Host-parasite relationships and intraspecific variation in Posthodiplostomum minimum (Trematoda: Diplostomatidae)

Normal 0 false false false EN-US X-NONE X-NONE MicrosoftInternetExplorer4 /* Style Definitions */ table.MsoNormalTable {mso-style-name:"Table Normal"; mso-tstyle-rowband-size:0; mso-tstyle-colband-size:0; mso-style-noshow:yes; mso-style-priority:99; mso-style-qformat:yes; mso-style-parent:""; mso-padding-alt:0in 5.4pt 0in 5.4pt; mso-para-margin:0in; mso-para-margin-bottom:.0001pt; mso-pagination:widow-orphan; font-size:11.0pt; font-family:"Calibri","sans-serif"; mso-ascii-font-family:Calibri; mso-ascii-theme-font:minor-latin; mso-fareast-font-family:"Times New Roman"; mso-fareast-theme-font:minor-fareast; mso-hansi-font-family:Calibri; mso-hansi-theme-font:minor-latin; mso-bidi-font-family:"Times New Roman"; mso-bidi-theme-font:minor-bidi;} A variety of amphibian, reptilian, avian, and mammalian hosts were used in experimental development of Posthodiplostomum minimum. As a result of this study much host - induced morphological variation was noted in several organs of attachment. Variations in the oral sucker ranged from a well - developed muscular organ to a weakly developed oral slit. Acetabular development ranged from well - developed to reduced forms lacking apical musculature, tegumental spines, and sensory structures. The holdfast organ showed marked reduction in most poikilothermic hosts.        

Host-induced morphological variations in the strigeoid trematode Posthodiplostomum minimum (Trematoda: Diplostomatidae). III. organs of attachment

Normal 0 false false false EN-US X-NONE X-NONE MicrosoftInternetExplorer4 /* Style Definitions */ table.MsoNormalTable {mso-style-name:"Table Normal"; mso-tstyle-rowband-size:0; mso-tstyle-colband-size:0; mso-style-noshow:yes; mso-style-priority:99; mso-style-qformat:yes; mso-style-parent:""; mso-padding-alt:0in 5.4pt 0in 5.4pt; mso-para-margin:0in; mso-para-margin-bottom:.0001pt; mso-pagination:widow-orphan; font-size:11.0pt; font-family:"Calibri","sans-serif"; mso-ascii-font-family:Calibri; mso-ascii-theme-font:minor-latin; mso-fareast-font-family:"Times New Roman"; mso-fareast-theme-font:minor-fareast; mso-hansi-font-family:Calibri; mso-hansi-theme-font:minor-latin; mso-bidi-font-family:"Times New Roman"; mso-bidi-theme-font:minor-bidi;} A variety of amphibian, reptilian, avian, and mammalian hosts were used in experimental development of Posthodiplostomum minimum. As a result of this study much host - induced morphological variation was noted in several organs of attachment. Variations in the oral sucker ranged from a well - developed muscular organ to a weakly developed oral slit. Acetabular development ranged from well - developed to reduced forms lacking apical musculature, tegumental spines, and sensory structures. The holdfast organ showed marked reduction in most poikilothermic hosts.        

Host-induced morphological variations in the strigeoid trematode Posthodiplostomum minimum (Trematoda: Diplostomatidae). II. Body measurements and tegument modifications

