3 groups of sites and their total densities

## 1. Introduction

The climate fluctuates and changes naturally, and adding the common problems of land transformation and deforestation, its impact can be very harsh on the natural environment, and cause a decline in the biodiversity of plants and animals. * Aloe dichotoma*, common name Quiver tree, is an important part of the arid regions, such as Namaqualand and Bushmanland in South Africa, and in arid parts of southern Namibia. This succulent tree species occurs in rocky areas, and it can grow quite rapidly under the right conditions. Succulents are able to survive long periods of drought conditions, due to the fact succulent plants has special water-storing tissue which makes part of the plant fleshy, and the Quiver tree has succulent leaf and stem (Van Wyk and Smith, 1996).

The Quiver tree has a 200 year life span, and can grow up to 9 meters tall, and it occurs in summer and winter rainfall regions, and can live under a variety of climatic conditions (Fig. 1). The Quiver tree is important to the ecosystem due to the fact that it is as a source of moisture for a wide variety of mammals, birds, and insects. Foden’s detailed study of the demographic data of the Quiver trees show that negligible recruitment has occurred in certain populations for 50 years, and the effects of non-climatic variables, such as herbivory, competition, seed availability, fungal pathogens, plant collection... are very small (Foden, 2002).

Today, the Quiver trees are threatened by agricultural expansion, overgrazing, and mining, as well as droughts and other climate changes (Foden, 2002). Climate changes is one of the major factors affecting the existence of Quiver trees, while the Quiver tree will unlikely to be affected by small climatic fluctuations, but will be affected larger or long term climatic changes. The Quiver tree can potentially provide a good indication of long term climate changes in the arid regions (Foden, 2002).

Previous onsite observations show that Quiver trees are very sensitive to temperature changes, and does not do well under extreme hot and dry conditions. Observations has also shown that the Quiver trees might be responding to higher temperatures by shifting its distribution range towards higher and higher altitudes, showing a preference for slightly cooler regions (Midgley et al., 2009).

To have a complete picture of the Quiver tree’s response to recent climatic changes, samples of Quiver trees were collected from their distributional range in arid Namibia and South Africa, and this is a continuing project funded by the South African National Biodiversity Institute. However, data uncertainty accompanied the sample collections as well.

In 2001 and 2002, Wendy Foden and various assistants collected Quiver trees sample data across the whole range, sampling 53 sites in detail. In 2008 Graeme Ellis re-sampled a subset of the population, sampling 41 sites. In 2009, Res Altwegg and Cory Merow did a thorough analysis and comparison of between the 2 sets of data, for 35 sites, excluding certain sites due to lack of data for comparisons.

In this chapter, we are going one step further, that is, to try to complete all the missing data values, which will allow us to do a more complete comparison. The incomplete data issue is complicated on many fronts:

While the 2001-2002 data are the most complete, however, there are several sites with missing variables from the 53 sample sites.

The 2008 data is a subset of the original 2001-2002 data, covering 41 sites, and the 2008 data variables are not the same as the 2001-2002 data variables.

The 2009 analysed data comparison between 2001-2002 and 2008 data is for 35 sites, with 18 sites uncalculated due to missing data.

With all 3 datasets, missing data is a major part of the problem, which renders the 3 datasets incomplete and only partially comparable.

Of course, another sample collection study would be ideal, but to due lack of funding and trained professionals, this is not possible at this stage. In any case, a full usage should be made of the 2002 and 2008 data. In Fig. 2, the Quiver trees sample sites are shown, the Quiver tree’s distribution extending over the arid regions in Namibia and South Africa. As one can see from the figure, the 2008 study is a subset of the original 2002 samples.

## 2. Impreciseness in quiver tree‘s sample data

To investigate the climate change impacts on the Quiver’s spatial distribution from 2002 to 2008, we must have the Quiver‘s population evolution information. We as biodiversity scientists need to reveal the climate change impacts on plant species based on the data collected. Only solid data-oriented analysis can provide near-true information to the public and governmental decision-making body. In this case, the Quiver tree’s dataset is not complete enough to perform a solid data-oriented analysis because of the impreciseness features of the dataset.

