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58 results for “Chrysomela”
Santa Barbara Coastal site, station Mohawk Reef, Santa Barbara Channel, study of animal density of Sebastes chrysomelas in units of numberPerMeterSquared on a yearly timescale
The EcoTrends project was established in 2004 by Dr. Debra Peters (Jornada Basin LTER, USDA-ARS Jornada Experimental Range) and Dr. Ariel Lugo (Luquillo LTER, USDA-FS Luquillo Experimental Forest) to support the collection and analysis of long-term ecological datasets. The project is a large synthesis effort focused on improving the accessibility and use of long-term data. At present, there are ~50 state and federally funded research sites that are participating and contributing to the EcoTrends project, including all 26 Long-Term Ecological Research (LTER) sites and sites funded by the USDA Agriculture Research Service (ARS), USDA Forest Service, US Department of Energy, US Geological Survey (USGS) and numerous universities. Data from the EcoTrends project are available through an exploratory web portal (http://www.ecotrends.info). This web portal enables the continuation of data compilation and accessibility by users through an interactive web application. Ongoing data compilation is updated through both manual and automatic processing as part of the LTER Provenance Aware Synthesis Tracking Architecture (PASTA). The web portal is a collaboration between the Jornada LTER and the LTER Network Office. The following dataset from Santa Barbara Coastal (SBC) contains animal density of Sebastes chrysomelas measurements in numberPerMeterSquared units and were aggregated to a yearly timescale.
Santa Barbara Coastal site, station Naples Reef, Santa Barbara Channel, study of animal density of Sebastes chrysomelas in units of numberPerMeterSquared on a yearly timescale
The EcoTrends project was established in 2004 by Dr. Debra Peters (Jornada Basin LTER, USDA-ARS Jornada Experimental Range) and Dr. Ariel Lugo (Luquillo LTER, USDA-FS Luquillo Experimental Forest) to support the collection and analysis of long-term ecological datasets. The project is a large synthesis effort focused on improving the accessibility and use of long-term data. At present, there are ~50 state and federally funded research sites that are participating and contributing to the EcoTrends project, including all 26 Long-Term Ecological Research (LTER) sites and sites funded by the USDA Agriculture Research Service (ARS), USDA Forest Service, US Department of Energy, US Geological Survey (USGS) and numerous universities. Data from the EcoTrends project are available through an exploratory web portal (http://www.ecotrends.info). This web portal enables the continuation of data compilation and accessibility by users through an interactive web application. Ongoing data compilation is updated through both manual and automatic processing as part of the LTER Provenance Aware Synthesis Tracking Architecture (PASTA). The web portal is a collaboration between the Jornada LTER and the LTER Network Office. The following dataset from Santa Barbara Coastal (SBC) contains animal density of Sebastes chrysomelas measurements in numberPerMeterSquared units and were aggregated to a yearly timescale.
Figure 15 in Maratus nubilis, a new peacock spider in the chrysomelas group from southwestern Australia (Araneae: Salticidae: Euophryini)
Figure 15 (continued from previous page). Living immature (instar III or IV) Maratus nubilis.
Figure 14 in Maratus nubilis, a new peacock spider in the chrysomelas group from southwestern Australia (Araneae: Salticidae: Euophryini)
Figure 14. Living emergent (instar II) Maratus nubilis.
Figure 12 in Maratus nubilis, a new peacock spider in the chrysomelas group from southwestern Australia (Araneae: Salticidae: Euophryini)
Figure 12 (continued from previous page). Female paratypes for Maratus nubilis in alcohol.
Figure 11 in Maratus nubilis, a new peacock spider in the chrysomelas group from southwestern Australia (Araneae: Salticidae: Euophryini)
Figure 11. Ventral view of living female paratypes for Maratus nubilis.
Figure 10 in Maratus nubilis, a new peacock spider in the chrysomelas group from southwestern Australia (Araneae: Salticidae: Euophryini)
Figure 10 (continued from previous page). Living female paratypes for Maratus nubilis.
Figure 10 in Maratus nubilis, a new peacock spider in the chrysomelas group from southwestern Australia (Araneae: Salticidae: Euophryini)
Figure 10 (continued on next page). Living female paratypes for Maratus nubilis.
