Relevant bibliographies by topics / Lachlan River (N.S.W.)

Academic literature on the topic 'Lachlan River (N.S.W.)'

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Published: 4 June 2021
Last updated: 20 February 2023

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Journal articles on the topic "Lachlan River (N.S.W.)":

1

Wilkins, Colin, and Mike Quayle. "Structural Control of High-Grade Gold Shoots at the Reward Mine, Hill End, New South Wales, Australia." Economic Geology 116, no. 4 (June 1, 2021): 909–35. http://dx.doi.org/10.5382/econgeo.4807.

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Abstract The Reward mine at Hill End hosts structurally controlled orogenic gold mineralization in moderately S plunging, high-grade gold shoots located at the intersection between a late, steeply W dipping reverse fault zone and E-dipping, bedding-parallel, laminated quartz veins (the Paxton’s vein system). The mineralized bedding-parallel veins are contained within the middle Silurian to Middle Devonian age, turbidite-dominated Hill End trough forming part of the Lachlan orogen in New South Wales. The Hill End trough was deformed in the Middle Devonian (Tabberabberan orogeny), forming tight, N-S–trending, macroscopic D2 folds (Hill End anticline) with S2 slaty cleavage and associated bedding-parallel veins. Structural analysis indicates that the D2 flexural-slip folding mechanism formed bedding-parallel movement zones that contained flexural-slip duplexes, bedding-parallel veins, and saddle reefs in the fold hinges. Bedding-parallel veins are concentrated in weak, narrow shale beds between competent sandstones with dip angles up to 70° indicating that the flexural slip along bedding occurred on unfavorably oriented planes until fold lockup. Gold was precipitated during folding, with fluid-flow concentrated along bedding, as fold limbs rotated, and hosted by bedding-parallel veins and associated structures. However, the gold is sporadically developed, often with subeconomic grades, and is associated with quartz, muscovite, chlorite, carbonates, pyrrhotite, and pyrite. East-west shortening of the Hill End trough resumed during the Late Devonian to early Carboniferous (Kanimblan orogeny), producing a series of steeply W dipping reverse faults that crosscut the eastern limb of the Hill End anticline. Where W-dipping reverse faults intersected major E-dipping bedding-parallel veins, gold (now associated with galena and sphalerite) was precipitated in a network of brittle fractures contained within the veins, forming moderately S plunging, high-grade gold shoots. Only where major bedding-parallel veins were intersected, displaced, and fractured by late W-dipping reverse faults is there a potential for localization of high-grade gold shoots (>10 g/t). A revised structural history for the Hill End area not only explains the location of gold shoots in the Reward mine but allows previous geochemical, dating, and isotope studies to be better understood, with the discordant W-dipping reverse faults likely acting as feeder structures introducing gold-bearing fluids sourced within deeply buried Ordovician volcanic units below the Hill End trough. A comparison is made between gold mineralization, structural style, and timing at Hill End in the eastern Lachlan orogen with the gold deposits of Victoria, in the western Lachlan orogen. Structural styles are similar where gold mineralization is formed during folding and reverse faulting during periods of regional east-west shortening. However, at Hill End, flexural-slip folding-related weakly mineralized bedding-parallel veins are reactivated to a lesser degree once folds lock up (cf. the Bendigo zone deposits in Victoria) due to the earlier effects of fold-related flattening and boudinage. The second stage of gold mineralization was formed by an array of crosscutting, steeply W dipping reverse faults fracturing preexisting bedding-parallel veins that developed high-grade gold shoots. Deformation and gold mineralization in the western Lachlan orogen started in the Late Ordovician to middle Silurian Benambran orogeny and continued with more deposits forming in the Bindian (Early Devonian) and Tabberabberan (late Early-Middle Devonian) orogenies. This differs from the Hill End trough in the eastern Lachlan orogen, where deformation and mineralization started in the Tabberabberan orogeny and culminated with the formation of high-grade gold shoots at Hill End during renewed compression in the early Carboniferous Kanimblan orogeny.
2

ERWIN, TERRY L. "The beetle family Carabidae of Costa Rica: The genus Epikastea Liebke of the Plochonida Group, with new Neotropical species and notes on their way of life (Insecta: Coleoptera, Lebiini, Agrina)." Zootaxa 790, no. 1 (December 22, 2004): 1. http://dx.doi.org/10.11646/zootaxa.790.1.1.

