took place on the 13/09/2022.</p> <p>Measuring platelet function: new strategies for precision medicine to prevent thrombosis - Prof Jon Gibbins (University of Reading).</p> <p>Bio: Jon Gibbins is Professor of Cell Biology within the School of Biological Sciences at the University and is Director of the Institute for Cardiovascular and Metabolic Research. He is a graduate of the University, obtaining a degree in Pathobiology with Chemistry in 1991 and a PhD in Molecular Endocrinology in 1995. Following a period of postdoctoral research at the Oxford University, he returned to Reading in 1998 as a lecturer. Jon has established an internationally leading research group that studies blood clotting, with a particular focus on the development of more effective clinical strategies for the prevention and treatment of heart attacks and strokes, and thrombosis associated with infection. Jon values greatly working in an active, engaging and successful school, in which all aspects of biology are represented, and he champions cross-disciplinary working to approach today’s most challenging and pressing questions in new ways. He believes strongly in widening participation and improving levels of equity, diversity and inclusion across our institution.</p> <p>Further details on this event can be found at: https://futurebloodtesting.org/event/13-14-09-2022/</p> <p>This video is an output from the Future Blood Testing Network which is funded by EPSRC under Grant Number EP/W000652/1</p> <p>YouTube Link: https://youtu.be/8vJZ_WO-dvk</p>
Fig. 3 in Life strategies and function of dissepiments in rugose coral Catactotoechus instabilis from the Lower Devonian of Morocco
Fig. 3. Schematic drawing of constriction and rejuvenescence phenomena showing their axial and lateral types.
Fig. 7 in Life strategies and function of dissepiments in rugose coral Catactotoechus instabilis from the Lower Devonian of Morocco
Fig. 7. Successive transversal sections showing development of lonsdaleoid dissepiments in two corallites of rugose coral Catactotoechus instabilis Berkowski, 2008, Hamar Laghdad (Morocco), Emsian. A. Specimen UAM Tc/B HD3/200; A1, juvenile stage of growth showing interaction with auloporoid coral; note dissepiment on this side; A2, next stage showing one row of lonsdaleoid dissepiment−extension phase of growth; A3, mature stage of growth showing increase in development of dissepiments in constriction phase of growth; note that diameter of central lumen (aulos) is narrowed. B. Specimen UAM Tc/B HD3/201; B1, constriction phase of growth showing irregular lonsdaleoid dissepiments narrowing septal area; note invaginations of dissepiment in places where septal crests are formed; B2, extension phase of growth showing decrease of lonsdaleoid dissepimentarium and expansion of septal area.
Fig. 6 in Life strategies and function of dissepiments in rugose coral Catactotoechus instabilis from the Lower Devonian of Morocco
Fig. 6. Schematic drawing showing successive stages of formation of lonsdaleoid dissepiments. A–D. Smaller dissepiment created between septal pockets. E–H. Larger dissepiment created in place with septal pocket, disrupting septal growth. Note hydrostatic pressure (HP) between basal ectoderm and skeletal structures is here responsible for the pushing up the ectoderm and shaping the dissepiment. Morphological nomenclature refers to all figures (A–H).
Fig. 5 in Life strategies and function of dissepiments in rugose coral Catactotoechus instabilis from the Lower Devonian of Morocco
Fig. 5. Well preserved calices of the rugose coral Catactotoechus instabilis Berkowski, 2008, Hamar Laghdad (Morocco), Emsian. A. Specimen UAM Tc/B HD3/217 showing inner calicular structures of extending calice after rejuvenescence; note well developed septa of both orders. B. Specimen UAM Tc/B HD3/212 showing increase of large lonsdaleoid dissepiments formation and simultaneous constriction and shifting of the septal apparatus; note large dissepiment covering previously formed septa. C. Specimen UAM Tc/B HD3/211 showing strong and abrupt constriction of the corallite; note that the wall of rejuvenated part of the corallite is surrounded by a new wall and dissepiments outside it are not fully developed.
Fig. 2 in Life strategies and function of dissepiments in rugose coral Catactotoechus instabilis from the Lower Devonian of Morocco
Fig. 2. External characters of the corallites of rugose coral Catactotoechus instabilis Berkowski, 2008, Hamar Laghdad (Morocco), Emsian. A. Specimen UAM Tc/B HD3/232 showing attachment to auloporid tabulate coral (below). B. Specimen UAM Tc/B {?}3/242 showing attachment to fragment of the crinoid stem. C. Specimen UAM Tc/B HD3/217 showing two corallites attached to each other, note expansion phase of growth after rejuvenescence in calicular part (above). D. Specimen UAM Tc/B HD3/238 showing weak constriction phase, note lack of attachment structures. E. Specimen UAM Tc/B HD3/237 showing successive constrictions and expansions during growth as well as deflection of growth direction in the juvenile stage; note lack of attachment structures. F. Specimen UAM Tc/B HD3/233 showing attached juvenile specimen on external wall near calice causing deflection of growth of calicular part of the corallite, note well developed attachment structure (talon). G. Specimen UAM Tc/B HD3/214 showing rejuvenescence and deflection of growth caused by settlement and growth of 3 juvenile specimens on the left part of calicular rim (competition).
Fig. 1. A in Life strategies and function of dissepiments in rugose coral Catactotoechus instabilis from the Lower Devonian of Morocco
Fig. 1. A. Simplified geologic map of northeastern Anti−Atlas, Devonian rocks and Hamar Laghdad are indicated. B. Outcrop marked by star in circle on southeastern slope of the mound 3 (view from the east). Separated lithologic units marked as roman numbers in squares: I, Saheb el Rhassel Group (Kess−Kess Formation); II, Amerboh Group (marly nodular limestone); III, Amerboh Group (marly shale with marly limestone intercalations); IV, Bou Tchrafine Group. C. Detailed geological map of Hamar Laghdad with distribution of particular types of Devonian rocks. Star in circle indicates outcrop, where studied corals were collected. Drawings A and C courtesy of Bełka (1998 and unpublished)—updated here.
Code Appendix: Do Seed Dispersal Strategies Reflect Adaptation to Environmental Variability? Functional Ecology, 2023
<p>This code appendix contains all of the R code and data for the manuscript:<br> <br> Van Den Elzen, C. L., N. Sigman, and N. C. Emery. 2023. Do Seed Dispersal Strategies Reflect Adaptation to Environmental Variability?. Functional Ecology (Manuscript ID: FE-2022-00850).<br> <br> Abstract: </p> <p>1. Dispersal is one of the primary mechanisms by which organisms adapt to spatial and temporal variation in the environment. Theory predicts that increasing spatiotemporal variation drives selection for offspring dispersal away from their natal habitat and one another. However, due to inherent difficulties in measuring dispersal in plant systems, there are few empirical tests of the extent to which this hypothesis can explain variation in seed dispersal strategies.</p> <p>2. In this study, we characterized and compared the dispersal patterns of three closely related plant species that segregate across gradients in spatiotemporal variation in seasonal wetlands.</p> <p>3. We tracked individual seeds as they dispersed in their natural habitats to measure seed dispersal distance (the distance traveled from the maternal plant) and inter-seed spread (distances between dispersed seeds), and to identify the plant traits causing within-species variation in seed dispersal. We also evaluated the seed traits causing within-species variation in seed flight distance and terminal velocity in a wind tunnel and a drop tube, respectively.</p> <p>4. We found that average seed dispersal distance was lowest in the species that occupies the most spatiotemporally variable habitat, contradicting our predictions; however, inter-seed spread was lowest in the species from the least variable habitat, which aligned with our expectations.</p> <p>5. The maternal plant and seed traits explaining intraspecific variation in seed dispersal varied among species as well as the method used to measure dispersal potential. Two traits had non-intuitive effects on dispersal, including pappus size, which reduced seed flight distance in two of the focal taxa.</p> <p>6. Overall, our results indicate that the differences we detected in seed dispersal among three closely related plant taxa can be only partially explained by current patterns of environmental variability in their respective habitats, and that the traits driving within species variation in seed dispersal can evolve rapidly and change with the environmental context in which they are measured.</p>
Effects of climate change on the distribution of plant species and plant functional strategies on the Canary Islands
<p>Occurrence data:</p> <p>We used occurrence data from the Banco de Datos de Biodiversidad de Canarias, an open-access database, for single-island endemic (SIE; n = 325), archipelago endemic (AE; n = 234) and definitely non-endemic native (NEN; n = 149) extant seed plant species (excluding subspecies), in a raster of 500 m x 500 m grid cells covering the Canary Islands (<a href="https://www.biodiversidadcanarias.es/biota/">https://www.biodiversidadcanarias.es/biota/</a>) [<em>accessed 14/03/2022</em>]. The database includes all species listed in the checklist of the Banco de Datos de Biodiversidad de Canarias, across 31,628 grid cell assemblages. Species range in occurrence from 1 to 4,466 cells. We only retrieved occurrences for which a species has been certainly observed or collected (precision level 1 of four levels). The Banco de Datos de Biodiversidad de Canarias provides presence-only information that is spatially biased by sampling effort (Hortal et al., 2007). However, the sampling bias of SIEs, AEs, and NENs is less than for species overall because studies incorporated into the database involved focus on, and extensive sampling of, endemic and non-endemic native species (<a href="https://www.biodiversidadcanarias.es/biota/documentos">https://www.biodiversidadcanarias.es/biota/documentos</a>). We considered a species (pseudo-)absent if it was not recorded at a site, although we recognise that there is debate as to whether this truly represents absences.</p>
Assessing the vulnerability of plant functional trait strategies to climate change
Open the record for dataset details and reuse information.
Studies of NH4+ and NO3- uptake ability of subalpine plants and resource-use strategy identified by their functional traits
<p>Data for the preprint "Studies of NH4+ and NO3- uptake ability of subalpine plants and resource-use strategy identified by their functional traits.”, by Legay N. , Grassein F., Arnoldi C., Segura R., Laîné P., Lavorel S., Clément J.C.</p>
The functional role of sibling aggression and "best of a bad job" strategies in cichlid juveniles
Siblings often compete for limited resources such as food provided by their parents. However, although several functions of non-lethal sibling (non-siblicidal) aggression have been proposed, there is currently little empirical evidence for these, apart from food monopolization. Here, we investigated the functions of non-lethal sibling aggression in the biparental-caring territorial herbivorous cichlid Varibilichromis moorii. We found that the juveniles of this species are highly aggressive and that larger juveniles are more aggressive toward their smaller siblings. Larger juveniles feed on algae more frequently than smaller siblings, thereby indicating a dominance hierarchy. Sibling aggression decreased when algae in the nest was experimentally removed. Furthermore, removal of smaller juveniles decreased sibling aggression among the remaining larger juveniles, whereas removal of larger juveniles increased aggression among smaller juveniles. The algal feeding rate of juveniles only increased when larger individuals were removed from the nest. Moreover, larger juveniles attained higher growth rates and remained in natal nests longer than smaller individuals. Our results indicate that sibling aggression may facilitate the monopolization of resources by larger juveniles and extend the parental care period. Interestingly, a small sub-set of juveniles were observed to migrate to other nests. These juveniles were larger than those of the host brood, and their growth rate increased within the new nests. We suggest that subordinate juveniles may disperse from natal nests and sneak into new nests to enhance their rank, which may represent a novel example of a "best of a bad job" strategy associated with sibling competition.
