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2,775 results for “G×E”
F I G U R E 6 in Reproductive biology of the electric lanternfish Electrona risso (Myctophidae) and the bigscale fishes Melamphaes polylepis and Scopelogadus mizolepis (Melamphaidae)
F I G U R E 6 Gonado-somatic index of females of (a) Electrona risso, (b) Melamphaes polylepis, and (c) Scopelogadus mizolepis, per reproductive phase. I, immature; II, early developing; III, developing; IV, spawning capable; V, actively spawning (see also Table 1). All neighboring values differ significantly (p <0.05).
F I G U R E 4 in Reproductive biology of the electric lanternfish Electrona risso (Myctophidae) and the bigscale fishes Melamphaes polylepis and Scopelogadus mizolepis (Melamphaidae)
F I G U R E 4 Melamphaes polylepis ovarian development. Reproductive phases based on Table 1. Macroscopic development in female gonads (left panels) and histological cross-sections of ovaries (right panels). CA, cortical alveoli oocyte; GVBD, germinal vesicle (nucleus) breakdown oocyte; nu, nucleus; PG, primary growth oocyte; POF, postovulatory follicle; Vtg1–3, primary to tertiary vitellogenic oocyte; yg, yolk granules; yv, yolk vesicle. Photography by A. Knorrn.
F I G U R E 2 in Biological information on a rare pelagic fish, black ruff Centrolophus niger, caught in Icelandic waters: Distribution, feeding, and otoliths
F I G U R E 2 Location of sampling stations of the Icelandic component of the International Ecosystem Summer Survey of the Nordic Seas 2009–2021. Stations where black ruff Centrolophus niger (Gmelin, 1789) were caught are shown in Black. The main surface currents in the Northeast Atlantic are shown in the final panel; the cold East Greenland current (green) and the warm Atlantic current (red) (Blindheim & Østerhus, 2005).
F I G U R E 3 in Reproductive biology of the electric lanternfish Electrona risso (Myctophidae) and the bigscale fishes Melamphaes polylepis and Scopelogadus mizolepis (Melamphaidae)
F I G U R E 3 Electrona risso ovarian development. Reproductive phases based on Table 1. Macroscopic development in female gonads (left panels) and histological cross-sections of ovaries (right panels). A, atresia; CA, cortical alveoli oocyte; GVBD, germinal vesicle (nucleus) breakdown oocyte; GVM, germinal vesicle migration oocyte; HYD, hydrated oocyte; PG, primary growth oocyte; Vtg1–3, primary to tertiary vitellogenic oocyte; yg, yolk granules; yv, yolk vesicle. Photography by K. Wieben.
F I G U R E 1 in Reproductive biology of the electric lanternfish Electrona risso (Myctophidae) and the bigscale fishes Melamphaes polylepis and Scopelogadus mizolepis (Melamphaidae)
F I G U R E 1 Mesopelagic net sampling stations (circles) and locations where (a) Electrona risso, (b) Melamphaes polylepis, and (c) Scopelogadus mizolepis were caught (black circles) in the eastern Central Atlantic during the 383rd cruise of the FFS Walther Herwig III in March and April 2015. Land mass is shown in light gray and ocean in dark gray.
F I G U R E 5 in Heterochrony and the evolution of the longjaw mudsucker (Gobiidae, Teleostei)
F I G U R E 5 Hypothesized phylogeny and inferred patterns of heterochrony between Eucylcogobius and Gillichthys.
F I G U R E 2 in Heterochrony and the evolution of the longjaw mudsucker (Gobiidae, Teleostei)
F I G U R E 2 Scatter plot of principal component 1 score (representative of body size) for all three species against (a) log-transformed total jaw length and (b) log-transformed free maxilla length. Linear trendline shown as lines matching the colors for each species. Sex is shown with different shapes for each species.
