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1,085 results for “Documentation”
FIGURES 153–157 in Documenting new and little known leaf-mining Nepticulidae from middle and southwestern areas of the Asian continent
FIGURES 153–157. Female genitalia of Ectoedemia orbiculata Diškus, Remeikis & Stonis, sp. nov. 153, paratype, genitalia slide no. AD487; 154, same, genitalia slide no. RA270; 155–157, details of genitalia, paratype, genitalia slide RA272 (ZIN)
FIGURES 158–166 in Documenting new and little known leaf-mining Nepticulidae from middle and southwestern areas of the Asian continent
FIGURES 158–166. Male genitalia of Ectoedemia spp. 158, E. jacutica Puplesis, paratype, genitalia slide no. AN539 (ZIN); 159, E. insignata Puplesis, gnathos, genitalia slide no. AN464; 160, same, pseuduncus, slide AN467; 161, same, capsule with phallus removed, slide no. AN467; 162, same, slide AN464; 163, phallus, slide no. AN467; 164, 165, same, slide no. AN464; 166, transtilla, slide no. AN467 (ZIN)
FIGURES 230–235 in Documenting new and little known leaf-mining Nepticulidae from middle and southwestern areas of the Asian continent
FIGURES 230–235. Female genitalia of Acalyptris nasutus Diškus & Navickaitė, sp. nov. 230, holotype, slide no. AD485, apophyses and vaginal sclerite; 231, same, paratype, slide no. AD479; 232, general view, holotype, slide no. AD485; 233, same, paratype, slide no. AD479; 234, coils and vesicle of ductus spermathecae, holotype, slide no. AD485; 235, same, general view (ZIN). Note: the slides in Figs 230, 231, and 234 were photographed old, 10 years after they been prepared; slides in Figs 232, 233, and 235 were photographed freshly made, immediately after their preparation in Euparal
FIGURES 73–80 in Documenting new and little known leaf-mining Nepticulidae from middle and southwestern areas of the Asian continent
FIGURES 73–80. Male adults of Ectoedemia spp. 73, holotype of E. ingloria Puplesis, general view (ZIN); 74, same, hindwing upper side; 75, 76, same, forewing underside; 77, 78, holotype of E. tadshikiella Puplesis, general view (ZIN); 79, same, fore- wing underside; 80, same, hindwing upper side.
FIGURES 174–178 in Documenting new and little known leaf-mining Nepticulidae from middle and southwestern areas of the Asian continent
FIGURES 174–178. Genitalia of Ectoedemia spinosella (de Joannis) (= E. albiformae Puplesis & Diškus). 174, holotype of E. albiformae, male genitalia, capsule with phallus removed, slide no. AD422; 175, same, pseuduncus; 176, same, gnathos; 177, same, phallus; 178, paratype of E. albiformae, female genitalia, slide no. AD423 (ZIN)
FIGURES 53–57 in Documenting new and little known leaf-mining Nepticulidae from middle and southwestern areas of the Asian continent
FIGURES 53–57. Male adult of Ectoedemia jacutica Puplesis, holotype (ZIN). 53, forewing upper side; 54, forewing underside; 55–57, hindwing upper side
FIGURES 113–121 in Documenting new and little known leaf-mining Nepticulidae from middle and southwestern areas of the Asian continent
FIGURES 113–121. Male genitalia of Stigmella alilediella Diškus & Navickaitė, sp. nov., holotype, genitalia slide no. AD488 (ZIN). 113, 114, capsule with phallus removed; 115, gnathos; 116–118, phallus; 119, 120, cornuti; 121, capsule with phallus removed
FIGURES 224–229 in Documenting new and little known leaf-mining Nepticulidae from middle and southwestern areas of the Asian continent
