Corpus Engine Towards a reproducible .science file.
← All .science files

pmid:30008725

Sex-Dependent Variation of Pumpkin (Cucurbita maxima cv. Big Max) Nectar and Nectaries as Determined by Proteomics and Metabolomics.

Elizabeth C Chatt · Patrick von Aderkas · Clay J Carter · Derek Smith · Monica Elliott · Basil J Nikolau

Frontiers in plant science · 2018 doi:10.3389/fpls.2018.00860

Paper

complete

Experiment

partial

Data

partial

Analysis

partial

Execution

absent

Execution evidence has not yet been added to this .science file. Explore its methods, data and open questions to plan the next step.
Record details sci_version · id · kind · revision · content_hash · schema · created_at · updated_at · generator
id
pmid:30008725
kind
science-record
content_hash
sha256:ee42ca1bdc8a782ab7b144b3dd9180da8151309626684f924e924c87d77cde9f
schema
https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json
created_at
2026-11-01T15:40:35Z
updated_at
2026-11-01T21:59:56Z
generator object · 2 fields
name
corpus-assay-engine
run_id
reading-sci-2026-11-01
paper object · 10 fields
state
complete
title
Sex-Dependent Variation of Pumpkin (Cucurbita maxima cv. Big Max) Nectar and Nectaries as Determined by Proteomics and Metabolomics.
doi
10.3389/fpls.2018.00860
pmid
30008725
authors array · 6 items
[0]
Elizabeth C Chatt
[1]
Patrick von Aderkas
[2]
Clay J Carter
[3]
Derek Smith
[4]
Monica Elliott
[5]
Basil J Nikolau
journal
Frontiers in plant science
year
2018
abstract
Nectar is a floral reward that sustains mutualisms with pollinators, which in turn, improves fruit set. While it is known that nectar is a chemically complex solution, extensive identification and quantification of this complexity has been lacking. Cucurbita maxima cv. Big Max, like many cucurbits, is monoecious with separate male and female flowers. Attraction of bees to the flowers through the reward of nectar is essential for reproductive success in this economically valuable crop. In this study, the sex-dependent variation in composition of male and female nectar and the nectaries were defined using a combination of GC-MS based metabolomics and LC-MS/MS based proteomics. Metabolomics analysis of nectar detected 88 metabolites, of which 40 were positively identified, and includes sugars, sugar alcohols, aromatics, diols, organic acids, and amino acids. There are differences in 29 metabolites between male and female nectar. The nectar proteome consists of 45 proteins, of which 70% overlap between nectar types. Only two proteins are unique to female nectar, and 10 are specific to male nectar. The nectary proteome data, accessible at ProteomeXchange with identifier PXD009810, contained 339 identifiable proteins, 71% of which were descriptively annotatable by homology to Plantae. The abundance of 45 proteins differs significantly between male and female nectaries, as determined by iTRAQ labeling. This rich dataset significantly expands the known complexity of nectar composition, supports the hypothesis of H+-driven nectar solute export, and provides genetic and chemical targets to understand plant-pollinator interactions.
claims array · 3 items
[0] object · 6 fields
id
claim-method
statement
Relative metabolite concentrations between male and female nectars were compared using a two-tailed independent samples t-test with resulting p-values corrected for multiple testing using the Benjamini and Hochberg’s method. A Mann Whitney test with Benjamini and Hochberg method for multiple testing correction was used to calculate p-values based on the log fold change of protein abundance between male and female nectaries.
kind
methodological
target
null
evidence array · 1 item
[0] object · 3 fields
asset
source:pmid:30008725
locator
sections[12] "Statistical Analyses" paragraph 2
quote
Relative metabolite concentrations between male and female nectars were compared using a two-tailed independent samples t-test with resulting p-values corrected for multiple testing using the Benjamini and Hochberg’s method. A Mann Whitney test with Benjamini and Hochberg method for multiple testing correction was used to calculate p-values based on the log fold change of protein abundance between male and female nectaries.
state
complete
[1] object · 6 fields
id
claim-data-access
statement
The mass spectrometry proteomics data have been deposited to the ProteomeXchange Consortium1 via PRIDE (Vizcaíno et al., 2016) partner repository, with the dataset identifier PXD009810 and 10.6019/PXD009810.
kind
methodological
target
null