F I G U R E 3 in Heterochrony and the evolution of the longjaw mudsucker (Gobiidae, Teleostei)
F I G U R E 3 Scatter plot of principal component 1 score (representative of body size) for mature and juvenile (a) Gillichthys mirabilis against log-transformed total jaw length, (b) G. mirabilis against log-transformed free maxilla length, (c) Gillichthys seta against log-transformed total jaw length, (d) G. seta against log-transformed free maxilla length, (e) Eucyclogobius newberryi against log-transformed total jaw length, and (f) E. newberryi against log-transformed free maxilla length. Linear trendlines shown with corresponding equations matching the colors for each sex.
F I G U R E 3 in Migration patterns and navigation cues of Atlantic salmon post-smolts migrating from 12 rivers through the coastal zones around the Irish Sea
F I G U R E 3 The binomial General Linear Model (GLM) model showing the effect of minimum migration distance (Distance [km]) from the exit of smolts natal river/estuary to monitoring line B on the probability of migration success (measured as minimum migration success) of Atlantic salmon (Salmo salar) post-smolt through the Irish Sea. The shaded region is the 95% confidence interval of the final model.
F I G U R E 4 in Heterochrony and the evolution of the longjaw mudsucker (Gobiidae, Teleostei)
F I G U R E 4 Scatterplot of principal components 1 and 2 from a principal component analysis of sexually mature Gillichthys mirabilis, Gillichthys seta, and Eucyclogobius newberryi (morphometric data adjusted using allometric- Burnaby transformation). Ellipses represent 95% confidence intervals.
F I G U R E 1 in Heterochrony and the evolution of the longjaw mudsucker (Gobiidae, Teleostei)
F I G U R E 1 Photos of a preserved Gillichthys mirabilis (a) unlabeled and (b) with labeled landmarks used in geometric morphometric analysis (in blue): (1) anterior tip of nasal bone, (2) first dorsal-fin spine insertion, (3) insertion of first element of second dorsal fin, (4) upper tip of dorsal hypural plate, (5) lower tip of ventral hypural plate, (6) first anal-fin spine insertion, and (7) pelvic-fin spine base. Additional measurements used in geometric morphometric analysis (in green): (1) head length from snout to farthest posterior point of the operculum, (2) head length from snout to dorsal operculum insertion, (3) total upper jaw length, (4) free maxilla length or the posterior portion of the maxilla that is not attached to the head, (5) maximum maxilla depth, and (6) body depth at the origin of the anal fin.
F I G U R E 7 Total length v in Biological information on a rare pelagic fish, black ruff Centrolophus niger, caught in Icelandic waters: Distribution, feeding, and otoliths
F I G U R E 7 Total length v. (a) frozen weight, (b) fork length, (c) and standard length and frozen weight v. (d) thawed weight for black ruff Centrolophus niger (Gmelin, 1789). (a) Nonlinear and (b–d) linear regression models are shown (a–d) as well as x = y line (d).
F I G U R E 2 in Scaling of fast-start performance and its thermal dependence in mummichog Fundulus heteroclitus
F I G U R E 2 Representative kinematics for fast-starts in small (41 mm SL) and large (66 mm SL) adult mummichogs controlling for temperature. The top panel shows frames from high-speed videos at 10 ms intervals. To facilitate interpretation, original videos have been cropped to the same spatial dimensions and rotated to standardize starting orientation and escape direction (but note that digitization used unmodified videos). The graph in the bottom panel shows the angular displacement of the head (triangles) and the linear displacement of the fish center of mass (circles) for the trials depicted in the video frames, which were maximum performance trials for the small (filled shapes) and large (open shapes) fish tested at their acclimation temperature (24 C). The curve for head rotation was truncated at its maximum value to highlight the difference in time to form the initial C-bend. The curve for linear displacement continued until the end of stage 2 of the fast-start. Whereas small fish had higher rotation rates and executed the fast-start in less time, small and large fish moved their bodies over similar distances given equal amounts of time.
F I G U R E 4 in Biological information on a rare pelagic fish, black ruff Centrolophus niger, caught in Icelandic waters: Distribution, feeding, and otoliths
F I G U R E 4 Temperature profiles from the CTD probe at each station of the Icelandic part of the International Ecosystem Summer Survey of the Nordic Seas (IESSNS) where black ruff Centrolophus niger (Gmelin, 1789) were caught.