Dataset for Ongole at al. - Functional traits predict tree-level phenological strategies in a mesic Indian savanna
<p>Leaf phenology influences terrestrial primary production by determining the period of carbon uptake. While dominant leaf habit (evergreen/deciduous) is predictable at large scales based on environmental factors, there is substantial variability in the timing of key events such as leaf flush and senescence at smaller site-level scales. How much of this variability is explained by species functional traits related to a plant's carbon economy? We monitored leaf phenology for 113 individual trees of eleven dominant species in an Indian mesic savanna. Specifically, we related leaf functional traits and wood density to the (i) timing of leaf flush, leaf maturity, peak canopy and senescence, (ii) duration of leaf deployment, (iii) duration from start of senescence to leaflessness, and (iv) time to attainment of peak mature canopy following leaf flush. We expected species that use resources conservatively (low specific leaf area (SLA), high leaf dry matter content, low leaf nitrogen and high wood density) to senesce later and retain their leaves longer. For all species, leaflessness was most pronounced in early dry season and leaf flushing occurred in the late dry season. Species with high leaf carbon and dry matter content showed earlier leaf maturation, attained peak mature canopies sooner and deployed leaves longer. Species with high SLA, leaf nitrogen and low wood density showed earlier senescence but relationships were weak. In this savanna, phenology at fine scales was indeed associated with species functional traits relating to carbon investment, but these relationships were strong only when intra-specific variation in phenology was low.</p>
Freshwater invertebrates - diversity and function of stream macroinvertebrates: Effects of habitat conversion and strategies for conservation
<b>Description: </b><p>Freshwater invertebrate communities from stream sites along a habitat disturbance gradient (including old growth forest, logged forest, oil palm with riparian buffers, and oil palm with no buffers) within the SAFE Project experimental area, SAFE surrounding area, Maliau Basin, and Danum Valley.</p><p><b>Project: </b>This dataset was collected as part of the following SAFE research project: <a href="https://www.safeproject.net/projects/project_view/121"><b>Diversity and function of stream macroinvertebrates: Effects of habitat conversion and strategies for conservation</b></a></p><p><b>Funding: </b>These data were collected as part of research funded by: </p><ul><li>Sime Darby Foundation (Research, SAFE Project)</li><li>NERC (Studentship, 1122589.0)</li><li>Proforest (Research)</li><li>Varley Gradwell Travelling Fellowship (Research)</li><li>Tim Whitmore Fund (Research)</li><li>Panton Trust (Research)</li><li>Cambridge University Commonwealth Fund (Research)</li></ul><p>This dataset is released under the CC-BY 4.0 licence, requiring that you cite the dataset in any outputs, but has the additional condition that you acknowledge the contribution of these funders in any outputs.</p><p></p><p><b>Permits: </b>These data were collected under permit from the following authorities:</p><ul><li>Sabah Biodiversity Centre (SABC) (Research licence JKM/MBS.1000-2/2(37))</li><li>Sabah Biodiversity Centre (SABC) (Research licence JKM/MBS.1000-2/2(68))</li><li>Sabah Biodiversity Centre (SABC) (Research licence JKM/MBS:1000-2/2(230))</li></ul><p></p><p><b>XML metadata: </b>GEMINI compliant metadata for this dataset is available <a href="https://www.safeproject.net/datasets/xml_metadata?id=6368114">here</a></p><p><b>Files: </b>This consists of 1 file: 2_Luke_Inverts_V4_mfh.xlsx</p><p><b>2_Luke_Inverts_V4_mfh.xlsx</b></p><p>This file contains dataset metadata and 7 data tables:</p><ol><li><p><b>Water striders (Gerromorpha)</b> (described in worksheet Gerro)</p><p>Description: Manually captured waterstriders. Rows represent potential functional group/body size x sample site/date combinations, but not each combination had individuals collected.</p><p>Number of fields: 66</p><p>Number of data rows: 33905</p><p>Fields: </p><ul><li><b>Locations</b>: Transect sampled (Field type: location)</li><li><b>Stream</b>: Stream IDs of where the bugs were collected (Field type: id)</li><li><b>Distance</b>: The 10-m section of the stream transect where bugs were collected (Field type: replicate)</li><li><b>CollectionDate</b>: Dates of when the bugs were collected (Field type: date)</li><li><b>Time</b>: The times of when the bugs were collected (Field type: replicate)</li><li><b>PotCode</b>: Pot ID. For example, 1 of 1 means there is only 1 pot for a particular Distance, 1 of 2 means it is the first pot out of 2 for a particular Distance, and so on (Field type: replicate)</li><li><b>ID</b>: The ID number for the pots, each Distance can consists of 1 to 3 pots of samples and each pot has its own ID (Field type: id)</li><li><b>HabitatType</b>: Habitat type (Field type: categorical)</li><li><b>HabitatTypeReplicate</b>: Replicate IDs for the habitat types. For example, the ID for stream 0m at 40-50m as the first replicate for LF/ Logged Forest is LF1.1, while for stream 0m at 20-30m is LF1.2, and so on (Field type: replicate)</li><li><b>SortDate</b>: Dates of when sortings were done (Field type: comments)</li><li><b>Family</b>: Family of the bugs collected (Field type: taxa)</li><li><b>Group</b>: Groups of the bugs based on body forms: 1) CGP (Cylindrostethinae, Gerrinae, and Ptilomerinae), 2) Halobatinae, and 3) Veliidae (Field type: taxa)</li><li><b>LifeStage</b>: Life stage of the bugs collected: either Juvenile (J) or Adult (A) (Field type: categorical trait)</li><li><b>Length</b>: The body length of the bugs collected (rounded) (Field type: numeric trait)</li><li><b>LengthRange</b>: The body length range of the bugs collected (Field type: id)</li><li><b>PredictedBiomass</b>: The predicted biomass of the bugs collected, calculated using power regression equations. Zeros indicate groups for which no individuals were present. a. Group CGP = Abundance in any of the cell from column W until BO * (0.04 * (the cell of the Column O (needs to be at the same row as the Abundance cell chosen from any of the column W until BO)/ representing the body length ^ 2.271)), b. Group Halobatinae = the same as above but with 0.072 and 2.218 as the coefficient a and b respectively, c. Group Veliidae = the same as above but with 0.041 and 2.32 as the coefficient a and b respectively. (Field type: numeric)</li><li><b>AdultWing</b>: Adult bug's ID based on the presence of wings (if the individual insect is a juvenile, the cell says 'None', instead of 'Winged' or 'Wingless') (Field type: categorical trait)</li><li><b>AdultWingAbund</b>: Adult bug's abundance based on the presence of wings (Field type: abundance)</li><li><b>PtilomeraMF</b>: Ptilomera sp. IDs based on sex: either male or female (Field type: categorical trait)</li><li><b>Note</b>: Notes about people who have sorted the bugs before Martina Harianja (if no one hasn't worked on a particular sample, it's written as 'None') (Field type: comments)</li><li><b>PtilomeraMFAbund</b>: Abundance of either male or female adult Ptilomera sp. (Field type: abundance)</li><li><b>4spot</b>: Abundance (Field type: abundance)</li><li><b>C.scrutator</b>: Abundance (Field type: abundance)</li><li><b>Cylindrosthetus.sp.</b>: Abundance (Field type: abundance)</li><li><b>Limnometra.sp.</b>: Abundance (Field type: abundance)</li><li><b>Metrocoris.sp.1</b>: Abundance (Field type: abundance)</li><li><b>Metrocoris.sp.2</b>: Abundance (Field type: abundance)</li><li><b>Morphospecies15</b>: Abundance (Field type: abundance)</li><li><b>Morphospecies20</b>: Abundance (Field type: abundance)</li><li><b>Morphospecies24</b>: Abundance (Field type: abundance)</li><li><b>Morphospecies25</b>: Abundance (Field type: abundance)</li><li><b>Morphospecies27</b>: Abundance (Field type: abundance)</li><li><b>Morphospecies28</b>: Abundance (Field type: abundance)</li><li><b>Morphospecies29</b>: Abundance (Field type: abundance)</li><li><b>Morphospecies30</b>: Abundance (Field type: abundance)</li><li><b>Morphospecies31</b>: Abundance (Field type: abundance)</li><li><b>Morphospecies33</b>: Abundance (Field type: abundance)</li><li><b>Morphospecies34</b>: Abundance (Field type: abundance)</li><li><b>Morphospecies35</b>: Abundance (Field type: abundance)</li><li><b>Morphospecies36</b>: Abundance (Field type: abundance)</li><li><b>Morphospecies37</b>: Abundance (Field type: abundance)</li><li><b>Morphospecies38</b>: Abundance (Field type: abundance)</li><li><b>Morphospecies4</b>: Abundance (Field type: abundance)</li><li><b>Morphospecies40</b>: Abundance (Field type: abundance)</li><li><b>Morphospecies41</b>: Abundance (Field type: abundance)</li><li><b>Morphospecies42</b>: Abundance (Field type: abundance)</li><li><b>Morphospecies43</b>: Abundance (Field type: abundance)</li><li><b>Morphospecies44</b>: Abundance (Field type: abundance)</li><li><b>Morphospecies45</b>: Abundance (Field type: abundance)</li><li><b>Morphospecies46</b>: Abundance (Field type: abundance)</li><li><b>Morphospecies47</b>: Abundance (Field type: abundance)</li><li><b>Morphospecies6</b>: Abundance (Field type: abundance)</li><li><b>Morphospecies7</b>: Abundance (Field type: abundance)</li><li><b>Morphospecies7.sp.2</b>: Abundance (Field type: abundance)</li><li><b>Potamometropsis.sp.