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2,798 results for “Chironomidae”
Figure 5 in SEASONAL VARIATION IN THE CHIRONOMIDAE (DIPTERA) COMMUNITIES OF TWO FAROESE STREAMS Abstract
Figure 5. Seasonal variation of the chironomid community of Sundsá. Bar labels refer to month and year. Species acronyms as in Table 2.
Figure 4 in SEASONAL VARIATION IN THE CHIRONOMIDAE (DIPTERA) COMMUNITIES OF TWO FAROESE STREAMS Abstract
Figure 4. Seasonal variation of the chironomid community of Matará. Bar labels refer to month and year. Species acronyms as in Table 2.
Figure 3 in SEASONAL VARIATION IN THE CHIRONOMIDAE (DIPTERA) COMMUNITIES OF TWO FAROESE STREAMS Abstract
Figure 3. Average density of chironomid larvae per sampling occasion in relation to water temperature. The larger stream Sundsá in green and the smaller stream Matará in blue dots. Standard Deviation lies between 141 and 5944 but is not shown for the sake of clarity.
Figure 2 in SEASONAL VARIATION IN THE CHIRONOMIDAE (DIPTERA) COMMUNITIES OF TWO FAROESE STREAMS Abstract
Figure 2. Daily temperature changes in Sundsá and Matará over a year. Water temperature of Sundsá (in green) and Matará (in blue) follow air temperature (black).
Figure 7 in SEASONAL VARIATION IN THE CHIRONOMIDAE (DIPTERA) COMMUNITIES OF TWO FAROESE STREAMS Abstract
Figure 7. Relative abundance of Tvetenia calvescens life stages (instars I, II, III and IV) in the smaller stream Matará (blue) and larger stream Sundsá (green). Black lines indicate emergence of adults.
Figure 4 in TEMPORAL PARTITIONING OF CHIRONOMIDAE EMERGENCE IN AN INSULAR, TROPICAL RAINFOREST STREAM Abstract
Figure 4. Monthly emergence of abundant Tanypodinae taxa (>1% of total abundance). Shaded area indicates dry season.
Figure 7 in TEMPORAL PARTITIONING OF CHIRONOMIDAE EMERGENCE IN AN INSULAR, TROPICAL RAINFOREST STREAM Abstract
Figure 7. Dissimilarities (Bray-Curtis) between monthly samples of emerging Chironomidae for (a) Quebrada Prieta (USA; Puerto Rico) and (b) Kalengo River (Democratic Republic of the Congo). Grey circles are individual paired months and black circles are the average dissimilarities of all pairs of samples separated by the same number of months.
Figure 3 in TEMPORAL PARTITIONING OF CHIRONOMIDAE EMERGENCE IN AN INSULAR, TROPICAL RAINFOREST STREAM Abstract
Figure 3. Monthly total abundance (a) and taxa richness (b) of emerging Chironomidae from Quebrada Prieta. Shaded area indicates dry season.
Figure 1 in TEMPORAL PARTITIONING OF CHIRONOMIDAE EMERGENCE IN AN INSULAR, TROPICAL RAINFOREST STREAM Abstract
Figure 1. Average monthly water temperature (a) and rainfall (b) from stations near the sample site on Quebrada Prieta. Circles are average values of water temperature (1983-2018) and rainfall (1975-2021) with error bars representing standard deviation. Grey bars are data for February 1990 through January 1991. Water temperature data are from a downstream station in Quebrada Sonadora (McDowell 2021) and rainfall data are from the El Verde Field Station (Ramirez 2021).
Figure 6 in TEMPORAL PARTITIONING OF CHIRONOMIDAE EMERGENCE IN AN INSULAR, TROPICAL RAINFOREST STREAM Abstract
Figure 6. Monthly emergence of abundant Chironominae taxa (>1% of total abundance). Shaded area indicates dry season.
Figure 5 in TEMPORAL PARTITIONING OF CHIRONOMIDAE EMERGENCE IN AN INSULAR, TROPICAL RAINFOREST STREAM Abstract
Figure 5. Monthly emergence of abundant Orthocladiinae taxa (>1% of total abundance). Shaded area indicates dry season.
Figure 6 in A New Species Of Petalocladius Sublette & Wirth, 1972 (Diptera, Chironomidae, Orthocladiinae) From The Dominican Republic, With An Emended Generic Diagnosis
Figure 6. Position of Petalocladius (marked in red) in the phylogenetic tree of Orthocladiinae, reconstructed with Bayesian inference (all posterior probabilities of the nodes are displayed, regardless of the value). This is a majority rule consensus tree based on morphology only.