F I G U R E 1 in Global warming is projected to lead to increased freshwater growth potential and changes in pace of life in Atlantic salmon Salmo salar
F I G U R E 1 Location of electrofishing sites (green circles) and fish traps (red circles) in the Burrishoole catchment, Co. Mayo, Ireland.
F I G U R E 1 in High summer temperatures are associated with poorer performance of underyearling Atlantic salmon (Salmo salar) in upland streams
F I G U R E 1 (a) Locations of sampling sites (circles) in the river Conon catchment, Northern Scotland. The map depicts the area within the black box in the inset map. (b) Daily maximum temperatures recorded in each stream during the study period (points represent the daily highest temperature for the entire stream, so may be either from the upper or lower sampling sites). Red values indicate temperatures>23 C, considered stressful to Atlantic salmon, while yellow values indicate temperatures between 20 C and 23 C, and blue values indicate temperatures <20 C. (c) Density and (d) biomass of underyearling Atlantic salmon, Salmo salar (both on a natural logarithmic scale, ± standard error) in relation to duration of peak temperatures (degree hours above 23 C) at sites in the River Conon catchment (n = 63 sections sampled across six sites in 2 years, 589 fish). All sites had the same initial density and genetic composition of eggs. Temperature: 0–20, 20–23, and>23. Year and sampling position: 2020 Downstream, 2020 Upstream, 2021 Downstream, and 2021 Upstream. Stream: Blackwater, Rannoch, and Vaich.
РИС. 2. Места нахождениЯ Amuranodonta kijaensis на территории Хинганского Заповедника, АмурскаЯ обл.: А. Схема расположениЯ лесничеств: 1 – Антоновское, 2 – Лебединское, 3 – Хинганское. B. ТопографическаЯ карта Антоновского вдхр. у пос. Архара. С, D. Топографические карты и спутниковый снимок оЗ. Яценково на территории Антоновского лесничества. E–G. ТопографическаЯ карта и спутниковый снимок оЗ. ПереШеечное на территории Лебединского лесничества. МасШтабные линейки: 20 км (А), 4 км (В, Е), 5 км (С), 1 км (D, G), 2 км (F). FIG. 2. Localities of Amuranodonta kijaensis in the Khingansky Reserve, Amur Region: A. Layout of forestry areas: 1 – Antonovsky, 2 – Lebedinsky, 3 – Khingansky. B. Topographic map of Antonovskoe Reservoir near Arkhara village. C, D. Topographic maps and satellite image of Yatsenkovo lake, Antonovsky forestry. E–G. Topographic map and satellite image of Peresheechnoe lake, Lebedinsky forestry. Scale bars: 20 km (A), 4 km (B, E), 5 km (C), 1 km (D, G), 2 km (F). in Новые данные об охранЯемом пресноводном двустворчатом моллюске Amuranodonta kijaensis Moskvicheva, 1973 (Unionidae, Anodontinae)
РИС. 2. Места нахождениЯ Amuranodonta kijaensis на территории Хинганского Заповедника, АмурскаЯ обл.: А. Схема расположениЯ лесничеств: 1 – Антоновское, 2 – Лебединское, 3 – Хинганское. B. ТопографическаЯ карта Антоновского вдхр. у пос. Архара. С, D. Топографические карты и спутниковый снимок оЗ. Яценково на территории Антоновского лесничества. E–G. ТопографическаЯ карта и спутниковый снимок оЗ. ПереШеечное на территории Лебединского лесничества. МасШтабные линейки: 20 км (А), 4 км (В, Е), 5 км (С), 1 км (D, G), 2 км (F). FIG. 2. Localities of Amuranodonta kijaensis in the Khingansky Reserve, Amur Region: A. Layout of forestry areas: 1 – Antonovsky, 2 – Lebedinsky, 3 – Khingansky. B. Topographic map of Antonovskoe Reservoir near Arkhara village. C, D. Topographic maps and satellite image of Yatsenkovo lake, Antonovsky forestry. E–G. Topographic map and satellite image of Peresheechnoe lake, Lebedinsky forestry. Scale bars: 20 km (A), 4 km (B, E), 5 km (C), 1 km (D, G), 2 km (F).