</b>: Abundance (Field type: abundance)</li><li><b>Ptilomera.sp.</b>: Abundance (Field type: abundance)</li><li><b>Rhagovelia.sp.</b>: Abundance (Field type: abundance)</li><li><b>Rhagovelia.sp.2</b>: Abundance (Field type: abundance)</li><li><b>Rhagovelia.sp.3</b>: Abundance (Field type: abundance)</li><li><b>Rheumatogonus.sp.1</b>: Abundance (Field type: abundance)</li><li><b>Rheumatogonus.sp.2</b>: Abundance (Field type: abundance)</li><li><b>Strongylovelia.sp.</b>: Abundance (Field type: abundance)</li><li><b>Tenagogonus.sp.1</b>: Abundance (Field type: abundance)</li><li><b>Tenagogonus.sp.2</b>: Abundance (Field type: abundance)</li><li><b>Ventidius.sp.</b>: Abundance (Field type: abundance)</li><li><b>Ventidius.sp.2</b>: Abundance (Field type: abundance)</li></ul></li><li><p><b>10m Chironomids</b> (described in worksheet Chiron_10m)</p><p>Description: Sampled from the streambed using a Surber sampler in 2012/2013. Suber sample had quadrat area of 0.33m2 and 250 μm mesh net. Sampling done at regularly spaced points along the 200m long dragonfly transects.</p><p>Number of fields: 51</p><p>Number of data rows: 151</p><p>Fields: </p><ul><li><b>Locations</b>: Location within the SAFE landscape (Field type: location)</li><li><b>Stream</b>: Stream name (Field type: id)</li><li><b>Distance</b>: Distance along the stream transect (Field type: numeric)</li><li><b>StreamDistance</b>: Stream and distance ID (Field type: id)</li><li><b>PointLocation</b>: Point location on stream transect (Field type: location)</li><li><b>SampleDate</b>: Date sample was collected (Field type: date)</li><li><b>SampleTime</b>: Time sample was collected (Field type: time)</li><li><b>Cladotanytarsus6teeth</b>: Cladotanytarsus6teeth abundance (Field type: abundance)</li><li><b>Cladotanytarsus5teeth</b>: Cladotanytarsus5teeth abundance (Field type: abundance)</li><li><b>Orthocladius</b>: Orthocladius abundance (Field type: abundance)</li><li><b>CricotopusWorn</b>: CricotopusWorn abundance (Field type: abundance)</li><li><b>CricotopusCylindraceus</b>: CricotopusCylindraceus abundance (Field type: abundance)</li><li><b>CricotopusOliveri</b>: CricotopusOliveri abundance (Field type: abundance)</li><li><b>Thienemanniella</b>: Thienemanniella abundance (Field type: abundance)</li><li><b>Thienemanniella2</b>: Thienemanniella2 abundance (Field type: abundance)</li><li><b>KelianA</b>: KelianA abundance (Field type: abundance)</li><li><b>KelianB</b>: KelianB abundance (Field type: abundance)</li><li><b>KelianC</b>: KelianC abundance (Field type: abundance)</li><li><b>TanytarsusMendax</b>: TanytarsusMendax abundance (Field type: abundance)</li><li><b>TanytarsusNemorosus</b>: TanytarsusNemorosus abundance (Field type: abundance)</li><li><b>PolypedilumType2</b>: PolypedilumType2 abundance (Field type: abundance)</li><li><b>PolypedilumConvictum</b>: PolypedilumConvictum abundance (Field type: abundance)</li><li><b>PolypedilumSp3</b>: PolypedilumSp3 abundance (Field type: abundance)</li><li><b>Chironomini1stInstar</b>: Chironomini1stInstar abundance (Field type: abundance)</li><li><b>ChironominiGenusB</b>: ChironominiGenusB abundance (Field type: abundance)</li><li><b>ChironominiPhoto1</b>: ChironominiPhoto1 abundance (Field type: abundance)</li><li><b>ChironominiPhoto2</b>: ChironominiPhoto2 abundance (Field type: abundance)</li><li><b>ChironominiPhoto3</b>: ChironominiPhoto3 abundance (Field type: abundance)</li><li><b>ChironominiPhoto5</b>: ChironominiPhoto5 abundance (Field type: abundance)</li><li><b>CorynoneuraLobata</b>: CorynoneuraLobata abundance (Field type: abundance)</li><li><b>Thienemannimyia</b>: Thienemannimyia abundance (Field type: abundance)</li><li><b>Parametriocnemus</b>: Parametriocnemus abundance (Field type: abundance)</li><li><b>Ceratopogonidae</b>: Ceratopogonidae abundance (Field type: abundance)</li><li><b>Cardiocladius</b>: Cardiocladius abundance (Field type: abundance)</li><li><b>Ablabesmyia</b>: Ablabesmyia abundance (Field type: abundance)</li><li><b>Stenochironomus</b>: Stenochironomus abundance (Field type: abundance)</li><li><b>Cryptochironomus</b>: Cryptochironomus abundance (Field type: abundance)</li><li><b>Nanocladius</b>: Nanocladius abundance (Field type: abundance)</li><li><b>Stictochironomus</b>: Stictochironomus abundance (Field type: abundance)</li><li><b>Nilotanypus</b>: Nilotanypus abundance (Field type: abundance)</li><li><b>Rheotanytarsus</b>: Rheotanytarsus abundance (Field type: abundance)</li><li><b>RheocricotopusChalybeatus</b>: RheocricotopusChalybeatus abundance (Field type: abundance)</li><li><b>Dicrotendipes</b>: Dicrotendipes abundance (Field type: abundance)</li><li><b>Paratendipes</b>: Paratendipes abundance (Field type: abundance)</li><li><b>Pseudorthocladius</b>: Pseudorthocladius abundance (Field type: abundance)</li><li><b>Kiefferulus</b>: Kiefferulus abundance (Field type: abundance)</li><li><b>Paracladopelma</b>: Paracladopelma abundance (Field type: abundance)</li><li><b>Microtendipes</b>: Microtendipes abundance (Field type: abundance)</li><li><b>Eukiefferiella</b>: Eukiefferiella abundance (Field type: abundance)</li><li><b>Diamesinae</b>: Diamesinae abundance (Field type: abundance)</li><li><b>TanytarsiniSurfaceTooth</b>: TanytarsiniSurfaceTooth abundance (Field type: abundance)</li></ul></li><li><p><b>10m Ephemeroptera, Plecoptera, Tricoptera (EPT)</b> (described in worksheet EPTabun_10m)</p><p>Description: Sampled from the streambed using a Surber sampler in 2012/2013. Suber sample had quadrat area of 0.33m2 and 250 μm mesh net. Sampling done at regularly spaced points along the 200m long dragonfly transects.</p><p>Number of fields: 34</p><p>Number of data rows: 78</p><p>Fields: </p><ul><li><b>Locations</b>: Location within the SAFE landscape (Field type: location)</li><li><b>Stream</b>: Stream name (Field type: id)</li><li><b>StreamDistance</b>: Distance along the stream transect (Field type: id)</li><li><b>Distance</b>: Stream and distance ID (Field type: id)</li><li><b>PointLocation</b>: Point location on stream transect (Field type: location)</li><li><b>SampleDate</b>: Date sample was collected (Field type: date)</li><li><b>SampleTime</b>: Time sample was collected (Field type: time)</li><li><b>Baetidae</b>: Baetidae abundance (Field type: abundance)</li><li><b>Leptophlebiidae</b>: Leptophlebiidae abundance (Field type: abundance)</li><li><b>Heptageniidae</b>: Heptageniidae abundance (Field type: abundance)</li><li><b>Caenidae</b>: Caenidae abundance (Field type: abundance)</li><li><b>Tricorythidae</b>: Tricorythidae abundance (Field type: abundance)</li><li><b>Euthyplociidae</b>: Euthyplociidae abundance (Field type: abundance)</li><li><b>Potamanthidae</b>: Potamanthidae abundance (Field type: abundance)</li><li><b>Oligoneuriidae</b>: Oligoneuriidae abundance (Field type: abundance)</li><li><b>Ephemeridae</b>: Ephemeridae abundance (Field type: abundance)</li><li><b>EphemUnknown</b>: EphemUnknown abundance (Field type: abundance)</li><li><b>Perlidae</b>: Perlidae abundance (Field type: abundance)</li><li><b>Nemouridae</b>: Nemouridae abundance (Field type: abundance)</li><li><b>Leuctridae</b>: Leuctridae abundance (Field type: abundance)</li><li><b>Peltoperlidae</b>: Peltoperlidae abundance (Field type: abundance)</li><li><b>PlecopUnkown</b>: PlecopUnkown abundance (Field type: abundance)</li><li><b>Dipsuedopsidae</b>: Dipsuedopsidae abundance (Field type: abundance)</li><li><b>Hydropsychidae</b>: Hydropsychidae abundance (Field type: abundance)</li><li><b>Leptoceridae</b>: Leptoceridae abundance (Field type: abundance)</li><li><b>Xiphocentronidae</b>: Xiphocentronidae abundance (Field type: abundance)</li><li><b>Polycentropodidae</b>: Polycentropodidae abundance (Field type: abundance)</li><li><b>Psychomyiidae</b>: Psychomyiidae abundance (Field type: abundance)</li><li><b>Ecnomidae</b>: Ecnomidae abundance (Field type: abundance)</li><li><b>Philopotamidae</b>: Philopotamidae abundance (Field type: abundance)</li><li><b>Hydroptilidae</b>: Hydroptilidae abundance (Field type: abundance)</li><li><b>Lepidostomatidae</b>: Lepidostomatidae abundance (Field type: abundance)</li><li><b>Calamoceratidae</b>: Calamoceratidae abundance (Field type: abundance)</li><li><b>TrichopUnknown</b>: TrichopUnknown abundance (Field type: abundance)</li></ul></li><li><p><b>10m Odonata nymphs</b> (described in worksheet OdonataNymph)</p><p>Description: Sampled from the streambed using a Surber sampler in 2012/2013. Suber sample had quadrat area of 0.33m2 and 250 μm mesh net. Sampling done at regularly spaced points along the 200m long dragonfly transects.