Figure 6 in Maratus nubilis, a new peacock spider in the chrysomelas group from southwestern Australia (Araneae: Salticidae: Euophryini)
Figure 6. Ventral view of living male types for Maratus nubilis.
On following pages: 489. Coues's Marsh Rice Rat (Oryzomys couesi); 490. White-bellied Marsh Rice Rat (Oryzomys albiventer), 491. Nicaraguan Marsh Rice Rat (Oryzomys dimidiatus); 492. Gorgas's Marsh Rice Rat (Oryzomys gorgasi, 493. Santiago Galapagos Mouse (Nesoryzomys swarthi); 494. Small Fernandina Galapagos Mouse (Nesoryzomys fernandinae); 495. Large Fernandina Galapagos Mouse (Nesoryzomys narboroughi); 496. Galapagos Rice Rat (Aegialomys galapagoensis); 497 Yellowish Rice Rat (Aegialomys xanthaeolus); 498. Baron's Rice Rat (Aegialomys baroni); 499. Ica Rice Rat (Aegialomys ica); 500. Alfaro's Water Rat (Sigmodontomys alfari); 501. Harris's Rice Water Rat (Tanyuromys aphrastus); 502. Black-and-Yellow Rice Rat (Melanomys chrysomelas); 503. Cinnamon-rufous Rice Rat (Melanomys idoneus); 504. Colombian Rice Rat (Melanomys columbianus); 505. Dusky Rice Rat (Melanomys caliginosus); 506. Robust Dark Rice Rat (Melanomys robustulus); 507. Zuniga's Dark Rice Rat (Melanomys zunigae); 508. Intermediate Lesser Grass Mouse (Microakodontomys transitorius); 509. Lagoa Santa Pink-lipped Mouse (Bibimys labiosus); 510. Chacoan Pink-lipped Mouse (Bibimys chacoensis); 511. Torres's Pink-lipped Mouse (Bibimys torresi), 512. Brazilian Swamp Rat (Scapteromys meridionalis); 513. Argentinean Swamp Rat (Scapteromys aquaticus); 514. Uruguay Swamp Rat (Scapteromys tumidus); 515. Cerrado Giant Rat (Gyldenstolpia planaltensis); 516. Fossorial Giant Rat (Gyldenstolpia fronto); 517. Woolly Giant Rat (Kunsia tomentosus); 518. Andean Rat (Lenoxus apicalis); 519. Atlantic Forest Burrowing Mouse (Blarinomys breviceps); 520. Gray-bellied Brucie (Brucepattersonius griserufescens); 521. Short-tailed Brucie (Brucepattersonius soricinus); 522. Ihering's Brucie (Brucepattersonius iheringi). in Cricetidae
On following pages: 489. Coues's Marsh Rice Rat (Oryzomys couesi); 490. White-bellied Marsh Rice Rat (Oryzomys albiventer), 491. Nicaraguan Marsh Rice Rat (Oryzomys dimidiatus); 492. Gorgas's Marsh Rice Rat (Oryzomys gorgasi, 493. Santiago Galapagos Mouse (Nesoryzomys swarthi); 494. Small Fernandina Galapagos Mouse (Nesoryzomys fernandinae); 495. Large Fernandina Galapagos Mouse (Nesoryzomys narboroughi); 496. Galapagos Rice Rat (Aegialomys galapagoensis); 497 Yellowish Rice Rat (Aegialomys xanthaeolus); 498. Baron's Rice Rat (Aegialomys baroni); 499. Ica Rice Rat (Aegialomys ica); 500. Alfaro's Water Rat (Sigmodontomys alfari); 501. Harris's Rice Water Rat (Tanyuromys aphrastus); 502. Black-and-Yellow Rice Rat (Melanomys chrysomelas); 503. Cinnamon-rufous Rice Rat (Melanomys idoneus); 504. Colombian Rice Rat (Melanomys columbianus); 505. Dusky Rice Rat (Melanomys caliginosus); 506. Robust Dark Rice Rat (Melanomys robustulus); 507. Zuniga's Dark Rice Rat (Melanomys zunigae); 508. Intermediate Lesser Grass Mouse (Microakodontomys transitorius); 509. Lagoa Santa Pink-lipped Mouse (Bibimys labiosus); 510. Chacoan Pink-lipped Mouse (Bibimys chacoensis); 511. Torres's Pink-lipped Mouse (Bibimys torresi), 512. Brazilian Swamp Rat (Scapteromys meridionalis); 513. Argentinean Swamp Rat (Scapteromys aquaticus); 514. Uruguay Swamp Rat (Scapteromys tumidus); 515. Cerrado Giant Rat (Gyldenstolpia planaltensis); 516. Fossorial Giant Rat (Gyldenstolpia fronto); 517. Woolly Giant Rat (Kunsia tomentosus); 518. Andean Rat (Lenoxus apicalis); 519. Atlantic Forest Burrowing Mouse (Blarinomys breviceps); 520. Gray-bellied Brucie (Brucepattersonius griserufescens); 521. Short-tailed Brucie (Brucepattersonius soricinus); 522. Ihering's Brucie (Brucepattersonius iheringi).
