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<article xmlns:xlink="http://www.w3.org/1999/xlink">
  <front>
    <journal-meta />
    <article-meta>
      <title-group>
        <article-title>Pl@ntNet's participation at LifeCLEF 2014 Plant Identi cation Task</article-title>
      </title-group>
      <contrib-group>
        <contrib contrib-type="author">
          <string-name>Herve Goeau</string-name>
          <xref ref-type="aff" rid="aff4">4</xref>
        </contrib>
        <contrib contrib-type="author">
          <string-name>Alexis Joly</string-name>
          <xref ref-type="aff" rid="aff4">4</xref>
          <xref ref-type="aff" rid="aff5">5</xref>
        </contrib>
        <contrib contrib-type="author">
          <string-name>Itheri Yahiaoui</string-name>
          <xref ref-type="aff" rid="aff4">4</xref>
        </contrib>
        <contrib contrib-type="author">
          <string-name>Vera Bakic</string-name>
          <xref ref-type="aff" rid="aff4">4</xref>
        </contrib>
        <contrib contrib-type="author">
          <string-name>Anne Verroust-Blondet</string-name>
          <xref ref-type="aff" rid="aff4">4</xref>
        </contrib>
        <contrib contrib-type="author">
          <string-name>Pierre Bonnet</string-name>
          <email>pierre.bonnet@cirad.fr</email>
          <xref ref-type="aff" rid="aff1">1</xref>
        </contrib>
        <contrib contrib-type="author">
          <string-name>Daniel Barthelemy</string-name>
          <email>daniel.barthelemy@cirad.fr</email>
          <xref ref-type="aff" rid="aff0">0</xref>
        </contrib>
        <contrib contrib-type="author">
          <string-name>Nozha Boujemaa</string-name>
          <email>nozha.boujemaa@inria.fr</email>
          <xref ref-type="aff" rid="aff2">2</xref>
        </contrib>
        <contrib contrib-type="author">
          <string-name>Jean-Francois Molino</string-name>
          <email>jean-francois.molino@ird.fr</email>
          <xref ref-type="aff" rid="aff3">3</xref>
        </contrib>
        <aff id="aff0">
          <label>0</label>
          <institution>CIRAD, BIOS Direction and INRA, UMR AMAP</institution>
          ,
          <addr-line>F-34398</addr-line>
          ,
          <country country="FR">France</country>
        </aff>
        <aff id="aff1">
          <label>1</label>
          <institution>CIRAD, UMR AMAP</institution>
          ,
          <country country="FR">France</country>
        </aff>
        <aff id="aff2">
          <label>2</label>
          <institution>INRIA, Direction of Saclay Center</institution>
        </aff>
        <aff id="aff3">
          <label>3</label>
          <institution>IRD</institution>
          ,
          <addr-line>UMR AMAP</addr-line>
          ,
          <country country="FR">France</country>
        </aff>
        <aff id="aff4">
          <label>4</label>
          <institution>Inria</institution>
          ,
          <country country="FR">France</country>
        </aff>
        <aff id="aff5">
          <label>5</label>
          <institution>LIRMM</institution>
          ,
          <addr-line>Montpellier</addr-line>
          ,
          <country country="FR">France</country>
        </aff>
      </contrib-group>
      <fpage>724</fpage>
      <lpage>737</lpage>
      <abstract>
        <p>This paper describes the participation of Inria within the Pl@ntNet project7 at the LifeCLEF2014 plant identi cation task. The aim of the task was to produce a list of relevant species for each plant observation in a test dataset according to a training dataset. Each plant observation contains several annotated pictures with organ/view tags: Flower, Leaf, Fruit, Stem, Branch, Entire, Scan (exclusively of leaf). Our system treated independently each category of organ/view and then a late hierarchical fusion is used in order to combine the results on visual content analysis from the most local level analysis in pictures to the highest level related to a plant observation. For the photographs of owers, leaves, fruits, stems, branches and entire views of plants, a large scale matching approach of local features extracted using di erent spatial constraints is used. For scans, the method combines the large scale matching approach with shape descriptors and geometric parameters on shape boundary. Then, several fusion methods are experimented through the four submitted runs in order to combine hierarchically the local responses to the nal response at the plant observation level. The four submitted runs obtained good results and got the 4th to the 7th place over 27 submitted runs by 10 participating teams.</p>