evidence array · 1 item
[0] object · 3 fields
asset
source:pmid:30008725
locator
sections[11] "Proteomics Data Processing" paragraph 2
quote
The mass spectrometry proteomics data have been deposited to the ProteomeXchange Consortium1 via PRIDE (Vizcaíno et al., 2016) partner repository, with the dataset identifier PXD009810 and 10.6019/PXD009810.
state
complete
[2] object · 6 fields
id
claim-target-result
statement
Male and female nectar differed significantly in 29 metabolites, with metabolite comparisons using two-tailed independent-samples t-tests followed by Benjamini–Hochberg multiple-testing correction; the proteomics source data are accessible through ProteomeXchange via PRIDE under PXD009810.
kind
quantitative
target object · 4 fields
value
71
unit
per cent
tolerance
null
source
The nectary proteome data, accessible at ProteomeXchange with identifier PXD009810, contained 339 identifiable proteins, 71% of which were descriptively annotatable by homology to Plantae.
evidence array · 2 items
[0] object · 3 fields
asset
source:pmid:30008725
locator
sections[15] "GC-MS Identification of Nectar Metabolites" paragraph 2
quote
A total of 29 analytes were found to differ significantly in abundance between male and female nectar (Figure 3).
[1] object · 3 fields
asset
source:pmid:30008725
locator
sections[0] "Abstract" paragraph 1
quote
The nectary proteome data, accessible at ProteomeXchange with identifier PXD009810, contained 339 identifiable proteins, 71% of which were descriptively annotatable by homology to Plantae.
state
complete
gaps array · 0 items
experiment object · 8 fields
state
partial
objective
Male and female nectar differed significantly in 29 metabolites, with metabolite comparisons using two-tailed independent-samples t-tests followed by Benjamini–Hochberg multiple-testing correction; the proteomics source data are accessible through ProteomeXchange via PRIDE under PXD009810.
steps array · 3 items
[0] object · 13 fields
id
read_published_estimate
order
1
name
Read the published estimate from the source
kind
other
state
complete
blocked_on
null
description
The claim, method and evidence span published with the source article.
parameters object · 0 fields
inputs array · 1 item
[0]
source:pmid:30008725
outputs array · 1 item
[0]
the published estimate and its evidence
instruments array · 0 items
reagents array · 0 items
[1] object · 13 fields
id
obtain_source_data
order
2
name
Obtain the source data from the named repository
kind
data-preparation
state
blocked
blocked_on
data:accession_absent
description
The GEO series accession resolves and its sample accessions are listed. This lane did not download the dataset or read its licence.
parameters object · 0 fields
inputs array · 0 items
outputs array · 1 item
[0]
the source data with its repository provenance
instruments array · 0 items
reagents array · 0 items
[2] object · 13 fields
id
run_analysis
order
3
name
Run the published analysis
kind
analysis
state
blocked
blocked_on
method:group_comparison_mann_whitney
description
Apply the paper's statistical method to the resolved series and compare the result with the published target.
parameters object · 0 fields
inputs array · 0 items
outputs array · 1 item
[0]
the replicated result and its comparison
instruments array · 0 items
reagents array · 0 items
materials array · 0 items
instruments array · 0 items
reagents array · 0 items
conditions object · 0 fields
gaps array · 2 items
[0]
step:run_analysis blocked on method:group_comparison_mann_whitney
[1]
step:obtain_source_data blocked on data:accession_absent
data object · 3 fields
state
partial
assets array · 2 items
[0] object · 15 fields
id
source:pmid:30008725
role
manuscript
format
xml
media_type
application/xml
uri
https://doi.org/10.3389/fpls.2018.00860
sha256
sha256:41e36e916f11664cc84d615d73dc133a16f0bf3354cfa2da6f04d27c1de761e3
bytes
55416
access
open
state
resolved
reader
null
reader_status
reader_required
identifier
10.3389/fpls.2018.00860
version
null
note
Full article fetched from PMC; the checksum covers the rendered section body, not the original XML bytes.
structure object · 4 fields
pmcid
PMC6034135
source
europe_pmc_fulltext
coverage
whole_body
text_hash_scope
rendered_section_body
[1] object · 16 fields
id
asset:table:pmid:30008725:1
role
table
format
jats-table
media_type
application/vnd.jats.table+json
uri
null
sha256
sha256:f8f827eab16f3df1e90bbe1aa18eda4e688a3781eb7bc434c3d77fedd7d8060d
bytes
1649
access
open
state
verified
reader
read_table
reader_status
available
identifier
