197,055 research outputs found

    Two new species of the Drosophila serido sibling set (Diptera, Drosophilidae)

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    Drosophila antonietae sp. nov. and D. gouveai sp. nov. are members of the D. buzzatii cluster of the D. repleta species group of the genus Drosophila. They can be distinguished from their cryptic species, D. borborema Vilela & Sene, 1977, D. koepferae Fontdevila & Wasserman, 1988, D. serido Vilela & Sene, 1977, and D. seriema Tidon-Sklorz & Sene, 1995 by morphological, genetic and ecological criteria.Em processament

    Cryptosepalum korupense Van Der Burgt & Poundje & Sene 2014, sp. nov.

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    Cryptosepalum korupense Burgt, sp. nov. (Figs 1-4) Cryptosepalum korupense, sp. nov. is related to Cryptosepalum staudtii Harms. Cryptosepalum korupense, sp. nov. has (10-)14-21(-26) pairs of leaflets; C. staudtii has 10-14(-16) pairs of leaflets. The leaflets of C. korupense, sp. nov. are divided by the midvein into two unequal parts; near the apex of the leaflet, the proximal part (the part closest to the twig) is 3-4 × wider than the distal part (the part furthest from the twig). In C. staudtii the proximal part of the leaflet near the apex is only 1-1.5 × wider than the distal part. The flowers of both species are more or less similar. The fruits of C. korupense, sp. nov. are 10-18 cm long; the fruits of C. staudtii are 6-10 cm long. TYPUS. — Cameroon. Southwest Region, south of Mundemba, forest near village Besingi, about 1 km downstream of bridge over Idu river, on the south bank, 4°55’16’’N, 8°54’04’’E, alt. 50 m, young fruits, 12.III.2007, van der Burgt & Motoh 922 (holo-, K [K000460356]; iso-, BR, G, MO, P, SCA, WAG, YA). PARATYPI. — Cameroon. Southwest Region, Korup National Park, south of P transect, 4°59’N, 8°49’E, alt. 100 m, sterile, 28.III.2004, van der Burgt & Eyakwe 681 (WAG, YA); same loc., 5°0’N, 8°48’E, alt. 100 m, seedlings, 25.V.2007, van der Burgt & Motoh 941 (BR, G, K, MO, P, SCA, WAG, YA); Korup National Park, P transect to Isangele Road, 4°58’N, 8°50’E, alt. 100 m, fr.& seedlings, 21.II.2008, van der Burgt, Pearce, Poundje & Yombo 1126 (K, MO, P, WAG, YA); Near Besingi village, about 1 km downstream of bridge over Idu river, 4°55’16’’N, 8°54’04’’E, alt. 50 m, sterile, 14.IX.2006, van der Burgt & Motoh 848 (K, MO, P, WAG, YA); same loc., fr., 20.V.2007, van der Burgt & Motoh 931 (K, MO, WAG, YA); same loc., fr., 29.IV.2007, Motoh 1 (BR, K, MO, P, WAG, YA); same loc., seeds, 30.VII.2007, Motoh 3 (K, YA); near Besingi village, about 1 km upstream of bridge over Idu river, 4°55’20’’N, 8°54’37’’E, alt. 50 m, 2.II.2010, Motoh 6 (K, YA); Mount Cameroon, Mokoko forest above Bonja village, 4°28’N, 9°06’E, alt. 100 m, sterile, 24.III.1993, Tchouto (Mbatchou) 621 (K, SCA); Mount Cameroon, Onge River, 4°18’N, 9°01’E, alt. 200 m, sterile, 10.X.1993, Tchouto (Mbatchou) 773 (K, SCA); Mount Cameroon, Mokoko, 4°27’N, 9°04’E, alt. 300 m, sterile, 22.V.1994, Thomas 10049 (SCA). DISTRIBUTION. — Cryptosepalum korupense, sp. nov. is endemic in the Southwest Region in Cameroon (Fig. 3). The species was found in southern Korup National Park, in the forest on the banks of the Idu River near the village Besingi, and in the lowland forest northwest of Mount Cameroon. Three large plots have been made in southern Korup National Park; but C. korupense, sp. nov. was not found in any of these plots. These three plots are the plots “P”, 82.5 ha and “NW”, 56.25 ha (Newbery et al. 2013); and the plot “KFDP”, 50 ha (Kenfack et al. 2006). The new species seems to be rare in southern Korup National Park (van der Burgt & Eyakwe 2010); which can also be concluded from the mapping of Microberlinia bisulcata trees. Three large groves of M. bisulcata have been mapped (one grove only partly); the area of forest mapped in and close to these groves is c. 7.9 km 2 (Newbery & van der Burgt unpubl. data). Within this area no C. korupense, sp. nov. trees were found. In addition, c. 66 km of parallel transect lines at 500 m distance to each other were walked along in southern Korup (Newbery & van der Burgt, unpubl. data). Any mature C. korupense, sp. nov. tree standing at less than 25 m from these transects would likely have been found by way