      </abstract>
      <kwd-group>
        <kwd>Pl@ntNet</kwd>
        <kwd>Inria</kwd>
        <kwd>LifeCLEF</kwd>
        <kwd>plant</kwd>
        <kwd>leaves</kwd>
        <kwd>owers</kwd>
        <kwd>fruits</kwd>
        <kwd>stem</kwd>
        <kwd>bark</kwd>
        <kwd>scan</kwd>
        <kwd>branch</kwd>
        <kwd>multi-organ</kwd>
        <kwd>image</kwd>
        <kwd>collection</kwd>
        <kwd>identi cation</kwd>
        <kwd>classi cation</kwd>
        <kwd>evaluation</kwd>
        <kwd>benchmark</kwd>
      </kwd-group>
    </article-meta>
  </front>
  <body>
    <sec id="sec-1">
      <title>-</title>
      <p>The plant identi cation task of LifeCLEF2014 [?] [?] was organized as a plant
species retrieval task over 500 species with visual content being the main
available information. The aim of the task was to produce a list of relevant species
for each observation in a test dataset containing 8163 plant observations based
on 13146 images, where each observation can contain several pictures of
detailed views on various organs: Flower, Fruit, Leaf, Stem, Entire, Branch and
Scan (scans or scan-like pictures of leaf exclusively). The training dataset
contains numerous plant observations related to 47815 images tagged with these
organ/view information.</p>
      <p>We present in this paper the methods used in order to produce the four
submitted runs by Inria within the PlantNet project. It is based more or less on
the same system used during our previous participations to the
ImageCLEF20112013 plant tasks [?] but with some improvements mainly related to new types
of combination of image list results provided by the di erent image queries from
a same plant observation.
2</p>
    </sec>
    <sec id="sec-2">
      <title>Description of the system</title>
      <p>Each tested observation can potentially contain several pictures on several
organs/views. Our system treated independently each organ/view and then a late
hierarchical fusion framework is used in order to combine the visual content
analysis from the most local level in pictures to the highest level related to one
same plant observation.</p>
      <p>{ local level (see subsection ??): we extract various types of local features
around interest points on training and test images. Then, considering one
single test image with one organ/view tag, and only one type of feature,
we search the knn local features in the training dataset with the same
organs/views tag, and combine them in order to obtain a ranked training image
list.
{ image level: (late fusion of features, see subsection ??) then we combine
the ranked training image list produced for all types of features.
{ multi-image level: (see subsection ??) the results from multiple test images
from a same plant observation within a same organ/view are combined.
{ multi-image level: (see subsection ??) the results from several organs/views
from a same plant observation are combined.
{ observation level: (see subsection ??) the combined results are transformed
in a ranked list of species.
2.1</p>
      <sec id="sec-2-1">
        <title>Local level: large scale matching approach</title>
      </sec>
      <sec id="sec-2-2">
        <title>Interest points detection (Run 1, 2, 3 &amp; 4 )</title>
        <p>We explored the fact that in most cases, one organ or one group of organs, is
generally centred in the pictures of the dataset. Harris corners were used at four
distinct resolutions with multiple orientations ([?]). In addition, as in [?], to
minimize the e ect of the cluttered background, a rhomboid-shaped mask was
applied to the input image and we used a Gaussian-like distribution in a 7x7
grid in order to take more points at the center of the pictures (the gure ??(a)
illustrates the detected points). About 100 points per image were output, and
according to the multiple-orientations, between 150 and 200 local features are
extracted in patches around these points (see subsection??), depending of the
visual content of the picture analysed.</p>
      </sec>
      <sec id="sec-2-3">
        <title>Local features extraction (Run 1, 2, 3 &amp; 4 )</title>
        <p>Several local features are extracted around each interest point from an oriented
