scholarly journals DYNAMICS AND PREDICTION OF DIAMETRIC STRUCTURE IN TWO ATLANTIC FOREST FRAGMENTS IN NORTHEASTERN BRAZIL

2016 ◽  
Vol 40 (2) ◽  
pp. 307-317 ◽  
Author(s):  
Anderson Pedro Bernardina Batista ◽  
Maria Jesus Nogueira Rodal ◽  
José Antonio Aleixo da Silva ◽  
Ana Carolina Borges Lins e Silva ◽  
Francisco Tarcisio Alves Junior ◽  
...  

ABSTRACT Monitoring analyses aim to understand the processes that drive changes in forest structure and, along with prediction studies, may assist in the management planning and conservation of forest remnants. The objective of this study was to analyze the forest dynamics in two Atlantic rainforest fragments in Pernambuco, Brazil, and to predict their future forest diameter structure using the Markov chain model. We used continuous forest inventory data from three surveys in two forest fragments of 87 ha (F1) and 388 ha (F2). We calculated the annual rates of mortality and recruitment, the mean annual increment, and the basal area for each of the 3-year periods. Data from the first and second surveys were used to project the third inventory measurements, which were compared to the observed values in the permanent plots using chi-squared tests (a = 0.05). In F1, a decrease in the number of individuals was observed due to mortality rates being higher than recruitment rates; however, there was an increase in the basal area. In this fragment, the fit to the Markov model was adequate. In F2, there was an increase in both the basal area and the number of individuals during the 6-year period due to the recruitment rate exceeding the mortality rate. For this fragment, the fit of the model was unacceptable. Hence, for the studied fragments, the demographic rates influenced the stem density more than the floristic composition. Yet, even with these intense dynamics, both fragments showed active growth.

2017 ◽  
Vol 47 (8) ◽  
pp. 1066-1074 ◽  
Author(s):  
L.C. Melo ◽  
R. Schneider ◽  
R. Manso ◽  
J.-P. Saucier ◽  
M. Fortin

Survival analysis methods make better use of temporal information, accommodate multiple levels of explanatory variables, and are meant to deal with interval-censored data. In a context of harvest modeling, this approach could improve some known limitations. In this study, we used data from a network of permanent plots in the province of Quebec, Canada, as a real-world case study. We tested the potential of survival analysis to predict plot-level harvest probabilities from plot- and regional-level variables. The approach also included random effects to account for spatial correlations. The results showed the potential of survival analysis to provide annual predictions of harvest occurrence. Both regional and time-varying variables, as well as spatial patterns, had important effects on the probability of a plot to be harvested. Respectively, reductions in the annual allowable cut volumes led to a decrease in the harvest probabilities. Greater harvest probabilities were associated with the broadleaved dynamics class and higher values of basal area. In contrast, they were decreased by stem density and slope classes. The spatial random effect resulted in an improvement of the model fit. Our plot-level model improved some limitations reported in previous studies by taking the effect of a time-varying regional variable into account.


2017 ◽  
Vol 33 (4) ◽  
pp. 241-248 ◽  
Author(s):  
Sergio Javier Ceballos ◽  
Agustina Malizia

Abstract:Changes in density and basal area of lianas ≥2 cm diameter were monitored in two 1-ha permanent plots in a subtropical montane mature forest of north-western Argentina. Liana stems were identified and measured at 130 cm from the main rooting point in two censuses conducted in 2003 and 2015. Between censuses, the density of liana stems decreased 13.3%, while basal area increased 11.5%. Density and basal area decreased mainly among lianas of 2–3 cm diameter, but increased in lianas ≥4 cm diameter. Quechualia fulta (Asteraceae), Serjania meridionalis (Sapindaceae) and Chamissoa altissima (Amaranthaceae) suffered large reductions in stem density and basal area. Dissimilar responses of density and basal area of lianas might be a consequence of the suppression of anthropogenic disturbances (e.g. livestock browsing) and the decrease of treefall gap frequency in the studied forest in recent decades. Light-demanding liana species decreased and shade-tolerant species increased possibly in response to the decline in the light availability associated with forest recovery from past disturbance. Lianas increased in basal area to a lesser extent compared with reports from several tropical and subtropical forests where lianas are increasing dramatically.


2007 ◽  
Vol 37 (3) ◽  
pp. 598-606 ◽  
Author(s):  
Koichi Takahashi ◽  
Ken Arii ◽  
Martin J. Lechowicz

Comparing permanent plots censused in 1997 and again in 2005, we quantified the impact of a severe ice storm on forest composition and dynamics in an old-growth beech–maple forest in eastern Canada. Acer saccharum Marsh. and Fagus grandifolia Ehrh. accounted for 78% of stand basal area immediately before the January 1998 ice storm. By 2005, eight growing seasons after the ice storm, stand basal area had dropped from 49.1 m2/ha to 31.5 m2/ha, and total tree density (>1 cm diameter at breast height (DBH)) decreased from 6350 stems/ha to 3875 stems/ha. However, A. saccharum and F. grandifolia remained dominant, accounting for 74% of stand basal area. Detrended correspondence analysis of relative dominance ratios at each plot in 1997 and 2005 showed that community composition did not change much during this period for either understory (1 cm ≤ DBH < 10 cm) or canopy trees (DBH ≥ 10 cm). The ice storm did not lead to significant recruitment of saplings (DBH ≥ 1 cm), but appears to have only contributed more to the growth of already-established saplings. We conclude that the ice storm of 1998 substantially decreased stand basal area and stem density but did not act to change the overall species composition or tree diversity in this old-growth beech–maple forest.