of the usually abundant seedlings at this distance. This amounts to another 3.3 km 2 of forest mapped. Within this area three small groves were found; one group of 14 C. korupense, sp. nov. trees over 10 cm trunk diameter (Fig. 4) and two small groups of two trees each. The total amount of forest mapped is c. 11.2 km 2; within this area 18 C. korupense, sp. nov. trees over 10 cm trunk diameter were found. Of all trees over 50 cm trunk diameter in southern Korup National Park, one tree out of c. 3100 trees is C. korupense, sp. nov. However, because these surveys were based on seedlings, mature trees which produced few or no seedlings in the years before these surveys, as well as immature trees, may have been overlooked. In the forests near Besingi village ten Cryptosepalum korupense, sp. nov. trees with trunk diameters of 20-60 cm were recorded. All trees were found on the banks of the Idu River. This river is bordered by an oil palm plantation on one side and by a mosaic of subsistence farms and secondary forest on the other side. Along the river a strip of forest rich in rare forest species remains. This forest strip is a remnant of a once more continuous forest and has not been converted to farmland because of the often steep and rocky banks and variable water level. HABITAT. — Rainforest on well-drained soil; 50-300 m. ETYMOLOGY. — Named for Korup National Park where the species was first found. SEED DISPERSAL. — Trees of Cryptosepalum korupense, sp. nov. appear to grow in small groups. The only group that could be mapped completely had 14 trees over 10 cm trunk diameter (Fig. 4). Several other species of Caesalpinioideae are present within this group, as well as many trees from other families. The seeds of C. korupense, sp. nov. are dispersed by way of ballistic seed dispersal. The maximum ballistic dispersal distance is unknown but it is probably in the range of 50-70 m. This estimate is based on van der Burgt (1997) and on later observations by the first author on other Caesalpinioideae taxa with similar pod and seed size and thickness, and therefore presumably similar maximum dispersal distance. The tendency of trees of this species to grow in groups (Fig. 4) is probably related to the relatively short and strictly limited maximum dispersal distance of the ballistic seed dispersal method. CONSERVATION STATUS Cryptosepalum korupense, sp. nov. is assessed here as Endangered, B1ab(iii;v) C1 D, under the criteria of IUCN (2013). The extent of occurrence of C. korupense, sp. nov. is 802 km 2. The forests in the area between the known localities are severely fragmented. Outside Korup National Park, which is a protected area, there is continuing decline in quality of habitat and in the number of mature individuals, due to subsistence farming and the establishment of oil palm plantations. These facts lead to Endangered under IUCN criterion B1 (IUCN 2013). In total 28 trees have been recorded in two of the three localities (one locality, the lowland forests northwest of Mount Cameroon, was not visited but taken from herbarium sheets). Assuming that trees become mature at 30 cm trunk diameter, 20 of the 28 trees are mature. Much forest in the Southwest region remains unexplored for this species; therefore the number of mature trees is expected to be more than 50. However, in southern Korup National Park the species is very rare (see the paragraph on distribution); therefore the number of mature trees may be less than 250, is leading also to Endangered, under IUCN criterion D. The estimated number of mature trees, combined with the estimated decline of the species of at least 20% over two generations (which may be over 100 years), due to subsistence farming and the establishment of oil palm plantations, is leading also to Endangered, under IUCN criterion C1. DESCRIPTION Tree to 44 m high, trunk to 88 cm diameter at 1.3 m high, bole cylindrical to somewhat irregular in large trees, bark light grey-brown, smooth.Twigs densely tomentose to glabrescent, hairs curly, 0.3-0.7 mm long. Bud scales 14-18, caducous, distichous, not keeled, parallel-veined; proximal scale 1 mm long × 3 mm wide, distal scales progressively larger and relatively longer, to 40 × 18 mm, oblanceolate, bright dark pink; both surfaces sparsely hairy with hairs to 0.1 