and scaled patch: rotation invariant Local Binary Pattern (ri-LBP) [?]; SURF
[?] [?] (sums of 2D Haar wavelet responses); a 20-dim. Fourier histogram [?]; an
8-dim. Edge Orientation Histogram (EOH); a 27-bin weighted RGB histogram
(wght-RGB) [?], a 27-bin weighted LUV histogram (wght-LUV) and a 30-bin
HSV histogram. After a series of preliminary evaluations tests with the training
data, we concluded that not all type of local features should be used for all views
(see subsection ??). In the speci c case of Scan we used a concatenation of the
SURF, EOH, Fourier and a 16-dim. histogram based on the Hough transform
[?] (we will call these concatenated descriptors "SEFH").</p>
      </sec>
      <sec id="sec-2-4">
        <title>Visual index of local features (Run 1, 2, 3 &amp; 4 )</title>
        <p>For each type of view/organ, and for each type of features, local features are
computed, compressed and indexed using RMMH method [?,?] using a 256-bit
hash code, which led to a total of 43 unique hash tables (6 organs/views x 7
types of features + 1 separate table for scans), but around half of them are
nally considered for computing the submitted runs (see subsection ??).</p>
      </sec>
      <sec id="sec-2-5">
        <title>Local similarity search (Run 1, 2, 3 &amp; 4 )</title>
        <p>Considering a test image Iq, its associated organ/view, and considering one visual
index of one type of features, the local similarity search produces a response
list R composed of similar training images sorted by a score Si related to a
matching function on each training image i. Each local query feature q of the
image Iq is compressed with RMMH and its approximate k-nearest neighbors
are searched by probing multiple neighboring buckets in the consulted hash table
(according to the a posteriori multi-probe algorithm described in [?]). Two types
of votes and parameters of k were used through in the submitted runs in order
to produce scores and sort the training image response list: Vote On Best and
Ranking Dominate.</p>
        <p>
          Vote On Best (VOB) (Run 1, 2 &amp; 4 )
The score Si here is directly the number of matches between a training image Ii
and the query image Iq. More precisely it is the number of instances of image Ii
retrieved through the k = 30 nearest neighbors lists of each local feature of the
query image Q. Finally the list is limited to the 300 best training images.
Ranking Dominate(RD) (Run 3 )
This new vote introduces a more advanced image ranking method based on the
number of dominating local features. Inspired by the concept of top-k dominating
queries in the database domain [?], we consider that a given local feature x is
dominating another local feature y if it is closer to a query feature q (according
to the distance used as matching function). Two images I1 and I2 can then be
compared with reference to a query image Iq by counting the number of query
local features qi for which a local feature of I1 is dominating all features of I2
(or conversely). More precisely, images are ranked using a quick sort algorithm
based on the following comparison function:
n
f (I1; I2) = sgn(X sgn(ri1
i=1
ri2))
(
          <xref ref-type="bibr" rid="ref1">1</xref>
          )
where ri1 is the rank of the best match of I1 in the k-nns of qi and ri2 is the
rank of the best match of I1 in the k-nns of qi. One advantage of this ranking
function is that it is much less sensitive to the value of k. When k grows, the
ranking of the top-K images becomes more and more stable. Ideally, the image
ranking could even be computed from the complete rankings of all local features
in the dataset. But for e ciency reasons, this is clearly not manageable, and we
choose a value of k = 600.
2.2
        </p>
      </sec>
      <sec id="sec-2-6">
        <title>Shape boundary description on scans</title>
        <p>(Run 1, 2, 3 &amp; 4 )
In the case of leaf scans and scan-like pictures, additional boundary descriptors
are used since it has been showed to provide a consistent improvement of the
global performances in the previous ImageCLEF2011 dataset [?]. Involving a
rst step of automatic leaf boundary detection, these descriptors are the
Directional Fragment Histogram (DFH) describing the leaf margin, and several
geometric parameters embedded in one single vector (Shapes6) of 6 dim.
measuring 6 standard geometric parameters on the shape: rectangularity, convexity,
solidity, circularity, Sphericity and Ellipse variance.