</p><p>Number of fields: 29</p><p>Number of data rows: 151</p><p>Fields: </p><ul><li><b>Locations</b>: Location within the SAFE landscape (Field type: location)</li><li><b>Stream</b>: Stream name (Field type: id)</li><li><b>Distance</b>: Distance along the stream transect (Field type: numeric)</li><li><b>StreamDistance</b>: Stream and distance ID (Field type: id)</li><li><b>SiteCode</b>: Point location on stream transect (Field type: location)</li><li><b>Date</b>: Date sample was collected (Field type: date)</li><li><b>Time</b>: Time sample was collected (Field type: time)</li><li><b>ChlorogomphidaeChlorogomphus</b>: ChlorogomphidaeChlorogomphus abundance (Field type: abundance)</li><li><b>GomphidaeLeptogomphus</b>: GomphidaeLeptogomphus abundance (Field type: abundance)</li><li><b>GomphidaeMegalogomphus</b>: GomphidaeMegalogomphus abundance (Field type: abundance)</li><li><b>GomphidaeBurmagomphus</b>: GomphidaeBurmagomphus abundance (Field type: abundance)</li><li><b>GomphidaeOnychogomphus</b>: GomphidaeOnychogomphus abundance (Field type: abundance)</li><li><b>GomphidaeGomphidia</b>: GomphidaeGomphidia abundance (Field type: abundance)</li><li><b>GomphidaeSinogomphus</b>: GomphidaeSinogomphus abundance (Field type: abundance)</li><li><b>GomphidaeHeliogomphus</b>: GomphidaeHeliogomphus abundance (Field type: abundance)</li><li><b>GomphidaeIctinogomphus</b>: GomphidaeIctinogomphus abundance (Field type: abundance)</li><li><b>GomphidaeUnknown</b>: GomphidaeUnknown abundance (Field type: abundance)</li><li><b>MacromiidaeUnknown1</b>: MacromiidaeUnknown1 abundance (Field type: abundance)</li><li><b>MacromiidaeMacromia</b>: MacromiidaeMacromia abundance (Field type: abundance)</li><li><b>MacromiidaeUnknown2</b>: MacromiidaeUnknown2 abundance (Field type: abundance)</li><li><b>LibellulidaeUnknown</b>: LibellulidaeUnknown abundance (Field type: abundance)</li><li><b>LibellulidaeTrithemis</b>: LibellulidaeTrithemis abundance (Field type: abundance)</li><li><b>EuphaeidaeEuphaea</b>: EuphaeidaeEuphaea abundance (Field type: abundance)</li><li><b>CalopterygidaeVestalis</b>: CalopterygidaeVestalis abundance (Field type: abundance)</li><li><b>PhilosinidaeRhinagrion</b>: PhilosinidaeRhinagrion abundance (Field type: abundance)</li><li><b>PlatystictidaeUnknown</b>: PlatystictidaeUnknown abundance (Field type: abundance)</li><li><b>LestidaeUnknown</b>: LestidaeUnknown abundance (Field type: abundance)</li><li><b>ChlorocyphidaeUnknown</b>: ChlorocyphidaeUnknown abundance (Field type: abundance)</li><li><b>Unknown</b>: Unknown abundance (Field type: abundance)</li></ul></li><li><p><b>10m benthic insects, order-level</b> (described in worksheet Order_10m)</p><p>Description: Sampled from the streambed using a Surber sampler in 2012/2013. Suber sample had quadrat area of 0.33m2 and 250 μm mesh net. Sampling done at regularly spaced points along the 200m long dragonfly transects.</p><p>Number of fields: 34</p><p>Number of data rows: 151</p><p>Fields: </p><ul><li><b>Locations</b>: Location within the SAFE landscape (Field type: location)</li><li><b>Stream</b>: Stream name (Field type: id)</li><li><b>Distance</b>: Distance along the stream transect (Field type: numeric)</li><li><b>StreamDistance</b>: Stream and distance ID (Field type: id)</li><li><b>PointLocations</b>: Point location on stream transect (Field type: location)</li><li><b>SampleDate</b>: Date sample was collected (Field type: date)</li><li><b>SampleTime</b>: Time sample was collected (Field type: time)</li><li><b>EphemeropteraWhole</b>: EphemeropteraWhole abundance (Field type: abundance)</li><li><b>EphemeropteraPart</b>: EphemeropteraPart abundance (Field type: abundance)</li><li><b>Ephemeroptera</b>: Ephemeroptera abundance (Field type: abundance)</li><li><b>PlecopteraWhole</b>: PlecopteraWhole abundance (Field type: abundance)</li><li><b>PlecopteraPart</b>: PlecopteraPart abundance (Field type: abundance)</li><li><b>Plecoptera</b>: Plecoptera abundance (Field type: abundance)</li><li><b>TrichopteraWhole</b>: TrichopteraWhole abundance (Field type: abundance)</li><li><b>TrichopteraPart</b>: TrichopteraPart abundance (Field type: abundance)</li><li><b>Trichoptera</b>: Trichoptera abundance (Field type: abundance)</li><li><b>ColeopteraLarvaeWhole</b>: ColeopteraLarvaeWhole abundance (Field type: abundance)</li><li><b>ColeopteraLarvaePart</b>: ColeopteraLarvaePart abundance (Field type: abundance)</li><li><b>ColeopteraAdultWhole</b>: ColeopteraAdultWhole abundance (Field type: abundance)</li><li><b>ColeopteraAdultPart</b>: ColeopteraAdultPart abundance (Field type: abundance)</li><li><b>Coleoptera</b>: Coleoptera abundance (Field type: abundance)</li><li><b>DipteraWhole</b>: DipteraWhole abundance (Field type: abundance)</li><li><b>DipteraPart</b>: DipteraPart abundance (Field type: abundance)</li><li><b>Diptera</b>: Diptera abundance (Field type: abundance)</li><li><b>OdonataWhole</b>: OdonataWhole abundance (Field type: abundance)</li><li><b>OdonataPart</b>: OdonataPart abundance (Field type: abundance)</li><li><b>Odonata</b>: Odonata abundance (Field type: abundance)</li><li><b>Heteroptera</b>: Heteroptera abundance (Field type: abundance)</li><li><b>Mites</b>: Mites abundance (Field type: abundance)</li><li><b>Isopods</b>: Isopods abundance (Field type: abundance)</li><li><b>Worms</b>: Worms abundance (Field type: abundance)</li><li><b>OtherWhole</b>: OtherWhole abundance (Field type: abundance)</li><li><b>OtherPart</b>: OtherPart abundance (Field type: abundance)</li><li><b>Other</b>: Other abundance (Field type: abundance)</li></ul></li><li><p><b>10m bottle traps, for crabs, shrimps, snails</b> (described in worksheet Bottletraps_nov2015)</p><p>Description: Crabs, shrimps, snails. Sampled using bottle traps baited with fish/bread. Sampling done at regularly spaced points along the 200m long dragonfly transects. </p><p>Number of fields: 13</p><p>Number of data rows: 999</p><p>Fields: </p><ul><li><b>Locations</b>: Location within the SAFE landscape (Field type: location)</li><li><b>Stream</b>: Stream name (Field type: id)</li><li><b>Date</b>: Date trap set (Field type: date)</li><li><b>ArrivalTime</b>: Trap set time (Field type: time)</li><li><b>LeavingTime</b>: Trap collection time (Field type: time)</li><li><b>Weather</b>: Weather comments (Field type: comments)</li><li><b>People</b>: Observer (Field type: comments)</li><li><b>Distance</b>: Distance along the stream transect (Field type: numeric)</li><li><b>IDnumber</b>: Trap number (Field type: id)</li><li><b>Shrimps</b>: Shrimps abundance (Field type: abundance)</li><li><b>Snails</b>: Snails abundance (Field type: abundance)</li><li><b>Crabs</b>: Crabs abundance (Field type: abundance)</li><li><b>Fish</b>: Fish abundance (Field type: abundance)</li></ul></li><li><p><b>200m transects, adult dragonflies</b> (described in worksheet Dragonflies_2012_2013)</p><p>Description: Adult dragonflies. Caught along 200m long transects using butterfly nets. </p><p>Number of fields: 23</p><p>Number of data rows: 1872</p><p>Fields: </p><ul><li><b>Location</b>: Location within the SAFE landscape (Field type: location)</li><li><b>Stream</b>: Stream name (Field type: id)</li><li><b>Date</b>: Distance along the stream transect (Field type: date)</li><li><b>Weather</b>: Stream and distance ID (Field type: comments)</li><li><b>WeatherIssues</b>: Weather issues (0 - no issues, 1 - issues) (Field type: numeric)</li><li><b>PeopleIssues</b>: People issues (0 - no issues, 1 - issues) (Field type: numeric)</li><li><b>People</b>: Observers (Field type: comments)</li><li><b>DragonflyNo</b>: Dragonfly catch number per day (Field type: id)</li><li><b>UniqueID</b>: Individual dragonfly ID (Field type: id)</li><li><b>Time</b>: Time of catch (Field type: time)</li><li><b>Photos</b>: How many photos were taken of that individual dragonfly (in order to assist with photo sorting later on) (Field type: id)</li><li><b>HeadColour</b>: Head colour (Field type: comments)</li><li><b>ThoraxColour</b>: Thorax colour (Field type: comments)</li><li><b>AbdomenColour</b>: Abdomen colour (Field type: comments)</li><li><b>WingColour</b>: Wing colour (Field type: