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980 results for “Coping”
FIGURES 110–113. Pseudotremia johnholsingeri, n in Cave millipeds of the United States. X. New species and records of the genus Pseudotremia Cope. 2. Species from Virginia, USA (Diplopoda, Chordeumatida, Cleidogonidae)
FIGURES 110–113. Pseudotremia johnholsingeri, n. sp. Fig.110, ocelli. Fig. 111, metazonite, dorsal view. Fig. 112. Metazonite, lateral view. Fig. 113, gonopods and ninth legpair, ventral view.
FIGURES 53–58. Pseudotremia jaculohamatum, n in Cave millipeds of the United States. X. New species and records of the genus Pseudotremia Cope. 2. Species from Virginia, USA (Diplopoda, Chordeumatida, Cleidogonidae)
FIGURES 53–58. Pseudotremia jaculohamatum, n. sp. Fig. 53, diplosegment, dorsal view. Fig. 54, diplosegment, lateral view. Fig. 55, gonopods, anterior view; as, apical spine; cc, colpocoxite; lap, lateral angiocoxal process; map, median angiocoxal process; vcp, ventral colpocoxite process. Fig. 56, gonopods, lateral view; labels as in fig. 55 and sas, subapical spine. Fig. 57, gonopods, ventral view. Fig. 58, legpair seven, anterior view.
FIGURES 92–98 in Cave millipeds of the United States. X. New species and records of the genus Pseudotremia Cope. 2. Species from Virginia, USA (Diplopoda, Chordeumatida, Cleidogonidae)
FIGURES 92–98. New species of Pseudotremia. Figs. 92–97, Pseudotremia piscator, n. sp. Fig. 92, ocelli. Fig. 93, metazonite, lateral view. Fig. 94, gonopods, lateral view. Fig. 95, gonopods, anterior view. Fig. 96, gonopods, ventral view. Fig. 97, right ninth leg, anterior view. Fig. 98, P. culveri, n. sp., eleventh coxae, posterior view.
FIGURES 46–52 in Cave millipeds of the United States. X. New species and records of the genus Pseudotremia Cope. 2. Species from Virginia, USA (Diplopoda, Chordeumatida, Cleidogonidae)
FIGURES 46–52. New species of Pseudotremia. Fig. 46, gonopods of Pseudotremia glaber, n. sp., lateral view. Figs. 47–50, P. f e r g u s o n i, n. sp. Fig. 47, ocelli. Fig. 48, metazonite, dorsal view. Fig. 49, metazonite, lateral view. Fig. 50, gonopods, ventral view; cc, colpocoxites; dcp, dorsal colpocoxite process; lap, lateral angiocoxite process; map, median angiocoxite process. Fig. 51, right ninth leg, anterior view. Fig. 52, P. jaculohamatum, n. sp., right ninth leg, anterior view.
FIGURES 101–109 in Cave millipeds of the United States. X. New species and records of the genus Pseudotremia Cope. 2. Species from Virginia, USA (Diplopoda, Chordeumatida, Cleidogonidae)
FIGURES 101–109. New species of Pseudotremia. Figs. 101–104, Pseudotremia culveri, n. sp. Fig. 101, ocelli. Fig. 102, metazonite, dorsal view. Fig. 103, left ninth leg, anterior view. Fig. 104, metazonite, lateral view. Figs. 105–109, Pseudotremia salfodina, n. sp. Fig. 105, left ninth leg, anterior view. Fig. 106, gonopods, lateral view. Fig. 107, gonopods, anterior view. Fig. 108, gonopods, ventral view. Fig. 109, ocelli.
FIGURES 39–45 in Cave millipeds of the United States. X. New species and records of the genus Pseudotremia Cope. 2. Species from Virginia, USA (Diplopoda, Chordeumatida, Cleidogonidae)
FIGURES 39–45. New species of Pseudotremia. Fig. 39, gonopods of Pseudotremia peponocranium, n. sp., ventral view. Figs. 40–45. Pseudotremia glaber, n. sp. Fig. 40, ocelli. Fig. 41, metazonite, dorsal view. Fig. 42, female genitalia, ventral view. Fig. 43, gonopods, anterior view. Fig. 44, gonopods, ventral view. Fig. 45, right ninth leg, anterior view.
FIGURES 32–38 in Cave millipeds of the United States. X. New species and records of the genus Pseudotremia Cope. 2. Species from Virginia, USA (Diplopoda, Chordeumatida, Cleidogonidae)
FIGURES 32–38. New species of Pseudotremia. Figs. 32, 33, Pseudotremia orndorffi, n. sp. Fig. 32, gonopods, anterior view; lap, lateral angiocoxal process; map, median angiocoxal process. Fig. 33, gonopods, lateral view; labels as in fig. 32, and dcp, dorsal colpocoxite process; vcp, ventral colpocoxite process. Figs. 34–38, P. peponocranium, n. sp. Fig. 34, head of male, frontal view. Fig. 35, head of male, lateral view. Fig. 36, diplosegment, dorsal view. Fig. 37, gonopods, anterior view. Fig. 38, gonopods, lateral view.