Normal 0 false false false EN-US X-NONE X-NONE MicrosoftInternetExplorer4 /* Style Definitions */ table.MsoNormalTable {mso-style-name:"Table Normal"; mso-tstyle-rowband-size:0; mso-tstyle-colband-size:0; mso-style-noshow:yes; mso-style-priority:99; mso-style-qformat:yes; mso-style-parent:""; mso-padding-alt:0in 5.4pt 0in 5.4pt; mso-para-margin:0in; mso-para-margin-bottom:.0001pt; mso-pagination:widow-orphan; font-size:11.0pt; font-family:"Calibri","sans-serif"; mso-ascii-font-family:Calibri; mso-ascii-theme-font:minor-latin; mso-fareast-font-family:"Times New Roman"; mso-fareast-theme-font:minor-fareast; mso-hansi-font-family:Calibri; mso-hansi-theme-font:minor-latin; mso-bidi-font-family:"Times New Roman"; mso-bidi-theme-font:minor-bidi;} Extensive feeding experiments were undertaken to determine if physiological host specificity was a major characteristic of Posthodiplostomum minimum. This involved the feeding of experimentally infected sunfish livers containing metacercariae of P. minimum to amphibian, reptilian, avian and mammalian hosts. Host - induced morphological variations of adult P. minimum were shown to be associated with the genus and class of host employed as well as with the inherent variability of P. minimum exclusive of host factors. Morphological characters such as body size and shape and tegumental surface and spines are indicated as undergoing morphological variation. Of all the experimental definitive hosts used, avian and mammalian are the most suitable for normal development of P. minimum. Amphibian and reptilian hosts demonstrate marked variation in the adult worm development usually manifested by pronounced size decrease.     

Host-induced morphological variations in the strigeoid trematode Posthodiplostomum minimum (Trematoda: Diplostomatidae). IV. organs of reproduction (ovary and testes), vitelline gland, and egg

Normal 0 false false false EN-US X-NONE X-NONE MicrosoftInternetExplorer4 /* Style Definitions */ table.MsoNormalTable {mso-style-name:"Table Normal"; mso-tstyle-rowband-size:0; mso-tstyle-colband-size:0; mso-style-noshow:yes; mso-style-priority:99; mso-style-qformat:yes; mso-style-parent:""; mso-padding-alt:0in 5.4pt 0in 5.4pt; mso-para-margin:0in; mso-para-margin-bottom:.0001pt; mso-pagination:widow-orphan; font-size:11.0pt; font-family:"Calibri","sans-serif"; mso-ascii-font-family:Calibri; mso-ascii-theme-font:minor-latin; mso-fareast-font-family:"Times New Roman"; mso-fareast-theme-font:minor-fareast; mso-hansi-font-family:Calibri; mso-hansi-theme-font:minor-latin; mso-bidi-font-family:"Times New Roman"; mso-bidi-theme-font:minor-bidi;} A variety of amphibian, reptilian, avian, and mammalian hosts were used in experimental development of Posthodiplostomum minimum. Results of this study indicate that the organs of reproduction (testes and ovary) as well as the vitelline gland and egg underwent host - induced morphological variations. Due to the lack of host specificity of P. minimum as well as the overlap of reported egg and body sizes of species of Posthodiplostomum, it is apparent that several reported species are not valid.     

Robber flies of Utah (Diptera: Asilidae)

Reported are 158 species of Asilidae (Diptera) in 50 genera from Utah. Keys to subfamilies, genera, and species are given, along with information on seasonal and distributional occurrence in Utah. Seventy-six maps and 56 line drawings show the Utah distribution of each species and illustrate important characters used in the keys. A table summarizes the current status of names used in earlier state lists.     

Life cycle and reproductive pattern of Acrotrichis intermedia (Coleoptera: Ptiliidae) in experimental conditions

Summary

At different constant temperatures specimens of Acrotrichis intermedia (Gillm. 1845) (Coleoptera: Ptiliidae) were cultivated. The life cycle is described and data are given concerning egg production, oviposition, lifespan and duration of developmental stages.     

Life cycle of Huarpea fallax (Hymenoptera: Sapygidae) in a xeric forest in Argentina

This study describes the life cycle of Huarpea fallax (Hymenoptera: Sapygidae) in a xeric forest in La Pampa province, Argentina. This cleptoparasitic wasp attacks the nests of two species of leaf-cutter bees: Megachile catamarcensis and Anthidium vigintipunctatum, both belonging to the family Megachilidae. Nests of these bee species were obtained during a trap-nesting programme. Adult emergence showed a unimodal pattern indicating a univoltine life cycle. The period from egg-laying to adult emergence lasted for 10–13 months; however, one female took about 2 years to emerge, suggesting parsivoltinism. Most females attack one cell per host nest, the outermost cells being the ones most parasitized. However, the position of the attacked cells was variable. In this paper, although there were insufficient data to prove a correlation, the data suggest a positive trend between body size of sapygid wasps and their host bees.     