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Genus Epikastea Liebke 1936, of the Plochionida Group of Subtribe Agrina, Lebiini, with six species is revised. Subtribe Agrina consists of those species formerly included in the Subtribe Calleidina. The species of Epikastea Liebke 1936 are diagnosed, described, and illustrated. One species occurs in Costa Rica; five are new South American species and are here assigned to this genus. The five new species described are: Epikastea biolat Erwin, n. sp. (PER , MADRE DE DIOS, Rio Manu, BIOLAT Biodiversity Station, Pakitza Guard Station, 356m, 11 56 47 S, 071 17 00 W), Epikastea grace Erwin, n. sp. (PER , LORETO, Samiria River, Camp Manco Capac, 04 43 0 S, 074 18 0 W), Epikastea mancocapac Erwin, n. sp. (PER , LORETO, Samiria River, Camp Manco Capac, 04 43 0 S, 074 18 0 W), Epikastea piranha Erwin, n. sp. (ECUADOR. ORELLANA, Hauorani Territory, Camp Pira a, 0 39' 25.685" S, 76 27' 10.813" W), Epikastea poguei Erwin, n. sp. (PER , MADRE DE DIOS, Rio Manu, BIOLAT Biodiversity Station, Pakitza Guard Station, 356m, 11 56 47 S, 071 17 00 W). A definition of the Plochionida Group and an identification key to the Western Hemisphere genera included are provided. A key to the known species of Epikastea Liebke is given. Distribution data are provided for all species and a map is provided for the Costa Rican taxon. Adults of Epikastea Liebke have been found on rotting logs in rainforests and fogged from the canopy of tropical trees and palms.
3

Yang, Suhang, Jie Liang, Xiaodong Li, Yuru Yi, Ziqian Zhu, Xin Li, Xuwu Chen, Shuai Li, Yeqing Zhai, and Ziming Pei. "The Impacts of Hydrology and Climate on Hydrological Connectivity in a Complex River–Lake Floodplain System Based on High Spatiotemporal Resolution Images." Water 14, no. 12 (June 7, 2022): 1836. http://dx.doi.org/10.3390/w14121836.

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The drivers that determine the hydrological connectivity (HC) are complex and interrelated, and disentangling this complexity will improve the administration of the river–lake interconnection system. Dongting Lake, as a typical river–lake interconnected system, is freely connected with the Yangtze River and their HC plays a major role in keeping the system healthy. Climate, hydrology, and anthropogenic activities are associated with the HC. In this study, hydrological drivers were divided into the total flow of three inlets (T-flow) and the total flow of four tributaries (F-flow). To elucidate the HC of the Dongting Lake, HC was calculated by geostatistical methods in association with Sentinel-2 remote sensing images. Then, the structural equation model (SEM) was used to quantify the impacts of hydrology (F-flow, and T-flow) and meteorology (precipitation, evaporation, and temperature) on HC. The geostatistical analysis results demonstrated that the HC showed apparent seasonal change. For East and West Dongting Lake, the dominant element was north–south hydrological connectivity (N–S HC), and the restricted was west–east hydrological connectivity (W-E HC), but the dominant element was E–W HC and the restricted was N–S HC in South Dongting Lake. The results of SEM showed that N–S HC was mainly explained by T-flow (r = 0.49, p < 0.001) and F-flow (r = 0.28, p < 0.05). T-flow, temperature (r = 0.33, p < 0.05), and F-flow explained E–W HC. The finding of this work supports the management of both the Dongting Lake floodplain and other similar river–lake floodplain systems.
4

Campos, Paula Nepomuceno, Rosildo Santos Paiva, Ana Cristina Teixeira Bonecker, Nuno Filipe Alves Correia de Melo, Glauber David Almeida Palheta, Cristiane Teixeira Contente, and Caio Aguiar Rodrigues Ramos. "First occurrence of Dolicholagus longirostris larvae (Maul 1948) (Osmeriformes, Bathylagidae) near the mouth of the Amazon River." Biota Neotropica 7, no. 1 (2007): 217–19. http://dx.doi.org/10.1590/s1676-06032007000100026.