FIGURES 25–31 in Cave millipeds of the United States. X. New species and records of the genus Pseudotremia Cope. 2. Species from Virginia, USA (Diplopoda, Chordeumatida, Cleidogonidae)
FIGURES 25–31. New species of Pseudotremia. Fig. 25, gonopods of Pseudotremia pomarium, n. sp., lateral view; dcp, dorsal colpocoxite process; vcp, ventral colpocoxite process. Figs. 26–31, P. o rn d or ffi, n. sp. Fig. 26, lateral view of anterior end of female. Fig. 27, ocelli. Fig. 28, metazonite, dorsal view. Fig. 29, metazonite, lateral view. Fig. 30, gonopods, ventral view. Fig. 31, right leg 9, anterior view.
FIGURES 19–24. Pseudotremia pomarium, n in Cave millipeds of the United States. X. New species and records of the genus Pseudotremia Cope. 2. Species from Virginia, USA (Diplopoda, Chordeumatida, Cleidogonidae)
FIGURES 19–24. Pseudotremia pomarium, n. sp. Fig. 19, ocelli. Fig. 20, diplosegment, dorsal view. Fig. 21, diplosegment, lateral view. Fig. 22, gonopods, anterior view. Fig. 23, gonopods, ventral view; dcp, dorsal colpocoxite process; vcp, ventral colpocoxite process. Fig. 24, right ninth leg, anterior view.
FIGURES 73–79 in Cave millipeds of the United States. X. New species and records of the genus Pseudotremia Cope. 2. Species from Virginia, USA (Diplopoda, Chordeumatida, Cleidogonidae)
FIGURES 73–79. New and previously described species of Pseudotremia. Figs. 73–77, Pseudotremia ryensis, n. sp. Fig. 73, ocelli. Fig. 74, diplosegment, dorsal view. Fig. 75, gonopods, ventral view. Fig. 76, gonopods, anterior view. Fig. 77, right ninth leg, anterior view. Figs. 78, 79, P. n o d o s a. Fig. 78, right ninth leg, anterior view. Fig. 79, metazonite, lateral view.
FIGURES 15–18. Pseudotremia cerberus, n in Cave millipeds of the United States. X. New species and records of the genus Pseudotremia Cope. 2. Species from Virginia, USA (Diplopoda, Chordeumatida, Cleidogonidae)
FIGURES 15–18. Pseudotremia cerberus, n. sp. Fig. 15, ocelli. Fig. 16, gonopods, lateral view. Fig. 17, gonopods, anterior view. Fig. 18, right ninth leg, anterior view.
FIGURES 9–14. Pseudotremia contorta, n in Cave millipeds of the United States. X. New species and records of the genus Pseudotremia Cope. 2. Species from Virginia, USA (Diplopoda, Chordeumatida, Cleidogonidae)
FIGURES 9–14. Pseudotremia contorta, n. sp. Fig. 9, metazonite, dorsal view. Fig. 10, diplosegment, lateral view. Fig. 11, gonopods, lateral view. Fig. 12, gonopods, anterior view. Fig. 13, gonopods, ventral view. Fig. 14, legpair 9 with gonopod colpocoxites, anterior view; cc, colpocoxites of gonopods; cxpf, coxoprefemur; L9, right ninth leg.
FIGURES 1–8 in Cave millipeds of the United States. X. New species and records of the genus Pseudotremia Cope. 2. Species from Virginia, USA (Diplopoda, Chordeumatida, Cleidogonidae)
FIGURES 1–8. New species of Pseudotremia. Figs. 1–7, P. loomisi, n. sp. Fig. 1, ocelli. Fig. 2, metazonite, dorsal view. Fig. 3, diplosegment, lateral view. Fig. 4, gonopods, ventral view. Fig. 5, gonopods, anterior view. Fig. 6, gonopods, lateral view. Fig. 7, left ninth leg, posterior view. Fig. 8, ocelli of P. c o n t or ta, n. sp.