2.3</p>
      </sec>
      <sec id="sec-2-7">
        <title>Image level: late fusion of features</title>
        <p>At this step, we have now for each image query Iq several image training response
lists, one for each type of (local or global) features. The next step is now to
combine these responses in order to obtain a single response. Thus, we use a late
fusion approach with di erent methods experimented through the four submitted
runs.</p>
        <p>CIN and WP (Run 1 )
For a query image Iq, according to its organ/view, the basic algorithm applied
is: (i) starting from the retrieved lists of similar training images for each type
of feature, (ii) transform each list of images into a probability distribution by
species with an adaptive rule CIN (see below), (iii) merge probabilities for all
types of features with a Weighted Probability approach (WP).</p>
        <p>CIN It an adaptive KNN rule established in this particular context of plant
observations [?]. For converting an image response list to a species probability
distribution, we use this adaptive rule focusing on plant observations (rather than
images). Indeed, the more a species will be represented in a response through
various plants observed by distinct users at di erent dates and locations, the more
the associated images will be informative for predicting a species. In contrast,
numerous redundant near duplicate images from the same plant observation
will be less informative for predicting a species. Instead of using a basic KNN
rule focusing on images, we search for top-K00 classes (species) represented with
at least K0 di erent plant observations. The values of K0 and K00 are
determined empirically based on the given training database, and are constant for a
database: K0 is a percentage of the average size of the training class, while K00 is
a percentage of the number of training classes. The response R is scanned from
the most to the least similar image, the counter of the number of classes with at
least K0 images is incremented accordingly, and when we nd K00 such classes,
we stop the scanning of the response. The adaptive criterion is important in
order to avoid the noise in the nal response: (a) had we searched for a xed (and
not dependent on the training data) number of classes with at least K0 plant
observations, we would often output classes that are not relevant to ll-in the
pre-de ned requirement, or (b) had we output a xed number of most similar
classes, we would give more weight to the classes with small number of plant
observations and would not reward the fact that some classes are well represented
in terms of plant observations. Finally, our K00 per class resulted in the K per
image of 85, ranging from 15 to 205, for the most to the least di
erent-plantobservation-containing response; organ-wise, the values of K ranged from 66 for
Stem to 101 for Fruit.</p>
        <p>Moreover, to eliminate the redundant images, we consider only two most
similar images per one plant observation: the score per plant observation Sm is
the average of the image scores Si. The score for a class is the sum of the scores of
its plant observations Sm: this step actually favours the well-represented classes,
and penalizes the classes with small number of plant observations. Finally, the
classes with only one image coming from one plant observation are removed from
the list as outliers.
Weighted Probability combination (WP) At this step we have several species
probability distributions, one for each type of features and we use a weighted
fusion in order to obtain a nal probability distribution. Let us de ne F as a
set of local features and P (Cfk) as probability of class Ck for feature f 2 F . In
order to re ect the discriminating power of each local feature, we de ne the nal
probability:</p>
        <p>P (Ck) = X w(f ) P (Cfk)</p>
        <p>f2F
w(f ) = max P (Cfk)= X max P (Cfk)</p>
        <p>8k f2F 8k
where
BordaMNZ &amp; IrpMNZ (BordaMNZ: Run 2, 3 &amp; 4, IrpMNZ; Run 4 )
In [?] the authors proposed similarity ranking lists fusion algorithms in order to
merge some multi-feature similarity lists into a nal overall similarity ranking
list. They showed good performances on their experimental results with basic
algorithms working directly with the ranks, i.e. without complicated and empirical
transformation of similarity lists into probability distributions. We experimented
here with two algorithms in order to merge the image training response lists given
by each type of features into one single list: the Borda Count Algorithm taken
from social theory in voting, and the Inverse Rank Position Algorithm (Irp).
Basically a score is computed for each training image contained in the response
lists to combine, and then used for sorting a nal merged list of training images.</p>
        <p>Considering an image query Q, a training image Ii, and several image training
response lists R, one for each feature f from a set of available features F , the
score used in the Borda Count algorithm is the sum of the rank positions of the
training image in the lists to merge:</p>
        <p>Borda(Q; Ii) =</p>
        <p>F
X rankposition(Ii; f )
f=1
Irp(Q; Ii) =</p>
        <p>1
PF 1</p>
        <p>f=1 rankposition(Ii;f)
The score used in the Irp algorithm is the inverse of the sum of inverses of the
rank positions of the training image in the di erent lists to merge:
Like in the previous work mentioned in [?], we used the MNZ extension of these
two algorithms (BordaMNZ and IrpMNZ ) in order to heavily weights common
training images in the lists to combine. Indeed, the hypothesis is that di erent
lists contain similar sets of relevant training images while they contain di erent
sets of non-relevant training images. Basically, the weights are based on the
number of Non-Zero entries of each training images in the lists to combine, i.e.
the number of times a training image appears in the ranked lists.</p>
        <p>
          BordaM N Z(Q; Ii) = Borda(Q; Ii)
(
          <xref ref-type="bibr" rid="ref6">6</xref>
          )
(
          <xref ref-type="bibr" rid="ref2">2</xref>
          )
(
          <xref ref-type="bibr" rid="ref3">3</xref>
          )
(
          <xref ref-type="bibr" rid="ref4">4</xref>
          )
(
          <xref ref-type="bibr" rid="ref5">5</xref>
          )
where
found.