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The family Bathylagidae contains eight genera and 22 species, of which only five occur in the Southwest Atlantic. Until recently, only adult specimens of the bathylaginin Melanolagus bericoides had been recorded off southern Brazil, between the Santa Marta Cape and Rio Grande (31° S and 49° W). The present work reports the first occurrence of Dolicholagus longirostris larvae on the northern Brazilian coast, expanding its distribution in the Southwest Atlantic. The two specimens found were collected near the mouth of the Amazon River (02° 00' 19" N, 47° 03' 30" W, and 00° 49' 06" N, 46° 25' 09" W).
5

GARRISON, ROSSER W., and NATALIA VON ELLENRIEDER. "New species of the damselfly genus Argia from Mexico, Central America and Ecuador with an emphasis on Costa Rica (Insecta: Odonata: Coenagrionidae)." Zootaxa 4235, no. 1 (February 20, 2017): 1. http://dx.doi.org/10.11646/zootaxa.4235.1.1.

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Seven new species of Argia are described, five of which occur in Costa Rica: Argia calverti n. sp. (Holotype ♂, Costa Rica, Cartago Prov., Tapantí Reserve, 1,310 m, 6 vii 1963, F. G. Thompson leg., in FSCA); Argia carolus n. sp. (Holotype ♂, Costa Rica, San José Prov., El Rodeo Biological Reserve, 7 km W of Villa Colón, 9°54' N, 84°16' W, 561 m, 10–13 vii 1990, T. W. Donnelly leg., in FSCA); Argia elongata n. sp. (Holotype ♂, Costa Rica, Cartago Prov., Reventazón river, SE of Turrialba by highway 10, 9°52'56'' N, 83°38'49'' W, 561 m, 10 viii 1979, R. W. & J. A. Garrison leg., in CSCA); Argia haberi n. sp. (Holotype ♂, Costa Rica, San José Prov., Bosque del Tolomuco, km 118 on Pan American highway, in seeps and trickles through brushy pasture on forested hillside, 9°28'18'' N, 83°41'48'' W, 1,710 m, 27 iii 2006, F. Sibley leg., in FSCA); Argia schorri n. sp. (Holotype ♂, Costa Rica, Puntarenas Prov., 2.8 mi E of Golfito, 8°39' N, 83°7' W, 35 m, 4 vii 1967, O. S. Flint, Jr. & M. A. Ortiz B. leg., in USNM), and two which are so far only known from Mexico and Ecuador respectively: Argia rudolphi n. sp. (Holotype ♂, Mexico, Puebla State, Zihuateutla, Sierra de Huauchinango, La Unión, in drainage area, 20°14'25'' N, 97°53'38'' W, 596 m, 21 v 1987, R. Novelo & A. Gómez leg., in CSCA) and Argia schneideri n. sp. (Holotype ♂, Ecuador, Napo Prov., Las Palmas, on Anzu river in Napo river watershed, 11 xii 1936, W. Clark-MacIntyre leg., in UMMZ). All the new species, as well as closely related species needed for diagnosis including A. anceps Garrison, A. cupraurea Calvert, A. cuprea (Hagen), A. extranea (Hagen), A. fissa Selys, A. fulgida Navás, A. oenea Hagen in Selys, A. popoluca Calvert, A. rhoadsi Calvert, and A. westfalli Garrison, are illustrated and diagnosed from their congeners and their known distribution areas are mapped.
6

Jung, Thomas S., Troy D. Pretzlaw, and David W. Nagorsen. "Northern Range Extension of the Pygmy Shrew, Sorex hoyi, in the Yukon." Canadian Field-Naturalist 121, no. 1 (January 1, 2007): 94. http://dx.doi.org/10.22621/cfn.v121i1.402.

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A Pygmy Shrew, Sorex hoyi, was captured in a pitfall trap on the Blackstone River (65°04.6'N, 138°10.8'W) in central Yukon. This represents a northern range extension of about 110 km for S. hoyi in the Yukon.
7

Miller, J. J., T. W. Curtis, E. Bremer, D. S. Chanasyk, and W. D. Willms. "Evaluation of selected soil properties for indicating cattle activity at off-stream watering and river access sites in southern Alberta." Canadian Journal of Soil Science 93, no. 3 (August 2013): 343–58. http://dx.doi.org/10.4141/cjss2012-074.