Environmental site characteristics and incidence of chokecherry black knot in Utah

Normal 0 false false false EN-US X-NONE X-NONE MicrosoftInternetExplorer4 st1\:*{behavior:url(#ieooui) } /* Style Definitions */ table.MsoNormalTable {mso-style-name:"Table Normal"; mso-tstyle-rowband-size:0; mso-tstyle-colband-size:0; mso-style-noshow:yes; mso-style-priority:99; mso-style-qformat:yes; mso-style-parent:""; mso-padding-alt:0in 5.4pt 0in 5.4pt; mso-para-margin:0in; mso-para-margin-bottom:.0001pt; mso-pagination:widow-orphan; font-size:11.0pt; font-family:"Calibri","sans-serif"; mso-ascii-font-family:Calibri; mso-ascii-theme-font:minor-latin; mso-fareast-font-family:"Times New Roman"; mso-fareast-theme-font:minor-fareast; mso-hansi-font-family:Calibri; mso-hansi-theme-font:minor-latin; mso-bidi-font-family:"Times New Roman"; mso-bidi-theme-font:minor-bidi;} Black knot disease of chokecherries, induced by Dibotryon morbosum (Schw.) Th. & Syd., is widely distributed in Utah. The incidence of black knot was measured by determining the ratio of total black knot gall length to total stem length of plants and then expressing that value as a percentage of diseased stems in the sample plot. The environmental site factors measured were elevation, exposure, slope, soil pH, soil depth, distance to surface water, plant moisture stress, and associated vegetation. Numerical values were determined for each of these variables at each of 18 randomly located plots. Correlation coefficients for plant moisture stress and soil temperature were –.439 (p = .065) and –.440 (p = .055). Multiple regression analyses using plant moisture stress and soil temperature gave a regression coefficient of –.641 (p = .05). As plant moisture stress and soil temperature decreased, incidence of black knot increased.        

Littoral heterogeneity and diel behavior of white bass ( Morone chrysops ) and carp ( Cyprinus carpio ) in Utah Lake, Utah

Normal 0 false false false EN-US X-NONE X-NONE MicrosoftInternetExplorer4 st1\:*{behavior:url(#ieooui) } /* Style Definitions */ table.MsoNormalTable {mso-style-name:"Table Normal"; mso-tstyle-rowband-size:0; mso-tstyle-colband-size:0; mso-style-noshow:yes; mso-style-priority:99; mso-style-qformat:yes; mso-style-parent:""; mso-padding-alt:0in 5.4pt 0in 5.4pt; mso-para-margin:0in; mso-para-margin-bottom:.0001pt; mso-pagination:widow-orphan; font-size:11.0pt; font-family:"Calibri","sans-serif"; mso-ascii-font-family:Calibri; mso-ascii-theme-font:minor-latin; mso-fareast-font-family:"Times New Roman"; mso-fareast-theme-font:minor-fareast; mso-hansi-font-family:Calibri; mso-hansi-theme-font:minor-latin; mso-bidi-font-family:"Times New Roman"; mso-bidi-theme-font:minor-bidi;} Diel activity and association patterns of white bass ( Morone chrysops ) and carp ( Cyprinus carpio ) in Utah Lake, Utah, were studied over four 24-hr periods during August 1980. Fish were concurrently sampled from two adjacent littoral habitats. Significant differences existed in diel activity patterns in two of three size classes of white bass and in diel association patterns of white bass and carp between the two habitat areas. Differences in habitat structure, and in biological activity between the habitat types, are implicated as the primary determinants of overall diel activity of fish in these littoral areas.        