section[15]/table-wrap[1]#T1
version
null
note
Amino acids identified in Cucurbita maxima nectar reported as mean ± SE (n = 6).
structure object · 5 fields
pmcid
PMC6034135
section_index
15
section_title
GC-MS Identification of Nectar Metabolites
row_count
21
column_count
5
table object · 8 fields
label
Table 1
caption
Amino acids identified in Cucurbita maxima nectar reported as mean ± SE (n = 6).
rows array · 21 items
[0] array · 3 items
[0]
Amino Acid
[1]
Concentration (μM)
[2]
% of total amino acid
[1] array · 5 items
[0]
[1]
Female
[2]
Male
[3]
Female
[4]
Male
[2] array · 5 items
[0]
∗Alanine
[1]
117 ± 14
[2]
212 ± 40
[3]
42.8 ± 3.4
[4]
52.9 ± 3.4
[3] array · 5 items
[0]
∗Glycine
[1]
3.6 ± 0.7
[2]
7.6 ± 1.3
[3]
1.3 ± 0.2
[4]
1.9 ± 0.2
[4] array · 5 items
[0]
Serine
[1]
5.7 ± 1.4
[2]
9.5 ± 2.2
[3]
1.9 ± 0.4
[4]
2.4 ± 0.5
[5] array · 5 items
[0]
Proline
[1]
30.5 ± 4.6
[2]
45.2 ± 9.2
[3]
11.3 ± 1.6
[4]
12.6 ± 3.2
[6] array · 5 items
[0]
Asparagine
[1]
10.2 ± 1.8
[2]
7.7 ± 1.6
[3]
3.6 ± 0.4
[4]
2.1 ± 0.6
[7] array · 5 items
[0]
Aspartic acid
[1]
6.9 ± 2.8
[2]
5.2 ± 0.7
[3]
2.4 ± 0.8
[4]
1.4 ± 0.2
[8] array · 5 items
[0]
Glutamic acid
[1]
11.9 ± 2.4
[2]
12.5 ± 1.6
[3]
4.4 ± 0.9
[4]
3.3 ± 0.5
[9] array · 5 items
[0]
Tyrosine
[1]
0.52 ± 0.15
[2]
0.75 ± 0.17
[3]
0.17 ± 0.04
[4]
0.19 ± 0.04
[10] array · 5 items
[0]
∗Tryptophan
[1]
0.23 ± 0.07
[2]
0.57 ± 0.11
[3]
0.08 ± 0.02
[4]
0.16 ± 0.03
[11] array · 5 items
[0]
Valine
[1]
11.9 ± 1.7
[2]
14.4 ± 2.5
[3]
4.3 ± 0.4
[4]
3.6 ± 03
[12] array · 5 items
[0]
Leucine
[1]
3.4 ± 0.4
[2]
4.8 ± 1.4
[3]
1.2 ± 0.1
[4]
1.1 ± 0.2
[13] array · 5 items
[0]
Isoleucine
[1]
11.9 ± 2.0
[2]
11.8 ± 2.8
[3]
4.4 ± 0.7
[4]
2.9 ± 0.6
[14] array · 5 items
[0]
Threonine
[1]
1.3 ± 0.4
[2]
2.2 ± 0.3
[3]
0.48 ± 0.11
[4]
0.59 ± 0.09
[15] array · 5 items
[0]
Methionine
[1]
1.4 ± 0.3
[2]
1.9 ± 0.6
[3]
0.51 ± 0.10
[4]
0.45 ± 0.09
[16] array · 5 items
[0]
Phenylalanine
[1]
11.5 ± 1.8
[2]
14.0 ± 1.7
[3]
4.2 ± 0.6
[4]
3.6 ± 0.3
[17] array · 5 items
[0]
Lysine
[1]
0.24 ± 0.09
[2]
0.72 ± 0.31
[3]
0.09 ± 0.03
[4]
0.19 ± 0.08
[18] array · 5 items
[0]
β-Alanine
[1]
13.1 ± 2.7
[2]
15.5 ± 3.1
[3]
4.6 ± 0.7
[4]
4.4 ± 1.1
[19] array · 5 items
[0]
GABA
[1]
32.9 ± 4.3
[2]
21.8 ± 4.4
[3]
12.1 ± 1.3
[4]
5.9 ± 1.4
[20] array · 5 items
[0]
4-Hydroxyproline
[1]
0.87 ± 0.66
[2]
0.54 ± 0.12
[3]
0.33 ± 0.24
[4]
0.14 ± 0.03
locator
section[15]/table-wrap[1]#T1
gaps array · 0 items
analysis object · 4 fields
state
partial
methods array · 2 items
[0] object · 10 fields
id
method-1
family
group_comparison
specific
mann_whitney
label
Group comparison
dsl_operations array · 0 items
missing_operations array · 1 item
[0]
group_comparison_mann_whitney
expressible
false
parameters object · 0 fields
data_shapes array · 1 item
[0]
two_or_more_groups_continuous
evidence object · 3 fields
score
0.8
band
high
quote
Mann Whitney
[1] object · 10 fields
id
method-2
family
null
specific
null
label
Two-tailed independent samples t-test for relative metabolite concentrations; Mann–Whitney test for relative protein abundance.
dsl_operations array · 0 items
missing_operations array · 0 items
parameters object · 0 fields
data_shapes array · 0 items
evidence object · 3 fields
score
1
band
verbatim
quote
Relative metabolite concentrations between male and female nectars were compared using a two-tailed independent samples t-test with resulting p-values corrected for multiple testing using the Benjamini and Hochberg’s method. A Mann Whitney test with Benjamini and Hochberg method for multiple testing correction was used to calculate p-values based on the log fold change of protein abundance between male and female nectaries.
targets array · 1 item
[0] object · 8 fields
id
target-published-estimate
claim_id
claim-target-result
operation
group_comparison_mann_whitney
unit
per cent
tolerance
null
state
complete
note
The published estimate as the reader quoted it from the paper. No tolerance is published because the paper states none.
gaps array · 2 items
[0]
method.reader_named_unmapped
[1]
method.group_comparison_mann_whitney
capability object · 3 fields
state
complete
requirements array · 1 item
[0] object · 6 fields
capability_id
capability:computational_analysis
label
Computational analysis platform
assay_families array · 9 items
[0]
meta_analysis
[1]
machine_learning
[2]
survival_analysis
[3]
statistical_regression
[4]
pca
[5]
molecular_docking
[6]
network_analysis
[7]
differential_expression
[8]
gwas
candidate
Automated Assays Laravel application and simulated adapters
gaps array · 0 items