РИС. 5. Места находок Amuranodonta kijaensis: A. Зейское вдхр. В–D. Река Амур у с. Чныррах. E, F. ОЗеро ПереШеечное. G. ОЗеро Долгое. H. Антоновское вдхр. FIG. 5. Localities of Amuranodonta kijaensis: A. Zeya Reservoir. B–D. Amur River near Chnyrrakh village. E, F. Peresheechnoe lake. G. Dolgoe lake. H. Antonovskoe Reservoir. in Новые данные об охранЯемом пресноводном двустворчатом моллюске Amuranodonta kijaensis Moskvicheva, 1973 (Unionidae, Anodontinae)
РИС. 5. Места находок Amuranodonta kijaensis: A. Зейское вдхр. В–D. Река Амур у с. Чныррах. E, F. ОЗеро ПереШеечное. G. ОЗеро Долгое. H. Антоновское вдхр. FIG. 5. Localities of Amuranodonta kijaensis: A. Zeya Reservoir. B–D. Amur River near Chnyrrakh village. E, F. Peresheechnoe lake. G. Dolgoe lake. H. Antonovskoe Reservoir.
РИС. 1. Раковины ювенильных крымских клауЗиллид (A–C). A. Mentissa gracilicosta, г. КоШка, СимеиЗ, coll. В. Н. Попов, det. С. В. Леонов. B. Mentissa canalifera, окрестности с. Краснолесье, 23.08.2002, сoll.&det. С. В. Леонов. C. Cochlodina laminata, Артек «Дубрава», 27.05.1999, coll.?, det. С.В. Леонов. Раковины половоЗрелых Balea perversa (D–G). D. Между Виклебю и Ресмо, остров Эланд, ШвециЯ, 07.1958 (фото F. Welter-Shultes). Е. Девичий Замок, Палава, ЮжнаЯ МоравиЯ, ЧехиЯ, 26.09.1998 (фото M. Horsák). F. РаЗвалины Замка РейнграфенШтайн блиЗ Бад-Мюнстер-ам-Штайн, Рейнланд-Пфальц, ГерманиЯ (фото А. В. Сысоев). G. Яйла Южной Демерджи, АлуШта, Республика Крым, РоссиЯ, 14.11.2002, сoll. Н. М. Ковблюк, det. С. В. Леонов. Все иЗображениЯ в одном масШтабе. FIG. 1. Shells of juvenile Crimean clausillids (A–C). A. Mentissa gracilicosta, Koshka mountain, Simeiz, coll. V. N. Popov, det. S. V. Leonov. B. Mentissa canalifera, near Krasnolesye village, 23.08.2002, coll.&det. S. V. Leonov. C. Cochlodina laminata, Artek "Dubrava", 27.05.1999, coll.?, det. S.V. Leonov. Adult Balea perversa shells (D–G). D. Sweden, Öland, between Vickleby and Resmo, 07.1958 (photo F. Welter-Shultes). E. Dívčí hrad, South Moravia, Czech Republic, 26.09.1998 (photo by M. Horsák). F. Ruins of the Rheingrafenstein Castle near Bad Munster am Stein, Rheineland-Pfalz, Germany (photo by A.V. Sysoev). G. Yayla Yuzhnaya Demerdzhi, Alushta, Republic of Crimea, Russia, 14.11.2002, coll. N. M. Kovblyuk, det. S. V. Leonov. All images are at the same scale. in О достоверности находок Balea perversa (Gastropoda: Pulmonata: Clausiliidae) в Крыму
РИС. 1. Раковины ювенильных крымских клауЗиллид (A–C). A. Mentissa gracilicosta, г. КоШка, СимеиЗ, coll. В. Н. Попов, det. С. В. Леонов. B. Mentissa canalifera, окрестности с. Краснолесье, 23.08.2002, сoll.&det. С. В. Леонов. C. Cochlodina laminata, Артек «Дубрава», 27.05.1999, coll.?, det. С.