New Haplopappus variety in Utah (Compositae)

Normal 0 false false false EN-US X-NONE X-NONE MicrosoftInternetExplorer4 st1\:*{behavior:url(#ieooui) } /* Style Definitions */ table.MsoNormalTable {mso-style-name:"Table Normal"; mso-tstyle-rowband-size:0; mso-tstyle-colband-size:0; mso-style-noshow:yes; mso-style-priority:99; mso-style-qformat:yes; mso-style-parent:""; mso-padding-alt:0in 5.4pt 0in 5.4pt; mso-para-margin:0in; mso-para-margin-bottom:.0001pt; mso-pagination:widow-orphan; font-size:11.0pt; font-family:"Calibri","sans-serif"; mso-ascii-font-family:Calibri; mso-ascii-theme-font:minor-latin; mso-fareast-font-family:"Times New Roman"; mso-fareast-theme-font:minor-fareast; mso-hansi-font-family:Calibri; mso-hansi-theme-font:minor-latin; mso-bidi-font-family:"Times New Roman"; mso-bidi-theme-font:minor-bidi;} Reported as a new variety from the Green River Formation of Uintah and Duchesne counties, Utah, is Haplopappus armerioides (Nutt.) Gray var. gramineus Welsh & F. J. Smith.     

Life cycle variation and adaptation in jumping plant lice (Insecta: Hemiptera: Psylloidea): a global synthesis

This paper integrates the scattered information on the life histories of the jumping plant lice or psyllids, examining those aspects of their biology that contribute to successful life cycle completion. Variation in life history parameters is reviewed across the world's psyllids and the relative importance of phylogeny and environment, including host‐plant growth strategy, in determining life history strategies is assessed. Elements of life cycles considered include: development rate and voltinism, response to high temperature and drought, cold‐hardiness and overwintering strategy, seasonal polymorphism, diapause, metabolism, host‐plant selection and range, phenological and other adaptations to host plants, disease transmission and host amelioration, dispersal, reproduction and mate finding. Life history parameters are analyzed for 342 species. While a phylogenetic signal can be identified within the data, the main drivers for life history adaptation are environmental temperatures and water availability, acting directly on the psyllids or mediated through their host plants.     

Life cycle and population structure of the terrestrial isopod Hemilepistus klugii (Brandt, 1833) (Isopoda: Oniscidea) in Iran

The life cycle and population structure of Hemilepistus klugii were studied in a population in Varamin, Iran. The population was sampled monthly (or fortnightly during the breeding season) from February 2008 to June 2009 and a total of 7015 individuals, comprising 1069 males, 1079 females and 4867 juveniles, were collected. As in other Hemilepistus species, five distinct phenophases, namely pair formation, gestation, hatching, growth and stationary, were recorded during the life cycle of H. klugii. The overall sex ratio was 1 : 1 but varied over time. Ovigerous females were observed only in April, indicating a seasonal and very short breeding period. With a short lifespan after breeding, females demonstrated true semelparity. The mean cephalothorax width for ovigerous/post-ovigerous females was higher in 2008 than in 2009. These females attained the largest size in the population throughout the year. The number of eggs per female ranged from 28 to 147 (mean ± SE, 78 ± 1.8). There was a positive correlation between female size and fecundity. Recruitment occurred in late April and resulted in the highest population density in this month, whereas the lowest densities were observed during November to January. Despite a high percentage of ovigerous females carrying undeveloped eggs (72.3%), intramarsupial mortality was low (3.5%).     

Montia linearis (Portulacaceae): a new record for Utah

Montia linearis Dougl., a plant known from British Columbia to Montana, Nevada, and California, is reported from Utah.     

Utah plant types—historical perspective 1840 to 1981—annotated list, and bibliography