readiness object · 8 fields
state
blocked
tier
R4
blocked_on
data:accession_absent
axes object · 3 fields
method object · 5 fields
tier
R1
expressible
false
required_operations array · 0 items
missing_operations array · 1 item
[0]
group_comparison_mann_whitney
basis
The paper names the method it used and the corpus's method extractor maps it onto the DSL catalogue: mann_whitney.
capability object · 4 fields
tier
R1
capability_id
capability:computational_analysis
availability_state
owned
basis
The computational analysis is owned. The physical bench the paper used is not, so a physical validation cannot be run here.
data object · 6 fields
tier
R4
reachable
false
accessions array · 1 item
[0]
PXD009810 and 10.6019/PXD009810
resolved_accessions array · 0 items
statements array · 1 item
[0]
The mass spectrometry proteomics data have been deposited to the ProteomeXchange Consortium1 via PRIDE (Vizcaíno et al., 2016) partner repository, with the dataset identifier PXD009810 and 10.6019/PXD009810.
basis
The paper names PXD009810 and 10.6019/PXD009810, but the accession does not resolve in the repository (no reason recorded), so the data cannot be reached from here. No dataset was downloaded and no licence was read.
can_run object · 3 fields
dsl_operations array · 0 items
assets array · 2 items
[0]
source:pmid:30008725
[1]
asset:table:pmid:30008725:1
steps array · 0 items
must_build object · 5 fields
dsl_operations array · 1 item
[0] object · 3 fields
operation
group_comparison_mann_whitney
priority
null
converters array · 0 items
readers array · 0 items
capabilities array · 0 items
data_gaps array · 1 item
[0]
data:geo:None
gaps array · 1 item
[0]
data:accession_absent
review object · 5 fields
state
partial
machine_critique object · 5 fields
kind
extraction_review
reader object · 5 fields
model
MiniMax-M3.1-Flash
provider
minimax
provider_family
minimax
read_at
2026-10-31T18:35:15Z
independence
same_provider
evidence_check object · 2 fields
method
verbatim
availability
verbatim
calls
8
usage object · 3 fields
prompt_tokens
115641
completion_tokens
5487
cached_tokens
1576
stages array · 1 item
[0] object · 4 fields
id
extraction
state
complete
reader
MiniMax-M3.1-Flash
provider
minimax
gaps array · 3 items
[0]
review.independent_reader
[1]
review.machine_critique
[2]
review.human_critique
execution object · 5 fields
state
absent
status
not_run
mode
null
runs array · 0 items
gaps array · 1 item
[0]
execution.not_run
provenance object · 7 fields
entities array · 3 items
[0] object · 3 fields
id
pmid:30008725
type
paper
label
pmid:30008725
[1] object · 3 fields
id
source:pmid:30008725
type
manuscript
label
PMID 30008725 full text
[2] object · 3 fields
id
data:geo:None
type
dataset
label
GEO None
activities array · 3 items
[0] object · 4 fields
id
activity-reading-sci-2026-11-01
type
classification
used array · 3 items
[0] object · 3 fields
id
pmid:30008725
type
paper
label
pmid:30008725
[1] object · 3 fields
id
source:pmid:30008725
type
manuscript
label
PMID 30008725 full text
[2] object · 3 fields
id
data:geo:None
type
dataset
label
GEO None
agent
agent:corpus-assay-engine
[1] object · 4 fields
id
activity-read-30008725
type
extraction
used array · 1 item
[0]
source:pmid:30008725
agent
agent:minimax-reader
[2] object · 4 fields
id
activity-resolve-None
type
accession_resolution
used array · 1 item
[0]
data:geo:None
agent
agent:corpus-assay-engine
agents array · 2 items
[0] object · 3 fields
id
agent:corpus-assay-engine
type
software
label
Corpus assay engine
[1] object · 3 fields
id
agent:minimax-reader
type
software
label
MiniMax literature reader
source_run_id
reading-sci-2026-11-01
dsl_catalogue_fingerprint
343fb30756ba6ec3
capability_table_fingerprint
2cb3e42f047d2ecf
snapshot_id
ba34b49490d9bfaf
lineage object · 4 fields
parent_id
pmid:30008725
parent_hash
sha256:f5b0c56f809479312b325e4ffeb63b7ec31291043096bdd5860eebf175148d46
fork_of
null
gaps array · 8 items
[0]
execution.not_run
[1]
method.group_comparison_mann_whitney
[2]
method.reader_named_unmapped
[3]
review.human_critique
[4]
review.independent_reader
[5]
review.machine_critique
[6]
step:obtain_source_data blocked on data:accession_absent
[7]
step:run_analysis blocked on method:group_comparison_mann_whitney
assays array · 2 items
[0] object · 11 fields
role
data_generation
definition_id
mass_spectrometry
definition_version
99e1195c7d6f
required_operations array · 0 items
support_state
partial
source_hashes object · 1 field
assay_lexicon
99e1195c7d6f
confidence
0.99
evidence array · 4 items
[0]