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Miller, J. J., Curtis, T. W., Bremer, E., Chanasyk, D. S. and Willms, W. D. 2013. Evaluation of selected soil properties for indicating cattle activity at off-stream watering and river access sites in southern Alberta. Can. J. Soil Sci. 93: 343–358. Off-stream watering troughs may reduce surface water pollution by shifting nutrient distribution from natural watering sites along the river to around artificial water troughs some distance from the river. The objective of our study was to evaluate the suitability of nine soil properties for assessing the impacts of cattle activity adjacent to eight watering sites. Nine surface (0–5 cm) soil properties were evaluated along four 100-m transects at the five off-stream water troughs and three river access sites along the Lower Little Bow River in southern Alberta over 4 yr (2007–2010). The properties included P (total P, soil test P or STP), N (total N, NO3-N, NH4-N), total C, total C:total N ratio (TC:TN), chloride (Cl), and soil bulk density. Soil test P was significantly (P≤0.05) enriched at 65% of site-year comparisons, followed by total C (63%), NO3-N (55%), total P and TC:TN (50%). This suggested that these soil properties were relatively good indicators of cattle activity at the majority (>50%) of watering sites. Chloride was a valid indicator only in non-saline areas (100% of four non-saline sites). Total C and TC:TN ratios were not valid indicators in the calcareous soils at all sites because of possible confounding influence of inorganic C. Overall, we recommend Cl as an indicator of cattle activity at watering sites not affected by soil salinity and high natural Cl levels, and STP as the best overall indicator of cattle activity at off-stream watering sites and river access sites. Certain soil properties were also influenced by distance from watering site, stocking rate, precipitation, and age of water trough.
8

Fettuccia, D. C., V. M. F. da Silva, M. S. Rocha, and P. C. Simões-Lopes. "Sternum and appendicular skeleton: morphometric differences between the species of genus Sotalia (Cetacea: Delphinidae)." Journal of the Marine Biological Association of the United Kingdom 92, no. 8 (August 31, 2012): 1657–62. http://dx.doi.org/10.1017/s0025315412000604.

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Two distinct species have been recently recognized for the genus Sotalia: S. fluviatilis, occurring in the Amazon River basin, and S. guianensis, from Honduras (15°58′N and 85°42′W) to Santa Catarina State (Florianópolis, southern Brazil—27°35′S and 48°34′W). For the first time the sternum and the appendicular skeleton of the two species of the genus Sotalia are compared. A comparative osteological work was performed with marine samples (from the States of Ceará, north-eastern and Santa Catarina, southern regions of Brazil) and riverine samples (Amazonas State) in relation to metric characters (scapula, flipper and sternum). There was a clear distinction of two species in relation to postcranial skeleton in the morphometric analysis (canonical variate analysis) presented. The flipper and the glenoid cavity of the scapula were proportionally wider in the fluvial species. The sternum, however, was smaller in this species in relation to the maximum width of the manubrium. Nevertheless, this structure still needs to be further studied.
9

KANE, R. P. "Inter-annual variability of rainfalls in the Amazon basin and its vicinity." MAUSAM 58, no. 3 (November 26, 2021): 351–60. http://dx.doi.org/10.54302/mausam.v58i3.1330.

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An analysis of the rainfall series (12-month running means) of the 5° × 5° gridded data in the Amazon river basin and its vicinity (15° N – 20° S, 30° - 80° W) indicated that the rainfalls were highly variable both from year to year and from region to region. Correlations with even nearby regions hardly exceeded 0.50, though correlations were better (up to 0.70) in the regions near the eastern coast of Brazil. Moderate relationship with ENSO indices was obtained for the Amazon river basin and the regions to its north, and for NE Brazil, while moderate relationship with South Atlantic SST was obtained for NE Brazil and the region immediately to its west. All other relationships (with 30 hPa wind, North Atlantic Oscillation Index, etc.) were obscure.
10

PECK, STEWART B., and JOYCE COOK. "Systematics, distributions and bionomics of the Catopocerini (eyeless soil fungivore beetles) of North America (Coleoptera: Leiodidae: Catopocerinae)." Zootaxa 3077, no. 1 (October 28, 2011): 1. http://dx.doi.org/10.11646/zootaxa.3077.1.1.