FIGURES 224–229. Male genitalia of Acalyptris noctilucus Rocienė & Stonis, sp. nov. 224, holotype, genitalia slide no. AG128, capsule with phallus removed; 225, 226, same, phallus; 227, 228, paratype, genitalia slide AG126, capsule with phallus inside; 229, paratype, genitalia slide no. AG125, capsule with phallus and ventrally bent carina (ZIN)
FIGURES 46–52 in Documenting new and little known leaf-mining Nepticulidae from middle and southwestern areas of the Asian continent
FIGURES 46–52. Details of male adults of Ectoedemia orbiculata Diškus, Remeikis & Stonis, sp. nov. 46–48, forewing underside, paratype; 49–52, hindwing upper side, paratype (ZIN)
FIGURES 103–108 in Documenting new and little known leaf-mining Nepticulidae from middle and southwestern areas of the Asian continent
FIGURES 103–108. Male genitalia of Stigmella damocles Remeikis, sp. nov., holotype, genitalia slide no. AN459 (ZIN). 103, capsule with phallus removed; 104, phallus; 105, valvae; 106, phallus; 107, 108, capsule
FIGURES 198–205 in Documenting new and little known leaf-mining Nepticulidae from middle and southwestern areas of the Asian continent
FIGURES 198–205. Male genitalia of Ectoedemia tadshikiella Puplesis. 198, 199, capsule with phallus removed, holotype, slide no. AN456; 200, 201, gnathos, paratype, genitalia slide no. AN417; 202–204, capsule with phallus removed, holotype, slide no. AN456; 205, same, phallus (ZIN)
FIGURES 192–197 in Documenting new and little known leaf-mining Nepticulidae from middle and southwestern areas of the Asian continent
FIGURES 192–197. Male genitalia of Ectoedemia ingloria Puplesis (= E. rosiphila Puplesis, syn. nov.). 192–194, holotype of E. rosiphila, capsule with phallus removed, slide no. AN466; 195–197, same, phallus (ZIN)
FIGURES 16–28 in Documenting new and little known leaf-mining Nepticulidae from middle and southwestern areas of the Asian continent
FIGURES 16–28. Leaf mines of new species of Nepticulidae. 16, 17, Stigmella longa Remeikis & Stonis, sp. nov.; 18–21, Acalyptris brunipexus Stonis, Diškus & Remeikis, sp. nov.; 22–25, A. nasutus Diškus & Navickaitė, sp. nov.; 26–28, Ectoedemia orbiculata Diškus, Remeikis & Stonis, sp. nov.
FIGURES 143–152 in Documenting new and little known leaf-mining Nepticulidae from middle and southwestern areas of the Asian continent
FIGURES 143–152. Male genitalia of Ectoedemia orbiculata Diškus, Remeikis & Stonis, sp. nov. 143, paratype, slide no. RA271, capsule; 144, same, photographed freshly made in Euparal; 145, pseuduncus, paratype, slide no. RA271; 146, gnathos, paratype, slide no. RA271; 147, cornuti, holotype, slide no. AD489; 148, capsule, paratype, slide no. AG129; 149, apex of phal- lus, holotype, slide no. AD489; 150, same, paratype, slide no. AG129; 151, phallus, general view, holotype, slide no. AD489; 152, same, paratype, slide no. AG129 (ZIN)
FIGURES 167–173 in Documenting new and little known leaf-mining Nepticulidae from middle and southwestern areas of the Asian continent
FIGURES 167–173. Male genitalia of holotype of Ectoedemia insignata Puplesis, genitalia slide no. AD574 (ZIN). 167, pseuduncus; 168, gnathos; 169, valva, 170, 171, apex of phallus; 172, capsule with phallus removed; 173, phallus
FIGURES 130–136 in Documenting new and little known leaf-mining Nepticulidae from middle and southwestern areas of the Asian continent
FIGURES 130–136. Male genitalia of new Stigmella species. 130, 131, holotype of S. latilobata Diškus & Navickaitė, sp. nov., genitalia slide no. AD484, capsule with phallus inside; 132, same, phallus; 133, holotype of S. paniculata Diškus & Navickaitė, sp. nov., capsule with phallus inside; 134, same, uncus and gnathos; 135, same, cornuti; 136, same, valvae (ZIN).