g Max) Nectar and Nectaries as Determined by Proteomics and Metabolomics.
[1]
combination of GC-MS based metabolomics and LC-MS/MS based proteomics. Metabolomics analysis of n
[2]
gin were manually removed from datasets. The mass spectrometry proteomics data have been deposited to the P
[3]
GC-MS based metabolomics and LC-MS/MS based proteomics. Metabolomics analysis of nectar detected 88
order_basis
paper_text_order:59
id
assay:1
[1] object · 11 fields
role
analysis
definition_id
group_comparison
definition_version
f2132e96ae6c7a4e
required_operations array · 0 items
support_state
partial
source_hashes object · 1 field
dsl_catalogue
f2132e96ae6c7a4e
evidence array · 1 item
[0]
Mann Whitney
order_basis
consumes_earlier_output
id
assay:2
Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:30008725", "kind": "science-record", "revision": 7, "content_hash": "sha256:ee42ca1bdc8a782ab7b144b3dd9180da8151309626684f924e924c87d77cde9f", "created_at": "2026-11-01T15:40:35Z", "updated_at": "2026-11-01T21:59:56Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Sex-Dependent Variation of Pumpkin (Cucurbita maxima cv. Big Max) Nectar and Nectaries as Determined by Proteomics and Metabolomics.", "doi": "10.3389/fpls.2018.00860", "pmid": "30008725", "authors": ["Elizabeth C Chatt", "Patrick von Aderkas", "Clay J Carter", "Derek Smith", "Monica Elliott", "Basil J Nikolau"], "journal": "Frontiers in plant science", "year": 2018, "abstract": "Nectar is a floral reward that sustains mutualisms with pollinators, which in turn, improves fruit set. While it is known that nectar is a chemically complex solution, extensive identification and quantification of this complexity has been lacking. Cucurbita maxima cv. Big Max, like many cucurbits, is monoecious with separate male and female flowers. Attraction of bees to the flowers through the reward of nectar is essential for reproductive success in this economically valuable crop. In this study, the sex-dependent variation in composition of male and female nectar and the nectaries were defined using a combination of GC-MS based metabolomics and LC-MS/MS based proteomics. Metabolomics analysis of nectar detected 88 metabolites, of which 40 were positively identified, and includes sugars, sugar alcohols, aromatics, diols, organic acids, and amino acids. There are differences in 29 metabolites between male and female nectar. The nectar proteome consists of 45 proteins, of which 70% overlap between nectar types. Only two proteins are unique to female nectar, and 10 are specific to male nectar. The nectary proteome data, accessible at ProteomeXchange with identifier PXD009810, contained 339 identifiable proteins, 71% of which were descriptively annotatable by homology to Plantae. The abundance of 45 proteins differs significantly between male and female nectaries, as determined by iTRAQ labeling. This rich dataset significantly expands the known complexity of nectar composition, supports the hypothesis of H+-driven nectar solute export, and provides genetic and chemical targets to understand plant-pollinator interactions.", "claims": [{"id": "claim-method", "statement": "Relative metabolite concentrations between male and female nectars were compared using a two-tailed independent samples t-test with resulting p-values corrected for multiple testing using the Benjamini and Hochberg’s method. A Mann Whitney test with Benjamini and Hochberg method for multiple testing correction was used to calculate p-values based on the log fold change of protein abundance between male and female nectaries.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:30008725", "locator": "sections[12] \"Statistical Analyses\" paragraph 2", "quote": "Relative metabolite concentrations between male and female nectars were compared using a two-tailed independent samples t-test with resulting p-values corrected for multiple testing using the Benjamini and Hochberg’s method. A Mann Whitney test with Benjamini and Hochberg method for multiple testing correction was used to calculate p-values based on the log fold change of protein abundance between male and female nectaries."}], "state": "complete"}, {"id": "claim-data-access", "statement": "The mass spectrometry proteomics data have been deposited to the ProteomeXchange Consortium1 via PRIDE (Vizcaíno et al., 2016) partner repository, with the dataset identifier PXD009810 and 10.6019/PXD009810.