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Aphodius alabama, new species, collected in burrows of the southeastern pocket gopher Geomys pinetus Rafinesque, is described. Aphodius dyspistus Skelley & Woodruff, A. hubbelli S. & W., A. platypleurus S. & W., and A. tanytarsus S. & W., collected with A. alubarna, are all recorded from southeastern Alabama.
Experiment NA49 at the Cern SPS uses a large acceptance detector for a systematic study of particle yields and correlations in nucleus-nucleus, nucleon-nucleus and nucleon-nucleon collisions. Preliminary results for Pb+Pb collisions at 40, 80 and 158 A*GeV beam energy are shown and compared to measurements at lower and higher energies.
Rapidity distributions for $\Lambda$ and $\bar{\Lambda}$ hyperons in central Pb-Pb collisions at 40, 80 and 158 A$\cdot$GeV and for ${\rm K}_{s}^{0}$ mesons at 158 A$\cdot$GeV are presented. The lambda multiplicities are studied as a function of collision energy together with AGS and RHIC measurements and compared to model predictions. A different energy dependence of the $\Lambda/\pi$ and $\bar{\Lambda}/\pi$ is observed. The $\bar{\Lambda}/\Lambda$ ratio shows a steep increase with collision energy. Evidence for a $\bar{\Lambda}/\bar{\rm p}$ ratio greater than 1 is found at 40 A$\cdot$GeV.
Systematic revision of the genus Orodaliscoides Schmidt, 1913 (Coleoptera: Scarabaeidae: Aphodiinae)
(2012)
The species belonging to the genus Orodaliscoides Schmidt (Coleoptera: Scarabaeidae: Aphodiinae) are redescribed and figured. The following new combinations are proposed: Orodaliscoides fimbripes (Brown, 1928) and Orodaliscoides giulianii (Gordon, 1977).
Even in V1, where neurons have well characterized classical receptive fields (CRFs), it has been difficult to deduce which features of natural scenes stimuli they actually respond to. Forward models based upon CRF stimuli have had limited success in predicting the response of V1 neurons to natural scenes. As natural scenes exhibit complex spatial and temporal correlations, this could be due to surround effects that modulate the sensitivity of the CRF. Here, instead of attempting a forward model, we quantify the importance of the natural scenes surround for awake macaque monkeys by modeling it non-parametrically. We also quantify the influence of two forms of trial to trial variability. The first is related to the neuron’s own spike history. The second is related to ongoing mean field population activity reflected by the local field potential (LFP). We find that the surround produces strong temporal modulations in the firing rate that can be both suppressive and facilitative. Further, the LFP is found to induce a precise timing in spikes, which tend to be temporally localized on sharp LFP transients in the gamma frequency range. Using the pseudo R2 as a measure of model fit, we find that during natural scene viewing the CRF dominates, accounting for 60% of the fit, but that taken collectively the surround, spike history and LFP are almost as important, accounting for 40%. However, overall only a small proportion of V1 spiking statistics could be explained (R2~5%), even when the full stimulus, spike history and LFP were taken into account. This suggests that under natural scene conditions, the dominant influence on V1 neurons is not the stimulus, nor the mean field dynamics of the LFP, but the complex, incoherent dynamics of the network in which neurons are embedded.
Dilatitibialis Duverger (61 species) (Coleoptera: Coccinelidae: Coccidulinae; Hyperaspidini) is discussed, species described, illustrations provided, and a key to all recognized taxa included. Cleothera cognata Mulsant, Cleothera cruciferae Mulsant, Cleothera fuscomaculata Mulsant, Cleothera gaynoni Mulsant, Cleothera glyphica Mulsant, Cleothera jucunda Mulsant, Cleothera luteola Mulsant, Cleothera mulsanti Kirsch, Cleothera oseryi Mulsant, Cleothera poortmanni Mulsant, Cleothera scenica Mulsant, Cleothera semicincta Weise, Cleothera tropicalis Mulsant, Hinda guttipennis Weise, Hyperaspis carolinae Crotch, Hyperaspis ceciliae Crotch, Hyperaspis dilatata Crotch, Hyperaspis florifera Vogel, Hyperaspis gravabilis Brèthes, Hyperaspis hybridula Crotch, Hyperaspis laterinotata Brèthes, Hyperaspis silvani Crotch, and Hyperaspis suzannae Crotch are transferred to Dilatitibialis, becoming new combinations. Lectotypes are designated for D. boliviana, D. cognata, D. florifera, D. fuscomaculata, D. gaynoni, D. glyphica, D. gravabilis, D. guttipennis, D. luteola, D. jucunda, D. mulsanti. D. poortmanni, D. retigera, D. scenica, D. semicincta, and D. staudingeri. A total of 38 new species of Dilatitibialis are described: Dilatitibialis annie, D. carmen, D. cindy, D. connie, D. crystal, D. dawn, D. diana, D. edith, D. edna, D. elaine, D. ellen, D. emily, D. ethel, D. fallax, D. florence, D. gladys, D. grace, D. josephine, D. kim, D. lillian, D. lois, D. marjorie, D. norma, D. paula, D. peggy, D. phyllis, D. rita, D. robin, D. rosa, D. shannon, D. sheila, D. sherry, D. sylvia, D. thelma, D. tiffany, D. tina, D. tracy, and D. wendy. Corrections are made to titles of previous Parts of this series, as follows: South American Coccinellidae, Part XII (Gordon 2007) is changed to Part XIII; South American Coccinellidae, Part XII (Gordon et al. 2013) is changed to Part XIV.