Implementing standardized provider documentation in a tertiary epilepsy clinic: supplemental material
<p class="CxSpFirst"><b>Objective: </b>To incorporate standardized documentation into an epilepsy clinic and use these standardized data to compare patients' perception of epilepsy diagnosis to provider documentation.</p> <p class="CxSpMiddle"><b>Methods: </b>Using quality improvement methodology, we implemented interventions to increase documentation of epilepsy diagnosis, seizure frequency and type from 49.8% to 70% of adult non-employee patients seen by six providers over five months of routine clinical care. The main intervention consisted of an interactive SmartPhrase that mirrored a documentation template developed by the Epilepsy Learning Healthcare System. We assessed the weekly proportion of complete SmartPhrases among eligible patient-encounters with a statistical process control chart. We used a subset of patients with established epilepsy care linked to existing patient-reported survey data to examine the proportion of patient-to-provider agreement on epilepsy diagnosis (yes vs no/unsure). We also examined socio-demographic and clinical characteristics of patients who disagreed vs agreed with provider's documentation of epilepsy diagnosis.</p> <p><b>Results: </b>The median SmartPhrase weekly completion rate was 78%. Established patients disagreed with providers with respect to epilepsy diagnosis in 18.5% of encounters (κ = 0.13), indicating that they did not have, or were unsure if they had, epilepsy despite having a provider-documented epilepsy diagnosis. Patients who disagreed with providers were similar to those who agreed with respect to age, sex, ethnicity, marital status, seizure frequency, type, and other quality of life measures.</p> <p class="CxSpMiddle"><b>Conclusions: </b>This project supports the feasibility of implementing standardized documentation of data relevant to epilepsy care in a tertiary epilepsy clinic and highlights an opportunity for improvement in patient-provider communication.</p>
Multilevel Text Alignment with Cross-Document Attention
<p>This benchmark belongs to our EMNLP2020 paper: <a href="https://arxiv.org/abs/2010.01263">Multilevel Text Alignment with Cross-Document Attention</a>.</p>
Dispatches from the neighborhood watch: using citizen science and field survey data to document color morph frequency in space and time
<p>Heritable color polymorphisms have a long history of study in evolutionary biology, though they are less frequently examined today than in the past. These systems, where multiple discrete, visually identifiable color phenotypes co-occur in the same population, are valuable for tracking evolutionary change and ascertaining the relative importance of different evolutionary mechanisms. Here, we use a combination of citizen science data and field surveys in the Great Lakes region of North America to identify patterns of color morph frequencies in the eastern gray squirrel (<i>Sciurus carolinensis</i>). Using over 68,000 individual squirrel records from both large and small spatial scales, we identify the following patterns: (1) the melanistic (black) phenotype is often localized but nonetheless widespread throughout the Great Lakes region, occurring in all states and provinces sampled. (2) In Ohio, where intensive surveys were performed, there is a weak but significantly positive association between color morph frequency and geographic proximity of populations. Nonetheless, even nearby populations often had radically different frequencies of the melanistic morph, which ranged from 0 to 96%. These patterns were mosaic rather than clinal. (3) In the Wooster, Ohio population, which had over eight years of continuous data on color morph frequency representing nearly 40,000 records, we found that the frequency of the melanistic morph increased gradually over time on some survey routes but decreased or did not change over time on others. These differences were statistically significant and occurred at very small spatial scales (on the order of hundreds of meters). Together, these patterns are suggestive of genetic drift as an important mechanism of evolutionary change in this system. We argue that studies of color polymorphism are still quite valuable in advancing our understanding of fundamental evolutionary processes, especially when coupled with the growing availability of data from citizen science efforts.</p>
A Comparative Analysis of Temporal Long Text Similarity: Application to Financial Documents
<p>Textual Similarity on MD&A disclosure</p>
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Allen Brain Atlas
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DANDI Archive for NWB datasets
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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.
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