2004 ◽  
Vol 68 (2) ◽  
pp. 346 ◽  
Author(s):  
Keijan Wu ◽  
Naoise Nunan ◽  
John W. Crawford ◽  
Iain M. Young ◽  
Karl Ritz

Author(s):  
R. Jamuna

CpG islands (CGIs) play a vital role in genome analysis as genomic markers.  Identification of the CpG pair has contributed not only to the prediction of promoters but also to the understanding of the epigenetic causes of cancer. In the human genome [1] wherever the dinucleotides CG occurs the C nucleotide (cytosine) undergoes chemical modifications. There is a relatively high probability of this modification that mutates C into a T. For biologically important reasons the mutation modification process is suppressed in short stretches of the genome, such as ‘start’ regions. In these regions [2] predominant CpG dinucleotides are found than elsewhere. Such regions are called CpG islands. DNA methylation is an effective means by which gene expression is silenced. In normal cells, DNA methylation functions to prevent the expression of imprinted and inactive X chromosome genes. In cancerous cells, DNA methylation inactivates tumor-suppressor genes, as well as DNA repair genes, can disrupt cell-cycle regulation. The most current methods for identifying CGIs suffered from various limitations and involved a lot of human interventions. This paper gives an easy searching technique with data mining of Markov Chain in genes. Markov chain model has been applied to study the probability of occurrence of C-G pair in the given   gene sequence. Maximum Likelihood estimators for the transition probabilities for each model and analgously for the  model has been developed and log odds ratio that is calculated estimates the presence or absence of CpG is lands in the given gene which brings in many  facts for the cancer detection in human genome.


1970 ◽  
Vol 20 ◽  
Author(s):  
R. Goossens

Contribution to the automation of the calculations involving  the forest inventory with the aid of an office computer - In this contribution an attempt was made to perform the  calculations involving the forest inventory by means of an office computer  Olivetti P203.     The general program (flowchart 1), identical for all tree species except  for the values of the different parameters, occupies the tracks A and B of a  magnetic card used with this computer. For each tree species one magnetic  card is required, while some supplementary cards are used for the  subroutines. The first subroutine (flowchart 1) enables us to preserve  temporarily the subtotals between two tree species (mixed stands) and so  called special or stand cards (SC). After the last tree species the totals  per ha are calculated and printed on the former, the average trees occuring  on the line below. Appendix 1 gives an example of a similar form resulting  from calculations involving a sampling in a mixed stand consisting of Oak  (code 11), Red oak (code 12), Japanese larch (code 24) and Beech (code 13).  On this form we find from the left to the right: the diameter class (m), the  number of trees per ha, the basal area (m2/ha), the current annual increment  of the basal area (m2/year/ha), current annual volume increment (m3/year/ha),  the volume (m3/ha) and the money value of the standing trees (Bfr/ha). On the  line before the last, the totals of the quantities mentioned above and of all  the tree species together are to be found. The last line gives a survey of  the average values dg, g, ig, ig, v and w.     Besides this form each stand or plot has a so-called 'stand card SC' on  wich the totals cited above as well as the area of the stand or the plot and  its code are stored. Similar 'stand card' may replace in many cases  completely the classical index cards; moreover they have the advantage that  the data can be entered directly into the computer so that further  calculations, classifications or tabling can be carried out by means of an  appropriate program or subroutine. The subroutine 2 (flowchart 2) illustrates  the use of similar cards for a series of stands or eventually a complete  forest, the real values of the different quantities above are calculated and  tabled (taking into account the area). At the same time the general totals  and the general mean values per ha, as well as the average trees are  calculated and printed. Appendix 2 represents a form resulting from such  calculations by means of subroutine 2.


2020 ◽  
Vol 11 (1) ◽  
pp. 317
Author(s):  
Taewon Song ◽  
Taeyoon Kim

The representative media access control (MAC) mechanism of IEEE 802.11 is a distributed coordination function (DCF), which operates based on carrier-sense multiple access with collision avoidance (CSMA/CA) with binary exponential backoff. The next amendment of IEEE 802.11 being developed for future Wi-Fi by the task group-be is called IEEE 802.11be, where the multi-link operation is mainly discussed when it comes to MAC layer operation. The multi-link operation discussed in IEEE 802.11be allows multi-link devices to establish multiple links and operate them simultaneously. Since the medium access on a link may affect the other links, and the conventional MAC mechanism has just taken account of a single link, the DCF should be used after careful consideration for multi-link operation. In this paper, we summarize the DCFs being reviewed to support the multi-radio multi-link operation in IEEE 802.11be and analyze their performance using the Markov chain model. Throughout the extensive performance evaluation, we summarize each MAC protocol’s pros and cons and discuss essential findings of the candidate MAC protocols.


Author(s):  
Pavlos Kolias ◽  
Nikolaos Stavropoulos ◽  
Alexandra Papadopoulou ◽  
Theodoros Kostakidis

Coaches in basketball often need to know how specific rotation line-ups perform in either offense or defense and choose the most efficient formation, according to their specific needs. In this research, a sample of 1131 ball possession phases of Greek Basket League was utilized, in order to estimate the offensive and defensive performance of each formation. Offensive and defensive ratings for each formation were calculated as a function of points scored or received, respectively, over possessions, where possessions were estimated using a multiple regression model. Furthermore, a Markov chain model was implemented to estimate the probabilities of the associated formation’s performance in the long run. The model could allow us to distinguish between overperforming and underperforming formations and revealed the probabilities over the evolution of the game, for each formation to be in a specific rating category. The results indicated that the most dominant formation, in terms of offense, is Point Guard-Point Guard-Small Forward-Power Forward-Center, while defensively schema Point Guard-Shooting Guard-Small Forward-Center-Center had the highest rating. Such results provide information, which could operate as a supplementary tool for the coach’s decisions, related to which rotation line-up patterns are mostly suitable during a basketball game.


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