743 resultados para Chiasmolithus bidens
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The grains of chickpea consumed in Brazil are almost entirely imported. Considering that chickpeas presents conditions to be cultivated in some regions of Brazil, this study aimed to study interference of six weed plants (Amaranthus viridis, Bidens pilosa, Raphanus raphanistrum, Cyperus rotundus, Digitaria nuda and Eleusine indica) on the vegetative development of chickpeas. Thus, we evaluated the shoot length, number of leaves, leaf area, chlorophyll content and dry weight of leaves, stem and root of chickpeas. We observed a significant interference on the chickpeas'development in coexistence with weeds. Among the weeds, D. nuda, E. indica and A. viridis were the most aggressive, highlighting the need for early control of weeds when in cultivation of chickpeas in areas with a history of high density of these weeds. The leaf area of chickpeas was the most affected trait by the coexistence with weeds, affecting the development of the crop.
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The aim of this study was to evaluate the effect of low soil moisture on the efficacy of applying herbicides ametryn + clomazone, sulfentrazone and tebuthiuron in pre-emergence application submitted to simulated rainfalls at different time intervals after application in control of B. pilosa, C. echinatus and U. plantaginea plants. The experiment was carried out in pots with a capacity of 2.5 L in green-house conditions and experimental design was completely randomized with four replications, arranged in a 3x5 factorial (three herbicides and five rains intervals). The herbicides clomazone + ametryn (Sinerge EC) 5.0 L commercial product (cp) ha(-1), sulfentrazone (Boral 500 SC) 1.2 L cp ha(-1) and tebuthiuron (combine SC) 2.0 L cp ha(-1) were applied in pre-emergence and the precipitation of 20 mm were applied under de pots in five time intervals after the herbicide application (0h, 4h, 8h, 12h and 24hours). Visual evaluations of plants control that emerged plants were realized at 14 and 21 days after treatment application and the plant emergence percentage was calculated. The application of these three herbicides in dry soil then rain within 24 hours after application provided C. echinatus plants emergence, reduced B. pilosa emergency but in the end of the experiment effectively controlled these two species and U. plantaginea plants.
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A systematic re-evaluation of Vampyressa pusilla warrants the elevation of V. p. thyone from subspecies to species rank based on its distinction from the allopatric V. p. pusilla. Morphological, mensural, chromosomal, and mitochondrial differences define each of these two taxa as divergent lineages. Vampyressa pusilla is endemic to the Atlantic Forest of southeastern South America and V. thyone is found allopatrically in northwestern South America, Central America, and southern Mexico. A molecular phylogenetic analysis of the mtDNA ND3-4 gene region using restriction endonuclease cut sites resulted in a monophyletic, although weakly supported Vampyressa ingroup with Chiroderma, and a clade of Mesophylla and Ectophylla as successive basal outgroup lineages. The phylogeny within Vampyressa, with the exception of V. melissa which is most similar to V. thyone based on karyotypes and morphology, had a topology of ((pusilla + thyone) + ((brocki + nymphaea) + bidens))).
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Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
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In the first seven months of 2008, eighteen Cuvier’s beaked whales (Ziphius cavirostris), four Sowerby’s beaked whales (Mesoplodon bidens), five unidentified beaked whales and twenty-nine long-finned pilot whales (Globicephala melas) were reported stranded in the UK and Ireland. Decomposition of those animals investigated puts the predicted time of death at mid-January. Concerns that an unusual mortality event had taken place prompted further investigations. Most carcasses were too decomposed for necropsy. A summary of findings is presented here. Although the initial stranding of five Cuvier’s beaked whales in Scotland shared some similarities with atypical mass stranding events linked in time and space to mid-frequency naval sonars, there were two important differences with the remaining strandings during this period. First, the geographical range of the event was very wide and second, the strandings occurred over a prolonged period of several months. Both of these factors could be related to the fact that the mortalities occurred offshore and the carcasses drifted ashore. The cause(s) of this high number of strandings of mixed offshore cetacean species during this period remain undetermined.
