Large vision-language models (LVLMs) have demonstrated outstanding performance in many downstream tasks. However, LVLMs are trained on large-scale datasets, which can pose privacy risks if training images contain sensitive information. Therefore, it is important to detect whether an image is used to train the LVLM. Recent studies have investigated membership inference attacks (MIAs) against LVLMs, including detecting image-text pairs and single-modality content. In this work, we focus on detecting whether a target image is used to train the target LVLM. We design simple yet effective Image Corruption-Inspired Membership Inference Attacks (ICIMIA) against LVLMs, which are inspired by LVLM’s different sensitivity to image corruption for member and non-member images. We first perform an MIA method under the white-box setting, where we can obtain the embeddings of the image through the vision part of the target LVLM. The attacks are based on the embedding similarity between the image and its corrupted version. We further explore a more practical scenario where we have no knowledge about target LVLMs and we can only query the target LVLMs with an image and a textual instruction. We then conduct the attack by utilizing the output text embeddings’ similarity. Experiments on existing datasets validate the effectiveness of our proposed methods under those two different settings.

In-context learning (ICL) effectively conditions large language models (LLMs) for molecular tasks, such as property prediction and molecule captioning, by embedding carefully selected demonstration examples into the input prompt. This approach eliminates the computational overhead of extensive pre-training and fine-tuning. However, current prompt retrieval methods for molecular tasks rely on molecule feature similarity, such as Morgan fingerprints, which do not adequately capture the global molecular and atom-binding relationships. As a result, these methods fail to represent the full complexity of molecular structures during inference. Moreover, medium-sized LLMs, which offer simpler deployment requirements in specialized systems, have remained largely unexplored in the molecular ICL literature. To address these gaps, we propose a self-supervised learning technique, GAMIC (Graph-Aligned Molecular In-Context learning), which aligns global molecular structures, represented by graph neural networks (GNNs), with textual captions (descriptions) while leveraging local feature similarity through Morgan fingerprints. In addition, we introduce a Maximum Marginal Relevance (MMR) based diversity heuristic during retrieval to optimize input prompt demonstration samples. Our experimental findings using diverse benchmark datasets show GAMIC outperforms simple Morgan-based ICL retrieval methods across all tasks by up to 45%. Our code is available at: https://github.com/aliwister/mol-icl.

Scientific claim verification can help the researchers to easily find the target scientific papers with the sentence evidence from a large corpus for the given claim. Some existing works propose pipeline models on the three tasks of abstract retrieval, rationale selection and stance prediction. Such works have the problems of error propagation among the modules in the pipeline and lack of sharing valuable information among modules. We thus propose an approach, named as ARSJoint, that jointly learns the modules for the three tasks with a machine reading comprehension framework by including claim information. In addition, we enhance the information exchanges and constraints among tasks by proposing a regularization term between the sentence attention scores of abstract retrieval and the estimated outputs of rational selection. The experimental results on the benchmark dataset SciFact show that our approach outperforms the existing works.