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This paper is a review and revision of the tribe Catopocerini (Coleoptera: Leoididae: Catopocerinae) of North America. It covers the following genera: Catopocerus Motschulsky, 1870 with five species east of the Mississippi River and the resurrected genus Pinodytes Horn, 1880 with 42 species in North America west of the Mississippi River. All species in the tribe are eyeless and wingless inhabitants of forest soil and litter. Larvae and adults probably feed on subterranean fungi. Pinodytes Horn is resurrected to valid generic status. A neotype is assigned for Catopocerus politus Motschulsky. Lectotypes are designated for Catops cryptophagoides (Mannerheim, 1852) (which is transferred to Pinodytes), and Pinodytes pusio Horn, 1892. The following new synonym is recognized: Catopocerus ulkei Brown, 1933 = Catopocerus politus Motschulsky, 1870. The 33 new species and their distributions are as follows: Pinodytes angulatus (NW Oregon, USA), P. borealis (central Alaska, USA), P. chandleri (N California, USA), P. colorado (Colorado, USA), P. constrictus (S California, USA), P. contortus (E California, USA), P. delnorte (NW California, USA), P. eldorado (E California, USA), P. fresno (central California, USA), P. garibaldi (NW Oregon, USA), P. gibbosus (S California, USA), P. haidagwaii (Haida Gwaii (formerly Queen Charlotte) Islands, British Columbia, Canada), P. humboldtensis (NW California, USA), P. idaho (NW Idaho, USA), P. isabella (N Idaho, USA), P. klamathensis (SW Oregon and NW California, USA), P. losangeles (S California, USA), P. marinensis (W California, USA), P. minutus (central California, USA), P. monterey ( SW California, USA), P. newtoni (Ozarks region to E Texas, USA), P. orca (SW Oregon, USA), P. parvus (NW California, USA), P. punctatus (W Idaho and E Washington, USA), P. sanjacinto (S California, USA), P. sequoia ( S central California, USA), P. setosus ( SW Oregon and NW California, USA), P. shasta (N California, USA), P. shoshone (N Idaho, USA), P. sinuatus (SW Oregon, USA), P. spinus (N central California, USA), P. tehama (N California, USA), and P. tuolumne (E central California, USA). The following new combinations are established: Pinodytes capizzii (Hatch, 1957), ex Catopocerus; P. cryptophagoides (Mannerheim, 1852), ex Catopocerus; P. imbricatus (Hatch, 1957), ex Catopocerus; P. newelli (Hatch, 1957), ex Catopocerus; P. ovatus (Hatch, 1957), ex Catopocerus; P. pusio Horn, 1892, ex Catopocerus; P. rothi (Hatch, 1957), ex Catopocerus; P. subterraneus (Hatch, 1935), ex Catopocerus; P. tibialis (Hatch, 1957), ex Catopocerus.
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Journal articles

Book chapters on the topic "Lachlan River (N.S.W.)":

1

James, Simon. "What and Where? Revised Overview of Base Extent." In The Roman Military Base at Dura-Europos, Syria. Oxford University Press, 2019. http://dx.doi.org/10.1093/oso/9780198743569.003.0025.