Impreciseness is a fundamental and intrinsic feature in a solid data oriented spatial modelling exercises due to the observational data shortage and incompleteness. Facing the impreciseness reality the spatial statisticians often rely on expert's knowledge to compensate the inadequacy and in accuracy in collected observational data. Nevertheless, such a dependence on experts' knowledge engineering will still open a backdoor to pseudo-scientific believe or claim.

Impreciseness is referred to a term with an intrinsic property governed by an uncertain measure or an uncertainty distribution for each of the actual or hypothetical members of an uncertainty population (i.e., collection of expert's knowledge). An uncertainty process is a repeating process whose outcomes follow no describable deterministic pattern, but follow an uncertainty distribution, such that the uncertain measure of the occurrence of each outcome can be only approximated or calculated.

Definition 2.1: Impreciseness is an intrinsic property of a variable or an expert's knowledge being specified by an uncertainty measure.

In geo-statistics analyst communities it is seldom to mention uncertainty measure. It is true, spatial researchers are used to the term "uncertainty", which represents randomness in their eyes. Actually, this perception is wrong. Researchers have long realized the there are many forms of uncertainty, randomness is merely a member of uncertainty family. How can we differentiate different forms of uncertainty? The answer is fairly straght forward: the appropriate measure specifies a particular form of uncertainty. For example, probability measure specifies random uncertainty.

The uncertainty modelling without a measure specification will not have an rigorous mathematical foundations and consequently the modelling exercise is baseless and blindness. In other words, measure specification is the prerequisite to spatial data collection and analysis. For example, without Kolmogrov's (1950) three axioms of probability measure, randomness is not defined and thus statistical data analysis and inference has no foundation at all.

Notice that imprecise probability theory is a potential remedy to address the observational data inaccuracy and inadequacy because most the geo-statistics analysts are familiar with probability theory. However the imprecise probability based spatial modelling might be not feasible. Just as Utikin and Gurov (2000) has commented, “the probabilistic uncertainty model makes sense if the following three premises are satisfied: (i) an event is defined precisely; (ii) a large amount of statistical samples is available; (iii) probabilistic repetitiveness is embedded in the collected samples. This implies that the probabilistic assumption may be unreasonable in a wide scope of cases.”

It is therefore inevitably to seek another form of uncertainty theory to meet the impreciseness challenges. In the theoretical basket, interval uncertainty theory (Moore, 1966), fuzzy theory (Zadeh, 1965, 1978), grey theory (Deng, 1984), rough set theory (1982), upper and lower provisions or expectations (Walley, 1991), or Liu’s uncertainty theory (2007, 2010) may be chosen. Nevertheless, Liu’s (2007, 2010) uncertainty theory is the only one built on an axiomatic uncertain measure foundation and fully justified with mathematical rigor. Therefore it is logical to engage Liu’s (2007, 2010) uncertainty theory for guiding us to understand the intrinsic character of imprecise uncertainty and facilitate an accurate mathematical definition of impreciseness in order to establish the foundations for uncertainty spatial modelling under imprecise uncertainty environments.

## 3. Uncertain measure foundation

The Uncertainty Theory was founded by Liu in 2007 and refined in 2010 (Liu, 2007, 2010). Nowadays uncertainty theory has become a branch of mathematics.

A key concept in uncertainty theory is the uncertain measure: Let

Axiom 1: (Normality)

Axiom 2: (Self-Duality)

Axiom 3: (

Definition 3.1: (Liu, 2007, 2010) A set function * Axioms 1-4*is called an uncertain measure. The triple

Definition 3.2: (Liu, 2007, 2010) An uncertain variable is a measurable function ξ from an uncertainty space

Definition 3.3: (Liu, 2010) Let

Theorem 3.4: (Liu, 2007, 2010) Let

for any real numbers

Definition 3.5: (Liu, 2007, 2010) Let

provided that one of the two integrals exists at least.

Definition 3.6: (Liu, 2007, 2010) Let

Liu's uncertainty theory (Liu, 2007, 2010) does not define multivariate uncertainty distribution, (Guo, 2010; Guo et al., 2007), except for the independent uncertainty variables. Hence it is necessary to facilitate a framework for showing the preparation to define the uncertain covariance.