        </p>
        <p>
          IrpM N Z(Q; Ii) = Irp(Q; Ii)
(
          <xref ref-type="bibr" rid="ref7">7</xref>
          )
is the number of feature response lists in which a training image was
        </p>
      </sec>
      <sec id="sec-2-8">
        <title>2.4 Intermediate levels: multiple-images and organs/views</title>
        <p>At this step, we have now a knowledge at the image query level combining the
di erent type of features for each image query from a same observation plant
query Oq. This knowledge can be a probability distribution if the Weighted
Probability approach was used, or a ranked training image list if the BordaMNZ
or IrpMNZ methods were used. The image queries from a same plant Oq can
be related to the same or distinct organs and views showing di erent angles
of the plant and we try here to take advantage from the complementarity of
these views in order to compute a nal knowledge at the observation level. Next
combinations of knowledge are performed in this order:
{ image level to organ/view level (if the query plant Oq has several images
from one same organ/view Vq),
{ then, organ/view level to observation level (if the query plant Oq as several
organs V ).</p>
        <p>Only the Weighted Probability approach (Run 1 ) and the BordaMNZ
approach (Run 2, 3 &amp; 4 ) are used in these upper levels of combination following
the same formulas in previous subsections ??.</p>
        <p>For instance, at organ level with the Weighted Probability approach, given
several probability distributions from a set of di erent organs/views V , we apply
the same the weighted fusion used as in subsection ?? where local features F
are replaced by V .
2.5</p>
      </sec>
      <sec id="sec-2-9">
        <title>Observation level and decision: the nal knowledge to a species list</title>
        <p>(Run 1, 2, 3 &amp; 4 )
At this nal step, we have for one query observation plant Oq, a distribution of
probabilities if the Weighted Probability approach was used in the lower levels
of fusion (Run 1 ), or a nal list of training image response if the BordaMNZ
was used instead.</p>
        <p>In the case of the WP approach, the nal list of species is directly given by
the probability distribution following a decreasing order of probabilities. In the
case of the BordaMNZ approach, we use a last step for converting the image list
response into a probability distribution with the CIN rule (see previous section
??).
2.6</p>
      </sec>
      <sec id="sec-2-10">
        <title>Summary of the di erent submitted runs</title>
        <p>Preliminary evaluation and feature selection Considering the available
number of visual feature for each images and the distinct methods of
combinations, we supposed here that each type of organ/views has a its own relevant
subset of visual features exploited no necessarily with the same combination
method. We made some intensive preliminary evaluations on the training dataset
in order to nd these subsets and methods for each type of organ/views. We used
a Leave One (Observation) Out procedure: focusing on one organ/view, for
image from the training dataset, we use it as an internal query and excluded from
the returned ranked image response list all the images belonging to the same
plant observation as the query image, in order to remove a bias related to near
duplicate images form a same plant. We concluded that in most of the cases,
it was more or less the same subsets of features which was pointed out by the
3 fusion methods BordaMNZ, IrpMNZ and WP. Since the BordaMNZ
demonstrated the best performances for mostly every organ/view, we choose to select
its subset of visual features. As might be expected, color is dominant for the
ower but may lead to confusion for leaves, while texture plays an important
role for stems and fruits. The features nally selected are presented in table ??:</p>
        <p>SURF Fourier EOH riLbp wRGB wLUV HSV SEFH DFH Shapes6
Branch
Entire
Flower
Fruit
Leaf
Scan</p>
        <p>Stem</p>
      </sec>
      <sec id="sec-2-11">
        <title>Recap chart of the di erent submitted runs The Table 2 summary of the</title>
        <p>di erent methods used at each level of fusion for each submitted run.</p>
        <p>PlantNet Run 1 is actually more or less the same method used for the
submitted run Inria PlantNet Run 1 during the previous ImageCLEF 2013 Plant
Task [?]. We used this con guration as a baseline in order to see the score this
year despite 250 more new species, and to see if we can obtain better scores with
the 3 new approaches experimented in the 3 other submitted runs.</p>
        <p>PlantNet Run2 is the BordaMNZ version of the PlantNet Run 1, where
for each step of fusion we changed the Weighted Probability WP combination
method by the BordaMNZ method. In this way, only list responses are merged
at each step, and nally we use the CIN approach in order to obtain a list of
probability of species, and thus, a list of ranked of species according to these
probability values.</p>
        <p>PlantNet Run 3 is like the PlantNet Run2 except that we changed the local
responses combination with the Ranking Dominate vote (see previous subsection
??).</p>
        <p>PlantNet Run 4 is supposed to be the best con guration, where for each
level of combination we choose the best method according to the preliminary
evaluations on the training dataset. The BordaMNZ is most of the time the
retained method, except for scans and stem pictures at the feature combination
level for which we had noticed better performances with the IprMNZ
combination. At the time of writing the paper, we noticed a mistake with the Fruit
organ where we selected a Weighted Probability approach and which probably
gave bad combinations in upper level since image response lists were expected
instead of probability distributions.
