Evidence map›Paper›PMID 42740175›Full record

ArticleSensors (Basel, Switzerland)2026

Characterization of Latency Sources in a MicroPython-Based ESP32 Edge-Cloud Sensor Network.

Katarzyna Smelcerz

Abstract read
In one paragraph

Article in Sensors (Basel, Switzerland), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

1 author.

Katarzyna SmelcerzAGH University of Krakow, al. Mickiewicza 30, 30-059 Krakow, Poland.ORCID 0000-0002-7291-6136

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This paper presents the design and experimental characterization of a distributed ESP32/MicroPython edge-cloud sensing system with packet-level latency decomposition. Sensor nodes transmit periodic telemetry to an ESP32 gateway over ESP-NOW; the gateway appends reception and MQTT-publication timestamps and forwards records through a local Mosquitto bridge v2.1.2, EMQX Cloud v5, Telegraf v1.36.0, and InfluxDB Cloud Serverless (Storage Engine Version 3). A three-probe two-way gateway-referenced synchronization procedure provides corrected sender timestamps while exposing an interval-based synchronization-uncertainty diagnostic. The bridge-assisted campaign comprised three independent 30 min repetitions with one, three, and five active nodes. Across runs, mean gateway-referenced node-to-gateway latency was 23.17 ± 0.13 ms, 24.13 ± 0.12 ms, and 24.84 ± 0.47 ms, respectively; the corresponding p95 values were 28 ms, 33 ms, and 37-38 ms. Mean gateway-processing latency remained nearly unchanged at 13.31-13.46 ms. Exact full-run database-visible PDR was 100% in all one-node runs, 99.28-99.88% in the three-node runs, and 96.75-97.05% in the five-node runs. Independent GPIO/oscilloscope validation showed a reproducible positive software-to-hardware difference of 12.132 ± 1.819 ms across run means, so the local metric is interpreted as a gateway-referenced application-level delivery metric rather than unbiased physical one-way radio latency. Relative to aggregate end-to-end reporting, the instrumentation separates local, gateway, and downstream ingestion contributions rather than claiming a universally faster transport method. Quantitative performance and scaling claims are confined to the evaluated bridge-assisted configuration and controlled indoor periodic workload.

Indexed as

distributed sensor networksedge computingESP32ESP-NOWgateway processingInternet of Thingslatency decompositionMicroPythonMQTTtime synchronization

Identifiers

PMID42740175
PMCPMC13568285

What OpenQuestion holds

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.