High capacity for a dietary specialist consumer population to cope with increasing cyanobacterial blooms
<p><span>We present a common-garden experiment to study the feeding plasticity of a key deposit-feeder in the Baltic Sea, a low diversity system presenting a good model for studying local adaptations. Based on the latitudinal gradient in phytoplankton blooms, with a single diatom bloom (high nutritional quality) in the north and a diatom bloom followed by cyanobacteria bloom (low nutritional quality) in the south, we expected populations of the amphipod Monoporeia affinis to be dietary specialists in the north and generalists in the south. We tested this hypothesis using a combination of stable isotope tracers, trophic niche analyses, and various endpoints of growth and health status. We found that the toxin-producing cyanobacteria, when mixed with diatoms, were efficiently incorporated and used for growth by both populations. However, contrary to the expectations, the feeding plasticity was more pronounced in the northern population, indicating genetically-based divergence and suggesting that this population is capable of ecological adaptation to the climate-induced northward cyanobacteria expansion in this system. Results provide important understandings for adaptations to increasing cyanobacteria in a future warming world in both limnic and marine ecosystems by invertebrates, but are likely widely applicable to other consumers where questions on adaptations to altered food quality. </span></p>
FIG. 1 in Out with the Old, in with the New: Oviposition Preference Matches Larval Success in Cope's Gray Treefrog, Hyla chrysoscelis
FIG. 1. Total number of eggs per treatment (gray = New, black = Old) for each night oviposition occurred, and mean (± SE) number of eggs per New (dark gray) and Old (black) pools over the duration of the experiment.
MESA inlists for "Coping with loss: Stability of mass transfer from post-main-sequence donor stars"
<p>Binary model inlists for MESA, as used for the paper <a href="https://ui.adsabs.harvard.edu/abs/2023A%26A...669A..45T/abstract">Coping with loss: Stability of mass transfer from post-main-sequence donor stars</a> . The inlists provided here are pared-down, minimal working examples of the ones used in the publication. Due to the nature of the calculations, it was often needed to fine-tune inlists for specific systems by hand. For example, AGB models typically required the additional setting of <em>use_gold_tolerances = .false.</em></p> <p>These binary calculations start from a previously-evolved single star model for the donor stars. These can be found in the compressed folder titled "sstar_models_CWL.tar.xz". Please note that several parameters in the inlists will need to be adjusted accordingly, such as the configuration (initial orbit; mass ratio) of the binaries.</p> <p> </p> <p><strong>NOTE:</strong> to ensure that the mass-transfer calculation is fully conservative, add the following line to the <em>binary_controls</em> namelist in the <em>inlist_project</em> file:</p> <blockquote> <p>use_radiation_corrected_transfer_rate = .false.</p> </blockquote> <p>Further advice, code and/or files are available upon reasonable request to the authors (<a href="mailto:Karel.Temmink@ru.nl">contact: Karel Temmink</a>).</p>
Data for: Coping with abrasive food – diverging composition of radular teeth in two Porifera-consuming nudibranch species (Mollusca, Gastropoda)
<p><span>Molluscs forage with their radula, a chitinous membrane with teeth. Adaptations to hard or abrasive ingesta were well studied in Polyplacophora and Patellogastropoda, but for other taxa, there are large gaps in knowledge. Here, we investigated the nudibranch gastropods <em>Felimare</em> <em>picta</em> and <em>Doris</em> <em>pseudoargus</em>, both of which feed on Porifera. Tooth morphologies were documented by scanning electron microscopy and mechanical properties were tested by nanoindentation. We found that these parameters are rather similar in both species, indicating that teeth are similar in their function. To study the composition, teeth were visualized using confocal laser scanning microscopy (CLSM), to determine the degree of tanning, and analysed with energy-dispersive X-ray spectroscopy, to test the elemental composition. The emitted autofluorescence signal and the inorganic content differed between the species. This was especially prominent when studying the inner and outer tooth surfaces (leading and trailing edges). In <em>F. picta</em>, we detected high proportions of Si, whereas teeth of <em>D. pseudoargus</em> contained high amounts of Ca, which influenced the autofluorescence signal in CLSM. Employing nanoindentation, we determined high Young's modulus and hardness values for the leading edges of teeth, which relate to the Si- and Ca-content. This highlights that teeth with a similar morphology and mechanical properties can be mechanically enhanced via different chemical pathways in Nudibranchia.</span></p>
Optimising an Online Self-help Program for Coping With the Loss of a Spouse
ClinicalTrials.gov study NCT05280041. IPD Sharing: NO. Countries: 1. Publications: 12.
A Complex Intervention Study on a Palliative Rehabilitation Blended Learning Program to Support Relatives and Health Care Providers of People With ALS and Cognitive Impairments in Coping With Challeng
ClinicalTrials.gov study NCT04638608. IPD Sharing: NO. Countries: 1. Publications: 3.
Couples Coping With Alzheimer's Disease
ClinicalTrials.gov study NCT00438724. IPD Sharing: Not stated. Countries: 1. Publications: 4.
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