LetDefinition 3.7: Let

Definition 3.8: Let

Theorem 3.9: Let

Remark 3.10: Different from independent random variables

Remark 3.11: The formation of uncertain variance-covariance does touch the detailed functional form of multivariate uncertainty joint distribution. For practical applications, the form of multivariate uncertainty joint distribution is not necessarily available, but the paired uncertainty bivariate distribution must be given.

Similar to the concept of stochastic process in probability theory, an uncertain process

(3) every increment

then

Theorem 3.13: Assuming that

where

## 4. Habitat measure

Note that the Quiver tree’s 2002 data subset contains percentage of dead trees, percentage of juvenile trees, the total density of trees, and the average age of dead trees. Also, Quiver tree‘s 2008 data subset contains population growth rate, survival reproductives, survival non-reproductives, and proportion juvenile. Considering the aim of this research: climate change impacts on the Quiver tree’s population, we select total density of tree (in 2002 data subset) and population growth rate (in 2008 data subset) as the our analysis data. We will build our model based on the total tree population size

where the

Notice that among 53 sites, 43 sites have total density observational values. Ten sites have missing values. That is, without total density observation {10,12,14,15,17,19,33,36,37,128} site number set.

For inexperienced go-statistics analysts, kriging method might be a choice for filling the ten missing vaules. Nevertheless, after examining the 2002 total density of tree‘s 43 observations, we found that geometric distance does not play a role in dertermining the value of the total density of trees. we can find out that the total density observations are not similar even for the very nearby sites geometrically within the same ecological sub-region. For example, Site, see Table 1.

From Table 1, it is obvious that for the Quiver tree‘s growth status,

The Quiver tree‘s growth status observations reveal a fact that the total density status is extremely sensitive to the ecological conditions of individual site area (or the area habitat). The graphical location and the isotropic distance will not offer much information, rather the Quiver tree‘s growth observation

Group/ site no. | Coordinates | Total density of trees | Geometric distance | Difference in total density | Density/ distance | ||

longitude | latitude | ||||||

1 | 40 | 21.64455 | -30.00486 | 36.41 | 1.1977228 | 65.42 | 54.62 |

42 | 22.83446 | -29.86828 | 101.83 | ||||

2 | 101 | 18.20583 | -30.15250 | 70.00 | 0.285919122 0.688683879 0.787944636 | 6.67 | 23.33 |

102 | 17.92017 | -30.14033 | 63.33 | 16.67 | 24.20 | ||

103 | 17.83583 | -29.45683 | 46.67 | 23.33 | 29.61 | ||

3 | 3 | 19.25749 | -27.49479 | 33.33 | 0.003999625 | 52.38 | 13096.47 |

4 | 19.26062 | -27.49230 | 54.17 |

The measure of habitat closeness can be defined by the habitat distance, which is a virtual distance indicating the aggregate ecological environment of an area. In such a circumstance, if we still impose conventional isotropic distance assumption to construct a kriging predictor, the prediction would be no sense at all.

It is logical to argue that in order to utilize the * n*observations

As to how to define the habitat distance measure, it depends upon the habitat spatial distribution pattern as well as the form of uncertainty governing the spatial process

In this study, we are going to calculate habitat distance in following three approaches:

(1) Grouping method. This approach classifies total density observations

It is logical to ignore those 3 groups because of extreme group variances, which should not accepted as habitat measures.

(2) Inverse-distance methods. Notice that there are ten sites without total density observations and thus their habitat measures cannot be determined. However, later we will see the empirical habitat measure is necessary for uncertain kriging.

In this paper, we propose two schemes for addressing the habitat measure at missing total density value site. The first one is the conventional inverse distance estimation. The second one is utilizing the empirical habitat distance for uncertain inverse distance estimation.