On following pages: 184. Magdalena Woodrat (Xenomys nelsoni); 185. Bushy-tailed Woodrat (Neotoma cinerea); 186. Sonoran Woodrat (Neotoma phenax); 187. Goldman's Woodrat (Neotoma goldmani); 188. Allegheny Woodrat (Neotoma magisten; 189. Eastern Woodrat (Neotoma floridanus); 190. White-throated Woodrat (Neotoma albigula); 191. Black-tailed Woodrat (Neotoma melanura); 192. White-toothed Woodrat (Neotoma leucodon): 193. Southern Plains Woodrat (Neotoma micropus); 194. Nelson's Woodrat (Neotoma nelsoni); 195. Bolanos Woodrat (Neotoma palatina); 196. Tamaulipan Woodrat (Neotoma angustapalata); 197. Mexican Woodrat (Neotoma mexicana); 198. Painted Woodrat (Neotoma picta); 199. Guatemala Woodrat (Neotoma ferruginea); 200. Nicaraguan Woodrat (Neotoma chrysomelas); 201. Stephens's Woodrat (Neotoma stephensi); 202. Dusky-footed Woodrat (Neotoma fuscipes); 203. Big-eared Woodrat (Neotoma macrotis); 204. Bryant's Woodrat (Neotoma bryant); 205. Angel de la Guarda Woodrat (Neotoma insularis); 206. Desert Woodrat (Neotoma lepida); 207. Arizona Woodrat (Neotoma devia). in Cricetidae
On following pages: 184. Magdalena Woodrat (Xenomys nelsoni); 185. Bushy-tailed Woodrat (Neotoma cinerea); 186. Sonoran Woodrat (Neotoma phenax); 187. Goldman's Woodrat (Neotoma goldmani); 188. Allegheny Woodrat (Neotoma magisten; 189. Eastern Woodrat (Neotoma floridanus); 190. White-throated Woodrat (Neotoma albigula); 191. Black-tailed Woodrat (Neotoma melanura); 192. White-toothed Woodrat (Neotoma leucodon): 193. Southern Plains Woodrat (Neotoma micropus); 194. Nelson's Woodrat (Neotoma nelsoni); 195. Bolanos Woodrat (Neotoma palatina); 196. Tamaulipan Woodrat (Neotoma angustapalata); 197. Mexican Woodrat (Neotoma mexicana); 198. Painted Woodrat (Neotoma picta); 199. Guatemala Woodrat (Neotoma ferruginea); 200. Nicaraguan Woodrat (Neotoma chrysomelas); 201. Stephens's Woodrat (Neotoma stephensi); 202. Dusky-footed Woodrat (Neotoma fuscipes); 203. Big-eared Woodrat (Neotoma macrotis); 204. Bryant's Woodrat (Neotoma bryant); 205. Angel de la Guarda Woodrat (Neotoma insularis); 206. Desert Woodrat (Neotoma lepida); 207. Arizona Woodrat (Neotoma devia).