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During the Paleocene-Eocene Thermal Maximum (PETM), rapid release of isotopically light C to the ocean-atmosphere system elevated the greenhouse effect and warmed temperatures by 5-7 °C for 105 yr. The response of the planktic ecosystems and productivity to the dramatic climate changes of the PETM may represent a significant feedback to the carbon cycle changes, but has been difficult to document. We examine Sr/Ca ratios in calcareous nannofossils in sediments spanning the PETM in three open ocean sites as a new approach to examine productivity and ecological shifts in calcifying plankton. The large heterogeneity in Sr/Ca among different nannofossil genera indicates that nannofossil Sr/Ca reflects primary productivity-driven geochemical signals and not diagenetic overprinting. Elevated Sr/Ca ratios in several genera and constant ratios in other genera suggest increased overall productivity in the Atlantic sector of the Southern Ocean during the PETM. Dominant nannofossil genera in tropical Atlantic and Pacific sites show Sr/Ca variations during the PETM which are comparable to background variability prior to the PETM. Despite acidification of the ocean there was not a productivity crisis among calcifying phytoplankton. We use the Pandora ocean box model to explore possible mechanisms for PETM productivity change. If independent proxy evidence for more stratified conditions in the Southern Ocean during the PETM is robust, then maintenance of stable or increased productivity there likely reflects increased nutrient inventories of the ocean. Increased nutrient inventories could have resulted from climatically enhanced weathering and would have important implications for burial rates of organic carbon and stabilization of climate and the carbon cycle.
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Composition and distribution of megabenthic communities around Svalbard were investigated in June/July 1991 with 20 Agassiz trawl and 5 bottom trawl hauls in depths between 100 and 2100 m. About 370 species, ranging from sponges to fish, were identified in the catches. Species numbers per station ranged from 21 to 86. Brittle stars, such as Ophiacantha bidentata, Ophiura sarsi and Ophiocten sericeum, were most important in terms of constancy and relative abundance in the catches. Other prominent faunal elements were eunephthyid alcyonarians, bivalves, shrimps, sea stars and fish (Gadidae, Zoarcidae, Cottidae). Multivariate analyses of the species and environmental data sets showed that the spatial distribution of the megabenthos was characterized by a pronounced depth zonation: abyssal, bathyal, off-shore shelf and fjordic communities were discriminated. However, a gradient in sediment properties, especially the organic carbon content, seemed to superimpose on the bathymetric pattern. Both main factors are interpreted as proxies of the average food availability, which is, hence, suggested to have the strongest influence in structuring megabenthic communities off Svalbard.
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A biostratigraphically complete (all nannofossil biozones present) Cretaceous/Tertiary boundary was recovered at Site 761 on the Wombat Plateau, northwest Australian margin, during Ocean Drilling Program Leg 122. A quantitative study of calcareous nannofossils on closely spaced samples across the boundary reveals a rapid change in assemblages in a similar fashion to other Cretaceous/Tertiary boundary sites. Nannofossil species were placed into three categories: Tertiary, Cretaceous, and 'survivors'. The rapid sequential turnover in these assemblages is as follows: Cretaceous species are abruptly replaced at the boundary by opportunistic survivor species, which in turn are abruptly replaced by newly evolved Tertiary taxa. The uppermost Maestrichtian assemblage is distinctly mid-latitudinal with few Micula murus and rare to few Nephrolithus frequens. The nannofossil assemblage immediately above the boundary is dominated by an abundance bloom of Cyclagelosphaera spp. No Thoracosphaera or Braarudosphaera abundance blooms are present as at many other localities. The change from a survivor- to Tertiary-dominated assemblage is coincident with the CPla/CPlb nannofossil subzonal boundary, which is marked by the simultaneous first occurrence of several species including Cruciplacolithus tenuis and C. primus. The latter is found to first occur below C. tenuis in the most complete Cretaceous/Tertiary sections. A hiatus between Subzones CPla and CPlb is interpreted to explain this discrepancy.