mm, margins with hairs to 1 mm. Stipules in pairs, free, caducous, parallel-veined, longpetioloid, oblanceolate, 20-40 × 1-10 mm; apex acute; indumentum similar to bud scales. Leaves alternate, paripinnate, (5.5-)7-11(-12) × (2-) 2.5- 3.2 cm; petiole 3-5 mm, without glands; rachis (4-)5.5-9.5(-11) cm long, densely tomentose, hairs curly, 0.3-0.7 mm long; upper and middle leaflet pairs opposite, lower pairs subopposite. Leaflets sessile, in (10-)14-21(-26) pairs; narrowly oblong, to 13-15 × 4-5 mm, base and apex asymmetric, apex emarginate; midvein dividing the leaflet into two unequal parts; at the base of the leaflet the proximal part (the part closest to the twig) is as wide as the distal part (the part furthest from the twig); near the apex of the leaflet the proximal part is 3-4 × wider than the distal part; leaflets glabrous both sides, caducous fringing hairs to 0.5 mm long, a few persistent hairs to 0.2 mm long on apex of midvein; glands 0-2, one gland positioned on distal part of leaflet, near the base and about midway between the midvein and the margin, on lowest leaflets also a gland on proximal part of leaflet. Inflorescence a raceme, axillary, one per node, 20-25-flowered, 5-7.5 cm long including a peduncle c. 2 cm long; densely tomentose, hairs curly, 0.3-0.7 mm long. Flowers Floral bract inserted at base of pedicel, caducous, lanceolate, c. 8 × 3 mm, indumentum similar to bud scales; pedicel 10-14 mm long, indumentum similar to inflorescence axis; bracteoles inserted at apex of pedicel, white, opposite, ovate, valvate, 6 × 5 mm, keeled, apex acute, mostly glabrous outside, short hairs outside near apex, on edge and inside; hypanthium campanulate, c. 0.8 mm deep, glabrous. Sepals 4, white, lanceolate; adaxial sepal 1-2 × 0.3-0.6 mm, sometimes bilobed, margins hairy; lateral sepals 0.2-1 × 0.3-0.4 mm; abaxial sepal 0.5-2 × 0.3-0.5mm. Adaxial petal white, glabrous, 6-7 mm long, 8 mm wide, claw 1 mm long; other petals absent. Stamens 3, filaments 8-9 mm long, glabrous, anthers oblong-elliptic, c. 2.2 × 1.5 mm. Staminodes 2-6, to 3 mm long. Ovary oblong, stipitate, 4.5 × 1.5 mm, glabrous, ovules 2-4; stipe 1-1.5 mm long, curled hairs to 1.5 mm long, placed on the sides; style 6-7 mm long, glabrous, stigma capitate. Pod oblong to obovate, glabrous, lacking surface sculpture; broadest towards apex, 10-18 × 3.5-5.5 × 0.3-0.8 cm, beak 3-8 mm long; upper suture broadened, to 3 mm wide per valve; containing 0-4 seeds. Seeds discoid, 22-28 × 16-22 × 4-5 mm. Seedling: hypocotyl 7.5-9.5 cm, epicotyl 2-3.5 cm, first pair of leaves opposite, leaves (6-)7.5- 10.5 × 2.5-3.5 cm, leaf rachis 6-10 cm, leaflets in (14-)16-22 pairs, to 18 × 6 mm. IDENTIFICATION NOTES The small, emarginate leaflets of Cryptosepalum korupense, sp. nov. have a unique character distinguishing them from all other West and Central African Caesalpinioideae species. The midvein divides the leaflet into two unequal parts; near the apex of the leaflet, the proximal part (the part closest to the twig; see Wieringa 1999: 40) is 3-4 × wider than the distal part (the part furthest from the twig). In other African Caesalpinioideae species with small, emarginate leaflets the proximal part of the leaflet near the apex is only 1-2 × wider than the distal part. This character can be used to distinguish C. korupense, sp. nov. from other species of Caesalpinioideae with small, emarginate leaflets; for example C. staudtii, Didelotia brevipaniculata J.Léonard, Microberlinia bisulcata and Plagiosiphon emarginatus. Flowering specimens of these species are easy to distinguish from C. korupense, sp. nov. (see Aubréville 1970). Cryptosepalum korupense, sp. nov. can be easily distinguished from the other tree species of Cryptosepalum, because the leaves have more pairs of leaflets than any of the other tree species: (10-)14-21(-26) pairs. Cryptosepalum staudtii has 10-14(-16) pairs of leaflets; the other tree species are unifoliolate, bifoliolate or tetrafoliolate.Published as part of Van Der Burgt, Xander M., Poundje, Maguy & Sene, Olivier, 2014, Cryptosepalum korupense Burgt, sp. nov. (Leguminosae, Caesalpinioideae), a tree species from the Southwest Region in Cameroon, pp. 73-81 in Adansonia (3) (3) 36 (1) on pages 76-80, DOI: 10.5252/a2014n1a7, http://zenodo.org/record/520844