The conventional inverse distance estimation. Table 5 summarizes the results (at

Group/ Site no. | Coordinates | Total density of trees | Habitat measure | ||

longitude | latitude | ||||

1 | 42 | 22.83446 | -29.86828 | 101.83 | 1.1112310 |

11 | 18.18643 | -26.21253 | 100.00 | ||

113 | 22.18500 | -29.06700 | 100.00 | ||

2 | 20 | 16.23986 | -25.59329 | 90.48 | 2.0052690 |

13 | 15.15805 | -21.48867 | 91.70 | ||

124 | 19.43333 | -28.83333 | 93.30 | ||

3 | 4 | 19.26062 | -27.49230 | 33.33 | 3.4715580 |

2 | 19.28217 | -28.66671 | 33.33 | ||

40 | 21.64455 | -30.00486 | 36.41 | ||

123 | 19.40000 | -28.98333 | 36.70 | ||

4 | 104 | 17.28650 | -28.30430 | 40.00 | 11.1111222 |

108 | 19.45333 | -28.10333 | 43.33 | ||

103 | 17.83583 | -29.45683 | 46.67 | ||

5 | 107 | 18.56950 | -27.68433 | 113.33 | 11.5226107 |

29 | 15.47427 | -26.58937 | 106.67 | ||

30 | 16.76122 | -27.03209 | 111.11 | ||

6 | 41 | 22.37461 | -29.29727 | 86.05 | 11.5534900 |

121 | 19.43333 | -29.06667 | 80.00 | ||

122 | 19.43333 | -29.06667 | 80.00 | ||

3 | 19.25749 | -27.49479 | 85.71 | ||

7 | 112 | 22.37000 | -28.93500 | 130.00 | 14.9633000 |

126 | 21.10000 | -29.40000 | 123.30 | ||

26 | 16.31455 | -27.64893 | 130.00 | ||

8 | 23 | 15.62385 | -26.99582 | 22.22 | 17.0993200 |

9 | 17.01403 | -26.66638 | 28.07 | ||

9 | 102 | 17.92017 | -30.14033 | 63.33 | 19.9113500 |

1 | 18.78301 | -28.71597 | 63.33 | ||

101 | 18.20583 | -30.15250 | 70.00 | ||

125 | 20.23333 | -28.61667 | 70.00 | ||

120 | 18.83333 | -30.70000 | 73.30 | ||

10 | 110 | 18.98883 | -31.10050 | 50.00 | 21.5049200 |

5 | 19.59336 | -26.79313 | 54.17 | ||

24 | 15.78774 | -27.31541 | 59.26 | ||

11 | 106 | 17.98333 | -26.40217 | 166.67 | 53.3333900 |

18 | 16.21400 | -23.95119 | 153.33 | ||

105 | 18.23967 | -26.47550 | 153.33 | ||

22 | 15.36674 | -26.88367 | 166.67 | ||

28 | 16.14727 | -26.54360 | 166.67 |

It is obvious that there are five sites left listed in Table 3.

Group/ site no. | Coordinates | Total density of trees | Group variance | ||

longitude | latitude | ||||

12 | 127 | 21.16667 | -29.08333 | 6.70 | |

13 | 34 | 16.77862 | -27.64536 | 282.61 | 1843.7403440 |

111 | 18.98567 | -31.10583 | 343.33 | ||

14 | 109 | 20.79000 | -28.74017 | 200.00 | 12482.0000000 |

21 | 16.31081 | -25.88543 | 252.17 |

Site no. | Coordinates | Predicted total density of trees | Predicted habitat measure | |

longitude | latitude | |||

15 | 14.57582 | -21.20986 | 103.2131 | 1.1112310 |

14 | 14.63088 | -21.26169 | 102.9913 | 1.1112310 |

12 | 15.21586 | -21.81786 | 102.3649 | 1.1112310 |

17 | 15.51133 | -23.30893 | 110.5426 | 11.5226107 |

19 | 16.39317 | -25.14609 | 115.2105 | 11.5226107 |

33 | 16.77479 | -27.94278 | 121.9919 | 14.9633000 |

36 | 17.47540 | -27.45209 | 106.7434 | 11.5226107 |

10 | 17.78013 | -25.87191 | 110.3903 | 11.5226107 |

37 | 17.80606 | -27.67034 | 101.0099 | 1.1112310 |

128 | 21.10000 | -28.95000 | 82.67477 | 11.5534900 |

From Table 4, we can see that since the estimated total density estimators are calculated in terms of graphical distances. Those estimators are empirical prior information. As to habitat measure, they are taking the values by comparing the estimated total density to the group total density values in Table 4. Definitely, the empirical habitat measures are not all accurate.