comments)</li><li><b>Pair</b>: Whether a male/female mating pair or not (knowing this could sometimes help with ID decisions later on, especially for females which are poorly known) (Field type: categorical)</li><li><b>Point10m</b>: Point of catch along the transect (10m intervals along he transect) (Field type: numeric)</li><li><b>Habitat</b>: Habitat type (Field type: comments)</li><li><b>Activity</b>: What was the dragon fly doing (Field type: comments)</li><li><b>DateIDing</b>: Date of ID (Field type: date)</li><li><b>PeopleIDing</b>: Person Iding (JA= James Austin, RD= Rory Dow, SHL = Sarah Luke) (Field type: categorical)</li><li><b>Species</b>: Species of dragonfly (Field type: taxa)</li><li><b>MaleFemale</b>: Sex of dragonfly (Field type: categorical)</li></ul></li></ol><p><b>Date range: </b>2011-07-03 to 2015-04-18</p><p><b>Latitudinal extent: </b>4.5755 to 4.9618</p><p><b>Longitudinal extent: </b>116.9641 to 117.7965</p><p><b>Taxonomic coverage: </b><br> All taxon names are validated against the GBIF backbone taxonomy. If a dataset uses a synonym, the accepted usage is shown followed by the dataset usage in brackets. Taxa that cannot be validated, including new species and other unknown taxa, morphospecies, functional groups and taxonomic levels not used in the GBIF backbone are shown in square brackets.</p><div> -  Animalia <br> -  -  Annelida <br> -  -  Arthropoda <br> -  -  -  Crabs <br> -  -  -  Insecta <br> -  -  -  -  Coleoptera <br> -  -  -  -  Coleoptera <br> -  -  -  -  Coleoptera <br> -  -  -  -  Coleoptera <br> -  -  -  -  Coleoptera <br> -  -  -  -  Diptera <br> -  -  -  -  -  Ceratopogonidae <br> -  -  -  -  -  Chironomidae <br> -  -  -  -  -  -  <i>Ablabesmyia</i> <br> -  -  -  -  -  -  <i>Cardiocladius</i> <br> -  -  -  -  -  -  Chironomini1stInstar <br> -  -  -  -  -  -  ChironominiGenusB <br> -  -  -  -  -  -  ChironominiPhoto1 <br> -  -  -  -  -  -  ChironominiPhoto2 <br> -  -  -  -  -  -  ChironominiPhoto3 <br> -  -  -  -  -  -  ChironominiPhoto5 <br> -  -  -  -  -  -  <i>Cladotanytarsus</i> <br> -  -  -  -  -  -  <i>Cladotanytarsus</i> <br> -  -  -  -  -  -  <i>Cricotopus</i> <br> -  -  -  -  -  -  -  <i>Cricotopus cylindraceus</i> <br> -  -  -  -  -  -  -  <i>Cricotopus olivetus</i> <br> -  -  -  -  -  -  <i>Cryptochironomus</i> <br> -  -  -  -  -  -  Diamesinae <br> -  -  -  -  -  -  <i>Dicrotendipes</i> <br> -  -  -  -  -  -  <i>Eukiefferiella</i> <br> -  -  -  -  -  -  KelianA <br> -  -  -  -  -  -  KelianB <br> -  -  -  -  -  -  KelianC <br> -  -  -  -  -  -  <i>Kiefferulus</i> <br> -  -  -  -  -  -  <i>Microtendipes</i> <br> -  -  -  -  -  -  <i>Nanocladius</i> <br> -  -  -  -  -  -  <i>Nilotanypus</i> <br> -  -  -  -  -  -  <i>Orthocladius</i> <br> -  -  -  -  -  -  <i>Paracladopelma</i> <br> -  -  -  -  -  -  <i>Parametriocnemus</i> <br> -  -  -  -  -  -  <i>Paratendipes</i> <br> -  -  -  -  -  -  <i>Polypedilum</i> <br> -  -  -  -  -  -  -  <i>Polypedilum convictum</i> <br> -  -  -  -  -  -  <i>Polypedilum</i> <br> -  -  -  -  -  -  -  <i>Polypedilum convictum</i> <br> -  -  -  -  -  -  <i>Pseudorthocladius</i> <br> -  -  -  -  -  -  <i>Rheotanytarsus</i> <br> -  -  -  -  -  -  <i>Stenochironomus</i> <br> -  -  -  -  -  -  <i>Stictochironomus</i> <br> -  -  -  -  -  -  TanytarsiniSurfaceTooth <br> -  -  -  -  -  -  <i>Thienemanniella</i> <br> -  -  -  -  -  -  <i>Thienemanniella</i> <br> -  -  -  -  -  -  <i>Thienemannimyia</i> <br> -  -  -  -  -  -  <i>Corynoneura</i> <br> -  -  -  -  -  -  -  <i>Corynoneura lobata</i> <br> -  -  -  -  -  -  <i>Tanytarsus</i> <br> -  -  -  -  -  -  -  <i>Tanytarsus mendax</i> <br> -  -  -  -  -  -  -  <i>Tanytarsus nemorosus</i> <br> -  -  -  -  -  -  <i>Rheocricotopus</i> <br> -  -  -  -  -  -  -  <i>Rheocricotopus chalybeatus</i> <br> -  -  -  -  Diptera <br> -  -  -  -  -  Ceratopogonidae <br> -  -  -  -  -  Chironomidae <br> -  -  -  -  -  -  <i>Ablabesmyia</i> <br> -  -  -  -  -  -  <i>Cardiocladius</i> <br> -  -  -  -  -  -  Chironomini1stInstar <br> -  -  -  -  -  -  ChironominiGenusB <br> -  -  -  -  -  -  ChironominiPhoto1 <br> -  -  -  -  -  -  ChironominiPhoto2 <br> -  -  -  -  -  -  ChironominiPhoto3 <br> -  -  -  -  -  -  ChironominiPhoto5 <br> -  -  -  -  -  -  <i>Cladotanytarsus</i> <br> -  -  -  -  -  -  <i>Cladotanytarsus</i> <br> -  -  -  -  -  -  <i>Cricotopus</i> <br> -  -  -  -  -  -  -  <i>Cricotopus cylindraceus</i> <br> -  -  -  -  -  -  -  <i>Cricotopus olivetus</i> <br> -  -  -  -  -  -  <i>Cryptochironomus</i> <br> -  -  -  -  -  -  Diamesinae <br> -  -  -  -  -  -  <i>Dicrotendipes</i> <br> -  -  -  -  -  -  <i>Eukiefferiella</i> <br> -  -  -  -  -  -  KelianA <br> -  -  -  -  -  -  KelianB <br> -  -  -  -  -  -  KelianC <br> -  -  -  -  -  -  <i>Kiefferulus</i> <br> -  -  -  -  -  -  <i>Microtendipes</i> <br> -  -  -  -  -  -  <i>Nanocladius</i> <br> -  -  -  -  -  -  <i>Nilotanypus</i> <br> -  -  -  -  -  -  <i>Orthocladius</i> <br> -  -  -  -  -  -  <i>Paracladopelma</i> <br> -  -  -  -  -  -  <i>Parametriocnemus</i> <br> -  -  -  -  -  -  <i>Paratendipes</i> <br> -  -  -  -  -  -  <i>Polypedilum</i> <br> -  -  -  -  -  -  -  <i>Polypedilum convictum</i> <br> -  -  -  -  -  -  <i>Polypedilum</i> <br> -  -  -  -  -  -  -  <i>Polypedilum convictum</i> <br> -  -  -  -  -  -  <i>Pseudorthocladius</i> <br> -  -  -  -  -  -  <i>Rheotanytarsus</i> <br> -  -  -  -  -  -  <i>Stenochironomus</i> <br> -  -  -  -  -  -  <i>Stictochironomus</i> <br> -  -  -  -  -  -  TanytarsiniSurfaceTooth <br> -  -  -  -  -  -  <i>Thienemanniella</i> <br> -  -  -  -  -  -  <i>Thienemanniella</i> <br> -  -  -  -  -  -  <i>Thienemannimyia</i> <br> -  -  -  -  -  -  <i>Corynoneura</i> <br> -  -  -  -  -  -  -  <i>Corynoneura lobata</i> <br> -  -  -  -  -  -  <i>Tanytarsus</i> <br> -  -  -  -  -  -  -  <i>Tanytarsus mendax</i> <br> -  -  -  -  -  -  -  <i>Tanytarsus nemorosus</i> <br> -  -  -  -  -  -  <i>Rheocricotopus</i> <br> -  -  -  -  -  -  -  <i>Rheocricotopus chalybeatus</i> <br> -  -  -  -  Diptera <br> -  -  -  -  -  Ceratopogonidae <br> -  -  -  -  -  Chironomidae <br> -  -  -  -  -  -  <i>Ablabesmyia</i> <br> -  -  -  -  -  -  <i>Cardiocladius</i> <br> -  -  -  -  -  -  Chironomini1stInstar <br> -  -  -  -  -  -  ChironominiGenusB <br> -  -  -  -  -  -  ChironominiPhoto1 <br> -  -  -  -  -  -  ChironominiPhoto2 <br> -  -  -  -  -  -  ChironominiPhoto3 <br> -  -  -  -  -  -  ChironominiPhoto5 <br> -  -  -  -  -  -  <i>Cladotanytarsus</i> <br> -  -  -  -  -  -  <i>Cladotanytarsus</i> <br> -  -  -  -  -  -  <i>Cricotopus</i> <br> -  -  -  -  -  -  -  <i>Cricotopus cylindraceus</i> <br> -  -  -  -  -  -  -  <i>Cricotopus olivetus</i> <br> -  -  -  -  -  -  <i>Cryptochironomus</i> <br> -  -  -  -  -  -  Diamesinae <br> -  -  -  -  -  -  <i>Dicrotendipes</i> <br> -  -  -  -  -  -  <i>Eukiefferiella</i> <br> -  -  -  -  -  -  KelianA <br> -  -  -  -  -  -  KelianB <br> -  -  -  -  -  -  KelianC <br> -  -  -  -  -  -  <i>Kiefferulus</i> <br> -  -  -  -  -  -  <i>Microtendipes</i> <br> -  -  -  -  -  -  <i>Nanocladius</i> <br> -  -  -  -  -  -  <i>Nilotanypus</i> <br> -  -  -  -  -  -  <i>Orthocladius</i> <br> -  -  -  -  -  -  <i>Paracladopelma</i> <br> -  -  -  -  -  -  <i>Parametriocnemus</i> <br> -  -  -  -  -  -  <i>Paratendipes</i> <br> -  -  -  -  -  -  <i>Polypedilum</i> <br> -  -  -  -  -  -  -  <i>Polypedilum convictum</i> <br> -  -  -  -  -  -  <i>Polypedilum</i> <br> -  -  -  -  -  -  -  <i>Polypedilum convictum</i> <br> -  -  -  -  -  -  <i>Pseudorthocladius</i> <br> -  -  -  -  -  -  <i>Rheotanytarsus</i> <br> -  -  -  -  -  -  <i>Stenochironomus</i> <br> -  -  -  -  -  -  <i>Stictochironomus</i> <br> -  -  -  -  -  -  TanytarsiniSurfaceTooth <br> -  -  -  -  -  -  <i>Thienemanniella</i> <br> -  -  -  -  -  -  <i>Thienemanniella</i> <br> -  -  -  -  -  -  <i>Thienemannimyia</i> <br> -  -  -  -  -  -  <i>Corynoneura</i> <br> -  -  -  -  -  -  -  <i>Corynoneura lobata</i> <br> -  -  -  -  -  -  <i>Tanytarsus</i> <br> -  -  -  -  -  -  -  <i>Tanytarsus mendax</i> <br> -  -  -  -  -  -  -  <i>Tanytarsus nemorosus</i> <br> -  -  -  -  -  -  <i>Rheocricotopus</i> <br> -  -  -  -  -  -  -  <i>Rheocricotopus chalybeatus</i> <br> -  -  -  -  Ephemeroptera <br> -  -  -  -  -  Baetidae <br> -  -  -  -  -  Caenidae <br> -  -  -  -  -  Ephemeridae <br> -  -  -  -  -  Ephemeridae <br> -  -  -  -  -  Euthyplociidae <br> -  -  -  -  -  Heptageniidae <br> -  -  -  -  -  Leptophlebiidae <br> -  -  -  -  -  Oligoneuriidae <br> -  -  -  -  -  Potamanthidae <br> -  -  -  -  -  Tricorythidae <br> -  -  -  -  Ephemeroptera <br> -  -  -  -  -  Baetidae <br> -  -  -  -  -  Caenidae <br> -  -  -  -  -  Ephemeridae <br> -  -  -  -  -  Ephemeridae <br> -  -  -  -  -  Euthyplociidae <br> -  -  -  -  -  Heptageniidae <br> -  -  -  -  -  Leptophlebiidae <br> -  -  -  -  -  Oligoneuriidae <br> -  -  -  -  -  Potamanthidae <br> -  -  -  -  -  Tricorythidae <br> -  -  -  -  Ephemeroptera <br> -  -  -  -  -  Baetidae <br> -  -  -  -  -  Caenidae <br> -  -  -  -  -  Ephemeridae <br> -  -  -  -  -  Ephemeridae <br> -  -  -  -  -  Euthyplociidae <br> -  -  -  -  -  Heptageniidae <br> -  -  -  -  -  Leptophlebiidae <br> -  -  -  -  -  Oligoneuriidae <br> -  -  -  -  -  Potamanthidae <br> -  -  -  -  -  Tricorythidae <br> -  -  -  -  Odonata <br> -  -  -  -  -  Chlorocyphidae <br> -  -  -  -  -  -  <i>Rhinocypha</i> <br> -  -  -  -  -  -  -  <i>Rhinocypha stygia</i> <br> -  -  -  -  -  -  -  <i>Rhinocypha aurofulgens</i> <br> -  -  -  -  -  -  -  <i>Rhinocypha humeralis</i> <br> -  -  -  -  -  -  -  <i>Rhinocypha stygia</i> <br> -  -  -  -  -  -  <i>Libellago</i> <br> -  -  -  -  -  -  -  <i>Libellago phaethon</i> <br> -  -  -  -  -  -  -  <i>Libellago semiopaca</i> <br> -  -  -  -  -  -  <i>Heliocypha</i> <br> -  -  -  -  -  -  -  <i>Heliocypha biseriata</i> <br> -  -  -  -  -  -  -  <i>Heliocypha biseriata</i> <br> -  -  -  -  -  Gomphidae <br> -  -  -  -  -  -  <i>Burmagomphus</i> <br> -  -  -  -  -  -  -  <i>Burmagomphus insularis</i> <br> -  -  -  -  -  -  <i>Gomphidia</i> <br> -  -  -  -  -  -  <i>Heliogomphus</i> <br> -  -  -  -  -  -  -  <i>Heliogomphus blandulus</i> <br> -  -  -  -  -  -  <i>Ictinogomphus</i> <br> -  -  -  -  -  -  <i>Leptogomphus</i> <br> -  -  -  -  -  -  -  <i>Leptogomphus williamsoni</i> <br> -  -  -  -  -  -  <i>Megalogomphus</i> <br> -  -  -  -  -  -  <i>Onychogomphus</i> <br> -  -  -  -  -  -  <i>Sinogomphus</i> <br> -  -  -  -  -  -  <i>Phaenandrogomphus</i> <br> -  -  -  -  -  -  -  <i>Phaenandrogomphus safei</i> <br> -  -  -  -  -  Lestidae <br> -  -  -  -  -  Libellulidae <br> -  -  -  -  -  -  <i>Trithemis</i> <br> -  -  -  -  -  -  -  <i>Trithemis aurora</i> <br> -  -  -  -  -  -  -  <i>Trithemis festiva</i> <br> -  -  -  -  -  -  <i>Orthetrum</i> <br> -  -  -  -  -  -  -  <i>Orthetrum chrysis</i> <br> -  -  -  -  -  -  -  <i>Orthetrum glaucum</i> <br> -  -  -  -  -  -  -  <i>Orthetrum testaceum</i> <br> -  -  -  -  -  -  -  <i>Orthetrum pruinosum</i> <br> -  -  -  -  -  -  -  -  <i>Orthetrum pruinosum schneideri</i> <br> -  -  -  -  -  -  <i>Tetrathemis</i> <br> -  -  -  -  -  -  <i>Lyriothemis</i> <br> -  -  -  -  -  -  -  <i>Lyriothemis cleis</i> <br> -  -  -  -  -  -  <i>Camacinia</i> <br> -  -  -  -  -  -  -  <i>Camacinia gigantea</i> <br> -  -  -  -  -  -  <i>Onychothemis</i> <br> -  -  -  -  -  -  -  <i>Onychothemis culminicola</i> <br> -  -  -  -  -  -  <i>Pantala</i> <br> -  -  -  -  -  -  -  <i>Pantala flavescens</i> <br> -  -  -  -  -  -  <i>Zygonyx</i> <br> -  -  -  -  -  -  -  <i>Zygonyx iris</i> <br> -  -  -  -  -  -  -  -  <i>Zygonyx iris errans</i> <br> -  -  -  -  -  -  <i>Cratilla</i> <br> -  -  -  -  -  -  -  <i>Cratilla lineata</i> <br> -  -  -  -  -  -  <i>Tyriobapta</i> <br> -  -  -  -  -  -  -  <i>Tyriobapta torrida</i> <br> -  -  -  -  -  -  <i>Neurothemis</i> <br> -  -  -  -  -  -  -  <i>Neurothemis fluctuans</i> <br> -  -  -  -  -  -  -  <i>Neurothemis ramburii</i> <br> -  -  -  -  -  Macromiidae <br> -  -  -  -  -  Macromiidae <br> -  -  -  -  -  Macromiidae <br> -  -  -  -  -  Platystictidae <br> -  -  -  -  -  -  <i>Drepanosticta</i> <br> -  -  -  -  -  -  -  <i>Drepanosticta actaeon</i> <br> -  -  -  -  -  -  -  <i>Drepanosticta rufostigma</i> <br> -  -  -  -  -  -  -  <i>Drepanosticta versicolor</i> <br> -  -  -  -  -  Megapodagrionidae <br> -  -  -  -  -  -  <i>Rhinagrion</i> <br> -  -  -  -  -  -  -  <i>Rhinagrion elopurae</i> <br> -  -  -  -  -  Amphipterygidae <br> -  -  -  -  -  -  <i>Devadatta</i> <br> -  -  -  -  -  -  -  <i>Devadatta tanduk</i> <br> -  -  -  -  -  Platycnemididae <br> -  -  -  -  -  -  <i>Coeliccia</i> <br> -  -  -  -  -  -  -  <i>Coeliccia arcuata</i> <br> -  -  -  -  -  -  -  <i>Coeliccia borneensis</i> <br> -  -  -  -  -  -  -  <i>Coeliccia cyaneothorax</i> <br> -  -  -  -  -  -  <i>Copera</i> <br> -  -  -  -  -  -  -  <i>Copera vittata</i> <br> -  -  -  -  -  Protoneuridae <br> -  -  -  -  -  -  <i>Prodasineura</i> <br> -  -  -  -  -  -  -  <i>Prodasineura hosei</i> <br> -  -  -  -  -  -  -  <i>Prodasineura verticalis</i> <br> -  -  -  -  -  Euphaeidae <br> -  -  -  -  -  -  <i>Euphaea</i> <br> -  -  -  -  -  -  -  <i>Euphaea impar</i> <br> -  -  -  -  -  -  -  <i>Euphaea subcostalis</i> <br> -  -  -  -  -  -  <i>Dysphaea</i> <br> -  -  -  -  -  -  -  <i>Dysphaea dimidiata</i> <br> -  -  -  -  -  -  -  <i>Dysphaea ulu</i> <br> -  -  -  -  -  Aeshnidae <br> -  -  -  -  -  -  <i>Tetracanthagyna</i> <br> -  -  -  -  -  -  -  <i>Tetracanthagyna degorsi</i> <br> -  -  -  -  -  Cordulegastridae <br> -  -  -  -  -  -  <i>Chlorogomphus</i> <br> -  -  -  -  -  Corduliidae <br> -  -  -  -  -  -  <i>Macromia</i> <br> -  -  -  -  -  -  -  <i>Macromia westwoodii</i> <br> -  -  -  -  -  -  <i>Macromidia</i> <br> -  -  -  -  -  -  -  <i>Macromidia fulva</i> <br> -  -  -  -  -  Coenagrionidae <br> -  -  -  -  -  -  <i>Pseudagrion</i> <br> -  -  -  -  -  -  -  <i>Pseudagrion pilidorsum</i> <br> -  -  -  -  -  -  <i>Agriocnemis</i> <br> -  -  -  -  -  -  -  <i>Agriocnemis femina</i> <br> -  -  -  -  -  -  <i>Stenagrion</i> <br> -  -  -  -  -  -  -  <i>Stenagrion dubium</i> <br> -  -  -  -  -  Calopterygidae <br> -  -  -  -  -  -  <i>Vestalis</i> <br> -  -  -  -  -  -  -  <i>Vestalis amaryllis</i> <br> -  -  -  -  -  -  -  <i>Vestalis amnicola</i> <br> -  -  -  -  -  -  -  <i>Vestalis amoena</i> <br> -  -  -  -  -  -  -  <i>Vestalis anacolosa</i> <br> -  -  -  -  -  -  <i>Vestalis</i> <br> -  -  -  -  -  -  -  <i>Vestalis amaryllis</i> <br> -  -  -  -  -  -  -  <i>Vestalis amnicola</i> <br> -  -  -  -  -  -  -  <i>Vestalis amoena</i> <br> -  -  -  -  -  -  -  <i>Vestalis anacolosa</i> <br> -  -  -  -  -  -  <i>Neurobasis</i> <br> -  -  -  -  -  -  -  <i>Neurobasis longipes</i> <br> -  -  -  -  Odonata <br> -  -  -  -  -  Chlorocyphidae <br> -  -  -  -  -  -  <i>Rhinocypha</i> <br> -  -  -  -  -  -  -  <i>Rhinocypha stygia</i> <br> -  -  -  -  -  -  -  <i>Rhinocypha aurofulgens</i> <br> -  -  -  -  -  -  -  <i>Rhinocypha humeralis</i> <br> -  -  -  -  -  -  -  <i>Rhinocypha stygia</i> <br> -  -  -  -  -  -  <i>Libellago</i> <br> -  -  -  -  -  -  -  <i>Libellago phaethon</i> <br> -  -  -  -  -  -  -  <i>Libellago semiopaca</i> <br> -  -  -  -  -  -  <i>Heliocypha</i> <br> -  -  -  -  -  -  -  <i>Heliocypha biseriata</i> <br> -  -  -  -  -  -  -  <i>Heliocypha biseriata</i> <br> -  -  -  -  -  Gomphidae <br> -  -  -  -  -  -  <i>Burmagomphus</i> <br> -  -  -  -  -  -  -  <i>Burmagomphus insularis</i> <br> -  -  -  -  -  -  <i>Gomphidia</i> <br> -  -  -  -  -  -  <i>Heliogomphus</i> <br> -  -  -  -  -  -  -  <i>Heliogomphus blandulus</i> <br> -  -  -  -  -  -  <i>Ictinogomphus</i> <br> -  -  -  -  -  -  <i>Leptogomphus</i> <br> -  -  -  -  -  -  -  <i>Leptogomphus williamsoni</i> <br> -  -  -  -  -  -  <i>Megalogomphus</i> <br> -  -  -  -  -  -  <i>Onychogomphus</i> <br> -  -  -  -  -  -  <i>Sinogomphus</i> <br> -  -  -  -  -  -  <i>Phaenandrogomphus</i> <br> -  -  -  -  -  -  -  <i>Phaenandrogomphus safei</i> <br> -  -  -  -  -  Lestidae <br> -  -  -  -  -  Libellulidae <br> -  -  -  -  -  -  <i>Trithemis</i> <br> -  -  -  -  -  -  -  <i>Trithemis aurora</i> <br> -  -  -  -  -  -  -  <i>Trithemis festiva</i> <br> -  -  -  -  -  -  <i>Orthetrum</i> <br> -  -  -  -  -  -  -  <i>Orthetrum chrysis</i> <br> -  -  -  -  -  -  -  <i>Orthetrum glaucum</i> <br> -  -  -  -  -  -  -  <i>Orthetrum testaceum</i> <br> -  -  -  -  -  -  -  <i>Orthetrum pruinosum</i> <br> -  -  -  -  -  -  -  -  <i>Orthetrum pruinosum schneideri</i> <br> -  -  -  -  -  -  <i>Tetrathemis</i> <br> -  -  -  -  -  -  <i>Lyriothemis</i> <br> -  -  -  -  -  -  -  <i>Lyriothemis cleis</i> <br> -  -  -  -  -  -  <i>Camacinia</i> <br> -  -  -  -  -  -  -  <i>Camacinia gigantea</i> <br> -  -  -  -  -  -  <i>Onychothemis</i> <br> -  -  -  -  -  -  -  <i>Onychothemis culminicola</i> <br> -  -  -  -  -  -  <i>Pantala</i> <br> -  -  -  -  -  -  -  <i>Pantala flavescens</i> <br> -  -  -  -  -  -  <i>Zygonyx</i> <br> -  -  -  -  -  -  -  <i>Zygonyx iris</i> <br> -  -  -  -  -  -  -  -  <i>Zygonyx iris errans</i> <br> -  -  -  -  -  -  <i>Cratilla</i> <br> -  -  -  -  -  -  -  <i>Cratilla lineata</i> <br> -  -  -  -  -  -  <i>Tyriobapta</i> <br> -  -  -  -  -  -  -  <i>Tyriobapta torrida</i> <br> -  -  -  -  -  -  <i>Neurothemis</i> <br> -  -  -  -  -  -  -  <i>Neurothemis fluctuans</i> <br> -  -  -  -  -  -  -  <i>Neurothemis ramburii</i> <br> -  -  -  -  -  Macromiidae <br> -  -  -  -  -  Macromiidae <br> -  -  -  -  -  Macromiidae <br> -  -  -  -  -  Platystictidae <br> -  -  -  -  -  -  <i>Drepanosticta</i> <br> -  -  -  -  -  -  -  <i>Drepanosticta actaeon</i> <br> -  -  -  -  -  -  -  <i>Drepanosticta rufostigma</i> <br> -  -  -  -  -  -  -  <i>Drepanosticta versicolor</i> <br> -  -  -  -  -  Megapodagrionidae <br> -  -  -  -  -  -  <i>Rhinagrion</i> <br> -  -  -  -  -  -  -  <i>Rhinagrion elopurae</i> <br> -  -  -  -  -  Amphipterygidae <br> -  -  -  -  -  -  <i>Devadatta</i> <br> -  -  -  -  -  -  -  <i>Devadatta tanduk</i> <br> -  -  -  -  -  Platycnemididae <br> -  -  -  -  -  -  <i>Coeliccia</i> <br> -  -  -  -  -  -  -  <i>Coeliccia arcuata</i> <br> -  -  -  -  -  -  -  <i>Coeliccia borneensis</i> <br> -  -  -  -  -  -  -  <i>Coeliccia cyaneothorax</i> <br> -  -  -  -  -  -  <i>Copera</i> <br> -  -  -  -  -  -  -  <i>Copera vittata</i> <br> -  -  -  -  -  Protoneuridae <br> -  -  -  -  -  -  <i>Prodasineura</i> <br> -  -  -  -  -  -  -  <i>Prodasineura hosei</i> <br> -  -  -  -  -  -  -  <i>Prodasineura verticalis</i> <br> -  -  -  -  -  Euphaeidae <br> -  -  -  -  -  -  <i>Euphaea</i> <br> -  -  -  -  -  -  -  <i>Euphaea impar</i> <br> -  -  -  -  -  -  -  <i>Euphaea subcostalis</i> <br> -  -  -  -  -  -  <i>Dysphaea</i> <br> -  -  -  -  -  -  -  <i>Dysphaea dimidiata</i> <br> -  -  -  -  -  -  -  <i>Dysphaea ulu</i> <br> -  -  -  -  -  Aeshnidae <br> -  -  -  -  -  -  <i>Tetracanthagyna</i> <br> -  -  -  -  -  -  -  <i>Tetracanthagyna degorsi</i> <br> -  -  -  -  -  Cordulegastridae <br> -  -  -  -  -  -  <i>Chlorogomphus</i> <br> -  -  -  -  -  Corduliidae <br> -  -  -  -  -  -  <i>Macromia</i> <br> -  -  -  -  -  -  -  <i>Macromia westwoodii</i> <br> -  -  -  -  -  -  <i>Macromidia</i> <br> -  -  -  -  -  -  -  <i>Macromidia fulva</i> <br> -  -  -  -  -  Coenagrionidae <br> -  -  -  -  -  -  <i>Pseudagrion</i> <br> -  -  -  -  -  -  -  <i>Pseudagrion pilidorsum</i> <br> -  -  -  -  -  -  <i>Agriocnemis</i> <br> -  -  -  -  -  -  -  <i>Agriocnemis femina</i> <br> -  -  -  -  -  -  <i>Stenagrion</i> <br> -  -  -  -  -  -  -  <i>Stenagrion dubium</i> <br> -  -  -  -  -  Calopterygidae <br> -  -  -  -  -  -  <i>Vestalis</i> <br> -  -  -  -  -  -  -  <i>Vestalis amaryllis</i> <br> -  -  -  -  -  -  -  <i>Vestalis amnicola</i> <br> -  -  -  -  -  -  -  <i>Vestalis amoena</i> <br> -  -  -  -  -  -  -  <i>Vestalis anacolosa</i> <br> -  -  -  -  -  -  <i>Vestalis</i> <br> -  -  -  -  -  -  -  <i>Vestalis amaryllis</i> <br> -  -  -  -  -  -  -  <i>Vestalis amnicola</i> <br> -  -  -  -  -  -  -  <i>Vestalis amoena</i> <br> -  -  -  -  -  -  -  <i>Vestalis anacolosa</i> <br> -  -  -  -  -  -  <i>Neurobasis</i> <br> -  -  -  -  -  -  -  <i>Neurobasis longipes</i> <br> -  -  -  -  Odonata <br> -  -  -  -  -  Chlorocyphidae <br> -  -  -  -  -  -  <i>Rhinocypha</i> <br> -  -  -  -  -  -  -  <i>Rhinocypha stygia</i> <br> -  -  -  -  -  -  -  <i>Rhinocypha aurofulgens</i> <br> -  -  -  -  -  -  -  <i>Rhinocypha humeralis</i> <br> -  -  -  -  -  -  -  <i>Rhinocypha stygia</i> <br> -  -  -  -  -  -  <i>Libellago</i> <br> -  -  -  -  -  -  -  <i>Libellago phaethon</i> <br> -  -  -  -  -  -  -  <i>Libellago semiopaca</i> <br> -  -  -  -  -  -  <i>Heliocypha</i> <br> -  -  -  -  -  -  -  <i>Heliocypha biseriata</i> <br> -  -  -  -  -  -  -  <i>Heliocypha biseriata</i> <br> -  -  -  -  -  Gomphidae <br> -  -  -  -  -  -  <i>Burmagomphus</i> <br> -  -  -  -  -  -  -  <i>Burmagomphus insularis</i> <br> -  -  -  -  -  -  <i>Gomphidia</i> <br> -  -  -  -  -  -  <i>Heliogomphus</i> <br> -  -  -  -  -  -  -  <i>Heliogomphus blandulus</i> <br> -  -  -  -  -  -  <i>Ictinogomphus</i> <br> -  -  -  -  -  -  <i>Leptogomphus</i> <br> -  -  -  -  -  -  -  <i>Leptogomphus williamsoni</i> <br> -  -  -  -  -  -  <i>Megalogomphus</i> <br> -  -  -  -  -  -  <i>Onychogomphus</i> <br> -  -  -  -  -  -  <i>Sinogomphus</i> <br> -  -  -  -  -  -  <i>Phaenandrogomphus</i> <br> -  -  -  -  -  -  -  <i>Phaenandrogomphus safei</i> <br> -  -  -  -  -  Lestidae <br> -  -  -  -  -  Libellulidae <br> -  -  -  -  -  -  <i>Trithemis</i> <br> -  -  -  -  -  -  -  <i>Trithemis aurora</i> <br> -  -  -  -  -  -  -  <i>Trithemis festiva</i> <br> -  -  -  -  -  -  <i>Orthetrum</i> <br> -  -  -  -  -  -  -  <i>Orthetrum chrysis</i> <br> -  -  -  -  -  -  -  <i>Orthetrum glaucum</i> <br> -  -  -  -  -  -  -  <i>Orthetrum testaceum</i> <br> -  -  -  -  -  -  -  <i>Orthetrum pruinosum</i> <br> -  -  -  -  -  -  -  -  <i>Orthetrum pruinosum schneideri</i> <br> -  -  -  -  -  -  <i>Tetrathemis</i> <br> -  -  -  -  -  -  <i>Lyriothemis</i> <br> -  -  -  -  -  -  -  <i>Lyriothemis cleis</i> <br> -  -  -  -  -  -  <i>Camacinia</i> <br> -  -  -  -  -  -  -  <i>Camacinia gigantea</i> <br> -  -  -  -  -  -  <i>Onychothemis</i> <br> -  -  -  -  -  -  -  <i>Onychothemis culminicola</i> <br> -  -  -  -  -  -  <i>Pantala</i> <br> -  -  -  -  -  -  -  <i>Pantala flavescens</i> <br> -  -  -  -  -  -  <i>Zygonyx</i> <br> -  -  -  -  -  -  -  <i>Zygonyx iris</i> <br> -  -  -  -  -  -  -  -  <i>Zygonyx iris errans</i> <br> -  -  -  -  -  -  <i>Cratilla</i> <br> -  -  -  -  -  -  -  <i>Cratilla lineata</i> <br> -  -  -  -  -  -  <i>Tyriobapta</i> <br> -  -  -  -  -  -  -  <i>Tyriobapta torrida</i> <br> -  -  -  -  -  -  <i>Neurothemis</i> <br> -  -  -  -  -  -  -  <i>Neurothemis fluctuans</i> <br> -  -  -  -  -  -  -  <i>Neurothemis ramburii</i> <br> -  -  -  -  -  Macromiidae <br> -  -  -  -  -  Macromiidae <br> -  -  -  -  -  Macromiidae <br> -  -  -  -  -  Platystictidae <br> -  -  -  -  -  -  <i>Drepanosticta</i> <br> -  -  -  -  -  -  -  <i>Drepanosticta actaeon</i> <br> -  -  -  -  -  -  -  <i>Drepanosticta rufostigma</i> <br> -  -  -  -  -  -  -  <i>Drepanosticta versicolor</i> <br> -  -  -  -  -  Megapodagrionidae <br> -  -  -  -  -  -  <i>Rhinagrion</i> <br> -  -  -  -  -  -  -  <i>Rhinagrion elopurae</i> <br> -  -  -  -  -  Amphipterygidae <br> -  -  -  -  -  -  <i>Devadatta</i> <br> -  -  -  -  -  -  -  <i>Devadatta tanduk</i> <br> -  -  -  -  -  Platycnemididae <br> -  -  -  -  -  -  <i>Coeliccia</i> <br> -  -  -  -  -  -  -  <i>Coeliccia arcuata</i> <br> -  -  -  -  -  -  -  <i>Coeliccia borneensis</i> <br> -  -  -  -  -  -  -  <i>Coeliccia cyaneothorax</i> <br> -  -  -  -  -  -  <i>Copera</i> <br> -  -  -  -  -  -  -  <i>Copera vittata</i> <br> -  -  -  -  -  Protoneuridae <br> -  -  -  -  -  -  <i>Prodasineura</i> <br> -  -  -  -  -  -  -  <i>Prodasineura hosei</i> <br> -  -  -  -  -  -  -  <i>Prodasineura verticalis</i> <br> -  -  -  -  -  Euphaeidae <br> -  -  -  -  -  -  <i>Euphaea</i> <br> -  -  -  -  -  -  -  <i>Euphaea impar</i> <br> -  -  -  -  -  -  -  <i>Euphaea subcostalis</i> <br> -  -  -  -  -  -  <i>Dysphaea</i> <br> -  -  -  -  -  -  -  <i>Dysphaea dimidiata</i> <br> -  -  -  -  -  -  -  <i>Dysphaea ulu</i> <br> -  -  -  -  -  Aeshnidae <br> -  -  -  -  -  -  <i>Tetracanthagyna</i> <br> -  -  -  -  -  -  -  <i>Tetracanthagyna degorsi</i> <br> -  -  -  -  -  Cordulegastridae <br> -  -  -  -  -  -  <i>Chlorogomphus</i> <br> -  -  -  -  -  Corduliidae <br> -  -  -  -  -  -  <i>Macromia</i> <br> -  -  -  -  -  -  -  <i>Macromia westwoodii</i> <br> -  -  -  -  -  -  <i>Macromidia</i> <br> -  -  -  -  -  -  -  <i>Macromidia fulva</i> <br> -  -  -  -  -  Coenagrionidae <br> -  -  -  -  -  -  <i>Pseudagrion</i> <br> -  -  -  -  -  -  -  <i>Pseudagrion pilidorsum</i> <br> -  -  -  -  -  -  <i>Agriocnemis</i> <br> -  -  -  -  -  -  -  <i>Agriocnemis femina</i> <br> -  -  -  -  -  -  <i>Stenagrion</i> <br> -  -  -  -  -  -  -  <i>Stenagrion dubium</i> <br> -  -  -  -  -  Calopterygidae <br> -  -  -  -  -  -  <i>Vestalis</i> <br> -  -  -  -  -  -  -  <i>Vestalis amaryllis</i> <br> -  -  -  -  -  -  -  <i>Vestalis amnicola</i> <br> -  -  -  -  -  -  -  <i>Vestalis amoena</i> <br> -  -  -  -  -  -  -  <i>Vestalis anacolosa</i> <br> -  -  -  -  -  -  <i>Vestalis</i> <br> -  -  -  -  -  -  -  <i>Vestalis amaryllis</i> <br> -  -  -  -  -  -  -  <i>Vestalis amnicola</i> <br> -  -  -  -  -  -  -  <i>Vestalis amoena</i> <br> -  -  -  -  -  -  -  <i>Vestalis anacolosa</i> <br> -  -  -  -  -  -  <i>Neurobasis</i> <br> -  -  -  -  -  -  -  <i>Neurobasis longipes</i> <br> -  -  -  -  Plecoptera <br> -  -  -  -  -  Leuctridae <br> -  -  -  -  -  Nemouridae <br> -  -  -  -  -  Peltoperlidae <br> -  -  -  -  -  Perlidae <br> -  -  -  -  Plecoptera <br> -  -  -  -  -  Leuctridae <br> -  -  -  -  -  Nemouridae <br> -  -  -  -  -  Peltoperlidae <br> -  -  -  -  -  Perlidae <br> -  -  -  -  Plecoptera <br> -  -  -  -  -  Leuctridae <br> -  -  -  -  -  Nemouridae <br> -  -  -  -  -  Peltoperlidae <br> -  -  -  -  -  Perlidae <br> -  -  -  -  Plecoptera <br> -  -  -  -  -  Leuctridae <br> -  -  -  -  -  Nemouridae <br> -  -  -  -  -  Peltoperlidae <br> -  -  -  -  -  Perlidae <br> -  -  -  -  Trichoptera <br> -  -  -  -  -  Calamoceratidae <br> -  -  -  -  -  Dipseudopsidae <br> -  -  -  -  -  