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An Eocene-Oligocene calcareous nannofossil biostratigraphic framework for Ocean Drilling Program (ODP) Site 748 in the southern Indian Ocean is established, which provides a foundation for this and future quantitative biogeographic studies. This biostratigraphic analysis, together with quantitative nannofossil data, enables a reinterpretation of the preliminary magnetostratigraphy and a new placement for magnetic Subchron CBN in the lowermost Oligocene. Calcareous nannofossil species diversity is low at Site 748 relative to lower latitude sites, with about 13 taxa in the middle Eocene, gradually decreasing to about 6 in the late Oligocene. There is, however, no apparent mass extinction at any stratigraphic level. Similarly, no mass extinctions were recorded at or near the Eocene/Oligocene boundary at Site 711 in the equatorial Indian Ocean. Species diversity at the equatorial site is significantly higher than at Site 748, with a maximum of 39 species in the middle Eocene and a minimum of 14 species in the late Oligocene. The abundance patterns of nannofossil taxa are also quite different at the two sites, with chiasmoliths, Isthmolithus recurvus, and Reticulofenestra daviesii abundant and restricted to the high-latitude site and Coccolithus formosus, discoasters, and sphenoliths abundant at the equatorial site but impoverished at the high-latitude site. This indicates a significant latitudinal biogeographic gradient between the equatorial site and the high-latitude site in the Indian Ocean for the middle Eocene-Oligocene interval. The abundance change of warm-water taxa is similar to that of species diversity at Site 711. There is a general trend of decreasing abundance of warm-water taxa from the middle Eocene through the early Oligocene at Site 711, suggesting a gradual cooling of the surface waters in the equatorial Indian Ocean. The abundance of warm-water taxa increased in the late Oligocene, in association with an increase in species diversity, and this may reflect a warming of the surface waters in the late Oligocene. An abrupt increase in the abundance of cool-water taxa (from ~20% to over 90%) occurred from 36.3 to 35.9 Ma at high-latitude Site 748. Coincident with this event was a ~1.0 per mil positive shift in the delta18O value of planktonic foraminifers and the occurrence of ice-rafted debris. This abrupt change in the nannofossil population is a useful biostratigraphic event for locating the bottom of magnetic Subchron C13N in the Southern Ocean. The sharp increase in cool-water taxa coeval with a large positive shift in delta18O values suggests that the high-latitude surface waters drastically cooled around 36.3-35.9 Ma. The temperature drop is estimated to be 4°C or more at Site 748 based on the nannofossil population change relative to the latitudinal biogeographic gradient established in the South Atlantic Ocean during previous studies. Consequently, much of the delta18O increase at Site 748 appears to be due to a temperature drop in the high latitudes rather than an ice-volume signal. The ~0.1 per mil delta18O increase not accounted for by the temperature drop is attributed to an ice-volume increase of 4.6 * 10**3 km**3, or 20% the size of the present Antarctic ice sheet.
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The opening of the Tasmanian Gateway between Australia and Antarctica has long been considered a critical element in the initiation of the Antarctic Circumpolar Current, thermal isolation of Antarctica, and Cenozoic global cooling. The timing for the opening of the gateway to shallow-water circulation and subsequently to deep-water circulation was poorly known, however, and the dating of these events was a major objective of ODP Leg 189. Nannofossil data from Leg 189 sites and DSDP Site 281 in the Tasmanian Gateway suggest a 41-42 Ma age for the initiation of widespread glauconite deposition in the region, which coincided with a sharp drop in sedimentation rate. This is interpreted to be the opening of the gateway to shallow-water circulation, which occurred within the middle of the 51-33 Ma long-term cooling. The change from siliciclastic sediments to pelagic carbonates, the most conspicuous sedimentological and paleontological change in the region for the last 70 Ma and presumably the indicator for the opening of the gateway to deep-water circulation, is dated at about 31 Ma. This event is more than 2 my younger than the major high-latitude cooling in the earliest Oligocene, and thus cannot be the cause for the latter.
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A pollen diagram from the Ahlequellmoor in the Solling area shows the history of vegetation and settlement over the last 7,800 years. In the early Atlantic period mixed deciduous forest with mainly Tilia together with Ulmus and Quercus grew in the area. In the late Atlantic period Quercus became most abundant. Fagus spread in the Sub-boreal period at about 2700 B.C. Since ca. 900 B.C. the Solling was covered by beech forests with some oak. In prehistoric times woodland grazing is indicated. Only in Medieval times are two settlements in the vicinity of the Ahlequellmoor reflected in the pollen diagram. The earlier one is dated to about A.D. 750-1020, and may be connected with the former Monastery of Hethis, which is thought to have existed close to the fen from A.D. 815 to 822. The second Medieval settlement dates to the 11th-12th century. The large-scale woodland destruction of late Medieval and modern times is not clearly visible. The silvicultural measures of the last 200 years are reflected by increasing values of spruce and grassland taxa.