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Archaeological evidence indicates that, during the final halfcentury of the life of the city, the area directly annexed by the military was significantly larger than the original excavators realized. In addition to concentrations of soldiers around the gates and defences, and at various places within the ‘civil’ town, the military came to control a single continuous swathe of the urban interior, comprising the entire N part of the walled area from the W defences to the river cliffs, and extending as far as the S end of the Citadel, plus the floor of the inner wadi right down to Lower Main St opposite the (by Durene standards) showy C3 bath, which it also apparently built. This area totals c.13.5 ha (c.33 acres)—a literal quarter of the intramural area which today covers c.52 ha (c.118 acres, measured from the CAD plan of the city by Dan Stewart; both city and base were slightly bigger in antiquity, before loss of the River Gate and parts of the Citadel). In its final form, the base included several distinct zones (Pl. XXIII). The NW part of the city had become a military enclosure, bounded on the E side by a continuous wall down the W side of G St, incorporating the street facades of the E3 bath and E4 house. On the S it was defined by the ‘camp wall’ from the city defences to D St; with no sign of a wall across blocks F5 or F7, the perimeter between D and F Sts is inferred. It must be presumed that, as to the W, the 8th-St-fronting properties of the two blocks were taken over, but that the party walls comprising the boundary with civil housing to the S was not further elaborated. These lines converged on the amphitheatre, which formed the corner of the enclosure. This perimeter of the NW enclosure involved physically blocking Wall, A, C, D, and 10th Sts. A major entrance was on 8th St, at G St between the amphitheatre and the E4 house.
2

James, Simon. "The Plateau Zone East of G St." In The Roman Military Base at Dura-Europos, Syria. Oxford University Press, 2019. http://dx.doi.org/10.1093/oso/9780198743569.003.0020.

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The N end of the city’s plateau zone E of G St, bounded by the N wadi, the river cliff, and the head of the inner wadi, comprising the remotest corner within the walls, also became part of the Roman military quarter. Here, as across the whole N part of the city, the stratigraphy is shallow, rarely deeper than a metre, with bedrock showing in places. Surface indications and magnetometry suggest that much of the region had been built up in pre-Roman times, although there may have been areas of open ground. The street grid had been substantially laid out here, especially H St which ran to the N city wall, but E of this line it seems partly to break down. In particular, in the nominal areas of projected block positions X1–X8, 10th St actually curved off-grid to the S, probably preserving the line of an early approach road to the N end of the Citadel before the stronghold was separated from the plateau by a great quarry and rebuilt. This far N region was presumably mostly residential before AD 165, except for two known sanctuaries beside H St: the so-called Dolicheneum in X7, and a temple of unknown dedication in X9. Under Roman rule it became dominated by insertion of the massive residence known as the ‘Palace of the dux ripae’, here referred to as the Roman Palace. Closures of both G and I Sts on the N side of 10th St, by the building of Roman structures across them, indicates that the zone N of this line became a military enclosure. This was accessible from the civil town only via an entrance on H St, and from the W part of the base area on the plateau, already enclosed by a boundary along the W side of G St, via a smaller entrance on the diverted line of ‘12th St’ at the N-most point of block E3. Within the re-entrant to the continuous base perimeter created by the G St and 10th St lines, more blocks appear to have been taken over by the military.
3

James, Simon. "How Did the Base Work?" In The Roman Military Base at Dura-Europos, Syria. Oxford University Press, 2019. http://dx.doi.org/10.1093/oso/9780198743569.003.0028.

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We now consider how the military base area operated, as a zone where a large number of people lived and worked on a routine basis. On one hand, to function it required the affordances of its internal communications, connections with the civil town, and access to roads, river, and lands beyond the walls; on the other, there was a need for surveillance and control of activities within the base, and of movements across its boundary. The most obvious part of the base boundary (Plate XXII) is the substantial mud brick wall ploughed across four blocks from the city defences just S of Tower 21, and blocking Wall, A, C, and D Sts, with a gate established at B St. How the S boundary was defined E of D St has always remained an issue. If it was necessary to build a wall at the W end, why was this not simply continued all the way to, e.g., the S end of the Citadel? Across blocks F7 and F5 it seems that the boundary of the military zone simply comprised party walls between military and civilian-occupied structures. The same was true within block B2, by the Citadel, although the boundary probably comprised building frontages along Lower Main St. On the plateau, as the camp wall may have been a subsequent local enhancement, except where the amphitheatre formed part of it, the boundary may generally have comprised the rear walls of military-held houses lining the S side of 8th St—probably all properties from the city wall to H St. The course of the boundary along the W side of the inner wadi is unknown, but the base is suggested, as along 8th St, to have incorporated at least all properties lining the S side of the Wadi Ascent Road, if not encompassing all blocks on the wadi slope—in which case the boundary here may rather have comprised property frontages on K St. The base area was split by site topography into two major zones, the flat plateau, and the N branch of the inner wadi around the Citadel. Each was further subdivided.
4

James, Simon. "The Wadi Zone Campus, Citadel, and C3 Bath." In The Roman Military Base at Dura-Europos, Syria. Oxford University Press, 2019. http://dx.doi.org/10.1093/oso/9780198743569.003.0021.