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:30008725", "locator": "sections[11] \"Proteomics Data Processing\" paragraph 2", "quote": "The mass spectrometry proteomics data have been deposited to the ProteomeXchange Consortium1 via PRIDE (Vizcaíno et al., 2016) partner repository, with the dataset identifier PXD009810 and 10.6019/PXD009810."}], "state": "complete"}, {"id": "claim-target-result", "statement": "Male and female nectar differed significantly in 29 metabolites, with metabolite comparisons using two-tailed independent-samples t-tests followed by Benjamini–Hochberg multiple-testing correction; the proteomics source data are accessible through ProteomeXchange via PRIDE under PXD009810.", "kind": "quantitative", "target": {"value": 71.0, "unit": "per cent", "tolerance": null, "source": "The nectary proteome data, accessible at ProteomeXchange with identifier PXD009810, contained 339 identifiable proteins, 71% of which were descriptively annotatable by homology to Plantae."}, "evidence": [{"asset": "source:pmid:30008725", "locator": "sections[15] \"GC-MS Identification of Nectar Metabolites\" paragraph 2", "quote": "A total of 29 analytes were found to differ significantly in abundance between male and female nectar (Figure 3)."}, {"asset": "source:pmid:30008725", "locator": "sections[0] \"Abstract\" paragraph 1", "quote": "The nectary proteome data, accessible at ProteomeXchange with identifier PXD009810, contained 339 identifiable proteins, 71% of which were descriptively annotatable by homology to Plantae."}], "state": "complete"}], "gaps": []}, "experiment": {"state": "partial", "objective": "Male and female nectar differed significantly in 29 metabolites, with metabolite comparisons using two-tailed independent-samples t-tests followed by Benjamini–Hochberg multiple-testing correction; the proteomics source data are accessible through ProteomeXchange via PRIDE under PXD009810.", "steps": [{"id": "read_published_estimate", "order": 1, "name": "Read the published estimate from the source", "kind": "other", "state": "complete", "blocked_on": null, "description": "The claim, method and evidence span published with the source article.", "duration_hours": null, "parameters": {}, "inputs": ["source:pmid:30008725"], "outputs": ["the published estimate and its evidence"], "instruments": [], "reagents": []}, {"id": "obtain_source_data", "order": 2, "name": "Obtain the source data from the named repository", "kind": "data-preparation", "state": "blocked", "blocked_on": "data:accession_absent", "description": "The GEO series accession resolves and its sample accessions are listed. This lane did not download the dataset or read its licence.", "duration_hours": null, "parameters": {}, "inputs": [], "outputs": ["the source data with its repository provenance"], "instruments": [], "reagents": []}, {"id": "run_analysis", "order": 3, "name": "Run the published analysis", "kind": "analysis", "state": "blocked", "blocked_on": "method:group_comparison_mann_whitney", "description": "Apply the paper's statistical method to the resolved series and compare the result with the published target.", "duration_hours": null, "parameters": {}, "inputs": [], "outputs": ["the replicated result and its comparison"], "instruments": [], "reagents": []}], "materials": [], "instruments": [], "reagents": [], "conditions": {}, "gaps": ["step:run_analysis blocked on method:group_comparison_mann_whitney", "step:obtain_source_data blocked on data:accession_absent"]}, "data": {"state": "partial", "assets": [{"id": "source:pmid:30008725", "role": "manuscript", "format": "xml", "media_type": "application/xml", "uri": "https://doi.org/10.3389/fpls.2018.00860", "sha256": "sha256:41e36e916f11664cc84d615d73dc133a16f0bf3354cfa2da6f04d27c1de761e3", "bytes": 55416, "access": "open", "state": "resolved", "reader": null, "reader_status": "reader_required", "identifier": "10.3389/fpls.2018.00860", "version": null, "note": "Full article fetched from PMC; the checksum covers the rendered section body, not the original XML bytes.", "structure": {"pmcid": "PMC6034135", "source": "europe_pmc_fulltext", "coverage": "whole_body", "text_hash_scope": "rendered_section_body"}}, {"id": "asset:table:pmid:30008725:1", "role": "table", "format": "jats-table", "media_type": "application/vnd.jats.table+json", "uri": null, "sha256": "sha256:f8f827eab16f3df1e90bbe1aa18eda4e688a3781eb7bc434c3d77fedd7d8060d", "bytes": 1649, "access": "open", "state": "verified", "reader": "read_table", "reader_status": "available", "identifier": "section[15]/table-wrap[1]#T1", "version": null, "note": "Amino acids identified in Cucurbita maxima nectar reported as mean ± SE (n = 6).", "structure": {"pmcid": "PMC6034135", "section_index": 15, "section_title": "GC-MS Identification of Nectar Metabolites", "row_count": 21, "column_count": 5}, "table": {"label": "Table 1", "caption": "Amino acids identified in Cucurbita maxima nectar reported as mean ± SE (n = 6).", "rows": [["Amino Acid", "Concentration (μM)", "% of total amino acid"], ["", "Female", "Male", "Female", "Male"], ["∗Alanine", "117 ± 14", "212 ± 40", "42.8 ± 3.4", "52.9 ± 3.4"], ["∗Glycine", "3.6 ± 0.7", "7.6 ± 1.3", "1.3 ± 0.2", "1.9 ± 0.2"], ["Serine", "5.7 ± 1.4", "9.5 ± 2.2", "1.9 ± 0.4", "2.4 ± 0.5"], ["Proline", "30.5 ± 4.6", "45.2 ± 9.2", "11.3 ± 1.6", "12.6 ± 3.2"], ["Asparagine", "10.2 ± 1.8", "7.7 ± 1.6", "3.6 ± 0.4", "2.1 ± 0.6"], ["Aspartic acid", "6.9 ± 2.8", "5.2 ± 0.7", "2.4 ± 0.8", "1.4 ± 0.2"], ["Glutamic acid", "11.9 ± 2.4", "12.5 ± 1.6", "4.4 ± 0.9", "3.3 ± 0.5"], ["Tyrosine", "0.52 ± 0.15", "0.75 ± 0.17", "0.17 ± 0.04", "0.19 ± 0.04"], ["∗Tryptophan", "0.23 ± 0.07", "0.57 ± 0.11", "0.08 ± 0.02", "0.16 ± 0.03"], ["Valine", "11.9 ± 1.7", "14.4 ± 2.5", "4.3 ± 0.4", "3.6 ± 03"], ["Leucine", "3.4 ± 0.4", "4.8 ± 1.4", "1.2 ± 0.1", "1.1 ± 0.2"], ["Isoleucine", "11.9 ± 2.0", "11.8 ± 2.8", "4.4 ± 0.7", "2.9 ± 0.6"], ["Threonine", "1.3 ± 0.4", "2.2 ± 0.3", "0.48 ± 0.11", "0.59 ± 0.09"], ["Methionine", "1.4 ± 0.3", "1.9 ± 0.6", "0.51 ± 0.10", "0.45 ± 0.09"], ["Phenylalanine", "11.5 ± 1.8", "14.0 ± 1.7", "4.2 ± 0.6", "3.6 ± 0.3"], ["Lysine", "0.24 ± 0.09", "0.72 ± 0.31", "0.09 ± 0.03", "0.19 ± 0.08"], ["β-Alanine", "13.1 ± 2.7", "15.5 ± 3.1", "4.6 ± 0.7", "4.4 ± 1.1"], ["GABA", "32.9 ± 4.3", "21.8 ± 4.4", "12.1 ± 1.3", "5.9 ± 1.4"], ["4-Hydroxyproline", "0.87 ± 0.66", "0.54 ± 0.12", "0.33 ± 0.24", "0.14 ± 0.03"]], "row_count": 21, "column_count": 5, "numeric_cells": 77, "header_rows": 2, "locator": "section[15]/table-wrap[1]#T1"}}], "gaps": []}, "analysis": {"state": "partial", "methods": [{"id": "method-1", "family": "group_comparison", "specific": "mann_whitney", "label": "Group comparison", "dsl_operations": [], "missing_operations": ["group_comparison_mann_whitney"], "expressible": false, "parameters": {}, "data_shapes": ["two_or_more_groups_continuous"], "evidence": {"score": 0.8, "band": "high", "quote": "Mann Whitney"}}, {"id": "method-2", "family": null, "specific": null, "label": "Two-tailed independent samples t-test for relative metabolite concentrations; Mann–Whitney test for relative protein abundance.", "dsl_operations": [], "missing_operations": [], "expressible": null, "parameters": {}, "data_shapes": [], "evidence": {"score": 1.0, "band": "verbatim", "quote": "Relative metabolite concentrations between male and female nectars were compared using a two-tailed independent samples t-test with resulting p-values corrected for multiple testing using the Benjamini and Hochberg’s method. A Mann Whitney test with Benjamini and Hochberg method for multiple testing correction was used to calculate p-values based on the log fold change of protein abundance between male and female nectaries."}}], "targets": [{"id": "target-published-estimate", "claim_id": "claim-target-result", "operation": "group_comparison_mann_whitney", "expected_value": 71.0, "unit": "per cent", "tolerance": null, "state": "complete", "note": "The published estimate as the reader quoted it from the paper. No tolerance is published because the paper states none."}], "gaps": ["method.reader_named_unmapped", "method.group_comparison_mann_whitney"]}, "capability": {"state": "complete", "requirements": [{"capability_id": "capability:computational_analysis", "label": "Computational analysis platform", "assay_families": ["meta_analysis", "machine_learning", "survival_analysis", "statistical_regression", "pca", "molecular_docking", "network_analysis", "differential_expression", "gwas"], "availability_state": "owned", "tier_unlocked": "R1", "candidate": "Automated Assays Laravel application and simulated adapters"}], "gaps": []}, "readiness": {"state": "blocked", "tier": "R4", "blocking_axis": "data", "blocked_on": "data:accession_absent", "axes": {"method": {"tier": "R1", "expressible": false, "required_operations": [], "missing_operations": ["group_comparison_mann_whitney"], "basis": "The paper names the method it used and the corpus's method extractor maps it onto the DSL catalogue: mann_whitney."}, "capability": {"tier": "R1", "capability_id": "capability:computational_analysis", "availability_state": "owned", "basis": "The computational analysis is owned. The physical bench the paper used is not, so a physical validation cannot be run here."