mound growth
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2017 ◽  
Vol 87 (2) ◽  
pp. 227-245 ◽  
Author(s):  
Jill Onken ◽  
Susan J. Smith ◽  
Manuel R. Palacios-Fest ◽  
Karen R. Adams

AbstractA late Holocene carbonate spring mound and associated wetland deposits at Cienega Amarilla, New Mexico, contain a 4000-yr record of geomorphic, paleoenvironmental, and hydroclimatic change on the southern Colorado Plateau. Forty-four14C dates support a century-scale chronostratigraphic framework. Pollen, plant macrofossil, mollusk, ostracode, and soil analyses indicate rapid spring mound growth and wetland expansion beginning ~2300 cal yr BP, followed by a pronounced decline in groundwater discharge (GWD) between ~1500 and 1000 cal yr BP. The isotopic composition of Cienega Amarilla springwater suggests GWD is driven primarily by winter precipitation. Historical climate data indicate that El Niño and warm Pacific Decadal Oscillation (PDO) conditions foster wetter-than-average winters in the Cienega Amarilla area, whereas dry winters are associated with La Niña conditions regardless of PDO phase. The ~2300–1500 cal yr BP Cienega Amarilla pluvial appears to represent an interval of peak, late Holocene cool-season precipitation that implies unusually strong or persistent El Niño–like and warm PDO–like conditions in the Pacific. Other southwestern paleoenvironmental records corroborate atypically wet conditions during this interval, and pluvial conditions related to increased winter precipitation likely fostered significant prehistoric cultural changes throughout the region, including increased sedentism, population, and dependence on agriculture.


2008 ◽  
Vol 68 (3) ◽  
pp. 529-533 ◽  
Author(s):  
MLT. Buschini ◽  
MAP. Abuabara ◽  
Miguel Petrere-Jr

In this research we proposed two mathematical models for Isoptera mound growth derived from the Von Bertalanffy growth curve, one appropriated for Nasutitermes coxipoensis, and a more general formulation. The mean height and the mean diameter of ten small colonies were measured each month for twelve months, from April, 1995 to April, 1996. Through these data, the monthly volumes were calculated for each of them. Then the growth in height and in volume was estimated and the models proposed.


2006 ◽  
Vol 74 (24) ◽  
Author(s):  
Serkan Zorba ◽  
Yonathan Shapir ◽  
Yongli Gao
Keyword(s):  

2002 ◽  
Vol 52 (3) ◽  
pp. 271-323 ◽  
Author(s):  
J. Ross Mackay

Abstract Growth data from precise surveys have been obtained for 11 pingos for periods ranging from 20 to 26 years. Most of the 1350 pingos, perhaps one quarter of the world's total, have grown up in the bottoms of drained lakes underlain by sands. Permafrost aggradation on the drained lake bottoms has resulted in pore water expulsion, solute rejection below the freezing front, a freezing point depression, and groundwater flow at below 0° C to one or more residual ponds, the sites of pingo growth. Sub-pingo water lenses underlie many growing pingos.The pure ice which grows by downward freezing in a sub-pingo water lens may be composed of seasonal growth bands which, like tree rings, are of potential use in the study of past climates. Growing pingos underlain by sub-pingo water lenses can often be identified by features such as peripheral pingo rupture, spring flow, frost mound growth, normal faulting, and oscillations in pingo height. Such features, and others, are associated with hydrofracturing and water loss from a sub-pingo water lens. Some of the data derived from the long-term study of pingo growth are relevant to the identification of collapse features, interpreted as paleo pingos, in areas now without permafrost.


2001 ◽  
Vol 482-485 ◽  
pp. 935-939 ◽  
Author(s):  
M. Aguilar ◽  
E. Anguiano ◽  
J.A. Aznárez ◽  
J.L. Sacedón

1997 ◽  
Vol 13 (1) ◽  
pp. 115-124 ◽  
Author(s):  
Tetsushi Inoue ◽  
Pisoot Vijarnsorn ◽  
Takuya Abe

ABSTRACTThe change of mound structure of the fungus growing termite, Macrotermes gilvus, which has no clear air passage system in the mound, was examined in relation to the mound growth in a rubber plantation of southern Thailand. The nest proper consisted of the hive with a royal chamber and nursery, and diffused chambers with fungus combs. The location of the hive became higher with the growth of the mound. Therefore, colonies with a very large mound utilize only the upper mound part and this may be due to the lack of air passage systems in this species. A colony with a very large mound is not in reality commensurately large in colony size and this may be the reason why the density of huge mounds of M. gilvus in Thailand is much higher than that of Macrotermes in Africa.


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