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From the junction of H and 8th Sts, which gave access to the twin main axes of the military base zone on the plateau, H St led S to the bulk of the civil town and ultimately to the Palmyrene Gate, the steppe plateau W of the city, and the roads W to Palmyra and NW up the Euphrates to Syria. The fourth side of the crossroads followed a curving course SE, down into the inner wadi, then snaking through the irregularly laid-out old lower town to the now-lost River Gate, portal to the Euphrates and its plain. Of most immediate significance is that the Wadi Ascent Road also linked the plateau military zone with what can now be seen as another major area of military control, in the old Citadel, and on the adjacent wadi floor. The N part of the wadi floor is now known to have accommodated two military-built temples, the larger of which, the A1 ‘Temple of the Roman Archers’, was axial to the long wadi floor, which in the Roman period appears to have comprised one of the largest areas of open ground inside the city walls. This is interpreted as the campus, or military assembly and training ground, extension of which was commemorated in an inscription found in the temple. In 2011, what is virtually certainly a second military temple was found in the wadi close by the first, built against the foundation of the Citadel. This is here referred to as the Military Zeus Temple. Behind the Temple of the Roman Archers was a lane leading from the Wadi Ascent Road to the N gate of the Citadel. It helped define a further de facto enclosure, effectively surrounded by other military-controlled areas and so also presumed to have been in military hands. The Citadel itself, while in Roman times already ruinous on the river side due to cliff falls, still formed part of the defences. Moreover the massive shell of its Hellenistic walls now also appears to have been adapted to yet more military accommodation, some of it two storeys or higher.
5

Brunini, Orivaldo, and Alice M. Grimm. "Agricultural Drought Phenomenon in Latin America with Focus on Brazil." In Monitoring and Predicting Agricultural Drought. Oxford University Press, 2005. http://dx.doi.org/10.1093/oso/9780195162349.003.0020.

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Abstract:
Latin America encompasses a vast territory between 12°30'N and 55°30'S latitude and between 29°W and 82°W longitude. This subcontinent has 13 countries with complex climatic conditions. Extremely humid weather is typical closer to the equator, while semiarid, arid, and desertic conditions prevail in the Bolivian and Chilean high plains. The wide variation in climatic conditions leads to distinct agricultural conditions across Latin America. For example, forests, equatorial fruits, and perennial vegetation exist throughout the Amazonian region. Farther from the equator, toward the Andes and at higher latitudes, there is a noticeable change in agricultural systems. There is a greater emphasis on growing cereal/grain crops in Argentina and Brazil. The countries that compose the Amazon River basin experience a higher amount of annual precipitation, and drought is not a characteristic phenomenon there, except during high-intensity El Niño years (Marengo et al., 2001). In contrast, drought is a regular event commonly observed in parts of Peru, Chile, Paraguay, Argentina (Scian and Donnari, 1996), Uruguay, and Brazil. The Atacama Desert in Chile is one of the most arid regions on the earth, where the average annual precipitation is as low as 0.8 mm in Arika or even 0.5 mm in other regions of this desert. Figure 12.2 provides a more detailed description on climatic conditions of Brazil. Although the average annual precipitation in the northeastern region is less than 300 mm, it exceeds 2500 mm in some other regions of Brazil (Grimm, 2003). Agricultural operations take place during the rainy season (March–October). The northeast region is drought prone, but the central, west, and southeast regions are traditionally grain-producing regions. In the northeast and central-west regions, water deficiency is higher, which seriously affects food production. Table 12.1 shows production losses in Brazil due to climate anomalies including droughts that occurred during 1978–1986 (Mota, 1979) and 1991–1994 (Rossetti, 2001). About 33% (about 50% in the northeast region) of these losses were attributed to droughts. Maize production also significantly declined due to drought that occurred during 1990–91, 1993–94, 1996–97, and 1997–98.
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