On following pages: 107. Cross-marked Langur (Presbytis chrysomelas); 108. White-fronted Langur (Presbytis frontata (Presbytis sabana); 112. Black-crested Sumatran Langur (Presbytis melalophos); 113. Black-and-white Langur (Presbytis); 109. Hose's Langur (Presbytis hosel); 110 canicrus.) Miller's Langur (Presbytis; 111. Sabah Grizzled Langur bicolon; 114 Presbytis. sumatrana Black) Sumatran; Langur 115 (. Mitered Langur (Presbytis mitrata). in Cercopithecidae
On following pages: 107. Cross-marked Langur (Presbytis chrysomelas); 108. White-fronted Langur (Presbytis frontata (Presbytis sabana); 112. Black-crested Sumatran Langur (Presbytis melalophos); 113. Black-and-white Langur (Presbytis); 109. Hose's Langur (Presbytis hosel); 110 canicrus.) Miller's Langur (Presbytis; 111. Sabah Grizzled Langur bicolon; 114 Presbytis. sumatrana Black) Sumatran; Langur 115 (. Mitered Langur (Presbytis mitrata).
Figure 3 in Maratus fimbriatus, a new peacock spider from the Darling Riverine Plains of New South Wales, with a review of the Maratus chrysomelas group (Araneae: Salticidae: Euophryini)
Figure 3. Two views of the underside of a male Maratus fimbriatus. From below, the fringes of
Data from: Genomic characterization of sex-identification markers in Sebastes carnatus and Sebastes chrysomelas rockfishes
Fish have evolved a variety of sex-determining (SD) systems including male heterogamy (XY), female heterogamy (ZW) and environmental SD. Little is known about SD mechanisms of Sebastes rockfishes, a highly speciose genus of importance to evolutionary and conservation biology. Here, we characterize the sex determination system in the sympatrically distributed sister species Sebastes chrysomelas and Sebastes carnatus. To identify sex-specific genotypic markers, double digest restriction site – associated DNA sequencing (ddRAD-seq) of genomic DNA from 40 sexed individuals of both species was performed. Loci were filtered for presence in all of the individuals of one sex, absence in the other sex and no heterozygosity. Of the 74 965 loci present in all males, 33 male-specific loci met the criteria in at least one species and 17 in both. Conversely, no female-specific loci were detected, together providing evidence of an XY sex determination system in both species. When aligned to a draft reference genome from Sebastes aleutianus, 26 sex-specific loci were interspersed among 1168 loci that were identical between sexes. The nascent Y chromosome averaged 5% divergence from the X chromosome and mapped to reference Sebastes genome scaffolds totalling 6.9Mbp in length. These scaffolds aligned to a single chromosome in three model fish genomes. Read coverage differences were also detected between sex-specific and autosomal loci. A PCR-RFLP assay validated the bioinformatic results and correctly identified sex of five additional individuals of known sex. A sex-determining gene in other teleosts gonadal soma-derived factor (gsdf) was present in the model fish chromosomes that spanned our sex-specific markers.
Data from: Genomic characterization of sex-identification markers in Sebastes carnatus and Sebastes chrysomelas rockfishes
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Figure 19. Sequential frames from a 25 in Maratus nubilis, a new peacock spider in the chrysomelas group from southwestern Australia (Araneae: Salticidae: Euophryini)
Figure 19. Sequential frames from a 25 fps video of the fan dance of a male Maratus nubilis. These frames illustrate slight movements of pedipalps and the flexion of legs III to the rear, at the tibiometatarsal joint, during this dance. One or both legs III may be flexed and at least partly concealed behind the fan, as shown here.
Figure 18 in Maratus nubilis, a new peacock spider in the chrysomelas group from southwestern Australia (Araneae: Salticidae: Euophryini)
Figure 18 (continued on next page). Sequential frames from a 100 fps video of the fan dance of a male Maratus nubilis.
Figure 10. Sequential photographs showing a in Maratus fimbriatus, a new peacock spider from the Darling Riverine Plains of New South Wales, with a review of the Maratus chrysomelas group (Araneae: Salticidae: Euophryini)
Figure 10. Sequential photographs showing a male (upper left) eliciting the attention of a female Maratus fimbriatus that subsequently (3) prepared to jump at him.
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