}, "data": {"tier": "R4", "reachable": false, "accessions": ["PXD009810 and 10.6019/PXD009810"], "resolved_accessions": [], "statements": ["The mass spectrometry proteomics data have been deposited to the ProteomeXchange Consortium1 via PRIDE (Vizcaíno et al., 2016) partner repository, with the dataset identifier PXD009810 and 10.6019/PXD009810."], "basis": "The paper names PXD009810 and 10.6019/PXD009810, but the accession does not resolve in the repository (no reason recorded), so the data cannot be reached from here. No dataset was downloaded and no licence was read."}}, "can_run": {"dsl_operations": [], "assets": ["source:pmid:30008725", "asset:table:pmid:30008725:1"], "steps": []}, "must_build": {"dsl_operations": [{"operation": "group_comparison_mann_whitney", "unlocks_papers": null, "priority": null}], "converters": [], "readers": [], "capabilities": [], "data_gaps": ["data:geo:None"]}, "gaps": ["data:accession_absent"]}, "review": {"state": "partial", "machine_critique": {"kind": "extraction_review", "reader": {"model": "MiniMax-M3.1-Flash", "provider": "minimax", "provider_family": "minimax", "read_at": "2026-10-31T18:35:15Z", "independence": "same_provider"}, "evidence_check": {"method": "verbatim", "availability": "verbatim"}, "calls": 8, "usage": {"prompt_tokens": 115641, "completion_tokens": 5487, "cached_tokens": 1576}}, "human_critique": null, "stages": [{"id": "extraction", "state": "complete", "reader": "MiniMax-M3.1-Flash", "provider": "minimax"}], "gaps": ["review.independent_reader", "review.machine_critique", "review.human_critique"]}, "execution": {"state": "absent", "status": "not_run", "mode": null, "runs": [], "gaps": ["execution.not_run"]}, "provenance": {"entities": [{"id": "pmid:30008725", "type": "paper", "label": "pmid:30008725"}, {"id": "source:pmid:30008725", "type": "manuscript", "label": "PMID 30008725 full text"}, {"id": "data:geo:None", "type": "dataset", "label": "GEO None"}], "activities": [{"id": "activity-reading-sci-2026-11-01", "type": "classification", "used": [{"id": "pmid:30008725", "type": "paper", "label": "pmid:30008725"}, {"id": "source:pmid:30008725", "type": "manuscript", "label": "PMID 30008725 full text"}, {"id": "data:geo:None", "type": "dataset", "label": "GEO None"}], "agent": "agent:corpus-assay-engine"}, {"id": "activity-read-30008725", "type": "extraction", "used": ["source:pmid:30008725"], "agent": "agent:minimax-reader"}, {"id": "activity-resolve-None", "type": "accession_resolution", "used": ["data:geo:None"], "agent": "agent:corpus-assay-engine"}], "agents": [{"id": "agent:corpus-assay-engine", "type": "software", "label": "Corpus assay engine"}, {"id": "agent:minimax-reader", "type": "software", "label": "MiniMax literature reader"}], "source_run_id": "reading-sci-2026-11-01", "dsl_catalogue_fingerprint": "343fb30756ba6ec3", "capability_table_fingerprint": "2cb3e42f047d2ecf", "snapshot_id": "ba34b49490d9bfaf"}, "lineage": {"parent_id": "pmid:30008725", "parent_hash": "sha256:f5b0c56f809479312b325e4ffeb63b7ec31291043096bdd5860eebf175148d46", "fork_of": null, "generation": 6}, "gaps": ["execution.not_run", "method.group_comparison_mann_whitney", "method.reader_named_unmapped", "review.human_critique", "review.independent_reader", "review.machine_critique", "step:obtain_source_data blocked on data:accession_absent", "step:run_analysis blocked on method:group_comparison_mann_whitney"], "assays": [{"role": "data_generation", "definition_id": "mass_spectrometry", "definition_version": "99e1195c7d6f", "definition_digest": null, "required_operations": [], "support_state": "partial", "source_hashes": {"assay_lexicon": "99e1195c7d6f"}, "confidence": 0.99, "evidence": ["g Max) Nectar and Nectaries as Determined by Proteomics and Metabolomics.", "combination of GC-MS based metabolomics and LC-MS/MS based proteomics. Metabolomics analysis of n", "gin were manually removed from datasets. The mass spectrometry proteomics data have been deposited to the P", "GC-MS based metabolomics and LC-MS/MS based proteomics. Metabolomics analysis of nectar detected 88"], "order_basis": "paper_text_order:59", "id": "assay:1"}, {"role": "analysis", "definition_id": "group_comparison", "definition_version": "f2132e96ae6c7a4e", "definition_digest": null, "required_operations": [], "support_state": "partial", "source_hashes": {"dsl_catalogue": "f2132e96ae6c7a4e"}, "confidence": 0.8, "evidence": ["Mann Whitney"], "order_basis": "consumes_earlier_output", "id": "assay:2"}]}