В. Леонов. Раковины половоЗрелых Balea perversa (D–G). D. Между Виклебю и Ресмо, остров Эланд, ШвециЯ, 07.1958 (фото F. Welter-Shultes). Е. Девичий Замок, Палава, ЮжнаЯ МоравиЯ, ЧехиЯ, 26.09.1998 (фото M. Horsák). F. РаЗвалины Замка РейнграфенШтайн блиЗ Бад-Мюнстер-ам-Штайн, Рейнланд-Пфальц, ГерманиЯ (фото А. В. Сысоев). G. Яйла Южной Демерджи, АлуШта, Республика Крым, РоссиЯ, 14.11.2002, сoll. Н. М. Ковблюк, det. С. В. Леонов. Все иЗображениЯ в одном масШтабе. FIG. 1. Shells of juvenile Crimean clausillids (A–C). A. Mentissa gracilicosta, Koshka mountain, Simeiz, coll. V. N. Popov, det. S. V. Leonov. B. Mentissa canalifera, near Krasnolesye village, 23.08.2002, coll.&det. S. V. Leonov. C. Cochlodina laminata, Artek "Dubrava", 27.05.1999, coll.?, det. S.V. Leonov. Adult Balea perversa shells (D–G). D. Sweden, Öland, between Vickleby and Resmo, 07.1958 (photo F. Welter-Shultes). E. Dívčí hrad, South Moravia, Czech Republic, 26.09.1998 (photo by M. Horsák). F. Ruins of the Rheingrafenstein Castle near Bad Munster am Stein, Rheineland-Pfalz, Germany (photo by A.V. Sysoev). G. Yayla Yuzhnaya Demerdzhi, Alushta, Republic of Crimea, Russia, 14.11.2002, coll. N. M. Kovblyuk, det. S. V. Leonov. All images are at the same scale.
РИС. 3. Раковины Зрелых глохидиев Beringiana beringiana в раЗных ракурсах: А–С – Закрытые раковины, вид со стороны створки (А), вентрального угла (В) и лигамента (С); D–F – полностью открытые раковины, вид иЗнутри (D), снаруЖи (E) и боковых краев створок (F); G, H – приоткрытые раковины, стрелка укаЗывает на остатки волокон мускулаЗамыкателЯ. МасштабнаЯ линейка 100 мкм. СканируюЩаЯ ЭлектроннаЯ микроскопиЯ. FIG. 3. Mature glochidial shells of Beringiana beringiana from different angles of view: A–C – closed shells, view from the valve side (A), ventral angle (B), and ligament (C); D–F – open shells, interior view (D), exterior view (E), and from lateral margins of valves (F); G, H – ajar shells, the arrows indicate the remains of the adductor muscle fibers. Scale bar 100 µm. Scanning electron microscopy. in Первые данные о морфологии глохидиев двустворчатых моллюсков Beringiana beringiana (Bivalvia, Unionidae) оЗера Дальнее, Камчатка
РИС. 3. Раковины Зрелых глохидиев Beringiana beringiana в раЗных ракурсах: А–С – Закрытые раковины, вид со стороны створки (А), вентрального угла (В) и лигамента (С); D–F – полностью открытые раковины, вид иЗнутри (D), снаруЖи (E) и боковых краев створок (F); G, H – приоткрытые раковины, стрелка укаЗывает на остатки волокон мускулаЗамыкателЯ. МасштабнаЯ линейка 100 мкм. СканируюЩаЯ ЭлектроннаЯ микроскопиЯ. FIG. 3. Mature glochidial shells of Beringiana beringiana from different angles of view: A–C – closed shells, view from the valve side (A), ventral angle (B), and ligament (C); D–F – open shells, interior view (D), exterior view (E), and from lateral margins of valves (F); G, H – ajar shells, the arrows indicate the remains of the adductor muscle fibers. Scale bar 100 µm. Scanning electron microscopy.
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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.
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DANDI Archive for NWB datasets
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OpenNeuro
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