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opennotspecifiedDec 2006View details →

Fig. 4 in Observations on the Natural History, Development, Range, and Future of Eubulusparochus(Herbst) (Coleoptera: Curculionidae)

Fig. 4. Numbers of Eubulus parochus adults collected by date from Chittenden and Washington Counties of Vermont in 1997, 1998, and 1999. Dashed lines mark first day of the month for June, July, August, and September.

opennotspecifiedDec 2006View details →

Fig. 1. a in Observations on the Mating Behavior of Lasioderma serricorne(F.) Adults and Experiments on their Nutritional Requirements in dried Tobacco

Fig. 1. a) Lasioderma serricorne adults in ''end to end'' copulatory position (lateral view); b) V-shaped apodema with the loboid multicellular gland evident around it (after coloration).

Fig. 4 in Crioprosopus magnificus Leconte (Coleoptera: Cerambycidae) in Aguascalientes, Mexico: Biological Observations and Geographical Distribution

Fig. 4. Oviposition and egg hatching by Crioprosopus magnificus. A) Female ovipositing, B) Individual egg, C) Fine, red frass beneath the egg shell indicating egg eclosion, D) Close-up of the egg shell showing a small hole from which frass is expelled, E) Uncovered first instar.

Fig. 1 in Crioprosopus magnificus Leconte (Coleoptera: Cerambycidae) in Aguascalientes, Mexico: Biological Observations and Geographical Distribution

Fig. 1. Adult Crioprosopus magnificus that emerged from Quercus potosina in the Sierra Fria, Aguascalientes, Mexico. A) Females, B) Males. Scale bars = 1 cm.

Fig. 2 in Crioprosopus magnificus Leconte (Coleoptera: Cerambycidae) in Aguascalientes, Mexico: Biological Observations and Geographical Distribution

Fig. 2. Geographical extent of wood boring symptoms in oak trees and proven Crioprosopus magnificus adult emergence in Aguascalientes, Mexico. Wood boring occurrence is based on a sample size of 20 trees per site.

opennotspecifiedMar 2011View details →

Fig. 1. Camptocerus noel. A in Observations of the Biology of Camptocerus Dejean (Coleoptera: Curculionidae: Scolytinae) in Peru

Fig. 1. Camptocerus noel. A) Males aggregating and resting in a leaf near a felled Protium amazonicum tree; they made the holes in which they rest, B) Female resting in a leaf, C) Female boring through the leaf with undigested leaf cuttings.

Fig. 3 in Crioprosopus magnificus Leconte (Coleoptera: Cerambycidae) in Aguascalientes, Mexico: Biological Observations and Geographical Distribution

Fig. 3. Attack symptoms of Crioprosopus magnificus on Quercus potosina, Quercus grisea, and Quercus eduardii in the Sierra Fria, Aguascalientes, Mexico. A) Entrance hole, B) Abundant frass accumulation at the base of the tree, C) Transverse bole section showing larval galleries, D) Longitudinal bole section showing larval galleries, E) Exit hole.

Figure 4 in A new species of the Neotropical genus Beebeomyia (Diptera: Richardiidae) with observations of its biology on Dieffenbachia oerstedii (Araceae)

Figure 4. Detail of male section of the inflorescence of D. oerstedii. (A) flower bud open with eggs of Beebeomyia exposed on the edge of the bract; (B–C) larvae of Beebeomyia feeding on the male flowers and damage along the raquis. Arrows show eggs (A) and larvae (B, C).

Figure 1 in A new species of the Neotropical genus Beebeomyia (Diptera: Richardiidae) with observations of its biology on Dieffenbachia oerstedii (Araceae)

Figure 1. Adult morphology of Beebeomyia tuxtlaensis n. sp.: (A) general habitus of male, lateral view; (B) detail of head; (C) thorax, dorsal view; (D) wing pattern and venation; (E–F) morphology of the female ovipositor and the aculeus tip; (G) male terminalia in lateral view showing outer and medial surstyli; (H–I) male phallus showing basal spines and detail of the distiphallus.

Figure 3 in A new species of the Neotropical genus Beebeomyia (Diptera: Richardiidae) with observations of its biology on Dieffenbachia oerstedii (Araceae)

Figure 3. (A) general aspect of the host plant, D. oerstedii, showing flower buds open and closed; (B) distribution of the male (top) and female (bottom) flowers in the inflorescence; (C) flower bud with eggs located at the edge of the bract; (D–E) females of Beebeomyia tuxtlaensis ovipositing on the bud. Arrows show the eggs.