New taxa include: Cryptantha cinerea (Torr.) Cronq. var. arenicola Higgins & Welsh; Physaria chambersii Rollins var. sobolifera Welsh (Cruciferae); Phacelia demissa Gray var. minor N. D. Atwood (Hydrophyllaceae); Iris pariensis Welsh (Iridaceae); Astragalus preussii var. cutleri Barneby and Pediomelum aromaticum (Payson) Welsh var. tuhyi Welsh (Leguminosae); Abronia nana Wats. var. harrisii Welsh (Nyctaginaceae); Camissonia atwoodii Cronq. (Onagraceae); Habenaria zothecina Higgins & Welsh (Orchidaceae); Aqiiilegia formosa Fisch. in DC. var. fosteri Welsh (Ranunculaceae). New nomenclatural combinations include: Rhus aromatica Ait. var. simplicifolia (Greene) Cronq. (Anacardiaceae); Lomatium kingii (Wats.) Cronq., L. kingii var. alpinum (Wats.) Cronq. (Apiaceae); Cryptantha cinerea (Torr.) Cronq. var. laxa (Macbr.) Higgins; Mertensia lanceolata (Pursh) DC. var. nivalis (Wats.) Higgins (Boraginaceae); Opuntia erinacea Engelm. var. aurea (Baxter) Welsh (Cactaceae); Arenaria fendleri Gray var. aculeata (Wats.) Welsh, A. fendleri var. eastwoodiae (Rydb.) Welsh, Lychnis apetala L. var. kingii (Wats.) Welsh, Stellaria longipes Goldie var. monantha (Hulten) Welsh (Caryophyllaceae); Draba densifolia Nutt. ex T. & G. var. apiculata (C. L. Hitchc.) Welsh, D. oligosperma Hook. var. juniperina (Dorn) Welsh, Physaria acutifolia Rydb. var. stylosa (Rollins) Welsh, Thelypodiopsis sagittata (Nutt.) Schulz var. ovalifolia (Rydb.) Welsh (Cruciferae); Lotus plebeius (T. Brandg.) Barneby, Lupinus polyphyllus Lindl. in Edwards var. ammophilus (Greene) Barneby, L polyphyllus var. humicola (A. Nels.) Barneby, L. argenteus Pursh var. fulvomaculatus (Payson) Barneby, L. argenteus var. palmeri (Wats.) Barneby, Pediomelum aromaticum (Payson) Welsh, P. epipsilum (Barneby) Welsh, Psoralidium lanceolatum (Pursh) Rydb. var. stenophyllum (Rydb.) Welsh, and P. lanceolatum var. stenostachys (Rydb.) Welsh (Leguminosae); Mirabilis linearis (Pursh) Hiemerl var. decipiens (Standl.) Welsh (Nyctaginaceae); Camissonia boothii var. condensata (Munz) Cronq., C. boothii var. villosa (Wats.) Cronq., C. clavaeformis (Torr. & Frem.) Raven var. purpurascens (Wats.) Cronq., C. scapoidea (T. & G.) var. utahensis (Raven) Welsh, Oenothera caespitosa var. macroglottis (Rydb.) Cronq., Oe. caespitosa var. navajoensis (Wagner, Stockhouse, & Klein) Cronq., Oe. flava (A. Nels.) Garrett var. acutissima (W. L. Wagner) Welsh, and Oe. primiveris Gray var. bufonis (Jones) Cronq. (Onagraceae); Papaver radicatum Rottb. var. pygmaeum (Rydb.) Welsh (Papaveraceae); Dodecatheon pulchellum (Raf.) Merr. var. zionense (Eastw.) Welsh (Primulaceae); Aquilegia flavescens Wats. var. rubicunda (Tidestr.) Welsh, Delphinium andersonii Gray var. scaposum (Greene) Welsh, D. occidentalis (Wats.) Wats. var. barbeyi (Huth) Welsh, and Ranunculus andersonii Gray var. juniperinus (Jones) Welsh (Ranunculaceae); Purshia mexicana (D. Don) Welsh and P. mexicana var. stansburyi (Torr.) Welsh (Rosaceae); Galium mexicanum H.B.K. var. asperrimum (Gray) Higgins & Welsh (Rubiaceae); Castilleja parvula Rydb. var. revealii (N. Holmgren) N. D. Atwood and C. rhexifolia Rydb. var. sulphurea (Rydb.) N. D. Atwood (Scrophulariaceae).     

New taxa and nomenclatural changes in Utah Penstemon (Scrophulariaceae)

New taxa include Penstemon angustifolius Pursh var. dulcis Neese, P. leonardii Rydb. var. higginsii Neese, P. scariosus Pennel var. cyanomontanus Neese, and P. thompsoniae (Gray) Rydb. var. desperatus Neese. New nomenclatural combinations include: Penstemon acaulis L. O. Williams var. yampaensis (Penl.) Neese, P. duchesnensis (N. Holmgren) Neese, P. leonardii Rydb. var. patricus (N. Holmgren) Neese, and P. pachyphyllus Gray ex Rydb. var. mucronatus (N. Holmgren) Neese.