Cyrea Gordon and Canepari (121 species) and Tiphysa Mulsant (2 species) are discussed, species are described, illustrations are provided, and a key to all recognized species is included. New synonyms recognized are:
Hyperaspis arrowi var. darwini Brèthes = Cyrea arrowi (Brèthes); Hyperaspis trivittata Weise, Hyperaspis mundula Weise = Cyrea emiliae (Mulsant); Cleothera scapulata Mulsant, Cleothera mercabilis Mulsant, Hyperaspis iheringi Weise = Cyrea flavoguttata (Mulsant); Cleothera gracilis Mulsant = Cyrea hexastigma (Mulsant); Cleothera triacantha Mulsant = Cyrea novemsignata (Herbst); Cleothera distinguenda Mulsant = Cyrea ormanceayi (Mulsant); Cleothera sexnotata Brèthes = Cyrea quinquenotata (Mulsant); Cleothera schaufussi Vogel and Hyperaspis adelaida Gorham = Cyrea tessulata (Mulsant). A total of 76 new species of Cyrea are described: Cyrea agnes, C. allison, C.alma, C. annette, C. arlene, C. audrey, C. beatrice, C. bernice, C. bessie, C. brittany, C. carla, C. charlene, C. claudia, C. colleen, C. constance, C. courtney, C. dana, C. dolores, C. dora, C. eileen, C. ella, elsie, erica, georgia, gertrude, gina, glenda, heidi, holly, ida, jackie, jeanne, jeannette, jessie, jo, C. joy, C. june, C. katie, C. kristen, C. laurie, C. lillie, C. lucille, C. lucy, C. lydia, C. marcia, C. marian, C. marion, C. marlene, C. mattie, C. maureen, C. maxine, C. melanie, C. melinda, C. minnie, C. natalia, C. nellie, C. pearl, C. pseudospinalis, C. renee, C. roberta, C. rosemary, C. samantha, C. stacy, C. stella, C. sue, C. tamara, C. tanya, C. tara, C. terry, C. vanessa, C. vera, C. vicki, C. viola, C. vivian, C. willie, C. wilma, C. yolanda, C.
yvonne. Lectotypes here designated for C. collaris, C. compta, C. distinguenda, C. exclamationis, C. fasciata, C. ferruginiceps, C. flavoguttata, C. iheringi, C. languida, C. maculosa, C. melaneura, C. mundula, C. noticollis, C. novemsignata, C. ormanceayi, C. ornaticolis, C. quinquenotata, C. renifera, C. schaufussi, C. sexguttata, C. spinalis, C. tessulata, C. trepida, C. triacantha
Genera of Brachiacanthini (Coleoptera: Coccinellidae: Hyperaspidinae) are discussed and a key to all recognized genera provided. Cyrea, new genus, is proposed, and Serratitibia, new genus, is erected and revised, Cleothera Mulsant and Hinda Mulsant are recognized as valid genera and revised. Helesius caseyi Sicard is transferred to Hinda and recognized as a synonym of Hinda designata Mulsant, new synonymy. Brachiacantha brethesi (Korschefsky), Cleothera abendrothi Kirsch, Cleothera ambigua Mulsant, Cleothera bisquatuorpustulata Mulsant, Cleothera decemsignata Mulsant, Cleothera gaillardi Mulsant, Cleothera humerata Mulsant, Cleothera tortuosa Mulsant, Cleothera traili Brèthes, Cleothera uncinata Mulsant, Hinda joeli Almeida and Milléo, Hinda modesta Weise, Hinda regularis Kirsch, Hyperaspis aliciae Crotch, and Hyperaspis fraudulenta Kirsch are transferred to Serratitibia, becoming new combinations. One new species of Hinda, H. ecuadorica, is described. A total of 73 new species of Serratitibia are described: Serratitibia amanda, S. andrea, S. angela, S. anna, S. ashley, S. barbara, S. barclayi, S. betty, S. beverly, S. bonnie, S. brenda, S. cheryl, S. christine, S. cynthia, S. debra, S. denise, S. donna, S. doris, S. elizabeth, S. evelyn, S. frances, S. gloria, S. heather, S. helen, S. irene, S. jacqueline, S. janet, S. janice, S. jean, S. jennifer, S. joan, S. joyce, S. judith, S. judy, S. julie, S. karen, S. katherine, S. kathleen, S. kathy, S. kelly, S. kimberly, S. laura, S. linda, S. lisa, S. loreto, S. lori, S. louise, S. margaret, S. marilyn, S. mary, S. martha, S. melissa, S. michelle, S. mildred, S. nancy, S. nicole, S. pamela, S. paprzycki, S. patricia, S. quincemil, S. rachel, S. rebecca, S. rose, S. ruby, S. ruth, S. sarah, S. satipoensis, S. shirley, S. stephanie, S. susan, S. tammy, S. teresa, and S. virginia. Lectotypes are here designated for Serratitibia lividipes, S. gaillardi, S. decemsignata, S. abendrothi, and S. ambigua.
The new species Cephalocyclus majomaensis and Oscarinus cabreroi from Mexico are described and figured. While studying specimens from Mexico to complete a systematic revision of the Aphodiinae (Coleoptera: Scarabaeidae) of that region, we found a couple of species new to science. They belong to the genera Cephalocyclus Dellacasa, Gordon and Dellacasa, 1998 and Oscarinus Gordon and Skelley, 2007, and are described here.