(3) Uncertain canonical process regression methods. Because the Quiver tree‘s total density is very sensitive to local area ecological environments, it is logical to consider if some uncertain relationship between the observed total density and ecological environmental variables, say, annual temperature, and annual rainfall. Table 4 lists the data, from which a linear relationship between group average total density

The uncertain regression model takes a form:

where errors

Site no. | Coordinates | Predicted total density of trees | Predicted habitat measure | |

longitude | latitude | |||

15 | 14.57582 | -21.20986 | 110.3210 | 11.5226 |

14 | 14.63088 | -21.26169 | 26.5995 | 17.0993 |

12 | 15.21586 | -21.81786 | 55.0573 | 21.5049 |

17 | 15.51133 | -23.30893 | 83.5152 | 11.5535 |

19 | 16.39317 | -25.14609 | 8.72890 | 2.0582 |

33 | 16.77479 | -27.94278 | 147.0394 | 53.3334 |

36 | 17.47540 | -27.45209 | 72.2531 | 19.9114 |

10 | 17.78013 | -25.87191 | 20.9684 | 17.0993 |

37 | 17.80606 | -27.67034 | 29.9036 | 17.0993 |

128 | 21.10000 | -28.95000 | 101.3857 | 1.1112 |

However, it is necessary to mention that the uncertain regression model is carried on the group average total density against group average annual temperature and group annual rainfall and thus the predictability is limited although the model goodness-of fit (

Finally, we must emphasize that for any given spatial process

## 5. Uncertain kriging predictor

We first point out that kriging predictor is not intrinsic to the probabilistic spatial statistics. As long as variance, covariance, and semi-variogram concepts can be established on some uncertain theory, no matter it is Zadeh’s fuzzy theory, rough set theory, grey theory, random set theory, or interval theory, or Liu’s uncertainty theory, new kriging predictor can be solidly established with similar mathematical formulae as that of probabilistic ordinary kriging (Cressie, 1991). However, the geometric location

An uncertain semi-variogram is defined by

where

The uncertain kriging predictor is defined by

where

where

where

Theorem 5.1: Let

then,

where

Theorem 5.2: Let

Proof: It is noticed that for

However, at location

Definition 5.3: If geometric location

There is possibility that some

It is obvious that constraint

is truly kept and also all

We will calculate those uncertain kriging predictors for the ten sites {10,12,14,15,17,19,33,36, 37,128} without total density observations in following 4 steps.

Step 1: Determine the 10 neighbourhoods

where

Step 2: For each individual neighbourhood

Step 3: Calculate those uncertain semi-variograms

in terms of

Step 4: Calculate

Step 5: Calculate the kriging predictor

The upper bound

Step 6: Repeat Step 2 to Step 5, until all 10 uncertain kriging predictors are calculated. Then stop.

Table 7 summarizes uncertain kriging predictor values, and lists the no total density observation sties (similar to Table 6).

site no. | Coordinates | Uncertain kriging predicted total density of trees | |

longitude | latitude | ||

15 | 14.57582 | -21.20986 | 132.446 |

14 | 14.63088 | -21.26169 | 155.987 |

12 | 15.21586 | -21.81786 | 177.641 |

17 | 15.51133 | -23.30893 | 132.567 |

19 | 16.39317 | -25.14609 | 99.266 |

33 | 16.77479 | -27.94278 | 62.493 |

36 | 17.47540 | -27.45209 | 117.045 |

10 | 17.78013 | -25.87191 | 121.982 |

37 | 17.80606 | -27.67034 | 72.249 |

128 | 21.10000 | -28.95000 | 44.087 |

Next, we will use uncertain kriging methods to predict the missing values for the population growth rate. There are 18 sites without values: Site number {120,111,110,125,22,23,24,26,123,124,121,122,17,34,126,128,127,42}

site no. | Coordinates | Habitat measure | Uncertain kriging Predicted population growth rate | |