    FIG. 3 in Cryptosepalum korupense Burgt, sp. nov. (Leguminosae, Caesalpinioideae), a tree species from the Southwest Region in Cameroon

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    FIG. 3. ― Distribution of Cryptosepalum korupense Burgt, sp. nov.Published as part of Van Der Burgt, Xander M., Poundje, Maguy & Sene, Olivier, 2014, Cryptosepalum korupense Burgt, sp. nov. (Leguminosae, Caesalpinioideae), a tree species from the Southwest Region in Cameroon, pp. 73-81 in Adansonia (3) 36 (1) on page 78, DOI: 10.5252/a2014n1a7, http://zenodo.org/record/520844

    Sugarcane bagasse as alternative packing material for biofiltration of benzene polluted gaseous streams: a preliminary study

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    Removal of benzene vapor from gaseous streams was studied in two identically sized lab-scale biofiltration columns: one filled with a mixture of raw sugarcane bagasse and glass beads, and the other one packed with a mixture of ground sugarcane bagasse and glass beads, in the same volume ratio, as filter materials

    Dr. Duane M. Jackson, Morehouse College, July 2011

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    This video is a conversation with Dr. Duane M. Jackson. Dr. Jackson talks about his paper, "Recall and the Serial Position Effect: The Role of Primacy and Recency on Accounting Students' Performance." Jackie Daniel, AUC Woodruff Library, is the interviewer

    "Reflections on the subject of Emigration from Europe with a view to Settlement in the United States" By M. Carey.

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    "Reflections on the subject of Emigration from Europe with a view to Settlement in the United States: containing bried sketches of the moral and political character of those states. By M. Carey, member of the American philosophical, and of the American Antiquarian Society, and author of The Olive Branch, Cindiciae Hibernicae, essays on banking, on political economy, and on internal improvement. To which are now added the English editor's comments on the subject; together with Important Advice to Emigrants, and Cautions Against Impositions Practiced in the Outports

    Dispelling the Myths Behind First-author Citation Counts

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    We conducted a full-scale evaluative citation analysis study of scholars in the XML research field to explore just how different from each other author rankings resulting from different citation counting methods actually are, and to demonstrate the capability of emerging data and tools on the Web in supporting more realistic citation counting methods. Our results contest some common arguments for the continued use of first-author citation counts in the evaluation of scholars, such as high correlations between author rankings by first-author citation counts and other citation counting methods, and high costs of using more realistic citation counting methods that are not well-supported by the ISI databases. It is argued that increasingly available digital full text research papers make it possible for citation analysis studies to go beyond what the ISI databases have directly supported and to employ more sophisticated methods

    Dr. Glendon Swarthout

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    Hosted by Roger M. Busfield, MSU Assistant Professor of Speech and Theater, Meet the Author is designed to introduce a general audience to a contemporary author and their work through in-depth interviews. This episode features a conversation between Dr. Glendon Swarthout, prolific author and English professor at MSU, and assistant professors Sam S. Baskett and Theodore B. Strandness

    Simulation of thermal plant optimization and hydraulic aspects of thermal distribution loops for large campuses

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    Following an introduction, the author describes Texas A&M University and its utilities system. After that, the author presents how to construct simulation models for chilled water and heating hot water distribution systems. The simulation model was used in a $2.3 million Ross Street chilled water pipe replacement project at Texas A&M University. A second project conducted at the University of Texas at San Antonio was used as an example to demonstrate how to identify and design an optimal distribution system by using a simulation model. The author found that the minor losses of these closed loop thermal distribution systems are significantly higher than potable water distribution systems. In the second part of the report, the author presents the latest development of software called the Plant Optimization Program, which can simulate cogeneration plant operation, estimate its operation cost and provide optimized operation suggestions. The author also developed detailed simulation models for a gas turbine and heat recovery steam generator and identified significant potential savings. Finally, the author also used a steam turbine as an example to present a multi-regression method on constructing simulation models by using basic statistics and optimization algorithms. This report presents a survey of the author??s working experience at the Energy Systems Laboratory (ESL) at Texas A&M University during the period of January 2002 through March 2004. The purpose of the above work was to allow the author to become familiar with the practice of engineering. The result is that the author knows how to complete a project from start to finish and understands how both technical and nontechnical aspects of a project need to be considered in order to ensure a quality deliverable and bring a project to successful completion. This report concludes that the objectives of the internship were successfully accomplished and that the requirements for the degree of Degree of Engineering have been satisfied
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