Ecnomidae <br> -  -  -  -  -  Hydropsychidae <br> -  -  -  -  -  Hydroptilidae <br> -  -  -  -  -  Lepidostomatidae <br> -  -  -  -  -  Leptoceridae <br> -  -  -  -  -  Philopotamidae <br> -  -  -  -  -  Polycentropodidae <br> -  -  -  -  -  Psychomyiidae <br> -  -  -  -  -  Xiphocentronidae <br> -  -  -  -  Trichoptera <br> -  -  -  -  -  Calamoceratidae <br> -  -  -  -  -  Dipseudopsidae <br> -  -  -  -  -  Ecnomidae <br> -  -  -  -  -  Hydropsychidae <br> -  -  -  -  -  Hydroptilidae <br> -  -  -  -  -  Lepidostomatidae <br> -  -  -  -  -  Leptoceridae <br> -  -  -  -  -  Philopotamidae <br> -  -  -  -  -  Polycentropodidae <br> -  -  -  -  -  Psychomyiidae <br> -  -  -  -  -  Xiphocentronidae <br> -  -  -  -  Trichoptera <br> -  -  -  -  -  Calamoceratidae <br> -  -  -  -  -  Dipseudopsidae <br> -  -  -  -  -  Ecnomidae <br> -  -  -  -  -  Hydropsychidae <br> -  -  -  -  -  Hydroptilidae <br> -  -  -  -  -  Lepidostomatidae <br> -  -  -  -  -  Leptoceridae <br> -  -  -  -  -  Philopotamidae <br> -  -  -  -  -  Polycentropodidae <br> -  -  -  -  -  Psychomyiidae <br> -  -  -  -  -  Xiphocentronidae <br> -  -  -  -  Hemiptera <br> -  -  -  -  -  Heteroptera <br> -  -  -  -  -  Gerridae <br> -  -  -  -  -  -  Halobatinae <br> -  -  -  -  -  -  [4spot] <br> -  -  -  -  -  -  [Morphospecies15] <br> -  -  -  -  -  -  [Morphospecies25] <br> -  -  -  -  -  -  [Morphospecies27] <br> -  -  -  -  -  -  [Morphospecies28] <br> -  -  -  -  -  -  [Morphospecies29] <br> -  -  -  -  -  -  [Morphospecies33] <br> -  -  -  -  -  -  [Morphospecies34] <br> -  -  -  -  -  -  [Morphospecies35] <br> -  -  -  -  -  -  [Morphospecies42] <br> -  -  -  -  -  -  [Morphospecies46] <br> -  -  -  -  -  -  [Morphospecies47] <br> -  -  -  -  -  -  [Morphospecies6] <br> -  -  -  -  -  -  <i>Limnometra</i> <br> -  -  -  -  -  -  -  [Limnometra.sp.] <br> -  -  -  -  -  -  <i>Tenagogonus</i> <br> -  -  -  -  -  -  -  [Tenagogonus.sp.1] <br> -  -  -  -  -  -  -  [Tenagogonus.sp.2] <br> -  -  -  -  -  -  <i>Ptilomera</i> <br> -  -  -  -  -  -  -  [Ptilomera.sp.] <br> -  -  -  -  -  -  <i>Potamometropsis</i> <br> -  -  -  -  -  -  -  [Potamometropsis.sp.] <br> -  -  -  -  -  -  <i>Metrocoris</i> <br> -  -  -  -  -  -  -  [Metrocoris.sp.1] <br> -  -  -  -  -  -  -  [Metrocoris.sp.2] <br> -  -  -  -  -  -  <i>Cylindrostethus</i> <br> -  -  -  -  -  -  -  <i>Cylindrostethus scrutator</i> <br> -  -  -  -  -  -  -  [Cylindrostethus.sp.] <br> -  -  -  -  -  Veliidae <br> -  -  -  -  -  -  [Morphospecies20] <br> -  -  -  -  -  -  [Morphospecies24] <br> -  -  -  -  -  -  [Morphospecies30] <br> -  -  -  -  -  -  [Morphospecies31] <br> -  -  -  -  -  -  [Morphospecies36] <br> -  -  -  -  -  -  [Morphospecies37] <br> -  -  -  -  -  -  [Morphospecies38] <br> -  -  -  -  -  -  [Morphospecies4] <br> -  -  -  -  -  -  [Morphospecies40] <br> -  -  -  -  -  -  [Morphospecies41] <br> -  -  -  -  -  -  [Morphospecies43] <br> -  -  -  -  -  -  [Morphospecies44] <br> -  -  -  -  -  -  [Morphospecies45] <br> -  -  -  -  -  -  [Morphospecies7] <br> -  -  -  -  -  -  [Morphospecies7.sp.2] <br> -  -  -  -  -  -  <i>Rhagovelia</i> <br> -  -  -  -  -  -  -  [Rhagovelia.sp.] <br> -  -  -  -  -  -  -  [Rhagovelia.sp.2] <br> -  -  -  -  -  -  -  [Rhagovelia.sp.3] <br> -  -  -  -  -  -  <i>Strongylovelia</i> <br> -  -  -  -  -  -  -  [Strongylovelia.sp.] <br> -  -  -  -  -  Gerridae <br> -  -  -  -  -  -  Halobatinae <br> -  -  -  -  -  -  [4spot] <br> -  -  -  -  -  -  [Morphospecies15] <br> -  -  -  -  -  -  [Morphospecies25] <br> -  -  -  -  -  -  [Morphospecies27] <br> -  -  -  -  -  -  [Morphospecies28] <br> -  -  -  -  -  -  [Morphospecies29] <br> -  -  -  -  -  -  [Morphospecies33] <br> -  -  -  -  -  -  [Morphospecies34] <br> -  -  -  -  -  -  [Morphospecies35] <br> -  -  -  -  -  -  [Morphospecies42] <br> -  -  -  -  -  -  [Morphospecies46] <br> -  -  -  -  -  -  [Morphospecies47] <br> -  -  -  -  -  -  [Morphospecies6] <br> -  -  -  -  -  -  <i>Limnometra</i> <br> -  -  -  -  -  -  -  [Limnometra.sp.] <br> -  -  -  -  -  -  <i>Tenagogonus</i> <br> -  -  -  -  -  -  -  [Tenagogonus.sp.1] <br> -  -  -  -  -  -  -  [Tenagogonus.sp.2] <br> -  -  -  -  -  -  <i>Ptilomera</i> <br> -  -  -  -  -  -  -  [Ptilomera.sp.] <br> -  -  -  -  -  -  <i>Potamometropsis</i> <br> -  -  -  -  -  -  -  [Potamometropsis.sp.] <br> -  -  -  -  -  -  <i>Metrocoris</i> <br> -  -  -  -  -  -  -  [Metrocoris.sp.1] <br> -  -  -  -  -  -  -  [Metrocoris.sp.2] <br> -  -  -  -  -  -  <i>Cylindrostethus</i> <br> -  -  -  -  -  -  -  <i>Cylindrostethus scrutator</i> <br> -  -  -  -  -  -  -  [Cylindrostethus.sp.] <br> -  -  -  -  -  Macroveliidae <br> -  -  -  -  -  -  <i>Rheumatogonus</i> <br> -  -  -  -  -  -  -  [Rheumatogonus.sp.1] <br> -  -  -  -  -  -  -  [Rheumatogonus.sp.2] <br> -  -  -  -  -  -  <i>Ventidius</i> <br> -  -  -  -  -  -  -  [Ventidius.sp.] <br> -  -  -  -  -  -  -  [Ventidius.sp.2] <br> -  -  -  Shrimps <br> -  -  -  Arachnida <br> -  -  -  -  Mites <br> -  -  -  Malacostraca <br> -  -  -  -  Isopoda <br> -  -  Mollusca <br> -  -  -  Gastropoda <br> -  -  Chordata <br> -  -  -  Actinopterygii <br></div><p></p>
Slow practice and tempo management strategies in instrumental music learning: Investigating prevalence and cognitive functions
<p>This dataset corresponds to the publication of the same title and the following DOI: <a href="https://doi.org/10.1177%2F03057356211073481">https://doi.org/10.1177/03057356211073481</a></p> <p>The dataset contains 3 excel files. The file named QuantiativeSurveyDataClean_withKey contains all collected, unprocessed, cleaned data variables from the quantitative questionnaire. This includes all variables used for the principle components analysis. The file named ANOVA_data contains the variables used for the ANOVA analyses, and the file named regression_data contains the variables used for the regressions analyses. In all three files, descriptions of the variables can be found in the sheet titled "key", and the data can be found in the sheet titled "data".</p>
Data for: "Different dry-wet pulses favor different functional strategies: a test using tropical dry forest tree species" by Vega-Ramos, Flor, Cifuentes Gómez, Lucas, Pineda-García, Fernando, Dawson, Todd, Paz, Horacio
<p>These data represent those published in "Different dry-wet pulses favor different functional strategies: a test using tropical dry forest tree species" by Vega-Ramos, Flor, Cifuentes Gómez, Lucas, Pineda-García, Fernando, Dawson, Todd, Paz, Horacio</p>
Contrasting soil- and canopy-nurse effects on dependent species in metalliferous systems may be explained by dominant plant functional strategies
<p>Plant-plant interaction studies in metalliferous systems have focused either on the role of facilitation or on the negative effects of elemental allelopathy. However, no studies have investigated both of these effects in the same system, and their relationships with the functional strategy of the nurse species, although this is crucial for the ecological restoration of polluted sites.</p> <p>We assessed the effects of two dominant nurse species, with apparent contrasting strategies, on two target species on a slag heap in the Pyrenees (France). We quantified both long-term soil-engineering and short-term canopy effects on the growth of two target species. We also measured morphological traits and leaf metal concentration of the two nurse species and their effects on air moisture, temperature, and vapour pressure deficit.</p> <p>Nurse functional strategies, as inferred from morphological traits and leaf metal concentration seem to drive their long-term soil engineering effects on target species: Gypsophila repens, the relatively larger and more exploitative species with high leaf metal concentration, had negative long-term effects likely due to elemental allelopathy, whereas Minuartia verna, the relatively smaller and more conservative species with a lower amount of metals in leaves, had neutral long-term effects. Although Gypsophila repens had a slightly stronger positive effect on microclimate than Minuartia verna, this did not turn into higher short-term effects for the target species.</p> <p>Our study highlights the possible role of the nurse's functional strategies in driving the relative importance of long and short-term effects on target species in metalliferous systems. This knowledge is key to increasing our understanding of plant-plant interaction outcomes in metalliferous systems and our ability to restore polluted environments.</p>
ScienceDex guides
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These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
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.
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.