longitude | latitude | |||

120 | 18.83333 | -30.7 | 19.91135 | 1.02490171 |

111 | 18.98567 | -31.1058 | 1843.74 | 1.027150902 |

110 | 18.98883 | -31.1005 | 21.50492 | 1.025065854 |

125 | 20.23333 | -28.6167 | 19.91135 | 1.01815189 |

22 | 15.36674 | -26.8837 | 53.33339 | 0.995053254 |

23 | 15.62385 | -26.9958 | 17.09932 | 1.030192199 |

24 | 15.78774 | -27.3154 | 21.50492 | 1.036620495 |

26 | 16.31455 | -27.6489 | 14.9633 | 1.006659104 |

123 | 19.4 | -28.9833 | 3.471558 | 1.001714497 |

121 | 19.43333 | -28.8333 | 2.005269 | 1.004648936 |

124 | 19.43333 | -29.0667 | 11.55349 | 1.014237773 |

122 | 19.43333 | -29.0667 | 11.55349 | 1.014237773 |

17 | 15.51133 | -23.3089 | 11.5535 | 0.999365585 |

34 | 16.77862 | -27.6454 | 1843.74 | 1.000142274 |

126 | 21.1 | -29.4 | 14.9633 | 1.02687582 |

128 | 21.1 | -28.95 | 1.1112 | 1.014980439 |

127 | 21.16667 | -29.0833 | 2.0582 | 1.005842705 |

42 | 22.83446 | -29.8683 | 1.111231 | 1.003521691 |

## 6. Climate change impacts

Now we are ready to calculate the missing values of 2008 total density of trees, which are 25 sites. We utilize the compound growth rate formula:

Denote the Site

Therefore, if the total density

After the calculations, we have complete data of

The final uncertain predicted results together with the original sampled results of 2002 and 2008 are shown in the Fig. 3. The reason that they look exactly the same with absolutely no difference at all, is because the increase and decrease in total densities are so small, that they cannot be viewed just by looking at the intervals.

In Fig. 4 the Ordinary kriging prediction maps of sampled and predicted total density of Quiver trees in 2002 and 2008 are shown. Since the population increase and decrease are very small, which is why they are only reflected using kriging maps. However, the kriging maps are slightly distorted in value, due to re-calculations of sample and predicted values, and the average mean values are used.

Table 8 and Fig. 5 show the change in the total density of Quiver trees over a 6 year period, between 2002 and 2008.

Negative change ( | Positive change ( | unchanged ( | |

No. Of sites | 7 | 18 | 28 |

Percentages | 13.21% | 33.96% | 52.83% |

As one can see from the Fig. 5 change map, the change in total density of trees is very small. Most sample sites show no changes at all, with 18 sites show an increase of 1 to 9 trees, and 7 sites showing a decrease of 1 to 8 trees. These are small but definite changes in Quiver tree‘s total density over the 6 year period, between 2002 and 2008.

## 7. Conclusion

In this paper, we utilize the partially collected Quiver tree's sample data, 2002 and 2008 datasets, particularly, the total density of trees to evaluate the climate change impact on the Quiver tree‘s population. Because the data collection sites are only 53 and the Quiver tree‘s population size is extremely sensitive to it habitat environment, the conventional methodologies are not applicable. Based on our observations, we propose the habitat measure to catch up the closeness of the Quiver tree‘s population, which is later defining the habit distance of the tree‘s population. The habitat distance set is then regarded as the partner process index set. Therefore, we are able to engage Liu's Uncertainty theory for developing a new uncertain kriging approach to facilitate the prediction task: utilizing "complete" (53 values) data to perform the change evaluation. Once the missing values are filled, the evaluation of climate change can be performed. We are aware that our new prediction results have not had a validation process because of the time-constraint. In the future, it is necessary to engage the model accuracy and validation checking. Overall, there is a small but definite change in Quiver trees over the 6 year period, between 2002 and 2008, possibly due to climate changes over time.

Of course, monitoring the Quiver trees and using it as a climate change indicator, is a continuing process and effort for the South African National Biodiversity Institute. The results from this paper help to complete the missing data or un-sampled data, and would be useful for future comparisons, when another sample collection is made. The uncertain prediction methods and calculation process may be useful with other kinds of plant species data that displays similar problems, such as missing sample values. The predicted values together with the real sample values could be very useful in examining climate change impact over time and for studying the comparisons of plant species from different periods.

## Acknowledgments

Sincere thanks to Wendy Foden and Graeme Ellis for their contribution to Aloe dichotoma data collections, and to the South African National Biodiversity Institute for their support of the Aloe Project. This book chapter is supported financially by the National Research Foundation of South Africa (Ref. No. IFR2009090800013) and (Ref. No. IFR2011040400096).