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Two marshes near Muscotah and Arrington, Atchison County, northeastern Kansas, yielded a pollen sequence covering the last 25,000 yrs of vegetation development. The earliest pollen spectra are comparable with surface pollen spectra from southern Saskatchewan and southeastern Manitoba and might indicate a rather open vegetation but with some pine, spruce, and birch as the most important tree species, with local stands of alder and willow. This type of vegetation changed about 23,000 yrs ago to a spruce forest, which prevailed in the region until at least 15,000 yrs ago. Because of a hiatus, the vegetation changes resulting in the spread of a mixed deciduous forest and prairie, which was present in the region from 11,000 to 9,000 yrs ago, remain unknown. Prairie vegetation, with perhaps a few trees along the valleys, covered the region until about 5,000 yrs ago, when a re-expansion of deciduous trees began in the lowlands.
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Calcareous nannofossil assemblages were studied from Sites 699 and 703, drilled during ODP Leg 114 to the west and east, respectively, of the Mid-Atlantic Ridge in the subantarctic South Atlantic Ocean. Recovery at the two sites consists of an almost continuous sequence of upper Eocene-lower Oligocene sediments. This study describes the calcareous nannofossil assemblages at the transition between the Eocene and Oligocene and correlates these assemblages with those described in lower latitude sections. Quantitative analyses were performed on several important taxa in order to improve the biostratigraphic resolution and permit some paleoenvironmental interpretations. Several discrepancies were noted between the two sites and between the Eocene and Oligocene assemblages. The Eocene assemblages show a great number of species and warmer water conditions; the early Oligocene assemblages are less diversified and are indicative of cooler conditions. The Eocene/Oligocene boundary was not defined by planktonic foraminifers because of the strong dissolution, poor recovery, and drilling disturbances. On the other hand, the calcareous nannofossil assemblage allowed recognition of the interval where the Eocene/Oligocene boundary can possibly be placed.
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Lower Eocene calcareous nannofossil limestone cored at DSDP Site 612 on the middle slope off New Jersey represents an almost complete biostratigraphic sequence; only the lowest biozone (CP9a; NP10*) was not recovered. The thickness of the strata (198 m), the good preservation of the nannofossils, and the lack of long hiatuses justify the acceptance of this section as a lower Eocene reference for the western North Atlantic margin. The widely recognized and very similar nannofossil zonations of Martini (NP zones) and Bukry-Okada (CP zones) are emended slightly to make their lower Eocene biozones coeval; in addition, five new subzones are erected that subdivide zones CP10 and CPU (NP12 and NP13). Established biozone names are retained as they are altered little in concept, but alphanumeric code systems are changed somewhat by appending an asterisk (*) to identify zones that are emended. Zone CP10* (NP12*) is divided into two parts, the Lophodolithus nascens Subzone (CP10*a; NP12*a) and the Helicosphaera seminulum Subzone (CP10*b; NP12*b). Zone CPU* (NP13*) is divided into three parts, the Helicosphaera lophota Subzone (CP11*a; NP13*a), the Cyclicargolithuspseudogammation Subzone (CP11*b; NP13*b), and the Rhabdosphaera tenuis Subzone (CP11*c; NP13*c). At Site 612, a time-depth curve based on nannofossil datums dated in previous studies reveals a smoothly declining sediment accumulation rate, from 4.9 cm/10**3yr in CP10* (NP12*) to 2.8 cm/103 yr. in CP12* (NP14*). The ages of first-occurrence datums not previously dated are approximated by projection onto this timedepth curve and are as follows: Helicosphaera seminulum, 55.0 Ma; Helicosphaera lophota, 54.5 Ma; Cyclicargolithus pseudogammation, 53.7 Ma; Rhabdosphaera tenuis, 52.6 Ma; and Rhabdosphaera inflata, 50.2 Ma. At nearby Site 613 on the upper rise, strata of similar age, 139 m thick, contain an unconformity representing Subzone CPll*b (NP13*b) and a hiatus of approximately 1.1 m.y. duration. The sediment accumulation rate in the lower part of this section (9.7 cm/10**3yr.) is twice that observed for equivalent strata at Site 612. The hiatus and the heightened sediment accumulation rate at Site 613 probably represent the effects of episodic mass wasting on the early Eocene continental slope and rise.