Figure 7 in A New Species Of Petalocladius Sublette & Wirth, 1972 (Diptera, Chironomidae, Orthocladiinae) From The Dominican Republic, With An Emended Generic Diagnosis
Figure 7. Rouge plot of the frequency of placement of Petalocladius on a Bayesian tree from Fig. 6, based on the frequency of occurrence of Petalocladius in a given node, based on 50001 most congruent trees from the Bayesian analysis of the genus's morphology.
Figure 3 in A New Species Of Petalocladius Sublette & Wirth, 1972 (Diptera, Chironomidae, Orthocladiinae) From The Dominican Republic, With An Emended Generic Diagnosis
Figure 3. Petalocladius dominiensis Andersen & Baranov sp. n., male. A. Hypopygium, dorsal view. B. Inferior volsella. C. Apex of gonostylus, showing the megaseta.
Figure 5 in A New Species Of Petalocladius Sublette & Wirth, 1972 (Diptera, Chironomidae, Orthocladiinae) From The Dominican Republic, With An Emended Generic Diagnosis
Figure 5. The male of Petalocladius setosus Sublette & Wirth, 1972. A. Head. B. Thorax. C. Wing. D. Hypopygium, dorsal view. E. Inferior volsella. F. Apex of gonostylus. Photos: David Pecor, Smithsonian Institution.
Figure 1 in A New Species Of Petalocladius Sublette & Wirth, 1972 (Diptera, Chironomidae, Orthocladiinae) From The Dominican Republic, With An Emended Generic Diagnosis
Figure 1. Petalocladius dominiensis Andersen & Baranov sp. n., male. A. Palp. B. Thorax. C. Hypopygium, dorsal view. D. Hypopygium, ventral view.
Figure 6 in LIMNOPHYES KNISPELAE SP. N. AND L. SARTORII SP. N., TWO NEW CRENOPHILOUS SPECIES FROM THE SWISS ALPS (CHIRONOMIDAE, ORTHOCLADIINAE) Abstract
Figure 6. Type-locality of Limnophyes sartorii sp. n. at the inlet of the Immez Lake (Macun cirque, Eastern Alps, Swiss National Park, alt. 2616 m; photo J.L. Lods).
Figure 5 in LIMNOPHYES KNISPELAE SP. N. AND L. SARTORII SP. N., TWO NEW CRENOPHILOUS SPECIES FROM THE SWISS ALPS (CHIRONOMIDAE, ORTHOCLADIINAE) Abstract
Figure 5. Type-locality of Limnophyes knispelae sp. n. at the upper basin of the Rhône river (Gletschboden, Central Swiss Alps, alt. 1800 m; photo J.L. Lods).
Figure 1 in LIMNOPHYES KNISPELAE SP. N. AND L. SARTORII SP. N., TWO NEW CRENOPHILOUS SPECIES FROM THE SWISS ALPS (CHIRONOMIDAE, ORTHOCLADIINAE) Abstract
Figure 1. Male adult of Limnophyes knispelae sp. n. A) clypeus; B) palpomere 3; C) lobes of antepronotum; D) humeral pit with dorsocentrals and prealars; E) humeral area with humeral pit; F-G) distribution pattern of preepisternals; H) tergite IX and anal point in lateral view. The arrows indicate some distinguishing characters.
Figure 4 in LIMNOPHYES KNISPELAE SP. N. AND L. SARTORII SP. N., TWO NEW CRENOPHILOUS SPECIES FROM THE SWISS ALPS (CHIRONOMIDAE, ORTHOCLADIINAE) Abstract
Figure 4. Male adult and pupal exuviae of Limnophyes sartorii sp. n. Male adult: A) hypopygium in dorsal view; B) apodemes; C) virga, other aspect; E) gonostylus at acute angle; F) gonostylus at obtuse angle. Male pupal exuviae: G) frontal apotome; H) thoracic horn (reduced) and precorneals; I) dorsocentrals Dc 1 -Dc 4; J) segment VI in lateral view; K) details of caudal transverse rows of small hooklets; L) segment VIII and anal lobe in dorsal and ventral view; M) anal macroseta. The arrows indicate some distinguishing characters.
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Allen Brain Atlas
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International Brain Laboratory public data
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OpenNeuro
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