Submitted "image" runs For each submitted run, it was recommended but
not mandatory to submit a second set of run les detailing species prediction
at image level like in the previous ImageCLEF 2013 Plant Task [?]. The aim
was to see if the participants can take bene t from the combination of multiple
images from a same plant. In order to produce these complementary "image"
runs, we simplify the hierarchical fusion of treatment, stopping at the feature
combination level for one same image query (see Table 3). Unfortunately, we
encountered a problem during the generation of the le (Image) PlantNet Run
3 and we were not able to submit it.
3</p>
      </sec>
    </sec>
    <sec id="sec-3">
      <title>Results</title>
      <p>2. It is disappointing that the new Ranking Vote experimented in PlantNet Run
3 didn't show some improvement and is strangely very close to the second run
PlantNet Run 2. Finally, our supposed best run PlantNet Run 4, with the best
combination at each level of fusion, didn't show the best performances, but it is
still better of our baseline Run PlantNet 1. Table ?? resumes the scores obtained</p>
      <p>Run name Score
IBM AU Run 4 0,471
IBM AU Run 3 0,459
IBM AU Run 2 0,454
PlantNet Run 2 0,289
PlantNet Run 3 0,289
PlantNet Run 4 0,282</p>
      <p>PlantNet Run 1 0,278
for the rst 6 submitted runs out of 14 total. Figure ?? gives an overview of all
results obtained by the participants who submitted these optional runs. Our 3
submitted "image" runs by our team are in the top 6. For each method, like
for most of other methods used by the other participants, it highlights the fact
that we obtained some slightly improvement by combining the pictures and the
organs/views from a same plant observation query.</p>
      <p>Table ?? resumes the detailed scores by organs/views obtained for the rst
10 submitted runs out of 14 total and Figure ?? gives an overview of all results
obtained by the participants who submitted these optional runs. In most cases,
our 3 submitted "image" runs by our team are in the top 6, expect for the Entire
and Flower where the 4th run of IBM AU obtained best results, and for the Stem
where the FINKI team used some better approaches.
Inria within the PlantNet project submitted four runs, and 3 complementary
"image" runs, that used the same hierarchical fusion framework, and where each
run was related to distinct con gurations of methods. All the submitted runs
obtained good results and are ranked from the 4th to the 7th place compared to
the other submitted run, but clearly behind the best results obtained by the IBM
AU team. The rst run was more or less the same approach used in the previous
ImageCLEF 2013 plant identi cation task, and was considered as a baseline
in our work. We try to improve this approach with simple but e ective fusion
approaches of ranked lists of results based on the Borda Count and the Inverse
Fig. 3. Overview of the image scores of the LifeCLEF 2014 Plant Task compared with
the o cial scores related to observation.</p>
      <p>Run Branch Entire Flower Fruit Leaf Leaf Scan Stem
IBM AU Run 4 0,292 0,333 0,585 0,339 0,318 0,64 0,269
IBM AU Run 3 0,298 0,34 0,57 0,326 0,304 0,614 0,267
IBM AU Run 2 0,294 0,335 0,555 0,317 0,3 0,612 0,267
PlantNet Run 4 0,112 0,167 0,366 0,197 0,165 0,541 0,152
PlantNet Run 2 0,112 0,181 0,376 0,22 0,164 0,453 0,156
PlantNet Run 1 0,112 0,168 0,366 0,197 0,165 0,449 0,133
IBM AU Run 1 0,103 0,193 0,389 0,161 0,103 0,278 0,138
FINKI Run 1 0,088 0,117 0,255 0,177 0,16 0,4 0,157
FINKI Run 2 0,108 0,099 0,187 0,16 0,14 0,399 0,18</p>
      <p>FINKI Run 3 0,088 0,117 0,255 0,177 0,162 0,36 0,159</p>
      <p>Rank Position Algorithms. These two approaches performed slightly better, and
we obtained the best results for the full BordaMNZ approach.</p>
      <p>Acknowledgments. Part of this work was funded by the Agropolis foundation
through the project Pl@ntNet (http://www.plantnet-project.org/)</p>
    </sec>
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