Figure 2 in A new species of the Neotropical genus Beebeomyia (Diptera: Richardiidae) with observations of its biology on Dieffenbachia oerstedii (Araceae)

Figure 2. Assessment of the infestation levels produced by B. tuxtlaensis and a drosophilid species on (A) the male and (B) the female sections of the inflorescence of D. oerstedii.

Figure 5 in A new species of the Neotropical genus Beebeomyia (Diptera: Richardiidae) with observations of its biology on Dieffenbachia oerstedii (Araceae)

Figure 5. Detail of female section of the inflorescence of D. oerstedii. (A) cross section showing the female flowers; (B–C) damage produced by larvae of Beebeomyia inside the female flowers; (D) some ovaries damaged by the larvae, and pupae arranged in groups inside the bract. Arrows show larvae and pupae.

Synthetic Observation of Column Density Maps Derived from Cloud Factory Data via Radiative Transfer Simulations

This dataset contains synthetic observation data derived from Cloud Factory data, processed through radiative transfer simulations using POLARIS. The data focuses on several star-forming regions, providing valuable insights into the evolution of filaments within these areas. The dataset is presented at three different resolutions: high (0.25 pc/pixel), medium (0.5 pc/pixel), and low (1 pc/pixel), to cater to various analytical needs. Files labeled as RA, RB, and RC correspond to three distinct regions under study. Additionally, each file is tagged with a 's' followed by a number, indicating the snapshot sequence.

opennotspecifiedOct 2016View details →

Figure 7 in First observation and seasonal dynamics of the new invasive planktonic copepod Oithona davisae Ferrari and Orsi, 1984 along the southern Black Sea (Anatolian Coast)

Figure 7. Black Sea coastal current system (http://www.ims.metu.edu.tr/cv/oguz/circulation.htm). © Temel Oguz. Reproduced by permission of Temel Oguz. Permission to reuse must be obtained from the rightsholder.

opennotspecifiedOct 2016View details →

Figure 6 in First observation and seasonal dynamics of the new invasive planktonic copepod Oithona davisae Ferrari and Orsi, 1984 along the southern Black Sea (Anatolian Coast)

Figure 6. Major shipping lanes in the Black Sea http://www.marinevesseltraffic.com/2013/06/black-sea-marine-traffic.html. © Marine Vessel Traffic. Reproduced by permission of Marine Vessel Traffic. Permission to reuse must be obtained from the rightsholder.

opennotspecifiedOct 2016View details →

Figure 1 in First observation and seasonal dynamics of the new invasive planktonic copepod Oithona davisae Ferrari and Orsi, 1984 along the southern Black Sea (Anatolian Coast)

Figure 1. (●) Previous report sites of Oithona davisae (Altukhov et al. 2014), (▲) Time series stations and (+) sampling locations.

Replication package for: "Heat and observed economic activity in the rich urban tropics"

The data and code shared here pertain to an article that is forthcoming in the Economic Journal. Please consult the README file herein for details.

Hunting Down White Dwarf--Main Sequence Binaries Using Multi-Wavelength Observations

Identification of white dwarfs (WD) with main-sequence (MS) companions and characterization of their properties can put important constraints on our understanding of binary stellar evolution and guide the theoretical predictions for a wide range of interesting transient events relevant for, e.g., Rubin Observatory (LSST), ZTF, and LISA. In this study, we combine ultraviolet (UV) and optical color-magnitude diagrams (CMDs) to identify unresolved WD--MS binaries. In particular, we combine high-precision astrometric and photometric data in the optical from \gaia\ -DR3 and UV data from GALEX GR6/7 to identify 93 WD--MS candidates within 100 pc. Of these, 80 are newly identified. Using the Virtual Observatory SED Analyzer (VOSA) we fit the spectral energy distributions (SEDs) of all our candidates and derive stellar parameters, such as effective temperature, bolometric luminosity, and radius for both companions. We find that our identification method helps identify hotter and smaller WD companions (majority with ≥ 10,000 K and ≤ 0.02 R_Sun) relative to the WDs identified by past surveys. We infer that these WDs are relatively more massive (median ~0.76 M_Sun). We find that most of the MS companions in our binaries are of the K and M spectral types.

Data and codes for the self-consistent analysis of GUVI and SEE observations

This dataset contains the data and Matlab codes that can be used to reproduce all the figures in the following manuscript:Resolving some longstanding issues in far ultraviolet remote sensing: A self-consistent analysis of the GUVI and SEE observations on the TIMED mission

Internal tides vertical structure and steric sea surface height signature south of New Caledonia revealed by glider observations

Data to reproduce the figures of the preprint Internal tides vertical structure and steric sea surface height signature south of New Caledonia revealed by glider observations, submitted to Ocean Science